心毒素诱导的骨骼肌损伤引起合成代谢和应激信号以及肌纤维类型组成的深刻变化。

IF 1.8 3区 生物学 Q4 CELL BIOLOGY
Sebastiaan Dalle, Charlotte Hiroux, Chiel Poffé, Monique Ramaekers, Louise Deldicque, Katrien Koppo
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引用次数: 6

摘要

为了改善损伤后的肌肉愈合,了解肌肉再生过程中关键信号通路的相互作用是很重要的。为此,在小鼠胫骨前肌注射心脏毒素(CTX)或PBS,并于注射后2、5和12天处死。时间点分别代表再生过程的不同阶段,即破坏、修复和重塑。注射ctx 2天后,p-mTORC1信号和应激标志物如BiP和p-ERK1/2上调。Phospho-ERK1/2和p-mTORC1在第5天达到峰值,而BiP的表达向PBS水平下降。注射ctx后第2天和第5天,Phospho-FOXO下降,表明分解代谢信号增加。此外,ctx注入诱导了纤维类型组成的变化,其特征是在d2和d5时IIa型纤维的初始损失。d5出现新的IIb型纤维,d12恢复IIa型纤维。综上所述,ctx注射严重影响了肌肉代谢和组织学的关键调节因子。这些数据为旨在改善肌肉分子信号从而恢复的策略的发展提供了有用的信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cardiotoxin-induced skeletal muscle injury elicits profound changes in anabolic and stress signaling, and muscle fiber type composition.

To improve muscle healing upon injury, it is of importance to understand the interplay of key signaling pathways during muscle regeneration. To study this, mice were injected with cardiotoxin (CTX) or PBS in the Tibialis Anterior muscle and were sacrificed 2, 5 and 12 days upon injection. The time points represent different phases of the regeneration process, i.e. destruction, repair and remodeling, respectively. Two days upon CTX-injection, p-mTORC1 signaling and stress markers such as BiP and p-ERK1/2 were upregulated. Phospho-ERK1/2 and p-mTORC1 peaked at d5, while BiP expression decreased towards PBS levels. Phospho-FOXO decreased 2 and 5 days following CTX-injection, indicative of an increase in catabolic signaling. Furthermore, CTX-injection induced a shift in the fiber type composition, characterized by an initial loss in type IIa fibers at d2 and at d5. At d5, new type IIb fibers appeared, whereas type IIa fibers were recovered at d12. To conclude, CTX-injection severely affected key modulators of muscle metabolism and histology. These data provide useful information for the development of strategies that aim to improve muscle molecular signaling and thereby recovery.

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来源期刊
CiteScore
6.20
自引率
0.00%
发文量
21
审稿时长
>12 weeks
期刊介绍: The Journal of Muscle Research and Cell Motility has as its main aim the publication of original research which bears on either the excitation and contraction of muscle, the analysis of any one of the processes involved therein, the processes underlying contractility and motility of animal and plant cells, the toxicology and pharmacology related to contractility, or the formation, dynamics and turnover of contractile structures in muscle and non-muscle cells. Studies describing the impact of pathogenic mutations in genes encoding components of contractile structures in humans or animals are welcome, provided they offer mechanistic insight into the disease process or the underlying gene function. The policy of the Journal is to encourage any form of novel practical study whatever its specialist interest, as long as it falls within this broad field. Theoretical essays are welcome provided that they are concise and suggest practical ways in which they may be tested. Manuscripts reporting new mutations in known disease genes without validation and mechanistic insight will not be considered. It is the policy of the journal that cells lines, hybridomas and DNA clones should be made available by the developers to any qualified investigator. Submission of a manuscript for publication constitutes an agreement of the authors to abide by this principle.
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