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采用分泌组学分析鉴定人类运动诱导的肌肉因子。

Identification of human exercise-induced myokines using secretome analysis.

机构信息

Nutrition, Metabolism and Genomics Group, Division of Human Nutrition, Wageningen University, Wageningen, the Netherlands;

出版信息

Physiol Genomics. 2014 Apr 1;46(7):256-67. doi: 10.1152/physiolgenomics.00174.2013. Epub 2014 Feb 11.

Abstract

Endurance exercise is associated with significant improvements in cardio-metabolic risk parameters. A role for myokines has been hypothesized, yet limited information is available about myokines induced by acute endurance exercise in humans. Therefore, the aim of the study was to identify novel exercise-induced myokines in humans. To this end, we carried out a 1 h one-legged acute endurance exercise intervention in 12 male subjects and a 12 wk exercise training intervention in 18 male subjects. Muscle biopsies were taken before and after acute exercise or exercise training and were subjected to microarray-based analysis of secreted proteins (secretome). For acute exercise, secretome analysis resulted in a list of 86 putative myokines, which was reduced to 29 by applying a fold-change cut-off of 1.5. Based on that shortlist, a selection of putative myokines was measured in the plasma by ELISA or multiplex assay. From that selection, CX3CL1 (fractalkine) and CCL2 (MCP-1) increased at both mRNA and plasma levels. From the known myokines, only IL-6 and FGF 21 changed at the mRNA level, whereas none of the known myokines changed at the plasma level. Secretome analysis of exercise training intervention resulted in a list of 69 putative myokines. Comparing putative myokines altered by acute exercise and exercise training revealed a limited overlap of only 13 genes. In conclusion, this study identified CX3CL1 and CCL2 as myokines that were induced by acute exercise at the gene expression and plasma level and that may be involved in communication between skeletal muscle and other organs.

摘要

耐力运动与心血管代谢风险参数的显著改善有关。已经假设肌因子起作用,但关于人类急性耐力运动诱导的肌因子的信息有限。因此,本研究的目的是在人类中鉴定新的运动诱导的肌因子。为此,我们对 12 名男性受试者进行了 1 小时单腿急性耐力运动干预,对 18 名男性受试者进行了 12 周运动训练干预。在急性运动或运动训练前后采集肌肉活检,并进行基于微阵列的分泌蛋白(分泌组)分析。对于急性运动,分泌组分析产生了 86 种假定的肌因子列表,通过应用 1.5 的倍数变化截止值将其减少到 29。基于该短名单,通过 ELISA 或多重测定法在血浆中测量了一组假定的肌因子。在该选择中,CX3CL1(趋化因子)和 CCL2(MCP-1)在 mRNA 和血浆水平上均增加。在已知的肌因子中,只有 IL-6 和 FGF 21 在 mRNA 水平上发生变化,而没有已知的肌因子在血浆水平上发生变化。运动训练干预的分泌组分析产生了 69 种假定的肌因子列表。比较急性运动和运动训练改变的假定肌因子,只有 13 个基因的重叠有限。总之,本研究鉴定出 CX3CL1 和 CCL2 作为急性运动诱导的肌因子,在基因表达和血浆水平上诱导,并可能参与骨骼肌和其他器官之间的通讯。

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