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
[61]   Cell therapy in acute myocardial infarction: measures of efficacy [J].
Lunde, Ketil ;
Aakhus, Svend .
HEART, 2008, 94 (08) :969-970
[62]   Intracoronary injection of mononuclear bone marrow cells in acute myocardial infarction [J].
Lunde, Ketil ;
Solheim, Svein ;
Aakhus, Svend ;
Arnesen, Harald ;
Abdelnoor, Michael ;
Egeland, Torstein ;
Endresen, Knut ;
Ilebekk, Arnfinn ;
Mangschau, Arild ;
Fjeld, Jan G. ;
Smith, Hans Jorgen ;
Taraldsrud, Eli ;
Grogaard, Haakon Kiil ;
Bjornerheim, Reidar ;
Brekke, Magne ;
Mueller, Carl ;
Hopp, Einar ;
Ragnarsson, Asgrimur ;
Brinchmann, Jan E. ;
Forfang, Kolbjorn .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (12) :1199-1209
[63]   Sonic Hedgehog-Modified Human CD34+Cells Preserve Cardiac Function After Acute Myocardial Infarction [J].
Mackie, Alexander R. ;
Klyachko, Ekaterina ;
Thorne, Tina ;
Schultz, Kathryn M. ;
Millay, Meredith ;
Ito, Aiko ;
Kamide, Christine E. ;
Liu, Ting ;
Gupta, Rajesh ;
Sahoo, Susmita ;
Misener, Sol ;
Kishore, Raj ;
Losordo, Douglas W. .
CIRCULATION RESEARCH, 2012, 111 (03) :312-+
[64]   Transplantation of adipose tissue mesenchymal cells conjugated with VEGF-releasing microcarriers promotes repair in murine myocardial infarction [J].
Madonna, Rosalinda ;
Petrov, Lyubomir ;
Teberino, Maria Anna ;
Manzoli, Lamberto ;
Karam, Jean-Pierre ;
Renna, Francesca Vera ;
Ferdinandy, Peter ;
Montero-Menei, Claudia N. ;
Yla-Herttuala, Seppo ;
De Caterina, Raffaele .
CARDIOVASCULAR RESEARCH, 2015, 108 (01) :39-49
[65]   Intracoronary cardiosphere-derived cells for heart regeneration after myocardial infarction (CADUCEUS): a prospective, randomised phase 1 trial [J].
Makkar, Raj R. ;
Smith, Rachel R. ;
Cheng, Ke ;
Malliaras, Konstantinos ;
Thomson, Louise E. J. ;
Berman, Daniel ;
Czer, Lawrence S. C. ;
Marban, Linda ;
Mendizabal, Adam ;
Johnston, Peter V. ;
Russell, Stuart D. ;
Schuleri, Karl H. ;
Lardo, Albert C. ;
Gerstenblith, Gary ;
Marban, Eduardo .
LANCET, 2012, 379 (9819) :895-904
[66]   Generation of functional murine cardiac myocytes from induced pluripotent stem cells [J].
Mauritz, Christina ;
Schwanke, Kristin ;
Reppel, Michael ;
Neef, Stefan ;
Katsirntaki, Katherina ;
Maier, Lars S. ;
Nguemo, Filomain ;
Menke, Sandra ;
Haustein, Moritz ;
Hescheler, Juergen ;
Hasenfuss, Gerd ;
Martin, Ulrich .
CIRCULATION, 2008, 118 (05) :507-517
[67]   Induced pluripotent stem cell (iPSC)-derived Flk-1 progenitor cells engraft, differentiate, and improve heart function in a mouse model of acute myocardial infarction [J].
Mauritz, Christina ;
Martens, Andreas ;
Rojas, Sebastian V. ;
Schnick, Tilman ;
Rathert, Christian ;
Schecker, Natalie ;
Menke, Sandra ;
Glage, Silke ;
Zweigerdt, Robert ;
Haverich, Axel ;
Martin, Ulrich ;
Kutschka, Ingo .
EUROPEAN HEART JOURNAL, 2011, 32 (21) :2634-2641
[68]   The effect of encapsulation of cardiac stem cells within matrix-enriched hydrogel capsules on cell survival, post-ischemic cell retention and cardiac function [J].
Mayfield, Audrey E. ;
Tilokee, Everad L. ;
Latham, Nicholas ;
McNeill, Brian ;
Lam, Bu-Khanh ;
Ruel, Marc ;
Suuronen, Erik J. ;
Courtman, David W. ;
Stewart, Duncan J. ;
Davis, Darryl R. .
BIOMATERIALS, 2014, 35 (01) :133-142
[69]   Intracoronary bone marrow cell transfer after myocardial infarction: 5-year follow-up from the randomized-controlled BOOST trial [J].
Meyer, Gerd P. ;
Wollert, Kai C. ;
Lotz, Joachim ;
Pirr, Jens ;
Rager, Ulrike ;
Lippolt, Peter ;
Hahn, Andreas ;
Fichtner, Stephanie ;
Schaefer, Arnd ;
Arseniev, Lubomir ;
Ganser, Arnold ;
Drexler, Helmut .
EUROPEAN HEART JOURNAL, 2009, 30 (24) :2978-2984
[70]   Intracoronary bone marrow cell transfer after myocardial infarction - Eighteen months' follow-up data from the randomized, controlled BOOST (BOne marrOw transfer to enhance ST-elevation infarct regeneration) trial [J].
Meyer, GP ;
Wollert, KC ;
Lotz, J ;
Steffens, J ;
Lippolt, P ;
Fichtner, S ;
Hecker, H ;
Schaefer, A ;
Arseniev, L ;
Hertenstein, B ;
Ganser, A ;
Drexler, H .
CIRCULATION, 2006, 113 (10) :1287-1294