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Exocytotic Insertion of Calcium Channels Constrains Compensatory Endocytosis to Sites of Exocytosis
Proteins inserted into the cell surface by exocytosis are thought to be retrieved by compensatory endocytosis, suggesting that retrieval requires granule proteins. In sea urchin eggs, calcium influx through P-type calcium channels is required for retrieval, and the large size of sea urchin secretory...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2000
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2169375/ https://www.ncbi.nlm.nih.gov/pubmed/10684256 |
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author | Smith, Robert M. Baibakov, Boris Ikebuchi, Yoshihide White, Benjamin H. Lambert, Nevin A. Kaczmarek, Leonard K. Vogel, Steven S. |
author_facet | Smith, Robert M. Baibakov, Boris Ikebuchi, Yoshihide White, Benjamin H. Lambert, Nevin A. Kaczmarek, Leonard K. Vogel, Steven S. |
author_sort | Smith, Robert M. |
collection | PubMed |
description | Proteins inserted into the cell surface by exocytosis are thought to be retrieved by compensatory endocytosis, suggesting that retrieval requires granule proteins. In sea urchin eggs, calcium influx through P-type calcium channels is required for retrieval, and the large size of sea urchin secretory granules permits the direct observation of retrieval. Here we demonstrate that retrieval is limited to sites of prior exocytosis. We tested whether channel distribution can account for the localization of retrieval at exocytotic sites. We find that P-channels reside on secretory granules before fertilization, and are translocated to the egg surface by exocytosis. Our study provides strong evidence that the transitory insertion of P-type calcium channels in the surface membrane plays an obligatory role in the mechanism coupling exocytosis and compensatory endocytosis. |
format | Text |
id | pubmed-2169375 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21693752008-05-01 Exocytotic Insertion of Calcium Channels Constrains Compensatory Endocytosis to Sites of Exocytosis Smith, Robert M. Baibakov, Boris Ikebuchi, Yoshihide White, Benjamin H. Lambert, Nevin A. Kaczmarek, Leonard K. Vogel, Steven S. J Cell Biol Original Article Proteins inserted into the cell surface by exocytosis are thought to be retrieved by compensatory endocytosis, suggesting that retrieval requires granule proteins. In sea urchin eggs, calcium influx through P-type calcium channels is required for retrieval, and the large size of sea urchin secretory granules permits the direct observation of retrieval. Here we demonstrate that retrieval is limited to sites of prior exocytosis. We tested whether channel distribution can account for the localization of retrieval at exocytotic sites. We find that P-channels reside on secretory granules before fertilization, and are translocated to the egg surface by exocytosis. Our study provides strong evidence that the transitory insertion of P-type calcium channels in the surface membrane plays an obligatory role in the mechanism coupling exocytosis and compensatory endocytosis. The Rockefeller University Press 2000-02-21 /pmc/articles/PMC2169375/ /pubmed/10684256 Text en © 2000 The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Original Article Smith, Robert M. Baibakov, Boris Ikebuchi, Yoshihide White, Benjamin H. Lambert, Nevin A. Kaczmarek, Leonard K. Vogel, Steven S. Exocytotic Insertion of Calcium Channels Constrains Compensatory Endocytosis to Sites of Exocytosis |
title | Exocytotic Insertion of Calcium Channels Constrains Compensatory Endocytosis to Sites of Exocytosis |
title_full | Exocytotic Insertion of Calcium Channels Constrains Compensatory Endocytosis to Sites of Exocytosis |
title_fullStr | Exocytotic Insertion of Calcium Channels Constrains Compensatory Endocytosis to Sites of Exocytosis |
title_full_unstemmed | Exocytotic Insertion of Calcium Channels Constrains Compensatory Endocytosis to Sites of Exocytosis |
title_short | Exocytotic Insertion of Calcium Channels Constrains Compensatory Endocytosis to Sites of Exocytosis |
title_sort | exocytotic insertion of calcium channels constrains compensatory endocytosis to sites of exocytosis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2169375/ https://www.ncbi.nlm.nih.gov/pubmed/10684256 |
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