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人胎盘及滋养层细胞系中HLA II类相关肽转运体和蛋白酶体基因的表达

Expression of HLA class II-associated peptide transporter and proteasome genes in human placentas and trophoblast cell lines.

作者信息

Roby K F, Fei K, Yang Y, Hunt J S

机构信息

Department of Anatomy and Cell Biology, University of Kansas Medical Center, Kansas City 66160-7400.

出版信息

Immunology. 1994 Nov;83(3):444-8.

Abstract

Expression of HLA class I antigens is closely controlled in the placental trophoblast cells, which interface directly with maternal cells during pregnancy. In this study, the possibility that peptide transporter (TAP-1, TAP-2) or proteasome (LMP7) genes might be involved in regulating antigen expression in these or other cells that comprise placentas was investigated. Analysis by Northern blot hybridization showed that transcripts from all three genes were present in samples of first trimester and term placental RNA. TAP-1 and TAP-2 messages were consistently more abundant in early than in late gestation placentas, whereas the reverse was observed for LMP7 mRNA. Futher experiments were done on two trophoblast cell lines. One line, Jar, is negative for HLA class I, and the second, JEG-3, expresses HLA-G as well as other HLA class I genes. Both Jar and JEG-3 cells contained TAP-1, TAP-2 and LMP7 mRNA. With the exception of LMP7 in JEG-3 cells, message from all three genes was increased by treating the trophoblast cells with interferon-gamma. While no evidence was collected to support the postulate that the HLA class I negative status of some trophoblast cell subpopulations could be related to absent or dysfunctional TAP-1, TAP-2 or LMP7 mRNA, the data are consistent with the postulate that placental cell expression of HLA class I antigens could be influenced by the availability of peptide transporters and proteasome components.

摘要

人类白细胞抗原I类抗原(HLA class I antigens)的表达在胎盘滋养层细胞中受到严格调控,在孕期这些细胞直接与母体细胞接触。在本研究中,探讨了肽转运体(TAP - 1、TAP - 2)或蛋白酶体(LMP7)基因是否可能参与调节这些或构成胎盘的其他细胞中的抗原表达。通过Northern印迹杂交分析表明,在孕早期和足月胎盘RNA样本中均存在这三个基因的转录本。TAP - 1和TAP - 2的信使核糖核酸(mRNA)在妊娠早期胎盘样本中始终比晚期更为丰富,而LMP7 mRNA的情况则相反。对两种滋养层细胞系进行了进一步实验。一种细胞系Jar不表达HLA I类抗原,另一种JEG - 3则表达HLA - G以及其他HLA I类基因。Jar和JEG - 3细胞均含有TAP - 1、TAP - 2和LMP7 mRNA。除JEG - 3细胞中的LMP7外,用γ干扰素处理滋养层细胞后,所有这三个基因的信使核糖核酸均增加。虽然没有收集到证据支持某些滋养层细胞亚群的HLA I类抗原阴性状态可能与TAP - 1、TAP - 2或LMP7 mRNA缺失或功能异常有关这一假设,但这些数据与胎盘细胞HLA I类抗原表达可能受肽转运体和蛋白酶体成分可用性影响这一假设一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99fd/1415039/33abad963cdf/immunology00077-0119-a.jpg

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