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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2023
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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 |
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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 |
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