MHC Class I Heavy Chain mRNA Must Exceed a Threshold Level for the Reconstitution of Cell Surface Expression of Class I MHC Complexes in Cells Transformed by the Highly Oncogenic Adenovirus 12

MHC I级 与抗原处理相关的转运体 生物 主要组织相容性复合体 分子生物学 细胞毒性T细胞 转基因 细胞 基因 转染 基因表达 细胞生物学 体外 遗传学
作者
Sharon Vigodman Fromm,Sigal Winograd Mey-Tal,John E. Coligan,Chana Schechter,Rachel Ehrlich
出处
期刊:Journal of Biological Chemistry [Elsevier BV]
卷期号:273 (24): 15209-15216 被引量:9
标识
DOI:10.1074/jbc.273.24.15209
摘要

In primary embryonal fibroblasts from transgenic mice expressing H-2(b) genes and a miniature swine class I transgene (PD1), transformation with adenovirus 12 results in suppression of assembly and cell surface expression of all class I complexes. Cell surface expression of PD1 can be recovered by transfecting the cells with peptide transporter genes. However, reconstitution of the H-2Kb gene expression requires, in addition, a 2-fold increase in the steady state level of the H-2Kb mRNA that can be attained by treatment of the cells with interferons or by transfecting them with the H-2Kb gene. A detailed analyses of the biogenesis of class I molecules has revealed the steady state expression of free class I heavy chains that are not converted into conformed complexes even when peptide transporter genes are overexpressed. The fact that class I complex assembly seems to be highly inefficient in certain cell lines might be a major in vivo obstacle for the elimination of transformed or virus-infected cells by cytotoxic T lymphocytes, especially in view of the fact that the level of class I gene transcription is often down-regulated in cancer cells and/or that assembly of class I major histocompatibility complexes can be subverted by virus-encoded proteins.
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