Characterization and therapeutic applications of mesenchymal stem cells for regenerative medicine

被引:42
作者
Wang, Jie [2 ,4 ]
Chen, Zhuo [1 ,4 ,5 ]
Sun, Meiyan [3 ]
Xu, Huijing [3 ]
Gao, Yufei [1 ,4 ,5 ]
Liu, Jingwen [6 ]
Li, Miao [1 ,4 ,5 ]
机构
[1] Jilin Univ, China Japan Union Hosp, Dept Neurosurg, Changchun 130033, Peoples R China
[2] Jilin Univ, China Japan Union Hosp, Dept Neurol, Changchun 130033, Peoples R China
[3] Jilin Med Univ, Med Examinat Coll, Jilin 132013, Jilin, Peoples R China
[4] Jilin Univ, Jilin Prov Neurooncol Engn Lab, Changchun 130033, Peoples R China
[5] Jilin Univ, Jilin Prov Key Lab Neurooncol, Changchun 130033, Peoples R China
[6] Univ Houston, Dept Pharmacol & Pharmaceut Sci, Coll Pharm, Houston, TX 77030 USA
关键词
Mesenchymal stem cells (MSC); Cell-based therapy; Tissue engineering; Cell; Therapy; BONE-MARROW; ADIPOSE-TISSUE; STROMAL CELLS; MYOCARDIAL-INFARCTION; SHORT-TERM; LONG-TERM; TRANSPLANTATION; DIFFERENTIATION; EXPANSION; REPAIR;
D O I
10.1016/j.tice.2020.101330
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Background: Mesenchymal stem cells (MSCs) are multipotent, genomic stable, self-renewable, and culturally expandable adult stem cells. MSCs facilitate tissue development, maintenance and repair, and produce secretory factors that support engraftment and trophic functions, marking them an attractive option in cell therapy, regenerative medicine and tissue engineering. Method: In this review, we summarize the recent researches regarding the isolation and characterization of MSCs, therapeutic applications and advanced engineering techniques. We also discuss the advantages and limitations that remain to be overcome for MSCs based therapy. Results: It has been demonstrated that MSCs are able to modulate endogenous tissue and immune cells. Preclinical studies and early phase clinical trials have shown their great potential for tissue engineering of bone, cartilage, marrow stroma, muscle, fat, and other connective tissues. Conclusions: MSC-based therapy show considerable promise to rebuild damaged or diseased tissues, which could be a promising therapeutic method for regeneration medicine.
引用
收藏
页数:9
相关论文
共 122 条
[1]   Human mesenchymal stem cells modulate allogeneic immune cell responses [J].
Aggarwal, S ;
Pittenger, MF .
BLOOD, 2005, 105 (04) :1815-1822
[2]   Murine but not human mesenchymal stem cells generate osteosarcoma-like lesions in the lung [J].
Aguilar, Susana ;
Nye, Emma ;
Chan, Jerry ;
Loebinger, Michael ;
Spencer-Dene, Bradley ;
Fisk, Nick ;
Stamp, Gordon ;
Bonnet, Dominique ;
Janes, Sam M. .
STEM CELLS, 2007, 25 (06) :1586-1594
[3]   CD271 as a marker to identify mesenchymal stem cells from diverse sources before culture [J].
Alvarez-Viejo, Maria ;
Menendez-Menendez, Yolanda ;
Otero-Hernandez, Jesus .
WORLD JOURNAL OF STEM CELLS, 2015, 7 (02) :470-476
[4]  
Augello A, 2010, EUR CELLS MATER, V20, P121
[5]   Hepatocyte differentiation of mesenchymal stem cells from human adipose tissue in vitro promotes hepatic integration in vivo [J].
Aurich, H. ;
Sgodda, M. ;
Kaltwasser, P. ;
Vetter, M. ;
Weise, A. ;
Liehr, T. ;
Brulport, M. ;
Hengstler, J. G. ;
Dollinger, M. M. ;
Fleig, W. E. ;
Christ, B. .
GUT, 2009, 58 (04) :570-581
[6]   Platelet-derived growth factor receptors regulate mesenchymal stem cell fate: implications for neovascularization [J].
Ball, Stephen G. ;
Shuttleworth, C. Adrian ;
Kielty, Cay M. .
EXPERT OPINION ON BIOLOGICAL THERAPY, 2010, 10 (01) :57-71
[7]  
Ballini A, 2019, EUR REV MED PHARMACO, V23, P2916, DOI 10.26355/eurrev_201904_17570
[8]   Tumor Specific Recruitment and Reprogramming of Mesenchymal Stem Cells in Tumorigenesis [J].
Berger, Liron ;
Shamai, Yeela ;
Skorecki, Karl L. ;
Tzukerman, Maty .
STEM CELLS, 2016, 34 (04) :1011-1026
[9]   A rapid and efficient method for expansion of human mesenchymal stem cells [J].
Both, Sanne K. ;
Van der Muijsenberg, Adrie J. C. ;
Van Blitterswijk, Clemens A. ;
De Boer, Jan ;
De Bruijn, Joost D. .
TISSUE ENGINEERING, 2007, 13 (01) :3-9
[10]   MESENCHYMAL STEM-CELLS IN IN BONE-DEVELOPMENT, BONE REPAIR, AND SKELETAL REGENERATION THERAPY [J].
BRUDER, SP ;
FINK, DJ ;
CAPLAN, AI .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1994, 56 (03) :283-294