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Qa-2抗原在小鼠植入前胚胎中的表达模式及其与Ped基因表型的相关性。

The expression pattern of the Qa-2 antigen in mouse preimplantation embryos and its correlation with the Ped gene phenotype.

作者信息

McElhinny A S, Kadow N, Warner C M

机构信息

Department of Biology, Northeastern University, Boston, MA 02115, USA.

出版信息

Mol Hum Reprod. 1998 Oct;4(10):966-71. doi: 10.1093/molehr/4.10.966.

Abstract

The Qa-2 antigen, the product of the Ped (Preimplantation embryo development) gene, is a glycosylphosphatidylinositol-linked cell surface protein encoded in the Q region of the mouse major histocompatibility complex (MHC). Ped fast (Qa-2+) mouse strains have significantly higher preimplantation embryo cleavage rates both in vivo and in vitro than Ped slow (Qa-2-) mice. In this study, we determined whether the Ped fast phenotype of blastocysts is due to an increased number of blastomeres in the trophectoderm (TE), the inner cell mass (ICM), or both. We also analysed the Ped gene expression pattern, both at the mRNA and at the protein level, in these lineages. Blastocysts were collected from the congenic mouse strains B6.K2 (Qa-2 +) and B6.K1 (Qa-2-). We performed reverse transcription-polymerase chain reaction (PCR) and Immuno-PCR and found that the Ped gene is expressed at the mRNA and protein level in whole embryos and in isolated ICM cells. Lastly, we differentially stained embryos from these strains and found that B6.K2 blastocysts had significantly higher cell numbers (P < 0.05) in both the ICM and in the TE than B6.K1 blastocysts. These results suggest that Qa-2 expression in both the TE and the ICM of blastocysts directly contributes to the Ped phenotype.

摘要

Qa-2抗原是Ped(植入前胚胎发育)基因的产物,是一种糖基磷脂酰肌醇连接的细胞表面蛋白,由小鼠主要组织相容性复合体(MHC)的Q区域编码。与Ped缓慢(Qa-2-)小鼠相比,Ped快速(Qa-2+)小鼠品系在体内和体外的植入前胚胎分裂率均显著更高。在本研究中,我们确定了囊胚的Ped快速表型是否归因于滋养外胚层(TE)、内细胞团(ICM)或两者中卵裂球数量的增加。我们还分析了这些谱系中Ped基因在mRNA和蛋白质水平上的表达模式。从同基因小鼠品系B6.K2(Qa-2+)和B6.K1(Qa-2-)收集囊胚。我们进行了逆转录聚合酶链反应(PCR)和免疫PCR,发现Ped基因在整个胚胎和分离的ICM细胞中均在mRNA和蛋白质水平上表达。最后,我们对这些品系的胚胎进行了差异染色,发现B6.K2囊胚的ICM和TE中的细胞数量均显著高于B6.K1囊胚(P<0.05)。这些结果表明,囊胚的TE和ICM中Qa-2的表达直接促成了Ped表型。

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