Literature DB >> 28852855

How does the stimulus define exocytosis in adrenal chromaffin cells?

Fernando D Marengo1, Ana M Cárdenas2.   

Abstract

The extent and type of hormones and active peptides secreted by the chromaffin cells of the adrenal medulla have to be adjusted to physiological requirements. The chromaffin cell secretory activity is controlled by the splanchnic nerve firing frequency, which goes from approximately 0.5 Hz in basal conditions to more than 15 Hz in stress. Thus, these neuroendocrine cells maintain a tonic release of catecholamines under resting conditions, massively discharge intravesicular transmitters in response to stress, or adequately respond to moderate stimuli. In order to adjust the secretory response to the stimulus, the adrenal chromaffin cells have an appropriate organization of Ca2+ channels, secretory granules pools, and sets of proteins dedicated to selectively control different steps of the secretion process, such as the traffic, docking, priming and fusion of the chromaffin granules. Among the molecules implicated in such events are the soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) proteins, Ca2+ sensors like Munc13 and synaptotagmin-1, chaperon proteins such as Munc18, and the actomyosin complex. In the present review, we discuss how these different actors contribute to the extent and maintenance of the stimulus-dependent exocytosis in the adrenal chromaffin cells.

Entities:  

Keywords:  Catecholamines; Chromaffin cells; Exocytosis; Vesicle pools; Voltage-dependent Ca2+ channels

Mesh:

Substances:

Year:  2017        PMID: 28852855     DOI: 10.1007/s00424-017-2052-5

Source DB:  PubMed          Journal:  Pflugers Arch        ISSN: 0031-6768            Impact factor:   3.657


  150 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2010-10-18       Impact factor: 11.205

2.  Munc18-1: sequential interactions with the fusion machinery stimulate vesicle docking and priming.

Authors:  Attila Gulyás-Kovács; Heidi de Wit; Ira Milosevic; Olexiy Kochubey; Ruud Toonen; Jürgen Klingauf; Matthijs Verhage; Jakob B Sørensen
Journal:  J Neurosci       Date:  2007-08-08       Impact factor: 6.167

Review 3.  Annexins: linking Ca2+ signalling to membrane dynamics.

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Journal:  Nat Rev Mol Cell Biol       Date:  2005-06       Impact factor: 94.444

4.  Action potentials in the rat chromaffin cell and effects of acetylcholine.

Authors:  B L Brandt; S Hagiwara; Y Kidokoro; S Miyazaki
Journal:  J Physiol       Date:  1976-12       Impact factor: 5.182

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Journal:  Neuron       Date:  1995-02       Impact factor: 17.173

6.  P/Q Ca2+ channels are functionally coupled to exocytosis of the immediately releasable pool in mouse chromaffin cells.

Authors:  Yanina D Alvarez; Lorena I Ibañez; Osvaldo D Uchitel; Fernando D Marengo
Journal:  Cell Calcium       Date:  2007-06-11       Impact factor: 6.817

7.  Juxtamembrane tryptophans of synaptobrevin 2 control the process of membrane fusion.

Authors:  Qinghua Fang; Ying Zhao; Manfred Lindau
Journal:  FEBS Lett       Date:  2012-11-21       Impact factor: 4.124

8.  Munc13 mediates the transition from the closed syntaxin-Munc18 complex to the SNARE complex.

Authors:  Cong Ma; Wei Li; Yibin Xu; Josep Rizo
Journal:  Nat Struct Mol Biol       Date:  2011-04-17       Impact factor: 15.369

9.  Synaptotagmin-1 C2B domain interacts simultaneously with SNAREs and membranes to promote membrane fusion.

Authors:  Shen Wang; Yun Li; Cong Ma
Journal:  Elife       Date:  2016-04-15       Impact factor: 8.140

10.  Architecture of the synaptotagmin-SNARE machinery for neuronal exocytosis.

Authors:  Qiangjun Zhou; Ying Lai; Taulant Bacaj; Minglei Zhao; Artem Y Lyubimov; Monarin Uervirojnangkoorn; Oliver B Zeldin; Aaron S Brewster; Nicholas K Sauter; Aina E Cohen; S Michael Soltis; Roberto Alonso-Mori; Matthieu Chollet; Henrik T Lemke; Richard A Pfuetzner; Ucheor B Choi; William I Weis; Jiajie Diao; Thomas C Südhof; Axel T Brunger
Journal:  Nature       Date:  2015-08-17       Impact factor: 49.962

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  7 in total

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Journal:  Methods Mol Biol       Date:  2021

2.  Membrane Capacitance Measurements of Stimulus-Evoked Exocytosis in Adrenal Chromaffin Cells.

Authors:  Elizabeth P Seward; Robert C Wykes
Journal:  Methods Mol Biol       Date:  2023

3.  Isolation and Purification of Chromaffin Granules from Adrenal Glands and Cultured Neuroendocrine Cells.

Authors:  Arlek González-Jamett; María Constanza Maldifassi; Ana María Cárdenas
Journal:  Methods Mol Biol       Date:  2023

Review 4.  Intricacies of the Molecular Machinery of Catecholamine Biosynthesis and Secretion by Chromaffin Cells of the Normal Adrenal Medulla and in Pheochromocytoma and Paraganglioma.

Authors:  Annika M A Berends; Graeme Eisenhofer; Lauren Fishbein; Anouk N A V D Horst-Schrivers; Ido P Kema; Thera P Links; Jacques W M Lenders; Michiel N Kerstens
Journal:  Cancers (Basel)       Date:  2019-08-06       Impact factor: 6.639

5.  HIF2α regulates the synthesis and release of epinephrine in the adrenal medulla.

Authors:  Deepika Watts; Nicole Bechmann; Ana Meneses; Ioanna K Poutakidou; Denise Kaden; Catleen Conrad; Anja Krüger; Johanna Stein; Ali El-Armouche; Triantafyllos Chavakis; Graeme Eisenhofer; Mirko Peitzsch; Ben Wielockx
Journal:  J Mol Med (Berl)       Date:  2021-09-04       Impact factor: 4.599

6.  Gain-of-Function Dynamin-2 Mutations Linked to Centronuclear Myopathy Impair Ca2+-Induced Exocytosis in Human Myoblasts.

Authors:  Lucas Bayonés; María José Guerra-Fernández; Fernando Hinostroza; Ximena Báez-Matus; Jacqueline Vásquez-Navarrete; Luciana I Gallo; Sergio Parra; Agustín D Martínez; Arlek González-Jamett; Fernando D Marengo; Ana M Cárdenas
Journal:  Int J Mol Sci       Date:  2022-09-08       Impact factor: 6.208

7.  Simultaneous Quantification of Vesicle Size and Catecholamine Content by Resistive Pulses in Nanopores and Vesicle Impact Electrochemical Cytometry.

Authors:  Xin-Wei Zhang; Amir Hatamie; Andrew G Ewing
Journal:  J Am Chem Soc       Date:  2020-02-24       Impact factor: 15.419

  7 in total

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