Keratinocyte growth inhibition by high-dose epidermal growth factor is mediated by transforming growth factor β autoinduction: A negative feedback mechanism for keratinocyte growth

Kenshi Yamasaki, Nobuko Toriu, Yasushi Hanakawa, Yuji Shirakata, Koji Sayama, Atsushi Takayanagi, Masafumi Ohtsubo, Shinobu Gamou, Nobuyoshi Shimizu, Makiko Fujii, Kohei Miyazono, Koji Hashimoto

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27 Citations (Scopus)

Abstract

The epidermal growth factor receptor and its ligands initiate a major signaling pathway that regulates keratinocyte growth in an autocrine manner. It is well known that high doses of epidermal growth factor receptor ligands inhibit keratinocyte growth. Recently, signal transducers and activators of transcription 1-dependent p21Waf1/Cip1 induction were reported to be involved in high-dose epidermal growth factor-dependent cell growth arrest in the A431 squamous cell carcinoma cell line; however, transfection of dominant-negative signal transducers and activators of transcription 1 adenovirus vector did not block epidermal growth factor-induced growth inhibition in normal human keratinocytes. As transforming growth factor β is a potent inhibitor of keratinocyte proliferation, we hypothesized that transforming growth factor β contributes to epidermal growth factor-mediated keratinocyte growth inhibition. Epidermal growth factor concentrations of 10 ng per ml enhanced transforming growth factor β1 mRNA expression from 3 to 6 h post-stimulation. Enzyme-linked immunosorbent assay analysis detected 150 pg per ml of transforming growth factor β1 in the culture medium of keratinocytes incubated with 10 and 100 ng per ml epidermal growth factor, whereas 0.1 and 1.0 ng per ml epidermal growth factor slightly enhance transforming growth factor β1 production. Epidermal growth factor (100 ng per ml) upregulated luciferase activity of p3TP-lux, which contains three tandem transforming growth factor β-Smad signaling responsive elements, 6-fold compared with unstimulated cells. The epidermal growth factor-dependent induction of p3TP-lux luciferase activity was disrupted by transfection of the dominant negative form of transforming growth factor β type I receptor adenovirus vector (AxdnALK5), which suggests that epidermal growth factor-induced transforming growth factor β acts in an autocrine manner in keratinocytes. Moreover, transfection of AxdnALK5 completely blocked the growth inhibition induced by 100 ng per ml of epidermal growth factor in normal keratinocytes. These data demonstrate that an autocrine transforming growth factor β1-ALK5 pathway is a negative feedback mechanism for epidermal growth factor-induced normal human keratinocyte growth.

Original languageEnglish
Pages (from-to)1030-1037
Number of pages8
JournalJournal of Investigative Dermatology
Volume120
Issue number6
DOIs
Publication statusPublished - 2003 Jun 1

Keywords

  • Activators of transcription
  • Activin receptor-like kinase
  • Epidermal growth factor
  • Keratinocyte
  • Signal transducers
  • Transforming growth factor β

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Dermatology
  • Cell Biology

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    Yamasaki, K., Toriu, N., Hanakawa, Y., Shirakata, Y., Sayama, K., Takayanagi, A., Ohtsubo, M., Gamou, S., Shimizu, N., Fujii, M., Miyazono, K., & Hashimoto, K. (2003). Keratinocyte growth inhibition by high-dose epidermal growth factor is mediated by transforming growth factor β autoinduction: A negative feedback mechanism for keratinocyte growth. Journal of Investigative Dermatology, 120(6), 1030-1037. https://doi.org/10.1046/j.1523-1747.2003.12239.x