Format

Send to

Choose Destination
FEBS Lett. 1996 Apr 29;385(1-2):4-6.

Cytokines activate the nuclear factor kappa B (NF-kappa B) and induce nitric oxide production in human pancreatic islets.

Author information

1
Department of Medical Cell Biology, Uppsala University, Sweden. malin.flodstrom@medcellbriol.uu.se

Abstract

We studied the ability of cytokines to activate the nuclear transcription factor NF-kappaB in human pancreatic islets and the putative role of NF-kappaB for cytokine-induced NO production. Brief exposure (20 min) of human islets of Langerhans to a combination of interleukin-1beta + interferon-gamma + tumor necrosis factor-alpha induced a 2.6-fold increase in nuclear NF-kappaB activity in gel shift analysis. This increase was prevented by the NF-kappaB inhibitor, pyrrolidine dithiocarbamate (PDTC), which also counteracted NO production by human islets exposed for 14 h to the cytokine combination. High concentrations of interleukin-1beta alone (150 and 250 U/ml) increased NF-kappaB nuclear binding but failed to induce NO formation in human islets. The present data are the first to demonstrate that cytokines activate NF-kappaB in primary adult human pancreatic islets and suggest that activation of NF-kappaB may be a necessary but not sufficient signal for cytokine-induced iNOS expression in human islets of Langerhans.

PMID:
8641463
DOI:
10.1016/0014-5793(96)00337-7
[Indexed for MEDLINE]
Free full text

Supplemental Content

Full text links

Icon for Wiley
Loading ...
Support Center