Lambracht-Washington Doris, Düvel Heike, Hänisch Lisa, Dinkel Astrid, Wonigeit Kurt
Transplantationslabor der Klinik für Visceral- und Transplantationschirurgie, Medizinische Hochschule Hannover, 30625 Hannover, Germany.
Immunogenetics. 2004 Apr;56(1):28-37. doi: 10.1007/s00251-004-0650-9. Epub 2004 Mar 19.
RT1.L class I antigens have originally been identified in LEW rats by LEW.1LV3-anti-LEW.1LM1 antisera and have been classified as nonclassical. We report now that LEW.1LV3-anti-LEW.1LM1 antisera react with three different antigens, termed RT1.L1, RT1.L2, and RT1.L3. This was found by serological analysis of a panel of transfectants expressing different class I genes of strain LEW with a LEW.1LV3-anti-LEW.1LM1 antiserum and two monoclonal antibodies (mAbs HT20 and HT21) generated in the same strain combination. The antiserum reacted with all three antigens: the two mAbs with RT1.L1 and RT1.L2, respectively. Sequence analysis showed that the genes encoding RT1.L1, RT1.L2, and RT1.L3 cluster together in a phylogenetic analysis of rat and mouse alpha(1)-alpha(2) sequences and that they share an unusual MHC class I promoter in which Enhancer A and B, as well as the interferon response element (IRE), are missing. Exchange of the promoter in RT1.L2 against the classical RT1.A promoter resulted in high surface expression in appropriate transfectants, indicating that the deviant promoter is responsible for the weak surface expression of the RT1.L2 gene. The very similar promoter structures of RT1.L1 and RT1.L3 are likely to contribute also to the weak expression of these genes. As RT1.L3 maps closely to the deletion in the mutant haplotype lm1, the RT1.L family can be located in the class I region extending from Bat1 to Pou5f1. Different from other allogeneic mAbs detecting known class I molecules encoded by genes of the RT1.C/E region, HT20 and HT21 react with a wide panel of strains carrying different RT1 haplotypes. This suggests that nonclassical class I genes of the RT1.L family are present in most RT1 haplotypes.
RT1.L I类抗原最初是通过LEW.1LV3抗LEW.1LM1抗血清在LEW大鼠中鉴定出来的,并被归类为非经典抗原。我们现在报告,LEW.1LV3抗LEW.1LM1抗血清与三种不同的抗原发生反应,分别称为RT1.L1、RT1.L2和RT1.L3。这是通过对一组表达LEW品系不同I类基因的转染子进行血清学分析发现的,使用的是LEW.1LV3抗LEW.1LM1抗血清以及在相同品系组合中产生的两种单克隆抗体(mAb HT20和HT21)。该抗血清与所有三种抗原发生反应:两种单克隆抗体分别与RT1.L1和RT1.L2发生反应。序列分析表明,在大鼠和小鼠α(1)-α(2)序列的系统发育分析中,编码RT1.L1、RT1.L2和RT1.L3的基因聚集在一起,并且它们共享一个不寻常的MHC I类启动子,其中增强子A和B以及干扰素反应元件(IRE)缺失。将RT1.L2中的启动子替换为经典的RT1.A启动子,导致在合适的转染子中高表面表达,表明异常的启动子是RT1.L2基因表面表达较弱的原因。RT1.L1和RT1.L3非常相似的启动子结构可能也导致了这些基因的弱表达。由于RT1.L3紧密定位在突变单倍型lm1的缺失区域,RT1.L家族可以定位在从Bat1到Pou5f1的I类区域。与检测由RT1.C/E区域基因编码的已知I类分子的其他同种异体单克隆抗体不同,HT20和HT21与携带不同RT1单倍型的多种品系发生反应。这表明RT1.L家族的非经典I类基因存在于大多数RT1单倍型中。