α3 β4 Nicotinic Receptors Are Components of the Secretory Machinery Clusters in Chromaffin Cells

ABSTRACT: The heteromeric assembly of α3 and β4 subunits of acetylcholine nicotinic receptors (nAChRs) seems to mediate the secretory response in bovine chromaffin cells. However, there is no information about the localization of these nAChRs in relationship with the secretory active zones in this c...

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Detalles Bibliográficos
Autores: Villanueva, José, Criado Herrero, Manuel, Giménez Molina, Yolanda, González Vélez, Virginia, Gil Gómez, Amparo|||0000-0002-7449-4205, Gutiérrez Pérez, Luis Miguel
Tipo de recurso: artículo
Fecha de publicación:2022
País:España
Institución:Universidad de Cantabria (UC)
Repositorio:UCrea Repositorio Abierto de la Universidad de Cantabria
Idioma:inglés
OAI Identifier:oai:repositorio.unican.es:10902/25712
Acceso en línea:http://hdl.handle.net/10902/25712
Access Level:acceso abierto
Palabra clave:Chromaffin cells
Exocytosis
Α3 β4 acetylcholine nicotinic receptor
SNAP-25
DBH
Secretory machinery
Particle-based methods
Modeling of calcium dynamics
Descripción
Sumario:ABSTRACT: The heteromeric assembly of α3 and β4 subunits of acetylcholine nicotinic receptors (nAChRs) seems to mediate the secretory response in bovine chromaffin cells. However, there is no information about the localization of these nAChRs in relationship with the secretory active zones in this cellular model. The present work presents the first evidence that, in fact, a population of these receptors is associated through the F-actin cytoskeleton with exocytotic machinery components, as detected by SNAP-25 labeling. Furthermore, we also prove that, upon stimulation, the probabilityto find α3β4 nAChRs very close to exocytotic events increases with randomized distributions, thus substantiating the clear dynamic behavior of these receptors during the secretory process. Modeling on secretory dynamics and secretory component distributions supports the idea that α3β4 nAChRcluster mobility could help with improving the efficiency of the secretory response of chromaffin cells. Our study is limited by the use of conventional confocal microscopy; in this sense, a strengthening to our conclusions could come from the use of super-resolution microscopy techniques in the near future.