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SOX17-positive rete testis epithelium is required for Sertoli valve formation and normal spermiogenesis in the male mouse

Seminiferous tubules (STs) in the mammalian testes are connected to the rete testis (RT) via a Sertoli valve (SV). Spermatozoa produced in the STs are released into the tubular luminal fluid and passively transported through the SV into the RT. However, the physiological functions of the RT and SV r...

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Autores principales: Uchida, Aya, Imaimatsu, Kenya, Suzuki, Honoka, Han, Xiao, Ushioda, Hiroki, Uemura, Mami, Imura-Kishi, Kasane, Hiramatsu, Ryuji, Takase, Hinako M., Hirate, Yoshikazu, Ogura, Atsuo, Kanai-Azuma, Masami, Kudo, Akihiko, Kanai, Yoshiakira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9772346/
https://www.ncbi.nlm.nih.gov/pubmed/36543770
http://dx.doi.org/10.1038/s41467-022-35465-1
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author Uchida, Aya
Imaimatsu, Kenya
Suzuki, Honoka
Han, Xiao
Ushioda, Hiroki
Uemura, Mami
Imura-Kishi, Kasane
Hiramatsu, Ryuji
Takase, Hinako M.
Hirate, Yoshikazu
Ogura, Atsuo
Kanai-Azuma, Masami
Kudo, Akihiko
Kanai, Yoshiakira
author_facet Uchida, Aya
Imaimatsu, Kenya
Suzuki, Honoka
Han, Xiao
Ushioda, Hiroki
Uemura, Mami
Imura-Kishi, Kasane
Hiramatsu, Ryuji
Takase, Hinako M.
Hirate, Yoshikazu
Ogura, Atsuo
Kanai-Azuma, Masami
Kudo, Akihiko
Kanai, Yoshiakira
author_sort Uchida, Aya
collection PubMed
description Seminiferous tubules (STs) in the mammalian testes are connected to the rete testis (RT) via a Sertoli valve (SV). Spermatozoa produced in the STs are released into the tubular luminal fluid and passively transported through the SV into the RT. However, the physiological functions of the RT and SV remain unclear. Here, we identified the expression of Sox17 in RT epithelia. The SV valve was disrupted before puberty in RT-specific Sox17 conditional knockout (Sox17-cKO) male mice. This induced a backflow of RT fluid into the STs, which caused aberrant detachment of immature spermatids. RT of Sox17-cKO mice had reduced expression levels of various growth factor genes, which presumably support SV formation. When transplanted next to the Sox17(+) RT, Sertoli cells of Sox17-cKO mice reconstructed the SV and supported proper spermiogenesis in the STs. This study highlights the novel and unexpected modulatory roles of the RT in SV valve formation and spermatogenesis in mouse testes, as a downstream action of Sox17.
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spelling pubmed-97723462022-12-23 SOX17-positive rete testis epithelium is required for Sertoli valve formation and normal spermiogenesis in the male mouse Uchida, Aya Imaimatsu, Kenya Suzuki, Honoka Han, Xiao Ushioda, Hiroki Uemura, Mami Imura-Kishi, Kasane Hiramatsu, Ryuji Takase, Hinako M. Hirate, Yoshikazu Ogura, Atsuo Kanai-Azuma, Masami Kudo, Akihiko Kanai, Yoshiakira Nat Commun Article Seminiferous tubules (STs) in the mammalian testes are connected to the rete testis (RT) via a Sertoli valve (SV). Spermatozoa produced in the STs are released into the tubular luminal fluid and passively transported through the SV into the RT. However, the physiological functions of the RT and SV remain unclear. Here, we identified the expression of Sox17 in RT epithelia. The SV valve was disrupted before puberty in RT-specific Sox17 conditional knockout (Sox17-cKO) male mice. This induced a backflow of RT fluid into the STs, which caused aberrant detachment of immature spermatids. RT of Sox17-cKO mice had reduced expression levels of various growth factor genes, which presumably support SV formation. When transplanted next to the Sox17(+) RT, Sertoli cells of Sox17-cKO mice reconstructed the SV and supported proper spermiogenesis in the STs. This study highlights the novel and unexpected modulatory roles of the RT in SV valve formation and spermatogenesis in mouse testes, as a downstream action of Sox17. Nature Publishing Group UK 2022-12-21 /pmc/articles/PMC9772346/ /pubmed/36543770 http://dx.doi.org/10.1038/s41467-022-35465-1 Text en © The Author(s) 2022 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 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Uchida, Aya
Imaimatsu, Kenya
Suzuki, Honoka
Han, Xiao
Ushioda, Hiroki
Uemura, Mami
Imura-Kishi, Kasane
Hiramatsu, Ryuji
Takase, Hinako M.
Hirate, Yoshikazu
Ogura, Atsuo
Kanai-Azuma, Masami
Kudo, Akihiko
Kanai, Yoshiakira
SOX17-positive rete testis epithelium is required for Sertoli valve formation and normal spermiogenesis in the male mouse
title SOX17-positive rete testis epithelium is required for Sertoli valve formation and normal spermiogenesis in the male mouse
title_full SOX17-positive rete testis epithelium is required for Sertoli valve formation and normal spermiogenesis in the male mouse
title_fullStr SOX17-positive rete testis epithelium is required for Sertoli valve formation and normal spermiogenesis in the male mouse
title_full_unstemmed SOX17-positive rete testis epithelium is required for Sertoli valve formation and normal spermiogenesis in the male mouse
title_short SOX17-positive rete testis epithelium is required for Sertoli valve formation and normal spermiogenesis in the male mouse
title_sort sox17-positive rete testis epithelium is required for sertoli valve formation and normal spermiogenesis in the male mouse
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9772346/
https://www.ncbi.nlm.nih.gov/pubmed/36543770
http://dx.doi.org/10.1038/s41467-022-35465-1
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