Schochetman G, Arthur L O, Long C W, Massey R J
J Virol. 1979 Oct;32(1):131-9. doi: 10.1128/JVI.32.1.131-139.1979.
Sera from C3H mammary tumor-bearing mice contain cytotoxic antibodies for mouse mammary tumor virus (MMTV)-producing cells, based on (51)Cr release in a complement-dependent serum cytotoxicity assay. The cytotoxic antibodies could be absorbed by purified C3H MMTV gp52 and C3H MMTV-infected cat cells (C3H [MMTV] CrFK) containing cell surface MMTV gp52. However, purified MMTV p27 and uninfected CrFK cat cells were negative. Absorption of the sera with GR (MMTV) CrFK cells also removed all of the cytotoxicity, whereas absorption with RIII (MMTV) CrFK cells was negative, even though all three infected cat cells contained equivalent amounts of gp52. The same C3H cytotoxic sera also neutralized the focus-forming capacity of a C3H MMTV pseudotype of Kirsten sarcoma virus containing MMTV gp52. In contrast, sera from mammary tumor-bearing GR and RIII mice did not neutralize the pseudotype. Furthermore, neutralization could be achieved only by anti-gp52 but not by anti-gp36, -p27, -p14, or -p10 C3H MMTV sera. The gp52's of C3H, GR, and RIII MMTV could also be distinguished by using a type-specific competition radioimmunoassay employing (125)I-gp52 of C3H MMTV and a hyperimmune rabbit anti-C3H MMTV serum. To demonstrate these differences directly, we studied the primary structure of gp52 on the surface of the C3H, GR, and RIII (MMTV) CrFK cells. Two-dimensional tryptic peptide maps of the cell surface lactoper-oxidase-catalyzed iodinated gp52's revealed a greater number of peptides common to the gp52's of C3H and GR MMTVs than to RIII MMTV gp52. These results demonstrate that gp52 is a major target antigen for both cytotoxic and neutralizing antibodies, that the cell surface and virion-associated gp52's of C3H, GR, and RIII MMTV contain both group- and type-specific determinants, and that C3H and GR MMTV gp52's are antigenically more related to each other than to RIII MMTV gp52. Furthermore, C3H mammary tumor-bearing mice develop type-specific antibodies capable of recognizing unique gp52 determinants and, therefore, are able to distinguish the gp52 of C3H MMTV from the gp52's of GR and RIII MMTV.
在补体依赖的血清细胞毒性试验中,基于(51)铬释放量,来自携带C3H乳腺肿瘤小鼠的血清含有针对产生小鼠乳腺肿瘤病毒(MMTV)的细胞的细胞毒性抗体。细胞毒性抗体可被纯化的C3H MMTV gp52和含有细胞表面MMTV gp52的C3H MMTV感染的猫细胞(C3H [MMTV] CrFK)吸收。然而,纯化的MMTV p27和未感染的CrFK猫细胞呈阴性。用GR(MMTV)CrFK细胞吸收血清也消除了所有细胞毒性,而用RIII(MMTV)CrFK细胞吸收则呈阴性,尽管所有三种感染的猫细胞都含有等量的gp52。相同的C3H细胞毒性血清也中和了含有MMTV gp52的 Kirsten 肉瘤病毒C3H MMTV假型的集落形成能力。相比之下,来自携带乳腺肿瘤的GR和RIII小鼠的血清不能中和该假型。此外,中和作用只能通过抗gp52实现,而不能通过抗C3H MMTV血清中的抗gp36、-p27、-p14或-p10实现。C3H、GR和RIII MMTV的gp52也可以通过使用一种类型特异性竞争放射免疫测定法来区分,该方法采用C3H MMTV的(125)I-gp52和超免疫兔抗C3H MMTV血清。为了直接证明这些差异,我们研究了C3H、GR和RIII(MMTV)CrFK细胞表面gp52的一级结构。细胞表面乳过氧化物酶催化碘化的gp52的二维胰蛋白酶肽图显示,C3H和GR MMTV的gp52共有的肽比RIII MMTV gp52更多。这些结果表明,gp52是细胞毒性和中和抗体的主要靶抗原,C3H、GR和RIII MMTV的细胞表面和病毒体相关的gp52含有组特异性和型特异性决定簇,并且C3H和GR MMTV gp52在抗原性上彼此之间的关系比与RIII MMTV gp52更密切。此外,携带C3H乳腺肿瘤的小鼠产生能够识别独特gp52决定簇的型特异性抗体,因此能够区分C3H MMTV的gp52与GR和RIII MMTV的gp52。