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Study of Tnp1, Tekt1, and Plzf Genes Expression During an in vitro Three-Dimensional Neonatal Male Mice Testis Culture
BACKGROUND: In vitro spermatogenesis has a long research history beginning in the early 20(th) century. This organ culture method was therefore abandoned, and alternative cell culture methods were chosen by many researchers. Here, whether Tnp1, Tekt1, and Plzf, which play a crucial role in spermatog...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Pasteur Institute
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5949128/ https://www.ncbi.nlm.nih.gov/pubmed/29397043 http://dx.doi.org/10.22034/ibj.22.4.258 |
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author | Alrahel, Ahmad Movahedin, Mansoureh Mazaheri, Zohre Amidi, Fardin |
author_facet | Alrahel, Ahmad Movahedin, Mansoureh Mazaheri, Zohre Amidi, Fardin |
author_sort | Alrahel, Ahmad |
collection | PubMed |
description | BACKGROUND: In vitro spermatogenesis has a long research history beginning in the early 20(th) century. This organ culture method was therefore abandoned, and alternative cell culture methods were chosen by many researchers. Here, whether Tnp1, Tekt1, and Plzf, which play a crucial role in spermatogenesis, can be expressed during testis organ culture was assessed. METHODS: Testes of 10 mouse pups were first removed, and the testis tissue was then separated into smaller pieces of seminiferous tubules. The size of the pieces was arbitrary; approximately 1 mg in weight or 1 mm(3) in size when compacted. Afterwards, the testis tissue fragments (1–3) were transferred to the hexahedrons, incubated in a culture incubator and cultured for 12 weeks. Histological assessment and molecular evaluation were carried out at the end of the study. RESULTS: The results showed that the expression of Tekt1 as a mitotic gene in mouse pups decreased significantly (p ≤ 0.05) in comparison to adult mouse testis. Meanwhile, the expression of Tnp1 as a meiotic gene increased significantly (p ≤ 0.05) as compared to neonate mouse testis at the beginning of the culture. The expression of Plzf showed no significant difference during the 12 weeks of culture (p ≥ 0.05). Based on histological study, different types of spermatocytes and post-meiotic stages of germ cells could not be detected. CONCLUSION: This kind of three-dimensional culture can induce expression of post-meiotic gene, Tnp1, but only at the molecular level and not beyond meiosis. |
format | Online Article Text |
id | pubmed-5949128 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Pasteur Institute |
record_format | MEDLINE/PubMed |
spelling | pubmed-59491282018-07-01 Study of Tnp1, Tekt1, and Plzf Genes Expression During an in vitro Three-Dimensional Neonatal Male Mice Testis Culture Alrahel, Ahmad Movahedin, Mansoureh Mazaheri, Zohre Amidi, Fardin Iran Biomed J Full Length BACKGROUND: In vitro spermatogenesis has a long research history beginning in the early 20(th) century. This organ culture method was therefore abandoned, and alternative cell culture methods were chosen by many researchers. Here, whether Tnp1, Tekt1, and Plzf, which play a crucial role in spermatogenesis, can be expressed during testis organ culture was assessed. METHODS: Testes of 10 mouse pups were first removed, and the testis tissue was then separated into smaller pieces of seminiferous tubules. The size of the pieces was arbitrary; approximately 1 mg in weight or 1 mm(3) in size when compacted. Afterwards, the testis tissue fragments (1–3) were transferred to the hexahedrons, incubated in a culture incubator and cultured for 12 weeks. Histological assessment and molecular evaluation were carried out at the end of the study. RESULTS: The results showed that the expression of Tekt1 as a mitotic gene in mouse pups decreased significantly (p ≤ 0.05) in comparison to adult mouse testis. Meanwhile, the expression of Tnp1 as a meiotic gene increased significantly (p ≤ 0.05) as compared to neonate mouse testis at the beginning of the culture. The expression of Plzf showed no significant difference during the 12 weeks of culture (p ≥ 0.05). Based on histological study, different types of spermatocytes and post-meiotic stages of germ cells could not be detected. CONCLUSION: This kind of three-dimensional culture can induce expression of post-meiotic gene, Tnp1, but only at the molecular level and not beyond meiosis. Pasteur Institute 2018-07 /pmc/articles/PMC5949128/ /pubmed/29397043 http://dx.doi.org/10.22034/ibj.22.4.258 Text en Copyright: © Iranian Biomedical Journal http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Length Alrahel, Ahmad Movahedin, Mansoureh Mazaheri, Zohre Amidi, Fardin Study of Tnp1, Tekt1, and Plzf Genes Expression During an in vitro Three-Dimensional Neonatal Male Mice Testis Culture |
title | Study of Tnp1, Tekt1, and Plzf Genes Expression During an in vitro Three-Dimensional Neonatal Male Mice Testis Culture |
title_full | Study of Tnp1, Tekt1, and Plzf Genes Expression During an in vitro Three-Dimensional Neonatal Male Mice Testis Culture |
title_fullStr | Study of Tnp1, Tekt1, and Plzf Genes Expression During an in vitro Three-Dimensional Neonatal Male Mice Testis Culture |
title_full_unstemmed | Study of Tnp1, Tekt1, and Plzf Genes Expression During an in vitro Three-Dimensional Neonatal Male Mice Testis Culture |
title_short | Study of Tnp1, Tekt1, and Plzf Genes Expression During an in vitro Three-Dimensional Neonatal Male Mice Testis Culture |
title_sort | study of tnp1, tekt1, and plzf genes expression during an in vitro three-dimensional neonatal male mice testis culture |
topic | Full Length |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5949128/ https://www.ncbi.nlm.nih.gov/pubmed/29397043 http://dx.doi.org/10.22034/ibj.22.4.258 |
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