Literature DB >> 9276499

Punctate appearance of dopamine-beta-hydroxylase on the chromaffin cell surface reflects the fusion of individual chromaffin granules upon exocytosis.

P F Wick1, J M Trenkle, R W Holz.   

Abstract

A secretion from cultured bovine chromaffin cells was stimulated to examine the pattern of exocytotic fusion on the plasma membrane. Confocal microscopy revealed that dopamine-beta-hydroxylase immunofluorescence in intact cells stimulated for 20s with the nicotinic agonist 1,1-dimethyl-4-phenylpiperazinium was almost entirely punctate and evenly distributed on the cell surface. The basis for the fine, punctate appearance of dopamine-beta-hydroxylase was investigated. Dopamine-beta-hydroxylase presentation on the surface of permeabilized cells stimulated with 1-30 microM Ca2+ was punctate and similar to that on the plasma membrane of intact cells. The fluorescence intensities of both surface dopamine-beta-hydroxylase sites and internal chromaffin granules were estimated by computerized digital image analysis. The surface area of punctate surface dopamine-beta-hydroxylase (0.218 +/- 0.013 microm2, mean +/- S.E.M.) is similar to the surface area of a 0.28 microm diameter chromaffin granule (0.25 microm2). The average fluorescence intensity integrated over the area of the surface spots was 25-30% of the average chromaffin granule intensity, a fraction that is similar to the published values of 40-50% of the dopamine-beta-hydroxylase in the chromaffin granule being membrane bound. The surface density of the spots is consistent with the number of granules undergoing exocytosis. The spots do not tend to be clumped. The key conclusions from this work are that each individual punctate site of dopamine-beta-hydroxylase represents the fusion of a single chromaffin granule and that the distribution of dopamine-beta-hydroxylase spots over the cell surface is extensive and random, suggesting that each individual granule associates with its own release site.

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Year:  1997        PMID: 9276499     DOI: 10.1016/s0306-4522(97)00062-6

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  13 in total

1.  A current activated on depletion of intracellular Ca2+ stores can regulate exocytosis in adrenal chromaffin cells.

Authors:  A F Fomina; M C Nowycky
Journal:  J Neurosci       Date:  1999-05-15       Impact factor: 6.167

2.  Visualization of regulated exocytosis with a granule-membrane probe using total internal reflection microscopy.

Authors:  Miriam W Allersma; Li Wang; Daniel Axelrod; Ronald W Holz
Journal:  Mol Biol Cell       Date:  2004-07-28       Impact factor: 4.138

3.  Inhibition of N and PQ calcium channels by calcium entry through L channels in chromaffin cells.

Authors:  Juliana M Rosa; Luis Gandía; Antonio G García
Journal:  Pflugers Arch       Date:  2009-04-04       Impact factor: 3.657

4.  A nibbling mechanism for clathrin-mediated retrieval of secretory granule membrane after exocytosis.

Authors:  Mary A Bittner; Rachel L Aikman; Ronald W Holz
Journal:  J Biol Chem       Date:  2013-02-05       Impact factor: 5.157

5.  Restriction of secretory granule motion near the plasma membrane of chromaffin cells.

Authors:  L M Johns; E S Levitan; E A Shelden; R W Holz; D Axelrod
Journal:  J Cell Biol       Date:  2001-04-02       Impact factor: 10.539

6.  Secretory granules are recaptured largely intact after stimulated exocytosis in cultured endocrine cells.

Authors:  Justin W Taraska; David Perrais; Mica Ohara-Imaizumi; Shinya Nagamatsu; Wolfhard Almers
Journal:  Proc Natl Acad Sci U S A       Date:  2003-01-21       Impact factor: 11.205

7.  Localized topological changes of the plasma membrane upon exocytosis visualized by polarized TIRFM.

Authors:  Arun Anantharam; Bibiana Onoa; Robert H Edwards; Ronald W Holz; Daniel Axelrod
Journal:  J Cell Biol       Date:  2010-02-08       Impact factor: 10.539

8.  Trafficking and fusion of neuropeptide Y-containing dense-core granules in astrocytes.

Authors:  Prabhu Ramamoorthy; Matthew D Whim
Journal:  J Neurosci       Date:  2008-12-17       Impact factor: 6.167

9.  Recapture after exocytosis causes differential retention of protein in granules of bovine chromaffin cells.

Authors:  David Perrais; Ingo C Kleppe; Justin W Taraska; Wolfhard Almers
Journal:  J Physiol       Date:  2004-08-05       Impact factor: 5.182

10.  Kv2.1 cell surface clusters are insertion platforms for ion channel delivery to the plasma membrane.

Authors:  Emily Deutsch; Aubrey V Weigel; Elizabeth J Akin; Phil Fox; Gentry Hansen; Christopher J Haberkorn; Rob Loftus; Diego Krapf; Michael M Tamkun
Journal:  Mol Biol Cell       Date:  2012-05-30       Impact factor: 4.138

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