期刊文献+

运动适应的细胞信号调控:线粒体的角色转换及其研究展望 被引量:14

Cell Signaling for Exercise-Induced Adaptation:ARole Transition of Mitochondria
下载PDF
导出
摘要 线粒体不仅是真核细胞的能量工厂,更是细胞信号转导的调控中心。转换线粒体的功能定位,探索线粒体能量代谢与信号转导之间的偶联机制,将有助于揭示运动与生理适应的链接通路。许多慢性疾病的病理基础可归因于线粒体与真核细胞之间共生关系异常,即以能量换营养的交易出现阻滞,运动有助于整合或恢复这种共生关系。因为运动不仅促进线粒体生物发生(正向适应),也诱导细胞自噬(含线粒体自噬),未来以"自噬"为标志的"逆向适应"研究将更全面地揭示线粒体质量控制的机理,这将进一步丰富运动适应的细胞信号调控理论以及线粒体相关疾病的病理机制。 Mitochondria is not only a eukaryotic cell energy plant,but also the regulation center of cell signal transduction.It is important to convert the traditional mitochondrial function and explore the crosstalk of mitochondrial energy metabolism and signal transduction for revealing the theory of adaption of physical activity.It is the abnormal symbiotic relationship between mitochondria and eukaryotic cells that may inducepathologyof many chronic diseases.That is,the trade of energy for food is retarded.The effect of exercise on mitochondrial quality control involves not onlymitochondrialbiogenesis and dynamics(forward adaptation),but alsothe induction of autophagy(mitophagy).In the near future,autophagy,regarded as a"reverse adaptation",may further disclose the underlying mechanisms of Mitochondrial Quality Control,the future resultswill enrich the relationship between exercise adaption and signal regulation,and provide more understandingsfor mitochondria-related diseases.
出处 《体育科学》 CSSCI 北大核心 2013年第7期65-69,共5页 China Sport Science
基金 国家自然科学基金资助项目(31171142)
关键词 线粒体 信号转导 自噬 生物发生 运动适应 mitochondria signal transduction autophagy biogenesis exercise adaptation
  • 相关文献

参考文献46

二级参考文献227

共引文献81

同被引文献177

  • 1Jiankang Liu Institute of Mitochondrial Biology and Medicine, Xi’an Jiaotong University School of Life Science and Technology, Xi’an 710049, China.Targeting mitochondrial biogenesis for preventing and treating insulin resistance in diabetes and obesity:Hope from natural mitochondrial nutrients[J].生物物理学报,2009,25(S1):100-100. 被引量:24
  • 2AMBROS V. The functions of animal microRNAs[J]. Nature,2004,431(7006):350-355. 被引量:1
  • 3ANDERSON C, CATOE H, WERNER R. MIR-206 regulatesconnexin43 expression during skeletal muscle development [ J ].Nucleic Acids Res,2006,34(20) :5863-5871. 被引量:1
  • 4AOI W,ICHIKAWA H, MUNE K, et al. Muscleenriched mi-croRNA miR-486 decreases in circulation in response to exercisein young men[J]. Front Physiol,2013,4(11) :80. 被引量:1
  • 5BAGGISH A L, HALE A, WEINER R B,et a l. Dynamic regula- tion of circulating microRNA during acute exhaustive exercise and sustained aerobic exercise training[J]. J Phys, 2011,589 (Pt 16) : 3983-3994. 被引量:1
  • 6BANZET S, CHENNAOUI M, GIRARD 0,et al. Changes incirculating microRNAs levels with exercise modality [J]. J ApplPhys,2013,115(9) :1237-1244. 被引量:1
  • 7BARRES R,YAN J,EGAN B? et al. Acute exercise remodelspromoter methylation in human skeletal muscle [J]. Cell Metab-olism,2012,15(3) :405-411. 被引量:1
  • 8BOUTZ P L,CHAWLA G,STOIOV P,et al. MicroRNAs regu- late the expression of the alternative splicing faetor nPTB during muscle development[J]. Genes Dev 2007,21 (1) : 71-84. 被引量:1
  • 9BYE A,ROSJO H,ASPENES S T,etal. Circulating microRNAsand aerobic fitness-the HUNT-Study [J]. PLoS ONE, 2013,8(2):e57496. 被引量:1
  • 10CHEN C Z,LI L, LODISH H F,et al. MicroRNAs modulatehematopoietic lineage differentiation [J], Sci? 2004 ?303 (5654):83-86. 被引量:1

引证文献14

二级引证文献79

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部