PT  - JOURNAL ARTICLE
AU  - Zhiyong Liu
AU  - Enquan Xu
AU  - Hien Tran Zhao
AU  - Tracy Cole
AU  - Andrew B. West
TI  - LRRK2 and Rab10 Coordinate Macropinocytosis to Mediate Immunological Responses in Phagocytes
AID  - 10.1101/2020.01.30.926840
DP  - 2020 Jan 01
TA  - bioRxiv
PG  - 2020.01.30.926840
4099  - http://biorxiv.org/content/early/2020/03/05/2020.01.30.926840.short
4100  - http://biorxiv.org/content/early/2020/03/05/2020.01.30.926840.full
AB  - Genetic variation in LRRK2 associates with susceptibility to Parkinson’s disease, Crohn’s disease, and mycobacteria infection, with high expression of LRRK2, and the LRRK2 kinase substrate Rab10, in phagocytic cells in the immune system. In mouse and human primary monocyte-derived macrophages, dendritic cells, and microglia-like cells, we find that Rab10 specifically regulates a specialized form of endocytosis known as macropinocytosis, without affecting phagocytosis or clathrin-mediated endocytosis. LRRK2 phosphorylates cytoplasmic PI(3,4,5)P3-positive GTP-Rab10 early macropinosomes, before EEA1 and Rab5 recruitment occurs. Macropinosome cargo in macrophages includes CCR5, CD11b, and MHCII, with LRRK2-phosphorylation of Rab10 potently blocking EHBP1L1-mediated recycling tubules and cargo turnover. EHBP1L1 over-expression competitively inhibits LRRK2-phosphorylation of Rab10, mimicking the effects of LRRK2 kinase inhibition in promoting cargo recycling. Both Rab10 knockdown and LRRK2 kinase inhibition potently suppresses the maturation of macropinosome-derived CCR5-loaded signaling endosomes important for CCL5-induced AKT-activation and chemotaxis. These data support a novel axis in the endolysosomal system whereby LRRK2-mediated Rab10 phosphorylation stalls vesicle fast-recycling to promote PI3K-AKT signal transduction.