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氧化损伤或完整 C2C12 肌管释放的细胞外囊泡促进向肌生成的不同反应汇聚。

Extracellular Vesicles Released by Oxidatively Injured or Intact C2C12 Myotubes Promote Distinct Responses Converging toward Myogenesis.

机构信息

Department of Biomolecular Sciences, University of Urbino Carlo Bo, Via I Maggetti, 26, 61029 Urbino, Italy.

出版信息

Int J Mol Sci. 2017 Nov 22;18(11):2488. doi: 10.3390/ijms18112488.

DOI:10.3390/ijms18112488
PMID:29165341
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5713454/
Abstract

Myogenic differentiation is triggered, among other situations, in response to muscle damage for regenerative purposes. It has been shown that during myogenic differentiation, myotubes release extracellular vesicles (EVs) which participate in the signalling pattern of the microenvironment. Here we investigated whether EVs released by myotubes exposed or not to mild oxidative stress modulate the behaviour of targeted differentiating myoblasts and macrophages to promote myogenesis. We found that EVs released by oxidatively challenged myotubes (H₂O₂-EVs) are characterized by an increased loading of nucleic acids, mainly DNA. In addition, incubation of myoblasts with H₂O₂-EVs resulted in a significant decrease of myotube diameter, myogenin mRNA levels and myosin heavy chain expression along with an upregulation of proliferating cell nuclear antigen: these effects collectively lead to an increase of recipient myoblast proliferation. Notably, the EVs from untreated myotubes induced an opposite trend in myoblasts, that is, a slight pro-differentiation effect. Finally, H₂O₂-EVs were capable of eliciting an increased interleukin 6 mRNA expression in RAW264.7 macrophages. Notably, this is the first demonstration that myotubes communicate with surrounding macrophages via EV release. Collectively, the data reported herein suggest that myotubes, depending on their conditions, release EVs carrying differential signals which could contribute to finely and coherently orchestrate the muscle regeneration process.

摘要

肌发生分化是在多种情况下被触发的,其中包括为了再生目的对肌肉损伤的反应。已经表明,在肌发生分化过程中,肌管释放细胞外囊泡(EVs),这些 EVs 参与微环境的信号模式。在这里,我们研究了暴露于或不暴露于轻度氧化应激的肌管释放的 EV 是否调节靶分化成肌细胞和巨噬细胞的行为,以促进肌发生。我们发现,氧化应激肌管释放的 EV(H₂O₂-EVs)的特征是核酸(主要是 DNA)的负载增加。此外,用 H₂O₂-EVs 孵育成肌细胞导致肌管直径、肌生成素 mRNA 水平和肌球蛋白重链表达显著降低,同时增殖细胞核抗原上调:这些效应共同导致受体成肌细胞增殖增加。值得注意的是,未处理的肌管 EV 诱导成肌细胞产生相反的趋势,即轻微的促分化作用。最后,H₂O₂-EVs 能够引起 RAW264.7 巨噬细胞中白细胞介素 6 mRNA 表达的增加。值得注意的是,这是首次证明肌管通过 EV 释放与周围巨噬细胞进行通讯。总之,本文报道的数据表明,肌管根据其状态释放携带不同信号的 EV,这些信号可能有助于精细而协调地调控肌肉再生过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a38/5713454/e21dd19c8f63/ijms-18-02488-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a38/5713454/8860f171cce3/ijms-18-02488-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a38/5713454/a2fc476b3f10/ijms-18-02488-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a38/5713454/218154b852c5/ijms-18-02488-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a38/5713454/e21dd19c8f63/ijms-18-02488-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a38/5713454/8860f171cce3/ijms-18-02488-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a38/5713454/a2fc476b3f10/ijms-18-02488-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a38/5713454/218154b852c5/ijms-18-02488-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a38/5713454/e21dd19c8f63/ijms-18-02488-g004.jpg

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