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G3BP2, a stress granule assembly factor, is dispensable for spermatogenesis in mice
BACKGROUND: Spermatogenesis is a complex process that includes mitosis, meiosis, and spermiogenesis. During spermatogenesis, genetic factors play a vital role inthe formation of properly functioning sperm. GTPase-activating protein (SH3 domain)-binding protein 2 (G3BP2) is known to take part in immu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9248785/ https://www.ncbi.nlm.nih.gov/pubmed/35782098 http://dx.doi.org/10.7717/peerj.13532 |
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author | Yun, Damin Zhou, Liwei Shi, Jie Li, Xinyao Wu, Xiaolong Sun, Fei |
author_facet | Yun, Damin Zhou, Liwei Shi, Jie Li, Xinyao Wu, Xiaolong Sun, Fei |
author_sort | Yun, Damin |
collection | PubMed |
description | BACKGROUND: Spermatogenesis is a complex process that includes mitosis, meiosis, and spermiogenesis. During spermatogenesis, genetic factors play a vital role inthe formation of properly functioning sperm. GTPase-activating protein (SH3 domain)-binding protein 2 (G3BP2) is known to take part in immune responses, mRNA transport, and stress-granule assembly. However, its role in male fertility is unclear. Here, we generated a G3bp2 conditional knockout (cKO) mouse model to explore the function of G3BP2 in male fertility. METHODS: Polymerase chain reaction (PCR) and western blotting (WB) were used to confirm testis-specific G3bp2 knockout. Hematoxylin-eosin (HE) staining to observe testicular morphology and epididymal structure. Computer-aided sperm analysis (CASA) to detect sperm concentration and motility. Terminal deoxynucleotidyl transferase-dUTP nick-end labeling (TUNEL) assay was used to detect apoptotic cells. RESULTS: We found that cKO male mice are fertile with the normal morphology of the testis and sperm. Additionally, CASA of the semen from cKO mice showed that they all had a similar sperm concentration and motility. In addition, sperm from these mice exhibited a similar morphology. But the tunnel assay revealed increased apoptosis in their testes relative to the level in the wild type (WT). CONCLUSION: Together, our data demonstrate that G3BP2 is dispensable for spermatogenesis and male fertility in mice albeit with the increased germ-cell apoptosis. |
format | Online Article Text |
id | pubmed-9248785 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92487852022-07-02 G3BP2, a stress granule assembly factor, is dispensable for spermatogenesis in mice Yun, Damin Zhou, Liwei Shi, Jie Li, Xinyao Wu, Xiaolong Sun, Fei PeerJ Cell Biology BACKGROUND: Spermatogenesis is a complex process that includes mitosis, meiosis, and spermiogenesis. During spermatogenesis, genetic factors play a vital role inthe formation of properly functioning sperm. GTPase-activating protein (SH3 domain)-binding protein 2 (G3BP2) is known to take part in immune responses, mRNA transport, and stress-granule assembly. However, its role in male fertility is unclear. Here, we generated a G3bp2 conditional knockout (cKO) mouse model to explore the function of G3BP2 in male fertility. METHODS: Polymerase chain reaction (PCR) and western blotting (WB) were used to confirm testis-specific G3bp2 knockout. Hematoxylin-eosin (HE) staining to observe testicular morphology and epididymal structure. Computer-aided sperm analysis (CASA) to detect sperm concentration and motility. Terminal deoxynucleotidyl transferase-dUTP nick-end labeling (TUNEL) assay was used to detect apoptotic cells. RESULTS: We found that cKO male mice are fertile with the normal morphology of the testis and sperm. Additionally, CASA of the semen from cKO mice showed that they all had a similar sperm concentration and motility. In addition, sperm from these mice exhibited a similar morphology. But the tunnel assay revealed increased apoptosis in their testes relative to the level in the wild type (WT). CONCLUSION: Together, our data demonstrate that G3BP2 is dispensable for spermatogenesis and male fertility in mice albeit with the increased germ-cell apoptosis. PeerJ Inc. 2022-06-28 /pmc/articles/PMC9248785/ /pubmed/35782098 http://dx.doi.org/10.7717/peerj.13532 Text en © 2022 Yun et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Cell Biology Yun, Damin Zhou, Liwei Shi, Jie Li, Xinyao Wu, Xiaolong Sun, Fei G3BP2, a stress granule assembly factor, is dispensable for spermatogenesis in mice |
title | G3BP2, a stress granule assembly factor, is dispensable for spermatogenesis in mice |
title_full | G3BP2, a stress granule assembly factor, is dispensable for spermatogenesis in mice |
title_fullStr | G3BP2, a stress granule assembly factor, is dispensable for spermatogenesis in mice |
title_full_unstemmed | G3BP2, a stress granule assembly factor, is dispensable for spermatogenesis in mice |
title_short | G3BP2, a stress granule assembly factor, is dispensable for spermatogenesis in mice |
title_sort | g3bp2, a stress granule assembly factor, is dispensable for spermatogenesis in mice |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9248785/ https://www.ncbi.nlm.nih.gov/pubmed/35782098 http://dx.doi.org/10.7717/peerj.13532 |
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