Literature DB >> 3315031

How calcium may cause exocytosis in sea urchin eggs.

M Whitaker1.   

Abstract

The process of secretory granule-plasma membrane fusion can be studied in sea urchin eggs. Micromolar calcium concentrations are all that is required to bring about exocytosis in vitro. I discuss recent experiments with sea urchin eggs that concentrate on the biophysical aspects of granule-membrane fusion. The backbone of biological membranes is the lipid bilayer. Sea urchin egg membrane lipids have negatively charged head groups that give rise to an electrical potential at the bilayer-water interface. We have found that this surface potential can affect the calcium required for exocytosis. Effects on the surface potential may also explain why drugs like trifluoperazine and tetracaine inhibit exocytosis: they absorb to the bilayer and reduce the surface potential. The membrane lipids may also be crucial to the formation of the exocytotic pore through which the secretory granule contents are released. We have measured calcium-induced production of the lipid, diacylglycerol. This lipid can induce a phase transition that will promote fusion of apposed lipid bilayers. The process of exocytosis involves the secretory granule core as well as the lipids of the membrane. The osmotic properties of the granule contents lead to swelling of the granule during exocytosis. Swelling promotes the dispersal of the contents as they are extruded through the exocytotic pore. The movements of water and ions during exocytosis may also stabilize the transient fusion intermediate and consolidate the exocytotic pore as fusion occurs.

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Year:  1987        PMID: 3315031     DOI: 10.1007/BF01362502

Source DB:  PubMed          Journal:  Biosci Rep        ISSN: 0144-8463            Impact factor:   3.840


  8 in total

Review 1.  Membrane fusion.

Authors:  K N Burger; A J Verkleij
Journal:  Experientia       Date:  1990-06-15

2.  Cell surface complexes ('cortices') isolated from Paramecium tetraurelia cells as a model system for analysing exocytosis in vitro in conjunction with microinjection studies.

Authors:  C J Lumpert; H Kersken; H Plattner
Journal:  Biochem J       Date:  1990-08-01       Impact factor: 3.857

3.  Limitations of the octadecylrhodamine dequenching assay for membrane fusion.

Authors:  T Stegmann; J G Orsel; J D Jamieson; P J Padfield
Journal:  Biochem J       Date:  1995-05-01       Impact factor: 3.857

4.  sn-1,2-diacylglycerol and choline increase after fertilization in Xenopus laevis.

Authors:  B J Stith; K Woronoff; R Espinoza; T Smart
Journal:  Mol Biol Cell       Date:  1997-04       Impact factor: 4.138

5.  Actin cytoskeleton and calcium-ATPase in the process of abomasal mucus secretion in cattle.

Authors:  M Schessner; B Schnorr
Journal:  Cell Tissue Res       Date:  1990-04       Impact factor: 5.249

6.  The role of diacylglycerol in the exocytosis of the sperm acrosome. Studies using diacylglycerol lipase and diacylglycerol kinase inhibitors and exogenous diacylglycerols.

Authors:  E R Roldan; R A Harrison
Journal:  Biochem J       Date:  1992-02-01       Impact factor: 3.857

7.  The N-ethylmaleimide-sensitive protein thiol groups necessary for sea-urchin egg cortical-granule exocytosis are highly exposed to the medium and are required for triggering by Ca2+.

Authors:  T Whalley; A Sokoloff
Journal:  Biochem J       Date:  1994-09-01       Impact factor: 3.857

8.  Phosphoprotein inhibition of calcium-stimulated exocytosis in sea urchin eggs.

Authors:  T Whalley; I Crossley; M Whitaker
Journal:  J Cell Biol       Date:  1991-05       Impact factor: 10.539

  8 in total

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