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
[1]   Induced regeneration-the progress and promise of direct reprogramming for heart repair [J].
Addis, Russell C. ;
Epstein, Jonathan A. .
NATURE MEDICINE, 2013, 19 (07) :829-836
[2]   ACETYLATION + METHYLATION OF HISTONES + THEIR POSSIBLE ROLE IN REGULATION OF RNA SYNTHESIS [J].
ALLFREY, VG ;
FAULKNER, R ;
MIRSKY, AE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1964, 51 (05) :786-+
[3]   Direct Reprogramming of Adult Human Fibroblasts to Functional Neurons under Defined Conditions [J].
Ambasudhan, Rajesh ;
Talantova, Maria ;
Coleman, Ronald ;
Yuan, Xu ;
Zhu, Saiyong ;
Lipton, Stuart A. ;
Ding, Sheng .
CELL STEM CELL, 2011, 9 (02) :113-118
[4]   Generation of pluripotent stem cells from adult mouse liver and stomach cells [J].
Aoi, Takashi ;
Yae, Kojiro ;
Nakagawa, Masato ;
Ichisaka, Tomoko ;
Okita, Keisuke ;
Takahashi, Kazutoshi ;
Chiba, Tsutomu ;
Yamanaka, Shinya .
SCIENCE, 2008, 321 (5889) :699-702
[5]   STUDIES ON THE CHEMICAL NATURE OF THE SUBSTANCE INDUCING TRANSFORMATION OF PNEUMOCOCCAL TYPES INDUCTION OF TRANSFORMATION BY A DESOXYRIBONUCLEIC ACID FRACTION ISOLATED FROM PNEUMOCOCCUS TYPE III [J].
Avery, Oswald T. ;
MacLeod, Colin M. ;
McCarty, Maclyn .
JOURNAL OF EXPERIMENTAL MEDICINE, 1944, 79 (02) :137-158
[6]   Epigenetic Memory and Preferential Lineage-Specific Differentiation in Induced Pluripotent Stem Cells Derived from Human Pancreatic Islet Beta Cells [J].
Bar-Nur, Ori ;
Russ, Holger A. ;
Efrat, Shimon ;
Benvenisty, Nissim .
CELL STEM CELL, 2011, 9 (01) :17-23
[7]   Neural subtype specification of fertilization and nuclear transfer embryonic stem cells and application in parkinsonian mice [J].
Barberi, T ;
Klivenyi, P ;
Calingasan, NY ;
Lee, H ;
Kawamata, H ;
Loonam, K ;
Perrier, AL ;
Bruses, J ;
Rubio, ME ;
Topf, N ;
Tabar, V ;
Harrison, NL ;
Beal, MF ;
Moore, MAS ;
Studer, L .
NATURE BIOTECHNOLOGY, 2003, 21 (10) :1200-1207
[8]   Concise Review: Managing Genotoxicity in the Therapeutic Modification of Stem Cells [J].
Baum, Christopher ;
Modlich, Ute ;
Goehring, Gudrun ;
Schlegelberger, Brigitte .
STEM CELLS, 2011, 29 (10) :1479-1484
[9]   USE OF RESTRICTION ENZYMES TO STUDY EUKARYOTIC DNA METHYLATION .1. METHYLATION PATTERN IN RIBOSOMAL DNA FROM XENOPUS-LAEVIS [J].
BIRD, AP ;
SOUTHERN, EM .
JOURNAL OF MOLECULAR BIOLOGY, 1978, 118 (01) :27-47
[10]   Differentiation of pluripotent embryonic stem cells into cardiomyocytes [J].
Boheler, KR ;
Czyz, J ;
Tweedie, D ;
Yang, HT ;
Anisimov, SV ;
Wobus, AM .
CIRCULATION RESEARCH, 2002, 91 (03) :189-201