Stang E, Kartenbeck J, Parton R G
Department of Physiology and Pharmacology, University of Queensland, Brisbane, Australia.
Mol Biol Cell. 1997 Jan;8(1):47-57. doi: 10.1091/mbc.8.1.47.
Simian virus 40 (SV40) has been shown to enter mammalian cells via uncoated plasma membrane invaginations. Viral particles subsequently appear within the endoplasmic reticulum. In the present study, we have examined the surface binding and internalization of SV40 by immunoelectron microscopy. We show that SV40 associates with surface pits which have the characteristics of caveolae and are labeled with antibodies to the caveolar marker protein, caveolin-1. SV40 is believed to use major histocompatibility complex (MHC) class I molecules as cell surface receptors. Using a number of MHC class I-specific monoclonal antibodies, we found that both viral infection and association of virus with caveolae were strongly reduced by preincubation with anti-MHC class I antibodies. Because binding of SV40 to MHC class I molecules may induce clustering, we investigated whether antibody cross-linked class I molecules also redistributed to caveolae. Clusters of MHC class I molecules were indeed shown to be specifically associated with caveolin-labeled surface pits. Taken together, the results suggest that SV40 may make use of MHC class I molecule clustering and the caveolae pathway to enter mammalian cells.
猴病毒40(SV40)已被证明可通过未包被的质膜内陷进入哺乳动物细胞。病毒颗粒随后出现在内质网中。在本研究中,我们通过免疫电子显微镜检查了SV40的表面结合和内化过程。我们发现SV40与具有小窝特征的表面凹陷相关联,并且这些凹陷被针对小窝标记蛋白小窝蛋白-1的抗体标记。据信SV40利用主要组织相容性复合体(MHC)I类分子作为细胞表面受体。使用多种MHC I类特异性单克隆抗体,我们发现与抗MHC I类抗体预孵育会强烈降低病毒感染以及病毒与小窝的关联。由于SV40与MHC I类分子的结合可能诱导聚集,我们研究了抗体交联的I类分子是否也重新分布到小窝中。事实上,MHC I类分子簇确实显示与小窝蛋白标记的表面凹陷特异性相关。综上所述,结果表明SV40可能利用MHC I类分子聚集和小窝途径进入哺乳动物细胞。