沃尔夫拉姆综合征中的内质网-线粒体锁定现象

IF 4.3 2区 生物学 Q2 CELL BIOLOGY Cell calcium Pub Date : 2024-09-12 DOI:10.1016/j.ceca.2024.102955
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引用次数: 0

摘要

沃尔夫拉姆综合征(WS)是一种无法治愈的常染色体隐性遗传疾病,最初被描述为线粒体病。在最近的一项研究中,Liiv 及其同事发现,在 WS 模型中,内质网(ER)到线粒体的钙穿梭障碍是线粒体功能障碍的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Endoplasmic reticulum-mitochondria lockdown in Wolfram syndrome

Wolfram syndrome (WS) is an incurable autosomal recessive disorder originally described as a mitochondriopathy. In a recent work, Liiv and colleagues found that an impaired endoplasmic reticulum (ER)-to-mitochondria calcium shuttling underlies mitochondrial dysfunction in WS models.

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来源期刊
Cell calcium
Cell calcium 生物-细胞生物学
CiteScore
8.70
自引率
5.00%
发文量
115
审稿时长
35 days
期刊介绍: Cell Calcium covers the field of calcium metabolism and signalling in living systems, from aspects including inorganic chemistry, physiology, molecular biology and pathology. Topic themes include: Roles of calcium in regulating cellular events such as apoptosis, necrosis and organelle remodelling Influence of calcium regulation in affecting health and disease outcomes
期刊最新文献
Endoplasmic reticulum-mitochondria lockdown in Wolfram syndrome Editorial Board In memoriam of Shun-ichi Miyazaki 1941–2024 Unveiling the intricate role of S100A1 in regulating RyR1 activity: A commentary on “Structural insights into the regulation of RyR1 by S100A1” The quest to map STIM1 activation in granular detail
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