The conserved phosphoinositide 3-kinase pathway determines heart size in mice

被引:502
作者
Shioi, T
Kang, PM
Douglas, PS
Hampe, J
Yballe, CM
Lawitts, J
Cantley, LC
Izumo, S [1 ]
机构
[1] Beth Israel Deaconess Med Ctr, Div Cardiovasc, Div Signal Transduct, Boston, MA 02215 USA
[2] Beth Israel Deaconess Med Ctr, Div Cardiovasc, Transgen Facil, Boston, MA 02215 USA
[3] Harvard Univ, Sch Med, Dept Med, Boston, MA 02215 USA
[4] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02215 USA
关键词
cell size; heart; hypertrophy; phosphoinositide; 3-kinase; transgenic mice;
D O I
10.1093/emboj/19.11.2537
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
Phosphoinositide 3-kinase (PI3K) has been shown to regulate cell and organ size in Drosophila, but the role of PI3K in vertebrates in vivo is not well understood. To examine the role of PI3K in intact mammalian tissue, we have created and characterized transgenic mice expressing constitutively active or dominant-negative mutants of PI3K in the heart. Cardiac-specific expression of constitutively active PI3K resulted in mice with larger hearts, while dominant-negative PI3K resulted in mice with smaller hearts, The increase or decrease in heart size was associated with comparable increase or decrease in myocyte size, Cardiomyopathic changes, such as myocyte necrosis, apoptosis, interstitial fibrosis or contractile dysfunction, were not observed in either of the transgenic mice, Thus, the PI3K pathway is necessary and sufficient to promote organ growth in mammals.
引用
收藏
页码:2537 / 2548
页数:12
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