| Literature DB >> 26885862 |
Yuanyuan Li1, Yu Wang1, Liyun Zou2, Xiangyu Tang3, Yi Yang1, Li Ma1, Qingzhu Jia1, Qingshan Ni1, Siqi Liu4, Lizhang Tang1, Regina Lin4, Elizabeth Wong4, Wei Sun1, Liting Wang1, Quanfang Wei1, Haiying Ran1, Liqun Zhang1, Hengning Lian1, Wei Huang1, Yuzhang Wu2, Qi-Jing Li5, Ying Wan6.
Abstract
Dendritic cells (DCs) orchestrate complex membrane trafficking through an interconnected transportation network linked together by Rab GTPases. Through a tandem affinity purification strategy and mass spectrometry, we depicted an interactomic landscape of major members of the mammalian Rab GTPase family. When complemented with imaging tools, this proteomic analysis provided a global view of intracellular membrane organization. Driven by this analysis, we investigated dynamic changes to the Rab32 subnetwork in DCs induced by L. monocytogenes infection and uncovered an essential role of this subnetwork in controlling the intracellular proliferation of L. monocytogenes. Mechanistically, Rab32 formed a persistent complex with two interacting proteins, PHB and PHB2, to encompass bacteria both during early phagosome formation and after L. monocytogenes escaped the original containment vacuole. Collectively, we have provided a functional compartmentalization overview and an organizational framework of intracellular Rab-mediated vesicle trafficking that can serve as a resource for future investigations.Entities:
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Year: 2016 PMID: 26885862 DOI: 10.1016/j.immuni.2016.01.027
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745