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Ankrd31 in Sperm and Epididymal Integrity
Ankyrin proteins (ANKRD) are key mediators linking membrane and sub-membranous cytoskeletal proteins. Recent findings have highlighted a new role of ANKRD31 during spermatogenesis, elucidating its involvement in meiotic recombination and male germ cell progression. Following testicular differentiati...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607815/ https://www.ncbi.nlm.nih.gov/pubmed/34820371 http://dx.doi.org/10.3389/fcell.2021.741975 |
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author | Manfrevola, Francesco Martinez, Guillaume Coutton, Charles Rocco, Domenico Reynaud, Karine Le Vern, Yves Froment, Pascal Beauclair, Linda Aubert, Denise Pierantoni, Riccardo Chianese, Rosanna Guillou, Florian |
author_facet | Manfrevola, Francesco Martinez, Guillaume Coutton, Charles Rocco, Domenico Reynaud, Karine Le Vern, Yves Froment, Pascal Beauclair, Linda Aubert, Denise Pierantoni, Riccardo Chianese, Rosanna Guillou, Florian |
author_sort | Manfrevola, Francesco |
collection | PubMed |
description | Ankyrin proteins (ANKRD) are key mediators linking membrane and sub-membranous cytoskeletal proteins. Recent findings have highlighted a new role of ANKRD31 during spermatogenesis, elucidating its involvement in meiotic recombination and male germ cell progression. Following testicular differentiation, spermatozoa (SPZ) enter into the epididymis, where they undergo several biochemical and enzymatic changes. The epididymal epithelium is characterized by cell-to-cell junctions that are able to form the blood-epididymal barrier (BEB). This intricate epithelial structure provides the optimal microenvironment needed for epididymal sperm maturation. To date, no notions have been reported regarding a putative role of ANKRD31 in correct BEB formation. In our work, we generated an Ankrd31 knockout male mouse model (Ankrd31(–/–)) and characterized its reproductive phenotype. Ankrd31(–/–) mice were infertile and exhibited oligo-astheno-teratozoospermia (a low number of immotile SPZ with abnormal morphological features). In addition, a complete deregulation of BEB was found in Ankrd31(–/–), due to cell-to-cell junction anomalies. In order to suggest that BEB deregulation may depend on Ankrd31 gene deletion, we showed the physical interaction among ANKRD31 and some epithelial junction proteins in wild-type (WT) epididymides. In conclusion, the current work shows a key role of ANKRD31 in the control of germ cell progression as well as sperm and epididymal integrity. |
format | Online Article Text |
id | pubmed-8607815 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86078152021-11-23 Ankrd31 in Sperm and Epididymal Integrity Manfrevola, Francesco Martinez, Guillaume Coutton, Charles Rocco, Domenico Reynaud, Karine Le Vern, Yves Froment, Pascal Beauclair, Linda Aubert, Denise Pierantoni, Riccardo Chianese, Rosanna Guillou, Florian Front Cell Dev Biol Cell and Developmental Biology Ankyrin proteins (ANKRD) are key mediators linking membrane and sub-membranous cytoskeletal proteins. Recent findings have highlighted a new role of ANKRD31 during spermatogenesis, elucidating its involvement in meiotic recombination and male germ cell progression. Following testicular differentiation, spermatozoa (SPZ) enter into the epididymis, where they undergo several biochemical and enzymatic changes. The epididymal epithelium is characterized by cell-to-cell junctions that are able to form the blood-epididymal barrier (BEB). This intricate epithelial structure provides the optimal microenvironment needed for epididymal sperm maturation. To date, no notions have been reported regarding a putative role of ANKRD31 in correct BEB formation. In our work, we generated an Ankrd31 knockout male mouse model (Ankrd31(–/–)) and characterized its reproductive phenotype. Ankrd31(–/–) mice were infertile and exhibited oligo-astheno-teratozoospermia (a low number of immotile SPZ with abnormal morphological features). In addition, a complete deregulation of BEB was found in Ankrd31(–/–), due to cell-to-cell junction anomalies. In order to suggest that BEB deregulation may depend on Ankrd31 gene deletion, we showed the physical interaction among ANKRD31 and some epithelial junction proteins in wild-type (WT) epididymides. In conclusion, the current work shows a key role of ANKRD31 in the control of germ cell progression as well as sperm and epididymal integrity. Frontiers Media S.A. 2021-11-08 /pmc/articles/PMC8607815/ /pubmed/34820371 http://dx.doi.org/10.3389/fcell.2021.741975 Text en Copyright © 2021 Manfrevola, Martinez, Coutton, Rocco, Reynaud, Le Vern, Froment, Beauclair, Aubert, Pierantoni, Chianese and Guillou. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Manfrevola, Francesco Martinez, Guillaume Coutton, Charles Rocco, Domenico Reynaud, Karine Le Vern, Yves Froment, Pascal Beauclair, Linda Aubert, Denise Pierantoni, Riccardo Chianese, Rosanna Guillou, Florian Ankrd31 in Sperm and Epididymal Integrity |
title | Ankrd31 in Sperm and Epididymal Integrity |
title_full | Ankrd31 in Sperm and Epididymal Integrity |
title_fullStr | Ankrd31 in Sperm and Epididymal Integrity |
title_full_unstemmed | Ankrd31 in Sperm and Epididymal Integrity |
title_short | Ankrd31 in Sperm and Epididymal Integrity |
title_sort | ankrd31 in sperm and epididymal integrity |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607815/ https://www.ncbi.nlm.nih.gov/pubmed/34820371 http://dx.doi.org/10.3389/fcell.2021.741975 |
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