Sasseville V G, Newman W, Brodie S J, Hesterberg P, Pauley D, Ringler D J
Department of Pathology, Harvard Medical School, New England Regional Primate Research Center, Southborough, Massachusetts.
Am J Pathol. 1994 Jan;144(1):27-40.
Because the mechanisms associated with recruitment of monocytes to brain in AIDS encephalitis are unknown, we used tissues from rhesus monkeys infected with simian immunodeficiency virus (SIV) to examine the relative contributions of various adhesion pathways in mediating monocyte adhesion to endothelium from encephalitic brain. Using a modified Stamper and Woodruff tissue adhesion assay, we found that the human monocytic cell lines, THP-1 and U937, and the B cell line, Ramos, preferentially bound to brain vessels from monkeys with AIDS encephalitis. Using a combined tissue adhesion/immunohistochemistry approach, these cells only bound to vessels expressing vascular cell adhesion molecule-1 (VCAM-1). Furthermore, pretreatment of tissues with antibodies to VCAM-1 or cell lines with antibodies to VLA-4 (CD49d) inhibited adhesion by more than 70%. Intercellular adhesion molecule-1 (ICAM-1)/beta 2 integrin interactions were not significant in mediating cell adhesion to the vasculature in encephalitic simian brain using a cell line (JY) capable of binding rhesus monkey ICAM-1. In addition, selectin-mediated interactions did not significantly contribute to cell binding to encephalitic brain as there was no immunohistochemical expression of E-selectin and P-selectin in either normal or encephalitic brain, nor was there a demonstrable adhesive effect from L-selectin using L-selectin-transfected 300.19 cells on simian encephalitic brain. These results demonstrate that using the tissue adhesion assay, THP-1, U937, and Ramos cells bind to vessels in brain from animals with AIDS encephalitis using VCAM-1/alpha 4 beta 1 integrin interactions and suggest that VCAM-1 and VLA-4 may be integral for monocyte recruitment to the central nervous system during the development of AIDS encephalitis.
由于艾滋病脑炎中单核细胞募集至脑的相关机制尚不清楚,我们利用感染了猴免疫缺陷病毒(SIV)的恒河猴组织,来研究各种黏附途径在介导单核细胞黏附于脑炎猴脑内皮细胞过程中的相对作用。通过改良的斯坦珀和伍德拉夫组织黏附试验,我们发现人单核细胞系THP-1和U937以及B细胞系Ramos优先黏附于患艾滋病脑炎猴的脑血管。采用组织黏附/免疫组织化学联合方法,这些细胞仅黏附于表达血管细胞黏附分子-1(VCAM-1)的血管。此外,用抗VCAM-1抗体预处理组织或用抗VLA-4(CD49d)抗体处理细胞系,可使黏附减少70%以上。使用能够结合恒河猴ICAM-1的细胞系(JY),细胞间黏附分子-1(ICAM-1)/β2整合素相互作用在介导细胞黏附于脑炎猴脑脉管系统中并不显著。此外,选择素介导的相互作用对细胞黏附于脑炎脑的作用不显著,因为在正常脑或脑炎脑中均无E选择素和P选择素的免疫组织化学表达,使用转染L选择素的300.19细胞对猴脑炎脑也未显示出明显的黏附作用。这些结果表明,通过组织黏附试验,THP-1、U937和Ramos细胞利用VCAM-1/α4β1整合素相互作用黏附于患艾滋病脑炎动物脑内的血管,提示VCAM-1和VLA-4可能在艾滋病脑炎发生过程中单核细胞募集至中枢神经系统方面起重要作用。