Cargando…
miR-1285-3p targets TPI1 to regulate the glycolysis metabolism signaling pathway of Tibetan sheep Sertoli cells
Glycolysis in Sertoli cells (SCs) can provide energy substrates for the development of spermatogenic cells. Triose phosphate isomerase 1 (TPI1) is one of the key catalytic enzymes involved in glycolysis. However, the biological function of TPI1 in SCs and its role in glycolytic metabolic pathways ar...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9499212/ https://www.ncbi.nlm.nih.gov/pubmed/36137140 http://dx.doi.org/10.1371/journal.pone.0270364 |
_version_ | 1784794940992126976 |
---|---|
author | An, Xuejiao Li, Taotao Chen, Nana Wang, Huihui Su, Manchun Shi, Huibin Duan, Xinming Ma, Youji |
author_facet | An, Xuejiao Li, Taotao Chen, Nana Wang, Huihui Su, Manchun Shi, Huibin Duan, Xinming Ma, Youji |
author_sort | An, Xuejiao |
collection | PubMed |
description | Glycolysis in Sertoli cells (SCs) can provide energy substrates for the development of spermatogenic cells. Triose phosphate isomerase 1 (TPI1) is one of the key catalytic enzymes involved in glycolysis. However, the biological function of TPI1 in SCs and its role in glycolytic metabolic pathways are poorly understood. On the basis of a previous research, we isolated primary SCs from Tibetan sheep, and overexpressed TPI1 gene to determine its effect on the proliferation, glycolysis, and apoptosis of SCs. Secondly, we investigated the relationship between TPI1 and miR-1285-3p, and whether miR-1285-3p regulates the proliferation and apoptosis of SCs, and participates in glycolysis by targeting TPI1. Results showed that overexpression of TPI1 increased the proliferation rate and decreased apoptosis of SCs. In addition, overexpression of TPI1 altered glycolysis and metabolism signaling pathways and significantly increased amount of the final product lactic acid. Further analysis showed that miR-1285-3p inhibited TPI1 by directly targeting its 3’untranslated region. Overexpression of miR-1285-3p suppressed the proliferation of SCs, and this effect was partially reversed by restoration of TPI1 expression. In summary, this study shows that the miR-1285-3p/TPI1 axis regulates glycolysis in SCs. These findings add to our understanding on the regulation of spermatogenesis in sheep and other mammals. |
format | Online Article Text |
id | pubmed-9499212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-94992122022-09-23 miR-1285-3p targets TPI1 to regulate the glycolysis metabolism signaling pathway of Tibetan sheep Sertoli cells An, Xuejiao Li, Taotao Chen, Nana Wang, Huihui Su, Manchun Shi, Huibin Duan, Xinming Ma, Youji PLoS One Research Article Glycolysis in Sertoli cells (SCs) can provide energy substrates for the development of spermatogenic cells. Triose phosphate isomerase 1 (TPI1) is one of the key catalytic enzymes involved in glycolysis. However, the biological function of TPI1 in SCs and its role in glycolytic metabolic pathways are poorly understood. On the basis of a previous research, we isolated primary SCs from Tibetan sheep, and overexpressed TPI1 gene to determine its effect on the proliferation, glycolysis, and apoptosis of SCs. Secondly, we investigated the relationship between TPI1 and miR-1285-3p, and whether miR-1285-3p regulates the proliferation and apoptosis of SCs, and participates in glycolysis by targeting TPI1. Results showed that overexpression of TPI1 increased the proliferation rate and decreased apoptosis of SCs. In addition, overexpression of TPI1 altered glycolysis and metabolism signaling pathways and significantly increased amount of the final product lactic acid. Further analysis showed that miR-1285-3p inhibited TPI1 by directly targeting its 3’untranslated region. Overexpression of miR-1285-3p suppressed the proliferation of SCs, and this effect was partially reversed by restoration of TPI1 expression. In summary, this study shows that the miR-1285-3p/TPI1 axis regulates glycolysis in SCs. These findings add to our understanding on the regulation of spermatogenesis in sheep and other mammals. Public Library of Science 2022-09-22 /pmc/articles/PMC9499212/ /pubmed/36137140 http://dx.doi.org/10.1371/journal.pone.0270364 Text en © 2022 An 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, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article An, Xuejiao Li, Taotao Chen, Nana Wang, Huihui Su, Manchun Shi, Huibin Duan, Xinming Ma, Youji miR-1285-3p targets TPI1 to regulate the glycolysis metabolism signaling pathway of Tibetan sheep Sertoli cells |
title | miR-1285-3p targets TPI1 to regulate the glycolysis metabolism signaling pathway of Tibetan sheep Sertoli cells |
title_full | miR-1285-3p targets TPI1 to regulate the glycolysis metabolism signaling pathway of Tibetan sheep Sertoli cells |
title_fullStr | miR-1285-3p targets TPI1 to regulate the glycolysis metabolism signaling pathway of Tibetan sheep Sertoli cells |
title_full_unstemmed | miR-1285-3p targets TPI1 to regulate the glycolysis metabolism signaling pathway of Tibetan sheep Sertoli cells |
title_short | miR-1285-3p targets TPI1 to regulate the glycolysis metabolism signaling pathway of Tibetan sheep Sertoli cells |
title_sort | mir-1285-3p targets tpi1 to regulate the glycolysis metabolism signaling pathway of tibetan sheep sertoli cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9499212/ https://www.ncbi.nlm.nih.gov/pubmed/36137140 http://dx.doi.org/10.1371/journal.pone.0270364 |
work_keys_str_mv | AT anxuejiao mir12853ptargetstpi1toregulatetheglycolysismetabolismsignalingpathwayoftibetansheepsertolicells AT litaotao mir12853ptargetstpi1toregulatetheglycolysismetabolismsignalingpathwayoftibetansheepsertolicells AT chennana mir12853ptargetstpi1toregulatetheglycolysismetabolismsignalingpathwayoftibetansheepsertolicells AT wanghuihui mir12853ptargetstpi1toregulatetheglycolysismetabolismsignalingpathwayoftibetansheepsertolicells AT sumanchun mir12853ptargetstpi1toregulatetheglycolysismetabolismsignalingpathwayoftibetansheepsertolicells AT shihuibin mir12853ptargetstpi1toregulatetheglycolysismetabolismsignalingpathwayoftibetansheepsertolicells AT duanxinming mir12853ptargetstpi1toregulatetheglycolysismetabolismsignalingpathwayoftibetansheepsertolicells AT mayouji mir12853ptargetstpi1toregulatetheglycolysismetabolismsignalingpathwayoftibetansheepsertolicells |