Cited by 710Hair Growth and DisordersAngiogenesis and VEGF in Cancerdental development and anomalies

Control of hair growth and follicle size by VEGF-mediated angiogenesis

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Yano, Kiichiro, Brown, Lawrence F., Detmar, Michael·2001·Journal of Clinical Investigation

Abstract

The murine hair follicle undergoes pronounced cyclic expansion and regression, leading to rapidly changing demands for its vascular support. Our study aimed to quantify the cyclic changes of perifollicular vascularization and to characterize the biological role of VEGF for hair growth, angiogenesis, and follicle cycling. We found a significant increase in perifollicular vascularization during the growth phase (anagen) of the hair cycle, followed by regression of angiogenic blood vessels during the involution (catagen) and the resting (telogen) phase. Perifollicular angiogenesis was temporally and spatially correlated with upregulation of VEGF mRNA expression by follicular keratinocytes of the outer root sheath, but not by dermal papilla cells. Transgenic overexpression of VEGF in outer root sheath keratinocytes of hair follicles strongly induced perifollicular vascularization, resulting in accelerated hair regrowth after depilation and in increased size of hair follicles and hair shafts. Conversely, systemic treatment with a neutralizing anti-VEGF antibody led to hair growth retardation and reduced hair follicle size. No effects of VEGF treatment or VEGF blockade were observed in mouse vibrissa organ cultures, which lack a functional vascular system. These results identify VEGF as a major mediator of hair follicle growth and cycling and provide the first direct evidence that improved follicle vascularization promotes hair growth and increases hair follicle and hair size.

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  • VSKOs can be used as a tool to investigate the interaction of hair follicles with vasculature, as well as hair-related pathologies.

    “VSKOs can also be used as a tool to investigate the interaction of hair follicles with vasculature, as well as hair‐related pathologies.[ 75 , 76 ]”

    From Coordinated Development of Immune Cell Populations in Vascularized Skin Organoids from Human Induced Pluripotent Stem Cells (2025) · cites this paper as [75]

    The Introduction and Discussion (page unavailable) show that perifollicular blood vessels affect hair growth and discuss a possible role for vascularization in hair-loss disorders. The study used mice and isolated vibrissa follicles, not VSKOs, so it does not establish that VSKOs can be used to investigate those interactions or pathologies. (LLM, conf=0.84)

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  • SKOs appeared to maintain hair follicle development after vascularization, with perifollicular vascularization consistently observed throughout the VSKO as seen in vivo.

    “Whilst the VSKOs were co‐cultured on an ALI to recapitulate the external environment human skin is exposed to, SKOs appeared to maintain hair follicle development after vascularization, where perifollicular vascularization was consistently observed throughout the VSKO as seen in vivo.[ 75 ]”
  • Endothelial differentiation was evaluated with observation of DLL4+ arterial capillaries and EMCN+ venous capillaries, highlighting appropriate recapitulation of a blood vessel as seen in vivo.

    “Additionally, endothelial differentiation was evaluated with an observation of DLL4+ arterial capillaries and EMCN+ venous capillaries, highlighting the appropriate recapitulation of a blood vessel as seen in vivo.[ 74 , 75 ]”

    From Coordinated Development of Immune Cell Populations in Vascularized Skin Organoids from Human Induced Pluripotent Stem Cells (2025) · cites this paper as [75]

    The Methods section (page unavailable) describes assessing perifollicular vessels with CD31 staining, and the Discussion describes vascular remodeling during the murine hair cycle. Searches for DLL4, EMCN, and arterial or venous capillaries found no passage evaluating differentiation with those markers or claiming that they demonstrate recapitulation of a blood vessel in vivo. (LLM, conf=0.76)

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Cites

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Research works printed but not linked: 3

  1. Durward, A., and Rudall, K.M. 1958. The vascularity and patterns of growth of hair follicles. In The biology of hair growth. W. Montagna and R.A. Ellis, editors. Academic Press. New York, New York, USA. 189-218.
  2. Dry, F.W. 1926. The coat of the mouse (mus musculus). Journal of Genetics. 16:287-340.
  3. Streit, M., et al. 1999. Thrombospondin-2: a potent endogenous inhibitor of tumor growth and angiogenesis. Proc. Natl. Acad. Sci. USA. 96:14888-14893.

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Authors
Yano, K., Brown, L. F., & Detmar, M.
Affiliations
  • Massachusetts General Hospital (US)
  • Beth Israel Deaconess Medical Center (US)
  • Harvard University (US)
Corresponding author
Detmar, Michael
Venue
Journal of Clinical Investigation
Published
2001-02-15
Volume
107
Issue
4
Pages
409-417
ISSN
0021-9738 (ISSN-L)
OpenAlex
W2042690168
Cited by
710
References
0
Citations by year
2026: 55 · 2025: 54 · 2024: 46 · 2023: 49 · 2022: 59 · 2021: 52 · 2020: 41 · 2019: 36 · 2018: 27 · 2017: 32 · 2016: 22 · 2015: 38 · 2014: 19 · 2013: 21 · 2012: 14
FWCI
18.39
Type
journal article
Language
en
Open access
Locations
  • Journal of Clinical Investigation (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Massachusetts General Hospital
  • National Institutes of Health (99-23901)
  • National Cancer Institute (R01CA069184, CA 86410, CA69184, R01CA086410, 99-23901)
Topics
  • Health Sciences › Medicine › Urology › Hair Growth and Disorders
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Angiogenesis and VEGF in Cancer
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › dental development and anomalies
Keywords
vascular endothelial growth factor, angiogenesis, hair follicle, hair growth, hair cycle, anagen, catagen, telogen, dermal papilla, anti-VEGF antibody
MeSH terms
Animals, Female, Hair, Lymphokines, Mice, Inbred C57BL, Endothelial Growth Factors, Hair Follicle, Neovascularization, Physiologic, Vascular Endothelial Growth Factors, Vascular Endothelial Growth Factor A, Mice

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