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定量评估伊朗多发性硬化症患者 CXCL8 及其受体(CXCR1 和 CXCR2)基因的表达。

Quantitative evaluation of CXCL8 and its receptors (CXCR1 and CXCR2) gene expression in Iranian patients with multiple sclerosis.

机构信息

Neurosciences Research Center, Tabriz University of Medical Sciences , Tabriz , Islamic Republic of Iran .

出版信息

Immunol Invest. 2013;42(8):737-48. doi: 10.3109/08820139.2013.812652. Epub 2013 Jul 22.

Abstract

CXCL8 and its receptors (CXCR1 and CXCR2) play important roles in CNS development, neuronal survival, modulation of excitability, and neuroimmune response. The aim of this study is to evaluate gene expression of CXCL8 and CXCR1/CXCR2 in peripheral blood cells (PBCs) of Iranian patients with relapsing remitting (RR) form of Multiple sclerosis (MS). We explored the mRNA expression of CXCL8 and its receptors in PBCs of 49 RR-MS patients in remitting status and 60 healthy controls by quantitative Real-Time PCR. Median expression of CXCL8 mRNA in peripheral blood of MS patients decreased more than 3-fold compared to control group (p < 0.001), while there were not significant differences in CXCR1 and CXCR2 gene expression between MS patients and healthy subjects (p = 0.159 and p = 0.248, respectively). There was a significant negative correlation of CXCR2 expression with EDSS (rs = -0.432, p = 0.004). It appears that decreased expression of CXCL8 may lead to a raised risk of MS.

摘要

CXCL8 及其受体(CXCR1 和 CXCR2)在中枢神经系统发育、神经元存活、兴奋性调节和神经免疫反应中发挥重要作用。本研究旨在评估 CXCL8 和 CXCR1/CXCR2 在伊朗复发缓解型多发性硬化症(RR-MS)患者外周血细胞(PBC)中的基因表达。我们通过定量实时 PCR 研究了 49 例缓解期 RR-MS 患者和 60 例健康对照者 PBC 中 CXCL8 和其受体的 mRNA 表达。与对照组相比,MS 患者外周血中 CXCL8 mRNA 的中位数表达降低了 3 倍以上(p<0.001),而 MS 患者与健康受试者之间的 CXCR1 和 CXCR2 基因表达无显著差异(p=0.159 和 p=0.248,分别)。CXCR2 表达与 EDSS 呈显著负相关(rs=-0.432,p=0.004)。CXCL8 表达降低似乎会增加 MS 的发病风险。

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