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Calcium Signaling and Meiotic Exit at Fertilization in Xenopus Egg
Calcium is a universal messenger that mediates egg activation at fertilization in all sexually reproducing species studied. However, signaling pathways leading to calcium generation and the mechanisms of calcium-induced exit from meiotic arrest vary substantially among species. Here, we review the p...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227238/ https://www.ncbi.nlm.nih.gov/pubmed/25322156 http://dx.doi.org/10.3390/ijms151018659 |
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author | Tokmakov, Alexander A. Stefanov, Vasily E. Iwasaki, Tetsushi Sato, Ken-Ichi Fukami, Yasuo |
author_facet | Tokmakov, Alexander A. Stefanov, Vasily E. Iwasaki, Tetsushi Sato, Ken-Ichi Fukami, Yasuo |
author_sort | Tokmakov, Alexander A. |
collection | PubMed |
description | Calcium is a universal messenger that mediates egg activation at fertilization in all sexually reproducing species studied. However, signaling pathways leading to calcium generation and the mechanisms of calcium-induced exit from meiotic arrest vary substantially among species. Here, we review the pathways of calcium signaling and the mechanisms of meiotic exit at fertilization in the eggs of the established developmental model, African clawed frog, Xenopus laevis. We also discuss calcium involvement in the early fertilization-induced events in Xenopus egg, such as membrane depolarization, the increase in intracellular pH, cortical granule exocytosis, cortical contraction, contraction wave, cortical rotation, reformation of the nuclear envelope, sperm chromatin decondensation and sister chromatid segregation. |
format | Online Article Text |
id | pubmed-4227238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-42272382014-11-12 Calcium Signaling and Meiotic Exit at Fertilization in Xenopus Egg Tokmakov, Alexander A. Stefanov, Vasily E. Iwasaki, Tetsushi Sato, Ken-Ichi Fukami, Yasuo Int J Mol Sci Review Calcium is a universal messenger that mediates egg activation at fertilization in all sexually reproducing species studied. However, signaling pathways leading to calcium generation and the mechanisms of calcium-induced exit from meiotic arrest vary substantially among species. Here, we review the pathways of calcium signaling and the mechanisms of meiotic exit at fertilization in the eggs of the established developmental model, African clawed frog, Xenopus laevis. We also discuss calcium involvement in the early fertilization-induced events in Xenopus egg, such as membrane depolarization, the increase in intracellular pH, cortical granule exocytosis, cortical contraction, contraction wave, cortical rotation, reformation of the nuclear envelope, sperm chromatin decondensation and sister chromatid segregation. MDPI 2014-10-15 /pmc/articles/PMC4227238/ /pubmed/25322156 http://dx.doi.org/10.3390/ijms151018659 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Tokmakov, Alexander A. Stefanov, Vasily E. Iwasaki, Tetsushi Sato, Ken-Ichi Fukami, Yasuo Calcium Signaling and Meiotic Exit at Fertilization in Xenopus Egg |
title | Calcium Signaling and Meiotic Exit at Fertilization in Xenopus Egg |
title_full | Calcium Signaling and Meiotic Exit at Fertilization in Xenopus Egg |
title_fullStr | Calcium Signaling and Meiotic Exit at Fertilization in Xenopus Egg |
title_full_unstemmed | Calcium Signaling and Meiotic Exit at Fertilization in Xenopus Egg |
title_short | Calcium Signaling and Meiotic Exit at Fertilization in Xenopus Egg |
title_sort | calcium signaling and meiotic exit at fertilization in xenopus egg |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227238/ https://www.ncbi.nlm.nih.gov/pubmed/25322156 http://dx.doi.org/10.3390/ijms151018659 |
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