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Expression and regulation of ICAM-1 and VCAM-1 in streptococcal-cell-wall-induced hepatic granuloma

机译:ICAM-1和VCAM-1在链球菌细胞壁诱导的肝肉芽肿中的表达和调控

摘要

Hepatic granulomas are induced by a single intraperitoneal injection of streptococcal cell wall (SCW) into female Lewis rats. This inflammatory response has a biphasic course with an early accumulation of polymorphonuclear leukocytes in the liver followed by infiltration of mononuclear phagocytes. The expression of adhesion molecules may contribute to the recruitment of leukocytes to the liver. Therefore, in this study I investigated the expression and regulation of intercellular adhesion molecule-1 (ICAM-1) and vascular adhesion molecule-1 (VCAM-1) on liver endothelial cells in a SCW rat model and in primary endothelial cell cultures treated with cytokines IL-1β, IL-6, IFN-γ, TNF-α and lipopolysaccharide (LPS). Immunohistochemical staining demonstrated that ICAM-1 was constitutively expressed on sinusoidal lining cells. Enhanced ICAM-1 expression was observed 3, 14 and 28 days after SCW injection. There was a gradation of ICAM-1 staining intensity with the strongest staining in periportal area. In primary endothelial cell culture, cells up-regulated surface ICAM-1 expression in response to cytokines in the following order: IL-1β + IFN-γ + TNF-α > IFN-γ + TNF-α > TNF-α + IL-1β or IFN-γ + IL-1β > TNF-α >IFN-γ > IL-1β. ICAM-1 was also up-regulated by LPS. Cytokine and LPS activated liver endothelial cells also increased ICAM-1 mRNA expression. The induction profile of ICAM-1 mRNA was identical to the profile of ICAM-1 expression on the cell surface. This parallel suggests that the increased surface ICAM-1 expression is associated with the increased ICAM-1 mRNA level. Interestingly, IL-6 had no effect on either surface ICAM-1 or mRNA production. Primary endothelial cell culture constitutively expressed both 7 domain (3.7 kb) and 3 domain (1.6 kb) VCAM-1 mRNAs. IL-1β, IL-6 and IFN-γ did not significantly affect VCAM-1 mRNA expression. TNF-α and LPS up-regulated 7 domain mRNA level 6 and 10 fold respectively with no effects on 3 domain mRNA expression. The most striking affects were induced by IFN-γ + TNF-α. This study suggests that the expression of ICAM-1 and VCAM-1 on liver endothelial cells could play an important role in the recruitment of leukocytes into the liver during SCW-induced hepatic inflammation. TNF-α was found to be produced by endothelial cells and may be one of the reasons for the chronicity of this lesion.
机译:腹腔注射链球菌细胞壁(SCW)到雌性Lewis大鼠中可诱发肝肉芽肿。这种炎性反应具有双相过程,肝中多形核白细胞的早期积累,随后是单核吞噬细胞的浸润。粘附分子的表达可能有助于白细胞向肝脏的募集。因此,在这项研究中,我研究了SCW大鼠模型和经EGF处理的原代内皮细胞培养物中细胞间粘附分子1(ICAM-1)和血管粘附分子1(VCAM-1)在肝内皮细胞中的表达和调控。细胞因子IL-1β,IL-6,IFN-γ,TNF-α和脂多糖(LPS)。免疫组织化学染色显示ICAM-1在正弦内衬细胞上组成性表达。注射SCW后3、14和28天观察到ICAM-1表达增强。在门静脉周围区域,ICAM-1染色强度呈渐变,染色最强。在原代内皮细胞培养中,细胞按照以下顺序上调响应细胞因子的表面ICAM-1表达:IL-1β+IFN-γ+TNF-α>IFN-γ+TNF-α>TNF-α+ IL- 1β或IFN-γ+IL-1β>TNF-α>IFN-γ>IL-1β。 ICAM-1也被LPS上调。细胞因子和LPS激活的肝内皮细胞也增加了ICAM-1 mRNA表达。 ICAM-1 mRNA的诱导概况与细胞表面上ICAM-1表达的概况相同。这种平行表明,表面ICAM-1表达的增加与ICAM-1 mRNA水平的增加有关。有趣的是,IL-6对表面ICAM-1或mRNA的产生均无影响。原代内皮细胞培养成分性表达7个域(3.7 kb)和3个域(1.6 kb)VCAM-1 mRNA。 IL-1β,IL-6和IFN-γ不会显着影响VCAM-1 mRNA的表达。 TNF-α和LPS分别上调7个域的mRNA水平6倍和10倍,而对3个域的mRNA表达无影响。最明显的影响是由IFN-γ+TNF-α引起的。这项研究表明,在SCW诱导的肝炎过程中,肝内皮细胞上ICAM-1和VCAM-1的表达可能在白细胞募集到肝脏中起重要作用。发现TNF-α是由内皮细胞产生的,并且可能是该病变的慢性的原因之一。

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    Xie Lei;

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  • 年度 1996
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