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...

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Main Authors: David Melamed, Daniel Kalderon
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2020-11-01
Series:eLife
Subjects:
Wnt
Online Access:https://elifesciences.org/articles/61204
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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
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