VAP‐SCRN1 interaction regulates dynamic endoplasmic reticulum remodeling and presynaptic function

• Feline W Lindhout ^[1] ; Yujie Cao ^[1] ; Josta T Kevenaar ^[1] ; Anna Bodzęta ^[1] ; Riccardo Stucchi ^[1] ; Maria M Boumpoutsari ^[1] ; Eugene A Katrukha ^[1] ; Maarten Altelaar ^[2] ; Harold D MacGillavry ^[1] ; Casper C Hoogenraad ^[1]
  1. [1] Utrecht University

     Utrecht University

     Países Bajos

     
  2. [2] 2 Biomolecular Mass Spectrometry and Proteomics Bijvoet Center for Biomolecular Research and Utrecht Institute for Pharmaceutical Sciences Utrecht University Utrecht The Netherlands
• Localización: EMBO journal: European Molecular Biology Organization, ISSN 0261-4189, Vol. 38, Nº. 20, 2019
• Idioma: inglés
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• Resumen

  • In neurons, the continuous and dynamic endoplasmic reticulum (ER) network extends throughout the axon, and its dysfunction causes various axonopathies. However, it remains largely unknown how ER integrity and remodeling modulate presynaptic function in mammalian neurons. Here, we demonstrated that ER membrane receptors VAPA and VAPB are involved in modulating the synaptic vesicle (SV) cycle. VAP interacts with secernin‐1 (SCRN1) at the ER membrane via a single FFAT‐like motif. Similar to VAP, loss of SCRN1 or SCRN1‐VAP interactions resulted in impaired SV cycling. Consistently, SCRN1 or VAP depletion was accompanied by decreased action potential‐evoked Ca2+ responses. Additionally, we found that VAP‐SCRN1 interactions play an important role in maintaining ER continuity and dynamics, as well as presynaptic Ca2+ homeostasis. Based on these findings, we propose a model where the ER‐localized VAP‐SCRN1 interactions provide a novel control mechanism to tune ER remodeling and thereby modulate Ca2+ dynamics and SV cycling at presynaptic sites. These data provide new insights into the molecular mechanisms controlling ER structure and dynamics, and highlight the relevance of ER function for SV cycling.