Warner C M, Gollnick S O
Department of Biology, Northeastern University, Boston, Massachusetts 02115.
Biol Reprod. 1993 May;48(5):1082-7. doi: 10.1095/biolreprod48.5.1082.
Genes in the major histocompatibility complex (MHC) have been shown to play a role in development and reproduction. In the mouse, class I MHC proteins are expressed on oocytes and preimplantation embryos. Each mouse strain contains multiple class I genes located in the classical regions, K and D, and the nonclassical regions, Q and TL, of the mouse MHC, the H-2 complex. This study was undertaken to evaluate the expression of the classical class I MHC antigen, H-2K, on preimplantation mouse embryos. Through use of appropriate monoclonal antibodies (mAb) and an ELISA procedure, it was shown that H-2K antigens are detectable on oocytes and blastocyst-stage embryos, but not on 2-cell or 8-cell embryos. This pattern of expression is different from that reported in previous studies showing expression of total class I antigens and the nonclassical MHC antigen, Qa-2, on all stages of preimplantation embryos, including 2-cell- and 8-cell-stage embryos. To analyze the nature of the H-2K protein on blastocysts, H-2K antigens were isolated from an H-2K overproducing cell line (RDM-4) and used in blocking experiments. It was found that the purified antigen blocked binding to tissue culture cells by 54% and to embryos by 68%. Therefore, H-2K antigens on tissue culture cells and embryos appear to be very similar, but perhaps not identical. Thus escape of embryos from surveillance by the maternal immune system may not be effected by the expression of a different or embryonic form of MHC antigens.
主要组织相容性复合体(MHC)中的基因已被证明在发育和繁殖过程中发挥作用。在小鼠中,I类MHC蛋白在卵母细胞和植入前胚胎上表达。每个小鼠品系在小鼠MHC即H-2复合体的经典区域K和D以及非经典区域Q和TL中都包含多个I类基因。本研究旨在评估经典I类MHC抗原H-2K在植入前小鼠胚胎上的表达情况。通过使用合适的单克隆抗体(mAb)和酶联免疫吸附测定程序,结果显示H-2K抗原在卵母细胞和囊胚期胚胎上可检测到,但在2细胞或8细胞胚胎上未检测到。这种表达模式与先前研究报道的不同,先前研究表明在植入前胚胎的所有阶段,包括2细胞和8细胞阶段胚胎,都有总I类抗原和非经典MHC抗原Qa-2的表达。为了分析囊胚上H-2K蛋白的性质,从H-2K过量产生细胞系(RDM-4)中分离出H-2K抗原并用于阻断实验。结果发现,纯化的抗原使与组织培养细胞的结合减少了54%,与胚胎的结合减少了68%。因此,组织培养细胞和胚胎上的H-2K抗原似乎非常相似,但可能并不完全相同。因此,胚胎逃避母体免疫系统监视可能不是由不同或胚胎形式的MHC抗原的表达所导致的。