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Biomechanical control of lysosomal secretion via the VAMP7 hub: a tug‐of‐war mechanism between VARP and LRRK1
Author(s) -
Galli Thierry,
Wang Guan,
Nola Sébastien,
Bovio Simone,
CoppeyMoisan Maïtté,
Lafont Frank
Publication year - 2018
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.2018.32.1_supplement.542.10
Subject(s) - secretion , lysosome , exocytosis , microbiology and biotechnology , chemistry , biology , biochemistry , enzyme
The rigidity of the cell environment can vary tremendously between tissues and in pathological conditions. How this property may affect intracellular membrane dynamics is still largely unknown. Here, using atomic force microscopy, we found that cells deficient in the secretory lysosome v‐SNARE VAMP7 were impaired in adapting to substrate rigidity. Conversely VAMP7‐mediated secretion was stimulated by more rigid substrate and this regulation depended on the Longin domain of VAMP7. We further found that the Longin domain bound the kinase and retrograde trafficking adaptor LRRK1 and LRRK1 negatively regulated VAMP7‐mediated exocytosis. Conversely, VARP, a VAMP7‐ and kinesin 1‐interacting protein, further controlled the availability for secretion of peripheral VAMP7 vesicles and response of cells to mechanical constraints. We propose a mechanism whereby biomechanical constraints regulate VAMP7‐dependent lysosomal secretion via LRRK1 and VARP tug‐of‐war control of the peripheral readily‐releasable pool of secretory lysosomes. Support or Funding Information Work in our group was funded by grants from INSERM, CNRS, Association Française contre les Myopathies (Research Grant 16612), the French National Research Agency (Neuro ImmunoSynapse ANR‐13‐BSV2‐0018‐02), the Ecole des Neurosciences de Paris (ENP), the Fondation pour la Recherche Médicale (FRM), Who am I? Labex (Idex ANR‐11‐IDEX‐0005‐01), awards of the Association Robert Debré pour la Recherche Médicale to T.G. and fellowship from the Region Ile‐de‐France in the framework of DIM Cerveau&Pensée and from FRM (FDT20150532766) to G.W. We acknowledge the ImagoSeine facility, and the France BioImaging infrastructure supported by ANR (10‐EQPX‐04‐01) and the EU‐FEDER (12,001,407) as part of “Investments of the future” program. This abstract is from the Experimental Biology 2018 Meeting. There is no full text article associated with this abstract published in The FASEB Journal .