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高糖诱导淋巴细胞中促炎细胞因子和趋化因子基因的表达:IL-17 家族基因表达的分子机制。

High glucose driven expression of pro-inflammatory cytokine and chemokine genes in lymphocytes: molecular mechanisms of IL-17 family gene expression.

机构信息

Department of Biomedical Science, Bharathidasan University, Tiruchirappalli 620 024, Tamilnadu, India.

Department of Biomedical Science, Bharathidasan University, Tiruchirappalli 620 024, Tamilnadu, India.

出版信息

Cell Signal. 2014 Mar;26(3):528-39. doi: 10.1016/j.cellsig.2013.11.031. Epub 2013 Dec 2.

Abstract

High glucose is an independent risk factor that alters the expression pattern of cytokines/chemokine leading to leukocyte activation in diabetes. Fluctuation of cytokine milieu in lymphocytes may lead to differentiation into a particular subset. Our objectives were to profile high glucose induced inflammatory gene expression in lymphocytes, to examine in vivo relevance in diabetes and to identify the key transcription factors and signaling pathways involved. Cytokine gene arrays and T-helper (Th1/Th2/Th17) cytokine profiler RT(2)-PCR arrays used for cytokine expression profiling followed by validation using Real Time-qPCR and relative RT-PCR in Jurkat T-lymphocytes, peripheral blood lymphocytes (PBLCs) from normal and diabetes subjects. Luciferase reporter plasmid, pharmacological inhibitors and mutant plasmids were used for promoter activation and signaling pathway studies. High glucose induced gene profiling in Jurkat T-lymphocytes showed significantly increased expression of 64 proinflammatory genes including IL-6 and IL-17A and most of these genes were Nuclear Factor (NF)-κB and AP-1 regulated. RT(2)-PCR array results suggested the transcriptional activation of IL-17 and its downstream signaling in Jurkat T-lymphocytes upon high glucose treatment. Candidate genes like Interleukin (IL)-17A, IL-17E IL-17F and IL-6 were up-regulated in both Jurkat T-lymphocytes and PBLCs from normal and diabetes subjects. This high glucose induced cytokine expression was due to promoter activation. Pharmacology inhibitor studies showed the involvement of NF-κB, protein kinase-C, p38 Mitogen activated protein kinase; Janus activated kinase-signal transducer and activator of transcription and extracellular regulated kinase signaling pathways. Further, high glucose treatment increased the adhesion of lymphocytes to human umbilical vein endothelial cells. These results show that IL-17 cytokines are induced by high glucose via key signaling pathways leading to lymphocyte activation and relevant to the pathogenesis of diabetic complications like atherosclerosis.

摘要

高血糖是一种独立的风险因素,它改变了细胞因子/趋化因子的表达模式,导致糖尿病患者白细胞活化。淋巴细胞中细胞因子微环境的波动可能导致其分化为特定亚群。我们的目标是分析高血糖诱导淋巴细胞中炎症基因的表达,研究其在糖尿病中的体内相关性,并确定涉及的关键转录因子和信号通路。我们使用细胞因子基因芯片和 T 辅助(Th1/Th2/Th17)细胞因子分析 RT(2)-PCR 芯片来分析细胞因子表达谱,然后使用 Jurkat T 淋巴细胞、正常和糖尿病患者的外周血淋巴细胞(PBLC)进行实时 qPCR 和相对 RT-PCR 验证。我们还使用荧光素酶报告质粒、药理学抑制剂和突变质粒进行启动子激活和信号通路研究。高葡萄糖诱导 Jurkat T 淋巴细胞基因谱显示,包括 IL-6 和 IL-17A 在内的 64 种促炎基因的表达显著增加,其中大多数基因受核因子(NF)-κB 和 AP-1 调控。RT(2)-PCR 阵列结果表明,高葡萄糖处理后 Jurkat T 淋巴细胞中 IL-17 及其下游信号的转录激活。候选基因如白细胞介素(IL)-17A、IL-17E、IL-17F 和 IL-6 在正常和糖尿病患者的 Jurkat T 淋巴细胞和 PBLC 中均上调。这种高葡萄糖诱导的细胞因子表达是由于启动子激活。药理学抑制剂研究表明,NF-κB、蛋白激酶 C、p38 丝裂原活化蛋白激酶;Janus 激活激酶-信号转导和转录激活因子和细胞外调节激酶信号通路参与其中。此外,高葡萄糖处理增加了淋巴细胞与人脐静脉内皮细胞的黏附。这些结果表明,IL-17 细胞因子通过关键信号通路被高葡萄糖诱导,导致淋巴细胞活化,并与糖尿病并发症(如动脉粥样硬化)的发病机制相关。

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