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干燥综合征患者小唾液腺中的血管内皮细胞和淋巴细胞黏附分子

Vascular endothelium and lymphocyte adhesion molecules in minor salivary glands of patients with Sjogren's syndrome.

作者信息

Aziz K E, McCluskey P J, Montanaro A, Wakefield D

机构信息

Department of Immunopathology, Prince Henry Hospital, Little Bay, NSW, Australia.

出版信息

J Clin Lab Immunol. 1992 Jan;37(1):39-49.

PMID:1339235
Abstract

The aim of this study was to examine the distribution and types of adhesion molecules expressed over endothelial cells and the ligands present on lymphocytes which infiltrate exocrine glands in patients with Sjogren's syndrome. Minor salivary gland biopsies were examined from twelve patients with Sjogren's syndrome and eight normal subjects for the presence of adhesion molecules using monoclonal antibodies and an Indirect Immunoperoxidase technique. There was an increased expression of intercellular adhesion molecule-1 (ICAM-1, CD54) on endothelial cells, lymphocytes, fibroblasts and salivary gland epithelial cells. In addition we documented the expression of endothelial leukocyte adhesion molecule-1 (ELAM-1) on endothelial cells in salivary glands from patients but not the controls. Many of the endothelial cells expressing these adhesion molecules in patients with Sjogren's syndrome had the morphological appearance of high endothelial venules. V-CAM-1 was shown to be present in some of the salivary biopsies from patients with Sjogren's syndrome. Lymphocytes infiltrating salivary glands strongly express LFA-1 (CD11a/CD18) molecules. Some infiltrating lymphocytes, and most monocytes, expressed C3bi-R (CD11b/CD18) and the p150.95 (CD11c/CD18) antigens on their cell surface. The results of this study reveal the enhanced expression of vascular endothelial and lymphocyte adhesion molecules on the minor salivary glands of patients with Sjogren's syndrome. The presence of such receptors and their putative ligands indicate an important role for these molecules in the pathogenesis of Sjogren's syndrome.

摘要

本研究的目的是检测干燥综合征患者外分泌腺中浸润淋巴细胞上的配体以及内皮细胞上表达的黏附分子的分布和类型。使用单克隆抗体和间接免疫过氧化物酶技术,对12例干燥综合征患者和8名正常受试者的小唾液腺活检组织进行黏附分子检测。细胞间黏附分子-1(ICAM-1,CD54)在内皮细胞、淋巴细胞、成纤维细胞和唾液腺上皮细胞上的表达增加。此外,我们记录了患者唾液腺内皮细胞上内皮白细胞黏附分子-1(ELAM-1)的表达,而对照组未检测到。干燥综合征患者中许多表达这些黏附分子的内皮细胞具有高内皮微静脉的形态学特征。血管细胞黏附分子-1(V-CAM-1)在部分干燥综合征患者的唾液活检组织中被检测到。浸润唾液腺的淋巴细胞强烈表达淋巴细胞功能相关抗原-1(LFA-1,CD11a/CD18)分子。一些浸润淋巴细胞以及大多数单核细胞在其细胞表面表达C3bi受体(CD11b/CD18)和p150.95(CD11c/CD18)抗原。本研究结果显示,干燥综合征患者小唾液腺上血管内皮和淋巴细胞黏附分子的表达增强。这些受体及其假定配体的存在表明这些分子在干燥综合征发病机制中起重要作用。

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