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首页> 外文期刊>Cell biology international. >Macrophage depletion impairs skeletal muscle regeneration: The roles of regulatory factors for muscle regeneration
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Macrophage depletion impairs skeletal muscle regeneration: The roles of regulatory factors for muscle regeneration

机译:巨噬细胞耗尽损害骨骼肌再生:调节因素为肌肉再生的作用

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Though macrophages are essential for skeletal muscle regeneration, which is a complex process, the roles and mechanisms of the macrophages in the process of muscle regeneration are still not fully understood. The objective of this study is to explore the roles of macrophages and the mechanisms involved in the regeneration of injured skeletal muscle. One hundred and twelve C57BL/6 mice were randomly divided into muscle contusion and macrophages depleted groups. Their gastrocnemius muscles were harvested at the time points of 12h, 1, 3, 5, 7, 14d post-injury. The changes in skeletal muscle morphology were assessed by hematoxylin and eosin (HE) stain. The gene expression was analyzed by real-time polymerase chain reaction. The data showed that CL-liposomes treatment did affect the expression of myogenic regulatory factors (MyoD, myogenin) after injury. In addition, CL-liposomes treatment decreased the expression of regulatory factors of muscle regeneration (HGF, uPA, COX-2, IGF-1, MGF, FGF6) and increased the expression of inflammatory cytokines (TGF-beta 1, TNF-alpha, IL-1 beta, RANTES) in the late stage of regeneration. Moreover, there were significant correlations between macrophages and some regulatory factors (such as HGF, uPA) for muscle regeneration. These results suggested that macrophages depletion impairs skeletal muscle regeneration and that the regulatory factors for muscle regeneration may play important roles in this process.
机译:尽管巨噬细胞对骨骼肌再生至关重要,这是一个复杂的过程,但巨噬细胞在肌肉再生过程中的作用和机制仍不完全清楚。本研究的目的是探讨巨噬细胞在损伤骨骼肌再生中的作用及其机制。112只C57BL/6小鼠随机分为肌肉挫伤组和巨噬细胞缺失组。分别于伤后12小时、1天、3天、5天、7天、14天采集腓肠肌。苏木精-伊红(HE)染色观察骨骼肌形态学变化。用实时聚合酶链反应分析基因表达。数据显示,CL脂质体治疗确实影响了损伤后肌源性调节因子(MyoD、肌生成素)的表达。此外,CL脂质体治疗降低了肌肉再生调节因子(HGF、uPA、COX-2、IGF-1、MGF、FGF6)的表达,并增加了再生后期炎性细胞因子(TGFβ1、TNFα、IL-1β、RANTES)的表达。此外,巨噬细胞与某些肌肉再生调节因子(如HGF、uPA)之间存在显著相关性。这些结果表明,巨噬细胞耗竭会损害骨骼肌再生,而肌肉再生的调节因子可能在这一过程中发挥重要作用。

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