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The association of ODF4 with AK1 and AK2 in mice is essential for fertility through its contribution to flagellar shape

Normal sperm flagellar shape and movement are essential for fertilization. The integral protein outer dense fiber 4 (ODF4) localizes to ODFs, but its function remains unclear. Adenylate kinase (AK) is a phosphotransferase that catalyzes the interconversion and controls the concentration equilibrium...

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Autores principales: Ito, Chizuru, Makino, Tsukasa, Mutoh, Tohru, Kikkawa, Masahide, Toshimori, Kiyotaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941515/
https://www.ncbi.nlm.nih.gov/pubmed/36804949
http://dx.doi.org/10.1038/s41598-023-28177-z
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author Ito, Chizuru
Makino, Tsukasa
Mutoh, Tohru
Kikkawa, Masahide
Toshimori, Kiyotaka
author_facet Ito, Chizuru
Makino, Tsukasa
Mutoh, Tohru
Kikkawa, Masahide
Toshimori, Kiyotaka
author_sort Ito, Chizuru
collection PubMed
description Normal sperm flagellar shape and movement are essential for fertilization. The integral protein outer dense fiber 4 (ODF4) localizes to ODFs, but its function remains unclear. Adenylate kinase (AK) is a phosphotransferase that catalyzes the interconversion and controls the concentration equilibrium of adenine nucleotides. AK shuttles ATP to energy-consuming sites. Here, we report on the relationship of flagellar shape and movement with ODF4, AK1 and AK2 by using Odf4-deletion (Odf4(−/−)) mice. Soluble ODF4 is coimmunoprecipitated with AK1 and AK2 in Odf4(+/+) spermatozoa. ODF4, AK1 and AK2 localize to whole flagella (plasmalemma, mitochondria, ODFs, and residual cytoplasmic droplets (CDs)), principal pieces, and midpieces, respectively. Odf4(−/−) sperm flagella lose ODF4 and reduce AK1 and AK2 but produce ATP. The flagellum is bent (hairpin flagellum) with a large CD in the midpiece. There is no motility in the midpiece, but the principal piece is motile. Odf4(−/−) spermatozoa progress backward and fail to ascend in the uterus. Thus, Odf4(−/−) males are infertile owing to abnormal flagellar shape and movement caused mainly by the loss of ODF4 with AK1 and AK2. This study is supported by the rescue experiment; the abnormalities and male infertility caused by Odf4 deletion were reversed by Odf4 restoration.
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spelling pubmed-99415152023-02-22 The association of ODF4 with AK1 and AK2 in mice is essential for fertility through its contribution to flagellar shape Ito, Chizuru Makino, Tsukasa Mutoh, Tohru Kikkawa, Masahide Toshimori, Kiyotaka Sci Rep Article Normal sperm flagellar shape and movement are essential for fertilization. The integral protein outer dense fiber 4 (ODF4) localizes to ODFs, but its function remains unclear. Adenylate kinase (AK) is a phosphotransferase that catalyzes the interconversion and controls the concentration equilibrium of adenine nucleotides. AK shuttles ATP to energy-consuming sites. Here, we report on the relationship of flagellar shape and movement with ODF4, AK1 and AK2 by using Odf4-deletion (Odf4(−/−)) mice. Soluble ODF4 is coimmunoprecipitated with AK1 and AK2 in Odf4(+/+) spermatozoa. ODF4, AK1 and AK2 localize to whole flagella (plasmalemma, mitochondria, ODFs, and residual cytoplasmic droplets (CDs)), principal pieces, and midpieces, respectively. Odf4(−/−) sperm flagella lose ODF4 and reduce AK1 and AK2 but produce ATP. The flagellum is bent (hairpin flagellum) with a large CD in the midpiece. There is no motility in the midpiece, but the principal piece is motile. Odf4(−/−) spermatozoa progress backward and fail to ascend in the uterus. Thus, Odf4(−/−) males are infertile owing to abnormal flagellar shape and movement caused mainly by the loss of ODF4 with AK1 and AK2. This study is supported by the rescue experiment; the abnormalities and male infertility caused by Odf4 deletion were reversed by Odf4 restoration. Nature Publishing Group UK 2023-02-20 /pmc/articles/PMC9941515/ /pubmed/36804949 http://dx.doi.org/10.1038/s41598-023-28177-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ito, Chizuru
Makino, Tsukasa
Mutoh, Tohru
Kikkawa, Masahide
Toshimori, Kiyotaka
The association of ODF4 with AK1 and AK2 in mice is essential for fertility through its contribution to flagellar shape
title The association of ODF4 with AK1 and AK2 in mice is essential for fertility through its contribution to flagellar shape
title_full The association of ODF4 with AK1 and AK2 in mice is essential for fertility through its contribution to flagellar shape
title_fullStr The association of ODF4 with AK1 and AK2 in mice is essential for fertility through its contribution to flagellar shape
title_full_unstemmed The association of ODF4 with AK1 and AK2 in mice is essential for fertility through its contribution to flagellar shape
title_short The association of ODF4 with AK1 and AK2 in mice is essential for fertility through its contribution to flagellar shape
title_sort association of odf4 with ak1 and ak2 in mice is essential for fertility through its contribution to flagellar shape
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941515/
https://www.ncbi.nlm.nih.gov/pubmed/36804949
http://dx.doi.org/10.1038/s41598-023-28177-z
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