Hilgers J, Sonnenberg A, Nusse R
Br J Cancer. 1980 Oct;42(4):542-50. doi: 10.1038/bjc.1980.278.
The MLr antigen, a mammary tumour virus-induced antigen on the surface of GR thymic lymphoma cells (GRSL) can be modulated from the cell surface upon incubation with specific antiserum for 1-2 h at 37 degrees C, followed by washing the cells. In contrast, a number of other cell-surface antigens on these GRSL cells cannot be modulated under similar conditions. These antigens include histocompatibility antigens of the H-2 complex (H-2.8 of the K-end and H-2dx(D) of the H-2dx haplotype) and two thymic markers, TL1.2 and Thy1.2. Antigenic modulation of MLr as tested by trypan-blue exclusion and by chromium51 release does not lead to a measurable change in the expression of H-2K, H-2D, TL and Thy1.2 antigens. These results could be confirmed by absorption analysis. The latter analysis showed that the number of antigenic sites per cell are about the same for MLr and the two H-2 antigens, while TL antigens are scarcer and Thy1.2 antigens are more abundant. The procedure of antigenic modulation showed that the MLr antigen resides on MTVgp52, the major protein of the envelope. There was no evidence of internal proteins, such as MTVp27, on the surface of GRSL cells.
MLr抗原是GR胸腺淋巴瘤细胞(GRSL)表面的一种乳腺肿瘤病毒诱导抗原,在37℃下与特异性抗血清孵育1 - 2小时,随后洗涤细胞,该抗原可从细胞表面被调控。相比之下,这些GRSL细胞上的许多其他细胞表面抗原在类似条件下不能被调控。这些抗原包括H - 2复合体的组织相容性抗原(K端的H - 2.8和H - 2dx单倍型的H - 2dx(D))以及两种胸腺标志物TL1.2和Thy1.2。通过台盼蓝排斥试验和铬51释放试验检测的MLr抗原调控,不会导致H - 2K、H - 2D、TL和Thy1.2抗原表达出现可测量的变化。这些结果可通过吸收分析得到证实。后者分析表明,每个细胞上MLr和两种H - 2抗原的抗原位点数量大致相同,而TL抗原较少,Thy1.2抗原较多。抗原调控过程表明,MLr抗原存在于包膜的主要蛋白MTVgp52上。没有证据表明GRSL细胞表面存在诸如MTVp27等内部蛋白。