Leis Martina, Marschall Manfred, Stamminger Thomas
Institut für Klinische und Molekulare Virologie, Schlossgarten 4, 91054 Erlangen, Germany.
J Gen Virol. 2004 Jul;85(Pt 7):1995-2000. doi: 10.1099/vir.0.79818-0.
The deregulation of cellular adhesion molecules by human cytomegalovirus (HCMV) appears to be correlated with the development of vascular disease. In this study, it was investigated whether the expression of Thy-1 (CD90), a member of the immunoglobulin superfamily of adhesion molecules with constitutive expression on fibroblast cells, is modulated following infection with HCMV. It was observed that Thy-1 cell surface expression decreased significantly during the course of infection. Addition of neutralizing antibodies, as well as UV inactivation of virus, prevented Thy-1 downregulation. In contrast, inhibition of virus replication by cidofovir did not alter Thy-1 regulation by HCMV, indicating that immediate-early (IE) and/or early (E) gene products are responsible. Interestingly, after infection of fibroblasts with a recombinant GFP-expressing virus, infected as well as non-infected cells showed a reduced Thy-1 cell surface expression. From these findings, it is concluded that IE or E gene products of HCMV induce a so far unidentified soluble factor that mediates Thy-1 downregulation.
人巨细胞病毒(HCMV)对细胞黏附分子的失调似乎与血管疾病的发展相关。在本研究中,研究了Thy-1(CD90)的表达情况,Thy-1是黏附分子免疫球蛋白超家族的成员,在成纤维细胞上组成性表达,在感染HCMV后其表达是否受到调节。观察到在感染过程中Thy-1细胞表面表达显著降低。添加中和抗体以及病毒的紫外线灭活可阻止Thy-1下调。相反,西多福韦抑制病毒复制并未改变HCMV对Thy-1的调节,表明立即早期(IE)和/或早期(E)基因产物起作用。有趣的是,用表达重组绿色荧光蛋白的病毒感染成纤维细胞后,感染和未感染的细胞均显示Thy-1细胞表面表达降低。从这些发现得出结论,HCMV的IE或E基因产物诱导了一种迄今未鉴定的可溶性因子,该因子介导Thy-1下调。