Nanoscale molecular architecture controls calcium diffusion and ER replenishment in dendritic spines

Autor: David Mazaud, Alexis Bemelmans, Lilia Kushnireva, David Holcman, Kanishka Basnayake, Nathalie Rouach, Eduard Korkotian
Přispěvatelé: Basnayake, Kanishka [0000-0001-8772-1158], Kushnireva, Lilia [0000-0002-6107-5052], Bemelmans, Alexis [0000-0001-7605-5225], Rouach, Nathalie [0000-0002-5574-888X], Korkotian, Eduard [0000-0001-5515-3387], Holcman, David [0000-0001-9854-5014], Apollo - University of Cambridge Repository, Center for Interdisciplinary Research in Biology, College de France, CNRS, INSERM, PSL Research University, 75231 Paris, France. (CIRB)
Rok vydání: 2021
Předmět:
Zdroj: Science Advances
Science Advances, American Association for the Advancement of Science (AAAS), 2021, 7 (38), ⟨10.1126/sciadv.abh1376⟩
ISSN: 2375-2548
DOI: 10.17863/cam.77003
Popis: Dendritic spines are critical components of neuronal synapses as they receive and transform synaptic inputs into a succession of calcium-regulated biochemical events. The spine apparatus (SA), an extension of smooth endoplasmic reticulum, regulates slow and fast calcium dynamics in spines. Calcium release events deplete SA calcium ion reservoir rapidly, yet the next cycle of signaling requires its replenishment. How spines achieve this replenishment without triggering calcium release remains unclear. Using computational modeling, calcium and STED superresolution imaging, we show that the SA replenishment involves the store-operated calcium entry pathway during spontaneous calcium transients. We identified two main conditions for SA replenishment without depletion: a small amplitude and a slow timescale for calcium influx, and a close proximity between SA and plasma membranes. Thereby, spine’s nanoscale organization separates SA replenishment from depletion. We further conclude that spine’s receptor organization also determines the calcium dynamics during the induction of long-term synaptic changes.
Databáze: OpenAIRE