Epstein R L, Powers M L, Weiner H L
J Immunol. 1981 Nov;127(5):1800-3.
We have previously shown that there are receptors for the hemagglutinin of reovirus type 3 on a subset of both murine T and B cells. Using purified reovirus type 3 particles as a ligand, followed by FITC-labeled antiviral antibody we have now been able to demonstrate viral induced capping of the reovirus receptor on both B and T cells. Kinetic studies and inhibition experiments using cytochalasin B and colchicine demonstrate that reovirus-induced capping of the viral receptor on both B and T cells has characteristics identical to the capping of immunoglobulin on B cells by anti-immunoglobulin reagents. Removal of the viral receptor and reexpression after overnight culture was demonstrated after membrane treatment by proteolytic enzymes (trypsin, pronase) or after viral induced modulation of receptor. Protein synthesis was required for reexpression since cyclohexamide prevented the reexpression of receptor in culture. Co-capping studies utilizing 2-color immunofluorescence failed to identify and association between the reovirus receptor and a variety of known surface structures on either B or T cells, but demonstrated independent modulation of the viral receptor from other surface structures. These studies suggest that the lymphocyte surface binding site for reovirus type 3 is a distinct structure that behaves identically in capping studies of both B and T cells, is protein in nature, and is intimately linked to the cell cytoskeleton.
我们之前已经表明,在小鼠T细胞和B细胞的一个亚群上存在3型呼肠孤病毒血凝素的受体。使用纯化的3型呼肠孤病毒颗粒作为配体,随后用异硫氰酸荧光素标记的抗病毒抗体,我们现在能够证明病毒诱导B细胞和T细胞上呼肠孤病毒受体的帽化。动力学研究以及使用细胞松弛素B和秋水仙碱的抑制实验表明,呼肠孤病毒诱导的B细胞和T细胞上病毒受体的帽化具有与抗免疫球蛋白试剂诱导的B细胞上免疫球蛋白帽化相同的特征。在用蛋白水解酶(胰蛋白酶、链霉蛋白酶)进行膜处理后或在病毒诱导受体调节后,过夜培养后证明病毒受体被去除并重新表达。由于环己酰亚胺阻止培养物中受体的重新表达,因此重新表达需要蛋白质合成。利用双色免疫荧光的共帽化研究未能确定呼肠孤病毒受体与B细胞或T细胞上各种已知表面结构之间的关联,但证明病毒受体与其他表面结构的独立调节。这些研究表明,3型呼肠孤病毒的淋巴细胞表面结合位点是一种独特的结构,在B细胞和T细胞的帽化研究中表现相同,本质上是蛋白质,并且与细胞骨架密切相关。