NFAT interactions with the vasoactive intestinal peptide cytokine response element

Aviva Symes, Tom Gearan, J. Stephen Fink

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

The vasoactive intestinal peptide cytokine response element (VIP CyRE) is responsible for mediating the transcriptional induction of the VIP gene to the neuropoietic cytokines leukemia inhibitory factor (LIF) and ciliary neurotrophic factor (CNTF). In investigating the sequence and function of the CyRE, we found a region of DNA with homology to the distal NFAT site in the IL-2 promoter. In this paper we characterize this sequence and show that the VIP NFAT site recognizes T cell NFAT with similar affinity to the previously characterized IL-2 NFAT site. However, despite its location in the middle of the CyRE, we find no CNTF/LIF induced binding to it. Instead we show that in NBFL neuroblastoma cells, the calcium ionophore A23187 induces a protein to bind to the VIP NFAT site. This A23187-mediated induction of nuclear protein binding to an NFAT oligonucleotide is dependent on extracellular calcium but not dependent on de novo protein synthesis. Thus, this protein has the characteristics of an NFAT-like protein and is recognized by an NFAT3- specific antiserum suggesting that it is indeed an NFAT protein. The location of the NFAT site in the VIP CyRE suggests that this may be one mechanism through which different signaling pathways engage in cross talk to alter VIP gene transcription.
Original languageAmerican English
Pages (from-to)93-104
Number of pages12
JournalJournal of Neuroscience Research
Volume52
Issue number1
DOIs
StatePublished - Jan 1998

Keywords

  • Calcium
  • Leukemia inhibitory factor
  • NFAT
  • Transcription factors
  • VIP

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