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通过蛋白激酶Cδ-p38激酶连接的级联反应上调血管细胞黏附分子-1介导肿瘤坏死因子-α诱导的肺气道上皮白细胞黏附和迁移。

VCAM-1 upregulation via PKCdelta-p38 kinase-linked cascade mediates the TNF-alpha-induced leukocyte adhesion and emigration in the lung airway epithelium.

作者信息

Woo Chang-Hoon, Lim Jae-Hyang, Kim Jae-Hong

机构信息

School of Life Sciences and Biotechnology, Korea University, 5-1 Anam-dong, Sungbuk-gu, Seoul, 136-701, Korea.

出版信息

Am J Physiol Lung Cell Mol Physiol. 2005 Feb;288(2):L307-16. doi: 10.1152/ajplung.00105.2004. Epub 2004 Oct 15.

Abstract

Vascular cell adhesion molecule (VCAM)-1 plays a central role in the recruitment of inflammatory cells, and its expression is rapidly induced by proinflammatory cytokines such as TNF-alpha. In the present study, we show that pretreatment with rottlerin, a specific inhibitor of protein kinase C (PKC)-delta, or transient transfection with antisense PKCdelta oligonucleotides significantly inhibits TNF-alpha-induced expression of VCAM-1, but not of intercellular adhesion molecule (ICAM)-1 in human lung epithelium A549 cells. In addition, TNF-alpha was shown to induce the expression of VCAM-1 in a p38 kinase-dependent manner; also, TNF-alpha-induced p38 kinase activation was blocked by inhibition of PKCdelta, suggesting that p38 kinase is apparently situated downstream of PKCdelta in the TNF-alpha-signaling pathway to VCAM-1 expression. Notably, inhibition of the PKCdelta-p38 kinase cascade also attenuated the TNF-alpha-induced adhesion of neutrophils to lung epithelium and the trafficking of leukocytes across the epithelium into the airway lumen in vivo. Together, these findings indicate that signaling via PKCdelta-p38 kinase-linked cascade specifically induces expression of VCAM-1 in lung epithelium in response to TNF-alpha and that this effect is both functionally and clinically significant.

摘要

血管细胞黏附分子(VCAM)-1在炎症细胞募集中起核心作用,其表达可被肿瘤坏死因子-α(TNF-α)等促炎细胞因子迅速诱导。在本研究中,我们发现,用蛋白激酶C(PKC)-δ的特异性抑制剂rottlerin预处理,或用反义PKCδ寡核苷酸进行瞬时转染,可显著抑制TNF-α诱导的人肺上皮A549细胞中VCAM-1的表达,但不影响细胞间黏附分子(ICAM)-1的表达。此外,TNF-α以p38激酶依赖的方式诱导VCAM-1的表达;而且,PKCδ的抑制可阻断TNF-α诱导的p38激酶激活,这表明在TNF-α信号通路中,p38激酶显然位于PKCδ的下游,参与调控VCAM-1的表达。值得注意的是,抑制PKCδ-p38激酶级联反应也减弱了TNF-α诱导的中性粒细胞与肺上皮的黏附以及体内白细胞穿过上皮进入气道腔的迁移。这些发现共同表明,通过PKCδ-p38激酶连接的级联反应进行的信号传导可特异性地诱导肺上皮中VCAM-1的表达,以响应TNF-α,并且这种作用在功能和临床上都具有重要意义。

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