M. Cavicchi et Bjr. Whittle, Potentiation of cytokine induced iNOS expression in the human intestinal epithelial cell line, DLD-1, by cyclic AMP, GUT, 45(3), 1999, pp. 367-374
Background-Nitric oxide production by the inducible isoform of nitric oxide
synthase (iNOS) is thought to play a role in the pathogenesis of inflammat
ory bowel disease along with other proinflammatory mediators.
Aims-To examine the effects of cAMP, an intracellular mediator of several p
roinflammatory mediators, on iNOS expression in the human intestinal epithe
lial cell line, DLD-1.
Methods-iNOS activity was assessed by measuring the NO stable oxidative pro
duct NO2-. iNOS protein expression and iNOS mRNA levels were determined by
western blotting and northern blotting, respectively.
Results-iNOS activity, protein, and mRNA were induced by a combination of i
nterleukin 1 beta (0.5-5 ng/ml), interferon gamma (20-200 u/ml), and tumour
necrosis factor cr (10-100 ng/ml). The cytokine induced NOS activity was p
otentiated by N-6,2'-O-dibutyryladenosine 3':5'-cyclic monophosphate and 8-
bromoadenosine 3':5'-cyclic monophosphate (0.1-1 mM), and the adenylate cyc
lase activator, forskolin (1-100 mu M). This activity was inhibited by the
selective iNOS inhibitor, 1400W (0.1-100 mu M) These agents increased iNOS
protein. The cAMP analogues potentiated iNOS at the transcriptional level a
s shown by effects of actinomycin D (5 mu g/ml) and northern blot analyses;
the nuclear factor (NF) KB inhibitor, pyrrolidine dithiocarbamate (10-200
mu M), significantly reduced this potentiation. The cAMP potentiated iNOS a
ctivity was inhibited by the tyrosine kinase inhibitor, A25 (10-200 mu M) a
nd the Janus activated kinase 2 inhibitor, B42 (10-200 mu M).
Conclusions-Increased intracellular cAMP is a potent stimulus of iNOS expre
ssion in combination with cytokines in DLD-1 cells, acting at the transcrip
tional level and involving NF-KB and the JAK-STAT pathways. Thus, proinflam
matory mediators that increase cAMP levels may augment iNOS expression and
NO production.