Jurisicova A, Casper R F, MacLusky N J, Mills G B, Librach C L
Department of Obstetrics and Gynecology, Toronto Hospital Research Institute, ON, Canada.
Proc Natl Acad Sci U S A. 1996 Jan 9;93(1):161-5. doi: 10.1073/pnas.93.1.161.
HLA-G is a nonclassical class I major histocompatibility complex molecule with a restricted pattern of expression that includes the placental extravillus cytotrophoblast cells in direct contact with maternal tissues. Circumstantial evidence suggests that HLA-G may play a role in protection of the semiallogeneic human fetus. We examined whether HLA-G is expressed during the critical period of preimplantation human development and whether expression of this molecule could be correlated with the cleavage rate of embryos. Using reverse transcription PCR on surplus human embryos and unfertilized oocytes from patients undergoing in vitro fertilization we detected HLA-G heavy chain mRNA in 40% of 148 of blastocysts tested. The presence of HLA-G mRNA was also detected in unfertilized oocytes and in early embryos, but not in control cumulus oophorus cells. beta 2-Microglobulin mRNA was also found in those embryos expressing HLA-G. In concordance with our mRNA data, a similar proportion of embryos stained positive for HLA-G utilizing a specific monoclonal antibody. Interestingly, expression of HLA-G mRNA was associated with an increased cleavage rate, as compared to embryos lacking HLA-G transcript. Thus, HLA-G could be a functional homologue of the mouse Qa-2 antigen, which has been implicated in differences in the rate of preimplantation embryo development. To our knowledge, the presence of HLA-G mRNA and protein in human preimplantation embryos and oocytes has not been reported previously. The correlation of HLA-G mRNA expression with cleavage rate suggests that this molecule may play an important role in human pre-embryo development.
HLA - G是一种非经典的I类主要组织相容性复合体分子,其表达模式受限,包括与母体组织直接接触的胎盘绒毛外细胞滋养层细胞。间接证据表明,HLA - G可能在保护半同种异体人类胎儿中发挥作用。我们研究了HLA - G在人类植入前发育的关键时期是否表达,以及该分子的表达是否与胚胎的分裂率相关。通过对接受体外受精患者的多余人类胚胎和未受精卵母细胞进行逆转录PCR,我们在148个测试囊胚中的40%检测到了HLA - G重链mRNA。在未受精卵母细胞和早期胚胎中也检测到了HLA - G mRNA的存在,但在对照卵丘细胞中未检测到。在那些表达HLA - G的胚胎中也发现了β2 -微球蛋白mRNA。与我们的mRNA数据一致,利用特异性单克隆抗体检测到相似比例的胚胎HLA - G染色呈阳性。有趣的是,与缺乏HLA - G转录本的胚胎相比,HLA - G mRNA的表达与分裂率增加相关。因此,HLA - G可能是小鼠Qa - 2抗原的功能同源物,后者与植入前胚胎发育速率的差异有关。据我们所知,此前尚未报道过人类植入前胚胎和卵母细胞中存在HLA - G mRNA和蛋白质。HLA - G mRNA表达与分裂率的相关性表明,该分子可能在人类胚胎前期发育中发挥重要作用。