首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >Monocyte adhesion to endothelium in simian immunodeficiency virus-induced AIDS encephalitis is mediated by vascular cell adhesion molecule-1/alpha 4 beta 1 integrin interactions.
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Monocyte adhesion to endothelium in simian immunodeficiency virus-induced AIDS encephalitis is mediated by vascular cell adhesion molecule-1/alpha 4 beta 1 integrin interactions.

机译:猿猴免疫缺陷病毒诱发的艾滋病性脑炎中单核细胞与内皮的粘附是通过血管细胞粘附分子-1 / alpha 4 beta 1整联蛋白相互作用来介导的。

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摘要

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.
机译:由于在艾滋病性脑炎中与单核细胞募集到大脑相关的机制尚不清楚,因此我们使用感染了猿猴免疫缺陷病毒(SIV)的恒河猴的组织来研究各种粘附途径在介导单核细胞与脑性脑血管内皮粘附中的相对作用。使用改良的Stamper和Woodruff组织粘附试验,我们发现人单核细胞系THP-1和U937,以及B细胞系Ramos优先与患有艾滋病脑炎的猴子的脑血管结合。使用组合的组织粘附/免疫组织化学方法,这些细胞仅与表达血管细胞粘附分子-1(VCAM-1)的血管结合。此外,用抗VCAM-1抗体预处理组织或用抗VLA-4(CD49d)抗体预处理细胞系可将粘连抑制70%以上。细胞间粘附分子1(ICAM-1)/β2整联蛋白的相互作用并不重要介导使用能够结合恒河猴ICAM-1的细胞系(JY)在脑性猿猴脑中与脉管系统的粘附。此外,选择素介导的相互作用不会显着促进细胞与脑性脑细胞的结合,因为在正常或脑性脑中均没有E-选择素和P-选择素的免疫组织化学表达,使用L-选择素也没有明显的粘附作用。 L-选择素转染的猴脑脑300.19细胞。这些结果表明,通过组织粘附试验,THP-1,U937和Ramos细胞通过VCAM-1 / alpha 4 beta 1整合素相互作用与艾滋病性脑炎动物的大脑血管结合,并提示VCAM-1和VLA-4可能是艾滋病脑炎发展过程中单核细胞募集到中枢神经系统所不可或缺的。

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