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Expression of polycystic ovary syndrome candidate genes in bovine fetal and adult ovarian somatic cells

Polycystic ovary syndrome (PCOS) is an endocrine metabolic disorder that appears to have a genetic predisposition and a fetal origin. The fetal ovary has two major somatic cell types shown previously to be of different cellular origins and different morphologies and to differentially express 15 gene...

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Autores principales: Liu, Menghe, Hummitzsch, Katja, Bastian, Nicole A, Hartanti, Monica D, Irving-Rodgers, Helen F, Anderson, Richard A, Rodgers, Raymond J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9782414/
https://www.ncbi.nlm.nih.gov/pubmed/36346793
http://dx.doi.org/10.1530/RAF-22-0068
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author Liu, Menghe
Hummitzsch, Katja
Bastian, Nicole A
Hartanti, Monica D
Irving-Rodgers, Helen F
Anderson, Richard A
Rodgers, Raymond J
author_facet Liu, Menghe
Hummitzsch, Katja
Bastian, Nicole A
Hartanti, Monica D
Irving-Rodgers, Helen F
Anderson, Richard A
Rodgers, Raymond J
author_sort Liu, Menghe
collection PubMed
description Polycystic ovary syndrome (PCOS) is an endocrine metabolic disorder that appears to have a genetic predisposition and a fetal origin. The fetal ovary has two major somatic cell types shown previously to be of different cellular origins and different morphologies and to differentially express 15 genes. In this study, we isolated the somatic gonadal ridge epithelial-like (GREL) cells (n  = 7) and ovarian fetal fibroblasts (n  = 6) by clonal expansion. Using qRT-PCR, we compared the gene expression levels of PCOS candidate genes with previous data on the expression levels in whole fetal ovaries across gestation. We also compared these levels with those in bovine adult ovarian cells including fibroblasts (n  = 4), granulosa cells (n  = 5) and surface epithelial cells (n  = 5). Adult cell types exhibited clear differences in the expression of most genes. In fetal ovarian cells, DENND1A and ERBB3 had significantly higher expression in GREL cells. HMGA2 and TGFB1I1 tended to have higher expression in fetal fibroblasts than GREL cells. The other 19 genes did not exhibit differences between GREL cells and fetal fibroblasts and FBN3, FSHB, LHCGR, FSHR and ZBTB16 were very lowly expressed in GREL cells and fibroblasts. The culture of fetal fibroblasts in EGF-containing medium resulted in lower expression of NEIL2 but higher expression of MAPRE1 compared to culture in the absence of EGF. Thus, the two fetal ovarian somatic cell types mostly lacked differential expression of PCOS candidate genes. LAY SUMMARY: Polycystic ovary syndrome (PCOS) is one of the most common reproductive problems. The cause is not known so there are no specific treatments or prevention strategies. We know it can be linked to issues that occur in the womb and that some people may be more likely to get PCOS due to their genetic makeup. Our recent studies showed that many of the genes linked to PCOS were found to be switched on in the fetal ovary and are likely to be involved in the development of the fetal ovary. In order to improve our understanding of PCOS, we need to identify the type of cells in the fetal ovary where these genes are switched on. In this study, we examined the PCOS genes in two types of cells that mature as the fetal ovary develops and found very little difference between them but bigger differences to their mature adult counterparts.
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spelling pubmed-97824142023-01-03 Expression of polycystic ovary syndrome candidate genes in bovine fetal and adult ovarian somatic cells Liu, Menghe Hummitzsch, Katja Bastian, Nicole A Hartanti, Monica D Irving-Rodgers, Helen F Anderson, Richard A Rodgers, Raymond J Reprod Fertil Research Polycystic ovary syndrome (PCOS) is an endocrine metabolic disorder that appears to have a genetic predisposition and a fetal origin. The fetal ovary has two major somatic cell types shown previously to be of different cellular origins and different morphologies and to differentially express 15 genes. In this study, we isolated the somatic gonadal ridge epithelial-like (GREL) cells (n  = 7) and ovarian fetal fibroblasts (n  = 6) by clonal expansion. Using qRT-PCR, we compared the gene expression levels of PCOS candidate genes with previous data on the expression levels in whole fetal ovaries across gestation. We also compared these levels with those in bovine adult ovarian cells including fibroblasts (n  = 4), granulosa cells (n  = 5) and surface epithelial cells (n  = 5). Adult cell types exhibited clear differences in the expression of most genes. In fetal ovarian cells, DENND1A and ERBB3 had significantly higher expression in GREL cells. HMGA2 and TGFB1I1 tended to have higher expression in fetal fibroblasts than GREL cells. The other 19 genes did not exhibit differences between GREL cells and fetal fibroblasts and FBN3, FSHB, LHCGR, FSHR and ZBTB16 were very lowly expressed in GREL cells and fibroblasts. The culture of fetal fibroblasts in EGF-containing medium resulted in lower expression of NEIL2 but higher expression of MAPRE1 compared to culture in the absence of EGF. Thus, the two fetal ovarian somatic cell types mostly lacked differential expression of PCOS candidate genes. LAY SUMMARY: Polycystic ovary syndrome (PCOS) is one of the most common reproductive problems. The cause is not known so there are no specific treatments or prevention strategies. We know it can be linked to issues that occur in the womb and that some people may be more likely to get PCOS due to their genetic makeup. Our recent studies showed that many of the genes linked to PCOS were found to be switched on in the fetal ovary and are likely to be involved in the development of the fetal ovary. In order to improve our understanding of PCOS, we need to identify the type of cells in the fetal ovary where these genes are switched on. In this study, we examined the PCOS genes in two types of cells that mature as the fetal ovary develops and found very little difference between them but bigger differences to their mature adult counterparts. Bioscientifica Ltd 2022-11-08 /pmc/articles/PMC9782414/ /pubmed/36346793 http://dx.doi.org/10.1530/RAF-22-0068 Text en © The authors https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. (https://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle Research
Liu, Menghe
Hummitzsch, Katja
Bastian, Nicole A
Hartanti, Monica D
Irving-Rodgers, Helen F
Anderson, Richard A
Rodgers, Raymond J
Expression of polycystic ovary syndrome candidate genes in bovine fetal and adult ovarian somatic cells
title Expression of polycystic ovary syndrome candidate genes in bovine fetal and adult ovarian somatic cells
title_full Expression of polycystic ovary syndrome candidate genes in bovine fetal and adult ovarian somatic cells
title_fullStr Expression of polycystic ovary syndrome candidate genes in bovine fetal and adult ovarian somatic cells
title_full_unstemmed Expression of polycystic ovary syndrome candidate genes in bovine fetal and adult ovarian somatic cells
title_short Expression of polycystic ovary syndrome candidate genes in bovine fetal and adult ovarian somatic cells
title_sort expression of polycystic ovary syndrome candidate genes in bovine fetal and adult ovarian somatic cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9782414/
https://www.ncbi.nlm.nih.gov/pubmed/36346793
http://dx.doi.org/10.1530/RAF-22-0068
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