Evidence map›Paper›PMID 36012367›Full record

ArticleInternational journal of molecular sciences2022

α3β4 Acetylcholine Nicotinic Receptors Are Components of the Secretory Machinery Clusters in Chromaffin Cells.

José Villanueva, Manuel Criado, Yolanda Giménez-Molina, Virginia González-Vélez, Amparo Gil, Luis Miguel Gutiérrez

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 52% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Article
  3. The Role of Nicotinic Receptors on CaCurrent issues in molecular biology · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

José VillanuevaInstituto de Neurociencias, CSIC-Universidad Miguel Hernández, Ctra de Valencia S/N, Sant Joan d'Alacant, 03550 Alicante, Spain.ORCID 0000-0002-4057-2113
Manuel CriadoInstituto de Neurociencias, CSIC-Universidad Miguel Hernández, Ctra de Valencia S/N, Sant Joan d'Alacant, 03550 Alicante, Spain.
Yolanda Giménez-MolinaInstituto de Neurociencias, CSIC-Universidad Miguel Hernández, Ctra de Valencia S/N, Sant Joan d'Alacant, 03550 Alicante, Spain.
Virginia González-VélezDepartamento Ciencias Básicas, UAM Azcapotzalco, México City 00810, México.
Amparo GilDepartamento de Matemática Aplicada y Ciencias de la Computación, Universidad de Cantabria, 39005 Santander, Spain.
Luis Miguel GutiérrezInstituto de Neurociencias, CSIC-Universidad Miguel Hernández, Ctra de Valencia S/N, Sant Joan d'Alacant, 03550 Alicante, Spain.ORCID 0000-0002-0512-7858
Instituto de Neurociencias · ESUniversidad de Cantabria · ES

Funding

Spanish Ministerio de Economía y Competitividad PID2020-114824GB-I00, MINECO, FEDER, UE
6 · The paper itself

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 probability to 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 nAChR cluster 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.

Indexed as

Chromaffin CellsReceptors, NicotinicAcetylcholineAnimalsBiological TransportCattleNicotinic AntagonistsAcetylcholineNicotinic AntagonistsReceptors, Nicotinicchromaffin cellsDBHexocytosismodeling of calcium dynamicsparticle-based methodssecretory machinerySNAP-25α3β4 acetylcholine nicotinic receptor

Identifiers

PMID36012367
PMCPMC9409273
OpenAlexW4291885579

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.