Stem Cell Technology in Cardiac Regeneration: A Pluripotent Stem Cell Promise

被引:70
作者
Duelen, Robin [1 ]
Sampaolesi, Maurilio [1 ,2 ]
机构
[1] Katholieke Univ Leuven, Dept Dev & Regenerat, Stem Cell Biol & Embryol Unit, Translat Cardiomyol Lab,Stem Cell Inst Leuven, B-3000 Leuven, Belgium
[2] Univ Pavia, Div Human Anat, Dept Publ Hlth Expt & Forens Med, I-27100 Pavia, Italy
关键词
Embryonic cardiomyogenesis; Heart regeneration; Stem cell-based therapy; Human pluripotent stem cell; Stem cell-derived exosome; ACUTE MYOCARDIAL-INFARCTION; LEFT-VENTRICULAR FUNCTION; BONE-MARROW-CELLS; ENGINEERED HEART-TISSUE; PROGENITOR CELLS; MONONUCLEAR-CELLS; INTRACORONARY INJECTION; ISCHEMIC ANGIOGENESIS; WNT/BETA-CATENIN; SOMATIC-CELLS;
D O I
10.1016/j.ebiom.2017.01.029
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Despite advances in cardiovascular biology and medical therapy, heart disorders are the leading cause of death worldwide. Cell-based regenerative therapies become a promising treatment for patients affected by heart failure, but also underline the need for reproducible results in preclinical and clinical studies for safety and efficacy. Enthusiasm has been tempered by poor engraftment, survival and differentiation of the injected adult stem cells. The crucial challenge is identification and selection of the most suitable stem cell type for cardiac regenerative medicine. Human pluripotent stem cells (PSCs) have emerged as attractive cell source to obtain cardiomyocytes (CMs), with potential applications, including drug discovery and toxicity screening, disease modelling and innovative cell therapies. Lessons from embryology offered important insights into the development of stem cell-derived CMs. However, the generation of a CM population, uniform in cardiac subtype, adult maturation and functional properties, is highly recommended. Moreover, hurdles regarding tumorigenesis, graft cell death, immune rejection and arrhythmogenesis need to be overcome in clinical practice. Here we highlight the recent progression in PSC technologies for the regeneration of injured heart. We review novel strategies that might overcome current obstacles in heart regenerative medicine, aiming at improving cell survival and functional integration after cell transplantation. (C) 2017 Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:30 / 40
页数:11
相关论文
共 116 条
[51]   Electromechanical integration of cardiomyocytes derived from human embryonic stem cells [J].
Kehat, I ;
Khimovich, L ;
Caspi, O ;
Gepstein, A ;
Shofti, R ;
Arbel, G ;
Huber, I ;
Satin, J ;
Itskovitz-Eldor, J ;
Gepstein, L .
NATURE BIOTECHNOLOGY, 2004, 22 (10) :1282-1289
[52]   Controlling Expansion and Cardiomyogenic Differentiation of Human Pluripotent Stem Cells in Scalable Suspension Culture [J].
Kempf, Henning ;
Olmer, Ruth ;
Kropp, Christina ;
Rueckert, Michael ;
Jara-Avaca, Monica ;
Robles-Diaz, Diana ;
Franke, Annika ;
Elliott, David A. ;
Wojciechowski, Daniel ;
Fischer, Martin ;
Lara, Angelica Roa ;
Kensah, George ;
Gruh, Ina ;
Haverich, Axel ;
Martin, Ulrich ;
Zweigerdt, Robert .
STEM CELL REPORTS, 2014, 3 (06) :1132-1146
[53]   Embryonic Stem Cell-Derived Exosomes Promote Endogenous Repair Mechanisms and Enhance Cardiac Function Following Myocardial Infarction [J].
Khan, Mohsin ;
Nickoloff, Emily ;
Abramova, Tatiana ;
Johnson, Jennifer ;
Verma, Suresh Kumar ;
Krishnamurthy, Prasanna ;
Mackie, Alexander Roy ;
Vaughan, Erin ;
Garikipati, Venkata Naga Srikanth ;
Benedict, Cynthia ;
Ramirez, Veronica ;
Lambers, Erin ;
Ito, Aiko ;
Gao, Erhe ;
Misener, Sol ;
Luongo, Timothy ;
Elrod, John ;
Qin, Gangjian ;
Houser, Steven R. ;
Koch, Walter J. ;
Kishore, Raj .
CIRCULATION RESEARCH, 2015, 117 (01) :52-64
[54]   Current status of pluripotent stem cells: moving the first therapies to the clinic [J].
Kimbrel, Erin A. ;
Lanza, Robert .
NATURE REVIEWS DRUG DISCOVERY, 2015, 14 (10) :681-692
[55]  
Kinder SJ, 2001, DEVELOPMENT, V128, P3623
[56]   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
[57]   Somatic transcriptome priming gates lineage-specific differentiation potential of human-induced pluripotent stem cell states [J].
Lee, Jong-Hee ;
Lee, Jung Bok ;
Shapovalova, Zoya ;
Fiebig-Comyn, Aline ;
Mitchell, Ryan R. ;
Laronde, Sarah ;
Szabo, Eva ;
Benoit, Yannick D. ;
Bhatia, Mickie .
NATURE COMMUNICATIONS, 2014, 5
[58]   Transplantation of progenitor cells and regeneration enhancement in acute myocardial infarction (TOPCARE-AMI): final 5-year results suggest long-term safety and efficacy [J].
Leistner, David M. ;
Fischer-Rasokat, Ulrich ;
Honold, Joerg ;
Seeger, Florian H. ;
Schaechinger, Volker ;
Lehmann, Ralf ;
Martin, Hans ;
Burck, Iris ;
Urbich, Carmen ;
Dimmeler, Stefanie ;
Zeiher, Andreas M. ;
Assmus, Birgit .
CLINICAL RESEARCH IN CARDIOLOGY, 2011, 100 (10) :925-934
[59]   Hotspots of aberrant epigenomic reprogramming in human induced pluripotent stem cells [J].
Lister, Ryan ;
Pelizzola, Mattia ;
Kida, Yasuyuki S. ;
Hawkins, R. David ;
Nery, Joseph R. ;
Hon, Gary ;
Antosiewicz-Bourget, Jessica ;
O'Malley, Ronan ;
Castanon, Rosa ;
Klugman, Sarit ;
Downes, Michael ;
Yu, Ruth ;
Stewart, Ron ;
Ren, Bing ;
Thomson, James A. ;
Evans, Ronald M. ;
Ecker, Joseph R. .
NATURE, 2011, 471 (7336) :68-U84
[60]   MicroRNA-155 prevents necrotic cell death in human cardiomyocyte progenitor cells via targeting RIP1 [J].
Liu, Jia ;
van Mil, Alain ;
Vrijsen, Krijn ;
Zhao, Jiajun ;
Gao, Ling ;
Metz, Corina H. G. ;
Goumans, Marie-Jose ;
Doevendans, Pieter A. ;
Sluijter, Joost P. G. .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2011, 15 (07) :1474-1482