Midkine induces epithelial-mesenchymal transition through Notch2/Jak2-Stat3 signaling in human keratinocytes

Cell Cycle. 2008 Jun 1;7(11):1613-22. doi: 10.4161/cc.7.11.5952. Epub 2008 Mar 16.

Abstract

Epithelial-to-mesenchymal transition (EMT) underlies cell plasticity and embryonic development and is frequently observed in advanced tumorigenesis. We demonstrated that midkine (MK), a retinoic acid-inducible heparin-binding mitogen, promotes EMT in immortalized HaCaT keratinocytes. We showed that MK binds to the Notch2 receptor in HaCaT keratinocytes. We further found that MK activates Notch2 signaling leading to protein/protein interactions between Hes1 and Jak2/Stat3 intermediates. We thus suggest that MK-induced cross talk of Notch2/Jak2/Stat3 signaling pathways can regulate cell plasticity and motility contributing to the EMT and later stages of tumorigenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Differentiation / physiology*
  • Cytokines / genetics*
  • Cytokines / metabolism
  • DNA Primers / genetics
  • Enzyme-Linked Immunosorbent Assay
  • Epithelial Cells / cytology
  • Epithelial Cells / drug effects*
  • Gene Expression Profiling
  • Humans
  • Immunoblotting
  • Janus Kinase 2 / metabolism
  • Keratinocytes / metabolism*
  • Mesoderm / cytology*
  • Microscopy, Fluorescence
  • Midkine
  • Neoplasms / metabolism*
  • Receptor, Notch2 / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction / physiology*
  • Two-Hybrid System Techniques

Substances

  • Cytokines
  • DNA Primers
  • NOTCH2 protein, human
  • Receptor, Notch2
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • Midkine
  • JAK2 protein, human
  • Janus Kinase 2