Single-Cell Transcriptomics Analysis of Human Small Antral Follicles
Human ovarian folliculogenesis is a highly regulated and complex process. Characterization of follicular cell signatures during this dynamic process is important to understand follicle fate (to grow, become dominant, or undergo atresia). The transcriptional signature of human oocytes and granulosa c...
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2021
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oai:doaj.org-article:e505a4facbd64435b1cd0d038ad3c6032021-11-11T17:22:36ZSingle-Cell Transcriptomics Analysis of Human Small Antral Follicles10.3390/ijms2221119551422-00671661-6596https://doaj.org/article/e505a4facbd64435b1cd0d038ad3c6032021-11-01T00:00:00Zhttps://www.mdpi.com/1422-0067/22/21/11955https://doaj.org/toc/1661-6596https://doaj.org/toc/1422-0067Human ovarian folliculogenesis is a highly regulated and complex process. Characterization of follicular cell signatures during this dynamic process is important to understand follicle fate (to grow, become dominant, or undergo atresia). The transcriptional signature of human oocytes and granulosa cells (GCs) in early-growing and ovulatory follicles have been previously described; however, that of oocytes with surrounding GCs in small antral follicles have not been studied yet. Here, we have generated a unique dataset of single-cell transcriptomics (SmartSeq2) consisting of the oocyte with surrounding GCs from several individual (non-dominant) small antral follicles isolated from adult human ovaries. We have identified two main types of (healthy) follicles, with a distinct oocyte and GC signature. Using the CellphoneDB algorithm, we then investigated the bi-directional ligand–receptor interactions regarding the transforming growth factor-β (TGFβ)/bone morphogenetic protein (BMP), wingless-type (MMTV)-integration site (WNT), NOTCH, and receptor tyrosine kinases (RTK) signaling pathways between oocyte and GCs within each antral follicle type. Our work not only revealed the diversity of small antral follicles, but also contributes to fill the gap in mapping the molecular landscape of human folliculogenesis and oogenesis.Xueying FanIoannis MoustakasMonika BialeckaJulieta S. del ValleArend W. OvereemLeoni A. LouweGonneke S. K. PilgramLucette A. J. van der WesterlakenHailiang MeiSusana M. Chuva de Sousa LopesMDPI AGarticlehuman adult ovaryoocytegranulosa cellantral folliclesingle-cell transcriptomicssignaling pathwaysBiology (General)QH301-705.5ChemistryQD1-999ENInternational Journal of Molecular Sciences, Vol 22, Iss 11955, p 11955 (2021) |
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human adult ovary oocyte granulosa cell antral follicle single-cell transcriptomics signaling pathways Biology (General) QH301-705.5 Chemistry QD1-999 |
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human adult ovary oocyte granulosa cell antral follicle single-cell transcriptomics signaling pathways Biology (General) QH301-705.5 Chemistry QD1-999 Xueying Fan Ioannis Moustakas Monika Bialecka Julieta S. del Valle Arend W. Overeem Leoni A. Louwe Gonneke S. K. Pilgram Lucette A. J. van der Westerlaken Hailiang Mei Susana M. Chuva de Sousa Lopes Single-Cell Transcriptomics Analysis of Human Small Antral Follicles |
description |
Human ovarian folliculogenesis is a highly regulated and complex process. Characterization of follicular cell signatures during this dynamic process is important to understand follicle fate (to grow, become dominant, or undergo atresia). The transcriptional signature of human oocytes and granulosa cells (GCs) in early-growing and ovulatory follicles have been previously described; however, that of oocytes with surrounding GCs in small antral follicles have not been studied yet. Here, we have generated a unique dataset of single-cell transcriptomics (SmartSeq2) consisting of the oocyte with surrounding GCs from several individual (non-dominant) small antral follicles isolated from adult human ovaries. We have identified two main types of (healthy) follicles, with a distinct oocyte and GC signature. Using the CellphoneDB algorithm, we then investigated the bi-directional ligand–receptor interactions regarding the transforming growth factor-β (TGFβ)/bone morphogenetic protein (BMP), wingless-type (MMTV)-integration site (WNT), NOTCH, and receptor tyrosine kinases (RTK) signaling pathways between oocyte and GCs within each antral follicle type. Our work not only revealed the diversity of small antral follicles, but also contributes to fill the gap in mapping the molecular landscape of human folliculogenesis and oogenesis. |
format |
article |
author |
Xueying Fan Ioannis Moustakas Monika Bialecka Julieta S. del Valle Arend W. Overeem Leoni A. Louwe Gonneke S. K. Pilgram Lucette A. J. van der Westerlaken Hailiang Mei Susana M. Chuva de Sousa Lopes |
author_facet |
Xueying Fan Ioannis Moustakas Monika Bialecka Julieta S. del Valle Arend W. Overeem Leoni A. Louwe Gonneke S. K. Pilgram Lucette A. J. van der Westerlaken Hailiang Mei Susana M. Chuva de Sousa Lopes |
author_sort |
Xueying Fan |
title |
Single-Cell Transcriptomics Analysis of Human Small Antral Follicles |
title_short |
Single-Cell Transcriptomics Analysis of Human Small Antral Follicles |
title_full |
Single-Cell Transcriptomics Analysis of Human Small Antral Follicles |
title_fullStr |
Single-Cell Transcriptomics Analysis of Human Small Antral Follicles |
title_full_unstemmed |
Single-Cell Transcriptomics Analysis of Human Small Antral Follicles |
title_sort |
single-cell transcriptomics analysis of human small antral follicles |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/e505a4facbd64435b1cd0d038ad3c603 |
work_keys_str_mv |
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_version_ |
1718432151367581696 |