Hair follicle dermal condensation forms via Fgf20 primed cell cycle exit, cell motility, and aggregation

Mesenchymal condensation is a critical step in organogenesis, yet the underlying molecular and cellular mechanisms remain poorly understood. The hair follicle dermal condensate is the precursor to the permanent mesenchymal unit of the hair follicle, the dermal papilla, which regulates hair cycling t...

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Main Authors: Leah C Biggs, Otto JM Mäkelä, Satu-Marja Myllymäki, Rishi Das Roy, Katja Närhi, Johanna Pispa, Tuija Mustonen, Marja L Mikkola
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2018-07-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/36468
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author Leah C Biggs
Otto JM Mäkelä
Satu-Marja Myllymäki
Rishi Das Roy
Katja Närhi
Johanna Pispa
Tuija Mustonen
Marja L Mikkola
author_facet Leah C Biggs
Otto JM Mäkelä
Satu-Marja Myllymäki
Rishi Das Roy
Katja Närhi
Johanna Pispa
Tuija Mustonen
Marja L Mikkola
author_sort Leah C Biggs
collection DOAJ
description Mesenchymal condensation is a critical step in organogenesis, yet the underlying molecular and cellular mechanisms remain poorly understood. The hair follicle dermal condensate is the precursor to the permanent mesenchymal unit of the hair follicle, the dermal papilla, which regulates hair cycling throughout life and bears hair inductive potential. Dermal condensate morphogenesis depends on epithelial Fibroblast Growth Factor 20 (Fgf20). Here, we combine mouse models with 3D and 4D microscopy to demonstrate that dermal condensates form de novo and via directional migration. We identify cell cycle exit and cell shape changes as early hallmarks of dermal condensate morphogenesis and find that Fgf20 primes these cellular behaviors and enhances cell motility and condensation. RNAseq profiling of immediate Fgf20 targets revealed induction of a subset of dermal condensate marker genes. Collectively, these data indicate that dermal condensation occurs via directed cell movement and that Fgf20 orchestrates the early cellular and molecular events.
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spelling doaj.art-7cd730ec9c4c493fadcff881c9fac35c2022-12-22T03:33:52ZengeLife Sciences Publications LtdeLife2050-084X2018-07-01710.7554/eLife.36468Hair follicle dermal condensation forms via Fgf20 primed cell cycle exit, cell motility, and aggregationLeah C Biggs0https://orcid.org/0000-0002-4990-8664Otto JM Mäkelä1https://orcid.org/0000-0001-6852-9814Satu-Marja Myllymäki2Rishi Das Roy3https://orcid.org/0000-0002-3276-7279Katja Närhi4Johanna Pispa5Tuija Mustonen6https://orcid.org/0000-0002-2429-5064Marja L Mikkola7https://orcid.org/0000-0002-9890-3835Developmental Biology Program, Institute of Biotechnology, University of Helsinki, Helsinki, FinlandDevelopmental Biology Program, Institute of Biotechnology, University of Helsinki, Helsinki, FinlandDevelopmental Biology Program, Institute of Biotechnology, University of Helsinki, Helsinki, FinlandDevelopmental Biology Program, Institute of Biotechnology, University of Helsinki, Helsinki, FinlandDevelopmental Biology Program, Institute of Biotechnology, University of Helsinki, Helsinki, FinlandDevelopmental Biology Program, Institute of Biotechnology, University of Helsinki, Helsinki, FinlandDevelopmental Biology Program, Institute of Biotechnology, University of Helsinki, Helsinki, FinlandDevelopmental Biology Program, Institute of Biotechnology, University of Helsinki, Helsinki, FinlandMesenchymal condensation is a critical step in organogenesis, yet the underlying molecular and cellular mechanisms remain poorly understood. The hair follicle dermal condensate is the precursor to the permanent mesenchymal unit of the hair follicle, the dermal papilla, which regulates hair cycling throughout life and bears hair inductive potential. Dermal condensate morphogenesis depends on epithelial Fibroblast Growth Factor 20 (Fgf20). Here, we combine mouse models with 3D and 4D microscopy to demonstrate that dermal condensates form de novo and via directional migration. We identify cell cycle exit and cell shape changes as early hallmarks of dermal condensate morphogenesis and find that Fgf20 primes these cellular behaviors and enhances cell motility and condensation. RNAseq profiling of immediate Fgf20 targets revealed induction of a subset of dermal condensate marker genes. Collectively, these data indicate that dermal condensation occurs via directed cell movement and that Fgf20 orchestrates the early cellular and molecular events.https://elifesciences.org/articles/36468hair follicledermal condensateFgf20RNAseqlive imaging
spellingShingle Leah C Biggs
Otto JM Mäkelä
Satu-Marja Myllymäki
Rishi Das Roy
Katja Närhi
Johanna Pispa
Tuija Mustonen
Marja L Mikkola
Hair follicle dermal condensation forms via Fgf20 primed cell cycle exit, cell motility, and aggregation
eLife
hair follicle
dermal condensate
Fgf20
RNAseq
live imaging
title Hair follicle dermal condensation forms via Fgf20 primed cell cycle exit, cell motility, and aggregation
title_full Hair follicle dermal condensation forms via Fgf20 primed cell cycle exit, cell motility, and aggregation
title_fullStr Hair follicle dermal condensation forms via Fgf20 primed cell cycle exit, cell motility, and aggregation
title_full_unstemmed Hair follicle dermal condensation forms via Fgf20 primed cell cycle exit, cell motility, and aggregation
title_short Hair follicle dermal condensation forms via Fgf20 primed cell cycle exit, cell motility, and aggregation
title_sort hair follicle dermal condensation forms via fgf20 primed cell cycle exit cell motility and aggregation
topic hair follicle
dermal condensate
Fgf20
RNAseq
live imaging
url https://elifesciences.org/articles/36468
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