Integration of Notch 1 and calcineurin/NFAT signaling pathways in keratinocyte growth and differentiation control

Dev Cell. 2005 May;8(5):665-76. doi: 10.1016/j.devcel.2005.02.016.

Abstract

The Notch and Calcineurin/NFAT pathways have both been implicated in control of keratinocyte differentiation. Induction of the p21(WAF1/Cip1) gene by Notch 1 activation in differentiating keratinocytes is associated with direct targeting of the RBP-Jkappa protein to the p21 promoter. We show here that Notch 1 activation functions also through a second Calcineurin-dependent mechanism acting on the p21 TATA box-proximal region. Increased Calcineurin/NFAT activity by Notch signaling involves downregulation of Calcipressin, an endogenous Calcineurin inhibitor, through a HES-1-dependent mechanism. Besides control of the p21 gene, Calcineurin contributes significantly to the transcriptional response of keratinocytes to Notch 1 activation, both in vitro and in vivo. In fact, deletion of the Calcineurin B1 gene in the skin results in a cyclic alopecia phenotype, associated with altered expression of Notch-responsive genes involved in hair follicle structure and/or adhesion to the surrounding mesenchyme. Thus, an important interconnection exists between Notch 1 and Calcineurin-NFAT pathways in keratinocyte growth/differentiation control.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alopecia / etiology
  • Animals
  • Calcineurin / metabolism*
  • Calcineurin Inhibitors
  • Cell Cycle Proteins / genetics
  • Cell Differentiation
  • Cell Division
  • Cells, Cultured
  • Cyclin-Dependent Kinase Inhibitor p21
  • DNA-Binding Proteins / metabolism*
  • Down-Regulation
  • Gene Expression Regulation, Developmental
  • Keratinocytes / cytology*
  • Keratinocytes / metabolism*
  • Mice
  • Mice, Knockout
  • NFATC Transcription Factors
  • Nuclear Proteins / metabolism*
  • Phenotype
  • Promoter Regions, Genetic
  • Receptor, Notch1
  • Receptors, Cell Surface / metabolism*
  • Signal Transduction
  • Transcription Factors / metabolism*

Substances

  • Calcineurin Inhibitors
  • Cdkn1a protein, mouse
  • Cell Cycle Proteins
  • Cyclin-Dependent Kinase Inhibitor p21
  • DNA-Binding Proteins
  • NFATC Transcription Factors
  • Notch1 protein, mouse
  • Nuclear Proteins
  • Receptor, Notch1
  • Receptors, Cell Surface
  • Transcription Factors
  • Calcineurin