Literature DB >> 32562620

Fusion Pore Expansion and Contraction during Catecholamine Release from Endocrine Cells.

Meyer B Jackson1, Yu-Tien Hsiao2, Che-Wei Chang3.   

Abstract

Amperometry recording reveals the exocytosis of catecholamine from individual vesicles as a sequential process, typically beginning slowly with a prespike foot, accelerating sharply to initiate a spike, reaching a peak, and then decaying. This complex sequence reflects the interplay between diffusion, flux through a fusion pore, and possibly dissociation from a vesicle's dense core. In an effort to evaluate the impacts of these factors, a model was developed that combines diffusion with flux through a static pore. This model accurately recapitulated the rapid phase of a spike but generated relations between spike shape parameters that differed from the relations observed experimentally. To explore the possible role of fusion pore dynamics, a transformation of amperometry current was introduced that yields fusion pore permeability divided by vesicle volume (g/V). Applying this transform to individual fusion events yielded a highly characteristic time course. g/V initially tracks the current, increasing ∼15-fold from the prespike foot to the spike peak. After the peak, g/V unexpectedly declines and settles into a plateau that indicates the presence of a stable postspike pore. g/V of the postspike pore varies greatly between events and has an average that is ∼3.5-fold below the peak value and ∼4.5-fold above the prespike value. The postspike pore persists and is stable for tens of milliseconds, as long as catecholamine flux can be detected. Applying the g/V transform to rare events with two peaks revealed a stepwise increase in g/V during the second peak. The g/V transform offers an interpretation of amperometric current in terms of fusion pore dynamics and provides a, to our knowledge, new frameworkfor analyzing the actions of proteins that alter spike shape. The stable postspike pore follows from predictions of lipid bilayer elasticity and offers an explanation for previous reports of prolonged hormone retention within fusing vesicles.
Copyright © 2020 Biophysical Society. Published by Elsevier Inc. All rights reserved.

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Year:  2020        PMID: 32562620      PMCID: PMC7335939          DOI: 10.1016/j.bpj.2020.06.001

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  56 in total

1.  Synaptotagmin modulation of fusion pore kinetics in regulated exocytosis of dense-core vesicles.

Authors:  C T Wang; R Grishanin; C A Earles; P Y Chang; T F Martin; E R Chapman; M B Jackson
Journal:  Science       Date:  2001-11-02       Impact factor: 47.728

2.  Transmembrane segments of syntaxin line the fusion pore of Ca2+-triggered exocytosis.

Authors:  Xue Han; Chih-Tien Wang; Jihong Bai; Edwin R Chapman; Meyer B Jackson
Journal:  Science       Date:  2004-03-11       Impact factor: 47.728

3.  Subnanometer fusion pores in spontaneous exocytosis of peptidergic vesicles.

Authors:  Nina Vardjan; Matjaz Stenovec; Jernej Jorgacevski; Marko Kreft; Robert Zorec
Journal:  J Neurosci       Date:  2007-04-25       Impact factor: 6.167

4.  Secretory vesicles membrane area is regulated in tandem with quantal size in chromaffin cells.

Authors:  Liang-Wei Gong; Ismail Hafez; Guillermo Alvarez de Toledo; Manfred Lindau
Journal:  J Neurosci       Date:  2003-08-27       Impact factor: 6.167

5.  Entropic forces drive self-organization and membrane fusion by SNARE proteins.

Authors:  Hakhamanesh Mostafavi; Sathish Thiyagarajan; Benjamin S Stratton; Erdem Karatekin; Jason M Warner; James E Rothman; Ben O'Shaughnessy
Journal:  Proc Natl Acad Sci U S A       Date:  2017-05-10       Impact factor: 11.205

6.  Synaptotagmin IV modulation of vesicle size and fusion pores in PC12 cells.

Authors:  Zhenjie Zhang; Zhen Zhang; Meyer B Jackson
Journal:  Biophys J       Date:  2010-03-17       Impact factor: 4.033

7.  Myosin II contributes to fusion pore expansion during exocytosis.

Authors:  Patricia Neco; Carlos Fernández-Peruchena; Sergio Navas; Luis M Gutiérrez; Guillermo Alvarez de Toledo; Eva Alés
Journal:  J Biol Chem       Date:  2008-02-18       Impact factor: 5.157

8.  Regulation of the fusion pore conductance during exocytosis by cyclin-dependent kinase 5.

Authors:  Jeff W Barclay; Marcos Aldea; Tim J Craig; Alan Morgan; Robert D Burgoyne
Journal:  J Biol Chem       Date:  2004-07-23       Impact factor: 5.157

9.  The crucial role of chromogranins in storage and exocytosis revealed using chromaffin cells from chromogranin A null mouse.

Authors:  Monica S Montesinos; J David Machado; Marcial Camacho; Jesica Diaz; Yezer G Morales; Diego Alvarez de la Rosa; Emilia Carmona; Agustin Castañeyra; O Humberto Viveros; Daniel T O'Connor; Sushil K Mahata; Ricardo Borges
Journal:  J Neurosci       Date:  2008-03-26       Impact factor: 6.167

10.  Hemi-fused structure mediates and controls fusion and fission in live cells.

Authors:  Wei-Dong Zhao; Edaeni Hamid; Wonchul Shin; Peter J Wen; Evan S Krystofiak; Seth A Villarreal; Hsueh-Cheng Chiang; Bechara Kachar; Ling-Gang Wu
Journal:  Nature       Date:  2016-06-15       Impact factor: 49.962

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  2 in total

1.  Synaptophysin Regulates Fusion Pores and Exocytosis Mode in Chromaffin Cells.

Authors:  Che-Wei Chang; Yu-Tien Hsiao; Meyer B Jackson
Journal:  J Neurosci       Date:  2021-03-04       Impact factor: 6.167

2.  A two-subpopulation model that reflects heterogeneity of large dense core vesicles in exocytosis.

Authors:  Nan Qin; Zhixi Chen; Renhao Xue
Journal:  Cell Cycle       Date:  2022-01-22       Impact factor: 4.534

  2 in total

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