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首页> 外文期刊>Biochemical and Biophysical Research Communications >Role of inositol 1,4,5-trisphosphate receptor type 1 in ATP-induced nuclear Ca2+ signal and hypertrophy in atrial myocytes
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Role of inositol 1,4,5-trisphosphate receptor type 1 in ATP-induced nuclear Ca2+ signal and hypertrophy in atrial myocytes

机译:肌醇1,4,5-三磷酸受体型1在ATP诱导的核CA2 +信号和心房肌细胞中的肥大作用

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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.
机译:肌醇1,4,5-三磷酸酯受体类型1(IP(3)R1)在风雨肌中表达,但不在心室中,它们在临核中丰富。通过IP3发电化学信使ATP刺激,我们调查了IP(3)R1在HL-1心房肌细胞的局部CA2 +信号和细胞大小的规定中的作用。使用共聚焦CA2 +成像评估核和细胞溶质CA2 +信号显示,ATP(1mM)诱导的单选式核CA2 +的IP3产生,其次是细胞溶质CA2 +振荡。 IP3R1的遗传淘汰(KD)消除了单选性核CA2 +信号并减慢了ATP暴露时的细胞溶胶CA2 +振荡。延长ATP以及其他已知的嗜好激动剂(内皮素-1和苯妥肾上腺素)在野生型细胞中增加细胞尺寸,但不在IP(3)R1 KD细胞中增加。我们的数据表明,IP(3)R1介导核CA2 +水平的持续升高,促进细胞溶质CA2 +振荡对外部ATP的增加,并进一步表明核IP(3)R1在心房肥大中的可能作用。 (c)2018年Elsevier Inc.保留所有权利。

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