Therapeutic approaches for cardiac regeneration and repair

被引:381
作者
Hashimoto, Hisayuki [1 ,2 ]
Olson, Eric N. [1 ,2 ]
Bassel-Duby, Rhonda [1 ,2 ]
机构
[1] Univ Texas Southwestern Med Ctr Dallas, Dept Mol Biol, Hamon Ctr Regenerat Sci & Med, Dallas, TX 75390 USA
[2] Univ Texas Southwestern Med Ctr Dallas, Senator Paul D Wellstone Muscular Dystrophy Coope, Dallas, TX 75390 USA
关键词
PLURIPOTENT STEM-CELLS; MAMMALIAN HEART REGENERATION; ACUTE MYOCARDIAL-INFARCTION; CARDIOMYOCYTE DNA-SYNTHESIS; FIBROBLAST GROWTH FACTOR-2; CARDIOSPHERE-DERIVED CELLS; TO-MESENCHYMAL TRANSITION; LEFT-VENTRICULAR FUNCTION; LARGE ANIMAL-MODELS; PROGENITOR CELLS;
D O I
10.1038/s41569-018-0036-6
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Ischaemic heart disease is a leading cause of death worldwide. Injury to the heart is followed by loss of the damaged cardiomyocytes, which are replaced with fibrotic scar tissue. Depletion of cardiomyocytes results in decreased cardiac contraction, which leads to pathological cardiac dilatation, additional cardiomyocyte loss, and mechanical dysfunction, culminating in heart failure. This sequential reaction is defined as cardiac remodelling. Many therapies have focused on preventing the progressive process of cardiac remodelling to heart failure. However, after patients have developed end-stage heart failure, intervention is limited to heart transplantation. One of the main reasons for the dramatic injurious effect of cardiomyocyte loss is that the adult human heart has minimal regenerative capacity. In the past 2 decades, several strategies to repair the injured heart and improve heart function have been pursued, including cellular and noncellular therapies. In this Review, we discuss current therapeutic approaches for cardiac repair and regeneration, describing outcomes, limitations, and future prospects of preclinical and clinical trials of heart regeneration. Substantial progress has been made towards understanding the cellular and molecular mechanisms regulating heart regeneration, offering the potential to control cardiac remodelling and redirect the adult heart to a regenerative state.
引用
收藏
页码:585 / 600
页数:16
相关论文
共 211 条
[1]
Notch Inhibition Enhances Cardiac Reprogramming by Increasing MEF2C Transcriptional Activity [J].
Abad, Maria ;
Hashimoto, Hisayuki ;
Zhou, Huanyu ;
Morales, Maria Gabriela ;
Chen, Beibei ;
Bassel-Duby, Rhonda ;
Olson, Eric N. .
STEM CELL REPORTS, 2017, 8 (03) :548-560
[2]
Long-term (1 year) functional and histological results of autologous skeletal muscle cells transplantation in rat [J].
Al Attar, N ;
Carrion, C ;
Ghostine, S ;
Garcin, I ;
Vilquin, JT ;
Hagège, AA ;
Menasché, P .
CARDIOVASCULAR RESEARCH, 2003, 58 (01) :142-148
[3]
Delivery of siRNA to the mouse brain by systemic injection of targeted exosomes [J].
Alvarez-Erviti, Lydia ;
Seow, Yiqi ;
Yin, HaiFang ;
Betts, Corinne ;
Lakhal, Samira ;
Wood, Matthew J. A. .
NATURE BIOTECHNOLOGY, 2011, 29 (04) :341-U179
[4]
Amado LC, 2005, P NATL ACAD SCI USA, V102, P11474, DOI 10.1073/pnas.0504388102
[5]
Single-cut genome editing restores dystrophin expression in a new mouse model of muscular dystrophy [J].
Amoasii, Leonela ;
Long, Chengzu ;
Li, Hui ;
Mireault, Alex A. ;
Shelton, John M. ;
Sanchez-Ortiz, Efrain ;
McAnally, John R. ;
Bhattacharyya, Samadrita ;
Schmidt, Florian ;
Grimm, Dirk ;
Hauschka, Stephen D. ;
Bassel-Duby, Rhonda ;
Olson, Eric N. .
SCIENCE TRANSLATIONAL MEDICINE, 2017, 9 (418)
[6]
[Anonymous], 2014, LANCET, V383, P1279
[7]
Antonitsis Polychronis, 2007, Interact Cardiovasc Thorac Surg, V6, P593, DOI 10.1510/icvts.2007.157875
[8]
Mesenchymal stem cell-derived exosomes increase ATP levels, decrease oxidative stress and activate PI3K/Akt pathway to enhance myocardial viability and prevent adverse remodeling after myocardial ischemia/reperfusion injury [J].
Arslan, Fatih ;
Lai, Ruenn Chai ;
Smeets, Mirjam B. ;
Akeroyd, Lars ;
Choo, Andre ;
Aguor, Eissa N. E. ;
Timmers, Leo ;
van Rijen, Harold V. ;
Doevendans, Pieter A. ;
Pasterkamp, Gerard ;
Lim, Sai Kiang ;
de Kleijn, Dominique P. .
STEM CELL RESEARCH, 2013, 10 (03) :301-312
[9]
Macrophages are required for neonatal heart regeneration [J].
Aurora, Arin B. ;
Porrello, Enzo R. ;
Tan, Wei ;
Mahmoud, Ahmed I. ;
Hi, Joseph A. ;
Bassel-Duby, Rhonda ;
Sadek, Hesham A. ;
Olsonl, Eric N. .
JOURNAL OF CLINICAL INVESTIGATION, 2014, 124 (03) :1382-1392
[10]
MicroRNA-214 protects the mouse heart from ischemic injury by controlling Ca2+ overload and cell death [J].
Aurora, Arin B. ;
Mahmoud, Ahmed I. ;
Luo, Xiang ;
Johnson, Brett A. ;
van Rooij, Eva ;
Matsuzaki, Satoshi ;
Humphries, Kenneth M. ;
Hill, Joseph A. ;
Bassel-Duby, Rhonda ;
Sadek, Hesham A. ;
Olson, Eric N. .
JOURNAL OF CLINICAL INVESTIGATION, 2012, 122 (04) :1222-1232