TY - JOUR
AU - Iwatsubo, Takeshi
AB - SignificanceLRRK2, a protein kinase related to Parkinson’s disease, is implicated in the maintenance of lysosomes, and a subset of Rab GTPases has been identified as bona fide substrates of LRRK2. Here, we reveal a key stress-responsive pathway composed of Rab7L1, LRRK2, and phosphorylated Rab8/10 involved in lysosomal homeostasis. Lysosomal overload stress induces translocation of Rab7L1 and LRRK2 to lysosomes, where LRRK2 is activated, and stabilizes Rab8 and Rab10 through phosphorylation. The activation of this machinery protects against lysosomal enlargement and upregulates lysosomal secretion through Rab effectors, EHBP1 and EHBP1L1. These findings elucidate a novel regulatory mechanism of Rab GTPases by phosphorylation by LRRK2 in stressed lysosomes, which may also be involved in the pathomechanism of LRRK2-related disorders.
TI - LRRK2 and its substrate Rab GTPases are sequentially targeted onto stressed lysosomes and maintain their homeostasis
JF - Proceedings of the National Academy of Sciences of the United States of America
DO - 10.1073/pnas.1812196115
DA - 2018-09-12
UR - https://www.deepdyve.com/lp/pubmed-central/lrrk2-and-its-substrate-rab-gtpases-are-sequentially-targeted-onto-H2ORfMgwyK
SP - E9115
EP - E9124
VL - 115
IS - 39
DP - DeepDyve
ER -