银屑病SH2结构域蛋白酪氨酸磷酸酶的激活与炎症表达

Bui Kieu Trang, Nguyen Thi Kim Lien, Nguyen Thi Xuan
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摘要

银屑病是一种慢性自身免疫性疾病,其特征是角化细胞的异常增殖和分化以及炎症细胞浸润到炎症部位。斑块型牛皮癣是最常见的牛皮癣类型,影响高达80-90%的牛皮癣病例。炎症细胞中,髓系树突状细胞或朗格汉斯细胞是银屑病发病过程中主要的活化细胞,诱导幼稚T细胞活化并分化为辅助性T细胞(Th)1和Th17细胞。含有SH2结构域的蛋白酪氨酸磷酸酶(SHP)是参与细胞分化、生长和活化的几种蛋白磷酸化的负调节因子。慢性炎症促进肿瘤进展,其特征是致癌抗原的释放,包括甲胎蛋白(AFP)和癌抗原125 (CA125)进入血液和尿液。它们是常见的肿瘤标志物,可作为癌症发展和癌症患者生存的预测因子。为此,采集103例银屑病患者和46例健康人的血液样本。定量RT-PCR检测SHP1、SHP2 mRNA表达,ELISA检测血清IL-6、TNF-α、IFN-γ、IL-17A、AFP、CA125水平。结果,与对照组相比,患者组SHP1的mRNA表达水平较高,而SHP2的水平未发生变化。重要的是,银屑病患者CA125水平高于临床临界值35U/mL为15.6%,而健康人CA125水平低于35U/mL。此外,患者组血清TNF-α和IL-17A浓度显著升高。综上所述,银屑病患者SHP1基因表达及炎症反应存在显著差异。本研究进一步提示了SHP1在银屑病患者免疫细胞活化调节中的功能作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Activation of SH2 domain-containing protein tyrosine phosphatase and inflammatory expression in psoriasis
Psoriasis is a chronic autoimmune disease characterized by abnormal proliferation and differentiation of keratinocytes and infiltration of inflammatory cells into the site of inflammation. Plaque psoriasis is the most common type of psoriasis, affecting up to 80–90% of psoriasis cases. Among inflammatory cells, myeloid dendritic cells or Langerhans cells are mainly activated cells during the pathogenesis of psoriasis to induce activation and differentiation of naive T cells into T helper cells (Th)1 and Th17 cells. SH2 domain-containing protein tyrosine phosphatase (SHP) is a negative regulator of the phosphorylation of several proteins involved in cellular differentiation, growth and activation. Chronic inflammation promotes tumor progression, which is characterized by the release of carcinogenic antigens, including alpha-fetoprotein (AFP) and cancer antigen 125 (CA125) into blood and urine. They are common tumor markers to serve as predictors of cancer development and survival of cancer patients. To this end, blood samples of 103 psoriasis patients and 46 healthy subjects were collected. The mRNA expressions of SHP1 and SHP2 were examined by using quantitative RT-PCR and the serum levels of IL-6, TNF-α, IFN-γ, IL-17A, AFP and CA125 by ELISA. As a result, the mRNA level of SHP1 was higher expressed, whereas the level of SHP2 was unaltered in the patient group compared to the control individuals. Importantly, psoriasis patients had CA125 level higher than the clinical cutoff 35U/mL was 15.6%, while healthy individuals had CA125 level lower than 35U/mL. In addition, the serum TNF-α and IL-17A concentrations were significantly increased in the patient group. In conclusion, the results indicated the significant differences in expression of SHP1 gene and inflammatory response in psoriasis patients. This study further hint for investigations on the functional role of SHP1 in regulating activation of immune cells present in psoriasis patients.
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