UBASH3A和TIGIT基因在系统性硬化症中的表达水平。

Q3 Medicine
Aml A R Mohammed, Fatma S Abd-Elsamea, Maha S I Abdelrahman, Fatma M A Mohamed, Fatma Y A Abbas, Fatma M Helbawi
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引用次数: 0

摘要

系统性硬化症(SSc)是一种以过度纤维化、微血管狭窄和全身性临床表现为特征的自身免疫性疾病。自身免疫过程被认为可诱导T细胞活化,主要是cd4 T辅助细胞,并增强促炎和促纤维化细胞因子如白细胞介素(IL) 4和IL 13的产生。这些细胞因子有助于血管病变和过多的胶原合成。UBASH3a (Ubiquitin Associated and SH3 Domain Containing A)和TIGIT (T细胞免疫球蛋白和ITIM结构域)在限制不必要的T细胞激活和维持免疫耐受方面具有重要作用。我们的研究旨在探讨30名SSc患者与30名年龄和性别匹配的正常对照组的UBASH3A和TIGIT mRNA表达水平。我们通过实时定量逆转录聚合酶链反应检测从SSc患者和对照组外周血单个核细胞(PBMCs)中分离的总RNA的mRNA水平。我们使用RNA提取商用试剂盒。与对照组相比,SSc患者外周血中UBASH3A和TIGIT mRNA的表达水平显著升高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
UBASH3A and TIGIT genes expression levels in systemic sclerosis.

Systemic sclerosis (SSc) is an autoimmune disorder marked by excessive fibrosis, microvascular stenosis, and systemic clinical manifestations. An autoimmune process is believed to induce T-cell activation, mainly CD 4 T helper cells, and enhance production of proinflammatory and profibrotic cytokines such as interleukin (IL) 4 and IL 13. These cytokines contribute to vasculopathy and excessive collagen synthesis. UBASH3a (Ubiquitin Associated and SH3 Domain Containing A) and TIGIT (T cell immunoglobulin and ITIM domain) have an important role in limiting unwarranted T cell activation and maintaining immune tolerance. Our study aimed to explore UBASH3A and TIGIT mRNA expression levels in 30 SSc patients compared to 30 age and sex matched normal controls. We measured mRNA levels via real-time quantitative reverse transcription polymerase chain reaction in total RNA isolated from the peripheral blood mononuclear cells (PBMCs) of SSc patients and controls. We used RNA extraction commercial kits. The expression levels of UBASH3A and TIGIT mRNA were significantly higher in PBMCs from SSc patients compared to control subjects.

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CiteScore
1.20
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发文量
52
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