Cell phenotypic plasticity requires autophagic flux driven by YAP/TAZ mechanotransduction
Author(s) -
Antonio Totaro,
Qiuyu Zhuang,
Tito Panciera,
Giusy Battilana,
Luca Azzolin,
Giulia Brumana,
Alessandro Gandin,
Giovanna Brusatin,
Michelangelo Cordesi,
Stefano Piccolo
Publication year - 2019
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1908228116
Subject(s) - autophagy , microbiology and biotechnology , reprogramming , biology , mechanotransduction , regeneration (biology) , pi3k/akt/mtor pathway , cell , signal transduction , apoptosis , genetics
Significance We describe the convergence of autophagy with YAP/TAZ, 2 highly related transcriptional regulators playing essential roles in cell plasticity for tissue regeneration and cancer. We show that a key event in autophagy, the fusion of autophagosomal vesicles with lysosomes, is transcriptionally regulated by YAP/TAZ. At least in part, this is mediated by the YAP/TAZ target Armus, a protein of the RAB-GAP family. Consistently with YAP/TAZ being patterned by mechanical signals, we found that cellular mechanics, dictated by the physical properties of the ECM, potently regulate autophagy efficiency. The connection described here is crucial for YAP-mediated reprogramming of normal cells into stem-like cells and of benign tumor cells in cancer stem cells. Thus, nuclear reprogramming must go hand in hand with autophagy-mediated cytoplasmic restructuring.
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