Substance P induces TNF-alpha and IL-6 production through NFkB in peritoneal mast cells (Articolo in rivista)

Type
Label
  • Substance P induces TNF-alpha and IL-6 production through NFkB in peritoneal mast cells (Articolo in rivista) (literal)
Anno
  • 2003-01-01T00:00:00+01:00 (literal)
Alternative label
  • Azzolina A, Bongiovanni A, Lampiasi N. (2003)
    Substance P induces TNF-alpha and IL-6 production through NFkB in peritoneal mast cells
    in Biochimica et biophysica acta. Molecular cell research
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Azzolina A, Bongiovanni A, Lampiasi N. (literal)
Pagina inizio
  • 75 (literal)
Pagina fine
  • 83 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 1643 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • IBIM CNR (literal)
Titolo
  • Substance P induces TNF-alpha and IL-6 production through NFkB in peritoneal mast cells (literal)
Abstract
  • The neuropeptide Substance P (SP) is an important mediator of neuroimmunomodulatory activity. The aim of this study is to elucidate the mechanism used by SP to promote increased production of pro-inflammatory cytokines in fresh isolated rat peritoneal mast cells (rPMC). We have demonstrated that SP induces production of interleukin-6 (IL-6) in rPMC through the PI-3K, p42/44 and p38 MAP kinase pathways. SP-stimulated rPMC also exhibited an enhanced nuclear translocation of the nuclear factor kappa B (NF kappa B). The tumour necrosis factor-alpha (TNF-alpha) and IL-6 production was completely inhibited by using (E)-4-hydroxynonenal (HNE) as an inhibitor of I kappa B-alpha and -beta phosphorylation. Further, TNF-alpha and IL-6 expression was significantly inhibited by the oligonucleotides (ODNs) containing the NF kappa B element (NF kappa B decoy ODNs) but not by the scrambled control ODNs. These findings indicate that the NF kappa B pathway is involved in the transcriptional regulation of the TNF-alpha and IL-6 overexpression in primary SP-stimulated mast cells. (literal)
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