Concise Review: Mesenchymal Stem Cells and Translational Medicine: Emerging Issues

被引:262
作者
Ren, Guangwen [1 ,2 ]
Chen, Xiaodong [1 ]
Dong, Fengping [1 ]
Li, Wenzhao [1 ]
Ren, Xiaohui [1 ]
Zhang, Yanyun [1 ]
Shi, Yufang [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Chinese Acad Sci, Shanghai Inst Biol Sci, Key Lab Stem Cell Biol,Inst Hlth Sci,Sch Med, Shanghai 200025, Peoples R China
[2] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Child Hlth Inst New Jersey, New Brunswick, NJ USA
基金
美国国家卫生研究院;
关键词
Mesenchymal stem cells; Immunosuppression; Cell-based therapy; Translational medicine; SYSTEMIC-LUPUS-ERYTHEMATOSUS; VERSUS-HOST-DISEASE; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; BONE-MARROW; STROMAL CELLS; INFARCTED MYOCARDIUM; MULTIPLE-SCLEROSIS; PEDIATRIC-PATIENTS; STEROID-RESISTANT; INTERFERON-BETA;
D O I
10.5966/sctm.2011-0019
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Mesenchymal stem cells (MSCs) are emerging as a promising therapeutic approach of cell-based therapy for a wide range of autoimmune disorders and degenerative diseases. In preclinical and clinical studies, MSCs have been shown to be highly efficient in treating graft-versus-host disease, systemic lupus erythematosus, multiple sclerosis, type 1 diabetes, myocardial infarction, liver cirrhosis, inflammatory bowel disease, and other disorders. The underlying therapeutic mechanisms of MSCs include their homing efficiency to the tissue injury sites, their differentiation potential, their capability to produce a large amount of trophic factors, and their immunomodulatory effect. Because tissue damage sites are complicated milieus with distinct types of inflammatory cells and factors, available data have demonstrated that the properties of MSCs could be fundamentally influenced by the inflammatory elements. Thus, an understanding of the interaction between MSCs and the inflammatory microenvironment will provide critical information in revealing the precise in vivo mechanisms of MSC-mediated therapeutic effects and designing more practical protocols for clinical use of these cells. STEM CELLS TRANSLATIONAL MEDICINE 2012;1:51-58
引用
收藏
页码:51 / 58
页数:8
相关论文
共 108 条
[71]   IFN-γ activation of mesenchymal stem cells for treatment and prevention of graft versus host disease [J].
Polchert, David ;
Sobinsky, Justin ;
Douglas, G. W. ;
Kidd, Martha ;
Moadsiri, Ada ;
Reina, Eduardo ;
Genrich, Kristyn ;
Mehrotra, Swati ;
Setty, Suman ;
Smith, Brett ;
Bartholomew, Amelia .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2008, 38 (06) :1745-1755
[72]   Efficacy and Safety of Ex Vivo Cultured Adult Human Mesenchymal Stem Cells (Prochymal™) in Pediatric Patients with Severe Refractory Acute Graft-Versus-Host Disease in a Compassionate Use Study [J].
Prasad, Vinod K. ;
Lucas, Kenneth G. ;
Kleiner, Gary I. ;
Talano, Julie An M. ;
Jacobsohn, David ;
Broadwater, Gloria ;
Monroy, Rod ;
Kurtzberg, Joanne .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2011, 17 (04) :534-541
[73]   Defining the risks of mesenchymal stromal cell therapy [J].
Prockop, Darwin J. ;
Brenner, Malcolm ;
Fibbe, Willem E. ;
Horwitz, Edwin ;
Le Blanc, Katarina ;
Phinney, Donald G. ;
Simmons, Paul J. ;
Sensebe, Lug ;
Keating, Armand .
CYTOTHERAPY, 2010, 12 (05) :576-578
[74]   Mesenchymal Stromal Cells Ameliorate Experimental Autoimmune Encephalomyelitis by Inhibiting CD4 Th17 T Cells in a CC Chemokine Lisgand 2-Dependent Manner [J].
Rafei, Moutih ;
Campeau, Philippe A. ;
Aguilar-Mahecha, Adriana ;
Buchanan, Marguerite ;
Williams, Patrick ;
Birman, Elena ;
Yuan, Shala ;
Young, Yoon Kow ;
Boivin, Marie-Noelle ;
Forner, Kathy ;
Basik, Mark ;
Galipeau, Jacques .
JOURNAL OF IMMUNOLOGY, 2009, 182 (10) :5994-6002
[75]   First experience in the use of bone marrow mesenchymal stem cells for the treatment of a patient with deep skin burns [J].
Rasulov, MF ;
Vasil'chenkov, AV ;
Onishchenko, NA ;
Krasheninnikov, ME ;
Kravchenko, VI ;
Gorshenin, TL ;
Pidtsan, RE ;
Potapov, IV .
BULLETIN OF EXPERIMENTAL BIOLOGY AND MEDICINE, 2005, 139 (01) :141-144
[76]   Cancer gene therapy using mesenchymal stem cells expressing interferon-β in a mouse prostate cancer lung metastasis model [J].
Ren, C. ;
Kumar, S. ;
Chanda, D. ;
Kallman, L. ;
Chen, J. ;
Mountz, J. D. ;
Ponnazhagan, S. .
GENE THERAPY, 2008, 15 (21) :1446-1453
[77]   Therapeutic potential of mesenchymal stem cells producing interferon-α in a mouse melanoma lung metastasis model [J].
Ren, Changchun ;
Kumar, Sanjay ;
Chanda, Diptiman ;
Chen, Jian ;
Mountz, John D. ;
Ponnazhagan, Selvarangan .
STEM CELLS, 2008, 26 (09) :2332-2338
[78]   Mesenchymal stem cell-mediated immunosuppression occurs via concerted action of chemokines and nitric oxide [J].
Ren, Guangwen ;
Zhang, Liying ;
Zhao, Xin ;
Xu, Guangwu ;
Zhang, Yingyu ;
Roberts, Arthur I. ;
Zhao, Robert Chunhua ;
Shi, Yufang .
CELL STEM CELL, 2008, 2 (02) :141-150
[79]   Inflammatory Cytokine-Induced Intercellular Adhesion Molecule-1 and Vascular Cell Adhesion Molecule-1 in Mesenchymal Stem Cells Are Critical for Immunosuppression [J].
Ren, Guangwen ;
Zhao, Xin ;
Zhang, Liying ;
Zhang, Jimin ;
L'Huillier, Andrew ;
Ling, Weifang ;
Roberts, Arthur I. ;
Le, Anh D. ;
Shi, Songtao ;
Shao, Changshun ;
Shi, Yufang .
JOURNAL OF IMMUNOLOGY, 2010, 184 (05) :2321-2328
[80]   Species Variation in the Mechanisms of Mesenchymal Stem Cell-Mediated Immunosuppression [J].
Ren, Guangwen ;
Su, Juanjuan ;
Zhang, Liying ;
Zhao, Xin ;
Ling, Weifang ;
L'Huillie, Andrew ;
Zhang, Jimin ;
Lu, Yongqing ;
Roberts, Arthur I. ;
Ji, Weizhi ;
Zhang, Huatang ;
Rabson, Arnold B. ;
Shi, Yufang .
STEM CELLS, 2009, 27 (08) :1954-1962