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Filtering by: Creator Yoshida, Sei Remove constraint Creator: Yoshida, Sei Discipline Health Sciences Remove constraint Discipline: Health Sciences
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  • Growth factor signaling to mTORC1 by amino acid–laden macropinosomes

    Work
    Creator:
    Yoshida, Sei and Swanson, Joel A
    Description:
    The rapid activation of the mechanistic target of rapamycin complex-1 (mTORC1) by growth factors is increased by extracellular amino acids through yet-undefined mechanisms of amino acid transfer into endolysosomes. Because the endocytic process of macropinocytosis concentrates extracellular solutes into endolysosomes and is increased in cells stimulated by growth factors or tumor-promoting phorbol esters, we analyzed its role in amino acid–dependent activation of mTORC1. Here, we show that growth factor-dependent activation of mTORC1 by amino acids, but not glucose, requires macropinocytosis. In murine bone marrow–derived macrophages and murine embryonic fibroblasts stimulated with their cognate growth factors or with phorbol myristate acetate, activation of mTORC1 required an Akt-independent vesicular pathway of amino acid delivery into endolysosomes, mediated by the actin cytoskeleton. Macropinocytosis delivered small, fluorescent fluid-phase solutes into endolysosomes sufficiently fast to explain growth factor–mediated signaling by amino acids. Therefore, the amino acid–laden macropinosome is an essential and discrete unit of growth factor receptor signaling to mTORC1
    Keyword:
    growth factor signaling, Macropinosomes, and mTORC1
    Citation to related publication:
     http://jcb.rupress.org/content/211/1/159
    Discipline:
    Health Sciences
    Title:
    Growth factor signaling to mTORC1 by amino acid–laden macropinosomes