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Stromal cell-derived factor 1 regulates in vitro sperm migration towards the cumulus-oocyte complex in cattle
Sperm migration towards an oocyte in the female reproductive tract is an important step for successful fertilization. Although several sperm-chemotactic factors have been identified in mammals, it is unclear whether these chemoattractants contribute to sperm migration towards an oocyte that is the f...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7192438/ https://www.ncbi.nlm.nih.gov/pubmed/32353075 http://dx.doi.org/10.1371/journal.pone.0232536 |
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author | Umezu, Kohei Hara, Kenshiro Hiradate, Yuuki Numabe, Takashi Tanemura, Kentaro |
author_facet | Umezu, Kohei Hara, Kenshiro Hiradate, Yuuki Numabe, Takashi Tanemura, Kentaro |
author_sort | Umezu, Kohei |
collection | PubMed |
description | Sperm migration towards an oocyte in the female reproductive tract is an important step for successful fertilization. Although several sperm-chemotactic factors have been identified in mammals, it is unclear whether these chemoattractants contribute to sperm migration towards an oocyte that is the final destination for sperm. Furthermore, chemoattractants for bovine sperm are still undiscovered even though the follicular fluid attracts sperm in cattle. Here, we demonstrated that a single bovine cumulus-oocyte complex (COC) had the ability to attract sperm, suggesting that the COC secreted sperm chemoattractants. We identified stromal cell-derived factor 1 (SDF1), which was expressed in COCs, and its receptor CXCR4 in sperm, as a candidate. Our results showed that bovine sperm preferentially migrated to the area with a high SDF1 concentration and occasionally showed turn movements by asymmetric flagellar bends during the migration. We also demonstrated that increasing the intracellular Ca(2+) concentration via Ca(2+) channels was related to SDF1-induced sperm chemotaxis. Finally, a CXCR4 inhibitor significantly suppressed the in vitro bovine sperm migration towards a COC. Taken together, we propose that SDF1 is a chemotactic factor for bovine sperm to regulate their migration towards an oocyte via the CXCR4 receptor. |
format | Online Article Text |
id | pubmed-7192438 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-71924382020-05-11 Stromal cell-derived factor 1 regulates in vitro sperm migration towards the cumulus-oocyte complex in cattle Umezu, Kohei Hara, Kenshiro Hiradate, Yuuki Numabe, Takashi Tanemura, Kentaro PLoS One Research Article Sperm migration towards an oocyte in the female reproductive tract is an important step for successful fertilization. Although several sperm-chemotactic factors have been identified in mammals, it is unclear whether these chemoattractants contribute to sperm migration towards an oocyte that is the final destination for sperm. Furthermore, chemoattractants for bovine sperm are still undiscovered even though the follicular fluid attracts sperm in cattle. Here, we demonstrated that a single bovine cumulus-oocyte complex (COC) had the ability to attract sperm, suggesting that the COC secreted sperm chemoattractants. We identified stromal cell-derived factor 1 (SDF1), which was expressed in COCs, and its receptor CXCR4 in sperm, as a candidate. Our results showed that bovine sperm preferentially migrated to the area with a high SDF1 concentration and occasionally showed turn movements by asymmetric flagellar bends during the migration. We also demonstrated that increasing the intracellular Ca(2+) concentration via Ca(2+) channels was related to SDF1-induced sperm chemotaxis. Finally, a CXCR4 inhibitor significantly suppressed the in vitro bovine sperm migration towards a COC. Taken together, we propose that SDF1 is a chemotactic factor for bovine sperm to regulate their migration towards an oocyte via the CXCR4 receptor. Public Library of Science 2020-04-30 /pmc/articles/PMC7192438/ /pubmed/32353075 http://dx.doi.org/10.1371/journal.pone.0232536 Text en © 2020 Umezu et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Umezu, Kohei Hara, Kenshiro Hiradate, Yuuki Numabe, Takashi Tanemura, Kentaro Stromal cell-derived factor 1 regulates in vitro sperm migration towards the cumulus-oocyte complex in cattle |
title | Stromal cell-derived factor 1 regulates in vitro sperm migration towards the cumulus-oocyte complex in cattle |
title_full | Stromal cell-derived factor 1 regulates in vitro sperm migration towards the cumulus-oocyte complex in cattle |
title_fullStr | Stromal cell-derived factor 1 regulates in vitro sperm migration towards the cumulus-oocyte complex in cattle |
title_full_unstemmed | Stromal cell-derived factor 1 regulates in vitro sperm migration towards the cumulus-oocyte complex in cattle |
title_short | Stromal cell-derived factor 1 regulates in vitro sperm migration towards the cumulus-oocyte complex in cattle |
title_sort | stromal cell-derived factor 1 regulates in vitro sperm migration towards the cumulus-oocyte complex in cattle |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7192438/ https://www.ncbi.nlm.nih.gov/pubmed/32353075 http://dx.doi.org/10.1371/journal.pone.0232536 |
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