Name: cerenkov luminescence imaging of interscapular brown adipose tissue
Uploaded: 2014-10-07T13:00:00
Duration: 6 min 28 s
Description: Watch this Scientific Journal Video about Cerenkov Luminescence Imaging of Interscapular Brown Adipose Tissue at JoVE.com

The authors thank Perkin Elmer Company for supporting this publication. We also thank Alana Ross, B.S. for proofreading this manuscript.

Note: All animal studies should be performed under approved institutional protocols and animal care guidelines.
1. In Vivo CLI imaging BAT with 18F-FDG
1.1 Background Imaging:
<ol>
	<li>Before 18F-FDG injection, place four nude mice in an induction chamber that has been connected with isoflurane balanced with oxygen for 5 min to induce anesthesia. Then place the four anesthetized mice into the imaging apparatus.</li>
	<li>Acquire the background image with the following parameters: Open filter, f = 1, bin = 8, FOV = D, and exposure time = 120 sec, stage temperature = 37 &#176;C.</li>
</ol>
1.2 BAT Imaging with 18F-FGD:
<ol>
	<li>Inject the anesthetized mice with 280 &#181;Ci of 18F-FDG in PBS intravenously in the tail vein. After the injection, return the mice to a cage equipped with food and water. 
	Note: It is necessary to intravenously inject 18F-FDG to achieve a decent contrast around BAT area. Only a very weak contrast can be seen with the same amount of 18F-FDG if an intraperitoneal injection is used.</li>
	<li>Acquire CLI images at 30, 60, and 120 min after 18F-FDG injection with the same parameters as background imaging (step 1.1.2). For each imaging session, allow 5 min for the anesthesia reinduction.</li>
	<li>To quantify the signal to noise ratio (S/N), use the imaging software interface to draw two equal sized ellipse ROIs over the interscapular BAT and an area adjacent to the BAT (reference area) (Figure 1b).</li>
</ol>
1.3 Validation of the CLI Source:
<ol>
	<li>Anesthetize four mice and inject the mice with 280 &#181;Ci of 18F-FDG intravenously.</li>
	<li>Sacrifice the mice 60 min after the injection of 18F-FDG by injection of sodium pentobarbital (200 mg/kg, IP). Carefully remove the skin from the interscapular area. Image all of the mice with the same parameters as above (1.1.2), at the same time (Figure 2a).</li>
	<li>Carefully remove the interscapular white adipose tissue (WAT) and BAT, and then image the dissected mice with the same parameters (Figure 2b).</li>
	<li>From the CLI images, calculate the contribution from BAT by using two ROIs with the following equation: R(BAT) = (CLIa-CLIb)(BAT)/(CLIa-CLIb)(BAT-removed), where ROIa is for the interscapular area and ROIb is for the reference area (Figure 2b).</li>
</ol>
2. BAT Imaging Application
2.1 Monitoring Activation with NE
<ol>
	<li>Divide nude mice into two groups (n = 4 each).</li>
	<li>Inject one group with norepinephrine (NE) (50 &#181;l, 10mM) intraperitoneally. Use the second group as a non-activated control. After 30 min, anesthetize both groups with isoflurane for 5 min, and then intravenously inject each mouse with 18F-FDG (220 &#181;Ci). 
	Note: The intraperitoneal injection of NE should be 30 min before 18F-FDG injection to avoid dramatically agitating the mice.</li>
	<li>Image the mice 60 min after 18F-FDG injection using the same parameters as the above protocols.</li>
</ol>
2.2 Monitoring Activation Under Cold Exposure
<ol>
	<li>Measure the body temperatures of the mice in the cold room with a rectal thermometer. Temperatures should be about 30 &#176;C.</li>
	<li>Image the mice 60 min after 18F-FDG injection by using the same imaging parameters as the above protocols. Use mice that are kept at room temperature (25 &#176;C) as the controls, and image them with the same.</li>
	<li>For a cold exposure study, place the mice in a cold room (4 &#176;C) for 4 hr before 18F-FDG injection and return the mice to the cold room after each imaging session and after recovering from anesthesia.</li>
	<li>parameters as above.</li>
</ol>
2.3 Monitoring Deactivation of BAT Under Long Anesthesia
<ol>
	<li>For long anesthesia (60 - 70 min), inject mice intraperitoneally with ketamine/xylazine and keep them under anesthesia for 60 - 70 min at room temperature.</li>
	<li>Once the mice are anesthetized, inject 18F-FDG (220 &#181;Ci) intravenously via the tail vein.</li>
	<li>Image the mice 60 min after 18F-FDG injection by using the same parameters as the above protocols.</li>
</ol>
3. Spectral Unmixing and Multispectral Cerenkov Luminescence Tomography Studies
<ol>
	<li>Anesthetize a mouse for 5 min, and then inject 300 &#181;Ci 18F-FDG intravenously. Acquire multispectral images 60 min after 18F-FDG injection from the animal&#8217;s dorsal side with the following parameters: f = 1, bin = 16, acquisition time = 300 sec per filter, emission filters = 580, 600, 620, 640, 660 and 680 nm.</li>
	<li>Conduct spectral unmixing with Living Imaging 4.3.1 software and select two components (BAT and unspecific signals) and automatic unmixing (Figure 4).</li>
	<li>Conduct the 3D reconstruction according to the method reported by Kuo et al. 28,43. Incorporate the Cerenkov emission spectrum into the diffuse light propagation model, apply Tikhonov regularization in the NNLS (nonnegative least squares) optimization of the residuals, and generate the surface tomography (which is used for 3D image coregistration) from the structure light imaging (Figure 5). 
	Note: For multispectral CLI spectral unmixing and tomography, at least 5 images with different filters are needed.</li>
</ol>

<ol>
	<li>Cannon, B., Nedergaard, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Brown+adipose+tissue:+function+and+physiological+significance.">Brown adipose tissue: function and physiological significance.</a> Physiol. Rev. 84, 277-359 (2004).</li><li>Cypess, A. M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Identification+and+importance+of+brown+adipose+tissue+in+adult+humans.">Identification and importance of brown adipose tissue in adult humans.</a> New Eng. J. Med. 360, 1509-1517 (2009).</li><li>Nedergaard, J., Bengtsson, T., Cannon, B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Unexpected+evidence+for+active+brown+adipose+tissue+in+adult+humans.">Unexpected evidence for active brown adipose tissue in adult humans.</a> Amer. J. Physiol. Endocrinol. Metabolism. 293, 444-452 (2007).</li><li>Tseng, Y. H., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=New+role+of+bone+morphogenetic+protein+7+in+brown+adipogenesis+and+energy+expenditure.">New role of bone morphogenetic protein 7 in brown adipogenesis and energy expenditure.</a> Nature. 454, 1000-1004 (2008).</li><li>Zhang, H., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cross+talk+between+insulin+and+bone+morphogenetic+protein+signaling+systems+in+brown+adipogenesis.">Cross talk between insulin and bone morphogenetic protein signaling systems in brown adipogenesis.</a> Mol. Cell. Biol. 30, 4224-4233 (2010).</li><li>van Marken Lichtenbelt, W. D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cold-activated+brown+adipose+tissue+in+healthy+men.">Cold-activated brown adipose tissue in healthy men.</a> New Eng. J. Med. 360, 1500-1508 (2009).</li><li>Zingaretti, M. C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+presence+of+UCP1+demonstrates+that+metabolically+active+adipose+tissue+in+the+neck+of+adult+humans+truly+represents+brown+adipose+tissue.">The presence of UCP1 demonstrates that metabolically active adipose tissue in the neck of adult humans truly represents brown adipose tissue.</a> FASEB J. 23, 3113-3120 (2009).</li><li>Chen, Y. I., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Anatomical+and+Functional+Assessment+of+Brown+Adipose+Tissue+by+Magnetic+Resonance+Imaging.">Anatomical and Functional Assessment of Brown Adipose Tissue by Magnetic Resonance Imaging.</a> Obesity. 20, 1519-1526 (2012).</li><li>Chen, Y. C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Measurement+of+human+brown+adipose+tissue+volume+and+activity+using+anatomic+MR+imaging+and+functional+MR+imaging.">Measurement of human brown adipose tissue volume and activity using anatomic MR imaging and functional MR imaging.</a> J. Nucl. Med. 54, 1584-1587 (2013).</li><li>Bostrom, P., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+PGC1-alpha-dependent+myokine+that+drives+brown-fat-like+development+of+white+fat+and+thermogenesis.">A PGC1-alpha-dependent myokine that drives brown-fat-like development of white fat and thermogenesis.</a> Nature. 481, 463-468 (2012).</li><li>Yoneshiro, T., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Age-related+decrease+in+cold-activated+brown+adipose+tissue+and+accumulation+of+body+fat+in+healthy+humans.">Age-related decrease in cold-activated brown adipose tissue and accumulation of body fat in healthy humans.</a> Obesity. 19, 1755-1760 (2011).</li><li>Mattson, M. P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Perspective:+Does+brown+fat+protect+against+diseases+of+aging.">Perspective: Does brown fat protect against diseases of aging.</a> Ageing Res. Rev. 9, 69-76 (2010).</li><li>Stephens, M., Ludgate, M., Rees, D. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Brown+fat+and+obesity:+the+next+big+thing.">Brown fat and obesity: the next big thing.</a> Clin. endocrinol. 74, 661-670 (2011).</li><li>Harms, M., Seale, P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Brown+and+beige+fat:+development,+function+and+therapeutic+potential.">Brown and beige fat: development, function and therapeutic potential.</a> Nat. Med. 19, 1252-1263 (2013).</li><li>Farmer, S. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Obesity:+Be+cool,+lose+weight.">Obesity: Be cool, lose weight.</a> Nature. 458, 839-840 (2009).</li><li>Inokuma, K., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Uncoupling+protein+1+is+necessary+for+norepinephrine-induced+glucose+utilization+in+brown+adipose+tissue.">Uncoupling protein 1 is necessary for norepinephrine-induced glucose utilization in brown adipose tissue.</a> Diabetes. 54, 1385-1391 (2005).</li><li>Isler, D., Hill, H. P., Meier, M. K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Glucose+metabolism+in+isolated+brown+adipocytes+under+beta-adrenergic+stimulation.+Quantitative+contribution+of+glucose+to+total+thermogenesis.">Glucose metabolism in isolated brown adipocytes under beta-adrenergic stimulation. Quantitative contribution of glucose to total thermogenesis.</a> Biochem. J. 245, 789-793 (1987).</li><li>Robertson, R., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Optical+imaging+of+Cerenkov+light+generation+from+positron-emitting+radiotracers.">Optical imaging of Cerenkov light generation from positron-emitting radiotracers.</a> Phys. Med. Biol. 54, 355-365 (2009).</li><li>Spinelli, A. E., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cerenkov+radiation+allows+in+vivo+optical+imaging+of+positron+emitting+radiotracers.">Cerenkov radiation allows in vivo optical imaging of positron emitting radiotracers.</a> Phys. Med. Biol. 55, 483-495 (2010).</li><li>Liu, H., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Molecular+optical+imaging+with+radioactive+probes.">Molecular optical imaging with radioactive probes.</a> PloS One. 5, e9470 (2010).</li><li>Ran, C., Zhang, Z., Hooker, J., Moore, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=In+vivo+photoactivation+without+'light':+use+of+Cherenkov+radiation+to+overcome+the+penetration+limit+of+light.">In vivo photoactivation without 'light': use of Cherenkov radiation to overcome the penetration limit of light.</a> Mol. Imaging. Biol. 14, 156-162 (2012).</li><li>Dothager, R. S., Goiffon, R. J., Jackson, E., Harpstrite, S., Piwnica-Worms, D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cerenkov+radiation+energy+transfer+(CRET)+imaging:+a+novel+method+for+optical+imaging+of+PET+isotopes+in+biological+systems.">Cerenkov radiation energy transfer (CRET) imaging: a novel method for optical imaging of PET isotopes in biological systems.</a> PloS One. 5, e13300 (2010).</li><li>Ruggiero, A., Holland, J. P., Lewis, J. S., Grimm, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cerenkov+luminescence+imaging+of+medical+isotopes.">Cerenkov luminescence imaging of medical isotopes.</a> J. Nucl. Med. 51, 1123-1130 (2010).</li><li>Lewis, M. A., Kodibagkar, V. D., Oz, O. K., Mason, R. P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=On+the+potential+for+molecular+imaging+with+Cerenkov+luminescence.">On the potential for molecular imaging with Cerenkov luminescence.</a> Optics Letters. 35, 3889-3891 (2010).</li><li>Mitchell, G. S., Gill, R. K., Boucher, D. L., Li, C., Cherry, S. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=In+vivo+Cerenkov+luminescence+imaging:+a+new+tool+for+molecular+imaging.">In vivo Cerenkov luminescence imaging: a new tool for molecular imaging.</a> Philosophical transactions. Series A, Mathematical, physical, and engineering sciences. 369, 4605-4619 (2011).</li><li>Thorek, D. L., Ogirala, A., Beattie, B. J., Grimm, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Quantitative+imaging+of+disease+signatures+through+radioactive+decay+signal+conversion.">Quantitative imaging of disease signatures through radioactive decay signal conversion.</a> Nat. Med. 19, 1345-1350 (2013).</li><li>Holland, J. P., Normand, G., Ruggiero, A., Lewis, J. S., Grimm, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Intraoperative+imaging+of+positron+emission+tomographic+radiotracers+using+cerenkov+luminescence+emissions.">Intraoperative imaging of positron emission tomographic radiotracers using cerenkov luminescence emissions.</a> Mol. Imaging. 11, 1-10 (2012).</li><li>Spinelli, A. E., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Multispectral+Cerenkov+luminescence+tomography+for+small+animal+optical+imaging.">Multispectral Cerenkov luminescence tomography for small animal optical imaging.</a> Optics Express. 19, 12605-12618 (2011).</li><li>Xu, Y., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Proof-of-concept+study+of+monitoring+cancer+drug+therapy+with+cerenkov+luminescence+imaging.">Proof-of-concept study of monitoring cancer drug therapy with cerenkov luminescence imaging.</a> J. Nucl. Med. 53, 312-317 (2012).</li><li>Liu, H., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Intraoperative+imaging+of+tumors+using+cerenkov+luminescence+endoscopy:+a+feasibility+experimental+study.">Intraoperative imaging of tumors using cerenkov luminescence endoscopy: a feasibility experimental study.</a> J. Nucl. Med. 53, 1579-1584 (2012).</li><li>Thorek, D. L., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Positron+lymphography:+multimodal,+high-resolution,+dynamic+mapping+and+resection+of+lymph+nodes+after+intradermal+injection+of+18F-FDG.">Positron lymphography: multimodal, high-resolution, dynamic mapping and resection of lymph nodes after intradermal injection of 18F-FDG.</a> J. Nucl. Med. 53, 1438-1445 (2012).</li><li>Xu, Y., Liu, H., Cheng, Z. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Harnessing+the+power+of+radionuclides+for+optical+imaging:+Cerenkov+luminescence+imaging.">Harnessing the power of radionuclides for optical imaging: Cerenkov luminescence imaging.</a> J. Nucl. Med. 52, 2009-2018 (2011).</li><li>Spinelli, A. E., Marengo, M., Calandrino, R., Sbarbati, A., Boschi, F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Optical+imaging+of+radioisotopes:+a+novel+multimodal+approach+to+molecular+imaging.">Optical imaging of radioisotopes: a novel multimodal approach to molecular imaging.</a> Quart. J. Nucl. Med. Mol. Imaging. 56, 280-290 (2012).</li><li>Hu, Z., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Experimental+Cerenkov+luminescence+tomography+of+the+mouse+model+with+SPECT+imaging+validation.">Experimental Cerenkov luminescence tomography of the mouse model with SPECT imaging validation.</a> Optics Express. 18, 24441-24450 (2010).</li><li>Hu, Z., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cerenkov+luminescence+tomography+of+aminopeptidase+N+(APN/CD13)+expression+in+mice+bearing+HT1080+tumors.">Cerenkov luminescence tomography of aminopeptidase N (APN/CD13) expression in mice bearing HT1080 tumors.</a> Mol. Imag. 12, 173-181 (2013).</li><li>Zhong, J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cerenkov+luminescence+tomography+for+in+vivo+radiopharmaceutical+imaging.">Cerenkov luminescence tomography for in vivo radiopharmaceutical imaging.</a> Internatl. J. Biomed. Imaging. 2011, 641618 (2011).</li><li>Zhong, J., Qin, C., Yang, X., Chen, Z., Tian, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Fast-specific+tomography+imaging+via+Cerenkov+emission.">Fast-specific tomography imaging via Cerenkov emission.</a> Mol. Imaging. Biol. 14, 286-292 (2012).</li><li>Kothapalli, S. R., Liu, H., Liao, J. C., Cheng, Z., Gambhir, S. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Endoscopic+imaging+of+Cerenkov+luminescence.">Endoscopic imaging of Cerenkov luminescence.</a> Biomed. Optics Express. 3, 1215-1225 (2012).</li><li>Spinelli, A. E., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=First+human+Cerenkography.">First human Cerenkography.</a> J. Biomed. optics. 18, 20502 (2013).</li><li>Thorek, D. L., Riedl, C., Grimm, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Clinical+Cerenkov+Luminescence+Imaging+of+18F-FDG.">Clinical Cerenkov Luminescence Imaging of 18F-FDG.</a> J. Nucl. Med. 55, 1345-1350 (2014).</li><li>Fueger, B. J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Impact+of+animal+handling+on+the+results+of+18F-FDG+PET+studies+in+mice.">Impact of animal handling on the results of 18F-FDG PET studies in mice.</a> J. Nucl. Med. 47, 999-1006 (2006).</li><li>Zhang, X., Kuo, C., Moore, A., Ran, C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=In+vivo+optical+imaging+of+interscapular+brown+adipose+tissue+with+(18)F-FDG+via+Cerenkov+luminescence+imaging.">In vivo optical imaging of interscapular brown adipose tissue with (18)F-FDG via Cerenkov luminescence imaging.</a> PloS One. 8, e62007 (2013).</li><li>Kuo, C., Coquoz, O., Troy, T. L., Xu, H., Rice, B. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Three-dimensional+reconstruction+of+in+vivo+bioluminescent+sources+based+on+multispectral+imaging.">Three-dimensional reconstruction of in vivo bioluminescent sources based on multispectral imaging.</a> J. Biomed. Optics. 12, 024007 (2007).</li><li>Xu, X., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Exercise+ameliorates+high-fat+diet-induced+metabolic+and+vascular+dysfunction,+and+increases+adipocyte+progenitor+cell+population+in+brown+adipose+tissue.">Exercise ameliorates high-fat diet-induced metabolic and vascular dysfunction, and increases adipocyte progenitor cell population in brown adipose tissue.</a> Amer. J. Physiol. Regulatory, integrative and comparative physiology. 300, 1115-1125 (2011).</li></ol>

Publication of this video-article is supported by&#160;Perkin Elmer Company.

Research related to BAT has been conducted for several decades. Previously, it had been considered to have no significant physiologic relevance during human adulthood 1. However, recent large scale clinical PET imaging with 18F-FDG and other investigations have confirmed BAT is still present in the upper chest, neck and other locations in adults 2,3. Recent studies have strongly suggested that BAT plays an important role in obesity and diabetes 2,6. Other research also indicates that BAT plays important roles during the process of ageing 12 and that its activity could be enhanced through exercise 10,44.
Both in clinical human studies and preclinical research, PET imaging with 18F-FDG is the most used method to study BAT. However, for preclinical animal studies, PET is generally much more expensive than optical imaging. In this protocol, we demonstrate that CLI with 18F-FDG can be applied for optically imaging BAT in small animals. Like other optical imaging techniques, tissue penetrating limitation and low sensitivity for deep targets are the intrinsic limitations of CLI 25,32. Nonetheless, recently Spinelli et al. demonstrated that decent CLI signal could be observed with 10 mm tissue depth with 32P 28,43, and Thorek et al. showed that 16 mm penetration could be achieved in lymph nodes of patients after 18F-FDG injection 39,40. Compared to PET imaging, CLI can be performed with a relatively low cost imaging system. Recently, Thorek et al. demonstrated that significantly high sensitivity could be achieved with CLI as low amounts of 18F-FDG accumulated (about 2Ci) in the nodes of patients 39,40. In vitro testing indicated that CLI signal from 0.01 Ci 90Y was detectable in solution 25,32,33. Moreover, CLI also has the potential for high spatial resolution and the capacity for high throughput screening. In addition, CLI is easy to learn and use.
In the course of experiments, we found that CLI contrast of BAT with 18F-FDG is highly related to the injection methods. Intravenous injection of 18F-FDG can provide excellent contrast for interscapular BAT, while intraperitoneal injection with the same amount of 18F-FDG only showed a weak contrast in the BAT area.
Spectral unmixing, a very practical technique to separate two sets of signals, has been widely used in fluorescence imaging. It is well known that the uptake of 18F-FDG is not highly target-specific, and different targets/tissues have different light attenuation properties. We found the peak of the CLI spectrum of BAT is around 640 nm, and this data reflected the actual contexts of BAT. The 3D reconstruction of this protocol is very operable, because it can be performed with a commercially available optical imaging system based on the light diffusive properties of different wavelengths. With this approach, we can avoid the use of a specialized imaging system that requires multiple-angle view images for 3D reconstruction.
For both spectral unmixing and 3D reconstruction, a greater minimum of 600 photon counts from each image in BAT is required. To this end, large binning (bin = 16), small f stop (f = 1) and a long acquisition time (5 min) are needed for each image.
In summary, harnessing the unique location and shape of BAT and the significantly high uptake of 18F-FDG in BAT, we demonstrate how BAT in small animals can be optically imaged with 18F-FDG via the CLI technique. This method can be reliably used for imaging BAT and for monitoring BAT activation. Additionally, we also demonstrate that spectral unmixing and 3D reconstruction are practicable and 3D volume quantification is possible for future studies.

Brown adipose Tissue (BAT) is a special tissue for thermogenesis in mammals, and one of its major functions is to maintain the energy balance of the whole body through dissipating large amounts of chemical/food energy as heat 1. BAT&#8217;s most unique characteristics include plentiful uncoupling protein-1 (UCP-1) expression, abundant small oil droplets, a large number of mitochondria in a single cell, and significant vascularization in the tissue 2-5. These unique features strongly associate with the tissue&#8217;s important role in metabolism and energy expenditure. BAT was previously considered to be no longer present and possessing no significant physiological functions in adult humans 1, however recent PET/CT imaging investigations have clearly demonstrated that BAT still presents in human adults 2,3,6-9. An inverse correlation between BAT mass and body mass index (BMI) was established from several studies, and recent studies indicated that physical exercises could increase the mass of BAT. These results strongly suggest that the dysfunction of BAT is tightly associated with the pathologies of obesity and diabetes 2,6,10,11. In addition, mounting evidence indicates that the function of BAT is strongly related to various other pathologies such as neurodegenerative disease and cancer 3,7,12,13.
BAT activation, a process to increase thermogenesis, can be achieved under various conditions such as cold exposure, exercise, and drug treatment and gene manipulation 1,14,15. Cold exposure and norepinephrine treatment are the most used methods to activate BAT. Cold, which can be sensed by various mechanisms such as thermoreceptors in the skin, stimulates sympathetic nerves and leads to the release of norepinephrine (NE) to BAT. The released NE triggers UCP-1 to initialize thermogenesis to maintain the normal body temperature. Under this condition, the uptake of glucose also increases to provide more carbon sources for the increased metabolism in BAT 1,16,17. PET imaging with 18F-FDG has confirmed that the uptake of labeled glucose increased under cold conditions in human studies 6.
In terms of optical imaging, BAT is an ideal target. The interscapular BAT has a unique location in mice, situated away from larger organs such as the liver, heart, and stomach. Therefore, signal interference from these large organs is insignificant (Figure 1a). Meanwhile, the shallow location of interscapular BAT allows more signals to be captured by the detection camera. Moreover, BAT is a concentrated mass organ, which confines the light signal in certain areas. Additionally, the unique triangular physical shape of BAT makes it easy to distinguish from other tissues (Figure 1a).
Cerenkov luminescence imaging (CLI), a newly emerged molecular imaging technology 18-26, harnesses the luminescence generated from the + and - decay of radionuclides such as 18F and 131I in the medium. The charged particle (such as + and -) polarizes molecules while it travels in the medium 18-20, and luminescence/light is emitted when the polarized molecules relax back to equilibrium. The emitted luminescence is called Cerenkov Luminescence (CL). The unique spectral properties of CL include its broad spectrum throughout the ultraviolet (UV) and visible spectrum 18-20, and its inverse correlation between the intensity and the square of the wavelength (&#955;2). Both UV and visible ranges of the emitted light can be utilized for different applications. The UV portion of Cerenkov luminescence has been applied for in vivo photoactivation of caged luciferin 21, while the light emitted in the longer wavelength can be used for in vivo optical imaging 18,27-31.
For small animal studies, CLI imaging with an optical imaging system is faster and more cost effective than PET. Moreover, CLI can be applied for high throughput screening with an imaging system equipped with high throughput capacity. The advantages and disadvantages of this technology have been discussed in several reviews 25,32,33. 3D tomography of CLI has been intensively studied in several groups 28,34-37, and the applications of CLI for endoscopic imaging and intraoperative imaging have been successfully demonstrated in mice as well 30,38. In addition, Spinelli and Thorek et al. have demonstrated that CLI imaging could be applied to human subjects, thus the technology also has potential for clinical applications 39,40.
In the course of rediscovery of BAT in humans, PET images clearly indicated that a significant amount of 18F-FDG accumulated in BAT under certain conditions 2,3,6. In addition, PET imaging with mice also undoubtedly showed that BAT could be highlighted with 18F-FDG 4142. In this report, we demonstrate how Cerenkov luminescence emitted from 18F-FDG can be utilized for imaging BAT in small animals using an optical imaging system. Our approach provides a fast, cheap and convenient method of BAT imaging for small animals. This technique can be used as an alternative method for PET imaging with 18F-FDG, especially for laboratories without PET facilities.

<table border="0" cellpadding="0" cellspacing="0" width="885">
	<tbody>
		<tr height="42">
			<td height="42" style="height:42px;width:216px;">Name of Material/ Equipment</td>
			<td style="width:71px;">Company</td>
			<td style="width:119px;">Catalog Number</td>
			<td style="width:479px;">Comments/Description</td>
		</tr>
		<tr height="231">
			<td height="231" style="height:231px;width:216px;">Optical Imaging system</td>
			<td style="width:71px;">Perkin Elmer</td>
			<td style="width:119px;"></td>
			<td style="width:479px;">IVIS Spectrum is an optical imaging system that is equiped with very sensitive camera for Cerenkov Luminescence. Some instrumental information is listed below: CCD Sensor: Back thinned, back illuminated 
			CCD Size: 2.7cm x 2.7cm 
			Pixels: 2048 x 2048 
			Quantum Efficiency: 85% 
			Min detectable photons: 70 photons/s/sr/cm &#60; sup &#62; 2 &#60; /sup &#62; 
			Dark Current: &#60; 100 electrons/s/cm &#60; sup &#62; 2 &#60; /sup &#62; 
			Lens: f 0.95 50mm 
			CCD Cooling: Cooled to-90 degree.&#160;</td>
		</tr>
		<tr height="63">
			<td height="63" style="height:63px;width:216px;">18F-FDG</td>
			<td style="width:71px;">IBA Molecular</td>
			<td style="width:119px;"></td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">norepinephrine</td>
			<td style="width:71px;">Sigma</td>
			<td>N5785-250MG</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:216px;">Ketamine/Xylazine</td>
			<td style="width:71px;">Sigma</td>
			<td>K113-10ML</td>
			<td></td>
		</tr>
	</tbody>
</table>

cerenkov luminescence imaging of interscapular brown adipose tissue

Brown adipose tissue (BAT), widely known as a &#8220;good fat&#8221; plays pivotal roles for thermogenesis in mammals. This special tissue is closely related to metabolism and energy expenditure, and its dysfunction is one important contributor for obesity and diabetes. Contrary to previous belief, recent PET/CT imaging studies indicated the BAT depots are still present in human adults. PET imaging clearly shows that BAT has considerably high uptake of 18F-FDG under certain conditions. In this video report, we demonstrate that Cerenkov luminescence imaging (CLI) with 18F-FDG can be used to optically image BAT in small animals. BAT activation is observed after intraperitoneal injection of norepinephrine (NE) and cold treatment, and depression of BAT is induced by long anesthesia. Using multiple-filter Cerenkov luminescence imaging, spectral unmixing and 3D imaging reconstruction are demonstrated. Our results suggest that CLI with 18F-FDG is a practical technique for imaging BAT in small animals, and this technique can be used as a cheap, fast, and alternative imaging tool for BAT research.

In Figure 1, interscapular BAT (Figure 1a) was highlighted at all time points (30, 60, 120 min), and the contrast between BAT and the reference area can be easily observed (Figure 1b). Notably, the contour of the BAT image closely reflected its physical appearance, which has a triangular contour. The signal ratios between BAT and the reference area were 2.37, 2.49, and 2.53 fold at 30, 60, and 120 min after injection (Figure 1a).
From the step-wise dissection experiment, 85% of the signal at the interscapular site had originated from the BAT (Figure 2). However, there was still some residual signal located near the upper rim of the BAT, which probably originated from the BAT residual tissue and other adjacent tissues that include blood vessels and muscles.
It has been reported that BAT activation can be accomplished through Norepinephrine (NE) treatment and cold exposure 3,6. First, we observed BAT activation with NE in the same group of mice with and without NE treatment under short (5 min) isoflurane anesthesia. The data showed significantly higher CLI signal under the NE-treated condition (1.23 fold) than without NE treatment (Figure 3a).
In human studies, PET imaging showed that subjects under cold exposure had much higher 18F-FDG uptake in the BAT than those at room temperature 6. In this mice study, a 39% increase in 18F-FDG uptake was observed in the BAT of the animals treated with cold exposure (Figure 3b).
In mice, BAT activity can be influenced by different anesthesia regimens 3,41. For example, 18F-FDG uptake in BAT can be considerably decreased after one hour of anesthesia with ketamine 41. Comparing the 18F-FDG uptake in the same group of mice under short (5 min with isoflurane) and long anesthesia (70 min with ketamine/xylazine) regimens, a 54% decrease in 18F-FDG BAT uptake was observed in the group anesthetized with ketamine/xylazine (Figure 3c).
It is well known that heme-containing proteins (such as hemoglobin in blood and cytochrome c in mitochondria) can lead to significant light absorption, and it is expected that the abundant blood vessels in BAT 1 will change the spectrum of CLI, and the spectral shape from the BAT area will be different from other areas. Conceivably, spectral unmixing techniques allow us to separate the two CLI spectra. From Figure 4a, no particular area was highlighted from the unmixed image of component #1 (Unmix #1), and the corresponding spectrum (blue line in Figure 4d) closely resembled the emission spectrum of 18F in pure media, in which the CLI intensity is inversely correlated with the square of the wavelength 18,20. This data suggests that Unmix #1 represented an unspecific CLI signal, which is probably from very shallow depths, such as 18F-FDG accumulation in the skin. The peak of the unmixed #2 spectrum (red line) was around 640 nm, suggesting the signal was from the BAT. Interestingly, contrary to the significant attenuation of the intensity of CLI shorter than 640 nm, no dramatic decrease of intensity was observed once it reached its peak (red line in Figure 4), indicating better tissue penetration of the emitted light at longer wavelengths.
Multispectral Cerenkov luminescence tomography (msCLT) was used for the 3D reconstruction. msCLT has been previously reported by Kuo et al. 28,43, and is constructed from a set of 2D planar images acquired with a number of narrow bandpass filters (&#62;5 filters). The reconstructed 3D images are coregistered with surface tomography that is generated from the structure light, and the images reveal that a substantial portion of the CLI signal originated from interscapular BAT (Figure 5). Remarkably, the coronal image (Figure 5a) clearly outlines the two lobes of BAT, which closely resemble the triangle contour of the BAT shown in Figure 5e.
<img alt="Figure 1" fo:content-width="5in" src="/files/ftp_upload/51790/51790fig1highres.jpg" width="500" /> 
Figure 1: (a) Triangular contour of interscapular BAT (blue arrow) in a mouse; (left) BAT is covered with white adipose tissue, and (right) BAT is exposed. (b) CLI images of a mouse at 30 and 60 min after 18F-FDG (280 &#181;Ci) intravenous injection. The images clearly outline the contour of BAT. (c) Quantitative analysis of CLI signal from interscapular BAT area and a reference area. Reprint from reference 42. <a href="https://www.jove.com/files/ftp_upload/51790/51790fig1highres.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" fo:content-width="5in" src="/files/ftp_upload/51790/51790fig2highres.jpg" width="500" /> 
Figure 2: (a) Representative images of mice before (left) and after (right) BAT removal. (b) Quantification indicates that &#62;85% CLI originated from BAT. Reprint from reference 42. <a href="https://www.jove.com/files/ftp_upload/51790/51790fig2highres.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" fo:content-width="5in" src="/files/ftp_upload/51790/51790fig3highres.jpg" width="500" /> 
Figure 3: (a) Representative CLI images of BAT of mice with (left) and without (right) NE stimulation under short isoflurane anesthesia. (b) Quantitative analysis of the CLI signals from the two groups in (a) (n = 4 for each group). (c) Representative CLI images of BAT of mice with (left) and without (right) cold stimulation under short isoflurane anesthesia. (d) Quantitative analysis of the CLI signals from the two groups shown in (e) (n = 3 - 4 for each group). (e) Representative CLI images of BAT at 60 min after 18F-FDG injection under short isoflurane anesthesia (5 min) (left) and ketamine/xylazine anesthesia (70 min) (right). (f) Quantitative analysis of the CLI signals from the two groups shown in (g) (n = 4 for each group). Reprint from reference 42. <a href="https://www.jove.com/files/ftp_upload/51790/51790fig3highres.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 4" fo:content-width="5in" src="/files/ftp_upload/51790/51790fig4highres.jpg" width="500" /> 
Figure 4: Spectral unmixing for unspecific CLI and BAT CLI. (a) Unmix #1 shows that unspecific CLI signal from 18F-FDG is distributed over the whole body (the unmixed spectrum for this image is shown in (d) (blue line)). (b) Unmix #2 indicates that the majority of CLI at the interscapular site is from BAT (the unmixed spectrum is shown in (d) (red line)). The CLI peak is around 640 nm. (c) Merged image of Unmix #1 and #2. (d) The CLI spectra of Unmix #1 and #2. Reprint from reference 42. <a href="https://www.jove.com/files/ftp_upload/51790/51790fig4highres.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 5" fo:content-width="5in" src="/files/ftp_upload/51790/51790fig5highres.jpg" width="500" /> 
Figure 5: Multispectral Cerenkov luminescence tomography. (a - d) 3D reconstruction of the images. Interscapular BAT can be seen in coronal (a), sagittal (b), and transverse (c) views, as well as in the 3D image (d); (e) Physical BAT shape is shown (blue arrow) which correlates with reconstructed images. Reprint and adapt from reference 42. <a href="https://www.jove.com/files/ftp_upload/51790/51790fig5highres.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

Watch this Scientific Journal Video about Cerenkov Luminescence Imaging of Interscapular Brown Adipose Tissue at JoVE.com

Cerenkov Luminescence Imaging of Interscapular Brown Adipose Tissue

In this video report, we show the application of Cerenkov Luminescence Imaging (CLI) for interscapular brown adipose tissue in mice under activated and depressed conditions.

Brown adipose tissue (BAT), widely known as a &#8220;good fat&#8221; plays pivotal roles for thermogenesis in mammals. This special tissue is closely ...

cerenkov-luminescence-imaging-of-interscapular-brown-adipose-tissue

Research

JoVE Journal

Medicine

Cerenkov Luminescence Imaging (CLI) for Cancer Therapy Monitoring

In molecular imaging, positron emission tomography (PET) and optical imaging (OI) are two of the most important and thus most widely used modalities1-3. PET is characterized by its excellent sensitivity and quantification ability while OI is notable for non-radiation, relative low cost, short scanning time, high throughput, and wide availability to basic researchers. However, both modalities have their shortcomings as well. PET suffers from poor spatial resolution and high cost, while OI is mostly limited to preclinical applications because of its limited tissue penetration along with prominent scattering optical signals through the thickness of living tissues.
 Recently a bridge between PET and OI has emerged with the discovery of Cerenkov Luminescence Imaging (CLI)4-6. CLI is a new imaging modality that harnesses Cerenkov Radiation (CR) to image radionuclides with OI instruments. Russian Nobel laureate Alekseyevich Cerenkov and his colleagues originally discovered CR in 1934. It is a form of electromagnetic radiation emitted when a charged particle travels at a superluminal speed in a dielectric medium7,8. The charged particle, whether positron or electron, perturbs the electromagnetic field of the medium by displacing the electrons in its atoms. After passing of the disruption photons are emitted as the displaced electrons return to the ground state. For instance, one 18F decay was estimated to produce an average of 3 photons in water5. 
 Since its emergence, CLI has been investigated for its use in a variety of preclinical applications including in vivo tumor imaging, reporter gene imaging, radiotracer development, multimodality imaging, among others4,5,9,10,11. The most important reason why CLI has enjoyed much success so far is that this new technology takes advantage of the low cost and wide availability of OI to image radionuclides, which used to be imaged only by more expensive and less available nuclear imaging modalities such as PET.
 Here, we present the method of using CLI to monitor cancer drug therapy. Our group has recently investigated this new application and validated its feasibility by a proof-of-concept study12. We demonstrated that CLI and PET exhibited excellent correlations across different tumor xenografts and imaging probes. This is consistent with the overarching principle of CR that CLI essentially visualizes the same radionuclides as PET. We selected Bevacizumab (Avastin; Genentech/Roche) as our therapeutic agent because it is a well-known angiogenesis inhibitor13,14. Maturation of this technology in the near future can be envisioned to have a significant impact on preclinical drug development, screening, as well as therapy monitoring of patients receiving treatments.

Cerenkov Luminescence Imaging CLI for Cancer Therapy Monitoring

Use of Cerenkov Luminescence Imaging (CLI) for monitoring preclinical cancer treatment is described here. This method takes advantage of Cerenkov Radiation (CR) and optical imaging (OI) to visualize radiolabeled probes and thus provides an alternative to PET in preclinical therapeutic monitoring and drug screening.

In  molecular imaging, positron emission tomography (PET) and optical imaging (OI)  are two of the most important and thus most widely used modalities1-3. ...

Human Brown Adipose Tissue Depots Automatically Segmented by Positron Emission Tomography/Computed Tomography and Registered Magnetic Resonance Images

Reliably differentiating brown adipose tissue (BAT) from other tissues using a non-invasive imaging method is an important step toward studying BAT in humans. Detecting BAT is typically confirmed by the uptake of the injected radioactive tracer 18F-Fluorodeoxyglucose (18F-FDG) into adipose tissue depots, as measured by positron emission tomography/computed tomography (PET-CT) scans after exposing the subject to cold stimulus. Fat-water separated magnetic resonance imaging (MRI) has the ability to distinguish BAT without the use of a radioactive tracer. To date, MRI of BAT in adult humans has not been co-registered with cold-activated PET-CT. Therefore, this protocol uses 18F-FDG PET-CT scans to automatically generate a BAT mask, which is then applied to co-registered MRI scans of the same subject. This approach enables measurement of quantitative MRI properties of BAT without manual segmentation. BAT masks are created from two PET-CT scans: after exposure for 2 hr to either thermoneutral (TN) (24 &#176;C) or cold-activated (CA) (17 &#176;C) conditions. The TN and CA PET-CT scans are registered, and the PET standardized uptake and CT Hounsfield values are used to create a mask containing only BAT. CA and TN MRI scans are also acquired on the same subject and registered to the PET-CT scans in order to establish quantitative MRI properties within the automatically defined BAT mask. An advantage of this approach is that the segmentation is completely automated and is based on widely accepted methods for identification of activated BAT (PET-CT). The quantitative MRI properties of BAT established using this protocol can serve as the basis for an MRI-only BAT examination that avoids the radiation associated with PET-CT.

The method presented here uses 18F-Fluorodeoxyglucose (18F-FDG) positron emission tomography/computed tomography (PET-CT) and fat-water separated magnetic resonance imaging (MRI), each scanned following 2 hr exposure to thermoneutral (24 &#176;C) and cold conditions (17 &#176;C) in order to map brown adipose tissue (BAT) in adult human subjects.

Reliably differentiating brown adipose tissue (BAT) from other tissues using a non-invasive imaging method is an important step toward studying BAT in ...

Murine Isolated Heart Model of Myocardial Stunning Associated with Cardioplegic Arrest

The following protocol is of use to evaluate impaired cardiac function or myocardial stunning following moderate ischemic insults. The technique is useful for modeling ischemic injury associated with numerous clinically relevant phenomenon including cardiac surgery with cardioplegic arrest and cardiopulmonary bypass, off-pump CABG, transplant, angina, brief ischemia, etc. The protocol presents a general method to model hypothermic hyperkalemic cardioplegic arrest and reperfusion in rodent hearts focusing on measurement of myocardial contractile function. In brief, a mouse heart is perfused in langendorff mode, instrumented with an intraventricular balloon, and baseline cardiac functional parameters are recorded. Following stabilization, the heart is then subject to brief infusion of a cardioprotective hypothermic cardioplegia solution to initiate diastolic arrest. Cardioplegia is delivered intermittently over 2 hr. The heart is then reperfused and warmed to normothermic temperatures and recovery of myocardial function is monitored. Use of this protocol results in reliable depressed cardiac contractile function free from gross myocardial tissue damage in rodents.

The goal of this protocol to assess myocardial stunning following ischemic cardioplegic arrest in rodents.

The following protocol is of use to evaluate impaired cardiac function or myocardial stunning following moderate ischemic insults. The technique is useful ...

Encapsulation Thermogenic Preadipocytes for Transplantation into Adipose Tissue Depots

Cell encapsulation was developed to entrap viable cells within semi-permeable membranes. The engrafted encapsulated cells can exchange low molecular weight metabolites in tissues of the treated host to achieve long-term survival. The semipermeable membrane allows engrafted encapsulated cells to avoid rejection by the immune system. The encapsulation procedure was designed to enable a controlled release of bioactive compounds, such as insulin, other hormones, and cytokines. Here we describe a method for encapsulation of catabolic cells, which consume lipids for heat production and energy dissipation (thermogenesis) in the intra-abdominal adipose tissue of obese mice. Encapsulation of thermogenic catabolic cells may be potentially applicable to the prevention and treatment of obesity and type 2 diabetes. Another potential application of catabolic cells may include detoxification from alcohols or other toxic metabolites and environmental pollutants.

Here, we present a protocol for encapsulation of catabolic cells, which consume lipids for heat production in intra-abdominal adipose tissue and increase energy dissipation in obese mice.

Cell encapsulation was developed to entrap viable cells within semi-permeable membranes. The engrafted encapsulated cells can exchange low molecular ...

Assessment of Human Adipose Tissue Microvascular Function Using Videomicroscopy

While obesity is closely linked to the development of metabolic and cardiovascular disease, little is known about mechanisms that govern these processes. It is hypothesized that pro-atherogenic mediators released from fat tissues particularly in association with central/visceral adiposity may promote pathogenic vascular changes locally and systemically, and the notion that cardiovascular disease may be the consequence of adipose tissue dysfunction continues to evolve. Here, we describe a unique method of videomicroscopy that involves analysis of vasodilator and vasoconstrictor responses of intact small human arterioles removed from the adipose depot of living human subjects. Videomicroscopy is used to examine functional properties of isolated microvessels in response to pharmacological or physiological stimuli using a pressured system that mimics in vivo conditions. The technique is a useful approach to gain understanding of the pathophysiology and molecular mechanisms that contribute to vascular dysfunction locally within the adipose tissue milieu. Moreover, abnormalities in the adipose tissue microvasculature have also been linked with systemic diseases. We applied this technique to examine depot-specific vascular responses in obese subjects. We assessed endothelium-dependent vasodilation to both increased flow and acetylcholine in adipose arterioles (50 - 350 &#181;m internal diameter, 2 - 3 mm in length) isolated from two different adipose depots during bariatric surgery from the same individual. We demonstrated that arterioles from visceral fat exhibit impaired endothelium-dependent vasodilation compared to vessels isolated from the subcutaneous depot. The findings suggest that the visceral microenvironment is associated with vascular endothelial dysfunction which may be relevant to clinical observation linking increased visceral adiposity to systemic disease mechanisms. The videomicroscopy technique can be used to examine vascular phenotypes from different fat depots as well as compare findings across individuals with different degrees of obesity and metabolic dysfunction. The method can also be used to examine vascular responses longitudinally in response to clinical interventions.

Videomicroscopy systems are used to examine functional properties of isolated adipose tissue arterioles in response to physiological and pharmacological stimuli. This technique can be used to examine microvascular phenotypes in different adipose tissue domains in obese humans.

While obesity is closely linked to the development of metabolic and cardiovascular disease, little is known about mechanisms that govern these processes. ...

Autologous Microfractured and Purified Adipose Tissue for Arthroscopic Management of Osteochondral Lesions of the Talus

In recent years, regenerative techniques have been increasingly studied and used to treat osteochondral lesions of the talus. In particular, several studies have focused their attention on mesenchymal stem cells derived from adipose tissue. Adipose-derived stem cells (ADSCs) exhibit morphological characteristics and properties similar to other mesenchymal cells, and are able to differentiate into several cellular lines. Moreover, these cells are also widely available in the subcutaneous tissue, representing 10 - 30% of the normal body weight, with a concentration of 5,000 cells per gram of tissue.
In the presented technique, the first step involves harvesting ADSCs from the abdomen and a process of microfracture and purification; next, the surgical procedure is performed entirely arthroscopically, with less soft tissue dissection, better joint visualization, and a faster recovery compared with standard open procedures. Arthroscopy is characterized by a first phase in which the lesion is identified, isolated, and prepared with microperforations; the second step, performed dry, involves injection of adipose tissue at the level of the lesion.
Between January 2016 and September 2016, four patients underwent arthroscopic treatment of osteochondral lesion of the talus with microfractured and purified adipose tissue. All patients reported clinical improvement six months after surgery with no reported complications. Functional scores at the latest follow-up are encouraging and confirm that the technique provides reliable pain relief and improvements in patients with osteochondral lesion of the talus.

The aim of this study is to report a protocol for the arthroscopic treatment of osteochondral lesions of the talus using microfractured and purified adipose-derived stem cells.

In recent years, regenerative techniques have been increasingly studied and used to treat osteochondral lesions of the talus. In particular, several ...

Characterization of Immune Cells in Human Adipose Tissue by Using Flow Cytometry

Infiltration of immune cells in the subcutaneous and visceral adipose tissue (AT) deposits leads to a low-grade inflammation contributing to the development of obesity-associated complications such as type 2 diabetes. To quantitatively and qualitatively investigate the immune cell subsets in human AT deposits, we have developed a flow cytometry approach. The stromal vascular fraction (SVF), containing the immune cells, is isolated from subcutaneous and visceral AT biopsies by collagenase digestion. Adipocytes are removed after centrifugation. The SVF cells are stained for multiple membrane-bound markers selected to differentiate between immune cell subsets and analyzed using flow cytometry. As a result of this approach, pro- and anti-inflammatory macrophage subsets, dendritic cells (DCs), B-cells, CD4+ and CD8+ T-cells, and NK cells can be detected and quantified. This method gives detailed information about immune cells in AT and the amount of each specific subset. Since there are numerous fluorescent antibodies available, our flow cytometry approach can be adjusted to measure various other cellular and intracellular markers of interest.

This article describes a method to analyze immune cell content of adipose tissue by isolation of immune cells from adipose tissue and subsequent analysis using flow cytometry.

Infiltration of immune cells in the subcutaneous and visceral adipose tissue (AT) deposits leads to a low-grade inflammation contributing to the ...

Clinical Protocol of Producing Adipose Tissue-Derived Stromal Vascular Fraction for Potential Cartilage Regeneration

Osteoarthritis (OA) is one of the most common debilitating disorders.&#160;Recently, numerous attempts have been made to improve the functions of the knees by using different forms of mesenchymal stem cells (MSCs). In Korea, bone marrow concentrates and cord blood-derived stem cells have been approved by the Korean Food and Drug Administration (KFDA) for cartilage regeneration. In addition, an adipose tissue-derived stromal vascular fraction (SVF) has been allowed by the KFDA for joint injections in human patients. Autologous adipose tissue-derived SVF contains extracellular matrix (ECM) in addition to mesenchymal stem cells. ECM excretes various cytokines that, along with hyaluronic acid (HA) and platelet-rich plasma (PRP) activated by calcium chloride, may help MSCs to regenerate cartilage and improve knee functions. In this article, we presented a protocol to improve knee functions by regenerating cartilage-like tissue in human patients with OA. The result of the protocol was first reported in 2011 followed by a few additional publications. The protocol involves liposuction to obtain autologous lipoaspirates that are mixed with collagenase. This lipoaspirates-collagenase mixture is then cut and homogenized to remove large fibrous tissue that may clog up the needle during the injection. Afterwards, the mixture is incubated to obtain adipose tissue-derived SVF. The resulting adipose tissue-derived SVF, containing both adipose tissue-derived MSCs and remnants of ECM, is injected into knees of patients, combined with HA and calcium chloride activated PRP. Included are three cases of patients who were treated with our protocol resulting in improvement of knee pain, swelling, and range of motion along with MRI evidence of hyaline cartilage-like tissue.

Here, we present a protocol to produce an adipose tissue-derived stromal vascular fraction and its application to improve knee functions by regenerating cartilage-like tissue in human patients with osteoarthritis.

Osteoarthritis (OA) is one of the most common debilitating disorders.&#160;Recently, numerous attempts have been made to improve the functions of the ...

Whole Body and Regional Quantification of Active Human Brown Adipose Tissue Using 18F-FDG PET/CT

In endothermic animals, brown adipose tissue (BAT) is activated to produce heat for defending body temperature in response to cold. BAT&#39;s ability to expend energy has made it a potential target for novel therapies to ameliorate obesity and associated metabolic disorders in humans. Though this tissue has been well studied in small animals, BAT&#39;s thermogenic capacity in humans remains largely unknown due to the difficulties of measuring its volume, activity, and distribution. Identifying and quantifying active human BAT is commonly performed using 18F-Fluorodeoxyglucose (18F-FDG) positron emission tomography and computed tomography (PET/CT) scans following cold-exposure or pharmacological activation. Here we describe a detailed image-analysis approach to quantify total-body human BAT from 18F-FDG PET/CT scans using an open-source software. We demonstrate the drawing of user-specified regions of interest to identify metabolically active adipose tissue while avoiding common non-BAT tissues, to measure BAT volume and activity, and to further characterize its anatomical distribution. Although this rigorous approach is time-consuming, we believe it will ultimately provide a foundation to develop future automated BAT quantification algorithms.

Whole Body and Regional Quantification of Active Human Brown Adipose Tissue Using 18F-FDG PET/CT

Using free, open-source software, we have developed an analytical approach to quantify total and regional brown adipose tissue (BAT) volume and metabolic activity of BAT using 18F-FDG PET/CT.

In endothermic animals, brown adipose tissue (BAT) is activated to produce heat for defending body temperature in response to cold. BAT&#39;s ability to ...

Inguinal Subcutaneous White Adipose Tissue (ISWAT) Transplantation Model of Murine Islets

Pancreatic islet transplantation is a well-established therapeutic treatment for type 1 diabetes. The kidney capsule is the most commonly used site for islet transplantation in rodent models. However, the tight kidney capsule limits the transplantation of sufficient islets in large animals and humans. The inguinal subcutaneous white adipose tissue (ISWAT), a new subcutaneous space, was found to be a potentially valuable site for islet transplantation. This site has better blood supply than other subcutaneous spaces. Moreover, the ISWAT accommodates a larger islet mass than the kidney capsule, and transplantation into it is simple. This manuscript describes the procedure of mouse islet isolation and transplantation in the ISWAT site of syngeneic diabetic mouse recipients. Using this protocol, murine pancreatic islets were isolated by standard collagenase digestion and a basement membrane matrix hydrogel was used for fixing the purified islets in the ISWAT site. The blood glucose levels of the recipient mice were monitored for more than 100 days. Islet grafts were retrieved at day 100 after transplantation for histological analysis. The protocol for islet transplantation in the ISWAT site described in this manuscript is simple and effective.

Inguinal Subcutaneous White Adipose Tissue ISWAT Transplantation Model of Murine Islets

In this protocol, a method of murine islet isolation and transplantation into the inguinal subcutaneous white adipose tissue is described. Isolated syngeneic murine islets are transplanted into a murine recipient using a basement membrane hydrogel. The blood glucose level of the recipients is monitored, and histology analysis of the islet grafts is performed.

Pancreatic islet transplantation is a well-established therapeutic treatment for type 1 diabetes. The kidney capsule is the most commonly used site for ...