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Ascorbic acid promotes the reproductive function of porcine immature Sertoli cells through transcriptome reprogramming

Vitamin C (ascorbic acid, AA) can regulate antioxidation and affect many cellular processes. However, the effect of AA on the reproduction of male animals remains less explored. Here, we showed that by supplementing exogenous AA to porcine immature Sertoli cells (iSCs), AA could promote the prolifer...

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Autores principales: Yang, Yu-Wei, Chen, Lu, Mou, Qiao, Liang, Hao, Du, Zhi-Qiang, Yang, Cai-Xia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524525/
https://www.ncbi.nlm.nih.gov/pubmed/33007716
http://dx.doi.org/10.1016/j.theriogenology.2020.09.022
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author Yang, Yu-Wei
Chen, Lu
Mou, Qiao
Liang, Hao
Du, Zhi-Qiang
Yang, Cai-Xia
author_facet Yang, Yu-Wei
Chen, Lu
Mou, Qiao
Liang, Hao
Du, Zhi-Qiang
Yang, Cai-Xia
author_sort Yang, Yu-Wei
collection PubMed
description Vitamin C (ascorbic acid, AA) can regulate antioxidation and affect many cellular processes. However, the effect of AA on the reproduction of male animals remains less explored. Here, we showed that by supplementing exogenous AA to porcine immature Sertoli cells (iSCs), AA could promote the proliferation, suppress apoptosis, and decrease the global nucleic acid methylation (5 mC and m(6)A) levels of iSCs. After we profiled mRNA and long non-coding RNA (lncRNA) expression by transcriptome sequencing on iSCs (treated by 250 μM AA for 36 h), 1232 mRNAs and 937 lncRNAs were identified to be differentially expressed (DE). Gene enrichment analysis found multiple significantly enriched biological pathways, including oxidoreductase activity, cell proliferation and apoptosis, regulation of hormone level, regulation of catalytic activity, developmental process, ATP metabolism and reproductive process. Specifically, for the reproductive process, 49 up- and 36 down-regulated DE mRNAs (including highly expressed genes, such as Tfcp2l1, Hmgcs1, Mmp7, Fndc3a, and Zfp36l1) are involved. Moreover, AA supplementation could promote the secretion of anti-müllerian hormone, inhibin B and lactate, and enhance the activity of lactate dehydrogenase as well. Taken together, AA could promote the reproductive function of pig iSCs, potentially through reprogramming the global transcriptome, and elevating hormone secretion and metabolite production.
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spelling pubmed-75245252020-09-30 Ascorbic acid promotes the reproductive function of porcine immature Sertoli cells through transcriptome reprogramming Yang, Yu-Wei Chen, Lu Mou, Qiao Liang, Hao Du, Zhi-Qiang Yang, Cai-Xia Theriogenology Article Vitamin C (ascorbic acid, AA) can regulate antioxidation and affect many cellular processes. However, the effect of AA on the reproduction of male animals remains less explored. Here, we showed that by supplementing exogenous AA to porcine immature Sertoli cells (iSCs), AA could promote the proliferation, suppress apoptosis, and decrease the global nucleic acid methylation (5 mC and m(6)A) levels of iSCs. After we profiled mRNA and long non-coding RNA (lncRNA) expression by transcriptome sequencing on iSCs (treated by 250 μM AA for 36 h), 1232 mRNAs and 937 lncRNAs were identified to be differentially expressed (DE). Gene enrichment analysis found multiple significantly enriched biological pathways, including oxidoreductase activity, cell proliferation and apoptosis, regulation of hormone level, regulation of catalytic activity, developmental process, ATP metabolism and reproductive process. Specifically, for the reproductive process, 49 up- and 36 down-regulated DE mRNAs (including highly expressed genes, such as Tfcp2l1, Hmgcs1, Mmp7, Fndc3a, and Zfp36l1) are involved. Moreover, AA supplementation could promote the secretion of anti-müllerian hormone, inhibin B and lactate, and enhance the activity of lactate dehydrogenase as well. Taken together, AA could promote the reproductive function of pig iSCs, potentially through reprogramming the global transcriptome, and elevating hormone secretion and metabolite production. Elsevier Inc. 2020-12 2020-09-29 /pmc/articles/PMC7524525/ /pubmed/33007716 http://dx.doi.org/10.1016/j.theriogenology.2020.09.022 Text en © 2020 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Yang, Yu-Wei
Chen, Lu
Mou, Qiao
Liang, Hao
Du, Zhi-Qiang
Yang, Cai-Xia
Ascorbic acid promotes the reproductive function of porcine immature Sertoli cells through transcriptome reprogramming
title Ascorbic acid promotes the reproductive function of porcine immature Sertoli cells through transcriptome reprogramming
title_full Ascorbic acid promotes the reproductive function of porcine immature Sertoli cells through transcriptome reprogramming
title_fullStr Ascorbic acid promotes the reproductive function of porcine immature Sertoli cells through transcriptome reprogramming
title_full_unstemmed Ascorbic acid promotes the reproductive function of porcine immature Sertoli cells through transcriptome reprogramming
title_short Ascorbic acid promotes the reproductive function of porcine immature Sertoli cells through transcriptome reprogramming
title_sort ascorbic acid promotes the reproductive function of porcine immature sertoli cells through transcriptome reprogramming
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524525/
https://www.ncbi.nlm.nih.gov/pubmed/33007716
http://dx.doi.org/10.1016/j.theriogenology.2020.09.022
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