Apps Richard, Meng Zhaojing, Del Prete Gregory Q, Lifson Jeffrey D, Zhou Ming, Carrington Mary
Cancer and Inflammation Program, Leidos Biomedical Research, Inc., Frederick National Laboratory, Frederick, MD 21702;
Protein Characterization Laboratory, Cancer Research Technology Program, Leidos Biomedical Research, Inc., Frederick National Laboratory, Frederick, MD 21702;
J Immunol. 2015 Apr 15;194(8):3594-600. doi: 10.4049/jimmunol.1403234. Epub 2015 Mar 9.
The expression level of HLA class-I proteins is known to influence pathological outcomes: pathogens downregulate HLA to evade host immune responses, host inflammatory reactions upregulate HLA, and differences among people with regard to the steady-state expression levels of HLA associate with disease susceptibility. Yet precise quantification of relative expression levels of the various HLA loci is difficult because of the tremendous polymorphism of HLA. We report relative expression levels of HLA-A, HLA-B, HLA-C, and HLA-E proteins for the specific haplotype A02:01, B44:02, C*05:01, which were characterized using two independent methods based on flow cytometry and mass spectrometry. PBLs from normal donors showed that HLA-A and HLA-B proteins are expressed at similar levels, which are 13-18 times higher than HLA-C by flow cytometry and 4-5 times higher than HLA-C by mass spectrometry; these differences may reflect variation in the conformation or location of proteins detected. HLA-E was detected at a level 25 times lower than that of HLA-C by mass spectrometry. Primary CD4(+) T cells infected with HIV in vitro were also studied because HIV downregulates selective HLA types. HLA-A and HLA-B were reduced on HIV-infected cells by a magnitude that varied between cells in an infected culture. Averaging all infected cells from an individual showed HLA-A to be 1-3 times higher and HLA-B to be 2-5 times higher than HLA-C by flow cytometry. These results quantify substantial differences in expression levels of the proteins from different HLA loci, which are very likely physiologically significant on both uninfected and HIV-infected cells.
已知HLA-I类蛋白的表达水平会影响病理结果:病原体下调HLA以逃避宿主免疫反应,宿主炎症反应上调HLA,并且不同个体之间HLA稳态表达水平的差异与疾病易感性相关。然而,由于HLA具有巨大的多态性,精确量化各种HLA基因座的相对表达水平很困难。我们报告了特定单倍型A02:01、B44:02、C*05:01的HLA-A、HLA-B、HLA-C和HLA-E蛋白的相对表达水平,这些是使用基于流式细胞术和质谱的两种独立方法进行表征的。来自正常供体的外周血淋巴细胞显示,HLA-A和HLA-B蛋白的表达水平相似,通过流式细胞术检测,它们比HLA-C高13-18倍,通过质谱检测比HLA-C高4-5倍;这些差异可能反映了所检测蛋白质的构象或位置的变化。通过质谱检测到的HLA-E水平比HLA-C低25倍。还研究了体外感染HIV的原代CD4(+) T细胞,因为HIV会下调选择性HLA类型。在感染HIV的细胞上,HLA-A和HLA-B的降低幅度在感染培养物中的细胞之间有所不同。对来自个体的所有感染细胞进行平均显示,通过流式细胞术检测,HLA-A比HLA-C高1-3倍,HLA-B比HLA-C高2-5倍。这些结果量化了来自不同HLA基因座的蛋白质表达水平的显著差异,这在未感染和感染HIV的细胞上很可能具有生理意义。