Croy B A, Rossant J, Clark D A
J Reprod Fertil. 1985 Jul;74(2):479-89. doi: 10.1530/jrf.0.0740479.
The role of the immune system in promoting the midterm death of Mus caroli embryos transferred to the Mus musculus uterus was studied in vivo by transferring M. caroli blastocysts to recipients with altered immune status. Transfers of embryos to chimaeric mothers (Mus musculus in equilibrium Mus caroli), which were expected to be tolerant of species antigens, resulted in survival of M. musculus embryos but death of M. caroli embryos. The preferential survival of M. musculus embryos was explained by showing that M. musculus embryos can survive in the M. caroli uterus. Transfers to T cell-deficient mice of genotype nu/nu and to NK cell-deficient mice of genotype bg/bg as well as treatment of normal transfer recipients with Cyclosporin A or anti-Ia antiserum failed to prolong survival. However, immunization of recipients with M. caroli lymphocytes promoted more rapid and uniform failure of the interspecies pregnancy. Cytotoxic cells were detected in the resorbing embryos on Day 10.5 in immune pregnancies and on Day 12.5 in non-immune pregnancies and these cells were promiscuous in their pattern of lysis, showing equal reactivity against M. caroli, transfer recipient and 3rd party target cells. These experiments show that failure of M. caroli embryos in the M. musculus uterus is complex, but probably does not involve responses by classical cytotoxic T lymphocyte or natural killer cell pathways. Participation of the immune system in the resorption process, however, is confirmed and is associated with generation of promiscuous cytolytic cells.
通过将卡氏小鼠囊胚移植到免疫状态改变的受体体内,在体内研究了免疫系统在促进移植到小家鼠子宫内的卡氏小鼠胚胎中期死亡中的作用。将胚胎移植到嵌合母体(处于平衡状态的小家鼠和卡氏小鼠)中,预期它们会对物种抗原产生耐受性,结果小家鼠胚胎存活而卡氏小鼠胚胎死亡。小家鼠胚胎的优先存活通过证明小家鼠胚胎能够在卡氏小鼠子宫内存活得到了解释。将胚胎移植到基因型为nu/nu的T细胞缺陷小鼠和基因型为bg/bg的NK细胞缺陷小鼠中,以及用环孢菌素A或抗Ia抗血清处理正常移植受体,均未能延长胚胎存活时间。然而,用卡氏小鼠淋巴细胞免疫受体促进了种间妊娠更快且更一致地失败。在免疫妊娠的第10.5天和非免疫妊娠的第12.5天,在吸收胚胎中检测到细胞毒性细胞,这些细胞的裂解模式杂乱,对卡氏小鼠、移植受体和第三方靶细胞表现出同等反应性。这些实验表明,卡氏小鼠胚胎在小家鼠子宫内的失败是复杂的,但可能不涉及经典细胞毒性T淋巴细胞或自然杀伤细胞途径的反应。然而,免疫系统在吸收过程中的参与得到了证实,并且与杂乱溶细胞的产生有关。