| Literature DB >> 32690605 |
Marc R Block1, Molly Brunner1, Théo Ziegelmeyer1, Dominique Lallemand2, Mylène Pezet1, Genevieve Chevalier1, Philippe Rondé3, Cécile Gauthier-Rouviere4, Bernhard Wehrle-Haller5, Daniel Bouvard6.
Abstract
Yes-associated protein (YAP) signaling has emerged as a crucial pathway in several normal and pathological processes. Although the main upstream effectors that regulate its activity have been extensively studied, the role of the endosomal system has been far less characterized. Here, we identified the late endosomal/lysosomal adaptor MAPK and mTOR activator (LAMTOR) complex as an important regulator of YAP signaling in a preosteoblast cell line. We found that p18/LAMTOR1-mediated peripheral positioning of late endosomes allows delivery of SRC proto-oncogene, nonreceptor tyrosine kinase (SRC) to the plasma membrane and promotes activation of an SRC-dependent signaling cascade that controls YAP nuclear shuttling. Moreover, β1 integrin engagement and mechano-sensitive cues, such as external stiffness and related cell contractility, controlled LAMTOR targeting to the cell periphery and thereby late endosome recycling and had a major impact on YAP signaling. Our findings identify the late endosome recycling pathway as a key mechanism that controls YAP activity and explains YAP mechano-sensitivity.Entities:
Keywords: LAMTOR complex; SRC kinase; Yes-associated protein (YAP); cell adhesion; cell signaling; extracellular matrix (ECM); late endosomes; mechanosensing; vesicular trafficking
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Year: 2020 PMID: 32690605 PMCID: PMC7521633 DOI: 10.1074/jbc.RA120.013503
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157