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通过VAMP7枢纽对溶酶体分泌的生物力学控制:VARP与LRRK1之间的拔河较量。

Biomechanical Control of Lysosomal Secretion Via the VAMP7 Hub: A Tug-of-War between VARP and LRRK1.

作者信息

Wang Guan, Nola Sébastien, Bovio Simone, Bun Philippe, Coppey-Moisan Maïté, Lafont Frank, Galli Thierry

机构信息

Membrane Traffic in Health & Disease, Institut Jacques Monod, CNRS UMR7592, INSERM U950, Sorbonne Paris-Cité, Université Paris Diderot, Paris 75205, France; Membrane Traffic in Healthy & Diseased Brain, Center of Psychiatry and Neurosciences, INSERM U894, Sorbonne Paris-Cité, Université Paris Descartes, 102-108 rue de la Santé, Paris 75014, France.

Cellular Microbiology and Physics of Infection Group, Center for Infection and Immunity of Lille, CNRS UMR 8204, INSERM U1019, Institut Pasteur de Lille, Centre Hospitalier Régional de Lille, Université de Lille, Lille, France.

出版信息

iScience. 2018 Jun 29;4:127-143. doi: 10.1016/j.isci.2018.05.016. Epub 2018 May 29.

Abstract

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 show that cells deficient in the secretory lysosome v-SNARE VAMP7 are impaired in adaptation to substrate rigidity. Conversely, VAMP7-mediated secretion is stimulated by more rigid substrate and this regulation depends on the Longin domain of VAMP7. We further find that the Longin domain binds the kinase and retrograde trafficking adaptor LRRK1 and that LRRK1 negatively regulates VAMP7-mediated exocytosis. Conversely, VARP, a VAMP7- and kinesin 1-interacting protein, further controls the availability for secretion of peripheral VAMP7 vesicles and response of cells to mechanical constraints. LRRK1 and VARP interact with VAMP7 in a competitive manner. We propose a mechanism whereby biomechanical constraints regulate VAMP7-dependent lysosomal secretion via LRRK1 and VARP tug-of-war control of the peripheral pool of secretory lysosomes.

摘要

细胞环境的硬度在不同组织之间以及在病理条件下可能有极大差异。这种特性如何影响细胞内膜动力学在很大程度上仍不清楚。在这里,我们使用原子力显微镜表明,分泌性溶酶体v-SNARE蛋白VAMP7缺陷的细胞在适应底物硬度方面存在缺陷。相反,更硬的底物会刺激VAMP7介导的分泌,并且这种调节依赖于VAMP7的Longin结构域。我们进一步发现,Longin结构域与激酶和逆向运输衔接蛋白LRRK1结合,并且LRRK1负向调节VAMP7介导的胞吐作用。相反,VARP是一种与VAMP7和驱动蛋白1相互作用的蛋白,它进一步控制外周VAMP7囊泡的分泌可用性以及细胞对机械约束的反应。LRRK1和VARP以竞争性方式与VAMP7相互作用。我们提出了一种机制,即生物力学约束通过LRRK1和VARP对分泌性溶酶体外周池的拔河式控制来调节VAMP7依赖性溶酶体分泌。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8880/6147023/e03e156960a4/fx1.jpg

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