Lessons for cardiac regeneration and repair through development

被引:29
作者
Alexander, Jeffrey M. [1 ,2 ]
Bruneau, Benoit G. [1 ,2 ,3 ,4 ]
机构
[1] Gladstone Inst Cardiovasc Dis, San Francisco, CA 94158 USA
[2] Univ Calif San Francisco, Program Biomed Sci, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Inst Cardiovasc Res, San Francisco, CA 94143 USA
关键词
EMBRYONIC STEM-CELLS; CARDIOVASCULAR PROGENITOR CELLS; ZEBRAFISH HEART REGENERATION; SMOOTH-MUSCLE; BETA-CATENIN; MOUSE HEART; WNT; DIFFERENTIATION; CARDIOMYOCYTES; TRANSPLANTATION;
D O I
10.1016/j.molmed.2010.06.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cell-based regenerative strategies have the potential to revolutionize the way cardiovascular injury is treated, but successful therapies will require a precise understanding of the mechanisms that dictate cell fate, survival and differentiation. Recent advances in the study of cardiac development hold promise for unlocking the keys for successful therapies. Using mouse models and embryonic stem cells, researchers are uncovering cardiac progenitor cells in both embryonic and adult contexts. Furthermore, the signaling molecules and transcriptional regulators that govern these cells and their behavior are being revealed. Here, we focus on the recent advances in these areas of cardiac developmental research and their impact on the expanding field of regenerative medicine.
引用
收藏
页码:426 / 434
页数:9
相关论文
共 85 条
[61]   Skeletal muscle stem cells do not transdifferentiate into cardiomyocytes after cardiac grafting [J].
Reinecke, H ;
Poppa, V ;
Murry, CE .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2002, 34 (02) :241-249
[62]   Mesp1 expression is the earliest sign of cardiovascular development [J].
Saga, Y ;
Kitajima, S ;
Miyagawa-Tomita, S .
TRENDS IN CARDIOVASCULAR MEDICINE, 2000, 10 (08) :345-352
[63]   BMP2 is required for early heart development during a distinct time period [J].
Schlange, T ;
Andrée, B ;
Arnold, HH ;
Brand, T .
MECHANISMS OF DEVELOPMENT, 2000, 91 (1-2) :259-270
[64]   Wnt antagonism initiates cardiogenesis in Xenopus laevis [J].
Schneider, VA ;
Mercola, M .
GENES & DEVELOPMENT, 2001, 15 (03) :304-315
[65]   A role for bone morphogenetic proteins in the induction of cardiac myogenesis [J].
Schultheiss, TM ;
Burch, JBE ;
Lassar, AB .
GENES & DEVELOPMENT, 1997, 11 (04) :451-462
[66]   BMP signaling is required for heart formation in vertebrates [J].
Shi, YQ ;
Katsev, S ;
Cai, C ;
Evans, S .
DEVELOPMENTAL BIOLOGY, 2000, 224 (02) :226-237
[67]   Interrogating functional integration between injected pluripotent stem cell-derived cells and surrogate cardiac tissue [J].
Song, Hannah ;
Yoon, Charles ;
Kattman, Steven J. ;
Dengler, Jana ;
Masse, Stephane ;
Thavaratnam, Thushaanthini ;
Gewarges, Mena ;
Nanthakumar, Kumaraswamy ;
Rubart, Michael ;
Keller, Gordon M. ;
Radisic, Milica ;
Zandstra, Peter W. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (08) :3329-3334
[68]   Making or breaking the heart: From lineage determination to morphogenesis [J].
Srivastava, Deepak .
CELL, 2006, 126 (06) :1037-1048
[69]   Induction of pluripotent stem cells from adult human fibroblasts by defined factors [J].
Takahashi, Kazutoshi ;
Tanabe, Koji ;
Ohnuki, Mari ;
Narita, Megumi ;
Ichisaka, Tomoko ;
Tomoda, Kiichiro ;
Yamanaka, Shinya .
CELL, 2007, 131 (05) :861-872
[70]   Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors [J].
Takahashi, Kazutoshi ;
Yamanaka, Shinya .
CELL, 2006, 126 (04) :663-676