Hyldahl Robert D, Nelson Brad, Xin Ling, Welling Tyson, Groscost Logan, Hubal Monica J, Chipkin Stuart, Clarkson Priscilla M, Parcell Allen C
*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.
FASEB J. 2015 Jul;29(7):2894-904. doi: 10.1096/fj.14-266668. Epub 2015 Mar 25.
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.
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。