The expression of keratinocyte growth factor receptor (FGFR2-IIIb) correlates with the high proliferative rate of HaCaT keratinocytes

Exp Dermatol. 2006 Aug;15(8):596-605. doi: 10.1111/j.1600-0625.2006.00450.x.

Abstract

Keratinocyte growth factor receptor (KGFR = FGFR2-IIIb) is a tyrosine kinase receptor expressed by keratinocytes, which mediates the effects of fibroblast growth factors (FGF). There are contradictory data in the literature regarding the role of FGFR2-IIIb during the proliferation/differentiation programme of keratinocytes. In this study, we aimed to investigate whether overexpression of FGFR2-IIIb may have a role in the regulation of keratinocyte proliferation. We analysed the expression of FGFR2-IIIb in an in vitro HaCaT model system representing different stages of proliferation and differentiation of keratinocytes. Real-time RT-PCR and Western blot analyses demonstrated a correlation between FGFR2-IIIb mRNA and protein expression and the proportion of cells in S/G2/M phase in synchronized HaCaT keratinocytes and thus with proliferation activity (r = 0.96). After treatment with the antipsoriatic drug, dithranol, FGFR2-IIIb is downregulated dose dependently both at mRNA and protein levels. Moreover, when the rate of proliferation is decreased by the lack of cell attachment to the culturing surface, FGFR2-IIIb mRNA (P = 0.0315) and protein expressions were also reduced (P = 0.0242), while a differentiation marker, keratin 10, mRNA (P = 0.0003) and protein levels (P = 0.001) were increased (r = -0.92). Based on our results we conclude that FGFR2-IIIb expression in HaCaT keratinocytes corresponds with the proliferative activation of the cells and is not related to the differentiation programme.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anthralin / pharmacology
  • Cell Cycle
  • Cell Differentiation
  • Cell Proliferation
  • Dose-Response Relationship, Drug
  • Down-Regulation
  • Exons
  • Gene Expression Regulation*
  • Humans
  • Keratinocytes / cytology*
  • Models, Genetic
  • RNA, Messenger / metabolism
  • Receptor, Fibroblast Growth Factor, Type 2 / biosynthesis*
  • Receptor, Fibroblast Growth Factor, Type 2 / physiology
  • Time Factors

Substances

  • RNA, Messenger
  • Receptor, Fibroblast Growth Factor, Type 2
  • keratinocyte growth factor receptor
  • Anthralin