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蛋白质组学研究人类骨骼肌在 70 天头低位卧床休息前后、有无运动以及睾酮对抗措施的变化。

Proteomic investigation of human skeletal muscle before and after 70 days of head down bed rest with or without exercise and testosterone countermeasures.

机构信息

Department of Internal Medicine, The University of Texas Medical Branch, Galveston, TX, United States of America.

Department of Biochemistry and Molecular Biology, The University of Texas Medical Branch, Galveston, TX, United States of America.

出版信息

PLoS One. 2019 Jun 13;14(6):e0217690. doi: 10.1371/journal.pone.0217690. eCollection 2019.

Abstract

INTRODUCTION

Long-term head-down bed rest (HDBR) results in musculoskeletal losses similar to those observed during long-term space flight. Agents such as testosterone, in addition to regular exercise, are effective countermeasures for reducing loss of skeletal muscle mass and function.

OBJECTIVE

We investigated the skeletal muscle proteome of healthy men in response to long term HDBR alone (CON) and to HDBR with exercise (PEX) or exercise plus testosterone (TEX) countermeasures.

METHOD

Biopsies were performed on the vastus lateralis before (pre) HDBR and on HDBR days 32 (mid) and 64 (post). Extracted proteins from these skeletal muscle biopsies were subjected to 2-dimensional gel electrophoresis (2DE), stained for phosphoproteins (Pro-Q Diamond dye) and total proteins (Sypro Ruby dye). Proteins showing significant fold differences (t-test p ≤ 0.05) in abundance or phosphorylation state at mid or post were identified by mass spectroscopy (MS).

RESULTS

From a total of 932 protein spots, 130 spots were identified as potentially altered in terms of total protein or phosphoprotein levels due to HDBR and/or countermeasures, and 59 unique molecules emerged from MS analysis. Top canonical pathways identified through IPA included calcium signaling, actin cytoskeleton signaling, integrin linked kinase (ILK) signaling, and epithelial adherens junction signaling. Data from the pre-HDBR proteome supported the potential for predicting physiological post-HDBR responses such as the individual's potential for loss vs. maintenance of muscle mass and strength.

CONCLUSIONS

HDBR resulted in alterations to skeletal muscle abundances and phosphorylation of several structural and metabolic proteins. Inclusion of exercise alone or in combination with testosterone treatment modulated the proteomic responses towards cellular reorganization and hypertrophy, respectively. Finally, the baseline proteome may aid in the development of personalized countermeasures to mitigate health risks in astronauts as related to loss of muscle mass and function.

摘要

简介

长期卧床(HDBR)会导致类似于长期太空飞行中观察到的肌肉骨骼损失。除了常规运动外,睾酮等药物对于减少骨骼肌质量和功能的损失也是有效的对策。

目的

我们研究了健康男性在单独进行长期 HDBR(CON)以及进行 HDBR 运动(PEX)或运动加睾酮(TEX)对策时的骨骼肌蛋白质组。

方法

在 HDBR 之前(预)和 HDBR 第 32 天(中)和第 64 天(后)对股外侧肌进行活检。从这些骨骼肌活检中提取的蛋白质进行二维凝胶电泳(2DE),用磷酸蛋白(Pro-Q Diamond 染料)和总蛋白(Sypro Ruby 染料)染色。通过质谱分析(MS)鉴定丰度或磷酸化状态在中期或后期发生显著倍数变化(t 检验 p ≤ 0.05)的蛋白质。

结果

在总共 932 个蛋白质斑点中,有 130 个蛋白质斑点由于 HDBR 和/或对策而在总蛋白或磷酸蛋白水平上被认为发生了改变,通过 MS 分析发现了 59 个独特的分子。IPA 确定的主要经典途径包括钙信号、肌动蛋白细胞骨架信号、整合素连接激酶(ILK)信号和上皮黏着连接信号。来自 HDBR 前蛋白质组的数据支持预测生理 HDBR 后反应的潜力,例如个体丧失或维持肌肉质量和力量的潜力。

结论

HDBR 导致骨骼肌丰度和几种结构和代谢蛋白的磷酸化发生改变。单独运动或与睾酮治疗结合使用分别调节了蛋白质组对细胞重组和肥大的反应。最后,基线蛋白质组可能有助于制定个性化的对策,以减轻宇航员因肌肉质量和功能丧失而带来的健康风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3593/6563988/2baccd82007d/pone.0217690.g001.jpg

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