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首页> 外文期刊>Biological research for nursing >Macrophage Colony Stimulating Factor-Induced Macrophage Differentiation Influences Myotube Elongation
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Macrophage Colony Stimulating Factor-Induced Macrophage Differentiation Influences Myotube Elongation

机译:巨噬细胞集落刺激因子诱导的巨噬细胞分化影响肌管伸长。

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Background: Unaccustomed exercise, high-intensity dynamic sports activities, or the resumption of normal weight-bearing after a period of disuse can induce skeletal muscle injury, which activates an inflammatory response followed by muscle regeneration. Specific subsets of macrophages are involved in muscle regeneration. But the exact role of macrophage differentiation during muscle regeneration remains to be elucidated. Objective: The objective of the study was to examine the effect of macrophage colony stimulating factor (M-CSF)-differentiated, lipopolysaccharides (LPS)-stimulated-macrophage-conditioned medium on muscle-cell proliferation, fusion, and elongation, which are key events during muscle regeneration and myogenesis Method: Murine C2C12 myoblasts were cultured in conditioned medium obtained from PU5-1R macrophages that were (a) undifferentiated, unstimulated; (b) M-CSF-differentiated, unstimulated; (c) undifferentiated, LPS-stimulated; or (d) M-CSF-differentiated, LPS-stimulated. Myoblast proliferation ratio, nuclei number, and length were measured. Results: C2C12 cells cultured in conditioned medium from M-CSF-differentiated, LPS-stimulated macrophages had significantly more nuclei and greater length thancells cultured in conditioned medium from undifferentiated, LPS-stimulated macrophages. Dilution and denaturization of the M-CSF-differentiated, LPS-stimulated-macrophage medium prevented a marked increase in C2C12 nuclei number and length. However, the C2C12 myoblast proliferation ratio was significantly greater in conditioned medium from undifferentiated,LPSstimulated macrophages than in conditioned medium from M-CSF-differentiated, LPS-stimulated macrophages. Conclusions: M-CSF-differentiated, LPS-stimulated macrophages may influence myogenesis and the early and terminal stages of muscle regeneration. This knowledge may aid in developing therapies that will directly expedite muscle repair and lead to faster rehabilitationand reduced rehabilitation costs.
机译:背景:不习惯的运动,高强度的动态运动或一段时间不使用后恢复正常的负重会诱发骨骼肌损伤,从而激活炎症反应,继而引起肌肉再生。巨噬细胞的特定子集参与肌肉再生。但是巨噬细胞分化在肌肉再生过程中的确切作用仍有待阐明。目的:本研究的目的是研究巨噬细胞集落刺激因子(M-CSF)-分化的脂多糖(LPS)-刺激的巨噬细胞条件培养基对肌肉细胞增殖,融合和伸长的影响。肌肉再生和成肌过程中的事件方法:在从PU5-1R巨噬细胞获得的条件培养基中培养鼠C2C12成肌细胞,该条件是(a)未分化,未刺激; (b)M-CSF分化的,未刺激的; (c)未分化,受脂多糖刺激的;或(d)M-CSF分化,LPS刺激。测量成肌细胞增殖率,细胞核数目和长度。结果:在M-CSF分化的LPS刺激的巨噬细胞的条件培养基中培养的C2C12细胞比在未分化的LPS刺激的巨噬细胞的条件培养基中培养的细胞具有更多的核和更长的核。 M-CSF分化的LPS刺激的巨噬细胞培养基的稀释和变性阻止了C2C12核数目和长度的显着增加。但是,来自未分化的,经LPS刺激的巨噬细胞的条件培养基中的C2C12成肌细胞增殖比明显高于来自经M-CSF分化的,经LPS刺激的巨噬细胞的条件培养基中的C2C12成肌细胞增殖率。结论:M-CSF分化,LPS刺激的巨噬细胞可能影响肌肉再生以及肌肉再生的早期和晚期。这些知识可能有助于开发可以直接加速肌肉修复并导致更快康复和降低康复成本的疗法。

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