Takeuchi T, Amano K, Sekine H, Koide J, Abe T
Department of Internal Medicine, Saitama Medical Center, Saitama Medical School, Japan.
J Clin Invest. 1993 Dec;92(6):3008-16. doi: 10.1172/JCI116924.
Upregulation of integrin adhesive receptors has been implicated in various pathological conditions. We examined expression and function of integrin adhesive receptors on peripheral blood lymphocytes from patients with systemic lupus erythematosus (SLE), particularly those with the complication of vasculitis, and found that VLA-4 and LFA-1 expression was increased in SLE patients with vasculitis, while LFA-1 but not VLA-4 expression was increased in those without vasculitis. These results suggested a role of VLA-4 in the pathogenesis of vasculitis in SLE. Functional studies further demonstrated that adhesion to cytokine-activated human umbilical cord vein endothelial cells and to the CS-1 alternatively spliced domain of fibronectin was significantly increased in SLE patients with vasculitis. Analysis of the functional epitopes on the alpha 4 chain demonstrated that antigen densities of all the functional epitopes were increased in those with vasculitis, indicating that the increased expression of VLA-4 resulted from the increased number of VLA-4 molecules, and was not secondary to an increase in one particular functional epitope. Immunoprecipitation studies further support these results. Interestingly, high molecular weight bands associated with VLA-4 were observed in about half of the SLE patients with vasculitis. These results introduce a possibility that upregulation of integrin adhesive receptors has a potential role in the pathogenesis of vasculitis in SLE.
整合素黏附受体的上调与多种病理状况有关。我们检测了系统性红斑狼疮(SLE)患者外周血淋巴细胞上整合素黏附受体的表达及功能,尤其是那些伴有血管炎并发症的患者,发现血管炎型SLE患者的VLA - 4和LFA - 1表达增加,而无血管炎的患者LFA - 1表达增加但VLA - 4表达未增加。这些结果提示VLA - 4在SLE血管炎发病机制中起作用。功能研究进一步表明,血管炎型SLE患者对细胞因子激活的人脐静脉内皮细胞和纤连蛋白CS - 1可变剪接结构域的黏附显著增加。对α4链上功能表位的分析表明,血管炎患者所有功能表位的抗原密度均增加,这表明VLA - 4表达增加是由于VLA - 4分子数量增加,而非某一特定功能表位增加所致。免疫沉淀研究进一步支持了这些结果。有趣的是,在约一半的血管炎型SLE患者中观察到与VLA - 4相关的高分子量条带。这些结果提示整合素黏附受体上调在SLE血管炎发病机制中可能具有潜在作用。