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...
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Frontiers Media S.A.
2021
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oai:doaj.org-article:72516afd023148dc8113f3a40a111e022021-11-08T13:35:12ZAnkrd31 in Sperm and Epididymal Integrity2296-634X10.3389/fcell.2021.741975https://doaj.org/article/72516afd023148dc8113f3a40a111e022021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fcell.2021.741975/fullhttps://doaj.org/toc/2296-634XAnkyrin 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.Francesco ManfrevolaGuillaume MartinezGuillaume MartinezCharles CouttonCharles CouttonDomenico RoccoKarine ReynaudYves Le VernPascal FromentLinda BeauclairDenise AubertRiccardo PierantoniRosanna ChianeseFlorian GuillouFrontiers Media S.A.articleankyrinsspermatogenesissperm qualityblood-epididymal-barriermale infertilityBiology (General)QH301-705.5ENFrontiers in Cell and Developmental Biology, Vol 9 (2021) |
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ankyrins spermatogenesis sperm quality blood-epididymal-barrier male infertility Biology (General) QH301-705.5 |
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ankyrins spermatogenesis sperm quality blood-epididymal-barrier male infertility Biology (General) QH301-705.5 Francesco Manfrevola Guillaume Martinez Guillaume Martinez Charles Coutton Charles Coutton Domenico Rocco Karine Reynaud Yves Le Vern Pascal Froment Linda Beauclair Denise Aubert Riccardo Pierantoni Rosanna Chianese Florian Guillou Ankrd31 in Sperm and Epididymal Integrity |
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 |
article |
author |
Francesco Manfrevola Guillaume Martinez Guillaume Martinez Charles Coutton Charles Coutton Domenico Rocco Karine Reynaud Yves Le Vern Pascal Froment Linda Beauclair Denise Aubert Riccardo Pierantoni Rosanna Chianese Florian Guillou |
author_facet |
Francesco Manfrevola Guillaume Martinez Guillaume Martinez Charles Coutton Charles Coutton Domenico Rocco Karine Reynaud Yves Le Vern Pascal Froment Linda Beauclair Denise Aubert Riccardo Pierantoni Rosanna Chianese Florian Guillou |
author_sort |
Francesco Manfrevola |
title |
Ankrd31 in Sperm and Epididymal Integrity |
title_short |
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_sort |
ankrd31 in sperm and epididymal integrity |
publisher |
Frontiers Media S.A. |
publishDate |
2021 |
url |
https://doaj.org/article/72516afd023148dc8113f3a40a111e02 |
work_keys_str_mv |
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_version_ |
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