Identification of the mammalian VPS4A as a selective lipophagy receptor.

IF 14.3 Autophagy Pub Date : 2025-04-01 Epub Date: 2025-01-03 DOI:10.1080/15548627.2024.2441535
Dimitra Dialynaki, Daniel J Klionsky
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Abstract

Lipophagy is a selective type of autophagy where lipid droplets are targeted to the lysosome/vacuole for degradation. Even though lipophagy has been reported in various species, many questions remain unaddressed. How are the lipid droplets sequestered to the lysosome? What is the lipophagy receptor? How is this receptor regulated at a posttranslational level? A new collaborative study among several universities conducted on mouse and human hepatocytes sheds light on these questions, deciphering the lipophagy mechanism in the liver. In a recent paper, Das and colleagues identified VPS4A (vacuolar protein sorting 4 homolog A) as a selective receptor, providing new insights into the mechanistic pathway of lipophagy in mammals and its inverse association with steatotic liver diseases.

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哺乳动物VPS4A作为选择性脂噬受体的鉴定。
脂噬是一种选择性的自噬,其中脂滴被靶向溶酶体/液泡降解。尽管在许多物种中都有脂食现象的报道,但许多问题仍未得到解决。脂滴是如何与溶酶体隔离的?什么是脂噬受体?这种受体是如何在翻译后水平调控的?几所大学在小鼠和人类肝细胞上进行的一项新的合作研究揭示了这些问题,破译了肝脏中的脂肪吞噬机制。在最近的一篇论文中,Das及其同事发现VPS4A(液泡蛋白分类4同源物a)是一种选择性受体,为哺乳动物脂质吞噬的机制途径及其与脂肪变性肝病的负相关提供了新的见解。
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