TI-VAMP/VAMP7 is the SNARE of secretory lysosomes contributing to ATP secretion from astrocytes

被引:75
作者
Verderio, Claudia [1 ,2 ]
Cagnoli, Cinzia [1 ,2 ,3 ]
Bergami, Matteo [4 ]
Francolini, Maura [1 ,2 ,3 ]
Schenk, Ursula [1 ,2 ]
Colombo, Alessio [1 ,2 ]
Riganti, Loredana [1 ,2 ]
Frassoni, Carolina [5 ]
Zuccaro, Emanuela [4 ]
Danglot, Lydia [6 ,7 ]
Wilhelm, Claire [8 ,10 ]
Galli, Thierry [7 ]
Canossa, Marco [4 ]
Matteoli, Michela [1 ,2 ,9 ]
机构
[1] Univ Milan, Dept Med Pharmacol, I-20129 Milan, Italy
[2] Univ Milan, CNR Inst Neurosci, I-20129 Milan, Italy
[3] Fdn Filarete, I-20139 Milan, Italy
[4] Italian Inst Technol, Dept Neurosci & Brain Technol, I-16163 Genoa, Italy
[5] Fdn IRCCS Ist Neurol Carlo Besta, Epileptol & Expt Neurophysiol Unit, Milan, Italy
[6] INSERM, U950, F-75013 Paris, France
[7] Univ Denis Diderot Paris 7, CNRS, UMR7592, Inst Jacques Monod, F-75013 Paris, France
[8] CNRS, UMR 7057, Lab Mat & Syst Complexes MSC, Paris, France
[9] IRCCS Ist Clin Humanitas, Milan, Italy
[10] Univ Paris Diderot, Paris, France
关键词
Astrocytes; ATP; Cathepsin B; Secretory lysosomes; TI-VAMP/VAMP7; TI-VAMP; VESICULAR COMPARTMENT; PROTEIN EXPRESSION; EXOCYTOSIS; RELEASE; FUSION; TRIGGERS; PERMEABILIZATION; TRANSPORT; NEURONS;
D O I
10.1111/boc.201100070
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background information. ATP is the main transmitter stored and released from astrocytes under physiological and pathological conditions. Morphological and functional evidence suggest that besides secretory granules, secretory lysosomes release ATP. However, the molecular mechanisms involved in astrocytic lysosome fusion remain still unknown. Results. In the present study, we identify tetanus neurotoxin-insensitive vesicle-associated membrane protein (TI-VAMP, also called VAMP7) as the vesicular SNARE which mediates secretory lysosome exocytosis, contributing to release of both ATP and cathepsin B from glial cells. We also demonstrate that fusion of secretory lysosomes is triggered by slow and locally restricted calcium elevations, distinct from calcium spikes which induce the fusion of glutamate-containing clear vesicles. Downregulation of TI-VAMP/VAMP7 expression inhibited the fusion of ATP-storing vesicles and ATP-mediated calcium wave propagation. TI-VAMP/VAMP7 downregulation also significantly reduced secretion of cathepsin B from glioma. Conclusions. Given that sustained ATP release from glia upon injury greatly contributes to secondary brain damage and cathepsin B plays a critical role in glioma dissemination, TI-VAMP silencing can represent a novel strategy to control lysosome fusion in pathological conditions.
引用
收藏
页码:213 / 228
页数:16
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