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Sperm-borne phospholipase C zeta-1 ensures monospermic fertilization in mice
Sperm entry in mammalian oocytes triggers intracellular Ca(2+) oscillations that initiate resumption of the meiotic cell cycle and subsequent activations. Here, we show that phospholipase C zeta 1 (PLCζ1) is the long-sought sperm-borne oocyte activation factor (SOAF). Plcz1 gene knockout (KO) mouse...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5778054/ https://www.ncbi.nlm.nih.gov/pubmed/29358633 http://dx.doi.org/10.1038/s41598-018-19497-6 |
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author | Nozawa, Kaori Satouh, Yuhkoh Fujimoto, Takao Oji, Asami Ikawa, Masahito |
author_facet | Nozawa, Kaori Satouh, Yuhkoh Fujimoto, Takao Oji, Asami Ikawa, Masahito |
author_sort | Nozawa, Kaori |
collection | PubMed |
description | Sperm entry in mammalian oocytes triggers intracellular Ca(2+) oscillations that initiate resumption of the meiotic cell cycle and subsequent activations. Here, we show that phospholipase C zeta 1 (PLCζ1) is the long-sought sperm-borne oocyte activation factor (SOAF). Plcz1 gene knockout (KO) mouse spermatozoa fail to induce Ca(2+) changes in intracytoplasmic sperm injection (ICSI). In contrast to ICSI, Plcz1 KO spermatozoa induced atypical patterns of Ca(2+) changes in normal fertilizations, and most of the fertilized oocytes ceased development at the 1–2-cell stage because of oocyte activation failure or polyspermy. We further discovered that both zona pellucida block to polyspermy (ZPBP) and plasma membrane block to polyspermy (PMBP) were delayed in oocytes fertilized with Plcz1 KO spermatozoa. With the observation that polyspermy is rare in astacin-like metalloendopeptidase (Astl) KO female oocytes that lack ZPBP, we conclude that PMPB plays more critical role than ZPBP in vivo. Finally, we obtained healthy pups from male mice carrying human infertile PLCZ1 mutation by single sperm ICSI supplemented with Plcz1 mRNA injection. These results suggest that mammalian spermatozoa have a primitive oocyte activation mechanism and that PLCζ1 is a SOAF that ensures oocyte activation steps for monospermic fertilization in mammals. |
format | Online Article Text |
id | pubmed-5778054 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57780542018-01-31 Sperm-borne phospholipase C zeta-1 ensures monospermic fertilization in mice Nozawa, Kaori Satouh, Yuhkoh Fujimoto, Takao Oji, Asami Ikawa, Masahito Sci Rep Article Sperm entry in mammalian oocytes triggers intracellular Ca(2+) oscillations that initiate resumption of the meiotic cell cycle and subsequent activations. Here, we show that phospholipase C zeta 1 (PLCζ1) is the long-sought sperm-borne oocyte activation factor (SOAF). Plcz1 gene knockout (KO) mouse spermatozoa fail to induce Ca(2+) changes in intracytoplasmic sperm injection (ICSI). In contrast to ICSI, Plcz1 KO spermatozoa induced atypical patterns of Ca(2+) changes in normal fertilizations, and most of the fertilized oocytes ceased development at the 1–2-cell stage because of oocyte activation failure or polyspermy. We further discovered that both zona pellucida block to polyspermy (ZPBP) and plasma membrane block to polyspermy (PMBP) were delayed in oocytes fertilized with Plcz1 KO spermatozoa. With the observation that polyspermy is rare in astacin-like metalloendopeptidase (Astl) KO female oocytes that lack ZPBP, we conclude that PMPB plays more critical role than ZPBP in vivo. Finally, we obtained healthy pups from male mice carrying human infertile PLCZ1 mutation by single sperm ICSI supplemented with Plcz1 mRNA injection. These results suggest that mammalian spermatozoa have a primitive oocyte activation mechanism and that PLCζ1 is a SOAF that ensures oocyte activation steps for monospermic fertilization in mammals. Nature Publishing Group UK 2018-01-22 /pmc/articles/PMC5778054/ /pubmed/29358633 http://dx.doi.org/10.1038/s41598-018-19497-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Nozawa, Kaori Satouh, Yuhkoh Fujimoto, Takao Oji, Asami Ikawa, Masahito Sperm-borne phospholipase C zeta-1 ensures monospermic fertilization in mice |
title | Sperm-borne phospholipase C zeta-1 ensures monospermic fertilization in mice |
title_full | Sperm-borne phospholipase C zeta-1 ensures monospermic fertilization in mice |
title_fullStr | Sperm-borne phospholipase C zeta-1 ensures monospermic fertilization in mice |
title_full_unstemmed | Sperm-borne phospholipase C zeta-1 ensures monospermic fertilization in mice |
title_short | Sperm-borne phospholipase C zeta-1 ensures monospermic fertilization in mice |
title_sort | sperm-borne phospholipase c zeta-1 ensures monospermic fertilization in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5778054/ https://www.ncbi.nlm.nih.gov/pubmed/29358633 http://dx.doi.org/10.1038/s41598-018-19497-6 |
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