Cited by 206Hair Growth and DisordersDevelopmental Biology and Gene Regulationdental development and anomalies

Generation of the primary hair follicle pattern.

Open access
Mou, Chunyan, Jackson, Ben, Schneider, Pascal, Overbeek, Paul A., Headon, Denis J.·2006·Proceedings of the National Academy of Sciences

Abstract

Hair follicles are spaced apart from one another at regular intervals through the skin. Although follicles are predominantly epidermal structures, classical tissue recombination experiments indicated that the underlying dermis defines their location during development. Although many molecules involved in hair follicle formation have been identified, the molecular interactions that determine the emergent property of pattern formation have remained elusive. We have used embryonic skin cultures to dissect signaling responses and patterning outcomes as the skin spatially organizes itself. We find that ectodysplasin receptor (Edar)–bone morphogenetic protein (BMP) signaling and transcriptional interactions are central to generation of the primary hair follicle pattern, with restriction of responsiveness, rather than localization of an inducing ligand, being the key driver in this process. The crux of this patterning mechanism is rapid Edar-positive feedback in the epidermis coupled with induction of dermal BMP4/7 . The BMPs in turn repress epidermal Edar and hence follicle fate. Edar activation also induces connective tissue growth factor, an inhibitor of BMP signaling, allowing BMP action only at a distance from their site of synthesis. Consistent with this model, transgenic hyperactivation of Edar signaling leads to widespread overproduction of hair follicles. This Edar–BMP activation–inhibition mechanism appears to operate alongside a labile prepattern, suggesting that Edar-mediated stabilization of β-catenin active foci is a key event in determining definitive follicle locations.

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Crossref · 10.1073/pnas.0600825103

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  • Eda signaling is necessary for the development and patterning of epithelial placodes of many integumentary organs in both mouse and chick.

    “Eda signaling is necessary for the development and patterning of epithelial placodes of many integumentary organs in both the mouse and chick [19]–[22].”

    From Zebrafish eda and edar Mutants Reveal Conserved and Ancestral Roles of Ectodysplasin Signaling in Vertebrates (2008) · cites this paper as [20]

    The introduction (p. 1) says the Eda–Edar–Edaradd pathway is required for a specific subset of mouse hair follicles, and the Discussion (p. 5) says loss of Edar signaling blocks primary follicle formation. The paper does not establish necessity for placodes of many organs in both mouse and chick: its discussion of scales, feathers, and teeth is explicitly speculative. (LLM, conf=0.88)

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Research works printed but not linked: 6

  1. [22]Noramly, S. & Morgan, B. A. (1998) Development (Cambridge, U.K.) 125, 3775-3787.
  2. [32]Harris, M. P., Williamson, S., Fallon, J. F., Meinhardt, H. & Prum, R. O. (2005) Proc. Natl. Acad. Sci. USA 102, 11734-11739.
  3. [34]Andl, T., Ahn, K., Kairo, A., Chu, E. Y., Wine-Lee, L., Reddy, S. T., Croft, N. J., Cebra-Thomas, J. A., Metzger, D., Chambon, P., et al. (2004) Development (Cambridge, U.K.) 131, 2257-2268.
  4. [35]Ivkovic, S., Yoon, B. S., Popoff, S. N., Safadi, F. F., Libuda, D. E., Stephenson, R. C., Daluiski, A. & Lyons, K. M. (2003) Development (Cambridge, U.K.) 130, 2779-2791.
  5. [36]Schmidt-Ullrich, R., Tobin, D. J., Lenhard, D., Schneider, P., Paus, R. & Scheidereit, C. (2006) Development (Cambridge, U.K.) 133, 1045-1057.
  6. [39]Byrne, C., Tainsky, M. & Fuchs, E. (1994) Development (Cambridge, U.K.) 120, 2369-2383.

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Authors
Mou, C., Jackson, B., Schneider, P., Overbeek, P. A., & Headon, D. J.
Affiliations
  • University of Manchester (GB)
  • University of Lausanne (CH)
  • Baylor College of Medicine (US)
Venue
Proceedings of the National Academy of Sciences
Published
2006-06-13
Volume
103
Issue
24
Pages
9075-9080
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2145032231
Cited by
206
References
4
Citations by year
2026: 9 · 2025: 6 · 2024: 6 · 2023: 8 · 2022: 11 · 2021: 8 · 2020: 9 · 2019: 8 · 2018: 6 · 2017: 6 · 2016: 10 · 2015: 14 · 2014: 20 · 2013: 8 · 2012: 11
FWCI
16.19
Type
journal article
Language
en
Open access
Locations
  • Proceedings of the National Academy of Sciences (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • IRIS (submittedVersion)
  • Research Explorer (The University of Manchester) (submittedVersion)
  • SERVAL (Université de Lausanne) (submittedVersion, other-oa)
Funders
Wellcome Trust (075220)
Topics
  • Health Sciences › Medicine › Urology › Hair Growth and Disorders
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › dental development and anomalies
Keywords
EDAR, BMP signaling, connective tissue growth factor, positive feedback loop, β-catenin, prepattern
MeSH terms
Animals, Embryo, Mammalian, Female, Male, Mice, Transgenic, Morphogenesis, Skin, Transcription, Genetic, Signal Transduction, Transforming Growth Factor beta, In Situ Hybridization, Receptors, Tumor Necrosis Factor, Gene Expression Regulation, Developmental, Hair Follicle, Bone Morphogenetic Proteins, Body Patterning, Tissue Culture Techniques, Mice, Receptors, Ectodysplasin, Edar Receptor, Bone Morphogenetic Protein 4, Bone Morphogenetic Protein 7

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