The Rag-Ragulator Complex Regulates Lysosome Function and Phagocytic Flux in Microglia
Author(s) -
Kimberle Shen,
Harwin Sidik,
William S. Talbot
Publication year - 2016
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2015.12.055
Subject(s) - microglia , phagocytosis , lysosome , microbiology and biotechnology , zebrafish , biology , pi3k/akt/mtor pathway , mtorc1 , function (biology) , inflammation , signal transduction , immunology , gene , genetics , biochemistry , enzyme
Microglia are resident macrophages of the CNS that are essential for phagocytosis of apoptotic neurons and weak synapses during development. We show that RagA and Lamtor4, two components of the Rag-Ragulator complex, are essential regulators of lysosomes in microglia. In zebrafish lacking RagA function, microglia exhibit an expanded lysosomal compartment, but they are unable to properly digest apoptotic neuronal debris. Previous biochemical studies have placed the Rag-Ragulator complex upstream of mTORC1 activation in response to cellular nutrient availability. Nonetheless, RagA and mTOR mutant zebrafish have distinct phenotypes, indicating that the Rag-Ragulator complex has functions independent of mTOR signaling. Our analysis reveals an essential role of the Rag-Ragulator complex in proper lysosome function and phagocytic flux in microglia.
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