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Hyphal Orientation of Candida albicans Is Regulated by a Calcium-Dependent Mechanism
Eukaryotic cells from fungal hyphae to neurites that grow by polarized extension must coordinate cell growth and cell orientation to enable them to exhibit growth tropisms and to respond to relevant environmental cues. Such cells generally maintain a tip-high Ca(2+) cytoplasmic gradient, which is co...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1885950/ https://www.ncbi.nlm.nih.gov/pubmed/17275302 http://dx.doi.org/10.1016/j.cub.2006.12.043 |
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author | Brand, Alexandra Shanks, Scott Duncan, Vanessa M.S. Yang, Meng Mackenzie, Kevin Gow, Neil A.R. |
author_facet | Brand, Alexandra Shanks, Scott Duncan, Vanessa M.S. Yang, Meng Mackenzie, Kevin Gow, Neil A.R. |
author_sort | Brand, Alexandra |
collection | PubMed |
description | Eukaryotic cells from fungal hyphae to neurites that grow by polarized extension must coordinate cell growth and cell orientation to enable them to exhibit growth tropisms and to respond to relevant environmental cues. Such cells generally maintain a tip-high Ca(2+) cytoplasmic gradient, which is correlated with their ability to exhibit polarized tip growth and to respond to growth-directing extracellular signals 1, 2, 3, 4, 5. In yeast and other fungi, the polarisome, exocyst, Arp2/3, and Spitzenkörper protein complexes collectively orchestrate tip growth and cell polarity, but it is not clear whether these molecular complexes also regulate cell orientation or whether they are influenced by cytoplasmic Ca(2+) gradients. Hyphae of the human pathogenic fungus Candida albicans reorient their growth axis in response to underlying surface topography (thigmotropism) [6] and imposed electric fields (galvanotropism) [7]. The establishment and maintenance of directional growth in relation to these environmental cues was Ca(2+) dependent. Tropisms were attenuated in media containing low Ca(2+), or calcium-channel blockers, and in mutants where calcium channels or elements of the calcium signaling pathway were deleted. Therefore galvanotropism and thigmotropism may both be mediated by localized Ca(2+) influx at sites of polarized growth via Ca(2+) channels that are activated by appropriate environmental signals. |
format | Text |
id | pubmed-1885950 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-18859502007-06-11 Hyphal Orientation of Candida albicans Is Regulated by a Calcium-Dependent Mechanism Brand, Alexandra Shanks, Scott Duncan, Vanessa M.S. Yang, Meng Mackenzie, Kevin Gow, Neil A.R. Curr Biol Report Eukaryotic cells from fungal hyphae to neurites that grow by polarized extension must coordinate cell growth and cell orientation to enable them to exhibit growth tropisms and to respond to relevant environmental cues. Such cells generally maintain a tip-high Ca(2+) cytoplasmic gradient, which is correlated with their ability to exhibit polarized tip growth and to respond to growth-directing extracellular signals 1, 2, 3, 4, 5. In yeast and other fungi, the polarisome, exocyst, Arp2/3, and Spitzenkörper protein complexes collectively orchestrate tip growth and cell polarity, but it is not clear whether these molecular complexes also regulate cell orientation or whether they are influenced by cytoplasmic Ca(2+) gradients. Hyphae of the human pathogenic fungus Candida albicans reorient their growth axis in response to underlying surface topography (thigmotropism) [6] and imposed electric fields (galvanotropism) [7]. The establishment and maintenance of directional growth in relation to these environmental cues was Ca(2+) dependent. Tropisms were attenuated in media containing low Ca(2+), or calcium-channel blockers, and in mutants where calcium channels or elements of the calcium signaling pathway were deleted. Therefore galvanotropism and thigmotropism may both be mediated by localized Ca(2+) influx at sites of polarized growth via Ca(2+) channels that are activated by appropriate environmental signals. Cell Press 2007-02-20 /pmc/articles/PMC1885950/ /pubmed/17275302 http://dx.doi.org/10.1016/j.cub.2006.12.043 Text en © 2007 ELL & Excerpta Medica. https://creativecommons.org/licenses/by/3.0/This is an open access article under the CC BY license (https://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Report Brand, Alexandra Shanks, Scott Duncan, Vanessa M.S. Yang, Meng Mackenzie, Kevin Gow, Neil A.R. Hyphal Orientation of Candida albicans Is Regulated by a Calcium-Dependent Mechanism |
title | Hyphal Orientation of Candida albicans Is Regulated by a Calcium-Dependent Mechanism |
title_full | Hyphal Orientation of Candida albicans Is Regulated by a Calcium-Dependent Mechanism |
title_fullStr | Hyphal Orientation of Candida albicans Is Regulated by a Calcium-Dependent Mechanism |
title_full_unstemmed | Hyphal Orientation of Candida albicans Is Regulated by a Calcium-Dependent Mechanism |
title_short | Hyphal Orientation of Candida albicans Is Regulated by a Calcium-Dependent Mechanism |
title_sort | hyphal orientation of candida albicans is regulated by a calcium-dependent mechanism |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1885950/ https://www.ncbi.nlm.nih.gov/pubmed/17275302 http://dx.doi.org/10.1016/j.cub.2006.12.043 |
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