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TPA causes divergent responses of Ca2+-dependent and Ca2+-independent isoforms of PKC in the nuclei of Caco-2 cells

  • Brendan P. Frawley
  • , Xiao Ying Tien
  • , Susanne C. Hartmann
  • , Ramesh K. Wali
  • , Sharon M. Niedziela
  • , Nicholas O. Davidson
  • , Michael D. Sitrin
  • , Thomas A. Brasitus
  • , Marc Bissonnette
  • The University of Chicago

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

The present studies were undertaken to examine the expression of PKC isoforms within the nucleus of Caco-2 cells, a cell line widely used to investigate intestinal cell growth and differentiation, in order to begin to explore their roles in modulating gene expression. Purified nuclei were, therefore, prepared from Caco-2 cells and found to contain PKC-ζ, but not -α. The phorbol ester, 12-O-tetradecanoyl phorbol 13-acetate (TPA) caused an acute redistribution of PKC-α to the nucleus, but did not change the distribution of PKC-ζ. Chronic treatment with TPA down-regulated total PKC-α, but not -ζ. Moreover, in contrast to acute TPA treatment, after chronic treatment, nuclear PKC-α was no longer detectable, whereas nuclear PKC-ζ was unchanged. These studies demonstrate for the first time the constitutive expression and divergent responses to TPA of the Ca2+-dependent and Ca2+-independent isoforms of PKC in the nuclei of Caco-2 cells and suggest that these specific isoforms may be involved in modulating gene expression.

Original languageEnglish
Pages (from-to)301-305
Number of pages5
JournalBiochimica et Biophysica Acta - Molecular Cell Research
Volume1222
Issue number2
DOIs
StatePublished - Jun 30 1994

Keywords

  • Nuclear protein kinase C
  • Phorbol ester
  • Signal transduction

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