Role of inositol 1,4,5-trisphosphate receptor type 1 in ATP-induced nuclear Ca2+ signal and hypertrophy in atrial myocytes

被引:1
作者
Kim, Joon-Chul [1 ]
Son, Min-Jeong [1 ]
Le, Qui Anh [1 ]
Woo, Sun-Hee [1 ]
机构
[1] Chungnam Natl Univ, Coll Pharm, Lab Physiol, 99 Daehak Ro, Daejeon 34134, South Korea
基金
新加坡国家研究基金会;
关键词
IP(3)R1; Atrial myocytes; Nuclear Ca2+; ATP; Hypertrophy; RAT VENTRICULAR MYOCYTES; CARDIAC MYOCYTES; GENE-EXPRESSION; CELL-LINE; RELEASE; CALCIUM; ACTIVATION;
D O I
10.1016/j.bbrc.2018.08.084
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
Inositol 1,4,5-trisphosphate receptor type 1 (IP(3)R1) is expressed in atrial muscle, but not in ventricle, and they are abundant in the perinucleus. We investigated the role of IP(3)R1 in the regulations of local Ca2+ signal and cell size in HL-1 atrial myocytes under stimulation by IP3-generating chemical messenger, ATP. Assessment of nuclear and cytosolic Ca2+ signal using confocal Ca2+ imaging revealed that IP3 generation by ATP (1 mM) induced monophasic nuclear Ca2+ increase, followed by cytosolic Ca2+ oscillation. Genetic knock-down (KD) of IP3R1 eliminated the monophasic nuclear Ca2+ signal and slowed the cytosolic Ca2+ oscillation upon ATP exposure. Prolonged application of ATP as well as other known hypertrophic agonists (endothelin-1 and phenylephrine) increased cell size in wild-type cells, but not in IP(3)R1 KD cells. Our data indicate that IP(3)R1 mediates sustained elevation in nuclear Ca2+ level and facilitates cytosolic Ca2+ oscillation upon external ATP increase, and further suggests possible role of nuclear IP(3)R1 in atrial hypertrophy. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:2998 / 3002
页数:5
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