This study was funded by a Mosaic grant (017.009.009) from The Netherlands Organization for Scientific Research (NWO) and a Start grant (S-13-167C) for young investigators from the AO Foundation. Z.Y.R is supported by the National Institutes of Health (grant # AG021566, AG035377, NS090051).

本文所述的所有实验，按照荷兰法律和法规（RU-DEC 2013-205）批准由当地局从Radboud大学奈梅亨动物实验。 1.细胞外基质凝胶点<ol><li>隔离之前执行以下步骤之一天： <ol><li>解冻等分试样的细胞外基质凝胶（100微升），在4℃下至少为1.5小时。稀释在Dulbecco改良的Eagle氏培养基1:10用4500毫克/升葡萄糖，4mM的L-谷氨酰胺，和110毫克/毫升丙酮酸钠（DMEM）中。保持在4℃的细胞外基质凝胶在任何时候。注：突然的温度变化会导致不均匀的涂层和晶体的形成。 </li><li>保持在冰上的稀释细胞外基质凝胶溶液15分钟。 </li><li>预寒意20微升微量10分钟。 </li><li>把8孔室玻片的100毫米的培养皿和10分钟的盘转移到冷表面（ 例如一个冰柜包）。</li><li>使用预冷微量把在各一滴10μl的细胞外基质凝胶的井。保持培养皿上冰冷的表面至少在7分钟（ 图1A）。 </li><li>完全除去剩余的细胞外基质凝胶（ 图1B），并干燥该井在37℃下过夜。 </li></ol></li></ol>头部解剖2.肌（咬肌，二腹肌和吊具膀帆） <ol><li>解剖前，准备50毫升磷酸盐缓冲盐水（PBS）中补充有2％青霉素 - 链霉素（P / S）的。置于冰上。 </li><li>一位年轻的成年大鼠（9周），与CO 2 / O 2的安乐死后，斩首的头部和从头部取下的皮肤。头转移到冰冷的PBS，在50毫升管补充有2％P / S。 </li><li>咬肌（从第1鳃弓派生） <ol><li>将头一侧上一个硅胶垫和皮下ñ修复eedles（ 图2A）。 </li><li>确定腮腺和面神经（ 图2A）。揭露深筋膜覆盖腺体。切开筋膜，用剪刀切开取出腺体。确定外耳道。从茎乳孔追踪面神经并小心地用手术刀刀片第15号取出颞，颧，颊分支机构。 </li><li>通过去除筋膜释放咬肌浅头。确定咬肌两种浅表和深部负责人。跟踪浅表头，直到上颌骨颧突插入其厚腱腱膜。 </li><li>在颧突与直钳分开它的起源肌腱。用手术刀片15号或夹层剪刀，小心它的生活（ 图2B）削减它。 </li><li>解剖咬肌的肤浅头，直到它的角度插入和T的下半部分他侧向下颌骨的支的表面用手术刀刀片号15（ 图2C）。现在，完全去除肌肉。 </li></ol></li><li>二腹肌后腹（从第二鳃弓派生） <ol><li>将头在上的硅胶垫仰卧位置和与皮下注射针（ 图3A）固定。 </li><li>取出皮下脂肪既覆舌下和下颌下腺。接下来，除去浅筋膜，用剪刀清扫腺体。暴露二腹肌（前，后腹）。 </li><li>抓住后腹的前肌腱采用了直板钳，剪，小心翼翼地解剖它，直到它在鼓泡（ 图3B）的由来。做同样的对侧。 </li></ol></li><li>提腭帆肌（从第4个鳃弓派生） <ol><li>二腹肌后腹的解剖后，本地化舌骨肌，横向拉，并小心地将其删除（ 图4A）。 </li><li>本地化提腭帆是在插入鼓膜泡（ 图4A）的肌腱。仔细解剖，并削减其两侧。 </li><li>寻找气管和运行背后的食道。提起食道，并露出咽，喉和软腭。 </li><li>本地化软腭插入提腭帆所在的区域，并切断其松动（ 图4B）。 注意：直接解剖后，小心地从立体显微镜下每一块肌肉肌腱删除和结缔组织。迅速浸没在乙醇70％所有的样品，并将其转移到冰冷的PBS在15毫升管补充2％P / S。 </li></ol></li></ol> 3.隔离卫星细胞<ol><li>执行以下步骤准备从3组肌肉SC隔离： <ol><li>准备7.5毫升0.1％链霉蛋白酶的DMEM。过滤通过0.22微米的过滤器的溶液。预温热的水浴将溶液在37℃下分离之前10分钟。 </li><li>制备35的DMEM补充有10％马血清（HS）和1％P / S的溶液中。还预先温暖，在37℃的水浴中。 </li><li>制备其由DMEM中补充有20％牛胎儿血清（FBS），10％HS，1％P / S和1％鸡胚提取物（CEE）15毫升培养基。在水浴中预暖在37℃。 </li><li>预涂层6塑料移液器（10毫升）与HS和干燥使用前至少10分钟。 </li></ol></li><li>在培养罩，转移的每个肌成一个6孔板的孔中。使用解剖剪，肌肉小块约2毫米。要小心，不要讳言组织过多。 </li><li>小心加入2.5毫升0.1％的链霉蛋白酶溶液到每个孔中并在37℃进行60分钟。经过20，40和60分钟，轻轻摇动板。注：确切的所需时n中孵育取决于如年龄的动物和应变的因素。 </li><li>在显微镜下监视。检查肌肉片段和停止酶消化当纤维束得到松动外观（ 图5）。 </li><li>添加2.5的DMEM毫升补充有10％HS和1％P / S。转移到15毫升管和离心管，在400×g离心5分钟。弃去上清液倾析。 </li><li>加5的10ml DMEM补充有10％HS和1％P / S。吸取的溶液上下用10毫升塑料吸管（研磨）为至少20倍以均化该组织。 </li><li>离心管，在200×g离心4分钟。收集上清液并转移到15毫升管。 </li><li>加5的10ml DMEM补充有10％HS和1％P / S。吸管再次用10毫升塑料吸管，直到组织碎片通过吸管传递容易。 </li><li>离心管，在200×g离心4分钟，并收集在15ml试管上清液。 </li><li> PUT斯达康一个细胞过滤网（40微米）至50ml管中，并含有离解的细胞的上清液转移到过滤器。用1毫升的DMEM最大细胞恢复洗。 </li><li>离心管在1000×g离心10分钟，并弃用吸管将上清液。 </li><li>悬浮在300微升培养基中的颗粒和细胞计数在血球。 </li></ol>在细胞外基质凝胶点4分化卫星细胞<ol><li>稀释细胞悬浮液，以获得1.5×10 3个细胞于10微升培养基中。 </li><li>固定的腔室玻片用胶带盖和标记用黑色标记在对象玻璃的底侧的斑点。 </li><li>用微量，把一滴10微升细胞悬液到细胞外基质凝胶点。检查显微镜是否细胞悬液滴已正确放置当场下。孵育六个小时，在37℃。 </li><li>小心LY添加400μl的培养基（补充有20％胎牛血清，10％HS，1％P / S和1％CEE）的孵育三天，在37℃。 注：在这一点上，新鲜分离的SC受到大面积创伤（酶消化和苛刻的研磨），他们需要恢复。期间的前三天37.下一页不干扰细胞，培养基可根据实验的类型而改变。 细胞外基质凝胶斑点可以接种高细胞密度（1.5-2.5×10 3 /20μL）对分化测定。培养培养基（DMEM补充有20％胎牛血清，10％HS，1％P / S和1％鸡胚胎提取物）可以每三天更换。 </li><li>另外，如果扩张和传球需要按照下面的步骤： <ol><li>解冻等分试样的细胞外基质凝胶（500微升），在4℃下至少为1.5小时。在稀释DMEM 1:10，按照点1.1.1的建议。 </li><li>预寒意10毫升吸管10分钟在4＃176;℃。 </li><li>转移3 T75烧瓶在冷表面（ 例如一个冰柜包）10分钟。 </li><li>使用预冷吸管把1毫升细胞外基质凝胶到每个烧瓶中。检查的表面被完全覆盖。保持瓶在冰冷的表面至少在7分钟（ 图1A）。 </li><li>完全除去用10毫升吸管剩余细胞外基质凝胶和干井，在37℃进行1小时。 </li><li>计数后，重悬在新鲜分离的SCs在10ml培养基（DMEM补充有20％胎牛血清，10％HS，1％P / S和1％鸡胚胎提取物）中的预涂覆T75烧瓶和种子。 </li><li>三天后，改变培养基（和每三天），直到80％汇合为止。传代，用PBS洗T75烧瓶三次。下一步加入1 ml 0.25％胰蛋白酶溶液，孵育3分钟，在37℃。重悬的9ml培养基（DMEM补充有20％胎牛血清，10％HS，1％P / S和1％鸡胚提取物）和离心机在200×g离心5分钟。弃去上清液。计数后，重悬1×10 6个细胞在1000微升培养基并冷冻的细胞。 </li></ol></li></ol>

The authors have no conflicting interests to disclose.

雪旺从不同branchiomeric头肌从一个9周龄的Wistar大鼠和对细胞外基质凝胶斑点直接分离培养无需事先膨胀和传代。分离后，将细胞计数并接种在相同细胞密度。对于三种不同的肌肉的平行隔离，这种方法需要大约4小时。为了避免培养污染，一个关键的步骤是快速清洗酒精70％的肌肉解剖后。 期间的SC隔离它切割肌肉组织切成小块（约2mm），但避免过多切碎，因为这将导致由于细胞损伤的小细胞产量是重要的。此外，酶消化的持续时间必须小心地在显微镜下检查，以避免进一步的损害。消化的目的是离解的肌纤维。因为90％以上的分离的细胞的表达表达Pax7，没有进一步纯化是必须的（ 图6-8）。这避免了在其它方法，例如在未涂覆的菜肴14,37,38预镀，分馏上的Percoll 39,40额外的纯化步骤，或fluorescent-或磁性细胞分选41,43。对于研磨有必要促使组织碎片和枪头的开口之间的剪切，因为这可以使机械释放的雪旺。如果用10毫升吸管（直径尖端内：1毫米）的研磨是困难的，有5毫升（直径尖端内：2mm）的移液管可以首先使用。或者，玻璃巴斯德移液管可以在所希望的直径被切割和使用。这种方法简单，高效，允许SC从不同的肌肉样本的同时分离。 在培养板的SCs也可以涂有明胶或胶原蛋白，但我们以前的研究表明，细胞外基质凝胶是好得多的肌源性潜力的维护比胶原38。的细胞外基质凝胶斑点毫米级（10微升/ O 2毫米或20微升/Ø4 MM）允许增殖和SCS与细胞的数量有限的分化研究。为分化测定约8至20倍的细胞较少，需要相比于24孔板（直径15.6毫米），以及约80至200倍更少相比毫米至35毫米的培养皿中（直径35 MM）14,38。 由于细胞外基质凝胶是昂贵的，这种方法也更具有成本效益。此外，该室载玻片可由塑料盖来代替滑动，以进一步降低成本。为细胞外基质的凝胶的制备掩护腔室玻片过夜干燥是必不可少的。作为细胞外基质凝胶斑点是透明的，有必要使用背光来标记斑点在底侧。腔室载玻片固定在一个培养皿容易操纵。进一步的细胞培养扩张是没有必要的，它提供了学习的SMAL的雪旺的可能性LER肌肉或小的肌肉样本。可替代地， 例如 ，用于PCR或肌肉构建如果需要更多的细胞，新鲜分离的SCs可以首先在T75烧瓶如上所述扩大。 雪旺分离使用该协议不适合用于进一步纯化用分离后的流动立即术。有链霉蛋白酶消化导致表面的广泛消化抗原14。了用于细胞培养的马血清和胎牛血清首先必须正确表征隔离之前，因为不同的批号不同的影响成肌细胞增殖和分化。 在最近几年，有一种在从鳃弓和头的中胚层（ 例如眼外肌）24来自肌肉的兴趣与日俱增。已经清楚地表明，头和四肢肌肉具有高度不同的特性。从旧的动物咬肌似乎重新覃它们的再生能力与四肢肌肉25,26的比较。从种姓眼外肌具有强大的增殖和分化能力堪比从头部肌肉种姓，并显示出更大的潜力植入比四肢肌肉旺24。 光纤类型分布和肌球蛋白组合物之间的肌肉群，也物种之间变化。肌肉从第一鳃弓在人类起源同时包含慢速和快速纤维（IIA亚型和IIX），新生儿肌球蛋白和肌球蛋白典型的发展中国家心肌。在这些啮齿动物的肌肉含有约95％的快速纤维肌球蛋白IIa和IIb）44-46。研究禽流感的肌肉显示，从不同的肌纤维类型不同种姓的分化能力。从快速纤维只种姓分化成快肌纤维，而从慢纤维旺能分化成两种类型的纤维47。此外，旺中快肌的百分比纤维比在慢肌纤维48,49更低。这表明，纤维型分布，必须考虑到对研究上的肌肉在颅面区域。类似的腭裂的肌肉，在啮齿动物的LVP包含几乎完全快纤维50。出于这个原因，从LVP种姓适用于腭裂的领域临床前研究。 该协议提供了新的可能性，研究从branchiomeric头部肌肉或其他肌肉更小或更小的肌肉样本得到旺。这将有利于新的疗法的开发，以改善肌肉在颌面区域中的条件的再生如腭裂而且在影响较小的肌肉的其他条件。

An erratum was issue for <a href="http://www.jove.com/video/52802">Isolation and Characterization of Satellite Cells from Rat Head Branchiomeric Muscles</a>. The fourth figure was updated to explain the isolation of the LVP better.

Erratum: Isolation and Characterization of Satellite Cells from Rat Head Branchiomeric Muscles

约1：500至1：1000的新生儿表现出涉及唇部和/或腭（CLP）的一个裂口;因此，这是在人类1中最常见的先天畸形。软腭肌肉是软腭的讲话，吞咽，吸吮和在运作的关键。如果软腭的裂存在时，这些肌肉异常插入腭骨的后端。 软腭上下移动讲话时，防止空气逸出通过鼻子。在上颚裂儿童没有造成这一现象被称为腭咽功能障碍2,3此控制功能。虽然治疗方案是可变的，软腭修复手术发生在儿童早期（6-36个月龄）4。软腭的异常插入肌肉可手术矫正5-7，然而，在7％的腭咽功能障碍仍然存在，以30％的的患者2,3,8-10。 骨骼肌通过卫星细胞（SCS）的作用，以再生能力是公认11,12。在肌肉损伤，旺被激活并迁移到损伤部位。然后，他们增殖，分化和融合形成新的肌纤维或修复受损的人13。静态旺表达转录因子表达Pax7 14,15，而他们的后代，增殖成肌细胞，另外表达生肌决定因子1（MyoD基因）16。分化成肌细胞开始表达肌细胞（肌细胞生成素）17。成肌细胞的终末分化的标志是形成的肌纤维，和肌特异性蛋白质如肌球蛋白重链（MyHC的）16,18的表达。 最近，一些战略已经在再生医学中用于改善四肢肌肉19-23的肌肉再生。在具体研究branchiomeric头部肌肉也很重要，因为它是最近表明，它们从其它肌肉的不同在几个方面24。与肢体肌肉相反，曾有人建议，branchiomeric头部肌肉含有较少的SCs 25，再生速度慢，并损伤26除之后形成更多的纤维结缔组织，增殖从branchiomeric头部肌肉旺还表示其它转录因子。例如，TCF21，颅面肌肉形成的转录因子中强烈表达再生头部肌肉但几乎在再生肢体肌肉25。在CLP患者的软腭肌肉通常更小，更精心组织比较正常腭肌肉27,28。慢速和快速纤维都存在于软腭肌肉但慢纤维更丰富。与此相反，裂肌含有较高比例的快速纤维，并且还减小毛细管供给与正常软腭肌肉29-31对比。快纤维更容易收缩引起的损伤31-33。伴随毛细血管供血不足也可促进纤维化34,35。手术裂闭合后36所有这些方面可能有助于软腭肌肉穷人再生。鉴于此，一个协议的branchiomeric头肌的SCs的分离和表征是关键的。这提供了研究branchiomeric头部肌肉SC生物学的可能性。此外，可以开发基于组织工程的新疗法手术中电和其他条件损害颅面区域后，以促进肌肉再生。 在一般情况下，许旺可以肌肉组织14的离解后得到。切碎，酶消化，并研磨一般都需要从它们的小生释放旺。雪旺可通过预镀上的未涂覆的菜肴14,37,38进行纯化，果actionation上珀39,40，或fluorescent-或磁性细胞分选41-43。在这里，我们提出了一个新的经济和快速的协议，用于卫星细胞从年轻的成年大鼠branchiomeric头部肌肉的隔离。这个协议是基于一个先前的原稿14，并特别适用于小的组织样本。从代表肌肉旺从第1次，2 次 ，和第 4 次鳃弓始发的分离进行说明。分离后，低数量的卫星细胞都在毫米大小的细胞外基质凝胶点来研究其分化培养。这种方法避免了对旺的膨胀和传代的要求。

<table border="0" cellpadding="0" cellspacing="0">
	<tbody>
		<tr>
			<td>Hypodermic Needle 25G 0,5x25m</td>
			<td>BD Microlance</td>
			<td>300400</td>
			<td></td>
		</tr>
		<tr>
			<td>Dissecting scissors</td>
			<td>Braun</td>
			<td>BC154R</td>
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			<td>Micro forceps straight</td>
			<td>Braun</td>
			<td>BD330R</td>
			<td></td>
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			<td>Surgical Scalpel Blade No.15</td>
			<td>Swann-Morton</td>
			<td>0205</td>
			<td></td>
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		<tr>
			<td>Alcohol 70%</td>
			<td>Denteck</td>
			<td>2,010,005</td>
			<td></td>
		</tr>
		<tr>
			<td>Permanox Slide, 8 Chamber</td>
			<td>Thermo Scientific</td>
			<td>177445</td>
			<td></td>
		</tr>
		<tr>
			<td>6 well cell culture plate</td>
			<td>Greiner bio-one</td>
			<td>657160</td>
			<td></td>
		</tr>
		<tr>
			<td>Cell Culture Dishes (100 x 20 mm)</td>
			<td>Greiner bio-one</td>
			<td>664160</td>
			<td></td>
		</tr>
		<tr>
			<td>15 ml sterile conical centrifuge tube</td>
			<td>BD Biosciences</td>
			<td>352097</td>
			<td></td>
		</tr>
		<tr>
			<td>50 ml sterile conical centrifuge tube</td>
			<td>BD Biosciences</td>
			<td>352098</td>
			<td></td>
		</tr>
		<tr>
			<td>Cell strainer (40 &#956;m)</td>
			<td>Gibco</td>
			<td>431750</td>
			<td></td>
		</tr>
		<tr>
			<td>10 mL serological pipette</td>
			<td>Greiner bio-one</td>
			<td>607180</td>
			<td></td>
		</tr>
		<tr>
			<td>20&#181;L FT20</td>
			<td>Greiner bio-one</td>
			<td>774288</td>
			<td></td>
		</tr>
		<tr>
			<td>Matrigel, Phenol-Red Free</td>
			<td>BD Biosciences</td>
			<td>356237</td>
			<td>10 mL</td>
		</tr>
		<tr>
			<td>Pronase</td>
			<td>Calbiochem</td>
			<td>53702</td>
			<td>10KU</td>
		</tr>
		<tr>
			<td>Phosphate Buffered Saline</td>
			<td>Gibco</td>
			<td>14190-144</td>
			<td>500 mL</td>
		</tr>
		<tr>
			<td>Dulbecco&#39;s Modified Eagle Medium, high glucose, GlutaMAX Supplement, pyruvate&#160;</td>
			<td>Gibco</td>
			<td>10569-010</td>
			<td>500 mL</td>
		</tr>
		<tr>
			<td>Fetal Bovine Serum&#160;&#160;</td>
			<td>Fisher Scientific&#160;</td>
			<td>3600511</td>
			<td>500 mL</td>
		</tr>
		<tr>
			<td>Horse Serum</td>
			<td>Gibco</td>
			<td>26050088</td>
			<td>500 mL</td>
		</tr>
		<tr>
			<td>Penicillin-Streptomycin (10,000 U/mL)</td>
			<td>Gibco</td>
			<td>15140-122</td>
			<td>100 mL</td>
		</tr>
		<tr>
			<td>Chicken Embryo Extract</td>
			<td>MP Biomedicals</td>
			<td>2850145</td>
			<td>20 mL</td>
		</tr>
	</tbody>
</table>

isolation and characterization of satellite cells from rat head branchiomeric muscles

Fibrosis and defective muscle regeneration can hamper the functional recovery of the soft palate muscles after cleft palate repair. This causes persistent problems in speech, swallowing, and sucking. In vitro culture systems that allow the study of satellite cells (myogenic stem cells) from head muscles are crucial to develop new therapies based on tissue engineering to promote muscle regeneration after surgery. These systems will offer new perspectives for the treatment of cleft palate patients. A protocol for the isolation, culture and differentiation of satellite cells from head muscles is presented. The isolation is based on enzymatic digestion and trituration to release the satellite cells. In addition, this protocol comprises an innovative method using extracellular matrix gel coatings of millimeter size, which requires only low numbers of satellite cells for differentiation assays.

使用此协议，咬肌（一侧）得到0.8-1×10 6细胞，二腹肌（后腹）得到1.5-2×10 5个细胞，并提腭帆肌产量1-1.5×10 5个细胞。细胞产率取决于肌肉类型的动物，应变和年龄。对于这三个肌肉组间比较，新鲜分离的SCs接种在相同细胞密度（1.5×10 3个/ 10微升）。直接在分离后，90％以上的新鲜分离细胞的表达表达Pax7（ 图6）。 4日，7日和10文化沾满抗表达Pax7，MyoD的，肌细胞生成素和免疫MyHC的。五场任意使用每一个20X的目标培养计数。在第4天大同7和缪D被表达于所有的肌肉群（ 图6和图7和8），SatCs的但是从咬肌和二腹肌后代开始EXPRES唱肌细胞生成早于提腭帆肌（ 图9）。在第10天，肌细胞生成素的表达在所有组中是强烈减少（ 图9）。接种在细胞外基质凝胶点之后的几天，增殖细胞开始融合，形成多核肌管，这表达肌球蛋白重链。小肌管是在第7天（ 图10）清楚可见。在第10天，对肌管的抽搐可以观察到（ 视频1）。 <img alt="图1" src="/files/ftp_upload/52802/52802fig1.jpg" /> 图1：细胞外基质凝胶点在玻片（A）为了便于操作，将8孔室滑动到100毫米的培养皿。每个腔室中吸取10微升细胞外基质凝胶，并把它放在冷的表面（7分）。 （ 二）外过剩矩阵G后玻片埃尔被除去。 <img alt="图2" src="/files/ftp_upload/52802/52802fig2.jpg" /> 图2：动物的侧视图咬肌剖析 （ 一 ）负责人。耳（E），腮腺（P）和面神经（七）。 （ 二）咬肌（MS）和颞肌（T）的肤浅头腱肌腱膜（TE）。用镊子分离从其插入的肌腱。 （三）认真解剖肌肉，直到它的下颌骨升支插入。 E：耳，P：腮腺，VII：面神经，T：颞肌，MS：咬肌，特浅头：肌腱，熔点：咬肌深头。 <img alt="图3" src="/files/ftp_upload/52802/52802fig3.jpg" /> 图3：二腹肌后腹的夹层（。动物一）仰卧位头。本地化颌下腺（SG），咬肌（M），面神经（VII）和胸锁乳突肌（SCM）。取出颌下腺。 （ 二）本地化二腹肌前（AD）和后腹（PD）。采用了直板钳，取后腹的前肌腱，切开它，仔细解剖它，直到它在鼓泡（TY）的由来。 E：耳，SG：颌下腺，VII：面神经，M：咬肌，SMC：胸锁乳突肌，AD：前腹二腹肌，PD：后腹二腹肌，泰：鼓泡。 <img alt="图4" src="/files/ftp_upload/52802/52802fig4.jpg" /> 图4：上睑提腭帆肌的解剖（A）二腹肌（后腹）的解剖后，普遍的看法。舌骨肌（ST）和上睑提肌腱腭帆可以本地化。注气管（T）和食道（ES）运行它的后面。 （B）解除气管和食道咽（P）的被暴露之后。提上睑肌腭帆进入软腭的插入是现在可见。箭头指示解剖软腭与提腭帆肌肉在两侧。 E：耳，ST：舌骨肌，VII：面神经，M：咬肌，AD：前腹二腹肌，PD：后腹二腹肌，T：气管，ES：食道，P：咽部，提*腭帆肌。 <img alt="图5" src="/files/ftp_upload/52802/52802fig5.jpg" /> 图5：肌肉组织（A） 的前外观和（B）的酶消化用链霉蛋白酶后。注意，肌束出现酶消化后，以松开。 图6：大同7免疫染色新鲜分离的SCs，施加到细胞外基质凝胶在隔离结束时（初始组织消化后约6小时）。五场任意用一个10X的目标，平均每场210细胞计数。大约90％的细胞是大同7阳性。 DAPI：蓝色，表达Pax7：红色。比例尺，100微米。 <img alt="图7" src="/files/ftp_upload/52802/52802fig7highres.jpg" width="700" /> 图7：大同7，MyoD的免疫第4天，第7和10的培养物染色抗体表达Pax7和MyoD的免疫染色。 （A - C）和（D - F）4天的代表性显微照片和7个文化从咬肌。 （G和 H </stro纳克&gt;）表达Pax7 +和MyoD的+每显微镜视野核的数目进行计数，并表示为核的总数（DAPI）的百分比。 DAPI：蓝色，表达Pax7：红色，MyoD的：绿色。秤吧，100微米。 <a href="https://www.jove.com/files/ftp_upload/52802/52802fig7highres.jpg" target="_blank">请点击此处查看该图的放大版本。</a> <img alt="图8" src="/files/ftp_upload/52802/52802fig8highres.jpg" width="700" /> 图8：表达Pax7±/±MyoD基因分布在文化从单核细胞培养的咬肌，二腹肌和提腭帆肌（A - C）第4天，第7和第10文化沾满抗表达Pax7和MyoD的免疫染色。细胞的总数量是基于核的总数（DAPI）的。 （D）表达Pax7±/±MyoD基因的CEL量化数据LS。 <a href="https://www.jove.com/files/ftp_upload/52802/52802fig8highres.jpg" target="_blank">请点击此处查看该图的放大版本。</a> <img alt="图9" src="/files/ftp_upload/52802/52802fig9highres.jpg" width="700" /> 图9：肌细胞生成素的免疫染色天4,7和10的培养物染色抗肌细胞生成素。 （A - D）4天的代表性显微照片和7个文化从提腭帆肌。 （E）的肌细胞生成素+每显微镜视野核的数目进行计数，并表示为核的总数（DAPI）的百分比。 （F）数据肌细胞生成素+细胞的定量。 DAPI：蓝色，肌细胞生成素：绿色。秤吧，100微米。 <a href="https://www.jove.com/files/ftp_upload/52802/52802fig9highres.jpg" target="_blank">请点击此处查看该FIGUR的放大版本。</a>即<img alt="图10" src="/files/ftp_upload/52802/52802fig10.jpg" /> 图10：球蛋白重链免疫第4天，第7和10的培养物染色抗肌球蛋白重链（MyHC的）。第4天，7的代表性显微照片，并从二腹肌（DIG）肌肉10培养物。在7天，小肌管存在，而在第10天漫长而精心组织肌管是显而易见的。秤吧，200微米。 <a href="https://www.jove.com/files/ftp_upload/52802/52802fig10large.jpg" target="_blank">请点击此处查看该图的放大版本。</a> 视频1：肌管与抽动抽动肌管两个具有代表性的领域的例子显示了从天二腹肌10文化<a href="https://www.jove.com/files/ftp_upload/52802/Video1.mpg" target="_blank">请点击此处观看该视频。</a>

Watch this Scientific Journal Video about Isolation and Characterization of Satellite Cells from Rat Head Branchiomeric Muscles at JoVE.com

Isolation and Characterization of Satellite Cells from Rat Head Branchiomeric Muscles

这个协议描述了从一个9周龄大鼠branchiomeric头肌卫星细胞的分离。肌肉从不同的鳃弓起源。随后，卫星细胞在局部上光毫米大小来研究其分化培养。这种方法避免了卫星细胞的扩增和传代。

隔离和卫星细胞的表征鼠头Branchiomeric肌肉

Fibrosis and defective muscle regeneration can hamper the functional recovery of the soft palate muscles after cleft palate repair. This causes persistent ...

isolation-characterization-satellite-cells-from-rat-head

Research

JoVE Journal

Developmental Biology

10.8K 次观看.  Radboud University Medical Center. 这个协议描述了从一个9周龄大鼠branchiomeric头肌卫星细胞的分离。肌肉从不同的鳃弓起源。随后，卫星细胞在局部上光毫米大小来研究其分化培养。这种方法避免了卫星细胞的扩增和传代。 

视频: Isolation and Characterization of Satellite Cells from Rat Head Branchiomeric Muscles

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.

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.

从人类骨骼肌成肌原细胞和成纤维细胞的分离和定量免疫细胞化学表征

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

科研

发育生物学

Isolation of Neural Stem/Progenitor Cells from the Periventricular Region of the Adult Rat and Human Spinal Cord

Adult rat and human spinal cord neural stem/progenitor cells (NSPCs) cultured in growth factor-enriched medium allows for the proliferation of multipotent, self-renewing, and expandable neural stem cells. In serum conditions, these multipotent NSPCs will differentiate, generating neurons, astrocytes, and oligodendrocytes. The harvested tissue is enzymatically dissociated in a papain-EDTA solution and then mechanically dissociated and separated through a discontinuous density gradient to yield a single cell suspension which is plated in neurobasal medium supplemented with epidermal growth factor (EGF), basic fibroblast growth factor (bFGF), and heparin. Adult rat spinal cord NSPCs are cultured as free-floating neurospheres and adult human spinal cord NSPCs are grown as adherent cultures. Under these conditions, adult spinal cord NSPCs proliferate, express markers of precursor cells, and can be continuously expanded upon passage. These cells can be studied in vitro in response to various stimuli, and exogenous factors may be used to promote lineage restriction to examine neural stem cell differentiation. Multipotent NSPCs or their progeny can also be transplanted into various animal models to assess regenerative repair.

The adult mammalian spinal cord contains neural stem/progenitor cells (NSPCs) that can be isolated and expanded in culture. This protocol describes the harvesting, isolation, culture, and passaging of NSPCs generated from the periventricular region of the adult spinal cord from the rat and from human organ transplant donors.

从脑室周围地区的成年大鼠和人类脊髓神经分离干/祖细胞

Adult rat and human spinal cord neural stem/progenitor cells (NSPCs) cultured in growth factor-enriched medium allows for the proliferation 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.

分离和斑马鱼胚胎单细胞的表征

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

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.

从人类脐带和胎盘胎儿分离和鉴定间充质干细胞

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

Isolation of Type I and Type II Pericytes from Mouse Skeletal Muscles

Pericytes are perivascular multipotent cells that show heterogeneity in different organs or even within the same tissue. In skeletal muscles, there are at least two pericyte subpopulations (called type I and type II), which express different molecular markers and have distinct differentiation capabilities. Using NG2-DsRed and Nestin-GFP double-transgenic mice, type I (NG2-DsRed+Nestin-GFP-) and type II (NG2-DsRed+Nestin-GFP+) pericytes have been successfully isolated. However, the availability of these double-transgenic mice prevents the widespread use of this purification method. This work describes an alternative protocol that allows for the easy and simultaneous isolation of type I and type II pericytes from skeletal muscles. This protocol utilizes the fluorescence-activated cell sorting (FACS) technique and targets PDGFR&#946;, rather than NG2, together with the Nestin-GFP signal. Following isolation, type I and type II pericytes show distinct morphologies. In addition, type I and type II pericytes isolated with this new method, like those isolated from the double-transgenic mice, are adipogenic and myogenic, respectively. These results suggest that this protocol can be used to isolate pericyte subpopulations from skeletal muscles and possibly from other tissues.

This work describes a FACS-based protocol that allows for easy and simultaneous isolation of type I and type II pericytes from skeletal muscles.

从小鼠骨骼肌分离I型和II型周细胞

Pericytes are perivascular multipotent cells that show heterogeneity in different organs or even within the same tissue. In skeletal muscles, there are at ...

Isolation and Characterization of Primary Rat Valve Interstitial Cells: A New Model to Study Aortic Valve Calcification

Calcific aortic valve disease (CAVD) is characterized by the progressive thickening of the aortic valve leaflets. It is a condition frequently found in the elderly and end-stage renal disease (ESRD) patients, who commonly suffer from hyperphosphatemia and hypercalcemia. At present, there are no medication therapies that can stop its progression. The mechanisms that underlie this pathological process remain unclear. The aortic valve leaflet is composed of a thin layer of valve endothelial cells (VECs) on the outer surfaces of the aortic cusps, with valve interstitial cells (VICs) sandwiched between the VECs. The use of a rat model enables the in vitro study of ectopic calcification based on the in vivo physiopathological serum phosphate (Pi) and calcium (Ca) levels of patients who suffer from hyperphosphatemia and hypercalcemia. The described protocol details the isolation of a pure rat VIC population as shown by the expression of VIC markers: alpha-smooth muscle actin (&#945;-SMA) vimentin and tissue growth factor beta (TGF&#946;) 1 and 2, and the absence of cluster of differentiation (CD) 31, a VEC marker. By expanding these VICs, biochemical, genetic, and imaging studies can be performed to study and unravel the key mediators underpinning CAVD.

This protocol describes the isolation, culture, and calcification of rat-derived valve interstitial cells, a highly physiological in vitro model of calcific aortic valve disease (CAVD). Exploitation of this rat model facilitates CAVD research in exploring the cell and molecular mechanisms that underlie this complex pathological process.

原发性大鼠瓣膜间质细胞的分离与鉴定: 主动脉瓣钙化的新模型研究

Calcific aortic valve disease (CAVD) is characterized by the progressive thickening of the aortic valve leaflets. It is a condition frequently found in ...

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.

Pax7 和层粘连蛋白抗体免疫荧光法鉴定骨骼肌卫星细胞

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

Isolation and Characterization of Cardiac Mesenchymal Stromal Cells from Endomyocardial Bioptic Samples of Arrhythmogenic Cardiomyopathy Patients

A normal adult heart is composed of several different cell types, among which cardiac mesenchymal stromal cells represent an abundant population. The isolation of these cells offers the possibility of studying their involvement in cardiac diseases, and, in addition, provides a useful primary cell model to investigate biological mechanisms.
Here, the method for the isolation of C-MSC from arrhythmogenic cardiomyopathy patients&#39; bioptic samples is described. The endomyocardial biopsy sampling is guided in the right ventricular areas adjacent to the scar visualized by electro-anatomical mapping. The digestion of the biopsies in collagenase and their plating on a plastic dish in culture medium to allow C-MSC growth is described. The isolated cells can be expanded in culture for several passages. To confirm their mesenchymal phenotype, the description of immuno-phenotypical characterization is provided. C-MSC are able to differentiate into several cell types like adipocytes, chondrocytes, and osteoblasts: in the context of ACM, characterized by adipocyte deposits in patients&#39; hearts, the protocols for the adipogenic differentiation of C-MSC and the characterization of lipid droplet accumulation are described.

In this article, a method to isolate cardiac mesenchymal stromal cells from endomyocardial bioptic samples of arrhythmogenic cardiomyopathy patients is provided. Their characterization and the protocol to boost their adipogenic differentiation are described.

致心律失常心肌病患者心内膜心肌活检样间质基质细胞的分离与鉴定

A normal adult heart is composed of several different cell types, among which cardiac mesenchymal stromal cells represent an abundant population. The ...

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.

早产儿和足月婴儿脐带源性间充质干细胞的分离与鉴定

Mesenchymal stem cells (MSCs) have considerable therapeutic potential and attract increasing interest in the biomedical field. MSCs are originally ...

In Vitro Generation of Somite Derivatives from Human Induced Pluripotent Stem Cells

In response to signals such as WNTs, bone morphogenetic proteins (BMPs), and sonic hedgehog (SHH) secreted from surrounding tissues, somites (SMs) give rise to multiple cell types, including the myotome (MYO), sclerotome (SCL), dermatome (D), and syndetome (SYN), which in turn develop into skeletal muscle, axial skeleton, dorsal dermis, and axial tendon/ligament, respectively. Therefore, the generation of SMs and their derivatives from human induced pluripotent stem cells (iPSCs) is critical to obtain pluripotent stem cells (PSCs) for application in regenerative medicine and for disease research in the field of orthopedic surgery. Although the induction protocols for MYO and SCL from PSCs have been previously reported by several researchers, no study has yet demonstrated the induction of SYN and D from iPSCs. Therefore, efficient induction of fully competent SMs remains a major challenge. Here, we recapitulate human SM patterning with human iPSCs in vitro by mimicking the signaling environment during chick/mouse SM development, and report on methods of systematic induction of SM derivatives (MYO, SCL, D, and SYN) from human iPSCs under chemically defined conditions through the presomitic mesoderm (PSM) and SM states. Knowledge regarding chick/mouse&#160;SM development was successfully applied to the induction of SMs with human iPSCs. This method could be a novel tool for studying human somitogenesis and patterning without the use of embryos and for cell-based therapy and disease modeling.

We present here a protocol for the differentiation of human induced pluripotent stem cells into each somite derivative (myotome, sclerotome, dermatome, and syndetome) in chemically defined conditions, which has applications in future disease modeling and cell-based therapies in orthopedic surgery.

人诱导多能干细胞体外生成体细胞衍生物的研究

In response to signals such as WNTs, bone morphogenetic proteins (BMPs), and sonic hedgehog (SHH) secreted from surrounding tissues, somites (SMs) give ...