Durda P J, Gottlieb P D
J Exp Med. 1976 Aug 1;144(2):476-93. doi: 10.1084/jem.144.2.476.
Specific anti-Ly sera were employed to precipitate Ly antigens from Nonidet P-40 extracts of mouse thymocytes labeled with 125I using lactoperoxidase and with NaB3H4 using galactose oxidase. Thymocytes from mice of the congenic strains C57BL/6J (Ly-2.2, Ly-3.2 positive), C57BL/6Ly-2a, Ly-3a (Ly-2.1, Ly-3.1 positive) and C57BL/6-Ly-2a (Ly-2.1, Ly-3.2-positive) were used as sources of labeled antigens and as immune adsorbants to permit evaluation of the specificity of each anti-Ly serum employed. Results of sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) under reducing conditions are consistent with the Ly-3.1 antigen containing a glycoprotein subunit with an apparent mol wt of 35,000 daltons. Specific precipitates obtained using anti-Ly-2.1 serum yielded SDS-PAGE profiles identical to that obtained with anti-Ly-3.1 serum, suggesting that the Ly-2 and Ly-3 antigens have the same molecular weight distribution. The relationships of these results to the observed close genetic and topological linkage of Ly-2 and Ly-3 and to the genetic linkage of these loci with the IB-peptide marker, a mouse Bk-region polymorphism, are discussed.
使用特异性抗Ly血清从用乳过氧化物酶标记125I和用半乳糖氧化酶标记NaB3H4的小鼠胸腺细胞的Nonidet P - 40提取物中沉淀Ly抗原。同基因品系C57BL/6J(Ly - 2.2、Ly - 3.2阳性)、C57BL/6Ly - 2a、Ly - 3a(Ly - 2.1、Ly - 3.1阳性)和C57BL/6 - Ly - 2a(Ly - 2.1、Ly - 3.2阳性)小鼠的胸腺细胞用作标记抗原的来源和免疫吸附剂,以评估所使用的每种抗Ly血清的特异性。在还原条件下进行的十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳(SDS - PAGE)结果与Ly - 3.1抗原含有一个表观分子量为35,000道尔顿的糖蛋白亚基一致。使用抗Ly - 2.1血清获得的特异性沉淀物产生的SDS - PAGE图谱与使用抗Ly - 3.1血清获得的图谱相同,表明Ly - 2和Ly - 3抗原具有相同的分子量分布。讨论了这些结果与观察到的Ly - 2和Ly - 3紧密遗传和拓扑连锁以及这些基因座与IB - 肽标记(一种小鼠Bk区域多态性)的遗传连锁之间的关系。