Use of Mesenchymal Stem Cells for Therapy of Cardiac Disease

被引:365
作者
Karantalis, Vasileios [1 ]
Hare, Joshua M. [1 ]
机构
[1] Univ Miami, Miller Sch Med, Interdisciplinary Stem Cell Inst, Coral Gables, FL 33124 USA
基金
美国国家卫生研究院;
关键词
cell differentiation; mesenchymal stem cell; regeneration; stem cells; MARROW STROMAL CELLS; ACUTE MYOCARDIAL-INFARCTION; LEFT-VENTRICULAR FUNCTION; HUMAN BONE-MARROW; EXOSOME-MEDIATED TRANSFER; ENHANCE VASCULAR DENSITY; IMPROVE HEART FUNCTION; ISCHEMIC CARDIOMYOPATHY; PROGENITOR CELLS; PRECURSOR CELLS;
D O I
10.1161/CIRCRESAHA.116.303614
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Despite substantial clinical advances over the past 65 years, cardiovascular disease remains the leading cause of death in America. The past 15 years has witnessed major basic and translational interest in the use of stem and precursor cells as a therapeutic agent for chronically injured organs. Among the cell types under investigation, adult mesenchymal stem cells are widely studied, and in early stage, clinical studies show promise for repair and regeneration of cardiac tissues. The ability of mesenchymal stem cells to differentiate into mesoderm-and nonmesoderm-derived tissues, their immunomodulatory effects, their availability, and their key role in maintaining and replenishing endogenous stem cell niches have rendered them one of the most heavily investigated and clinically tested type of stem cell. Accumulating data from preclinical and early phase clinical trials document their safety when delivered as either autologous or allogeneic forms in a range of cardiovascular diseases, but also importantly define parameters of clinical efficacy that justify further investigation in larger clinical trials. Here, we review the biology of mesenchymal stem cells, their interaction with endogenous molecular and cellular pathways, and their modulation of immune responses. Additionally, we discuss factors that enhance their proliferative and regenerative ability and factors that may hinder their effectiveness in the clinical setting.
引用
收藏
页码:1413 / 1430
页数:18
相关论文
共 176 条
[1]
Miro1 regulates intercellular mitochondrial transport & enhances mesenchymal stem cell rescue efficacy [J].
Ahmad, Tanveer ;
Mukherjee, Shravani ;
Pattnaik, Bijay ;
Kumar, Manish ;
Singh, Suchita ;
Kumar, Manish ;
Rehman, Rakhshinda ;
Tiwari, Brijendra K. ;
Jha, Kumar A. ;
Barhanpurkar, Amruta P. ;
Wani, Mohan R. ;
Roy, Soumya S. ;
Mabalirajan, Ulaganathan ;
Ghosh, Balaram ;
Agrawal, Anurag .
EMBO JOURNAL, 2014, 33 (09) :994-1010
[2]
Fusion of bone-marrow-derived cells with Purkinje neurons, cardiomyocytes and hepatocytes [J].
Alvarez-Dolado, M ;
Pardal, R ;
Garcia-Vardugo, JM ;
Fike, JR ;
Lee, HO ;
Pfeffer, K ;
Lois, C ;
Morrison, SJ ;
Alvarez-Buylla, A .
NATURE, 2003, 425 (6961) :968-973
[3]
Amado LC, 2005, P NATL ACAD SCI USA, V102, P11474, DOI 10.1073/pnas.0504388102
[4]
Multimodality noninvasive imaging demonstrates in vivo cardiac regeneration after mesenchymal stem cell therapy [J].
Amado, Luciano C. ;
Schuleri, Karl H. ;
Saliaris, Anastasios P. ;
Boyle, Andrew J. ;
Helm, Robert ;
Oskouei, Behzad ;
Centola, Marco ;
Eneboe, Virginia ;
Young, Randell ;
Lima, Joao A. C. ;
Lardo, Albert C. ;
Heldman, Alan W. ;
Hare, Joshua M. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2006, 48 (10) :2116-2124
[5]
Concise Review: Circulating Endothelial Progenitor Cells for Vascular Medicine [J].
Asahara, Takayuki ;
Kawamoto, Atsuhiko ;
Masuda, Haruchika .
STEM CELLS, 2011, 29 (11) :1650-1655
[6]
Mesenchymal Precursor Cells as Adjunctive Therapy in Recipients of Contemporary Left Ventricular Assist Devices [J].
Ascheim, Deborah D. ;
Gelijns, Annetine C. ;
Goldstein, Daniel ;
Moye, Lemuel A. ;
Smedira, Nicholas ;
Lee, Sangjin ;
Klodell, Charles T. ;
Szady, Anita ;
Parides, Michael K. ;
Jeffries, Neal O. ;
Skerrett, Donna ;
Taylor, Doris A. ;
Rame, Eduardo ;
Milano, Carmelo ;
Rogers, Joseph G. ;
Lynch, Janine ;
Dewey, Todd ;
Eichhorn, Eric ;
Sun, Benjamin ;
Feldman, David ;
Simari, Robert ;
O'Gara, Patrick T. ;
Taddei-Peters, Wendy C. ;
Miller, Marissa A. ;
Naka, Yoshifumi ;
Bagiella, Emilia ;
Rose, Eric A. ;
Woo, Y. Joseph .
CIRCULATION, 2014, 129 (22) :2287-+
[7]
Systemic delivery of bone marrow-derived mesenchymal stem cells to the infarcted myocardium - Feasibility, cell migration, and body distribution [J].
Barbash, IM ;
Chouraqui, P ;
Baron, J ;
Feinberg, MS ;
Etzion, S ;
Tessone, A ;
Miller, L ;
Guetta, E ;
Zipori, D ;
Kedes, LH ;
Kloner, RA ;
Leor, J .
CIRCULATION, 2003, 108 (07) :863-868
[8]
Macrophage diversity in cardiac inflammation: A review [J].
Barin, Jobert G. ;
Rose, Noel R. ;
Cihakova, Daniela .
IMMUNOBIOLOGY, 2012, 217 (05) :468-475
[9]
Cardiopoietic Stem Cell Therapy in Heart Failure [J].
Bartunek, Jozef ;
Behfar, Atta ;
Dolatabadi, Dariouch ;
Vanderheyden, Marc ;
Ostojic, Miodrag ;
Dens, Jo ;
El Nakadi, Badih ;
Banovic, Marko ;
Beleslin, Branko ;
Vrolix, Mathias ;
Legrand, Victor ;
Vrints, Christian ;
Vanoverschelde, Jean Louis ;
Crespo-Diaz, Ruben ;
Homsy, Christian ;
Tendera, Michal ;
Waldman, Scott ;
Wijns, William ;
Terzic, Andre .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2013, 61 (23) :2329-2338
[10]
Isolation of functionally distinct mesenchymal stem cell subsets using antibodies against CD56, CD271, and mesenchymal stem cell antigen-1 [J].
Battula, Venkata Lokesh ;
Treml, Sabrina ;
Bareiss, Petra M. ;
Gieseke, Friederike ;
Roelofs, Helene ;
de Zwart, Peter ;
Mueller, Ingo ;
Schewe, Bernhard ;
Skutella, Thomas ;
Fibbe, Willem E. ;
Kanz, Lothar ;
Buehring, Hans-Joerg .
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2009, 94 (02) :173-184