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巨噬细胞条件培养基对小鼠和人类肌肉细胞的影响:增殖、分化及融合分析

Effects of Macrophage Conditioned-Medium on Murine and Human Muscle Cells: Analysis of Proliferation, Differentiation, and Fusion.

作者信息

Saclier Marielle, Theret Marine, Mounier Rémi, Chazaud Bénédicte

机构信息

Department of Biosciences, University of Milan, 20133, Milan, Italy.

Institut NeuroMyoGène, INMG, Université Claude Bernard Lyon 1, INSERM U1217, CNRS UMR5310, Villeurbanne, France.

出版信息

Methods Mol Biol. 2017;1556:317-327. doi: 10.1007/978-1-4939-6771-1_17.

DOI:10.1007/978-1-4939-6771-1_17
PMID:28247358
Abstract

Skeletal muscle is a highly plastic tissue, which is able to regenerate after an injury. Effective and complete regeneration requires interactions between myogenic precursor cells and several cell types such as macrophages . Bone marrow derived macrophages in mouse and monocyte-derived macrophages in human are useful tools to obtain macrophage populations that may be specifically activated/polarized in vitro (e.g., pro-inflammatory, anti-inflammatory, and alternatively activated macrophages ). In vitro , human or murine primary myogenic cells recapitulate the adult myogenesis program through proliferation, myogenic differentiation, and fusion. Macrophages being highly secreting cells, they act on various biological processes including adult myogenesis . Here, we present protocols to analyze in vitro the effect of macrophage-secreted factors on muscle cell proliferation or differentiation in both mouse and human.

摘要

骨骼肌是一种高度可塑性的组织,能够在损伤后再生。有效的完全再生需要成肌前体细胞与多种细胞类型(如巨噬细胞)之间的相互作用。小鼠中的骨髓来源巨噬细胞和人类中的单核细胞来源巨噬细胞是获得可在体外特异性激活/极化的巨噬细胞群体(如促炎性、抗炎性和替代性激活巨噬细胞)的有用工具。在体外,人类或小鼠原代成肌细胞通过增殖、成肌分化和融合来重现成年肌生成程序。巨噬细胞是高度分泌性细胞,它们作用于包括成年肌生成在内的各种生物学过程。在这里,我们展示了在体外分析巨噬细胞分泌因子对小鼠和人类肌肉细胞增殖或分化影响的方案。

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本文引用的文献

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Transcriptome-based network analysis reveals a spectrum model of human macrophage activation.基于转录组的网络分析揭示了人类巨噬细胞激活的谱模型。
Immunity. 2014 Feb 20;40(2):274-88. doi: 10.1016/j.immuni.2014.01.006. Epub 2014 Feb 13.
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AMPKα1 regulates macrophage skewing at the time of resolution of inflammation during skeletal muscle regeneration.AMPKα1 在骨骼肌再生过程中炎症消退时调节巨噬细胞的极化。
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Differentially activated macrophages orchestrate myogenic precursor cell fate during human skeletal muscle regeneration.
转录因子 Nfix 通过 RhoA-ROCK1 依赖的吞噬作用来调节骨骼肌再生过程中的巨噬细胞极化。
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The BACH1-HMOX1 Regulatory Axis Is Indispensable for Proper Macrophage Subtype Specification and Skeletal Muscle Regeneration.BACH1-HMOX1 调控轴对于正确的巨噬细胞亚型分化和骨骼肌再生是不可或缺的。
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差异激活的巨噬细胞在人类骨骼肌再生过程中协调成肌前体细胞命运。
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Inflammatory monocytes recruited after skeletal muscle injury switch into antiinflammatory macrophages to support myogenesis.骨骼肌损伤后募集的炎性单核细胞会转变为抗炎性巨噬细胞以支持肌生成。
J Exp Med. 2007 May 14;204(5):1057-69. doi: 10.1084/jem.20070075. Epub 2007 May 7.
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Satellite cells attract monocytes and use macrophages as a support to escape apoptosis and enhance muscle growth.卫星细胞吸引单核细胞,并利用巨噬细胞作为支持来逃避凋亡并增强肌肉生长。
J Cell Biol. 2003 Dec 8;163(5):1133-43. doi: 10.1083/jcb.200212046.
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Cultured myf5 null and myoD null muscle precursor cells display distinct growth defects.培养的Myf5基因缺失和MyoD基因缺失的肌肉前体细胞表现出明显的生长缺陷。
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Murine bone marrow-derived macrophages.
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