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T抗原抑制胚胎癌细胞来源的类胚体的着床。

T-Ag inhibits implantation by EC cell derived embryoid bodies.

作者信息

Espinosa A, Villarreal L P

机构信息

Department of Molecular Biology and Biochemistry, University of California, Irvine, USA.

出版信息

Virus Genes. 2000;20(3):195-200. doi: 10.1023/a:1008139126041.

Abstract

When introduced into EC cells of a blastocyst, polyomavirus (Py) T-Ag results in mice mosaic for T-Ag but otherwise essentially normal. It had been reported that SV40 T-Ag does not inhibit differentiation of F9 EC cells, but did inhibit endogenous retrovirus (ERV) production. We therefore sought to determine if Py T-Ag had any affect on EC derived embryoid body implantation onto mouse placenta. F9 EC cells were selected for T-Ag maintenance. Like the SV40 transformed cells, we show that these Py T-Ag selected EC cells no longer express IAP transcripts following differentiation into embryoid bodies. Normal and Py T-Ag selected F9 cells were differentiated into embryoid bodies then implanted into pseudopregnant mice. We observe, that normal F9 derived embryoid bodies underwent the initial stages of implantation whereas the Py T-Ag selected embryoid bodied did not implant. The implications of this observation with respect to trophectoderm and ERV function are discussed. We examine the idea that ERVs may be a required element for normal embryo implantation.

摘要

将多瘤病毒(Py)T抗原导入囊胚的内细胞团(EC)细胞后,会产生T抗原镶嵌的小鼠,但其他方面基本正常。据报道,SV40 T抗原不抑制F9 EC细胞的分化,但会抑制内源性逆转录病毒(ERV)的产生。因此,我们试图确定Py T抗原是否对源自EC的胚状体植入小鼠胎盘有任何影响。选择F9 EC细胞来维持T抗原表达。与SV40转化细胞一样,我们发现这些经Py T抗原选择的EC细胞在分化为胚状体后不再表达IAP转录本。将正常的和经Py T抗原选择的F9细胞分化为胚状体,然后植入假孕小鼠体内。我们观察到,源自正常F9的胚状体经历了植入的初始阶段,而经Py T抗原选择的胚状体则没有植入。讨论了这一观察结果对滋养外胚层和ERV功能的影响。我们探讨了ERV可能是正常胚胎植入所需元素的观点。

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