LAMTOR/Ragulator is a negative regulator of Arl8b- and BORC-dependent late endosomal positioning

LAMTOR/Ragulator 是 Arl8b 和 BORC 依赖性晚期内体定位的负调控因子。

阅读:2
作者:Przemyslaw A Filipek ,Mariana E G de Araujo ,Georg F Vogel ,Cedric H De Smet ,Daniela Eberharter ,Manuele Rebsamen ,Elena L Rudashevskaya ,Leopold Kremser ,Teodor Yordanov ,Philipp Tschaikner ,Barbara G Fürnrohr ,Stefan Lechner ,Theresia Dunzendorfer-Matt ,Klaus Scheffzek ,Keiryn L Bennett ,Giulio Superti-Furga ,Herbert H Lindner ,Taras Stasyk ,Lukas A Huber

Abstract

Signaling from lysosomes controls cellular clearance and energy metabolism. Lysosomal malfunction has been implicated in several pathologies, including neurodegeneration, cancer, infection, immunodeficiency, and obesity. Interestingly, many functions are dependent on the organelle position. Lysosomal motility requires the integration of extracellular and intracellular signals that converge on a competition between motor proteins that ultimately control lysosomal movement on microtubules. Here, we identify a novel upstream control mechanism of Arl8b-dependent lysosomal movement toward the periphery of the cell. We show that the C-terminal domain of lyspersin, a subunit of BLOC-1-related complex (BORC), is essential and sufficient for BORC-dependent recruitment of Arl8b to lysosomes. In addition, we establish lyspersin as the linker between BORC and late endosomal/lysosomal adaptor and mitogen activated protein kinase and mechanistic target of rapamycin activator (LAMTOR) complexes and show that epidermal growth factor stimulation decreases LAMTOR/BORC association, thereby promoting BORC- and Arl8b-dependent lysosomal centrifugal transport.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。