Sullivan Brian P, Nie Yaohui, Evans Sheelagh, Kargl Chris K, Hettinger Zach R, Garner Ron T, Hubal Monica J, Kuang Shihuan, Stout Julianne, Gavin Timothy P
Department of Health and Kinesiology, Purdue University, West Lafayette, Indiana, USA.
Department of Animal Sciences, Purdue University, West Lafayette, Indiana, USA.
Exp Physiol. 2022 May;107(5):462-475. doi: 10.1113/EP090062. Epub 2022 Apr 3.
What is the central question of this study? Is 1 week of exercise training sufficient to reduce local and systemic inflammation? Do obesity and short-term concurrent aerobic and resistance exercise training alter skeletal muscle extracellular vesicle (EV) contents? What is the main finding and its importance? Obesity alters skeletal muscle small EV microRNAs targeting inflammatory and growth pathways. Exercise training alters skeletal muscle small EV microRNAs targeting inflammatory pathways, indicative of reduced inflammation. Our findings provide support for the hypotheses that EVs play a vital role in intercellular communication during health and disease and that EVs mediate many of the beneficial effects of exercise.
Obesity is associated with chronic inflammation characterized by increased levels of inflammatory cytokines, whereas exercise training reduces inflammation. Small extracellular vesicles (EVs; 30-150 nm) participate in cell-to-cell communication in part through microRNA (miRNA) post-transcriptional regulation of mRNA. We examined whether obesity and concurrent aerobic and resistance exercise training alter skeletal muscle EV miRNA content and inflammatory signalling. Vastus lateralis biopsies were obtained from sedentary individuals with (OB) and without obesity (LN). Before and after 7 days of concurrent aerobic and resistance training, muscle-derived small EV miRNAs and whole-muscle mRNAs were measured. Pathway analysis revealed that obesity alters small EV miRNAs that target inflammatory (SERPINF1, death receptor and Gα ) and growth pathways (Wnt/β-catenin, PTEN, PI3K/AKT and IGF-1). In addition, exercise training alters small EV miRNAs in an anti-inflammatory manner, targeting the IL-10, IL-8, Toll-like receptor and nuclear factor-κB signalling pathways. In whole muscle, IL-8 mRNA was reduced by 50% and Jun mRNA by 25% after exercise training, consistent with the anti-inflammatory effects of exercise on skeletal muscle. Obesity and 7 days of concurrent exercise training differentially alter skeletal muscle-derived small EV miRNA contents targeting inflammatory and anabolic pathways.
本研究的核心问题是什么?1周的运动训练是否足以减轻局部和全身炎症?肥胖以及短期同时进行有氧和抗阻运动训练是否会改变骨骼肌细胞外囊泡(EV)的内容物?主要发现及其重要性是什么?肥胖会改变骨骼肌小EV中靶向炎症和生长途径的微小RNA。运动训练会改变骨骼肌小EV中靶向炎症途径的微小RNA,这表明炎症减轻。我们的研究结果支持以下假设:EV在健康和疾病期间的细胞间通讯中起着至关重要的作用,并且EV介导了运动的许多有益作用。
肥胖与以炎性细胞因子水平升高为特征的慢性炎症相关,而运动训练可减轻炎症。小细胞外囊泡(EV;30 - 150纳米)部分通过微小RNA(miRNA)对mRNA的转录后调控参与细胞间通讯。我们研究了肥胖以及同时进行有氧和抗阻运动训练是否会改变骨骼肌EV miRNA含量和炎症信号传导。从有肥胖(OB)和无肥胖(LN)的久坐不动个体中获取股外侧肌活检样本。在同时进行7天的有氧和抗阻训练前后,测量肌肉来源的小EV miRNA和全肌肉mRNA。通路分析显示,肥胖会改变靶向炎症(丝氨酸蛋白酶抑制剂F1、死亡受体和Gα)和生长途径(Wnt/β-连环蛋白、磷酸酶和张力蛋白同源物、磷脂酰肌醇-3-激酶/蛋白激酶B和胰岛素样生长因子-1)的小EV miRNA。此外,运动训练以抗炎方式改变小EV miRNA,靶向白细胞介素-10、白细胞介素-8、Toll样受体和核因子-κB信号通路。在全肌肉中,运动训练后白细胞介素-8 mRNA降低了50%,Jun mRNA降低了25%,这与运动对骨骼肌的抗炎作用一致。肥胖和7天的同时运动训练以不同方式改变骨骼肌来源的小EV miRNA含量,这些小EV miRNA靶向炎症和合成代谢途径。