Opposing JAK-STAT and Wnt signaling gradients define a stem cell domain by regulating differentiation at two borders
Many adult stem cell communities are maintained by population asymmetry, where stochastic behaviors of multiple individual cells collectively result in a balance between stem cell division and differentiation. We investigated how this is achieved for Drosophila Follicle Stem Cells (FSCs) by spatiall...
Main Authors: | , |
---|---|
Format: | Article |
Language: | English |
Published: |
eLife Sciences Publications Ltd
2020-11-01
|
Series: | eLife |
Subjects: | |
Online Access: | https://elifesciences.org/articles/61204 |
id |
doaj-cc21bfec516b46fea09e0d1f3d211251 |
---|---|
record_format |
Article |
spelling |
doaj-cc21bfec516b46fea09e0d1f3d2112512021-05-05T21:39:52ZengeLife Sciences Publications LtdeLife2050-084X2020-11-01910.7554/eLife.61204Opposing JAK-STAT and Wnt signaling gradients define a stem cell domain by regulating differentiation at two bordersDavid Melamed0https://orcid.org/0000-0002-2102-1340Daniel Kalderon1https://orcid.org/0000-0002-2149-0673Department of Biological Sciences, Columbia University, New York, United StatesDepartment of Biological Sciences, Columbia University, New York, United StatesMany adult stem cell communities are maintained by population asymmetry, where stochastic behaviors of multiple individual cells collectively result in a balance between stem cell division and differentiation. We investigated how this is achieved for Drosophila Follicle Stem Cells (FSCs) by spatially-restricted niche signals. FSCs produce transit-amplifying Follicle Cells (FCs) from their posterior face and quiescent Escort Cells (ECs) to their anterior. We show that JAK-STAT pathway activity, which declines from posterior to anterior, dictates the pattern of divisions over the FSC domain, promotes more posterior FSC locations and conversion to FCs, while opposing EC production. Wnt pathway activity declines from the anterior, promotes anterior FSC locations and EC production, and opposes FC production. The pathways combine to define a stem cell domain through concerted effects on FSC differentiation to ECs and FCs at either end of opposing signaling gradients, and impose a pattern of proliferation that matches derivative production.https://elifesciences.org/articles/61204Follicle Stem CellsStem CellsJAK-STATWntsignalingniche |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
David Melamed Daniel Kalderon |
spellingShingle |
David Melamed Daniel Kalderon Opposing JAK-STAT and Wnt signaling gradients define a stem cell domain by regulating differentiation at two borders eLife Follicle Stem Cells Stem Cells JAK-STAT Wnt signaling niche |
author_facet |
David Melamed Daniel Kalderon |
author_sort |
David Melamed |
title |
Opposing JAK-STAT and Wnt signaling gradients define a stem cell domain by regulating differentiation at two borders |
title_short |
Opposing JAK-STAT and Wnt signaling gradients define a stem cell domain by regulating differentiation at two borders |
title_full |
Opposing JAK-STAT and Wnt signaling gradients define a stem cell domain by regulating differentiation at two borders |
title_fullStr |
Opposing JAK-STAT and Wnt signaling gradients define a stem cell domain by regulating differentiation at two borders |
title_full_unstemmed |
Opposing JAK-STAT and Wnt signaling gradients define a stem cell domain by regulating differentiation at two borders |
title_sort |
opposing jak-stat and wnt signaling gradients define a stem cell domain by regulating differentiation at two borders |
publisher |
eLife Sciences Publications Ltd |
series |
eLife |
issn |
2050-084X |
publishDate |
2020-11-01 |
description |
Many adult stem cell communities are maintained by population asymmetry, where stochastic behaviors of multiple individual cells collectively result in a balance between stem cell division and differentiation. We investigated how this is achieved for Drosophila Follicle Stem Cells (FSCs) by spatially-restricted niche signals. FSCs produce transit-amplifying Follicle Cells (FCs) from their posterior face and quiescent Escort Cells (ECs) to their anterior. We show that JAK-STAT pathway activity, which declines from posterior to anterior, dictates the pattern of divisions over the FSC domain, promotes more posterior FSC locations and conversion to FCs, while opposing EC production. Wnt pathway activity declines from the anterior, promotes anterior FSC locations and EC production, and opposes FC production. The pathways combine to define a stem cell domain through concerted effects on FSC differentiation to ECs and FCs at either end of opposing signaling gradients, and impose a pattern of proliferation that matches derivative production. |
topic |
Follicle Stem Cells Stem Cells JAK-STAT Wnt signaling niche |
url |
https://elifesciences.org/articles/61204 |
work_keys_str_mv |
AT davidmelamed opposingjakstatandwntsignalinggradientsdefineastemcelldomainbyregulatingdifferentiationattwoborders AT danielkalderon opposingjakstatandwntsignalinggradientsdefineastemcelldomainbyregulatingdifferentiationattwoborders |
_version_ |
1721458045480861696 |