Regulation of the mitochondrial reactive oxygen species: Strategies to control mesenchymal stem cell fates ex vivo and in vivo

被引:56
作者
Hu, Chenxia [1 ]
Zhao, Lingfei [2 ,3 ]
Peng, Conggao [1 ]
Li, Lanjuan [1 ]
机构
[1] Zhejiang Univ, Affiliated Hosp 1, State Key Lab Diag & Treatment Infect Dis,Sch Med, Collaborat Innovat Ctr Diag & Treatment Infect Di, Hangzhou, Zhejiang, Peoples R China
[2] Zhejiang Univ, Affiliated Hosp 1, Coll Med, Kidney Dis Ctr, Hangzhou, Zhejiang, Peoples R China
[3] Zhejiang Univ, Inst Nephrol, Key Lab Kidney Dis Prevent & Control Technol, Hangzhou, Zhejiang, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
mesenchymal stem cell; multilineage; reactive oxygen species; regenerative medicine; self-renewal; MARROW STROMAL CELLS; INDUCED OXIDATIVE STRESS; HUMAN DENTAL-PULP; HYDROGEN-PEROXIDE; OSTEOGENIC DIFFERENTIATION; REPLICATIVE SENESCENCE; INDUCED APOPTOSIS; OSTEOBLASTIC DIFFERENTIATION; ADIPOCYTE DIFFERENTIATION; INFLAMMATORY RESPONSE;
D O I
10.1111/jcmm.13835
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mesenchymal stem cells (MSCs) are broadly used in cell-based regenerative medicine because of their self-renewal and multilineage potencies invitro and invivo. To ensure sufficient amounts of MSCs for therapeutic purposes, cells are generally cultured invitro for long-term expansion or specific terminal differentiation until cell transplantation. Although physiologically up-regulated reactive oxygen species (ROS) production is essential for maintenance of stem cell activities, abnormally high levels of ROS can harm MSCs both invitro and invivo. Overall, additional elucidation of the mechanisms by which physiological and pathological ROS are generated is necessary to better direct MSC fates and improve their therapeutic effects by controlling external ROS levels. In this review, we focus on the currently revealed ROS generation mechanisms and the regulatory routes for controlling their rates of proliferation, survival, senescence, apoptosis, and differentiation. A promising strategy in future regenerative medicine involves regulating ROS generation via various means to augment the therapeutic efficacy of MSCs, thus improving the prognosis of patients with terminal diseases.
引用
收藏
页码:5196 / 5207
页数:12
相关论文
共 137 条
[1]   Bioenergetics and the formation of mitochondrial reactive oxygen species [J].
Adam-Vizi, Vera ;
Chinopoulos, Christos .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2006, 27 (12) :639-645
[2]   The metabolic function of hepatocytes differentiated from human mesenchymal stem cells is inversely related to cellular glutathione levels [J].
Allameh, Abdolamir ;
Ahmadi-Ashtiani, Hamidreza ;
Aleagha, Mohammad Sajad Emami ;
Rastegar, Hossein .
CELL BIOCHEMISTRY AND FUNCTION, 2014, 32 (02) :194-200
[3]   TNF-α promotes survival and migration of MSCs under oxidative stress via NF-κB pathway to attenuate intimal hyperplasia in vein grafts [J].
Bai, Xiao ;
Xi, Jie ;
Bi, Yanwen ;
Zhao, Xin ;
Bing, Weidong ;
Meng, Xiangbin ;
Liu, Yimin ;
Zhu, Zhonglai ;
Song, Guangmin .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2017, 21 (09) :2077-2091
[4]   Vitamin E protects rat mesenchymal stem cells against hydrogen peroxide-induced oxidative stress in vitro and improves their therapeutic potential in surgically-induced rat model of osteoarthritis [J].
Bhatti, F. U. ;
Mehmood, A. ;
Latief, N. ;
Zahra, S. ;
Cho, H. ;
Khan, S. N. ;
Riazuddin, S. .
OSTEOARTHRITIS AND CARTILAGE, 2017, 25 (02) :321-331
[5]   Mitochondria and Reactive Oxygen Species: Physiology and Pathophysiology [J].
Bolisetty, Subhashini ;
Jaimes, Edgar A. .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2013, 14 (03) :6306-6344
[6]   Atmospheric Oxygen Inhibits Growth and Differentiation of Marrow-Derived Mouse Mesenchymal Stem Cells via a p53-Dependent Mechanism: Implications for Long-Term Culture Expansion [J].
Boregowda, Siddaraju V. ;
Krishnappa, Veena ;
Chambers, Jeremy W. ;
Lograsso, Philip V. ;
Lai, Wen-Tzu ;
Ortiz, Luis A. ;
Phinney, Donald G. .
STEM CELLS, 2012, 30 (05) :975-987
[7]   Interaction between ROS dependent DNA damage, mitochondria and p38 MAPK underlies senescence of human adult stem cells [J].
Borodkina, Aleksandra ;
Shatrova, Alla ;
Abushik, Polina ;
Nikolsky, Nikolay ;
Burova, Elena .
AGING-US, 2014, 6 (06) :481-495
[8]   CELLULAR PRODUCTION OF HYDROGEN-PEROXIDE [J].
BOVERIS, A ;
CHANCE, B ;
OSHINO, N .
BIOCHEMICAL JOURNAL, 1972, 128 (03) :617-&
[9]   Pigment epithelium-derived factor delays cellular senescence of human mesenchymal stem cells in vitro by reducing oxidative stress [J].
Cao, Yukun ;
Yang, Ting ;
Gu, Chunhu ;
Yi, Dinghua .
CELL BIOLOGY INTERNATIONAL, 2013, 37 (04) :305-313
[10]   Coordinated changes of mitochondrial biogenesis and antioxidant enzymes during osteogenic differentiation of human mesenchymal stem cells [J].
Chen, Chien-Tsun ;
Shih, Yu-Ru V. ;
Kuo, Tom K. ;
Lee, Oscar K. ;
Wei, Yau-Huei .
STEM CELLS, 2008, 26 (04) :960-968