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Defb19 regulates the migration of germ cell and is involved in male fertility
β-defensins are small antimicrobial peptides that play essential roles in male fertility. Although several members of the β-defensin family are preferentially expressed in the testis, their involvement in spermatogenesis remains elusive. In this study, we have characterized the expression and functi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682749/ https://www.ncbi.nlm.nih.gov/pubmed/36414976 http://dx.doi.org/10.1186/s13578-022-00924-1 |
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author | Jin, Jing Li, Xiaofeng Ye, Mei Qiao, Feng Chen, Hao Fok, Kin Lam |
author_facet | Jin, Jing Li, Xiaofeng Ye, Mei Qiao, Feng Chen, Hao Fok, Kin Lam |
author_sort | Jin, Jing |
collection | PubMed |
description | β-defensins are small antimicrobial peptides that play essential roles in male fertility. Although several members of the β-defensin family are preferentially expressed in the testis, their involvement in spermatogenesis remains elusive. In this study, we have characterized the expression and function of Defb19 in mouse testis. Our results showed that Defb19 is expressed in both Sertoli cells and germ cells. Overexpression of Defb19 in the 15P-1 Sertoli cell line decreases the expression of cell junction molecules and promotes the matrix adhesion and migration of Sertoli cells. Recombinant DEFB19 and conditioned medium of Defb19-overexpressed 15P-1 cells promote the migration of GC2-spd spermatocyte cell line. Knockout of Defb19 in mouse by CRISPR/Cas9 resulted in male subfertility with testicular and epididymal atrophy. A marked increase in apoptosis and a significant decrease in the sperm count were observed in the KO mice. Together, our study has uncovered an important role of Defb19 in male fertility by regulating the migration of both the Sertoli cells and the germ cells. Our study has shed new light on the functions of β-defensins in the testis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13578-022-00924-1. |
format | Online Article Text |
id | pubmed-9682749 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-96827492022-11-24 Defb19 regulates the migration of germ cell and is involved in male fertility Jin, Jing Li, Xiaofeng Ye, Mei Qiao, Feng Chen, Hao Fok, Kin Lam Cell Biosci Letter to the Editor β-defensins are small antimicrobial peptides that play essential roles in male fertility. Although several members of the β-defensin family are preferentially expressed in the testis, their involvement in spermatogenesis remains elusive. In this study, we have characterized the expression and function of Defb19 in mouse testis. Our results showed that Defb19 is expressed in both Sertoli cells and germ cells. Overexpression of Defb19 in the 15P-1 Sertoli cell line decreases the expression of cell junction molecules and promotes the matrix adhesion and migration of Sertoli cells. Recombinant DEFB19 and conditioned medium of Defb19-overexpressed 15P-1 cells promote the migration of GC2-spd spermatocyte cell line. Knockout of Defb19 in mouse by CRISPR/Cas9 resulted in male subfertility with testicular and epididymal atrophy. A marked increase in apoptosis and a significant decrease in the sperm count were observed in the KO mice. Together, our study has uncovered an important role of Defb19 in male fertility by regulating the migration of both the Sertoli cells and the germ cells. Our study has shed new light on the functions of β-defensins in the testis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13578-022-00924-1. BioMed Central 2022-11-22 /pmc/articles/PMC9682749/ /pubmed/36414976 http://dx.doi.org/10.1186/s13578-022-00924-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Letter to the Editor Jin, Jing Li, Xiaofeng Ye, Mei Qiao, Feng Chen, Hao Fok, Kin Lam Defb19 regulates the migration of germ cell and is involved in male fertility |
title | Defb19 regulates the migration of germ cell and is involved in male fertility |
title_full | Defb19 regulates the migration of germ cell and is involved in male fertility |
title_fullStr | Defb19 regulates the migration of germ cell and is involved in male fertility |
title_full_unstemmed | Defb19 regulates the migration of germ cell and is involved in male fertility |
title_short | Defb19 regulates the migration of germ cell and is involved in male fertility |
title_sort | defb19 regulates the migration of germ cell and is involved in male fertility |
topic | Letter to the Editor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682749/ https://www.ncbi.nlm.nih.gov/pubmed/36414976 http://dx.doi.org/10.1186/s13578-022-00924-1 |
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