Literature DB >> 21839720

Gap junction-mediated intercellular communication in the adrenal medulla: an additional ingredient of stimulus-secretion coupling regulation.

Claude Colomer1, Agnès O Martin, Michel G Desarménien, Nathalie C Guérineau.   

Abstract

The traditional understanding of stimulus-secretion coupling in adrenal neuroendocrine chromaffin cells states that catecholamines are released upon trans-synaptic sympathetic stimulation mediated by acetylcholine released from the splanchnic nerve terminals. Although this statement remains largely true, it deserves to be tempered. In addition to its neurogenic control, catecholamine secretion also depends on a local gap junction-mediated communication between chromaffin cells. We review here the insights gained since the first description of gap junctions in the adrenal medullary tissue. Adrenal stimulus-secretion coupling now appears far more intricate than was previously envisioned and its deciphering represents a challenge for neurobiologists engaged in the study of the regulation of neuroendocrine secretion. This article is part of a Special Issue entitled: The Communicating junctions, composition, structure and characteristics.
Copyright © 2011 Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 21839720     DOI: 10.1016/j.bbamem.2011.07.034

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  11 in total

1.  Pituitary adenylate cyclase-activating peptide enhances electrical coupling in the mouse adrenal medulla.

Authors:  Jacqueline Hill; Seong-Ki Lee; Prattana Samasilp; Corey Smith
Journal:  Am J Physiol Cell Physiol       Date:  2012-05-16       Impact factor: 4.249

Review 2.  Gap junction communication between chromaffin cells: the hidden face of adrenal stimulus-secretion coupling.

Authors:  Nathalie C Guérineau
Journal:  Pflugers Arch       Date:  2017-07-22       Impact factor: 3.657

Review 3.  Roles of connexins and pannexins in (neuro)endocrine physiology.

Authors:  David J Hodson; Christian Legros; Michel G Desarménien; Nathalie C Guérineau
Journal:  Cell Mol Life Sci       Date:  2015-06-18       Impact factor: 9.261

4.  Reduced calcium current density in female versus male mouse adrenal chromaffin cells in situ.

Authors:  Shyue-An Chan; Jacqueline Hill; Corey Smith
Journal:  Cell Calcium       Date:  2012-04-30       Impact factor: 6.817

Review 5.  Functional chromaffin cell plasticity in response to stress: focus on nicotinic, gap junction, and voltage-gated Ca2+ channels.

Authors:  Nathalie C Guérineau; Michel G Desarménien; Valentina Carabelli; Emilio Carbone
Journal:  J Mol Neurosci       Date:  2012-01-18       Impact factor: 3.444

6.  Basal and Stress-Induced Network Activity in the Adrenal Medulla In Vivo.

Authors:  Jose R Lopez Ruiz; Stephen A Ernst; Ronald W Holz; Edward L Stuenkel
Journal:  Front Endocrinol (Lausanne)       Date:  2022-06-20       Impact factor: 6.055

7.  Ca(V)1.3-driven SK channel activation regulates pacemaking and spike frequency adaptation in mouse chromaffin cells.

Authors:  David H F Vandael; Annalisa Zuccotti; Joerg Striessnig; Emilio Carbone
Journal:  J Neurosci       Date:  2012-11-14       Impact factor: 6.167

8.  Nicotinic receptor Alpha7 expression during mouse adrenal gland development.

Authors:  Lorise C Gahring; Elizabeth Myers; Sierra Palumbos; Scott W Rogers
Journal:  PLoS One       Date:  2014-08-05       Impact factor: 3.240

9.  Monitoring the Secretory Behavior of the Rat Adrenal Medulla by High-Performance Liquid Chromatography-Based Catecholamine Assay from Slice Supernatants.

Authors:  Frédéric De Nardi; Claudie Lefort; Dimitri Bréard; Pascal Richomme; Christian Legros; Nathalie C Guérineau
Journal:  Front Endocrinol (Lausanne)       Date:  2017-09-25       Impact factor: 5.555

Review 10.  Inflammatory Signaling in Hypertension: Regulation of Adrenal Catecholamine Biosynthesis.

Authors:  Collin J Byrne; Sandhya Khurana; Aseem Kumar; T C Tai
Journal:  Front Endocrinol (Lausanne)       Date:  2018-06-28       Impact factor: 5.555

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