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巨噬细胞耗竭会损害骨骼肌再生:促纤维化因子、炎症和氧化应激的作用。

Macrophage Depletion Impairs Skeletal Muscle Regeneration: the Roles of Pro-fibrotic Factors, Inflammation, and Oxidative Stress.

作者信息

Xiao Weihua, Liu Yu, Chen Peijie

机构信息

School of Kinesiology, Shanghai University of Sport, Shanghai, 200438, China.

出版信息

Inflammation. 2016 Dec;39(6):2016-2028. doi: 10.1007/s10753-016-0438-8.

Abstract

Muscle contusion is one of the most common muscle injuries in sports medicine. Macrophages play complex roles in the regeneration of skeletal muscle. However, the roles of macrophages, especially the mechanisms involved, in the regeneration of muscle contusion are still not fully understood. We hypothesize that the depletion of macrophages impairs skeletal muscle regeneration and that pro-fibrotic factors, inflammation, and oxidative stress may be involved in the process. To test these hypotheses, we constructed a muscle contusion injury and a macrophage depletion model and followed it up with morphological and gene expression analyses. The data showed that fibrotic scars were formed in the muscle of contusion injury, and they deteriorated in the mice of macrophage depletion. Furthermore, the sizes of regenerating myofibers were significantly reduced by macrophage depletion. Pro-fibrotic factors, inflammatory cytokines, chemokines, and oxidative stress-related enzymes increased significantly after muscle injury. Moreover, the expression of these factors was delayed by macrophage depletion. Most of them were still significantly higher in the later stage of regeneration. These results suggest that macrophage depletion impairs skeletal muscle regeneration and that pro-fibrotic factors, inflammation, and oxidative stress may play important roles in the process.

摘要

肌肉挫伤是运动医学中最常见的肌肉损伤之一。巨噬细胞在骨骼肌再生中发挥着复杂的作用。然而,巨噬细胞在肌肉挫伤再生中的作用,尤其是其涉及的机制,仍未完全明确。我们推测巨噬细胞的缺失会损害骨骼肌再生,并且促纤维化因子、炎症和氧化应激可能参与了这一过程。为了验证这些假设,我们构建了肌肉挫伤损伤和巨噬细胞缺失模型,并对其进行形态学和基因表达分析。数据显示,挫伤损伤的肌肉中形成了纤维化瘢痕,而在巨噬细胞缺失的小鼠中,这些瘢痕恶化。此外,巨噬细胞缺失显著减小了再生肌纤维的大小。肌肉损伤后,促纤维化因子、炎性细胞因子、趋化因子和氧化应激相关酶显著增加。此外,巨噬细胞缺失延迟了这些因子的表达。在再生后期,其中大多数因子仍显著高于正常水平。这些结果表明,巨噬细胞缺失会损害骨骼肌再生,并且促纤维化因子、炎症和氧化应激可能在这一过程中发挥重要作用。

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