Literature DB >> 9879835

Expression of vascular endothelial growth factor (VEGF) in various compartments of the human hair follicle.

U Kozlowska1, U Blume-Peytavi, V Kodelja, C Sommer, S Goerdt, S Majewski, S Jablonska, C E Orfanos.   

Abstract

Hair follicle vascularization appears to be closely related to the processes involved in hair cycle regulation, in which growth factors, cytokines and other bioactive molecules are involved. In particular, vascular endothelial growth factor (VEGF), essential for angiogenesis and vascular permeability, may be responsible for maintaining proper vasculature around the hair follicle during the anagen growth phase. The aim of our study was to compare the in vitro angiogenic capacity, i.e. the steady-state expression of the VEGF gene, of different cultured cell types derived from normal human hair follicles, corresponding to different follicular compartments. Human dermal papilla cells (DPC), fibrous sheath fibroblasts, dermal fibroblasts, and follicular and interfollicular keratinocytes were cultured and studied in vitro for VEGF expression at the mRNA level using RT-PCR, and for VEGF protein synthesis by radioimmunoprecipitation and immunocytochemistry. In vivo examination for VEGF expression in human terminal hair follicles was performed using immunohistochemical methods. In the present report the expression of four different VEGF molecular isoforms, differing in their angiogenic capacity, are described in different cultured follicular cell types for the first time. Cultured follicular cells strongly expressed mRNA of four VEGF molecular species identified as the 121-, 145-, 165- and 189-amino acid splice variants, the most prominent being the 121-amino acid molecule. DPC, and also other mesenchymal cells such as fibrous sheath fibroblasts and dermal fibroblasts, in vivo and in vitro strongly expressed VEGF mRNA and synthesized a 46-kDa VEGF protein, whereas follicular and interfollicular keratinocytes in vitro expressed lower levels of VEGF mRNA and proteins than mesenchymal cells. As the highest expression of VEGF was found in DPC, we suggest that DPC are mainly responsible for angiogenic processes possibly related to the human hair cycle.

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Year:  1998        PMID: 9879835     DOI: 10.1007/s004030050370

Source DB:  PubMed          Journal:  Arch Dermatol Res        ISSN: 0340-3696            Impact factor:   3.017


  25 in total

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Review 3.  [Biology of the human hair follicle. New knowledge and the clinical significance].

Authors:  A Vogt; U Blume-Peytavi
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4.  Hormones and the pilosebaceous unit.

Authors:  Wen-Chieh Chen; Christos C Zouboulis
Journal:  Dermatoendocrinol       Date:  2009-03

Review 5.  Explant culture: An advantageous method for isolation of mesenchymal stem cells from human tissues.

Authors:  Fatemeh Hendijani
Journal:  Cell Prolif       Date:  2017-02-01       Impact factor: 6.831

6.  Hair follicle stem cell cultures reveal self-organizing plasticity of stem cells and their progeny.

Authors:  Carlos Andrés Chacón-Martínez; Markus Klose; Catherin Niemann; Ingmar Glauche; Sara A Wickström
Journal:  EMBO J       Date:  2016-12-09       Impact factor: 11.598

7.  VEGF upregulates VEGF receptor-2 on human outer root sheath cells and stimulates proliferation through ERK pathway.

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

Authors:  K Yano; L F Brown; M Detmar
Journal:  J Clin Invest       Date:  2001-02       Impact factor: 14.808

9.  In vivo detection of human vascular endothelial growth factor promoter activity in transgenic mouse skin.

Authors:  J Kishimoto; R Ehama; Y Ge; T Kobayashi; T Nishiyama; M Detmar; R E Burgeson
Journal:  Am J Pathol       Date:  2000-07       Impact factor: 4.307

10.  Nitric oxide in the human hair follicle: constitutive and dihydrotestosterone-induced nitric oxide synthase expression and NO production in dermal papilla cells.

Authors:  Ronald Wolf; Gilbert Schönfelder; Martin Paul; Ulrike Blume-Peytavi
Journal:  J Mol Med (Berl)       Date:  2002-12-19       Impact factor: 4.599

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