Redline R W, Lu C Y
Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115.
Lab Invest. 1989 Jul;61(1):27-36.
An immunohistochemical study of the days 14-19 murine placenta and uterus using a panel of antibodies specific for maternal and paternal class I major histocompatibility complex (MHC) antigens, specific leukocyte subsets, and other lineage-specific markers was performed to elucidate the nature of the maternal tolerance of the fetal implant in the uterus. Fetally derived trophoblast lining maternal blood spaces lacked MHC antigens, but other interstitial trophoblasts expressed fetally derived polymorphic class I MHC determinants. The latter class I MHC-bearing trophoblasts were most prominent in the maternal decidua basalis where they were mixed with maternal cells. Our results identify two factors that may be relevant for understanding why these alloantigen-bearing fetal cells are not rejected by the mother: a paucity of la-bearing antigen presenting cells, macrophages, and mature T and B lymphocytes and the presence of large numbers of Thy-1+ asialo-GM-1+ CD4- CD8- bone marrow-derived (CLA/Ly5+) cells of maternal origin in the decidua basalis. These latter cells correspond to previously described granulated metrial gland cells that may be involved in local immunoregulation.
利用一组针对母本和父本I类主要组织相容性复合体(MHC)抗原、特定白细胞亚群及其他谱系特异性标志物的抗体,对第14 - 19天的小鼠胎盘和子宫进行了免疫组织化学研究,以阐明子宫内胎儿植入物的母体耐受性的本质。衬于母体血窦的胎儿来源的滋养层细胞缺乏MHC抗原,但其他间质滋养层细胞表达胎儿来源的多态性I类MHC决定簇。后一种携带I类MHC的滋养层细胞在母体基蜕膜中最为显著,它们与母体细胞混合存在。我们的研究结果确定了两个可能与理解为何这些携带同种异体抗原的胎儿细胞不被母体排斥相关的因素:缺乏携带Ia抗原的抗原呈递细胞、巨噬细胞以及成熟的T和B淋巴细胞,以及在基蜕膜中存在大量源自母体的Thy-1⁺ 去唾液酸神经节苷脂-1⁺ CD4⁻ CD8⁻ 骨髓来源(CLA/Ly5⁺)细胞。后一种细胞对应于先前描述的可能参与局部免疫调节的颗粒化子宫内膜腺细胞。