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Cellular Processes in Human Ovarian Follicles Are Regulated by Expression Profile of New Gene Markers—Clinical Approach
In the growing ovarian follicle, the maturing oocyte is accompanied by cumulus (CCs) and granulosa (GCs) cells. Currently, there remain many unanswered questions about the epithelial origin of these cells. Global and targeted gene transcript levels were assessed on 1, 7, 15, 30 days of culture for C...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745700/ https://www.ncbi.nlm.nih.gov/pubmed/35011815 http://dx.doi.org/10.3390/jcm11010073 |
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author | Chermuła, Błażej Kranc, Wiesława Celichowski, Piotr Stelmach, Bogusława Piotrowska-Kempisty, Hanna Mozdziak, Paul Pawelczyk, Leszek Spaczyński, Robert Zygmunt Kempisty, Bartosz |
author_facet | Chermuła, Błażej Kranc, Wiesława Celichowski, Piotr Stelmach, Bogusława Piotrowska-Kempisty, Hanna Mozdziak, Paul Pawelczyk, Leszek Spaczyński, Robert Zygmunt Kempisty, Bartosz |
author_sort | Chermuła, Błażej |
collection | PubMed |
description | In the growing ovarian follicle, the maturing oocyte is accompanied by cumulus (CCs) and granulosa (GCs) cells. Currently, there remain many unanswered questions about the epithelial origin of these cells. Global and targeted gene transcript levels were assessed on 1, 7, 15, 30 days of culture for CCs and GCs. Detailed analysis of the genes belonging to epithelial cell-associated ontological groups allowed us to assess a total of 168 genes expressed in CCs (97 genes) and GCs (71 genes) during long-term in vitro culture. Expression changes of the analyzed genes allowed the identification of the group of genes: TGFBR3, PTGS2, PRKX, AHI1, and IL11, whose expression decreased the most and the group of ANXA3, DKK1, CCND1, STC1, CAV1, and SFRP4 genes, whose expression significantly increased. These genes’ expression indicates CCs and GCs epithelialization processes and their epithelial origin. Expression change analysis of genes involved in epithelization processes in GCs and CCs during their in vitro culture made it possible to describe the most significantly altered of the 11 genes. Detailed analysis of gene expression in these two cell populations at different time intervals confirms their ovarian surface epithelial origin. Furthermore, some gene expression profiles appear to have tumorigenic properties, suggesting that granulosa cells may play a role in cancerogenesis. |
format | Online Article Text |
id | pubmed-8745700 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87457002022-01-11 Cellular Processes in Human Ovarian Follicles Are Regulated by Expression Profile of New Gene Markers—Clinical Approach Chermuła, Błażej Kranc, Wiesława Celichowski, Piotr Stelmach, Bogusława Piotrowska-Kempisty, Hanna Mozdziak, Paul Pawelczyk, Leszek Spaczyński, Robert Zygmunt Kempisty, Bartosz J Clin Med Article In the growing ovarian follicle, the maturing oocyte is accompanied by cumulus (CCs) and granulosa (GCs) cells. Currently, there remain many unanswered questions about the epithelial origin of these cells. Global and targeted gene transcript levels were assessed on 1, 7, 15, 30 days of culture for CCs and GCs. Detailed analysis of the genes belonging to epithelial cell-associated ontological groups allowed us to assess a total of 168 genes expressed in CCs (97 genes) and GCs (71 genes) during long-term in vitro culture. Expression changes of the analyzed genes allowed the identification of the group of genes: TGFBR3, PTGS2, PRKX, AHI1, and IL11, whose expression decreased the most and the group of ANXA3, DKK1, CCND1, STC1, CAV1, and SFRP4 genes, whose expression significantly increased. These genes’ expression indicates CCs and GCs epithelialization processes and their epithelial origin. Expression change analysis of genes involved in epithelization processes in GCs and CCs during their in vitro culture made it possible to describe the most significantly altered of the 11 genes. Detailed analysis of gene expression in these two cell populations at different time intervals confirms their ovarian surface epithelial origin. Furthermore, some gene expression profiles appear to have tumorigenic properties, suggesting that granulosa cells may play a role in cancerogenesis. MDPI 2021-12-24 /pmc/articles/PMC8745700/ /pubmed/35011815 http://dx.doi.org/10.3390/jcm11010073 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Chermuła, Błażej Kranc, Wiesława Celichowski, Piotr Stelmach, Bogusława Piotrowska-Kempisty, Hanna Mozdziak, Paul Pawelczyk, Leszek Spaczyński, Robert Zygmunt Kempisty, Bartosz Cellular Processes in Human Ovarian Follicles Are Regulated by Expression Profile of New Gene Markers—Clinical Approach |
title | Cellular Processes in Human Ovarian Follicles Are Regulated by Expression Profile of New Gene Markers—Clinical Approach |
title_full | Cellular Processes in Human Ovarian Follicles Are Regulated by Expression Profile of New Gene Markers—Clinical Approach |
title_fullStr | Cellular Processes in Human Ovarian Follicles Are Regulated by Expression Profile of New Gene Markers—Clinical Approach |
title_full_unstemmed | Cellular Processes in Human Ovarian Follicles Are Regulated by Expression Profile of New Gene Markers—Clinical Approach |
title_short | Cellular Processes in Human Ovarian Follicles Are Regulated by Expression Profile of New Gene Markers—Clinical Approach |
title_sort | cellular processes in human ovarian follicles are regulated by expression profile of new gene markers—clinical approach |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745700/ https://www.ncbi.nlm.nih.gov/pubmed/35011815 http://dx.doi.org/10.3390/jcm11010073 |
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