The authors wish to thank Carl Hobbs and Lindsey Majoram for their technical assistance, and Professor Pat Doherty for use of microscopy facilities. Dr. Agley was supported by a studentship from King&#8217;s College London. Funding from the Spurrell Trust is also acknowledged.

NOTE: For the studies performed in our lab all subjects gave their written, informed consent to participate and all experiments were performed with UK National Health Service Ethics Committee approval (London Research Ethics Committee; reference: 10/H0718/10) and in accordance with the Human Tissue Act and Declaration of Helsinki.
1. Initial Preparation Prior to Muscle Biopsy (15 min)
<ol>
	<li>Make human skeletal muscle growth medium. To a graduated sterile 50 ml conical tube add 2.5 ml of ...

<ol>
	<li>Mauro, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Satellite+cell+of+skeletal+muscle+fibres.">Satellite cell of skeletal muscle fibres.</a> J. Cell Biol. 9, 493-495 (1961).</li><li>Hawke, T. J., Garry, D. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Myogenic+satellite+cells:+physiology+to+molecular+biology.">Myogenic satellite cells: physiology to molecular biology.</a> J. Appl. Physiol. 91, 534-551 (2001).</li><li>Yin, H., Price, F., Rudnicki, M. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Satellite+Cells+and+the+Muscle+Stem+Cell+Niche.">Satellite Cells and the Muscle Stem Cell Niche.</a> Physiol. Rev. 93, 23-67 (2013).</li><li>Alsharidah, 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=Primary+human+muscle+precursor+cells+obtained+from+young+and+old+donors+produce+similar+proliferative,+differentiation+and+senescent+profiles+in+culture.">Primary human muscle precursor cells obtained from young and old donors produce similar proliferative, differentiation and senescent profiles in culture.</a> Aging Cell. 12, 333-344 (2013).</li><li>Agley, C. C., Rowlerson, A. M., Velloso, C. P., Lazarus, N. R., Harridge, S. D. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Human+skeletal+muscle+fibroblasts,+but+not+myogenic+cells,+readily+undergo+adipogenic+differentiation.">Human skeletal muscle fibroblasts, but not myogenic cells, readily undergo adipogenic differentiation.</a> J. Cell Sci. 126, 5610-5625 (2013).</li><li>Murphy, M. M., Lawson, J. A., Mathew, S. J., Hutcheson, D. A., Kardon, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Satellite+cells,+connective+tissue+fibroblasts+and+their+interactions+are+crucial+for+muscle+regeneration.">Satellite cells, connective tissue fibroblasts and their interactions are crucial for muscle regeneration.</a> Development. 138, 3625-3637 (2011).</li><li>Webster, C., Pavlath, G. K., Parks, D. R., Walsh, F. S., Blau, H. M. <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+human+myoblasts+with+the+fluorescence-activated+cell+sorter.">Isolation of human myoblasts with the fluorescence-activated cell sorter.</a> Exp. Cell Res. 174, 252-265 (1988).</li><li>Pasut, A., Jones, A. E., Rudnicki, M. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Isolation+and+Culture+of+Individual+Myofibers+and+their+Satellite+Cells+from+Adult+Skeletal+Muscle.">Isolation and Culture of Individual Myofibers and their Satellite Cells from Adult Skeletal Muscle.</a> J. Vis Exp. , e50074 (2013).</li><li>Kuang, S., Kuroda, K., Le Grand, F., Rudnicki, M. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Asymmetric+Self-Renewal+and+Commitment+of+Satellite+Stem+Cells+in+Muscle.">Asymmetric Self-Renewal and Commitment of Satellite Stem Cells in Muscle.</a> Cell. 129, 999-1010 (2007).</li><li>Mackey, A. 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=Assessment+of+satellite+cell+number+and+activity+status+in+human+skeletal+muscle+biopsies.">Assessment of satellite cell number and activity status in human skeletal muscle biopsies.</a> Muscle a d Nerve. 40, 455-465 (2009).</li><li>Stewart, J. 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=Characterization+of+proliferating+human+skeletal+muscle-derived+cells+in+vitro:+Differential+modulation+of+myoblast+markers+by+TGF-&#946;2.">Characterization of proliferating human skeletal muscle-derived cells in vitro: Differential modulation of myoblast markers by TGF-&#946;2.</a> J. Cell. Physiol. 196, 70-78 (2003).</li><li>Miltenyi, S., M&#252;ller, W., Weichel, W., Radbruch, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=High+gradient+magnetic+cell+separation+with+MACS.">High gradient magnetic cell separation with MACS.</a> Cytometry. 11, 231-238 (1990).</li><li>Clarke, C., Davies, S., Brooks, S. A., Schumacher, U. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Ch.+2.+Methods+in+Molecular+Medicine.">Ch. 2. Methods in Molecular Medicine.</a> Metastasis Research Protocols. 58, 17-23 (2001).</li><li>Gr&#252;tzkau, A., Radbruch, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Small+but+mighty:+How+the+MACS-technology+based+on+nanosized+superparamagnetic+particles+has+helped+to+analyze+the+immune+system+within+the+last+20+years.">Small but mighty: How the MACS-technology based on nanosized superparamagnetic particles has helped to analyze the immune system within the last 20 years.</a> Cytometry Part A. 77A, 643-647 (2010).</li><li>Tomlinson, M. J., Tomlinson, S., Yang, X. B., Kirkham, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cell+separation:+Terminology+and+practical+considerations.">Cell separation: Terminology and practical considerations.</a> Journal of Tissue Engineering. 4, (2013).</li><li>Agley, C. C., Velloso, C. P., Lazarus, N. R., Harridge, S. D. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=An+Image+Analysis+Method+for+the+Precise+Selection+and+Quantitation+of+Fluorescently+Labeled+Cellular+Constituents:+Application+to+the+Measurement+of+Human+Muscle+Cells+in+Culture.">An Image Analysis Method for the Precise Selection and Quantitation of Fluorescently Labeled Cellular Constituents: Application to the Measurement of Human Muscle Cells in Culture.</a> J. Histochem. Cytochem. 60, 428-438 (2012).</li><li>Danoviz, M., Yablonka-Reuveni, Z., DiMario, J. X. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Ch.+2.+Methods+in+Molecular+Biology.">Ch. 2. Methods in Molecular Biology.</a> Myogenesis. 798, 21-52 (2012).</li><li>Bergstr&#246;m, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Muscle+electrolytes+in+man.+Determined+by+neutron+activation+analysis+on+needle+biopsy+specimens.+A+study+on+normal+subjects,+kidney+patients,+and+patients+with+chronic+diarrhoea.">Muscle electrolytes in man. Determined by neutron activation analysis on needle biopsy specimens. A study on normal subjects, kidney patients, and patients with chronic diarrhoea.</a> Scand. J. Clin. Lab. Invest. 14, 7-100 (1962).</li><li>Chazaud, B., 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=Satellite+cells+attract+monocytes+and+use+macrophages+as+a+support+to+escape+apoptosis+and+enhance+muscle+growth.">Satellite cells attract monocytes and use macrophages as a support to escape apoptosis and enhance muscle growth.</a> The Journal of Cell Biology. 163, 1133-1143 (2003).</li><li>Abou-Khalil, 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=Autocrine+and+Paracrine+Angiopoietin+1/Tie-2+Signaling+Promotes+Muscle+Satellite+Cell+Self-Renewal.">Autocrine and Paracrine Angiopoietin 1/Tie-2 Signaling Promotes Muscle Satellite Cell Self-Renewal.</a> Cell Stem Cell. 5, 298-309 (2009).</li><li>Timpl, R., Kvonder Mark, . <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Role+of+laminin+and+fibronectin+in+selecting+myogenic+versus+fibrogenic+cells+from+skeletal+muscle+cells+in.">Role of laminin and fibronectin in selecting myogenic versus fibrogenic cells from skeletal muscle cells in.</a> 117, 628-635 (1986).</li><li>Lichtman, J. W., Conchello, J. -. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Fluorescence+microscopy.">Fluorescence microscopy.</a> Nat Meth. 2, 910-919 (2005).</li><li>Koopman, R., Schaart, G., Hesselink, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Optimisation+of+oil+red+O+staining+permits+combination+with+immunofluorescence+and+automated+quantification+of+lipids.">Optimisation of oil red O staining permits combination with immunofluorescence and automated quantification of lipids.</a> Histochem. Cell Biol. 116, 63-68 (2001).</li><li>Rossner, M., Yamada, K. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=What's+in+a+picture?+The+temptation+of+image+manipulation.">What's in a picture? The temptation of image manipulation.</a> The Journal of Cell Biology. 166, 11-15 (2004).</li><li>Zinchuk, V., Grossenbacher-Zinchuk, O. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Recent+advances+in+quantitative+colocalization+analysis:+Focus+on+neuroscience.">Recent advances in quantitative colocalization analysis: Focus on neuroscience.</a> Prog. Histochem. Cytochem. 44, 125-172 (2009).</li><li>Johnson, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Not+seeing+is+not+believing:+improving+the+visibility+of+your+fluorescence+images.">Not seeing is not believing: improving the visibility of your fluorescence images.</a> Mol. Biol. Cell. 23, 754-757 (2012).</li><li>Waters, J. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Accuracy+and+precision+in+quantitative+fluorescence+microscopy.">Accuracy and precision in quantitative fluorescence microscopy.</a> The Journal of Cell Biology. 185, 1135-1148 (2009).</li><li>Pawley, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+39+steps:+A+cautionary+tale+of+quantitative+3-D+fluorescence+microscopy.">The 39 steps: A cautionary tale of quantitative 3-D fluorescence microscopy.</a> Biotechniques. 28, 884-887 (2000).</li><li>Bolte, S., Cordeli&#232;res, F. P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+guided+tour+into+subcellular+colocalization+analysis+in+light+microscopy.">A guided tour into subcellular colocalization analysis in light microscopy.</a> J. Microsc. 224, 213-232 (2006).</li><li>Brown, C. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Fluorescence+microscopy+-+avoiding+the+pitfalls.">Fluorescence microscopy - avoiding the pitfalls.</a> J. Cell Sci. 120, 1703-1705 (2007).</li><li>Bareja, 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=Human+and+Mouse+Skeletal+Muscle+Stem+Cells:+Convergent+and+Divergent+Mechanisms+of+Myogenesis.">Human and Mouse Skeletal Muscle Stem Cells: Convergent and Divergent Mechanisms of Myogenesis.</a> PLoS ONE. 9, e90398 (2014).</li><li>Castiglioni, 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=Isolation+of+Progenitors+that+Exhibit+Myogenic/Osteogenic+Bipotency+In+by+Fluorescence-Activated+Cell+Sorting+from+Human+Fetal+Muscle.">Isolation of Progenitors that Exhibit Myogenic/Osteogenic Bipotency In by Fluorescence-Activated Cell Sorting from Human Fetal Muscle.</a> Stem Cell Reports. 2, 560 (2014).</li><li>Fukada, S. -. 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=CD90-positive+cells,+an+additional+cell+population,+produce+laminin+&#945;2+upon+transplantation+to+dy3k/dy3k+mice.">CD90-positive cells, an additional cell population, produce laminin &#945;2 upon transplantation to dy3k/dy3k mice.</a> Exp. Cell Res. 314, 193-203 (2008).</li><li>Stickland, N. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Muscle+development+in+the+human+fetus+as+exemplified+by+m.+sartorius:+a+quantitative+study.">Muscle development in the human fetus as exemplified by m. sartorius: a quantitative study.</a> J. Anat. 132, 557-579 (1981).</li></ol>

We have described an immunomagentic sorting procedure for the selective enrichment of human muscle-derived precursors from small samples of muscle biopsy material. This technique has been invaluable in our lab for overcoming the loss of human muscle-derived cultures to fibroblasts, but also for understanding the unique behavior of distinct populations of muscle-derived progenitors. Once purified myogenic cells can be investigated for changes in protein and/or gene expression, or used for downstream experiments.
<p cl...

The repair and regeneration of skeletal muscle requires the action of satellite cells1, the myogenic stem cells2,3. In vivo these cells exist in a reversibly quiescent state located between the sarcolemma and basal lamina of every myofibre, but become activated to proliferate, fuse and differentiate as muscle tissue is damaged, repaired and regenerated3. Satellite cells can be isolated from young and elderly human muscle biopsy samples using enzymatic digestion4 and their myogenic properties can subsequently be studied in primary culture5. The efficiency of this isolation process in regard to both yield and purity of cell population depends on the methods used and can vary from sample to sample. The two main adherent cell types obtained from enzymatic digestion are the satellite cells (now termed myogenic cells or muscle precursor cells), identified initially as CD56+/desmin cells, and muscle-derived fibroblasts, identified as CD56&#8211; and TE7+ cells5. Fibroblasts have a rapid proliferative rate and do not undergo irreversible growth arrest and terminal differentiation upon cell-cell contact like myogenic cells; thus in mixed populations, fibroblasts may overrun myogenic cells to dominate the culture.
Fibroblasts have often been viewed as an irritation for muscle biologists, however, there is now a growing interest in fibroblasts as cells worthy of study in their own right, particularly as they have been shown to have a cooperative role with myogenic cells during muscle repair6. The isolation and purification of different cell types from human muscle is thus an important methodological consideration when trying to investigate the innate behavior of both cell types in culture. Fluorescence-activated cell sorting (FACS) is a method by which cells can be sorted for further study and/or counted and analyzed. FACS has been shown to reliably enrich human myogenic cells, but the yield of cells for subsequent culture has thus far not been high7. Given the limited replication potential of somatic cells such as satellite cell-derived myogenic cells and the very poor proliferation and differentiation associated with senescence4, more gentle approaches are required. Single muscle fiber cultures offer another, less aggressive, means of obtaining murine satellite cells still resident in their sublaminal niche and after their activation in culture8,9. However, this is often not possible from human muscle biopsy material (because fibres can rarely be obtained from tendon to tendon) meaning that this technique may not be accessible to many research labs interested in studying human muscle-derived cells. Moreover, the single fiber technique only provides very limited cell numbers.
Here we describe a system of sorting based on the gentle enzymatic digestion of cells using collagenase and dispase followed by two successive rounds of magnetic activated cell sorting (MACS) which gives both a high purity (&#62;95% myogenic cells) and yield (~2.8 x 106 &#177; 8.87 x 105 cells/g tissue) for experiments in culture. CD56 is considered the gold standard surface marker for the identification of human satellite cells in situ10 and in vitro11 and provides the ideal surface marker candidate for bead attachment. In this approach CD56 antibodies conjugated to iron oxide and polysaccharide-containing superparamagnetic beads are bound to cells and passed through a high gradient magnetic cell separation column placed in a strong magnetic field12,13. The separation columns are filled with a matrix of ferromagnetic steel wool or iron spheres which serve to focus magnetic field lines towards their surface generating strong magnetic field gradients (~4tesla)14. In these columns even slightly magnetic cells are attracted and adsorbed to their surface14. Unbound (CD56&#8210;) cells pass through the column whereas CD56+ cells labeled with magnetic microbeads are retained until removal from the magnetic field12,15.
Cell suspensions from any stage of the sorting process can be plated at the desired density for further experimentation. Following a given intervention the cellular constituents can be identified using immunocytochemistry, imaged using wide-field or confocal fluorescence microscopy and analyzed quantitatively using an image analysis approach that allows rapid objective measurement of all labeled cells in any given image. In our laboratory we have used this double immunomagnetic sorting approach followed by image analysis16 to demonstrate that CD56&#8211; human fibroblasts readily transdifferentiate into adipocytes, whilst myogenic cells of satellite origin are highly resistant to this adipogenic conversion5.

<table border="0" cellpadding="0" cellspacing="0">
	<tbody>
		<tr height="19">
			<td height="19" style="height:19px;width:169px;">Collagenase&#160; D</td>
			<td style="width:111px;">Roche&#160;</td>
			<td style="width:89px;">11088866001</td>
			<td style="width:140px;"></td>
		</tr>
		<tr height="37">
			<td height="37" style="height:37px;width:169px;">Dispase II</td>
			<td style="width:111px;">Sigma</td>
			<td style="width:89px;">D4693-1G</td>
			<td style="width:140px;">Must be filter sterilized before use</td>
		</tr>
		<tr height="19">
			<td height="19" style="height:19px;width:169px;">Trypsin/EDTA</td>
			<td style="width:111px;">(Gibco) Invitrogen</td>
			<td style="width:89px;">15400-054</td>
			<td style="width:140px;"></td>
		</tr>
		<tr height="19">
			<td height="19" style="height:19px;width:169px;">100 micron cell strainer</td>
			<td style="width:111px;">BD Biosciences</td>
			<td style="width:89px;">352360</td>
			<td style="width:140px;"></td>
		</tr>
		<tr height="37">
			<td height="37" style="height:37px;width:169px;">Collagen solution ( 3 mg/ml in 0.1% acetic acid)</td>
			<td style="width:111px;">Sigma, Dorset, UK</td>
			<td style="width:89px;">C8919&#160;</td>
			<td style="width:140px;"></td>
		</tr>
		<tr height="37">
			<td height="37" style="height:37px;width:169px;">Minisart SRP15 syringe filter (0.2 micron)</td>
			<td style="width:111px;">Sartorius</td>
			<td style="width:89px;">17573ACK</td>
			<td style="width:140px;">Polytetrafluorethylene (PTFE) membrane</td>
		</tr>
		<tr height="55">
			<td height="55" style="height:55px;width:169px;">CD56 human Microbeads</td>
			<td style="width:111px;">Miltenyi Biotech</td>
			<td style="width:89px;">130-050-401</td>
			<td style="width:140px;">Be aware of the limited shelf life of microbeads</td>
		</tr>
		<tr height="37">
			<td height="37" style="height:37px;width:169px;">Anti- fibroblast Microbeads, human</td>
			<td style="width:111px;">Miltenyi Biotech</td>
			<td style="width:89px;">130-050-601</td>
			<td style="width:140px;"></td>
		</tr>
		<tr height="19">
			<td height="19" style="height:19px;width:169px;">40 &#956;m Pre-separation filters</td>
			<td style="width:111px;">Miltenyi Biotech</td>
			<td style="width:89px;">130-041-407</td>
			<td style="width:140px;"></td>
		</tr>
		<tr height="129">
			<td height="129" style="height:129px;width:169px;">Large Cell Collumns</td>
			<td style="width:111px;">Miltenyi Biotech</td>
			<td style="width:89px;">130-042-202</td>
			<td style="width:140px;">These columns come with a flow resistor. Use of the flow resistor is not necessary to obtain the high myogenic purities described here.</td>
		</tr>
		<tr height="19">
			<td height="19" style="height:19px;width:169px;">LS columns&#160;</td>
			<td style="width:111px;">Miltenyi Biotech</td>
			<td style="width:89px;">130-042-401</td>
			<td style="width:140px;"></td>
		</tr>
		<tr height="55">
			<td height="55" style="height:55px;width:169px;">MiniMacs Seperator</td>
			<td style="width:111px;">Miltenyi Biotech</td>
			<td style="width:89px;">130-042-102</td>
			<td style="width:140px;">This separator fits the large cell column but not the LS column.&#160;</td>
		</tr>
		<tr height="19">
			<td height="19" style="height:19px;width:169px;">MidiMACS</td>
			<td style="width:111px;">Miltenyi Biotech&#160;</td>
			<td style="width:89px;">130-042-302</td>
			<td style="width:140px;"></td>
		</tr>
		<tr height="19">
			<td height="19" style="height:19px;width:169px;">MACS multistand</td>
			<td style="width:111px;">Miltenyi Biotech</td>
			<td style="width:89px;">130-042-303</td>
			<td style="width:140px;"></td>
		</tr>
		<tr height="37">
			<td height="37" style="height:37px;width:169px;">BSA</td>
			<td style="width:111px;">Sigma</td>
			<td style="width:89px;"></td>
			<td style="width:140px;">Must be filter sterilized before use</td>
		</tr>
		<tr height="19">
			<td height="19" style="height:19px;width:169px;">Oil Red O</td>
			<td style="width:111px;">Sigma</td>
			<td style="width:89px;">O0625</td>
			<td style="width:140px;"></td>
		</tr>
		<tr height="19">
			<td height="19" style="height:19px;width:169px;">Triethyl phosphate</td>
			<td style="width:111px;">Sigma</td>
			<td style="width:89px;">538728</td>
			<td style="width:140px;"></td>
		</tr>
		<tr height="166">
			<td height="166" style="height:166px;width:169px;">Whatman Paper</td>
			<td style="width:111px;">Sigma</td>
			<td style="width:89px;">Z241121-1PAK</td>
			<td style="width:140px;">No. 42, Ashless. To prepare the filter fold the circular filter paper to make a semi circle, then fold the semi-circle in half again to form a cone shape. Fit the cone into a funnel for filtering.&#160;</td>
		</tr>
		<tr height="19">
			<td height="19" style="height:19px;width:169px;"></td>
			<td style="width:111px;"></td>
			<td style="width:89px;"></td>
			<td style="width:140px;"></td>
		</tr>
		<tr height="74">
			<td height="74" style="height:74px;width:169px;">ProLong Gold Antifade Reagent</td>
			<td style="width:111px;">Molecular Probes, Invitrogen</td>
			<td style="width:89px;">P36930</td>
			<td style="width:140px;">This can be purchased with or without DAPI and does not quench initial fluorescence.</td>
		</tr>
		<tr height="55">
			<td height="55" style="height:55px;width:169px;">AxioVision</td>
			<td style="width:111px;">Carl Zeiss</td>
			<td style="width:89px;">Contact Zeiss</td>
			<td style="width:140px;"></td>
		</tr>
		<tr height="52">
			<td height="52" style="height:52px;width:169px;">Adobe Photoshop CS5 Extended</td>
			<td style="width:111px;">Adobe (purchased from Pugh Computers)</td>
			<td>ADPH16982*&#160;</td>
			<td style="width:140px;"></td>
		</tr>
	</tbody>
</table>

isolation and quantitative immunocytochemical characterization of primary myogenic cells and fibroblasts from human skeletal muscle

The repair and regeneration of skeletal muscle requires the action of satellite cells, which are the resident muscle stem cells. These can be isolated from human muscle biopsy samples using enzymatic digestion and their myogenic properties studied in culture. Quantitatively, the two main adherent cell types obtained from enzymatic digestion are: (i) the satellite cells (termed myogenic cells or muscle precursor cells), identified initially as CD56+ and later as CD56+/desmin+ cells and (ii) muscle-derived fibroblasts, identified as CD56&#8211; and TE-7+. Fibroblasts proliferate very efficiently in culture and in mixed cell populations these cells may overrun myogenic cells to dominate the culture. The isolation and purification of different cell types from human muscle is thus an important methodological consideration when trying to investigate the innate behavior of either cell type in culture. Here we describe a system of sorting based on the gentle enzymatic digestion of cells using collagenase and dispase followed by magnetic activated cell sorting (MACS) which gives both a high purity (&#62;95% myogenic cells) and good yield (~2.8 x 106 &#177; 8.87 x 105 cells/g tissue after 7 days in vitro) for experiments in culture. This approach is based on incubating the mixed muscle-derived cell population with magnetic microbeads beads conjugated to an antibody against CD56 and then passing cells though a magnetic field. CD56+ cells bound to microbeads are retained by the field whereas CD56&#8211; cells pass unimpeded through the column. Cell suspensions from any stage of the sorting process can be plated and cultured. Following a given intervention, cell morphology, and the expression and localization of proteins including nuclear transcription factors can be quantified using immunofluorescent labeling with specific antibodies and an image processing and analysis package.

Purified myogenic cells and fibroblasts can be cultured in adipogenic differentiation medium for three days followed by adipogenic nutrition medium from anywhere between 7-30 days to assess their potential for adipogenesis. Using the purified cell populations, Oil Red O staining in combination with immunostaining for adipogenic and myogenic lineage markers showed that only the fibroblast fraction was capable of adipogenic differentiation (Figure 2). The massive accumulation of fat by the fibroblasts is v...

Watch this Scientific Journal Video about Isolation and Quantitative Immunocytochemical Characterization of Primary Myogenic Cells and Fibroblasts from Human Skeletal Muscle at JoVE.com

Isolation and Quantitative Immunocytochemical Characterization of Primary Myogenic Cells and Fibroblasts from Human Skeletal Muscle

The main adherent cell types derived from human muscle are myogenic cells and fibroblasts. Here, cell populations are enriched using magnetic-activated cell sorting based on the CD56 antigen. Subsequent immunolabelling with specific antibodies and use of image analysis techniques allows quantification of cytoplasmic and nuclear characteristics in individual cells.

The repair and regeneration of skeletal muscle requires the action of satellite cells, which are the resident muscle stem cells. These can be isolated ...

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Developmental Biology

15.8K 次观看.  King's College London. The main adherent cell types derived from human muscle are myogenic cells and fibroblasts. Here, cell populations are enriched using magnetic-activated cell sorting based on the CD56 antigen. Subsequent immunolabelling with specific antibodies and use of image analysis techniques allows quantification of cytoplasmic and nuclear characteristics in individual cells. 

视频: Isolation and Quantitative Immunocytochemical Characterization of Primary Myogenic Cells and Fibroblasts from Human Skeletal Muscle

The main adherent cell types derived from human muscle are myogenic cells and fibroblasts. Here, cell populations are enriched using magnetic-activated cell sorting based on the CD56 antigen. Subsequent immunolabelling with specific antibodies and use of image analysis techniques allows quantification of cytoplasmic and nuclear characteristics in individual cells.

preparation and culture of myogenic precursor cells/primary myoblasts from skeletal muscle of adult and aged humans

Preparation and Culture of Myogenic Precursor Cells/Primary Myoblasts from Skeletal Muscle of Adult and Aged Humans

This protocol describes a robust, reproducible and simple method of isolation and culture of myoblast progenitor cells from the skeletal muscle of adult and aged people. The muscles used here include foot and leg muscles. This approach enables the isolation of an enriched population of primary myoblasts for functional...

parallel measurement of circadian clock gene expression and hormone secretion in human primary cell cultures

Parallel Measurement of Circadian Clock Gene Expression and Hormone Secretion in Human Primary Cell Cultures

Here, we describe settings to monitor in parallel circadian bioluminescence and the secretory activity of human islet cells and primary myotubes. For this, we employed lentiviral gene delivery of a luciferase core clock reporter, followed by in vitro synchronization and collection of outflow medium by continuous cell...

isolation and characterization of exosomes from skeletal muscle fibroblasts

Isolation and Characterization of Exosomes from Skeletal Muscle Fibroblasts

This protocol illustrates the 1) the isolation and culture of primary fibroblasts from the adult mouse gastrocnemius muscle as well as 2) purification and characterization of exosomes using a differential ultracentrifugation method combined with sucrose density gradients followed by western blot...

isolation, culture, and characterization of primary schwann cells, keratinocytes, and fibroblasts from human foreskin

Isolation, Culture, and Characterization of Primary Schwann Cells, Keratinocytes, and Fibroblasts from Human Foreskin

The study of wound healing associated with musculoskeletal injury often requires the assessment of in vitro interactions between Schwann cells (SCs), keratinocytes, and fibroblasts. This protocol describes the isolation, culturing, and characterization of these primary cells from the human foreskin.

isolation, culture, characterization, and differentiation of human muscle progenitor cells from the skeletal muscle biopsy procedure

Isolation, Culture, Characterization, and Differentiation of Human Muscle Progenitor Cells from the Skeletal Muscle Biopsy Procedure

We present techniques for isolating, culturing, characterizing, and differentiating human primary muscle progenitor cells (hMPCs) obtained from skeletal muscle biopsy tissue. hMPCs obtained and characterized through these methods can be used to subsequently address research questions related to human myogenesis and skeletal muscle...

isolation, culture, and characterization of primary dermal fibroblasts from human keloid tissue

Isolation, Culture, and Characterization of Primary Dermal Fibroblasts from Human Keloid Tissue

This study describes an optimized protocol for establishing primary fibroblasts from keloid tissues that can effectively and steadily provide pure and viable...

identification, isolation, and characterization of fibro-adipogenic progenitors (faps) and myogenic progenitors (mps) in skeletal muscle in the rat

Identification, Isolation, and Characterization of Fibro-Adipogenic Progenitors FAPs and Myogenic Progenitors MPs in Skeletal Muscle in the Rat

This protocol outlines a method to isolate Fibro-adipogenic progenitors (FAPs) and myogenic progenitors (MPs) from rat skeletal muscle. Utilization of the rat in muscle injury models provides increased tissue availability from atrophic muscle for the analysis and a larger repertoire of validated methods to assess muscle strength and gait in free-moving...

Identification, Isolation, and Characterization of Fibro-Adipogenic Progenitors (FAPs) and Myogenic Progenitors (MPs) in Skeletal Muscle in the Rat

isolation and differentiation of primary myoblasts from mouse skeletal muscle explants

Isolation and Differentiation of Primary Myoblasts from Mouse Skeletal Muscle Explants

Myoblasts are proliferating precursor cells that differentiate to form polynucleated myotubes and eventually skeletal muscle myofibers. Here, we present a protocol for efficient isolation and culture of primary myoblasts from young adult mouse skeletal muscles. The method enables molecular, genetic, and metabolic studies of muscle cells in...

tissue processing and isolation of primary fibroblasts from the human vagina

This protocol demonstrates a reliable and effective technique to isolate primary fibroblasts from either premenopausal or postmenopausal human vaginal tissue. Existing protocols for vaginal fibroblast isolation do not consider the challenges of cell isolation from senescent tissue. Vaginal tissue was obtained from women after pelvic organ prolapse...

Tissue Processing and Isolation of Primary Fibroblasts from the Human Vagina

isolation of primary murine skeletal muscle microvascular endothelial cells

Isolation of Primary Murine Skeletal Muscle Microvascular Endothelial Cells

Microvascular endothelial cells of skeletal muscles (MMEC) shape the inner wall of muscle capillaries and regulate both, exchange of fluids/molecules and migration of (immune) cells between muscle tissue and blood. Isolation of primary murine MMEC, as described here, enables comprehensive in vitro investigations of the &#34;myovascular...

adult and embryonic skeletal muscle microexplant culture and isolation of skeletal muscle stem cells

Adult and Embryonic Skeletal Muscle Microexplant Culture and Isolation of Skeletal Muscle Stem Cells

The micro-dissected explants technique is a robust and reliable method for isolating proliferative skeletal muscle cells from juvenile, adult or embryonic muscles as a source of skeletal muscle stem cells. Uniquely, these cells have been clonally derived to produce skeletal muscle stem cell lines used for in vivo...

isolation and culture of individual myofibers and their satellite cells from adult skeletal muscle

Isolation and Culture of Individual Myofibers and their Satellite Cells from Adult Skeletal Muscle

Isolation and culture of myofibers is the gold standard in vitro system to study the transition of satellite cells through quiescence, activation and differentiation.  Importantly, the single myofiber culture system preserves the myofiber/stem cell association, which is an essential component of the muscle stem cell...

isolation of blood-vessel-derived multipotent precursors from human skeletal muscle

Isolation of Blood-vessel-derived Multipotent Precursors from Human Skeletal Muscle

Blood vessels within human skeletal muscle harbor several multi-lineage precursor populations that are ideal for regenerative applications. This isolation method allows simultaneous purification of three multipotent precursor cell populations respectively from three structural layers of blood vessels: myogenic endothelial cells from intima, pericytes from media, and adventitial cells from...

facs-isolation and culture of fibro-adipogenic progenitors and muscle stem cells from unperturbed and injured mouse skeletal muscle

FACS-Isolation and Culture of Fibro-Adipogenic Progenitors and Muscle Stem Cells from Unperturbed and Injured Mouse Skeletal Muscle

The precise identification of fibro-adipogenic progenitor cells (FAPs) and muscle stem cells (MuSCs) is critical to studying their biological function in physiological and pathological conditions. This protocol provides guidelines for the isolation, purification, and culture of FAPs and MuSCs from adult mouse muscles.

mitochondrial isolation from skeletal muscle

Mitochondrial Isolation from Skeletal Muscle

This protocol describes a procedure to study the respiration of mitochondria isolated from skeletal muscles. This method was adapted from Scorrano et al. (2007).  The mitochondrial isolation procedure requires about 2 hours.  The mitochondrial respiration can be completed in about 1...

isolation and characterization of adult cardiac fibroblasts and myofibroblasts

Isolation and Characterization of Adult Cardiac Fibroblasts and Myofibroblasts

Obtaining a pure population of fibroblasts is crucial to studying their role in wound repair and fibrosis. Described here is a detailed method to isolate fibroblasts and myofibroblasts from uninjured and injured mouse hearts followed by characterization of their purity and functionality by immunofluorescence, RTPCR, fluorescence-assisted cell sorting, and collagen gel...

isolation of single-fiber from freeze-dried human skeletal muscle

Isolation of Single-Fiber from Freeze-Dried Human Skeletal Muscle  

isolation and culture of primary synovial macrophages and fibroblasts from murine arthritis tissue

Author Spotlight: Isolation and Culture of Primary Synovial Macrophages and Fibroblasts from Murine Arthritis Tissue  

The present study provides a modified protocol to isolate synovial macrophages and fibroblasts from murine inflammatory arthritis tissue.

Isolation and Culture of Primary Synovial Macrophages and Fibroblasts from Murine Arthritis Tissue

isolation and culture of primary schwann cells from a human dermis

This video demonstrates a protocol for isolating and culturing Schwann cells from human dermis tissues. The human dermis contains various cell types, including fibroblasts and Schwann cells. After isolation, the cells are treated with an antimitotic agent to eliminate proliferating fibroblasts, resulting in a pure culture of Schwann...

Isolation and Culture of Primary Schwann Cells from a Human Dermis

Using Isolated Mitochondria from Minimal Quantities of Mouse Skeletal Muscle for High throughput Microplate Respiratory Measurements

Skeletal muscle mitochondria play a specific role in many disease pathologies. As such, the measurement of oxygen consumption as an indicator of mitochondrial function in this tissue has become more prevalent. Although many technologies and assays exist that measure mitochondrial respiratory pathways in a variety of cells, tissue and species, there is currently a void in the literature in regards to the compilation of these assays using isolated mitochondria from mouse skeletal muscle for use in microplate based technologies. Importantly, the use of microplate based respirometric assays is growing among mitochondrial biologists as it allows for high throughput measurements using minimal quantities of isolated mitochondria. Therefore, a collection of microplate based respirometric assays were developed that are able to assess mechanistic changes/adaptations in oxygen consumption in a commonly used animal model. The methods presented herein provide step-by-step instructions to perform these assays with an optimal amount of mitochondrial protein and reagents, and high precision as evidenced by the minimal variance across the dynamic range of each assay.

The methods presented provide step-by-step instructions for the performance of a collection of microplate based respirometric assays using isolated mitochondria from minimal quantities of mouse skeletal muscle. These assays are able to measure mechanistic changes/adaptations in mitochondrial oxygen consumption in a commonly used animal model.

Skeletal muscle mitochondria play a specific role in many disease pathologies. As such, the measurement of oxygen consumption as an indicator of ...

Isolation and Characterization of Single Cells from Zebrafish Embryos

The zebrafish (Danio rerio) is a powerful model organism to study vertebrate development. Though many aspects of zebrafish embryonic development have been described at the morphological level, little is known about the molecular basis of cellular changes that occur as the organism develops. With recent advancements in microfluidics and multiplexing technologies, it is now possible to characterize gene expression in single cells. This allows for investigation of heterogeneity between individual cells of specific cell populations to identify and classify cell subtypes, characterize intermediate states that occur during cell differentiation, and explore differential cellular responses to stimuli. This study describes a protocol to isolate viable, single cells from zebrafish embryos for high throughput multiplexing assays. This method may be rapidly applied to any zebrafish embryonic cell type with fluorescent markers. An extension of this method may also be used in combination with high throughput sequencing technologies to fully characterize the transcriptome of single cells. As proof of principle, the relative abundance of cardiac differentiation markers was assessed in isolated, single cells derived from nkx2.5 positive cardiac progenitors. By evaluation of gene expression at the single cell level and at a single time point, the data support a model in which cardiac progenitors coexist with differentiating progeny. The method and work flow described here is broadly applicable to the zebrafish research community, requiring only a labeled transgenic fish line and access to microfluidics technologies.

This protocol describes a method for isolating single cells from zebrafish embryos, enriching for cells of interest, capturing zebrafish cells in microfluidic based single cell multiplex systems, and assessing gene expression from single cells.

The zebrafish (Danio rerio) is a powerful model organism to study vertebrate development. Though many aspects of zebrafish embryonic development have been ...

Establishment of Proliferative Tetraploid Cells from Nontransformed Human Fibroblasts

Polyploid (mostly tetraploid) cells are often observed in preneoplastic lesions of human tissues and their chromosomal instability has been considered to be responsible for carcinogenesis in such tissues. Although proliferative polyploid cells are requisite for analyzing chromosomal instability of polyploid cells, creating such cells from nontransformed human cells is rather challenging. Induction of tetraploidy by chemical agents usually results in a mixture of diploid and tetraploid populations, and most studies employed fluorescence-activated cell sorting or cloning by limiting dilution to separate tetraploid from diploid cells. However, these procedures are time-consuming and laborious. The present report describes a relatively simple protocol to induce proliferative tetraploid cells from normal human fibroblasts with minimum contamination by diploid cells. Briefly, the protocol is comprised of the following steps: arresting cells in mitosis by demecolcine (DC), collecting mitotic cells after shaking off, incubating collected cells with DC for an additional 3 days, and incubating cells in drug-free medium (They resume proliferation as tetraploid cells within several days). Depending on cell type, the collection of mitotic cells by shaking off might be omitted. This protocol provides a simple and feasible method to establish proliferative tetraploid cells from normal human fibroblasts. Tetraploid cells established by this method could be a useful model for studying chromosome instability and the oncogenic potential of polyploid human cells.

Although proliferative polyploid cells are necessary to analyze chromosomal instability of polyploid cells, creating such cells from nontransformed human cells is not easy. The present report describes relatively simple procedures to establish proliferative tetraploid cells free of a diploid population from normal human fibroblasts.

Polyploid (mostly tetraploid) cells are often observed in preneoplastic lesions of human tissues and their chromosomal instability has been considered to ...

Skeletal muscle homeostasis depends on muscle growth (hypertrophy), atrophy and regeneration. During ageing and in several diseases, muscle wasting occurs. Loss of muscle mass and function is associated with muscle fiber type atrophy, fiber type switching, defective muscle regeneration associated with dysfunction of satellite cells, muscle stem cells, and other pathophysiological processes. These changes are associated with changes in intracellular as well as local and systemic niches. In addition to most commonly used rodent models of muscle ageing, there is a need to study muscle homeostasis and wasting using human models, which due to ethical implications, consist predominantly of in vitro cultures. Despite the wide use of human Myogenic Progenitor Cells (MPCs) and primary myoblasts in myogenesis, there is limited data on using human primary myoblast and myotube cultures to study molecular mechanisms regulating different aspects of age-associated muscle wasting, aiding in the validation of mechanisms of ageing proposed in rodent muscle. The use of human MPCs, primary myoblasts and myotubes isolated from adult and aged people, provides a physiologically relevant model of molecular mechanisms of processes associated with muscle growth, atrophy and regeneration. Here we describe in detail a robust, inexpensive, reproducible and efficient protocol for the isolation and maintenance of human MPCs&#160;and their progeny&#160;&#8212; myoblasts and myotubes from human muscle samples using enzymatic digestion. Furthermore, we have determined the passage number at which primary myoblasts from adult and aged people undergo senescence in an in vitro culture. Finally, we show the ability to transfect these myoblasts and the ability to characterize their proliferative and differentiation capacity and propose their suitability for performing functional studies of molecular mechanisms of myogenesis and muscle wasting in vitro.

This protocol describes a robust, reproducible and simple method of isolation and culture of myoblast progenitor cells from the skeletal muscle of adult and aged people. The muscles used here include foot and leg muscles. This approach enables the isolation of an enriched population of primary myoblasts for functional studies.

Skeletal muscle homeostasis depends on muscle growth (hypertrophy), atrophy and regeneration. During ageing and in several diseases, muscle wasting ...

Isolation and Characterization of Mesenchymal Stromal Cells from Human Umbilical Cord and Fetal Placenta

The human umbilical cord (UC) and placenta are non-invasive, primitive and abundant sources of mesenchymal stromal cells (MSCs) that have increasingly gained attention because they do not pose any ethical or moral concerns. Current methods to isolate MSCs from UC yield low amounts of cells with variable proliferation potentials. Since UC is an anatomically-complex organ, differences in MSC properties may be due to the differences in the anatomical regions of their isolation. In this study, we first dissected the cord/placenta samples into three discrete anatomical regions: UC, cord-placenta junction (CPJ), and fetal placenta (FP). Second, two distinct zones, cord lining (CL) and Wharton&#39;s jelly (WJ), were separated. The explant culture technique was then used to isolate cells from the four sources. The time required for the primary culture of cells from the explants varied depending on the source of the tissue. Outgrowth of the cells occurred within 3 - 4 days of the CPJ explants, whereas growth was observed after 7 - 10 days and 11 - 14 days from CL/WJ and FP explants, respectively. The isolated cells were adherent to plastic and displayed fibroblastoid morphology and surface markers, such as CD29, CD44, CD73, CD90, and CD105, similarly to bone marrow (BM)-derived MSCs. However, the colony-forming efficiency of the cells varied, with CPJ-MSCs and WJ-MSCs showing higher efficiency than BM-MSCs. MSCs from all four sources differentiated into adipogenic, chondrogenic, and osteogenic lineages, indicating that they were multipotent. CPJ-MSCs differentiated more efficiently in comparison to other MSC sources. These results suggest that the CPJ is the most potent anatomical region and yields a higher number of cells, with greater proliferation and self-renewal capacities in vitro. In conclusion, the comparative analysis of the MSCs from the four sources indicated that CPJ is a more promising source of MSCs for cell therapy, regenerative medicine, and tissue engineering.

Here, we present a protocol for the dissection of human umbilical cord (UC) and fetal placenta sample into cord lining (CL), Wharton&#39;s jelly (WJ), cord-placenta junction (CPJ), and fetal placenta (FP) for the isolation and characterization of mesenchymal stromal cells (MSCs) using the explant culture technique.

The human umbilical cord (UC) and placenta are non-invasive, primitive and abundant sources of mesenchymal stromal cells (MSCs) that have increasingly ...

Isolation of Human Myoblasts, Assessment of Myogenic Differentiation, and Store-operated Calcium Entry Measurement

Satellite cells (SC) are muscle stem cells located between the plasma membrane of muscle fibers and the surrounding basal lamina. They are essential for muscle regeneration. Upon injury, which occurs frequently in skeletal muscles, SCs are activated. They proliferate as myoblasts and differentiate to repair muscle lesions. Among many events that take place during muscle differentiation, cytosolic Ca2+ signals are of great importance. These Ca2+ signals arise from Ca2+ release from internal Ca2+ stores, as well as from Ca2+ entry from the extracellular space, particularly the store-operated Ca2+ entry (SOCE). This paper describes a methodology used to obtain a pure population of human myoblasts from muscle samples collected after orthopedic surgery. The tissue is mechanically and enzymatically digested, and the cells are amplified and then sorted by flow cytometry according to the presence of specific membrane markers. Once obtained, human myoblasts are expanded and committed to differentiate by removing growth factors from the culture medium. The expression levels of specific transcription factors and in vitro immunofluorescence are used to assess the myogenic differentiation process in control conditions and after silencing proteins involved in Ca2+ signaling. Finally, we detail the use of Fura-2 as a ratiometric Ca2+ probe that provides reliable and reproducible measurements of SOCE.

Here, we describe a methodology to obtain a pure population of human myoblasts from adult muscle tissue. These cells are used to study in vitro skeletal muscle differentiation and, in particular, to study proteins involved in Ca2+ signaling.

Satellite cells (SC) are muscle stem cells located between the plasma membrane of muscle fibers and the surrounding basal lamina. They are essential for ...

Identification of Skeletal Muscle Satellite Cells by Immunofluorescence with Pax7 and Laminin Antibodies

Immunofluorescence is an effective method that helps to identify different cell types on tissue sections. In order to study the desired cell population, antibodies for specific cell markers are applied on tissue sections. In adult skeletal muscle, satellite cells (SCs) are stem cells that contribute to muscle repair and regeneration. Therefore, it is important to visualize and trace the satellite cell population under different physiological conditions. In resting skeletal muscle, SCs reside between the basal lamina and myofiber plasma membrane. A commonly used marker for identifying SCs on the myofibers or in cell culture is the paired box protein Pax7. In this article, an optimized Pax7 immunofluorescence protocol on skeletal muscle sections is presented that minimizes non-specific staining and background. Another antibody that recognizes a protein (laminin) of the basal lamina was also added to help identify SCs. Similar protocols can also be used to perform double or triple labeling with Pax7 and antibodies for additional proteins of interest.

The precise identification of satellite cells is essential for studying their functions under various physiological and pathological conditions. This article presents a protocol to identify satellite cells on adult skeletal muscle sections by immunofluorescence-based staining.

Immunofluorescence is an effective method that helps to identify different cell types on tissue sections. In order to study the desired cell population, ...

The Isolation and Culture of Primary Epicardial Cells Derived from Human Adult and Fetal Heart Specimens

The epicardium, an epithelial cell layer covering the myocardium, has an essential role during cardiac development, as well as in the repair response of the heart after ischemic injury. When activated, epicardial cells undergo a process known as epithelial to mesenchymal transition (EMT) to provide cells to the regenerating myocardium. Furthermore, the epicardium contributes via secretion of essential paracrine factors. To fully appreciate the regenerative potential of the epicardium, a human cell model is required. Here we outline a novel cell culture model to derive primary epicardial derived cells (EPDCs) from human adult and fetal cardiac tissue. To isolate EPDCs, the epicardium is dissected from the outside of the heart specimen and processed into a single cell suspension. Next, EPDCs are plated and cultured in EPDC medium containing the ALK 5-kinase inhibitor SB431542 to maintain their epithelial phenotype. EMT is induced by stimulation with TGF&#946;. This method enables, for the first time, the study of the process of human epicardial EMT in a controlled setting, and facilitates gaining more insight in the secretome of EPDCs that may aid heart regeneration. Furthermore, this uniform approach allows for direct comparison of human adult and fetal epicardial behavior.

The epicardium plays a crucial role in the development and repair of the heart by providing cells and growth factors to the myocardial wall. Here, we describe a method to culture human primary epicardial cells that enables the study and comparison of their developmental and adult characteristics.

The epicardium, an epithelial cell layer covering the myocardium, has an essential role during cardiac development, as well as in the repair response of ...

RNA-based Reprogramming of Human Primary Fibroblasts into Induced Pluripotent Stem Cells

Induced pluripotent stem cells (iPSCs) have proven to be a valuable tool to study human development and disease. Further advancing iPSCs as a regenerative therapeutic requires a safe, robust, and expedient reprogramming protocol. Here, we present a clinically relevant, step-by-step protocol for the extremely high-efficiency reprogramming of human dermal fibroblasts into iPSCs using a non-integrating approach. The core of the protocol consists of expressing pluripotency factors (SOX2, KLF4, cMYC, LIN28A, NANOG, OCT4-MyoD fusion) from in vitro transcribed messenger RNAs synthesized with modified nucleotides (modified mRNAs). The reprogramming modified mRNAs are transfected into primary fibroblasts every 48 h together with mature embryonic stem cell-specific microRNA-367/302 mimics for two weeks. The resulting iPSC colonies can then be isolated and directly expanded in feeder-free conditions. To maximize efficiency and consistency of our reprogramming protocol across fibroblast samples, we have optimized various parameters including the RNA transfection regimen, timing of transfections, culture conditions, and seeding densities. Importantly, our method generates high-quality iPSCs from most fibroblast sources, including difficult-to-reprogram diseased, aged, and/or senescent samples.

Here we describe a clinically relevant, high-efficiency, feeder-free method to reprogram human primary fibroblasts into induced pluripotent stem cells using modified mRNAs encoding reprogramming factors and mature microRNA-367/302 mimics. Also included are methods to assess reprogramming efficiency, expand clonal iPSC colonies, and confirm expression of the pluripotency marker TRA-1-60.

Induced pluripotent stem cells (iPSCs) have proven to be a valuable tool to study human development and disease. Further advancing iPSCs as a regenerative ...

Isolation and Characterization of Human Umbilical Cord-derived Mesenchymal Stem Cells from Preterm and Term Infants

Mesenchymal stem cells (MSCs) have considerable therapeutic potential and attract increasing interest in the biomedical field. MSCs are originally isolated and characterized from bone marrow (BM), then acquired from tissues including adipose tissue, synovium, skin, dental pulp, and fetal appendages such as placenta, umbilical cord blood (UCB), and umbilical cord (UC). MSCs are a heterogeneous cell population with the capacity for (1) adherence to plastic in standard culture conditions, (2) surface marker expression of CD73+/CD90+/CD105+/CD45-/CD34-/CD14-/CD19-/HLA-DR- phenotypes, and (3) trilineage differentiation into adipocytes, osteocytes, and chondrocytes, as currently defined by the International Society for Cellular Therapy (ISCT). Although BM is the most widely used source of MSCs, the invasive nature of BM aspiration ethically limits its accessibility. Proliferation and differentiation capacity of MSCs obtained from BM generally decline with the age of the donor. In contrast, fetal MSCs obtained from UC have advantages such as vigorous proliferation and differentiation capacity. There is no ethical concern for UC sampling, as it is typically regarded as medical waste. Human UC starts to develop with continuing growth of the amniotic cavity at 4-8 weeks of gestation and keeps growing until reaching 50-60 cm in length, and it can be isolated during the whole newborn delivery period. To gain insight into the pathophysiology of intractable diseases, we have used UC-derived MSCs (UC-MSCs) from infants delivered at various gestational ages. In this protocol, we describe the isolation and characterization of UC-MSCs from fetuses/infants at 19-40 weeks of gestation.

Human umbilical cord (UC) can be obtained during the perinatal period as a result of preterm, term, and postterm delivery. In this protocol, we describe the isolation and characterization of UC-derived mesenchymal stem cells (UC-MSCs) from fetuses/infants at 19-40 weeks of gestation.