This work was supported by the National Institutes of Health (HL114669). CM is a recipient of a postdoctoral research fellowship grant awarded by the Myocarditis Foundation, NJ.

ETHICS STATEMENT:
All animal procedures were conducted in accordance with the guidelines for the Care and Use of Laboratory Animals and approved by the University of Nebraska-Lincoln, Lincoln, NE.
1. Induction of Experimental Autoimmune Myocarditis
<ol>
	<li>Prepare the peptide solution by dissolving Myhc-&#945; 334-352 in 1x phosphate-buffered saline to a final concentration of 2 mg/1.5 ml.</li>
	<li>Prepare the pertussis toxin (PT) by adding 1 ml of sterile 1x PBS to a vial containing 50 &#956;g of lyophilized PT to obtain a stock concentration of 50 ng/&#956;l. Take 20 &#956;l of the stock into a sterile 1.5 ml tube and add 980 &#956;l of sterile 1x PBS to obtain a working concentration of 1 ng/&#956;l.</li>
	<li>Prepare complete Freund&#8217;s adjuvant (CFA) by adding 40 mg of Mycobacterium&#160;tuberculosis H37Rv (MTB) extract to 10 ml of CFA to obtain a final concentration of 5 mg/ml.</li>
	<li>Prepare the peptide-CFA emulsion. NOTE: For EAM induction, the peptide-CFA emulsion was administered in 150 &#956;l containing 100 &#181;g of Myhc-&#945; 334-352 per animal. For example, to immunize ten mice use 1.5 ml of peptide-CFA emulsion containing 1 mg of Myhc-&#945; 334-352.
	<ol>
		<li>To prepare 1.5 ml of emulsion, aliquot 750 &#956;l of Myhc-&#945; 334-352 peptide solution in one 1.5 ml tube, and CFA supplemented with MTB into another 1.5 ml tube. Using a 3&#160;ml luer-lok syringe, draw the peptide solution first, followed by the CFA/MTB extract.</li>
		<li>Attach the syringe to a 3-way stopcock and connect the other outlet of the stopcock to an empty 3&#160;ml syringe. Adjust the patency of the stopcock so the peptide-CFA mixture flows from one syringe to the other with reasonably good resistance.</li>
		<li>Mix by pushing the contents from one syringe to the other repeatedly for ~1 min and then place the entire assembly on ice for ~3 min. Repeat this procedure a minimum of 10x.</li>
		<li>Determine the consistency of the emulsion by carefully placing a tiny droplet on still water in a 100 ml glass beaker. The droplet is not expected to disperse in water. If it does, continue mixing until the desired consistency is achieved.</li>
		<li>Transfer the contents of emulsion from 3 ml syringes into 1&#160;ml luer-lok syringes by replacing one of the two 3-ml syringes attached to the stopcock with the 1-ml syringe, and attach a 27 &#189; G needle to the 1&#160;ml syringe.</li>
	</ol>
	</li>
	<li>Inject 150 &#181;l of the peptide-CFA emulsion in split doses subcutaneously in the two inguinal regions of six-to-eight-week-old female A/J mice (~75 &#181;l each).</li>
	<li>Administer 100 &#956;l of PT suspension (100 ng) intraperitoneally to each animal on day 0 and day 2 postimmunization.</li>
	<li>Repeat the immunization procedure on day 7 by administering 150 &#181;l of peptide-CFA emulsion in split doses subcutaneously into either side of the sternum (~75 &#181;l each). Prepare this emulsion fresh as above. Then, on day 21, subject the animals to MRM imaging, see step 3.</li>
</ol>
2. Animal Handling
<ol>
	<li>Place each mouse in an anesthetic induction chamber containing 2% isoflurane-air mixture with a heating pad placed underneath to maintain warmth, and transfer the animal to a specially designed animal holder (Figure&#160;1).</li>
	<li>Immobilize the animal in the prone position on the animal holder so its snout fits into the nose cone to maintain anesthesia (Figure&#160;1). Secure the head of the mouse with a bite-bar attached to the front teeth of the mouse.</li>
	<li>Turn on the air blow heater with its outlet hose inserted in the scanner&#8217;s vertical bore to maintain the animal&#8217;s body temperature during the experiment.</li>
	<li>Maintain anesthesia at 0.5 to 2% isoflurane with a flow rate of 2 ml/min during the entire imaging session. Confirm anesthesia using the toe pinch method, no movement expected.</li>
	<li>Set up a pneumatic pillow sensor, mouse tail/ankle fiber optic pulse oximetry sensor, and rectal temperature probe to monitor respiration, heart rate and body temperature, respectively (Figure&#160;1). Note: Cardiac gating is performed through Pulse Oximetry, which allows noninvasive monitoring of arterial blood oxygen saturation. The pulse oximetry sensor should be attached to the left ankle, and the foot should be secured with a thread loop and taped to maintain the ankle in the sensor. MRM imaging is achieved by gating the respiration and cardiac signals without the use of any contrast agents.</li>
</ol>
3. Image Acquisition
<ol>
	<li>After preparing the animal (Figure&#160;1), place the mouse in the center of the MRM scanner with the heart positioned in the center of the field of view (FOV), where magnetic field homogeneity is maximum. NOTE: A wide-bore (89 mm)&#160;9.4 T vertical-bore magnet equipped with triple axis gradients of 100 G/cm and a 4 cm radio-frequency (RF) imaging coil is to be used to obtain high-resolution three-dimensional (3D) images. Note: Be sure to non-magnetic supplies when using an MRI scanner.&#160;</li>
	<li>Run the imaging interface and select &#8220;New Study&#8221; from the &#8220;Study Options&#8221; menu. Type &#8220;mtune&#8221; at the command bar and run it to pull up the &#8220;Tune GUI&#8221;. Then select &#8220;Start Probe Tune&#8221; and click on &#8220;Autoscale&#8221; button. The Tune GUI will change to show the RFsignal. Use the remote tune/match knobs at the end of the coil to tune the RF coil to the proton resonance frequency (400 MHz). On the &#8220;Start&#8221; tab go to the &#8220;Prescan&#8221; page to run the frequency and power calibration by clicking on the related buttons. Hit the XYZ (quick) button on the &#8216;Shim&#8221; tab of &#8220;Study&#8217; tab to pull up the shimming page. Go to the shim page, select all of the iterations, and hit the shim button to perform auto shimming.</li>
	<li>Select a scout sequence from the &#8220;Study&#8221; tab of the imaging interface to localize the mouse heart. On the &#8220;Acquire&#8221; tab change the FOV to 35 mm2 and keep the machine&#8217;s default settings. Click Start to run the sequence; adjust the position of the animal holder if the heart is not in the center of FOV, retune the RF coil and obtain the scout images again.</li>
	<li>Click the &#8220;GEMS&#8221; sequence button on the &#8220;Study&#8221; tab then enter the acquisition parameters on the corresponding &#8220;Acquire&#8221; tab to obtain two orthogonal planes along the short axis and long axis of the heart20,21. NOTE: Typical acquisition parameters for a gradient-echo scan are: slice thickness, 1 mm; repetition time (TR), 200 msec; echo time (TE), 2.67 msec (minimum); flip angle, 25&#176;; inplane matrix size, 128 x 128; FOV, 22 mm2; number of acquisitions, 4; and an approximate acquisition time of 1 min&#160;and 30 sec.</li>
	<li>On the &#8220;Adv&#8221; tab select the &#8220;CINE&#8221; sequence to collect the pulse oximetry-gated short-axis cine MR images in order to measure the LV anatomic and functional parameters. Adjust the position and angle of the imaging slices based on the long axis view of the heart by mouse hovering and dragging. Enter the following imaging parameters on the &#8220;Acquire&#8221; tab to obtain the gradient echo cine sequence: TR, 500 msec; TE, 5 msec; FOV, 22 mm2; acquisition matrix, 256 x 256; slice thickness, 1 mm; number of acquisitions, 8; number of frames, 6; and an acquisition time of ~17 min. Click start to begin the acquisition.</li>
	<li>Convert the acquired images to DICOM format using the &#8220;I/O&#8221; tab of the imaging software and transfer the corresponding files to the data center for processing.</li>
	<li>At the end of imaging procedure, allow the mice to recover from anesthesia within the filter-top cages. Do not leave the mice unattended until they regain sufficient consciousness to maintain sternal recumbency and keep them for further studies as needed.</li>
</ol>
4. Data Analysis of Cardiac Magnetic Resonance Microscopy Imaging
<ol>
	<li>Use Segment software to analyze the anatomic and functional parameters of the LV19. By loading the DICOM format cine images into the software using the &#8220;Open Image File(s)&#8221; submenu of the &#8220;File&#8221; menu. On the GUI select &#8216;MRGE&#8217; as the imaging technique, &#8216;Cine&#8217; as the image type and &#8216;short-axis mid-ventricular&#8217; as the image view plane.</li>
	<li>Specify the time frames to be used for end-diastole and end-systole through the &#8220;Set Current Timeframe to End Diastole&#8221; and &#8220;Set Current Timeframe to End Systole&#8221; submenus of the &#8220;Edit&#8221; menu respectively.</li>
	<li>First click the &#8220;LV&#8221; command button and then the &#8220;ENDO&#8221; and &#8220;EPI&#8221; command buttons on the bottom-right panel to manually draw the left ventricle endocardium and epicardium respectively. Remove the papillary muscles by hitting the corresponding command button in order to increase the accuracy of the calculations.</li>
	<li>Read the quantified LV parameters such as diastolic volume, systolic volume, stroke volume, and ejection fraction on the top-right panel. Click the &#8220;Misc&#8221; command button and then the &#8220;Measurement Caliper&#8221; command button to measure the LV parameters such as wall thickness, and ventricular diameter22.</li>
	<li>Click the &#8220;Save Both Image Stacks and Segmentation&#8221; submenu of the &#8220;File&#8221; menu to save the images, including the segmentations, in &#8216;.mat&#8217; format to reprocess the images as needed.</li>
</ol>

<ol>
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R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Pathogenesis+of+myocarditis+and+dilated+cardiomyopathy.">Pathogenesis of myocarditis and dilated cardiomyopathy.</a> Adv Immunol. 99, 95-114 (2008).</li><li>Donermeyer, 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=Myocarditis-inducing+epitope+of+myosin+binds+constitutively+and+stably+to+I-Ak+on+antigen-presenting+cells+in+the+heart.">Myocarditis-inducing epitope of myosin binds constitutively and stably to I-Ak on antigen-presenting cells in the heart.</a> J Exp Med. 182 (5), 1291-1300 (1995).</li><li>Gangaplara, A., 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=Coxsackievirus+B3+infection+leads+to+the+generation+of+cardiac+myosin+heavy+chain-alpha-reactive+CD4+T+cells+in+A/J+mice.">Coxsackievirus B3 infection leads to the generation of cardiac myosin heavy chain-alpha-reactive CD4 T cells in A/J mice.</a> Clin Immunol. 144 (3), 237-249 (2012).</li><li>Huber, S. A., Lodge, P. 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No conflicts of interests were declared.

This study describes the MRM procedure and its utility as a non-invasive tool to ascertain cardiac abnormalities in mice affected with autoimmune myocarditis. Since the histologic features of EAM resemble postinfectious myocarditis of humans, mouse models are commonly employed to delineate the immune mechanisms of myocardial injuries23-25. However, the animals affected with myocarditis appear clinically normal, and the diagnosis is made based on histology at the termination of experiments7. The anim...

Heart failure is the leading cause of deaths, and myocarditis is one predominant cause of heart failure in young adolescents1. Most patients affected with myocarditis remain asymptomatic and the disease is spontaneously resolved2. However, 10-20% of those affected can develop chronic disease, leading to dilated cardiomyopathy (DCM)3. Various animal models have been developed to study the immune pathogenesis of myocarditis. The disease can be induced in myocarditis-susceptible A/J and Balb/c mice by immunizing the animals with cardiac myosin heavy chain (Myhc)-&#945; or its immunodominant peptide fragments or by infecting with pathogens like coxsackievirus B3 4-9. This study involves Myhc-&#945; 334-352-induced myocarditis in A/J mice. Despite showing myocardial infiltrations, the myocarditis-affected animals appear clinically normal; diagnosis is based on histological evaluation of hearts for inflammation7 and echocardiography10.
Magnetic resonance microscopy (MRM) is a commonly used method to obtain cardiovascular imaging with high resolution three-dimensional planes, permitting assessment of functional details to the level of minute blood vessels (up to 10 &#956;m diameter), but this level of resolving power is not achievable with the routine magnetic resonance imaging (MRI) scanning procedure, in which, the resolution is generally obtained up to 1 mm11-14. MRM offers an advantage as it permits acquisition of high-resolution images and also to derive performance parameters in the early time points of disease process14. Clinically, MRM imaging has been extensively applied to study the functional parameters of diseased heart, lung or brain15-17. In this study, the use of an MRM technique as a non-invasive tool to ascertain cardiac abnormalities in A/J mice affected with autoimmune myocarditis is shown. Specifically, the MRM imaging allows quantification of functional parameters such as left ventricular (LV) end-diastolic volume and ejection fraction (EF) with reasonable accuracy18. The definitions of respective parameters are: LV end diastolic volume, volume of blood in the left ventricle at the end of diastolic cycle, and ejection fraction, stroke volume/end-diastolic volume. The data analysis is performed using the freely available Segment software developed for processing DICOM-compliant cardiovascular images acquired by magnetic resonance scanners19. The data revealed an increase in thickness of the LV wall in the myocarditic animals, corresponding to a decrease in LV end-diastolic volume, stroke volume and ejection fraction, as compared with these functional parameters in healthy mice.

<table border="0" cellpadding="0" cellspacing="0" width="1185">
	<tbody>
		<tr height="25">
			<td height="25" style="height:25px;width:509px;">Myhc-a 334-352 (DSAFDVLSFTAEEKAGVYK)</td>
			<td style="width:364px;">Neopeptide, Cambridge, MA</td>
			<td style="width:145px;"></td>
			<td style="width:167px;">Store at 4&#959;C</td>
		</tr>
		<tr height="25">
			<td height="25" style="height:25px;">CFA</td>
			<td style="width:364px;">Sigma Aldrich, St Louis, MO</td>
			<td style="width:145px;">5881</td>
			<td>Store at 4&#959;C</td>
		</tr>
		<tr height="25">
			<td height="25" style="height:25px;">MTB&#160; H37Rv extract&#160;</td>
			<td>Difco Laboratories, Detroit, MI</td>
			<td>231141</td>
			<td>Store at 4&#959;C</td>
		</tr>
		<tr height="25">
			<td height="25" style="height:25px;">PT</td>
			<td>List Biologicals Laboratories, Campbell, CA</td>
			<td>181</td>
			<td>Store at 4&#959;C</td>
		</tr>
		<tr height="25">
			<td height="25" style="height:25px;">1x PBS&#160;</td>
			<td>Corning, Manassas, VA</td>
			<td>21-040-CV</td>
			<td>Store at 4&#959;C</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Isoflurane&#160;</td>
			<td>Piramal Healthcare, Mumbai, India</td>
			<td>NDC66794-013-25</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Female A/J mice&#160;</td>
			<td>Jackson Laboratories, Bar Harbor, ME</td>
			<td>646</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Leur-lok sterile 1 ml syrringe</td>
			<td>BD, Franklin Lakes, NJ</td>
			<td>309628</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Leur-lok sterile 3 ml syrringe</td>
			<td>BD, Franklin Lakes, NJ</td>
			<td>309657</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Sterile needle, 18 G</td>
			<td>BD, Franklin Lakes, NJ</td>
			<td>305195</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Sterile needle, 27 1/2 G</td>
			<td>BD, Franklin Lakes, NJ</td>
			<td>305109</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">3-way stopcock&#160;</td>
			<td>Smiths Medical ASD, Inc. Dublin, OH</td>
			<td>MX5311L</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Kerlix gauze bandage rolls&#160;</td>
			<td>Covidien, Mansfield, MA</td>
			<td>6720</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Kimwipes</td>
			<td>Kimberly-Clark Professional, Roswell, GA</td>
			<td>34155</td>
			<td></td>
		</tr>
		<tr height="21">
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noninvasive assessment of cardiac abnormalities in experimental autoimmune myocarditis by magnetic resonance microscopy imaging in the mouse

Myocarditis is an inflammation of the myocardium, but only ~10% of those affected show clinical manifestations of the disease. To study the immune events of myocardial injuries, various mouse models of myocarditis have been widely used. This study involved experimental autoimmune myocarditis (EAM) induced with cardiac myosin heavy chain (Myhc)-&#945; 334-352 in A/J mice; the affected animals develop lymphocytic myocarditis but with no apparent clinical signs. In this model, the utility of magnetic resonance microscopy (MRM) as a non-invasive modality to determine the cardiac structural and functional changes in animals immunized with Myhc-&#945; 334-352 is shown. EAM and healthy mice were imaged using a 9.4 T (400 MHz) 89 mm vertical core bore scanner equipped with a 4 cm millipede radio-frequency imaging probe and 100 G/cm triple axis gradients. Cardiac images were acquired from anesthetized animals using a gradient-echo-based cine pulse sequence, and the animals were monitored by respiration and pulse oximetry. The analysis revealed an increase in the thickness of the ventricular wall in EAM mice, with a corresponding decrease in the interior diameter of ventricles, when compared with healthy mice. The data suggest that morphological and functional changes in the inflamed hearts can be non-invasively monitored by MRM in live animals. In conclusion, MRM offers an advantage of assessing the progression and regression of myocardial injuries in diseases caused by infectious agents, as well as response to therapies.

In this report, the utility of MRM technique as a non-invasive modality to determine the structural and functional changes in the hearts of animals affected with EAM is shown. Myocarditis was induced in A/J mice by immunizing the animals with Myhc-&#945; 334-352 in CFA7, and the animals were subjected to MRM experiments on day 21 post-immunization. The MRM imaging was performed on live animals under isoflurane anesthesia at 9.4 T (400 MHz for protons) using an 89&#160;mm vertical-bore magnet equipped with trip...

Watch this Scientific Journal Video about Noninvasive Assessment of Cardiac Abnormalities in Experimental Autoimmune Myocarditis by Magnetic Resonance Microscopy Imaging in the Mouse at JoVE.com

Noninvasive Assessment of Cardiac Abnormalities in Experimental Autoimmune Myocarditis by Magnetic Resonance Microscopy Imaging in the Mouse

This study demonstrates the successful establishment of magnetic resonance microscopy imaging as a non-invasive tool to assess the cardiac abnormalities in mice affected with autoimmune myocarditis. The data indicate that the technique can be used to monitor the disease-progression in live animals.

Myocarditis is an inflammation of the myocardium, but only ~10% of those affected show clinical manifestations of the disease. To study the immune events ...

noninvasive-assessment-cardiac-abnormalities-experimental-autoimmune

Research

JoVE Journal

Medicine

9.8K Views.  University of Nebraska-Lincoln. This study demonstrates the successful establishment of magnetic resonance microscopy imaging as a non-invasive tool to assess the cardiac abnormalities in mice affected with autoimmune myocarditis. The data indicate that the technique can be used to monitor the disease-progression in live animals.