首页> 美国卫生研究院文献>Gut >Is the intercellular adhesion molecule-1/leukocyte function associated antigen 1 pathway of leukocyte adhesion involved in the tissue damage of alcoholic hepatitis?
【2h】

Is the intercellular adhesion molecule-1/leukocyte function associated antigen 1 pathway of leukocyte adhesion involved in the tissue damage of alcoholic hepatitis?

机译:酒精性肝炎的组织损伤中是否涉及细胞间黏附分子-1 /白细胞功能相关的抗原1通路与白细胞黏附有关?

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Alcoholic hepatitis is characterised histologically by an intense inflammatory cell infiltrate made up predominantly of neutrophils but including other cell types, particularly lymphocytes. Leukocyte cytotoxicity requires cell adhesion, which is mediated via receptors on the leukocyte surface including leukocyte function associated antigen-1 (LFA-1) which binds to the ligand intercellular adhesion molecule-1 (ICAM-1) on the target cell. The distribution of ICAM-1 and LFA-1 expression in liver biopsy specimens from patients with alcoholic liver disease was examined to ascertain whether this pathway of leukocyte adhesion is involved in the tissue damage of alcoholic hepatitis. Specimens were stained for ICAM-1 and LFA-1 by a three step immunoalkaline-phosphatase method using monoclonal antibodies against ICAM-1 and LFA-1. LFA-1 staining on portal tract inflammatory cells and parenchymal inflammatory cells and ICAM-1 staining on liver components were examined. ICAM-1 expression on hepatocytes was significantly greater in alcoholic hepatitis compared with fatty liver (p less than 0.001) and normal controls (p less than 0.01). ICAM-1 expression correlated with the histological degree of hepatocellular damage (tau = 0.79; p = 0.0005) and parenchymal inflammation (tau = 0.65; p less than 0.001, and with LFA-1 expression on parenchymal leukocytes (tau = 0.63; p = 0.01). The ICAM-1/LFA-1 pathway may therefore be involved in leukocyte mediated tissue damage during alcoholic hepatitis.
机译:酒精性肝炎的组织学特征是强烈的炎症细胞浸润,主要由中性粒细胞组成,但包括其他细胞类型,尤其是淋巴细胞。白细胞的细胞毒性需要细胞粘附,这是通过白细胞表面上的受体介导的,该受体包括与靶细胞上的配体细胞间粘附分子-1(ICAM-1)结合的白细胞功能相关抗原-1(LFA-1)。检查酒精性肝病患者肝活检标本中ICAM-1和LFA-1表达的分布,以确定这种白细胞粘附途径是否与酒精性肝炎的组织损伤有关。使用针对ICAM-1和LFA-1的单克隆抗体,通过三步免疫碱性磷酸酶方法对标本进行ICAM-1和LFA-1染色。检查了门静脉炎性细胞和实质性炎性细胞的LFA-1染色以及肝成分的ICAM-1染色。与脂肪肝(p小于0.001)和正常对照组(p小于0.01)相比,酒精性肝炎中肝细胞ICAM-1的表达明显更高。 ICAM-1表达与肝细胞损伤的组织学程度(tau = 0.79; p = 0.0005)和实质性炎症(tau = 0.65; p小于0.001)以及与实质白细胞中的LFA-1表达相关(tau = 0.63; p = 0.01)。因此,ICAM-1 / LFA-1途径可能与酒精性肝炎期间白细胞介导的组织损伤有关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号