蛋白质稳态
拉布
GTP酶
细胞生物学
自噬
生物
小型GTPase
基因敲除
生物化学
信号转导
细胞凋亡
作者
Anne Feldmann,Fazilet Bekbulat,Heike Huesmann,Sarah Ulbrich,Jörg Tatzelt,Christian Behl,Andreas Kern
标识
DOI:10.1016/j.bbrc.2017.03.112
摘要
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.
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