The authors would like to acknowledge Bryan Bergman, PhD at University of Colorado for providing the image of the IMAT biopsy in Figure 1C from the MoTrIMAT study (R01AG077956). We are grateful for the Study of Muscle, Mobility and Aging providing the IMAT sample from which data is shown in the representative results section. The National Institute on Aging (NIA) funded the Study of Muscle, Mobility and Aging (SOMMA; R01AG059416) and its ancillary studies SOMMA AT (R01AG066474) and SOMMA Knee OA (R01AG070647). Study infrastructure support was funded in part by NIA Claude D. Pepper Older American Independence Centers at University of Pittsburgh (P30AG024827) and Wake Forest University (P30AG021332) and the Clinical and Translational Science Institutes, funded by the National Center for Advancing Translational Science, at Wake Forest University (UL1 0TR001420).

The sample used for this protocol was part of the Study of Muscle, Mobility, and Aging (SOMMA)15, which was approved by the Western IRB-Copernicus Group (WCG) Institutional Review Board and was carried out in accordance with the Declaration of Helsinki. Participants provided written informed consent for their participation in the study.
NOTE : This protocol is adapted from a previous protocol using 100 mg of human abdominal subcutaneous adipose tissue on a na...

Single Cell Nuclei Isolation from IMAT for Studying Gene Expression Profiles 

<ol>
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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=Reduced+physical+activity+increases+intermuscular+adipose+tissue+in+healthy+young+adults.">Reduced physical activity increases intermuscular adipose tissue in healthy young adults.</a> Am J Clin Nutr. 85 (2), 377-384 (2007).</li><li>Addison, O., Marcus, R. L., LaStayo, P. C., Ryan, A. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Intermuscular+fat:+A+review+of+the+consequences+and+causes.">Intermuscular fat: A review of the consequences and causes.</a> Int J Endocrinol. 2014, 309570 (2014).</li><li>Goodpaster, B. 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=Obesity,+regional+body+fat+distribution,+and+the+metabolic+syndrome+in+older+men+and+women.">Obesity, regional body fat distribution, and the metabolic syndrome in older men and women.</a> Arch Intern Med. 165 (7), 777-783 (2005).</li><li>Goodpaster, B. H., Thaete, F. L., Kelley, D. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Thigh+adipose+tissue+distribution+is+associated+with+insulin+resistance+in+obesity+and+in+type+2+diabetes+mellitus.">Thigh adipose tissue distribution is associated with insulin resistance in obesity and in type 2 diabetes mellitus.</a> Am J Clin Nutr. 71 (4), 885-892 (2000).</li><li>Goodpaster, B. 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=Association+between+regional+adipose+tissue+distribution+and+both+type+2+diabetes+and+impaired+glucose+tolerance+in+elderly+men.">Association between regional adipose tissue distribution and both type 2 diabetes and impaired glucose tolerance in elderly men.</a> Diabetes Care. 26 (2), 372-379 (2003).</li><li>Sachs, S., 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=Intermuscular+adipose+tissue+directly+modulates+skeletal+muscle+insulin+sensitivity+in+humans.">Intermuscular adipose tissue directly modulates skeletal muscle insulin sensitivity in humans.</a> Am J Physiol Endocrinol Metab. 316 (5), E866-E879 (2019).</li><li>Ford, H., Liu, Q., Fu, X., Strieder-Barboza, C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=White+adipose+tissue+heterogeneity+in+the+single-cell+era:+From+mice+and+humans+to+cattle.">White adipose tissue heterogeneity in the single-cell era: From mice and humans to cattle.</a> Biology (Basel). 12 (10), 1289 (2023).</li><li>Wang, 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=Single-nucleus+and+bulk+RNA+sequencing+reveal+cellular+and+transcriptional+mechanisms+underlying+lipid+dynamics+in+high+marbled+pork.">Single-nucleus and bulk RNA sequencing reveal cellular and transcriptional mechanisms underlying lipid dynamics in high marbled pork.</a> NPJ Sci Food. 7 (1), 23 (2023).</li><li>Li, 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=Identification+of+diverse+cell+populations+in+skeletal+muscles+and+biomarkers+for+intramuscular+fat+of+chicken+by+single-cell+RNA+sequencing.">Identification of diverse cell populations in skeletal muscles and biomarkers for intramuscular fat of chicken by single-cell RNA sequencing.</a> BMC Genomics. 21 (1), 752 (2020).</li><li>Lyu, P., Qi, Y., Tu, Z. J., Jiang, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Single-cell+RNA+sequencing+reveals+heterogeneity+of+cultured+bovine+satellite+cells.">Single-cell RNA sequencing reveals heterogeneity of cultured bovine satellite cells.</a> Front Genet. 12, 742077 (2021).</li><li>Fitzgerald, G., 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=MME++fibro-adipogenic+progenitors+are+the+dominant+adipogenic+population+during+fatty+infiltration+in+human+skeletal+muscle.">MME+ fibro-adipogenic progenitors are the dominant adipogenic population during fatty infiltration in human skeletal muscle.</a> Commun Biol. 6 (1), 111 (2023).</li><li>Cummings, S. 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=The+study+of+muscle,+mobility+and+aging+(SOMMA):+A+unique+cohort+study+about+the+cellular+biology+of+aging+and+age-related+loss+of+mobility.">The study of muscle, mobility and aging (SOMMA): A unique cohort study about the cellular biology of aging and age-related loss of mobility.</a> J Gerontol A Biol Sci Med Sci. 78 (11), 2083-2093 (2023).</li><li>Whytock, K. 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=Isolation+of+nuclei+from+frozen+human+subcutaneous+adipose+tissue+for+full-length+single-nuclei+transcriptional+profiling.">Isolation of nuclei from frozen human subcutaneous adipose tissue for full-length single-nuclei transcriptional profiling.</a> STAR Protoc. 4 (1), 102054 (2023).</li><li>10x Genomics. Chromium Single Cell 3' Reagent Kits User Guide (v3.1 Chemistry Dual Index), Document Number CG000315 RevE Available from: <a target="_blank" href="https://cdn.10xgenomics.com/image/upload/v1668017706/support-documents/CG000315_ChromiumNextGEMSingleCell3-_GeneExpression_v3.1_DualIndex__RevE.pdf">https://cdn.10xgenomics.com/image/upload/v1668017706/support-documents/CG000315_ChromiumNextGEMSingleCell3-_GeneExpression_v3.1_DualIndex__RevE.pdf</a> (2022)</li><li>Heumos, 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=Best+practices+for+single-cell+analysis+across+modalities.">Best practices for single-cell analysis across modalities.</a> Nat Rev Genet. 24 (1), 550-572 (2023).</li><li>Hao, 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=Dictionary+learning+for+integrative,+multimodal+and+scalable+single-cell+analysis.">Dictionary learning for integrative, multimodal and scalable single-cell analysis.</a> Nat Biotechnol. 42 (2), 293-304 (2023).</li><li>McGinnis, C. 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There are several inherent challenges to working with IMAT. In addition to its limited accessibility, the yield of sample material is often very scarce, and &#34;contamination&#34; of skeletal muscle is almost impossible to avoid. To obtain the best quality sample, one should penetrate the muscle fascia when inserting the biopsy needle (to make sure not to collect subcutaneous adipose tissue) and remove as much muscle tissue as possible by dissecting the sample under a microscope immediately after collection, followed by...

Intermuscular adipose tissue (IMAT) is an ectopic adipose depot residing between and around muscle fibers1. As described in detail in a recent review by Goodpaster et al., IMAT can be detected using high-resolution computed tomography (CT) and magnetic resonance imaging (MRI) (Figure 1A,B) and is found around and within muscle fibers throughout the entire body1. The quantity of IMAT varies greatly between individuals and is influenced by BMI, age, sex, race, and sedentariness2,3,4. Moreover, IMAT deposition is commonly seen in pathological conditions associated with muscle degeneration5, and numerous studies have documented increased IMAT mass in individuals with obesity, type 2 diabetes, metabolic syndrome, and insulin resistance6,7,8,9. Nonetheless, the cellular and biological properties of IMAT are only beginning to be unraveled. The limited accessibility and the variation in IMAT locations and content throughout the body have challenged the collection of samples from this unique adipose depot2. Moreover, samples are easily &#39;contaminated&#39; with skeletal muscle (SM) upon collection, making the separation between the biological contribution from the different tissues difficult to decipher (Figure 1C). To this end, single nuclei RNA sequencing (snRNA-seq), which has gained considerable attention during the last decade, serves as an ideal methodology to allow for the separation of IMAT- and SM-derived gene expression patterns with single-cell resolution. Moreover, nuclei isolation is particularly useful for adipose tissue due to the large lipid-laden adipocytes, which are impossible to dissociate into single-cell suspension without compromising the integrity of the cells. Lastly, this technology holds the potential to discover novel markers of IMAT-specific adipocytes and uncover the composition and presence of different progenitor cell populations, as well as study the variation of the cell composition in pathological and normal conditions.
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/66784/66784fig01.jpg" /> 
Figure 1: Images of IMAT. Representative magnetic resonance (MRI) image of IMAT from (A) a middle-aged lean female and (B) a middle-aged male with obesity. Red: subcutaneous adipose tissue, yellow: intermuscular adipose tissue, green: skeletal muscle, blue: bone. Image courtesy of Heather Cornnell, AdventHealth Translational Research Institute. (C) Fresh tissue sample with IMAT (encircled by dashed black line). Image courtesy of Meghan Hopf, AdventHealth Translational Research Institute and Bryan Bergman, University of Colorado. This figure has been modified with permission from Goodpaster et al.1. <a href="https://www.jove.com/files/ftp_upload/66784/66784fig01large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
A number of studies have been published from the livestock industry investigating the marbling of meat (IMAT in particular) in pigs, chickens, and cattle using single-cell (sc) and snRNA-seq10. These studies have identified several subpopulations of adipocytes and markers of potential progenitor cells of IMAT11,12,13; however, whether these cellular compositions translate to human IMAT is unknown. To our knowledge, only one study has looked into the cellular heterogeneity of human muscle with fatty infiltration, obtained from male patients with hip osteoarthritis, using snRNA-seq14. The investigators reported a small adipocyte population and several fibro-adipogenic progenitor (FAP) subpopulations within the large population of myonuclei14. Our study is the first to develop a method to directly interrogate IMAT manually dissected&#160;from human muscle for cellular composition using snRNA-seq.
Importantly, protocols for snRNA-seq need to be customized for the specific tissue studied, as the amount of tissue available and the physical properties of the specific tissue will dictate the optimal processing steps. The tissue yield for IMAT is typically small, often not exceeding 50 mg, even when performing ultrasound-guided biopsies. Hence, proper processing of this scarce tissue is essential. We believe that this protocol will serve as a valuable resource for researchers studying human IMAT.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>0.2 &#181;m corning syringe filters&#160;</td>
			<td>Millipore Sigma</td>
			<td>CLS431229</td>
			<td></td>
		</tr>
		<tr>
			<td>1.7 mL DNA LoBind tubes</td>
			<td>Eppendorf</td>
			<td>22431021</td>
			<td>low-bind tubes</td>
		</tr>
		<tr>
			<td>10% Tween 20</td>
			<td>Bio-Rad</td>
			<td>1662404</td>
			<td></td>
		</tr>
		<tr>
			<td>100x protease inhibitor</td>
			<td>Thermo Fisher Scientific</td>
			<td>78437</td>
			<td></td>
		</tr>
		<tr>
			<td>10X Magnetic Separator</td>
			<td>10X Genomics</td>
			<td>230003</td>
			<td></td>
		</tr>
		<tr>
			<td>10X Vortex Adapter</td>
			<td>10X Genomics</td>
			<td>330002</td>
			<td></td>
		</tr>
		<tr>
			<td>15 mL canonical tubes</td>
			<td>Sarstedt</td>
			<td>6,25,54,502</td>
			<td></td>
		</tr>
		<tr>
			<td>2100 Bioanalyzer&#160;</td>
			<td>Agilent</td>
			<td>G2939BA</td>
			<td></td>
		</tr>
		<tr>
			<td>50 mL conical tubes</td>
			<td>Sarstedt</td>
			<td>6,25,47,254</td>
			<td></td>
		</tr>
		<tr>
			<td>CellRanger</td>
			<td>Genomics</td>
			<td>N/A</td>
			<td></td>
		</tr>
		<tr>
			<td>Chromium iX accesory kit</td>
			<td>10X Genomics</td>
			<td>PN1000323</td>
			<td></td>
		</tr>
		<tr>
			<td>Chromium iX Controller</td>
			<td>10X Genomics</td>
			<td>PN1000326</td>
			<td></td>
		</tr>
		<tr>
			<td>Chromium Next GEM Chip G Single Cell Kit&#160;</td>
			<td>10X Genomics</td>
			<td>PN1000127</td>
			<td></td>
		</tr>
		<tr>
			<td>Chromium Next GEM Single Cell 3&#39;&#160; Kit v 3.1</td>
			<td>10X Genomics</td>
			<td>PN1000269</td>
			<td></td>
		</tr>
		<tr>
			<td>Chromium Next GEM Single Cell 3&#39; Gel Bead Kit v3.1&#160;</td>
			<td>10X Genomics</td>
			<td>PN1000129</td>
			<td></td>
		</tr>
		<tr>
			<td>Chromium Next GEM Single Cell GEM Kit v3.1</td>
			<td>10X Genomics</td>
			<td>PN1000130</td>
			<td></td>
		</tr>
		<tr>
			<td>Countess 3 Automated Cell Counter</td>
			<td>Thermo Fisher Scientific</td>
			<td>AMQAX2000</td>
			<td>Automated cell counter</td>
		</tr>
		<tr>
			<td>Countess cell counting chamber slides</td>
			<td>Thermo Fisher Scientific</td>
			<td>C10228</td>
			<td></td>
		</tr>
		<tr>
			<td>DoubletFinder</td>
			<td>R&#160;</td>
			<td>N/A</td>
			<td></td>
		</tr>
		<tr>
			<td>DPBS (no calcium, no magnesium)</td>
			<td>Thermo Fisher Scientific</td>
			<td>14190144</td>
			<td></td>
		</tr>
		<tr>
			<td>DTT</td>
			<td>Thermo Fisher Scientific</td>
			<td>R0861</td>
			<td></td>
		</tr>
		<tr>
			<td>Dual Index Kit TT Set A, 96 rxns</td>
			<td>10X Genomics</td>
			<td>PN1000215</td>
			<td></td>
		</tr>
		<tr>
			<td>Dynabeads MyOne SILANE&#160;</td>
			<td>10X Genomics</td>
			<td>PN2000048</td>
			<td></td>
		</tr>
		<tr>
			<td>Falcon 100 &#181;m Cell strainer</td>
			<td>Corning Life Science</td>
			<td>352360</td>
			<td></td>
		</tr>
		<tr>
			<td>Falcon 40 &#181;m Cell strainer</td>
			<td>Corning Life Science</td>
			<td>352340</td>
			<td></td>
		</tr>
		<tr>
			<td>Glycerin (glycerol), 50% (v/v) Aqueous Solution</td>
			<td>Ricca Chemical Company</td>
			<td>3290-32</td>
			<td></td>
		</tr>
		<tr>
			<td>KCL</td>
			<td>Thermo Fisher Scientific</td>
			<td>AM9640G</td>
			<td></td>
		</tr>
		<tr>
			<td>Library Construction Kit v3.1</td>
			<td>10X Genomics</td>
			<td>PN1000196</td>
			<td></td>
		</tr>
		<tr>
			<td>MACS SmartStrainers (30&#181;m)</td>
			<td>Miltenyi Biotec</td>
			<td>130-098-458</td>
			<td></td>
		</tr>
		<tr>
			<td>Mastercycler Nexus Gradient Thermal cycler</td>
			<td>Eppendorf</td>
			<td>6331000017</td>
			<td></td>
		</tr>
		<tr>
			<td>MgCl2</td>
			<td>Ambion</td>
			<td>AM9530G</td>
			<td></td>
		</tr>
		<tr>
			<td>Mortar and pestel</td>
			<td>Health care logistics&#160;</td>
			<td>14075</td>
			<td></td>
		</tr>
		<tr>
			<td>NucBlue Live Ready Probes Reagent</td>
			<td>Thermo Fisher Scientific</td>
			<td>R37605</td>
			<td></td>
		</tr>
		<tr>
			<td>Nuclease Free Water (not DEPC treated)</td>
			<td>Thermo Fisher Scientific</td>
			<td>AM9930</td>
			<td></td>
		</tr>
		<tr>
			<td>Probumin Bovine Serum Albumin Fatty Acid Free, Powder</td>
			<td>Sigma-Aldrich</td>
			<td>820024</td>
			<td></td>
		</tr>
		<tr>
			<td>Qiagen Buffer EB</td>
			<td>Qiagen</td>
			<td>19086</td>
			<td></td>
		</tr>
		<tr>
			<td>Ribolock RNAse inhibitor</td>
			<td>Thermo Fisher Scientific</td>
			<td>EO0382</td>
			<td></td>
		</tr>
		<tr>
			<td>Seurat</td>
			<td>R&#160;</td>
			<td>N/A</td>
			<td></td>
		</tr>
		<tr>
			<td>Sucrose</td>
			<td>Sigma-Aldrich</td>
			<td>S0389</td>
			<td></td>
		</tr>
		<tr>
			<td>SUPERasin 20 U/&#181;L</td>
			<td>Thermo Fisher Scientific</td>
			<td>AM2695</td>
			<td></td>
		</tr>
		<tr>
			<td>ThermoMixer C</td>
			<td>Eppendorf</td>
			<td>&#160;5382000015</td>
			<td></td>
		</tr>
		<tr>
			<td>Tissue homogenizer</td>
			<td>Glass-Col</td>
			<td>099C K54</td>
			<td></td>
		</tr>
		<tr>
			<td>Tris buffer pH 8.0</td>
			<td>Thermo Fisher Scientific</td>
			<td>AM9855G</td>
			<td></td>
		</tr>
		<tr>
			<td>Triton X-100</td>
			<td>Thermo Fisher Scientific</td>
			<td>AC327372500</td>
			<td></td>
		</tr>
		<tr>
			<td>UltraPure 0.5M EDTA pH 8.0</td>
			<td>Gibco</td>
			<td>15575020</td>
			<td></td>
		</tr>
	</tbody>
</table>

isolation of nuclei from human intermuscular adipose tissue and downstream single-nuclei rna sequencing

Intermuscular adipose tissue (IMAT) is a relatively understudied adipose depot located between muscle fibers. IMAT content increases with age and BMI and is associated with metabolic and muscle degenerative diseases; however, an understanding of the biological properties of IMAT and its interplay with the surrounding muscle fibers is severely lacking. In recent years, single-cell and nuclei RNA sequencing have provided us with cell type-specific atlases of several human tissues. However, the cellular composition of human IMAT remains largely unexplored due to the inherent challenges of its accessibility from biopsy collection in humans. In addition to the limited amount of tissue collected, the processing of human IMAT is complicated due to its proximity to skeletal muscle tissue and fascia. The lipid-laden nature of the adipocytes makes it incompatible with single-cell isolation. Hence, single nuclei RNA sequencing is optimal for obtaining high-dimensional transcriptomics at single-cell resolution and provides the potential to uncover the biology of this depot, including the exact cellular composition of IMAT. Here, we present a detailed protocol for nuclei isolation and library preparation of frozen human IMAT for single nuclei RNA sequencing. This protocol allows for the profiling of thousands of nuclei using a droplet-based approach, thus providing the capacity to detect rare and low-abundant cell types.

Author Spotlight: Deciphering the Cellular Mysteries of Intermuscular Adipose Tissue in Humans

Isolation of Nuclei from Human Intermuscular Adipose Tissue and Downstream Single-Nuclei RNA Sequencing

Our research group is trying to understand the cell composition and cell-specific transcriptional profiles of intermuscular adipose tissue or IMAT in humans. IMAT is actually an ectopic adipose depot residing between and around muscle fibers. Computed tomography and MRI have been able to quantify IMAT volume and have recently shown that it increases with both age and BMI, and is also associated with muscle degenerative diseases.In vitro secretome studies have recently shown that IMAT secreted proteins have the ability to influence insulin sensitivity, inflammatory profiles, and also contractile protein expressions in human skeletal muscle. The limited amount of IMAT tissue collected during biopsies and the lipid laden nature of adipocytes make this tissue incompatible with tissue digestion and single cell RNA-Seq. Therefore, we wanted to develop a protocol that performed nuclei isolation on small amounts of tissue that could then be used in downstream single nuclei RNA-Seq.This protocol will enable researchers to determine the compositional and cell-specific transcriptional alterations that occur in IMAT in different metabolic disease states and in response to interventions. We hope that this information will be crucial in developing new therapeutic strategies to help alleviate metabolic disease by either targeting IMAT directly or its secreted factors. The field severely lacks data on the biology of IMAT, its cellular origins, and communication with other cells, resident both within and outside of IMAT, as well as its molecular responses to lifestyle interventions, such as diet and exercise or pharmacotherapy.All of these are key research questions for our group.

This workflow was designed to guide the processing of frozen human IMAT samples to obtain gene expression profiles at single nuclei resolution, enabling cell type identification. Here, one representative IMAT sample from a participant in the SOMMA study is presented.
The first step of any analysis of snRNA-seq data is to evaluate the quality of the data to identify poor-quality nuclei, which should potentially be removed from the dataset. Importantly, the filtering steps and thresholds should ...

Read this Scientific Article Protocol about Author Spotlight: Deciphering the Cellular Mysteries of Intermuscular Adipose Tissue in Humans at JoVE.com

The biology of intermuscular adipose tissue (IMAT) is largely unexplored due to the limited accessibility of human tissue. Here, we present a detailed protocol for nuclei isolation and library preparation of frozen human IMAT for single nuclei RNA sequencing to identify the cellular composition of this unique adipose depot.

Intermuscular adipose tissue (IMAT) is a relatively understudied adipose depot located between muscle fibers. IMAT content increases with age and BMI and ...

isolation-nuclei-from-human-intermuscular-adipose-tissue-downstream

Research

JoVE Journal

Biology

360 ビュー.  AdventHealth. 私たちの研究グループでは、ヒトにおける筋肉間脂肪組織(IMAT)の細胞組成と細胞特異的な転写プロファイルの理解を目指しています。IMATは、実際には筋繊維の間や周囲に存在する異所性脂肪貯蔵庫です。コンピューター断層撮影とMRIは、IMATボリュームを定量化することができ、最近、年齢とBMIの両方で増加し、筋肉変性疾患にも関連していることが示されています。

ビデオ: 著者スポットライト:ヒトの筋肉間脂肪組織の細胞の謎を解読する

The biology of intermuscular adipose tissue (IMAT) is largely unexplored due to the limited accessibility of human tissue. Here, we present a detailed protocol for nuclei isolation and library preparation of frozen human IMAT for single nuclei RNA sequencing to identify the cellular composition of this unique adipose...

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measuring in vivo adipose tissue kinetics in humans using the deuterium (2h)-labeling approach

Measuring In Vivo Adipose Tissue Kinetics in Humans Using the Deuterium 2H-Labeling Approach

Presented here is a protocol to measure in vivo adipose tissue kinetics in humans using the deuterium (2H)-labeling...

Measuring In Vivo Adipose Tissue Kinetics in Humans Using the Deuterium (2H)-Labeling Approach

pulverization and homogenization of frozen human intermuscular adipose tissue samples for nuclei isolation

Pulverization and Homogenization of Frozen Human Intermuscular Adipose Tissue Samples for Nuclei Isolation

single-cell nuclei isolation from homogenized human intermuscular adipose tissue samples for rna sequencing

Single-Cell Nuclei Isolation from Homogenized Human Intermuscular Adipose Tissue Samples for RNA Sequencing

semi-automated isolation of the stromal vascular fraction from murine white adipose tissue using a tissue dissociator

Author Spotlight: Semi-Automated Isolation of the Stromal Vascular Fraction from Murine White Adipose Tissue Using a Tissue Dissociator  

This protocol describes the semi-automated isolation of the stromal vascular fraction (SVF) from murine adipose tissue to obtain preadipocytes and achieve adipocyte differentiation in vitro. Using a tissue dissociator for collagenase digestion reduces experimental variation and increases...

Semi-Automated Isolation of Murine White Adipose Tissue

dissection, histological processing, and gene expression analysis of murine supraclavicular brown adipose tissue

Author Spotlight: Optimizing Supraclavicular Brown Adipose Tissue Extraction for Genetic Analysis

Here, we provide a practical procedure for dissecting and performing histological and gene expression analyses of murine supraclavicular brown adipose...

Morphological and Molecular Characterization of the scBAT in Mice

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isolation, culture, and adipogenic induction of stromal vascular fraction-derived preadipocytes from mouse periaortic adipose tissue

Author Spotlight: The Significance of Isolation, Culture, and Adipogenic Induction of SVF-Derived Preadipocytes from Mouse Perivascular Adipose Tissue 

Here, we describe the isolation, culture, and adipogenic induction of stromal vascular fraction-derived preadipocytes from mouse periaortic adipose tissue, allowing for the study of perivascular adipose tissue function and its relationship with vascular...

Culturing Preadipocytes Isolated from Murine Perivascular Adipose Tissue

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studying adipose endothelial cell/adipocyte cross-talk in human subcutaneous adipose tissue

Author Spotlight: Insights into Cardiometabolic Diseases with Subcutaneous Adipose Tissue Microvasculature Studies 

Here, we describe a protocol for isolating, culturing, and phenotyping microvascular endothelial cells from human subcutaneous adipose tissue (hSATMVECs). Additionally, we describe an experimental model of hSATMVEC-adipocyte cross-talk.

Human SATMVECs: Isolation and Adipocyte Cross-Talk Studies

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isolation and identification of mesenchymal stem cells derived from adipose tissue of sprague dawley rats

Author Spotlight: Isolation and Identification of Mesenchymal Stem Cells Derived from Adipose Tissue of Sprague Dawley Rats  

This protocol describes a methodology for isolating and identifying adipose tissue-derived mesenchymal stem cells (MSCs) from Sprague Dawley rats.

Adipose Tissue-Derived Stem Cell Isolation and Characterization

using a combination of indirect calorimetry, infrared thermography, and blood glucose levels to measure brown adipose tissue thermogenesis in humans

Using a Combination of Indirect Calorimetry, Infrared Thermography, and Blood Glucose Levels to Measure Brown Adipose Tissue Thermogenesis in Humans

Here, we present a protocol to quantify the physiological significance of the impact of brown adipose tissue (BAT) activity on human metabolism. This is achieved by combining carbohydrate loading and indirect calorimetry with measurements of supraclavicular changes in temperature. This novel approach can help develop a pharmacological target for BAT thermogenesis in...

effects of desmodium caudatum on gastrointestinal hormones and intestinal flora in rats with gastritis

Author Spotlight: Exploring the Mysteries of Sichuan&#039;s Herbal Medicine in Chinese Medicine Research

The present protocol describes the method for analyzing intestinal flora using Illumina-based 16S rRNA gene sequencing and provides a framework for evaluating the effectiveness of herbal...

&lt;i&gt;Desmodium caudatum &lt;/i&gt; Decoction&#039;s Impact on Intestinal Microbiota of Rats

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isolation, in vitro expansion, and characterization of mesenchymal stem cells from mouse epididymal adipose tissue

Author Spotlight: Advancing Treatment Approaches with Adipose-Derived Stem Cells

The adipose tissue is an excellent source of mesenchymal stem cells. Here, we bring the step-by-step extraction, cultivation, and characterization of adipose tissue-derived stem cells (ADSCs) from Swiss mice epididymal adipose tissue.

Primary Culture of Adipose Tissue Derived Stem Cells from Mouse Epididymis

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fiber type identification of human skeletal muscle

Author Spotlight: Deciphering the Mysteries of Skeletal Muscle Fiber Types Using the MyDoBID Technique 

This protocol demonstrates single-fiber isolation from freeze-dried human skeletal muscle and fiber-type classification according to Myosin heavy chain (MHC) isoform using the dot blotting technique. Identified MHC I and II fiber samples can then be further analyzed for fiber type-specific differences in protein expression using western...

MyDoBID- A Novel Technique for Identifying Muscle Fiber Types Efficiently

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infrared thermography for the detection of changes in brown adipose tissue activity

Infrared Thermography for the Detection of Changes in Brown Adipose Tissue Activity

Here, we present a protocol for measuring brown adipose tissue activity after a meal in humans and laboratory...

isolation of adipose tissue immune cells

Isolation of Adipose Tissue Immune Cells

Adipose tissue (AT) is a site of intense immune cell activation and interaction.  Almost all cells of the immune system are present in AT and their ratios are altered by obesity.  Proper isolation, quantification, and characterization of AT immune cell populations are critical for understanding their role in immunometabolic...

Studying Adipose Endothelial Cell/Adipocyte Cross-Talk in Human Subcutaneous Adipose Tissue

3d modeling of the lateral ventricles and histological characterization of periventricular tissue in humans and mouse

3D Modeling of the Lateral Ventricles and Histological Characterization of Periventricular Tissue in Humans and Mouse

Using MRI scans (human), 3D imaging software, and immunohistological analysis, we document changes to the brain&#8217;s lateral ventricles. Longitudinal 3D mapping of lateral ventricle volume changes and characterization of periventricular cellular changes that occur in the human brain due to aging or disease are then modeled in mice.

chromatin immunoprecipitation of murine brown adipose tissue

Chromatin Immunoprecipitation of Murine Brown Adipose Tissue

Here we describe a protocol for efficient chromatin immunoprecipitation (ChIP) followed by high-throughput DNA sequencing (ChIP-seq) of brown adipose tissue (BAT) isolated from a mouse. This protocol is suitable for both mapping histone modifications and investigating genome-wide localization of non-histone proteins of interest in...