The role of mitochondrial dysfunction in mesenchymal stem cell senescence

被引:0
作者
Yibo Wang
Yunlong Liu
Erman Chen
Zhijun Pan
机构
[1] Zhejiang University School of Medicine,Department of Orthopedics, The Second Affiliated Hospital
来源
Cell and Tissue Research | 2020年 / 382卷
关键词
Senescence; Mesenchymal stem cells; Mitochondrial dysfunction; Reactive oxygen species; Mitophagy;
D O I
暂无
中图分类号
学科分类号
摘要
Mesenchymal stem cells (MSCs) hold enormous potential for the treatment of immune-related conditions and degenerative diseases, owing to their self-renewal and multilineage differentiation capabilities. Nevertheless, cellular senescence significantly impacts the quantity and quality of MSCs, limiting their clinical use. Mitochondria play essential roles in energy production by oxidative phosphorylation and metabolism of energy sources via the tricarboxylic acid cycle. Therefore, mitochondrial dysfunction is a primary cause of senescence in MSCs. Herein, we summarize the current knowledge regarding the mechanisms underlying mitochondrial dysfunction–associated cellular senescence. We also discuss potential methods to prevent or even reverse MSC senescence.
引用
收藏
页码:457 / 462
页数:5
相关论文
共 347 条
  • [1] Acosta JC(2013)A complex secretory program orchestrated by the inflammasome controls paracrine senescence Nat Cell Biol 15 978-990
  • [2] Banito A(2018)Neural stem cells from a mouse model of Rett syndrome are prone to senescence, show reduced capacity to cope with genotoxic stress, and are impaired in the differentiation process Exp Mol Med 50 1-1
  • [3] Wuestefeld T(2015)The HIV proteins Tat and Nef promote human bone marrow mesenchymal stem cell senescence and alter osteoblastic differentiation Aging Cell 14 534-546
  • [4] Georgilis A(2013)A complex of Cox4 and mitochondrial Hsp70 plays an important role in the assembly of the cytochrome c oxidase Mol Biol Cell 24 2609-2619
  • [5] Janich P(1997)Melatonin in humans N Engl J Med 336 186-195
  • [6] Morton JP(1990)Structure and function of cytochrome c oxidase Annu Rev Biochem 59 569-596
  • [7] Athineos D(2019)Mitochondrial dysfunction and cell senescence: deciphering a complex relationship FEBS Lett 593 1566-1579
  • [8] Kang TW(2018)Nuclear TP53: an unraveled function as transcriptional repressor of PINK1 Autophagy 14 1099-1101
  • [9] Lasitschka F(2015)Muscle heat shock protein 70 predicts insulin resistance with aging J Gerontol A Biol Sci Med Sci 70 155-162
  • [10] Andrulis M(2014)HSP72 is a mitochondrial stress sensor critical for Parkin action, oxidative metabolism, and insulin sensitivity in skeletal muscle Diabetes 63 1488-1505