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富含亮氨酸重复蛋白 10 对心脏 L 型钙通道的调节作用。

Cardiac L-type calcium channel regulation by Leucine-Rich Repeat-Containing Protein 10.

机构信息

Department of Medicine, School of Medicine and Public Health, University of Wisconsin - Madison, Madison, WI, USA.

Department of Cell and Regenerative Biology, School of Medicine and Public Health, University of Wisconsin - Madison, Madison, WI, USA.

出版信息

Channels (Austin). 2024 Dec;18(1):2355121. doi: 10.1080/19336950.2024.2355121. Epub 2024 May 19.

Abstract

L-type calcium channels (LTCCs), the major portal for Ca entry into cardiomyocytes, are essential for excitation-contraction coupling and thus play a central role in regulating overall cardiac function. LTCC function is finely tuned by multiple signaling pathways and accessory proteins. Leucine-rich repeat-containing protein 10 (LRRC10) is a little studied cardiomyocyte-specific protein recently identified as a modulator of LTCCs. LRRC10 exerts a remarkable effect on LTCC function, more than doubling L-type Ca current (I) amplitude in a heterologous expression system by altering the gating of the channels without changing their surface membrane expression. Genetic ablation of LRRC10 expression in mouse and zebrafish hearts leads to a significant reduction in I density and a slowly progressive dilated cardiomyopathy in mice. Rare sequence variants of LRRC10 have been identified in dilated cardiomyopathy and sudden unexplained nocturnal cardiac death syndrome, but these variants have not been clearly linked to disease. Nevertheless, the DCM-associated variant, I195T, converted LRRC10 from a I potentiator to a I suppressor, thus illustrating the wide dynamic range of LRRC10-mediated I regulation. This review focuses on the contemporary knowledge of LTCC modulation by LRRC10 and discusses potential directions for future investigations.

摘要

L 型钙通道(LTCCs)是 Ca 进入心肌细胞的主要门户,对于兴奋-收缩偶联至关重要,因此在调节整体心脏功能方面发挥着核心作用。LTCC 的功能受到多种信号通路和辅助蛋白的精细调节。富含亮氨酸重复蛋白 10(LRRC10)是一种最近被确定为 LTCC 调节剂的研究较少的心肌细胞特异性蛋白。LRRC10 对 LTCC 功能具有显著影响,通过改变通道的门控而不改变其细胞膜表达,使异源表达系统中的 L 型 Ca 电流(I)幅度增加一倍以上。LRRC10 在小鼠和斑马鱼心脏中的表达缺失导致 I 密度显著降低,并导致小鼠进行性扩张型心肌病。在扩张型心肌病和突发性不明原因夜间心脏死亡综合征中已鉴定出 LRRC10 的稀有序列变异体,但这些变异体与疾病尚未明确相关。然而,与 DCM 相关的变异体 I195T 将 LRRC10 从 I 增强剂转换为 I 抑制剂,从而说明了 LRRC10 介导的 I 调节的广泛动态范围。这篇综述重点介绍了 LRRC10 对 LTCC 调节的当代知识,并讨论了未来研究的潜在方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af88/11110685/2990627f62fa/KCHL_A_2355121_F0001_OC.jpg

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