Differences in the expression of neurokinin receptor in neural and bone marrow mesenchymal cells: implications for neuronal expansion from bone marrow cells

Neuropeptides. 2002 Feb;36(1):13-21. doi: 10.1054/npep.2002.0869.

Abstract

The neurokinin-1 (NK-1) receptor interacts with peptides that belong to the tachykinin family. NK-1 is inducible in bone marrow (BM) stroma. In neural cells, its expression is high to constitutive. Screening of three cDNA libraries indicated that this different in NK-1 expression in neural and BM cells could not be explained by differences in the cDNA sequence. Analyses the 5' flanking sequence in BM stroma and three neural cell lines indicated that sequence +1/+358 relative to the transcription start (TS) site could account for the differences in NK-1 expression. Particular cytokines could reverse the repressive effects of region +1/+358 in BM stroma. The effects of NF-kappa B and cAMP activators were studied in stromal cells using a dominant negative inhibitor of NF-kappa B (I kappa B) or a repressor of CRE activators (ICERII gamma). The results showed that their effects of these transcription factors depended on the stimulating cytokine. This study provides insight into the tissue-specific differences in the expression of the NK-1 gene.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 5' Untranslated Regions / genetics
  • Bone Marrow Cells / metabolism*
  • Cell Line / metabolism
  • Cyclic AMP / metabolism
  • Cytokines / pharmacology
  • DNA, Complementary / genetics
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation / physiology*
  • Genes, Reporter
  • Humans
  • Mesoderm / cytology
  • Mesoderm / metabolism*
  • NF-kappa B / metabolism
  • Neuroblastoma / pathology
  • Neurons / metabolism*
  • Organ Specificity
  • Receptors, Neurokinin-1 / biosynthesis*
  • Receptors, Neurokinin-1 / genetics
  • Recombinant Fusion Proteins / biosynthesis
  • Second Messenger Systems / drug effects
  • Stromal Cells / metabolism
  • Transcription, Genetic / drug effects
  • Tumor Cells, Cultured / metabolism

Substances

  • 5' Untranslated Regions
  • Cytokines
  • DNA, Complementary
  • NF-kappa B
  • Receptors, Neurokinin-1
  • Recombinant Fusion Proteins
  • Cyclic AMP