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首页> 外文期刊>Acta Histochemica: Zeitschrift fur Histologische Topochemie >Expression and localization analyses of the cholinergic anti-inflammatory pathway and a7nAchR in different tissues of rats with rheumatoid arthritis
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Expression and localization analyses of the cholinergic anti-inflammatory pathway and a7nAchR in different tissues of rats with rheumatoid arthritis

机译:类风湿性关节炎大鼠不同组织中胆碱能抗炎途径和A7NACHR的表达及定位分析

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Rheumatoid arthritis (RA) is a complicated chronic multisystem autoimmune disease, wherein the inflammatory cascade leads to vasospasm and osteoclastogenesis, which ultimately results in bone and cartilage destruction. In this study, we investigated the expression and localization of the alpha-7 nicotinic receptor (a7nAchR) gene CHRNA7 in the heart, liver, spleen, lung, kidney, and joints of the collagen-induced arthritis (CIA) rat model. The CHRNA7 mRNA and protein expression levels in these tissues of rats from CIA and normal groups were analyzed via real-time quantitative polymerase chain reaction (RT-qPCR) and western blotting, respectively. The cellular localization of CHRNA7 protein was determined via immunohistochemistry (IHC) assays. CHRNA7 was expressed at varying levels in different tissues of rats from the groups, among which joints showed significantly higher CHRNA7 expression levels than other tissues (P < 0.05). CIA rats had significantly higher CHRNA7 expression levels in the spleen and joints than the control group rats (P < 0.05). Positive expression signals for CHRNA7 were detected in various tissues of CIA and control group rats, among which strong positive signals were detected in joint fibroblast-like synoviocytes (FLSs), endothelial cells, stromal cells, and macrophages. Our results further confirmed the involvement of the CAP in the onset and development of inflammatory responses in RA, suggesting that CHRNA7 may be a new therapeutic target for RA. This study is of great clinical and theoretical significance for understanding the differential expression of CHRNA7 in various tissues and cholinergic anti-inflammatory pathway (CAP)-targeted treatment of RA.
机译:类风湿性关节炎(RA)是一种复杂的慢性多系统自身免疫疾病,其中炎症级联导致血管痉挛和骨质细胞发生,这最终导致骨和软骨破坏。在这项研究中,我们研究了胶原诱导的关节炎(CIA)大鼠模型的心脏,肝,脾,肺,肾脏和关节中α-7烟碱受体(A7NACHR)基因ChrNA7的表达和定位。通过实时定量聚合酶链反应(RT-QPCR)和Western印迹分析来自CIA和正常组的这些组织中的这些组织中的ChrNA7 mRNA和蛋白表达水平。通过免疫组织化学(IHC)测定法测定CHRNA7蛋白的细胞定位。 ChrNA7在来自组的大鼠的不同组织中的不同水平表达,其中关节显示比其他组织显着更高的ChRNA7表达水平(P <0.05)。 CIA大鼠在脾脏和关节中具有显着高于对照组大鼠的表达水平(P <0.05)。在CIA和对照组大鼠的各种组织中检测CHRNA7的阳性表达信号,其中在联合成纤维细胞样Synoviocytes(FLS),内皮细胞,基质细胞和巨噬细胞中检测到强阳性信号。我们的结果进一步证实了CAP参与RA中炎症反应的发作和开发,表明CHRNA7可能是RA的新治疗靶标。本研究具有巨大的临床和理论意义,用于了解ChrNA7在各种组织中ChrNA7的差异表达和胆碱能抗炎途径(帽) - RA治疗RA。

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