TY - JOUR
T1 - Tyrosine kinase activation is necessary for inducible nitric oxide synthase expression by interleukin-1β
AU - Tetsuka, T.
AU - Morrison, A. R.
PY - 1995
Y1 - 1995
N2 - The inflammatory cytokine interleukin-1 (IL-1) induces the inducible form of nitric oxide synthase (iNOS) with an increase in nitric oxide in rat mesangial cells. However, the cellular mechanisms that underlie the induction of iNOS by IL-1β in mesangial cells has not been clarified. Because we have shown that tyrosine kinase inhibitors attenuate IL-1β-induced cyclooxygenase expression and prostaglandin production, we investigated the effect of tyrosine kinase inhibitors on IL-1β-induced nitrite production and iNOS mRNA expression in rat mesangial cells. The tyrosine kinase inhibitors genistein and herbimycin A attenuated IL-1β-induced nitrite production in a dose- dependent manner. In addition, both of these inhibitors blocked IL-1β- induced iNOS mRNA expression. These data suggest that tyrosine kinase(s) plays a central role in IL-1β signaling to induce iNOS in rat mesangial cells.
AB - The inflammatory cytokine interleukin-1 (IL-1) induces the inducible form of nitric oxide synthase (iNOS) with an increase in nitric oxide in rat mesangial cells. However, the cellular mechanisms that underlie the induction of iNOS by IL-1β in mesangial cells has not been clarified. Because we have shown that tyrosine kinase inhibitors attenuate IL-1β-induced cyclooxygenase expression and prostaglandin production, we investigated the effect of tyrosine kinase inhibitors on IL-1β-induced nitrite production and iNOS mRNA expression in rat mesangial cells. The tyrosine kinase inhibitors genistein and herbimycin A attenuated IL-1β-induced nitrite production in a dose- dependent manner. In addition, both of these inhibitors blocked IL-1β- induced iNOS mRNA expression. These data suggest that tyrosine kinase(s) plays a central role in IL-1β signaling to induce iNOS in rat mesangial cells.
KW - interleukin-1
KW - protein tyrosine kinase
KW - signal transduction
UR - http://www.scopus.com/inward/record.url?scp=0028892988&partnerID=8YFLogxK
U2 - 10.1152/ajpcell.1995.269.1.c55
DO - 10.1152/ajpcell.1995.269.1.c55
M3 - Article
C2 - 7543244
AN - SCOPUS:0028892988
SN - 0363-6143
VL - 269
SP - C55-C59
JO - American Journal of Physiology - Cell Physiology
JF - American Journal of Physiology - Cell Physiology
IS - 1 38-1
ER -