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视网膜母细胞瘤蛋白对非小细胞肺癌细胞中HLA II类信使RNA干扰素-γ诱导性的凋亡非依赖性挽救。缺乏与HLA-DRA诱导的特定缺陷相关的表面II类表达。

Apoptosis-independent retinoblastoma protein rescue of HLA class II messenger RNA IFN-gamma inducibility in non-small cell lung carcinoma cells. Lack of surface class II expression associated with a specific defect in HLA-DRA induction.

作者信息

Lu Y, Boss J M, Hu S X, Xu H J, Blanck G

机构信息

Department of Biochemistry and Molecular Biology, University of South Florida College of Medicine, Tampa, 33612, USA.

出版信息

J Immunol. 1996 Apr 1;156(7):2495-502.

PMID:8786310
Abstract

Work from our laboratory indicates that HLA class II induction by IFN- gamma in the retinoblastoma (RB) protein-defective breast carcinoma line MDA-468-S4 (S4) requires reconstitution of functional RB. To determine whether RB is required for HLA class 11 expression in multiple tumor types, the RB-defective non-small cell lung carcinoma line H2009 and its RB-reconstituted subclones were examined for class II inducibility. Surface HLA-DR (DR) was not inducible by IFN-gamma in H2009. However, unlike the RB-reconstituted subclones of S4, DR surface expression was not detected in the H2009 RB-positive subclones. IFN-gamma induction of CIITA, a major regulator of class II transcription, suggested that H2009 retained at least part of the IFN-gamma signaling pathway leading to class II expression. Examination of class II mRNA indicated that IFN-gamma induction of RB was rescued in the RB-positive subclones of H2009, confirming the requirement for RB for HLA class II inducibility and revealing that RB is required for inducibility in developmentally distinct tumor types. However, DRA inducibility was not rescued in the H2009 RB-positive subclones, which explained the lack of surface DR induction in the RB-positive H2009 subclones. DPA and DPB were also only weakly inducible in the RB-reconstituted H2009 subclones, compared with the previously described, S4 RB-positive subclones. Finally, data reported here indicates that RB's ability to inhibit IFN-gamma-induced apoptosis is not a viable explanation for why RB expression rescues DRB inducibility in H2009.

摘要

我们实验室的研究表明,在视网膜母细胞瘤(RB)蛋白缺陷的乳腺癌细胞系MDA - 468 - S4(S4)中,γ干扰素诱导的HLA - II类分子表达需要功能性RB的重建。为了确定RB是否是多种肿瘤类型中HLA - I类分子表达所必需的,我们检测了RB缺陷的非小细胞肺癌细胞系H2009及其RB重建的亚克隆的II类分子诱导能力。在H2009中,γ干扰素不能诱导表面HLA - DR(DR)表达。然而,与S4的RB重建亚克隆不同,在H2009的RB阳性亚克隆中未检测到DR表面表达。II类转录的主要调节因子CIITA的γ干扰素诱导表明,H2009至少保留了部分导致II类分子表达的γ干扰素信号通路。对II类分子mRNA的检测表明,在H2009的RB阳性亚克隆中,γ干扰素对RB的诱导作用得到了恢复,这证实了RB对HLA - II类分子诱导的必要性,并揭示了RB在发育上不同的肿瘤类型中对诱导的必要性。然而,在H2009的RB阳性亚克隆中,DRA的诱导作用没有得到恢复,这解释了RB阳性的H2009亚克隆中表面DR诱导缺失的原因。与先前描述的S4 RB阳性亚克隆相比,DPA和DPB在RB重建的H2009亚克隆中也只是弱诱导。最后,本文报道的数据表明,RB抑制γ干扰素诱导的细胞凋亡的能力并不是RB表达挽救HLO09中DRB诱导能力的可行解释。

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