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JAK/STAT信号通路对血管平滑肌细胞中IFNγ和LPS刺激诱导的一氧化氮合酶的抑制作用。

Inhibition by the JAK/STAT pathway of IFNgamma- and LPS-stimulated nitric oxide synthase induction in vascular smooth muscle cells.

作者信息

Marrero M B, Venema V J, He H, Caldwell R B, Venema R C

机构信息

Vascular Biology Center, Medical College of Georgia, Augusta, Georgia, 30912, USA.

出版信息

Biochem Biophys Res Commun. 1998 Nov 18;252(2):508-12. doi: 10.1006/bbrc.1998.9678.

Abstract

Inducible nitric oxide synthase (iNOS) is induced in many cell types by cytokines and lipopolysaccharide (LPS). Cytokine signal transduction is believed to be mediated primarily through the JAK/STAT pathway. We therefore examined the effects of a JAK2-specific inhibitor, an antisense oligonucleotide to JAK2, and electroporation of neutralizing anti-STAT1 and anti-STAT3 antibodies on IFNgamma- and LPS-stimulated induction of iNOS in vascular smooth muscle cells. Unexpectedly, we found that the JAK/STAT pathway suppresses IFNgamma- and LPS-stimulated iNOS induction in these cells. In contrast, the JAK/STAT pathway appears to have a positive role in iNOS induction in RAW 264.7 macrophages.

摘要

诱导型一氧化氮合酶(iNOS)在许多细胞类型中可被细胞因子和脂多糖(LPS)诱导产生。细胞因子信号转导主要被认为是通过JAK/STAT途径介导的。因此,我们研究了JAK2特异性抑制剂、JAK2反义寡核苷酸以及中和性抗STAT1和抗STAT3抗体电穿孔对血管平滑肌细胞中IFNγ和LPS刺激的iNOS诱导作用的影响。出乎意料的是,我们发现JAK/STAT途径在这些细胞中抑制IFNγ和LPS刺激的iNOS诱导。相反,JAK/STAT途径似乎在RAW 264.7巨噬细胞的iNOS诱导中发挥积极作用。

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