The calcium release-activated calcium channel Orai1 represents a crucial component in hypertrophic compensation and the development of dilated cardiomyopathy

被引:27
|
作者
Horton, Jaime S. [1 ,2 ]
Buckley, Cadie L. [1 ,3 ]
Alvarez, Ernest M. [1 ,2 ]
Schorlemmer, Anita [1 ,3 ]
Stokes, Alexander J. [1 ,2 ,3 ,4 ]
机构
[1] Univ Hawaii, John A Burns Sch Med, Expt Med Lab, Honolulu, HI 96822 USA
[2] Univ Hawaii, John A Burns Sch Med, Dept Cell & Mol Biol, Honolulu, HI 96822 USA
[3] Univ Hawaii, Dept Mol Biosci & Bioengn, Honolulu, HI 96822 USA
[4] Chaminade Univ, Honolulu, HI USA
基金
美国国家卫生研究院;
关键词
CRACM1; Orai1; ICRAC; pressure overload; dilated cardiomyopathy; contraction coupling; apoptosis; OPERATED CA2+ ENTRY; CARDIAC-HYPERTROPHY; HEART-FAILURE; MICE LACKING; PORE SUBUNIT; MECHANISMS; PROTEINS; ABSENCE; GROWTH; TRPV1;
D O I
10.4161/chan.26581
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
As exceptionally calcium selective store-operated channels, Orai channels play a prominent role in cellular calcium signaling. While most studied in the immune system, we are beginning to recognize that Orai1 provides unique calcium signaling pathways in numerous tissue contexts. To assess the involvement of Orai1 in cardiac hypertrophy we used transverse aortic constriction to model pressure overload cardiac hypertrophy and heart failure in Orai1 deficient mice. We demonstrate that Orai1 deficient mice have significantly decreased survival in this pressure overload model. Transthoracic echocardiography reveals that Orai1 deficient mice develop rapid dilated cardiomyopathy, with greater loss of function, and histological and molecular data indicate that this pathology is associated with significant apoptosis, but not major differences in cellular hypertrophy, fibrosis, and some major hypertrophic makers. Orai1 represents a crucial calcium entry mechanism in the compensation of the heart to pressure overload over-load, and the development of dilated cardiomyopathy.
引用
收藏
页码:35 / 48
页数:14
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