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Identification of fish spermatogenic cells through high-throughput immunofluorescence against testis with an antibody set

Image-based identification and quantification of different types of spermatogenic cells is of great importance, not only for reproductive studies but also for genetic breeding. Here, we have developed antibodies against spermatogenesis-related proteins in zebrafish (Danio rerio), including Ddx4, Piw...

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Autores principales: Ye, Ding, Liu, Tao, Li, Yongming, Wang, Yaping, Hu, Wei, Zhu, Zuoyan, Sun, Yonghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10106697/
https://www.ncbi.nlm.nih.gov/pubmed/37077350
http://dx.doi.org/10.3389/fendo.2023.1044318
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author Ye, Ding
Liu, Tao
Li, Yongming
Wang, Yaping
Hu, Wei
Zhu, Zuoyan
Sun, Yonghua
author_facet Ye, Ding
Liu, Tao
Li, Yongming
Wang, Yaping
Hu, Wei
Zhu, Zuoyan
Sun, Yonghua
author_sort Ye, Ding
collection PubMed
description Image-based identification and quantification of different types of spermatogenic cells is of great importance, not only for reproductive studies but also for genetic breeding. Here, we have developed antibodies against spermatogenesis-related proteins in zebrafish (Danio rerio), including Ddx4, Piwil1, Sycp3, and Pcna, and a high-throughput method for immunofluorescence analysis of zebrafish testicular sections. By immunofluorescence analysis of zebrafish testes, our results demonstrate that the expression of Ddx4 decreases progressively during spermatogenesis, Piwil1 is strongly expressed in type A spermatogonia and moderately expressed in type B spermatogonia, and Sycp3 has distinct expression patterns in different subtypes of spermatocytes. Additionally, we observed polar expression of Sycp3 and Pcna in primary spermatocytes at the leptotene stage. By a triple staining of Ddx4, Sycp3, and Pcna, different types/subtypes of spermatogenic cells were easily characterized. We further demonstrated the practicality of our antibodies in other fish species, including Chinese rare minnow (Gobiocypris rarus), common carp (Cyprinus carpio), blunt snout bream (Megalobrama amblycephala), rice field eel (Monopterus albus) and grass carp (Ctenopharyngodon idella). Finally, we proposed an integrated criterion for identifying different types/subtypes of spermatogenic cells in zebrafish and other fishes using this high-throughput immunofluorescence approach based on these antibodies. Therefore, our study provides a simple, practical, and efficient tool for the study of spermatogenesis in fish species.
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spelling pubmed-101066972023-04-18 Identification of fish spermatogenic cells through high-throughput immunofluorescence against testis with an antibody set Ye, Ding Liu, Tao Li, Yongming Wang, Yaping Hu, Wei Zhu, Zuoyan Sun, Yonghua Front Endocrinol (Lausanne) Endocrinology Image-based identification and quantification of different types of spermatogenic cells is of great importance, not only for reproductive studies but also for genetic breeding. Here, we have developed antibodies against spermatogenesis-related proteins in zebrafish (Danio rerio), including Ddx4, Piwil1, Sycp3, and Pcna, and a high-throughput method for immunofluorescence analysis of zebrafish testicular sections. By immunofluorescence analysis of zebrafish testes, our results demonstrate that the expression of Ddx4 decreases progressively during spermatogenesis, Piwil1 is strongly expressed in type A spermatogonia and moderately expressed in type B spermatogonia, and Sycp3 has distinct expression patterns in different subtypes of spermatocytes. Additionally, we observed polar expression of Sycp3 and Pcna in primary spermatocytes at the leptotene stage. By a triple staining of Ddx4, Sycp3, and Pcna, different types/subtypes of spermatogenic cells were easily characterized. We further demonstrated the practicality of our antibodies in other fish species, including Chinese rare minnow (Gobiocypris rarus), common carp (Cyprinus carpio), blunt snout bream (Megalobrama amblycephala), rice field eel (Monopterus albus) and grass carp (Ctenopharyngodon idella). Finally, we proposed an integrated criterion for identifying different types/subtypes of spermatogenic cells in zebrafish and other fishes using this high-throughput immunofluorescence approach based on these antibodies. Therefore, our study provides a simple, practical, and efficient tool for the study of spermatogenesis in fish species. Frontiers Media S.A. 2023-04-03 /pmc/articles/PMC10106697/ /pubmed/37077350 http://dx.doi.org/10.3389/fendo.2023.1044318 Text en Copyright © 2023 Ye, Liu, Li, Wang, Hu, Zhu and Sun 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 Endocrinology
Ye, Ding
Liu, Tao
Li, Yongming
Wang, Yaping
Hu, Wei
Zhu, Zuoyan
Sun, Yonghua
Identification of fish spermatogenic cells through high-throughput immunofluorescence against testis with an antibody set
title Identification of fish spermatogenic cells through high-throughput immunofluorescence against testis with an antibody set
title_full Identification of fish spermatogenic cells through high-throughput immunofluorescence against testis with an antibody set
title_fullStr Identification of fish spermatogenic cells through high-throughput immunofluorescence against testis with an antibody set
title_full_unstemmed Identification of fish spermatogenic cells through high-throughput immunofluorescence against testis with an antibody set
title_short Identification of fish spermatogenic cells through high-throughput immunofluorescence against testis with an antibody set
title_sort identification of fish spermatogenic cells through high-throughput immunofluorescence against testis with an antibody set
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10106697/
https://www.ncbi.nlm.nih.gov/pubmed/37077350
http://dx.doi.org/10.3389/fendo.2023.1044318
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