Nonnenmacher H, Illinger D, Kuhry J G, Kirn A, Braunwald J
Institut de Virologie de la Faculté de Médecine, Unité INSERM U74, Strasbourg, France.
Biochem Biophys Res Commun. 1994 Nov 15;204(3):1299-304. doi: 10.1006/bbrc.1994.2604.
The aim of this study was to examine whether or not membrane fluidity directly influences infection by enveloped viruses, and, more precisely here, the susceptibility of A/J mouse hepatocytes to Mouse Hepatitis Virus type 3 (MHV3). We therefore studied, in parallel, the effects on hepatocyte membrane fluidity and on intracellular viral titre of two treatments, i) a hypercholesterolaemic diet to increase the hepatocyte membrane cholesterol content, ii) direct phosphatidylserine incorporation into hepatocyte membrane. Membrane fluidity was monitored on isolated hepatocytes by fluorescence anisotropy with TMA-DPH, and the viral titre was determined by plaque assay. The results clearly demonstrate that membrane fluidity is not directly involved in viral infection mechanisms.
本研究的目的是检验膜流动性是否直接影响包膜病毒的感染,更确切地说,是检验A/J小鼠肝细胞对3型小鼠肝炎病毒(MHV3)的易感性。因此,我们同时研究了两种处理对肝细胞膜流动性和细胞内病毒滴度的影响,i)高胆固醇饮食以增加肝细胞膜胆固醇含量,ii)将磷脂酰丝氨酸直接掺入肝细胞膜。通过使用TMA-DPH的荧光各向异性监测分离肝细胞的膜流动性,并通过噬斑测定法确定病毒滴度。结果清楚地表明,膜流动性并不直接参与病毒感染机制。