Somatic Cell Reprogramming into Cardiovascular Lineages

被引:7
作者
Chen, Jenny X. [1 ]
Plonowska, Karolina [2 ]
Wu, Sean M. [2 ,3 ,4 ]
机构
[1] Harvard Univ, Sch Med, Boston, MA USA
[2] Stanford Cardiovasc Inst, Stanford, CA USA
[3] Stanford Univ, Sch Med, Dept Med, Div Cardiovasc Med, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Inst Stem Cell Biol & Regenerat Med, Stanford, CA 94305 USA
关键词
cardiomyopathies; cardiomyopathy; heart disease; stem cells therapy; PLURIPOTENT STEM-CELLS; ZEBRAFISH HEART REGENERATION; ADULT HUMAN FIBROBLASTS; GENE-EXPRESSION; MOUSE FIBROBLASTS; DIRECT CONVERSION; NUCLEAR TRANSFER; DNA METHYLATION; FUNCTIONAL-PROPERTIES; HISTONE ACETYLATION;
D O I
10.1177/1074248414527641
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Ischemic cardiac disease is the leading cause of death in the developed world. The inability of the adult mammalian heart to adequately repair itself has motivated stem cell researchers to explore various strategies to regenerate cardiomyocytes after myocardial infarction. Over the past century, progressive gains in our knowledge about the cellular mechanisms governing fate determination have led to recent advances in cellular reprogramming. The identification of specific factors capable of inducing pluripotent phenotype in somatic cells as well as factors that can directly reprogram somatic cells into cardiomyocytes suggests the potential for these approaches to translate into clinical therapies in the future. Although conceptually appealing, the field of cell lineage reprogramming is in its infancy, and further research will be needed to improve the efficiency of the reprogramming process and the fidelity of the reprogrammed cells to their in vivo counterpart.
引用
收藏
页码:340 / 349
页数:10
相关论文
共 113 条
[11]   Adult mice generated from induced pluripotent stem cells [J].
Boland, Michael J. ;
Hazen, Jennifer L. ;
Nazor, Kristopher L. ;
Rodriguez, Alberto R. ;
Gifford, Wesley ;
Martin, Greg ;
Kupriyanov, Sergey ;
Baldwin, Kristin K. .
NATURE, 2009, 461 (7260) :91-U94
[12]   New sources of pancreatic β-cells [J].
Bonner-Weir, S ;
Weir, GC .
NATURE BIOTECHNOLOGY, 2005, 23 (07) :857-861
[13]  
BORNE SWM, 2009, NAT REV CARDIOL, V7, P30, DOI DOI 10.1038/NRCARDIO.2009.199
[14]   TRANSPLANTATION OF LIVING NUCLEI FROM BLASTULA CELLS INTO ENUCLEATED FROGS EGGS [J].
BRIGGS, R ;
KING, TJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1952, 38 (05) :455-463
[15]  
BRIGGS ROBERT, 1957, J MORPH, V100, P269, DOI 10.1002/jmor.1051000204
[16]   Direct generation of functional dopaminergic neurons from mouse and human fibroblasts [J].
Caiazzo, Massimiliano ;
Dell'Anno, Maria Teresa ;
Dvoretskova, Elena ;
Lazarevic, Dejan ;
Taverna, Stefano ;
Leo, Damiana ;
Sotnikova, Tatyana D. ;
Menegon, Andrea ;
Roncaglia, Paola ;
Colciago, Giorgia ;
Russo, Giovanni ;
Carninci, Piero ;
Pezzoli, Gianni ;
Gainetdinov, Raul R. ;
Gustincich, Stefano ;
Dityatev, Alexander ;
Broccoli, Vania .
NATURE, 2011, 476 (7359) :224-U151
[17]   Sheep cloned by nuclear transfer from a cultured cell line [J].
Campbell, KHS ;
McWhir, J ;
Ritchie, WA ;
Wilmut, I .
NATURE, 1996, 380 (6569) :64-66
[18]   Inefficient Reprogramming of Fibroblasts into Cardiomyocytes Using Gata4, Mef2c, and Tbx5 [J].
Chen, Jenny X. ;
Krane, Markus ;
Deutsch, Marcus-Andre ;
Wang, Li ;
Rav-Acha, Moshe ;
Gregoire, Serge ;
Engels, Marc C. ;
Rajarajan, Kuppusamy ;
Karra, Ravi ;
Abel, E. Dale ;
Wu, Joe C. ;
Milan, David ;
Wu, Sean M. .
CIRCULATION RESEARCH, 2012, 111 (01) :50-55
[19]   Induced Pluripotent Stem Cells and Embryonic Stem Cells Are Distinguished by Gene Expression Signatures [J].
Chin, Mark H. ;
Mason, Mike J. ;
Xie, Wei ;
Volinia, Stefano ;
Singer, Mike ;
Peterson, Cory ;
Ambartsumyan, Gayane ;
Aimiuwu, Otaren ;
Richter, Laura ;
Zhang, Jin ;
Khvorostov, Ivan ;
Ott, Vanessa ;
Grunstein, Michael ;
Lavon, Neta ;
Benvenisty, Nissim ;
Croce, Carlo M. ;
Clark, Amander T. ;
Baxter, Tim ;
Pyle, April D. ;
Teitell, Mike A. ;
Pelegrini, Matteo ;
Plath, Kathrin ;
Lowry, William E. .
CELL STEM CELL, 2009, 5 (01) :111-123
[20]   MYOD CONVERTS PRIMARY DERMAL FIBROBLASTS, CHONDROBLASTS, SMOOTH-MUSCLE, AND RETINAL PIGMENTED EPITHELIAL-CELLS INTO STRIATED MONONUCLEATED MYOBLASTS AND MULTINUCLEATED MYOTUBES [J].
CHOI, J ;
COSTA, ML ;
MERMELSTEIN, CS ;
CHAGAS, C ;
HOLTZER, S ;
HOLTZER, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (20) :7988-7992