| Literature DB >> 28342870 |
Anne Feldmann1, Fazilet Bekbulat2, Heike Huesmann3, Sarah Ulbrich4, Jörg Tatzelt5, Christian Behl6, Andreas Kern7.
Abstract
Macroautophagy is a conserved degradative pathway and its deterioration is linked to disturbances in cellular proteostasis and multiple diseases. Here, we show that the RAB GTPase RAB18 modulates autophagy in primary human fibroblasts. The knockdown of RAB18 results in a decreased autophagic activity, while its overexpression enhances the degradative pathway. Importantly, this function of RAB18 is dependent on RAB3GAP1 and RAB3GAP2, which might act as RAB GEFs and stimulate the activity of the RAB GTPase. Moreover, the knockdown of RAB18 deteriorates proteostasis and results in the intracellular accumulation of ubiquitinated degradation-prone proteins. Thus, the RAB GTPase RAB18 is a positive modulator of autophagy and is relevant for the maintenance of cellular proteostasis.Entities:
Keywords: Autophagy; Proteostasis; RAB18; RAB3GAP1; RAB3GAP2; Warburg Micro syndrome
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Year: 2017 PMID: 28342870 DOI: 10.1016/j.bbrc.2017.03.112
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575