Novel function of alpha(1D) L-type calcium channel in the atria

作者：Srivastava Ujala; Aromolaran Ademuyiwa S; Fabris Frank; Lazaro Deana; Kassotis John; Qu Yongxia; Boutjdir Mohamed^*

来源：Biochemical and Biophysical Research Communications, 2017, 482(4): 771-776.

DOI：10.1016/j.bbrc.2016.11.109

• Atria
• Brain natriuretic peptide
• Alpha(1D) calcium channel
• Atrial fibrillation

Ca entry through atrial L-type Calcium channels (alpha(1c) and alpha(1D)) play an important role in muscular contraction, regulation of gene expression, and release of hormones including atrial natriuretic peptide (ANP), and brain natriuretic peptide (BNP). alpha(1D) Ca channel is exclusively expressed in atria, and has been shown to play a key role in the pathogenesis of atrial fibrillation. Recent data have shown that the small conductance calcium-activated potassium channel, SK4 is also atrial specific and also contributes prominently to the secretion of ANP and BNP. However, its functional role in the heart is still poorly understood. Here we used alpha(1D) gene heterozygous (alpha(+/-)(1D)) mice and HL-1 cells to determine the functional contribution of SK4 channels to Mm dependent regulation of ANP and BNP secretion in response to endothelin (ET), and/or mechanical stretch. Immunoprecipitation with alpha(1D) specific antibody and western blotting with SK4 specific antibody on the immuno-precipitated protein complex showed a band at 50 KDa confirming the presence of SK4 in the complex and provided evidence of interaction between SK4 and alpha(1D) channels. Using RT-PCR, we observed a 2.9 fold decrease in expression of Cacna1d (gene encoding alpha(1D)) mRNA in atria from alpha(+/-)(1D) mice. The decrease in alp mRNA corresponded with a 4.2 fold decrease in Kcnn4 (gene encoding SK4) mRNA from alpha(+/-)(1D) mice. These changes were paralleled with a 77% decrease in BNP serum levels from alpha(+/-)(1D) mice. When alpha(1D) was knocked down in HL-1 cardiomyocytes using CRISPR/Cas9 technology, a 97% decrease in secreted BNP was observed even in cells subjected to stretch and endothelin. In conclusion, our data are first to show that alpha(1D) Ca and SK4 channels are coupled in the atria, and that deletion of alp leads to decreased SK4 mRNA and BNP secretion providing evidence for a novel role of am in atrial endocrine function. Elucidating the regulatory factors that underlie the secretory function of atria will identify novel therapeutic targets for treatment and prevention of cardiac arrhythmias such as atrial fibrillation. Published by Elsevier Inc.

• 出版日期2017-1-22