Chen Cai-Feng, Feng Xia, Liao Hui-Yu, Jin Wen-Jing, Zhang Jian, Wang Yu, Gong Lu-Lu, Liu Jing-Jun, Yuan Xiao-Hui, Zhao Bin-Bin, Zhang Ding, Chen Guo-Feng, Wan Ying, Guo Jian, Yan Hui-Ping, He You-Wen
1] MOH Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences &Peking Union Medical College, Beijing, People's Republic of China [2].
1] Center for Infection and Immunity, YouAn Hospital, The Beijing Capital Medical University, Beijing, China [2].
Sci Rep. 2014 Sep 15;4:6359. doi: 10.1038/srep06359.
T cell functional exhaustion during chronic hepatitis B virus (HBV) infection may contribute to the failed viral clearance; however, the underlying molecular mechanisms remain largely unknown. Here we demonstrate that jumonji domain-containing protein 6 (JMJD6) is a potential regulator of T cell proliferation during chronic HBV infection. The expression of JMJD6 was reduced in T lymphocytes in chronic hepatitis B (CHB) patients, and this reduction in JMJD6 expression was associated with impaired T cell proliferation. Moreover, silencing JMJD6 expression in primary human T cells impaired T cell proliferation. We found that JMJD6 promotes T cell proliferation by suppressing the mRNA expression of CDKN3. Furthermore, we have identified platelet derived growth factor-BB (PDGF-BB) as a regulator of JMJD6 expression. PDGF-BB downregulates JMJD6 expression and inhibits the proliferation of human primary T cells. Importantly, the expression levels of JMJD6 and PDGF-BB in lymphocytes from CHB patients were correlated with the degree of liver damage and the outcome of chronic HBV infection treatment. Our results demonstrate that PDGF-BB and JMJD6 regulate T cell function during chronic HBV infection and may provide insights for the treatment strategies for CHB patients.
慢性乙型肝炎病毒(HBV)感染期间T细胞功能耗竭可能导致病毒清除失败;然而,其潜在的分子机制仍 largely未知。在此,我们证明含jumonji结构域蛋白6(JMJD6)是慢性HBV感染期间T细胞增殖的潜在调节因子。慢性乙型肝炎(CHB)患者T淋巴细胞中JMJD6的表达降低,且JMJD6表达的这种降低与T细胞增殖受损相关。此外,在原代人T细胞中沉默JMJD6表达会损害T细胞增殖。我们发现JMJD6通过抑制CDKN3的mRNA表达促进T细胞增殖。此外,我们已确定血小板衍生生长因子-BB(PDGF-BB)是JMJD6表达的调节因子。PDGF-BB下调JMJD6表达并抑制人原代T细胞的增殖。重要的是,CHB患者淋巴细胞中JMJD6和PDGF-BB的表达水平与肝损伤程度及慢性HBV感染治疗结果相关。我们的结果表明,PDGF-BB和JMJD6在慢性HBV感染期间调节T细胞功能,并可能为CHB患者的治疗策略提供见解。