Comparison of Human Embryonic Stem Cell-Derived Cardiomyocytes, Cardiovascular Progenitors, and Bone Marrow Mononuclear Cells for Cardiac Repair

被引:75
作者
Fernandes, Sarah [1 ,2 ,3 ]
Chong, James J. H. [1 ,2 ,3 ,4 ,5 ]
Paige, Sharon L. [1 ,2 ,3 ]
Iwata, Mineo [8 ]
Torok-Storb, Beverly [8 ]
Keller, Gordon [9 ]
Reinecke, Hans [1 ,2 ,3 ]
Murry, Charles E. [1 ,2 ,3 ,6 ,7 ]
机构
[1] Univ Washington, Ctr Cardiovasc Biol, Seattle, WA 98109 USA
[2] Univ Washington, Inst Stem Cell & Regenerat Med, Seattle, WA 98109 USA
[3] Univ Washington, Dept Pathol, Seattle, WA 98109 USA
[4] Univ Sydney, Sch Med, Sydney, NSW 2006, Australia
[5] Univ Sydney, Westmead Millennium Inst Med Res, Sydney, NSW 2145, Australia
[6] Univ Washington, Dept Bioengn, Seattle, WA 98109 USA
[7] Univ Washington, Dept Med Cardiol, Seattle, WA 98109 USA
[8] Fred Hutchinson Canc Res Ctr, Seattle, WA 98109 USA
[9] Ontario Canc Inst, McEwen Ctr Regenerat Med, Toronto, ON M5G 2M9, Canada
来源
STEM CELL REPORTS | 2015年 / 5卷 / 05期
基金
英国医学研究理事会;
关键词
SKELETAL MYOBLAST TRANSPLANTATION; THERAPY; PERFORMANCE; INFARCTION;
D O I
10.1016/j.stemcr.2015.09.011
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Cardiomyocytes derived from human embryonic stem cells (hESC-CMs) can improve the contractility of injured hearts. We hypothesized that mesodermal cardiovascular progenitors (hESC-CVPs), capable of generating vascular cells in addition to cardiomyocytes, would provide superior repair by contributing to multiple components of myocardium. We performed a head-to-head comparison of hESC-CMs and hESC-CVPs and compared these with the most commonly used clinical cell type, human bone marrow mononuclear cells (hBM-MNCs). In a nude rat model of myocardial infarction, hESC-CMs and hESC-CVPs generated comparable grafts. Both similarly improved systolic function and ventricular dilation. Furthermore, only rare human vessels formed from hESC-CVPs. hBM-MNCs attenuated ventricular dilation and enhanced host vascularization without engrafting long-term or improving contractility. Thus, hESC-CMs and CVPs show similar efficacy for cardiac repair, and both are more efficient than hBM-MNCs. However, hESC-CVPs do not form larger grafts or more significant numbers of human vessels in the infarcted heart.
引用
收藏
页码:753 / 762
页数:10
相关论文
共 23 条
[1]   Transplantation of human embryonic stem cell-derived cardiomyocytes improves myocardiol performance in infrcted rat hearts [J].
Caspi, Oren ;
Huber, Irit ;
Kehat, Izhak ;
Habib, Manhal ;
Arbel, Gil ;
Gepstein, Amira ;
Yankelson, Lior ;
Aronson, Doron ;
Beyar, Rafael ;
Gepstein, Lior .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2007, 50 (19) :1884-1893
[2]   Human embryonic-stem-cell-derived cardiomyocytesregenerate non-humanprimate hearts [J].
Chong, James J. H. ;
Yang, Xiulan ;
Don, Creighton W. ;
Minami, Elina ;
Liu, Yen-Wen ;
Weyers, Jill J. ;
Mahoney, William M., Jr. ;
Van Biber, Benjamin ;
Cook, Savannah M. ;
Palpant, Nathan J. ;
Gantz, Jay A. ;
Fugate, James A. ;
Muskheli, Veronica ;
Gough, G. Michael ;
Vogel, Keith W. ;
Astley, Cliff A. ;
Hotchkiss, Charlotte E. ;
Baldessari, Audrey ;
Pabon, Lil ;
Reinecke, Hans ;
Gill, Edward A. ;
Nelson, Veronica ;
Kiem, Hans-Peter ;
Laflamme, Michael A. ;
Murry, Charles E. .
NATURE, 2014, 510 (7504) :273-+
[3]   Cell Therapy for Left Ventricular Dysfunction: An Overview for Cardiac Clinicians [J].
Chong, James J. H. .
HEART LUNG AND CIRCULATION, 2012, 21 (09) :532-542
[4]   Experience From Experimental Cell Transplantation Therapy of Myocardial Infarction: What Have We Learned? [J].
Dai, Wangde ;
Kay, Gregory L. ;
Jyrala, Aarne J. ;
Kloner, Robert A. .
CELL TRANSPLANTATION, 2013, 22 (03) :563-568
[5]   Human embryonic stem cell-derived cardiomyocytes engraft but do not alter cardiac remodeling after chronic infarction in rats [J].
Fernandes, S. ;
Naumova, A. V. ;
Zhu, W. Z. ;
Laflamme, M. A. ;
Gold, J. ;
Murry, C. E. .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2010, 49 (06) :941-949
[6]   Cell transplantation to prevent heart failure: A comparison of cell types [J].
Fujii, T ;
Yau, TM ;
Weisel, RD ;
Ohno, N ;
Mickle, DAG ;
Shiono, N ;
Ozawa, T ;
Matsubayashi, K ;
Li, RK .
ANNALS OF THORACIC SURGERY, 2003, 76 (06) :2062-2070
[7]   Regeneration Next: Toward Heart Stem Cell Therapeutics [J].
Hansson, Emil M. ;
Lindsay, Mark E. ;
Chien, Kenneth R. .
CELL STEM CELL, 2009, 5 (04) :364-377
[8]   Comparison of benefits on myocardial performance of cellular cardiomyoplasty with skeletal myoblasts and fibroblasts [J].
Hutcheson, KA ;
Atkins, BZ ;
Hueman, MT ;
Hopkins, MB ;
Glower, DD ;
Taylor, DA .
CELL TRANSPLANTATION, 2000, 9 (03) :359-368
[9]   Neovascularization of ischemic myocardium by human bone-marrow-derived angioblasts prevents cardiomyocyte apoptosis, reduces remodeling and improves cardiac function [J].
Kocher, AA ;
Schuster, MD ;
Szabolcs, MJ ;
Takuma, S ;
Burkhoff, D ;
Wang, J ;
Homma, S ;
Edwards, NM ;
Itescu, S .
NATURE MEDICINE, 2001, 7 (04) :430-436
[10]   Cardiomyocytes derived from human embryonic stem cells in pro-survival factors enhance function of infarcted rat hearts [J].
Laflamme, Michael A. ;
Chen, Kent Y. ;
Naumova, Anna V. ;
Muskheli, Veronica ;
Fugate, James A. ;
Dupras, Sarah K. ;
Reinecke, Hans ;
Xu, Chunhui ;
Hassanipour, Mohammad ;
Police, Shailaja ;
O'Sullivan, Chris ;
Collins, Lila ;
Chen, Yinhong ;
Minami, Elina ;
Gill, Edward A. ;
Ueno, Shuichi ;
Yuan, Chun ;
Gold, Joseph ;
Murry, Charles E. .
NATURE BIOTECHNOLOGY, 2007, 25 (09) :1015-1024