Modification of mesenchymal stem cells for cardiac regeneration

被引:94
作者
Song, Heesang [2 ]
Song, Byeong-Wook [3 ]
Cha, Min-Ji [3 ]
Choi, In-Geol [4 ]
Hwang, Ki-Chul [1 ]
机构
[1] Yonsei Univ, Coll Med, Cardiovasc Res Inst, Seoul 120752, South Korea
[2] Yonsei Univ, Res Inst Sci Aging, Seoul 120752, South Korea
[3] Yonsei Univ, Coll Med, Brain Korea Project Med Sci 21, Seoul 120752, South Korea
[4] Korea Univ, Div Biotechnol, Coll Life Sci & Biotechnol, Seoul 136701, South Korea
关键词
cardiac regenration; cell adhesion; cell survival; mesenchymal stem cell; INTEGRIN-LINKED KINASE; ENDOTHELIAL PROGENITOR CELLS; BONE-MARROW; GROWTH-FACTOR; STROMAL CELLS; INTRACORONARY TRANSPLANTATION; TISSUE TRANSGLUTAMINASE; ISCHEMIC-MYOCARDIUM; HEART-FAILURE; IN-VITRO;
D O I
10.1517/14712590903455997
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Importance of the field. Mesenchymal stem cells (MSCs) have the greatest potential for use in cell-based therapy of human heart diseases, especially in myocardial infarcts. The therapeutic potential of MSCs in myocardial repair is based on the ability of MSCs to directly differentiate into cardiac tissue and on the paracrine actions of factors released from MSCs. However, the major obstacle in the clinical application of MSC-based therapy is the poor viability of the transplanted cells due to harsh microenvironments like ischemia, inflammation and/or anoikis in the infarcted myocardium. Recently, various approaches have been implemented in an effort to improve the survival of implanted MSCs through ex vivo manipulation of MSCs. Areas covered in this review. Major obstacles in MSC-based therapy are discussed, along with recent advances for enhancing therapeutic potential of engrafted MSCs from the past decade. What the reader will gain: This review focuses primarily on ex vivo manipulation of MSCs before transplantation, which includes pretreatment, preconditioning and genetic modification of MSCs, and future directions. Take home message: Modification of MSCs before transplantation has developed into a promising option for enhancing the beneficial effects of MSC-based therapy for cardiac repair after myocardial infarction.
引用
收藏
页码:309 / 319
页数:11
相关论文
共 104 条
[1]   Tissue transglutaminase is an integrin-binding adhesion coreceptor for fibronectin [J].
Akimov, SS ;
Krylov, D ;
Fleischman, LF ;
Belkin, AM .
JOURNAL OF CELL BIOLOGY, 2000, 148 (04) :825-838
[2]   Endothelial progenitor cells for postnatal vasculogenesis [J].
Asahara, T ;
Kawamoto, A .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2004, 287 (03) :C572-C579
[3]   TNFR gene-modified mesenchymal stem cells attenuate inflammation and cardiac dysfunction following MI [J].
Bao, Cuiyu ;
Guo, Jun ;
Lin, Guosheng ;
Hu, Mingyan ;
Hu, Zhimin .
SCANDINAVIAN CARDIOVASCULAR JOURNAL, 2008, 42 (01) :56-62
[4]   Mesenchymal stem cells suppress lymphocyte proliferation in vitro and prolong skin graft survival in vivo [J].
Bartholomew, A ;
Sturgeon, C ;
Siatskas, M ;
Ferrer, K ;
McIntosh, K ;
Patil, S ;
Hardy, W ;
Devine, S ;
Ucker, D ;
Deans, R ;
Moseley, A ;
Hoffman, R .
EXPERIMENTAL HEMATOLOGY, 2002, 30 (01) :42-48
[5]   Epithelial stem cells: Turning over new leaves [J].
Blanpain, Cedric ;
Horsley, Valerie ;
Fuchs, Elaine .
CELL, 2007, 128 (03) :445-458
[6]   Mesenchymal Stem Cells Pretreated with Delivered Hph-1-Hsp70 Protein Are Protected from Hypoxia-Mediated Cell Death and Rescue Heart Functions from Myocardial Injury [J].
Chang, Woochul ;
Song, Byeong-Wook ;
Lim, Soyeon ;
Song, Heesang ;
Shim, Chi Young ;
Cha, Min-Ji ;
Ahn, Dong Hyuck ;
Jung, Young-Gook ;
Lee, Dong-Ho ;
Chung, Ji Hyung ;
Choi, Ki-Doo ;
Lee, Seung-Kyou ;
Chung, Namsik ;
Lee, Sang-Kyou ;
Jang, Yangsoo ;
Hwang, Ki-Chul .
STEM CELLS, 2009, 27 (09) :2283-2292
[7]   Lysophosphatidic acid protects mesenchymal stem cells against hypoxia and serum deprivation-induced apoptosis [J].
Chen, Jinghai ;
Baydoun, Anwar R. ;
Xu, Ruixia ;
Deng, Linzi ;
Liu, Xuebin ;
Zhu, Weiquan ;
Shi, Linhui ;
Cong, Xiangfeng ;
Hu, Shengshou ;
Chen, Xi .
STEM CELLS, 2008, 26 (01) :135-145
[8]   Effect on left ventricular function of intracoronary transplantation of autologous bone marrow mesenchymal stem cell in patients with acute myocardial infarction [J].
Chen, SL ;
Fang, W ;
Ye, F ;
Liu, YH ;
Qian, J ;
Shan, S ;
Zhang, J ;
Zhao, RCH ;
Liao, LM ;
Lin, S ;
Sun, JP .
AMERICAN JOURNAL OF CARDIOLOGY, 2004, 94 (01) :92-95
[9]   Cyclosporin A pre-incubation attenuates hypoxia/reoxygenation-induced apoptosis in mesenchymal stem cells [J].
Chen, T. -L. ;
Wang, J. -A. ;
Shi, H. ;
Gui, C. ;
Luo, R. -H. ;
Xie, X. -J. ;
Xiang, M. -X. ;
Zhang, X. ;
Cao, J. .
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 2008, 68 (07) :585-593
[10]   Targeted migration of mesenchymal stem cells modified with CXCR4 gene to infarcted myocardium improves cardiac performance [J].
Cheng, Zhaokang ;
Ou, Lailiang ;
Zhou, Xin ;
Li, Fei ;
Jia, Xiaohua ;
Zhang, Yinguo ;
Liu, Xiaolei ;
Li, Yuming ;
Ward, Christopher A. ;
Melo, Luis G. ;
Kong, Deling .
MOLECULAR THERAPY, 2008, 16 (03) :571-579