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The contractile vacuole in Ca(2+)-regulation in Dictyostelium: its essential function for cAMP-induced Ca(2+)-influx
BACKGROUND: cAMP-induced Ca(2+)-influx in Dictyostelium is controlled by at least two non-mitochondrial Ca(2+)-stores: acidic stores and the endoplasmic reticulum (ER). The acidic stores may comprise the contractile vacuole network (CV), the endosomal compartment and acidocalcisomes. Here the role o...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1513554/ https://www.ncbi.nlm.nih.gov/pubmed/16787542 http://dx.doi.org/10.1186/1471-213X-6-31 |
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author | Malchow, Dieter Lusche, Daniel F Schlatterer, Christina De Lozanne, Arturo Müller-Taubenberger, Annette |
author_facet | Malchow, Dieter Lusche, Daniel F Schlatterer, Christina De Lozanne, Arturo Müller-Taubenberger, Annette |
author_sort | Malchow, Dieter |
collection | PubMed |
description | BACKGROUND: cAMP-induced Ca(2+)-influx in Dictyostelium is controlled by at least two non-mitochondrial Ca(2+)-stores: acidic stores and the endoplasmic reticulum (ER). The acidic stores may comprise the contractile vacuole network (CV), the endosomal compartment and acidocalcisomes. Here the role of CV in respect to function as a potential Ca(2+)-store was investigated. RESULTS: Dajumin-GFP labeled contractile vacuoles were purified 7-fold by anti-GFP-antibodies in a magnetic field. The purified CV were shown for the first time to accumulate and release Ca(2+). Release of Ca(2+ )was elicited by arachidonic acid or the calmodulin antagonist W7, the latter due to inhibition of the pump. The characteristics of Ca(2+)-transport and Ca(2+)-release of CV were compared to similarly purified vesicles of the ER labeled by calnexin-GFP. Since the CV proved to be a highly efficient Ca(2+)-compartment we wanted to know whether or not it takes part in cAMP-induced Ca(2+)-influx. We made use of the LvsA(-)-mutant expected to display reduced Ca(2+)-transport due to loss of calmodulin. We found a severe reduction of cAMP-induced Ca(2+)-influx into whole cells. CONCLUSION: The contractile vacuoles in Dictyostelium represent a highly efficient acidic Ca(2+)-store that is required for cAMP-induced Ca(2+)-influx. |
format | Text |
id | pubmed-1513554 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-15135542006-07-22 The contractile vacuole in Ca(2+)-regulation in Dictyostelium: its essential function for cAMP-induced Ca(2+)-influx Malchow, Dieter Lusche, Daniel F Schlatterer, Christina De Lozanne, Arturo Müller-Taubenberger, Annette BMC Dev Biol Research Article BACKGROUND: cAMP-induced Ca(2+)-influx in Dictyostelium is controlled by at least two non-mitochondrial Ca(2+)-stores: acidic stores and the endoplasmic reticulum (ER). The acidic stores may comprise the contractile vacuole network (CV), the endosomal compartment and acidocalcisomes. Here the role of CV in respect to function as a potential Ca(2+)-store was investigated. RESULTS: Dajumin-GFP labeled contractile vacuoles were purified 7-fold by anti-GFP-antibodies in a magnetic field. The purified CV were shown for the first time to accumulate and release Ca(2+). Release of Ca(2+ )was elicited by arachidonic acid or the calmodulin antagonist W7, the latter due to inhibition of the pump. The characteristics of Ca(2+)-transport and Ca(2+)-release of CV were compared to similarly purified vesicles of the ER labeled by calnexin-GFP. Since the CV proved to be a highly efficient Ca(2+)-compartment we wanted to know whether or not it takes part in cAMP-induced Ca(2+)-influx. We made use of the LvsA(-)-mutant expected to display reduced Ca(2+)-transport due to loss of calmodulin. We found a severe reduction of cAMP-induced Ca(2+)-influx into whole cells. CONCLUSION: The contractile vacuoles in Dictyostelium represent a highly efficient acidic Ca(2+)-store that is required for cAMP-induced Ca(2+)-influx. BioMed Central 2006-06-20 /pmc/articles/PMC1513554/ /pubmed/16787542 http://dx.doi.org/10.1186/1471-213X-6-31 Text en Copyright © 2006 Malchow et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Malchow, Dieter Lusche, Daniel F Schlatterer, Christina De Lozanne, Arturo Müller-Taubenberger, Annette The contractile vacuole in Ca(2+)-regulation in Dictyostelium: its essential function for cAMP-induced Ca(2+)-influx |
title | The contractile vacuole in Ca(2+)-regulation in Dictyostelium: its essential function for cAMP-induced Ca(2+)-influx |
title_full | The contractile vacuole in Ca(2+)-regulation in Dictyostelium: its essential function for cAMP-induced Ca(2+)-influx |
title_fullStr | The contractile vacuole in Ca(2+)-regulation in Dictyostelium: its essential function for cAMP-induced Ca(2+)-influx |
title_full_unstemmed | The contractile vacuole in Ca(2+)-regulation in Dictyostelium: its essential function for cAMP-induced Ca(2+)-influx |
title_short | The contractile vacuole in Ca(2+)-regulation in Dictyostelium: its essential function for cAMP-induced Ca(2+)-influx |
title_sort | contractile vacuole in ca(2+)-regulation in dictyostelium: its essential function for camp-induced ca(2+)-influx |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1513554/ https://www.ncbi.nlm.nih.gov/pubmed/16787542 http://dx.doi.org/10.1186/1471-213X-6-31 |
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