Cargando…

Single-cell sequencing reveals suppressive transcriptional programs regulated by MIS/AMH in neonatal ovaries

Müllerian inhibiting substance (MIS/AMH), produced by granulosa cells of growing follicles, is an important regulator of folliculogenesis and follicle development. Treatment with exogenous MIS in mice suppresses follicle development and prevents ovulation. To investigate the mechanisms by which MIS...

Descripción completa

Detalles Bibliográficos
Autores principales: Meinsohn, Marie-Charlotte, Saatcioglu, Hatice D., Wei, Lina, Li, Yi, Horn, Heiko, Chauvin, Maeva, Kano, Motohiro, Nguyen, Ngoc Minh Phuong, Nagykery, Nicholas, Kashiwagi, Aki, Samore, Wesley R., Wang, Dan, Oliva, Esther, Gao, Guangping, Morris, Mary E., Donahoe, Patricia K., Pépin, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8157966/
https://www.ncbi.nlm.nih.gov/pubmed/33980714
http://dx.doi.org/10.1073/pnas.2100920118
_version_ 1783699790405566464
author Meinsohn, Marie-Charlotte
Saatcioglu, Hatice D.
Wei, Lina
Li, Yi
Horn, Heiko
Chauvin, Maeva
Kano, Motohiro
Nguyen, Ngoc Minh Phuong
Nagykery, Nicholas
Kashiwagi, Aki
Samore, Wesley R.
Wang, Dan
Oliva, Esther
Gao, Guangping
Morris, Mary E.
Donahoe, Patricia K.
Pépin, David
author_facet Meinsohn, Marie-Charlotte
Saatcioglu, Hatice D.
Wei, Lina
Li, Yi
Horn, Heiko
Chauvin, Maeva
Kano, Motohiro
Nguyen, Ngoc Minh Phuong
Nagykery, Nicholas
Kashiwagi, Aki
Samore, Wesley R.
Wang, Dan
Oliva, Esther
Gao, Guangping
Morris, Mary E.
Donahoe, Patricia K.
Pépin, David
author_sort Meinsohn, Marie-Charlotte
collection PubMed
description Müllerian inhibiting substance (MIS/AMH), produced by granulosa cells of growing follicles, is an important regulator of folliculogenesis and follicle development. Treatment with exogenous MIS in mice suppresses follicle development and prevents ovulation. To investigate the mechanisms by which MIS inhibits follicle development, we performed single-cell RNA sequencing of whole neonatal ovaries treated with MIS at birth and analyzed at postnatal day 6, coinciding with the first wave of follicle growth. We identified distinct transcriptional signatures associated with MIS responses in the ovarian cell types. MIS treatment inhibited proliferation in granulosa, surface epithelial, and stromal cell types of the ovary and elicited a unique signature of quiescence in granulosa cells. In addition to decreasing the number of growing preantral follicles, we found that MIS treatment uncoupled the maturation of germ cells and granulosa cells. In conclusion, MIS suppressed neonatal follicle development by inhibiting proliferation, imposing a quiescent cell state, and preventing granulosa cell differentiation.
format Online
Article
Text
id pubmed-8157966
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher National Academy of Sciences
record_format MEDLINE/PubMed
spelling pubmed-81579662021-05-28 Single-cell sequencing reveals suppressive transcriptional programs regulated by MIS/AMH in neonatal ovaries Meinsohn, Marie-Charlotte Saatcioglu, Hatice D. Wei, Lina Li, Yi Horn, Heiko Chauvin, Maeva Kano, Motohiro Nguyen, Ngoc Minh Phuong Nagykery, Nicholas Kashiwagi, Aki Samore, Wesley R. Wang, Dan Oliva, Esther Gao, Guangping Morris, Mary E. Donahoe, Patricia K. Pépin, David Proc Natl Acad Sci U S A Biological Sciences Müllerian inhibiting substance (MIS/AMH), produced by granulosa cells of growing follicles, is an important regulator of folliculogenesis and follicle development. Treatment with exogenous MIS in mice suppresses follicle development and prevents ovulation. To investigate the mechanisms by which MIS inhibits follicle development, we performed single-cell RNA sequencing of whole neonatal ovaries treated with MIS at birth and analyzed at postnatal day 6, coinciding with the first wave of follicle growth. We identified distinct transcriptional signatures associated with MIS responses in the ovarian cell types. MIS treatment inhibited proliferation in granulosa, surface epithelial, and stromal cell types of the ovary and elicited a unique signature of quiescence in granulosa cells. In addition to decreasing the number of growing preantral follicles, we found that MIS treatment uncoupled the maturation of germ cells and granulosa cells. In conclusion, MIS suppressed neonatal follicle development by inhibiting proliferation, imposing a quiescent cell state, and preventing granulosa cell differentiation. National Academy of Sciences 2021-05-18 2021-05-12 /pmc/articles/PMC8157966/ /pubmed/33980714 http://dx.doi.org/10.1073/pnas.2100920118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biological Sciences
Meinsohn, Marie-Charlotte
Saatcioglu, Hatice D.
Wei, Lina
Li, Yi
Horn, Heiko
Chauvin, Maeva
Kano, Motohiro
Nguyen, Ngoc Minh Phuong
Nagykery, Nicholas
Kashiwagi, Aki
Samore, Wesley R.
Wang, Dan
Oliva, Esther
Gao, Guangping
Morris, Mary E.
Donahoe, Patricia K.
Pépin, David
Single-cell sequencing reveals suppressive transcriptional programs regulated by MIS/AMH in neonatal ovaries
title Single-cell sequencing reveals suppressive transcriptional programs regulated by MIS/AMH in neonatal ovaries
title_full Single-cell sequencing reveals suppressive transcriptional programs regulated by MIS/AMH in neonatal ovaries
title_fullStr Single-cell sequencing reveals suppressive transcriptional programs regulated by MIS/AMH in neonatal ovaries
title_full_unstemmed Single-cell sequencing reveals suppressive transcriptional programs regulated by MIS/AMH in neonatal ovaries
title_short Single-cell sequencing reveals suppressive transcriptional programs regulated by MIS/AMH in neonatal ovaries
title_sort single-cell sequencing reveals suppressive transcriptional programs regulated by mis/amh in neonatal ovaries
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8157966/
https://www.ncbi.nlm.nih.gov/pubmed/33980714
http://dx.doi.org/10.1073/pnas.2100920118
work_keys_str_mv AT meinsohnmariecharlotte singlecellsequencingrevealssuppressivetranscriptionalprogramsregulatedbymisamhinneonatalovaries
AT saatciogluhaticed singlecellsequencingrevealssuppressivetranscriptionalprogramsregulatedbymisamhinneonatalovaries
AT weilina singlecellsequencingrevealssuppressivetranscriptionalprogramsregulatedbymisamhinneonatalovaries
AT liyi singlecellsequencingrevealssuppressivetranscriptionalprogramsregulatedbymisamhinneonatalovaries
AT hornheiko singlecellsequencingrevealssuppressivetranscriptionalprogramsregulatedbymisamhinneonatalovaries
AT chauvinmaeva singlecellsequencingrevealssuppressivetranscriptionalprogramsregulatedbymisamhinneonatalovaries
AT kanomotohiro singlecellsequencingrevealssuppressivetranscriptionalprogramsregulatedbymisamhinneonatalovaries
AT nguyenngocminhphuong singlecellsequencingrevealssuppressivetranscriptionalprogramsregulatedbymisamhinneonatalovaries
AT nagykerynicholas singlecellsequencingrevealssuppressivetranscriptionalprogramsregulatedbymisamhinneonatalovaries
AT kashiwagiaki singlecellsequencingrevealssuppressivetranscriptionalprogramsregulatedbymisamhinneonatalovaries
AT samorewesleyr singlecellsequencingrevealssuppressivetranscriptionalprogramsregulatedbymisamhinneonatalovaries
AT wangdan singlecellsequencingrevealssuppressivetranscriptionalprogramsregulatedbymisamhinneonatalovaries
AT olivaesther singlecellsequencingrevealssuppressivetranscriptionalprogramsregulatedbymisamhinneonatalovaries
AT gaoguangping singlecellsequencingrevealssuppressivetranscriptionalprogramsregulatedbymisamhinneonatalovaries
AT morrismarye singlecellsequencingrevealssuppressivetranscriptionalprogramsregulatedbymisamhinneonatalovaries
AT donahoepatriciak singlecellsequencingrevealssuppressivetranscriptionalprogramsregulatedbymisamhinneonatalovaries
AT pepindavid singlecellsequencingrevealssuppressivetranscriptionalprogramsregulatedbymisamhinneonatalovaries