Cargando…

Sequential events during the quiescence to proliferation transition establish patterns of follicle cell differentiation in the Drosophila ovary

Stem cells cycle between periods of quiescence and proliferation to promote tissue health. In Drosophila ovaries, quiescence to proliferation transitions of follicle stem cells (FSCs) are exquisitely feeding-dependent. Here, we demonstrate feeding-dependent induction of follicle cell differentiation...

Descripción completa

Detalles Bibliográficos
Autores principales: Lee, Eric H., Zinshteyn, Daniel, Miglo, Fred, Wang, Melissa Q., Reinach, Jessica, Chau, Cindy M., Grosstephan, Joseph M., Correa, Iliana, Costa, Kelly, Vargas, Alberto, Johnson, Aminah, Longo, Sheila M., Alexander, Jennifer I., O'Reilly, Alana M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9867896/
https://www.ncbi.nlm.nih.gov/pubmed/36524613
http://dx.doi.org/10.1242/bio.059625
_version_ 1784876437726035968
author Lee, Eric H.
Zinshteyn, Daniel
Miglo, Fred
Wang, Melissa Q.
Reinach, Jessica
Chau, Cindy M.
Grosstephan, Joseph M.
Correa, Iliana
Costa, Kelly
Vargas, Alberto
Johnson, Aminah
Longo, Sheila M.
Alexander, Jennifer I.
O'Reilly, Alana M.
author_facet Lee, Eric H.
Zinshteyn, Daniel
Miglo, Fred
Wang, Melissa Q.
Reinach, Jessica
Chau, Cindy M.
Grosstephan, Joseph M.
Correa, Iliana
Costa, Kelly
Vargas, Alberto
Johnson, Aminah
Longo, Sheila M.
Alexander, Jennifer I.
O'Reilly, Alana M.
author_sort Lee, Eric H.
collection PubMed
description Stem cells cycle between periods of quiescence and proliferation to promote tissue health. In Drosophila ovaries, quiescence to proliferation transitions of follicle stem cells (FSCs) are exquisitely feeding-dependent. Here, we demonstrate feeding-dependent induction of follicle cell differentiation markers, eyes absent (Eya) and castor (Cas) in FSCs, a patterning process that does not depend on proliferation induction. Instead, FSCs extend micron-scale cytoplasmic projections that dictate Eya-Cas patterning. We identify still life and sickie as necessary and sufficient for FSC projection growth and Eya-Cas induction. Our results suggest that sequential, interdependent events establish long-term differentiation patterns in follicle cell precursors, independently of FSC proliferation induction.
format Online
Article
Text
id pubmed-9867896
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher The Company of Biologists Ltd
record_format MEDLINE/PubMed
spelling pubmed-98678962023-01-23 Sequential events during the quiescence to proliferation transition establish patterns of follicle cell differentiation in the Drosophila ovary Lee, Eric H. Zinshteyn, Daniel Miglo, Fred Wang, Melissa Q. Reinach, Jessica Chau, Cindy M. Grosstephan, Joseph M. Correa, Iliana Costa, Kelly Vargas, Alberto Johnson, Aminah Longo, Sheila M. Alexander, Jennifer I. O'Reilly, Alana M. Biol Open Research Article Stem cells cycle between periods of quiescence and proliferation to promote tissue health. In Drosophila ovaries, quiescence to proliferation transitions of follicle stem cells (FSCs) are exquisitely feeding-dependent. Here, we demonstrate feeding-dependent induction of follicle cell differentiation markers, eyes absent (Eya) and castor (Cas) in FSCs, a patterning process that does not depend on proliferation induction. Instead, FSCs extend micron-scale cytoplasmic projections that dictate Eya-Cas patterning. We identify still life and sickie as necessary and sufficient for FSC projection growth and Eya-Cas induction. Our results suggest that sequential, interdependent events establish long-term differentiation patterns in follicle cell precursors, independently of FSC proliferation induction. The Company of Biologists Ltd 2023-01-12 /pmc/articles/PMC9867896/ /pubmed/36524613 http://dx.doi.org/10.1242/bio.059625 Text en © 2023. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Lee, Eric H.
Zinshteyn, Daniel
Miglo, Fred
Wang, Melissa Q.
Reinach, Jessica
Chau, Cindy M.
Grosstephan, Joseph M.
Correa, Iliana
Costa, Kelly
Vargas, Alberto
Johnson, Aminah
Longo, Sheila M.
Alexander, Jennifer I.
O'Reilly, Alana M.
Sequential events during the quiescence to proliferation transition establish patterns of follicle cell differentiation in the Drosophila ovary
title Sequential events during the quiescence to proliferation transition establish patterns of follicle cell differentiation in the Drosophila ovary
title_full Sequential events during the quiescence to proliferation transition establish patterns of follicle cell differentiation in the Drosophila ovary
title_fullStr Sequential events during the quiescence to proliferation transition establish patterns of follicle cell differentiation in the Drosophila ovary
title_full_unstemmed Sequential events during the quiescence to proliferation transition establish patterns of follicle cell differentiation in the Drosophila ovary
title_short Sequential events during the quiescence to proliferation transition establish patterns of follicle cell differentiation in the Drosophila ovary
title_sort sequential events during the quiescence to proliferation transition establish patterns of follicle cell differentiation in the drosophila ovary
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9867896/
https://www.ncbi.nlm.nih.gov/pubmed/36524613
http://dx.doi.org/10.1242/bio.059625
work_keys_str_mv AT leeerich sequentialeventsduringthequiescencetoproliferationtransitionestablishpatternsoffolliclecelldifferentiationinthedrosophilaovary
AT zinshteyndaniel sequentialeventsduringthequiescencetoproliferationtransitionestablishpatternsoffolliclecelldifferentiationinthedrosophilaovary
AT miglofred sequentialeventsduringthequiescencetoproliferationtransitionestablishpatternsoffolliclecelldifferentiationinthedrosophilaovary
AT wangmelissaq sequentialeventsduringthequiescencetoproliferationtransitionestablishpatternsoffolliclecelldifferentiationinthedrosophilaovary
AT reinachjessica sequentialeventsduringthequiescencetoproliferationtransitionestablishpatternsoffolliclecelldifferentiationinthedrosophilaovary
AT chaucindym sequentialeventsduringthequiescencetoproliferationtransitionestablishpatternsoffolliclecelldifferentiationinthedrosophilaovary
AT grosstephanjosephm sequentialeventsduringthequiescencetoproliferationtransitionestablishpatternsoffolliclecelldifferentiationinthedrosophilaovary
AT correailiana sequentialeventsduringthequiescencetoproliferationtransitionestablishpatternsoffolliclecelldifferentiationinthedrosophilaovary
AT costakelly sequentialeventsduringthequiescencetoproliferationtransitionestablishpatternsoffolliclecelldifferentiationinthedrosophilaovary
AT vargasalberto sequentialeventsduringthequiescencetoproliferationtransitionestablishpatternsoffolliclecelldifferentiationinthedrosophilaovary
AT johnsonaminah sequentialeventsduringthequiescencetoproliferationtransitionestablishpatternsoffolliclecelldifferentiationinthedrosophilaovary
AT longosheilam sequentialeventsduringthequiescencetoproliferationtransitionestablishpatternsoffolliclecelldifferentiationinthedrosophilaovary
AT alexanderjenniferi sequentialeventsduringthequiescencetoproliferationtransitionestablishpatternsoffolliclecelldifferentiationinthedrosophilaovary
AT oreillyalanam sequentialeventsduringthequiescencetoproliferationtransitionestablishpatternsoffolliclecelldifferentiationinthedrosophilaovary