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Release mode of large and small dense-core vesicles specified by different synaptotagmin isoforms in PC12 cells
Many cells release multiple substances in different proportions according to the specific character of a stimulus. PC12 cells, a model neuroendocrine cell line, express multiple isoforms of the exocytotic Ca(2+) sensor synaptotagmin. We show that these isoforms sort to populations of dense-core vesi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3128534/ https://www.ncbi.nlm.nih.gov/pubmed/21551071 http://dx.doi.org/10.1091/mbc.E11-02-0159 |
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author | Zhang, Zhen Wu, Yao Wang, Zhao Dunning, F. Mark Rehfuss, Jonathan Ramanan, Deepshika Chapman, Edwin R. Jackson, Meyer B. |
author_facet | Zhang, Zhen Wu, Yao Wang, Zhao Dunning, F. Mark Rehfuss, Jonathan Ramanan, Deepshika Chapman, Edwin R. Jackson, Meyer B. |
author_sort | Zhang, Zhen |
collection | PubMed |
description | Many cells release multiple substances in different proportions according to the specific character of a stimulus. PC12 cells, a model neuroendocrine cell line, express multiple isoforms of the exocytotic Ca(2+) sensor synaptotagmin. We show that these isoforms sort to populations of dense-core vesicles that differ in size. These synaptotagmins differ in their Ca(2+) sensitivities, their preference for full fusion or kiss-and-run, and their sensitivity to inhibition by synaptotagmin IV. In PC12 cells, vesicles that harbor these different synaptotagmin isoforms can be preferentially triggered to fuse by different forms of stimulation. The mode of fusion is specified by the synaptotagmin isoform activated, and because kiss-and-run exocytosis can filter small molecules through a size-limiting fusion pore, the activation of isoforms that favor kiss-and-run will select smaller molecules over larger molecules packaged in the same vesicle. Thus synaptotagmin isoforms can provide multiple levels of control in the release of different molecules from the same cell. |
format | Online Article Text |
id | pubmed-3128534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-31285342011-09-16 Release mode of large and small dense-core vesicles specified by different synaptotagmin isoforms in PC12 cells Zhang, Zhen Wu, Yao Wang, Zhao Dunning, F. Mark Rehfuss, Jonathan Ramanan, Deepshika Chapman, Edwin R. Jackson, Meyer B. Mol Biol Cell Articles Many cells release multiple substances in different proportions according to the specific character of a stimulus. PC12 cells, a model neuroendocrine cell line, express multiple isoforms of the exocytotic Ca(2+) sensor synaptotagmin. We show that these isoforms sort to populations of dense-core vesicles that differ in size. These synaptotagmins differ in their Ca(2+) sensitivities, their preference for full fusion or kiss-and-run, and their sensitivity to inhibition by synaptotagmin IV. In PC12 cells, vesicles that harbor these different synaptotagmin isoforms can be preferentially triggered to fuse by different forms of stimulation. The mode of fusion is specified by the synaptotagmin isoform activated, and because kiss-and-run exocytosis can filter small molecules through a size-limiting fusion pore, the activation of isoforms that favor kiss-and-run will select smaller molecules over larger molecules packaged in the same vesicle. Thus synaptotagmin isoforms can provide multiple levels of control in the release of different molecules from the same cell. The American Society for Cell Biology 2011-07-01 /pmc/articles/PMC3128534/ /pubmed/21551071 http://dx.doi.org/10.1091/mbc.E11-02-0159 Text en © 2011 Zhang et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society of Cell Biology. |
spellingShingle | Articles Zhang, Zhen Wu, Yao Wang, Zhao Dunning, F. Mark Rehfuss, Jonathan Ramanan, Deepshika Chapman, Edwin R. Jackson, Meyer B. Release mode of large and small dense-core vesicles specified by different synaptotagmin isoforms in PC12 cells |
title | Release mode of large and small dense-core vesicles specified by different synaptotagmin isoforms in PC12 cells |
title_full | Release mode of large and small dense-core vesicles specified by different synaptotagmin isoforms in PC12 cells |
title_fullStr | Release mode of large and small dense-core vesicles specified by different synaptotagmin isoforms in PC12 cells |
title_full_unstemmed | Release mode of large and small dense-core vesicles specified by different synaptotagmin isoforms in PC12 cells |
title_short | Release mode of large and small dense-core vesicles specified by different synaptotagmin isoforms in PC12 cells |
title_sort | release mode of large and small dense-core vesicles specified by different synaptotagmin isoforms in pc12 cells |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3128534/ https://www.ncbi.nlm.nih.gov/pubmed/21551071 http://dx.doi.org/10.1091/mbc.E11-02-0159 |
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