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Single‐cell profiling of transcriptomic changes during in vitro maturation of human oocytes
PURPOSE: In vitro maturation (IVM) of human oocytes offers an invaluable opportunity for infertility treatment. However, in vitro matured oocytes often show lower developmental abilities than their in vivo counterparts, and molecular mechanisms underlying successful maturation remain unclear. In thi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9084694/ https://www.ncbi.nlm.nih.gov/pubmed/35582522 http://dx.doi.org/10.1002/rmb2.12464 |
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author | Takeuchi, Hiroki Yamamoto, Mari Fukui, Megumi Inoue, Akihiro Maezawa, Tadashi Nishioka, Mikiko Kondo, Eiji Ikeda, Tomoaki Matsumoto, Kazuya Miyamoto, Kei |
author_facet | Takeuchi, Hiroki Yamamoto, Mari Fukui, Megumi Inoue, Akihiro Maezawa, Tadashi Nishioka, Mikiko Kondo, Eiji Ikeda, Tomoaki Matsumoto, Kazuya Miyamoto, Kei |
author_sort | Takeuchi, Hiroki |
collection | PubMed |
description | PURPOSE: In vitro maturation (IVM) of human oocytes offers an invaluable opportunity for infertility treatment. However, in vitro matured oocytes often show lower developmental abilities than their in vivo counterparts, and molecular mechanisms underlying successful maturation remain unclear. In this study, we investigated gene expression profiles of in vitro matured oocytes at the single‐cell level to gain mechanistic insight into IVM of human oocytes. METHODS: Human oocytes were retrieved by follicular puncture and in vitro matured. In total, 19 oocytes from 11 patients were collected and subjected to single‐cell RNA‐seq analyses. RESULTS: Global gene expression profiles were similar among oocytes at the same maturation stage, while a small number of oocytes showed distinct transcriptomes from those at the corresponding maturation stage. Differential gene expression analysis identified hundreds of transcripts that dynamically altered their expression during IVM, and we revealed molecular pathways and upstream regulators that may govern oocyte maturation. Furthermore, oocytes that were delayed in their maturation showed distinct transcriptomes. Finally, we identified genes whose transcripts were enriched in each stage of oocyte maturation. CONCLUSIONS: Our work uncovers transcriptomic changes during human oocyte IVM and the differential gene expression profile of each oocyte. |
format | Online Article Text |
id | pubmed-9084694 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90846942022-05-16 Single‐cell profiling of transcriptomic changes during in vitro maturation of human oocytes Takeuchi, Hiroki Yamamoto, Mari Fukui, Megumi Inoue, Akihiro Maezawa, Tadashi Nishioka, Mikiko Kondo, Eiji Ikeda, Tomoaki Matsumoto, Kazuya Miyamoto, Kei Reprod Med Biol Original Articles PURPOSE: In vitro maturation (IVM) of human oocytes offers an invaluable opportunity for infertility treatment. However, in vitro matured oocytes often show lower developmental abilities than their in vivo counterparts, and molecular mechanisms underlying successful maturation remain unclear. In this study, we investigated gene expression profiles of in vitro matured oocytes at the single‐cell level to gain mechanistic insight into IVM of human oocytes. METHODS: Human oocytes were retrieved by follicular puncture and in vitro matured. In total, 19 oocytes from 11 patients were collected and subjected to single‐cell RNA‐seq analyses. RESULTS: Global gene expression profiles were similar among oocytes at the same maturation stage, while a small number of oocytes showed distinct transcriptomes from those at the corresponding maturation stage. Differential gene expression analysis identified hundreds of transcripts that dynamically altered their expression during IVM, and we revealed molecular pathways and upstream regulators that may govern oocyte maturation. Furthermore, oocytes that were delayed in their maturation showed distinct transcriptomes. Finally, we identified genes whose transcripts were enriched in each stage of oocyte maturation. CONCLUSIONS: Our work uncovers transcriptomic changes during human oocyte IVM and the differential gene expression profile of each oocyte. John Wiley and Sons Inc. 2022-05-09 /pmc/articles/PMC9084694/ /pubmed/35582522 http://dx.doi.org/10.1002/rmb2.12464 Text en © 2022 The Authors. Reproductive Medicine and Biology published by John Wiley & Sons Australia, Ltd on behalf of Japan Society for Reproductive Medicine https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Takeuchi, Hiroki Yamamoto, Mari Fukui, Megumi Inoue, Akihiro Maezawa, Tadashi Nishioka, Mikiko Kondo, Eiji Ikeda, Tomoaki Matsumoto, Kazuya Miyamoto, Kei Single‐cell profiling of transcriptomic changes during in vitro maturation of human oocytes |
title | Single‐cell profiling of transcriptomic changes during in vitro maturation of human oocytes |
title_full | Single‐cell profiling of transcriptomic changes during in vitro maturation of human oocytes |
title_fullStr | Single‐cell profiling of transcriptomic changes during in vitro maturation of human oocytes |
title_full_unstemmed | Single‐cell profiling of transcriptomic changes during in vitro maturation of human oocytes |
title_short | Single‐cell profiling of transcriptomic changes during in vitro maturation of human oocytes |
title_sort | single‐cell profiling of transcriptomic changes during in vitro maturation of human oocytes |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9084694/ https://www.ncbi.nlm.nih.gov/pubmed/35582522 http://dx.doi.org/10.1002/rmb2.12464 |
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