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细胞外基质重塑及其在人体肌肉延长收缩后的保护性适应中的作用。

Extracellular matrix remodeling and its contribution to protective adaptation following lengthening contractions in human muscle.

作者信息

Hyldahl Robert D, Nelson Brad, Xin Ling, Welling Tyson, Groscost Logan, Hubal Monica J, Chipkin Stuart, Clarkson Priscilla M, Parcell Allen C

机构信息

*Department of Exercise Sciences, Brigham Young University, Provo, Utah, USA; Department of Natural Sciences, Ohio Dominican University, Columbus, Ohio, USA; Department of Kinesiology, University of Massachusetts Amherst, Massachusetts, USA; and Department of Integrative Systems Biology, George Washington University, Washington, DC, USA

*Department of Exercise Sciences, Brigham Young University, Provo, Utah, USA; Department of Natural Sciences, Ohio Dominican University, Columbus, Ohio, USA; Department of Kinesiology, University of Massachusetts Amherst, Massachusetts, USA; and Department of Integrative Systems Biology, George Washington University, Washington, DC, USA.

出版信息

FASEB J. 2015 Jul;29(7):2894-904. doi: 10.1096/fj.14-266668. Epub 2015 Mar 25.

Abstract

This study determined the contribution of extracellular matrix (ECM) remodeling to the protective adaptation of human skeletal muscle known as the repeated-bout effect (RBE). Muscle biopsies were obtained 3 hours, 2 days, and 27 days following an initial bout (B1) of lengthening contractions (LCs) and 2 days following a repeated bout (B2) in 2 separate studies. Biopsies from the nonexercised legs served as controls. In the first study, global transcriptomic analysis indicated widespread changes in ECM structural, deadhesive, and signaling transcripts, 3 hours following LC. To determine if ECM remodeling is involved in the RBE, we conducted a second study by use of a repeated-bout paradigm. TNC immunoreactivity increased 10.8-fold following B1, was attenuated following B2, and positively correlated with LC-induced strength loss (r(2) = 0.45; P = 0.009). Expression of collagen I, III, and IV (COL1A1, COL3A1, COL4A1) transcripts was unchanged early but increased 5.7 ± 2.5-, 3.2 ± 0.9-, and 2.1 ± 0.4-fold (P < 0.05), respectively, 27 days post-B1 and were unaffected by B2. Likewise, TGF-β signaling demonstrated a delayed response following LC. Satellite cell content increased 80% (P < 0.05) 2 days post-B1 (P < 0.05), remained elevated 27 days post-B1, and was unaffected by B2. Collectively, the data suggest sequential ECM remodeling characterized by early deadhesion and delayed reconstructive activity that appear to contribute to the RBE.

摘要

本研究确定了细胞外基质(ECM)重塑对人类骨骼肌保护性适应(即重复运动效应,RBE)的作用。在两项独立研究中,分别于初次延长收缩(LC)运动(B1)后3小时、2天和27天以及重复运动(B2)后2天采集肌肉活检样本。未运动腿部的活检样本作为对照。在第一项研究中,整体转录组分析表明,LC运动后3小时,ECM结构、去黏附及信号转导转录本出现广泛变化。为确定ECM重塑是否参与RBE,我们采用重复运动范式进行了第二项研究。肌腱蛋白C(TNC)免疫反应性在B1后增加了10.8倍,在B2后减弱,且与LC诱导的力量损失呈正相关(r² = 0.45;P = 0.009)。I型、III型和IV型胶原(COL1A1、COL3A1、COL4A1)转录本的表达早期未发生变化,但在B1后27天分别增加了5.7±2.5倍、3.2±0.9倍和2.1±0.4倍(P<0.05),且不受B2影响。同样,转化生长因子-β(TGF-β)信号在LC运动后表现出延迟反应。卫星细胞含量在B1后2天增加了80%(P<0.05),在B1后27天仍保持升高,且不受B2影响。总体而言,数据表明ECM重塑具有先后顺序,其特征为早期去黏附及延迟的重建活动,这似乎对RBE有促进作用。

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