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格雷夫斯眼病患者眼后结缔组织中选择素和免疫球蛋白超家族型黏附分子的原位表达升高。

Elevated expression in situ of selectin and immunoglobulin superfamily type adhesion molecules in retroocular connective tissues from patients with Graves' ophthalmopathy.

作者信息

Heufelder A E, Bahn R S

机构信息

Department of Internal Medicine, Mayo Clinic/Foundation, Rochester, MN 55905.

出版信息

Clin Exp Immunol. 1993 Mar;91(3):381-9. doi: 10.1111/j.1365-2249.1993.tb05913.x.

Abstract

Activation of certain adhesion molecules within vascular endothelium and the surrounding extravascular space is a critical event in the recruitment and targeting of an inflammatory response or autoimmune attack to a particular tissue site. We have recently demonstrated that the adhesion of lymphocytes to cultured retroocular fibroblasts obtained from patients with Graves' ophthalmopathy (GO) is mediated predominantly by the interaction of lymphocyte function-associated antigen-1 (LFA-1), expressed on lymphocytes, with intercellular adhesion molecule-1 (ICAM-1), expressed by these cells following exposure to interferon-gamma (IFN-gamma), tumour necrosis factor-alpha (TNF-alpha), IL-1 alpha or purified thyroid-stimulating immunoglobulins. We now report the expression and localization in situ of several adhesion molecules, ICAM-1, endothelial leucocyte adhesion molecule-1 (ELAM-1), vascular cell adhesion molecule-1 (VCAM-1), and LFA-3 in retroocular tissues derived from patients with severe GO (n = 4) and normal individuals (n = 3). Serial cryostat sections of tissue specimens were processed for immunoperoxidase staining using various MoAbs against ICAM-1, ELAM-1, VCAM-1 and LFA-3. In addition, consecutive sections were stained with MoAbs against LFA-1, CD45RO (UCHL-1)DR-human leucocyte antigen (HLA-DR), CD11b/CD18 (Mac-1), and CD11c/CD18 (p150,95). In GO-retroocular tissues, strong immunoreactivity for ICAM-1 and LFA-3 was detected in blood vessels (> 90%), in perimysial fibroblasts surrounding extraocular muscle fibres, and in connective tissue distinct from extraocular muscle. No ICAM-1 or LFA-3 immunoreactivity was present in extraocular muscle cells themselves. ICAM-1 and LFA-3 immunoreactivity in normal tissues was minimal or absent both in connective and muscle tissues. Vascular endothelium was strongly positive for ELAM-1 and VCAM-1 in GO-retroocular tissues, while VCAM-1 immunoreactivity was minimal (< 5% of blood vessels) and ELAM-1 immunoreactivity was generally absent in normal retroocular tissue. LFA-1-expressing, activated mononuclear cells and memory T lymphocytes (CD3+/CD45RO+) were only detected in GO-retrocular tissues, and were mainly localized around blood vessels and in areas of ICAM-1-expressing connective and perimysial tissue. HLA-DR expression was restricted to GO-tissue specimens, with strong immunoreactivity detected in blood vessels, macrophages and connective tissue and perimysial fibroblasts. No HLA-DR was detectable in extraocular muscle cells. In conclusion, infiltration of the orbit in GO by mononuclear cells, and their targeting within the orbit, may depend upon the coordinate expression of certain adhesion and MHC molecules.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

血管内皮及周围血管外间隙中某些黏附分子的激活是炎症反应或自身免疫攻击募集并靶向特定组织部位的关键事件。我们最近证实,淋巴细胞与从格雷夫斯眼病(GO)患者获取的培养的眼后成纤维细胞的黏附主要由淋巴细胞上表达的淋巴细胞功能相关抗原-1(LFA-1)与这些细胞在暴露于干扰素-γ(IFN-γ)、肿瘤坏死因子-α(TNF-α)、IL-1α或纯化的促甲状腺素免疫球蛋白后表达的细胞间黏附分子-1(ICAM-1)相互作用介导。我们现在报告在重度GO患者(n = 4)和正常个体(n = 3)的眼后组织中几种黏附分子ICAM-1、内皮白细胞黏附分子-1(ELAM-1)、血管细胞黏附分子-1(VCAM-1)和淋巴细胞功能相关抗原-3(LFA-3)的原位表达和定位。使用针对ICAM-1、ELAM-1、VCAM-1和LFA-3的各种单克隆抗体对组织标本的连续冰冻切片进行免疫过氧化物酶染色处理。此外,连续切片用针对LFA-1、CD45RO(UCHL-1)、DR-人类白细胞抗原(HLA-DR)、CD11b/CD18(Mac-1)和CD11c/CD18(p150,95)的单克隆抗体染色。在GO眼后组织中,在血管(> 90%)、眼外肌纤维周围的肌周成纤维细胞以及与眼外肌不同的结缔组织中检测到ICAM-1和LFA-3的强免疫反应性。眼外肌细胞本身未检测到ICAM-1或LFA-3免疫反应性。正常组织中结缔组织和肌肉组织的ICAM-1和LFA-3免疫反应性最小或不存在。GO眼后组织中的血管内皮对ELAM-1和VCAM-1呈强阳性,而正常眼后组织中VCAM-1免疫反应性最小(< 5%的血管)且ELAM-1免疫反应性通常不存在。仅在GO眼后组织中检测到表达LFA-1的活化单核细胞和记忆T淋巴细胞(CD3+/CD45RO+),且主要定位于血管周围以及表达ICAM-1的结缔组织和肌周组织区域。HLA-DR表达仅限于GO组织标本,在血管、巨噬细胞、结缔组织和肌周成纤维细胞中检测到强免疫反应性。眼外肌细胞中未检测到HLA-DR。总之,GO中单核细胞浸润眼眶及其在眼眶内的靶向作用可能取决于某些黏附分子和主要组织相容性复合体分子的协同表达。(摘要截短于400字)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ca/1554712/2a08beb2b442/clinexpimmunol00041-0043-a.jpg

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