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慢性肾病中,单核细胞中SOCS3表达增加以及淋巴细胞中SOCS1表达增加与肾功能的进行性丧失和心血管危险因素相关。

Increased expression of SOCS3 in monocytes and SOCS1 in lymphocytes correlates with progressive loss of renal function and cardiovascular risk factors in chronic kidney disease.

作者信息

Rastmanesh M Mehdi, Bluyssen Hans A R, Joles Jaap A, Boer Peter, Willekes Nel, Braam Branko

机构信息

Department of Nephrology and Hypertension, University Medical Center Utrecht, The Netherlands.

出版信息

Eur J Pharmacol. 2008 Sep 28;593(1-3):99-104. doi: 10.1016/j.ejphar.2008.07.013. Epub 2008 Jul 12.

Abstract

Inflammation, an independent cardiovascular disease risk factor is common in patients with chronic kidney disease. Suppressors of cytokine signaling (SOCS) are induced by cytokines in a variety of cells and modulate inflammatory responses. We hypothesized that in chronic kidney disease, SOCS expression in peripheral blood mononuclear cells is increased, and related to inflammation and renal function. We also tested correlations between SOCS expression and biomarkers and risk factors of cardiovascular disease. Whether monocytes and lymphocytes differentially respond to interleukin-6 (IL-6) was tested ex vivo. Monocytes and lymphocytes were isolated from peripheral blood of chronic kidney disease patients (n=9) and controls (n=11). In three other healthy subjects, whole blood was incubated with IL-6 before cell isolation. SOCS expression was assessed by real-time quantitative PCR. Plasma cytokines were measured as well as pulse wave velocity. SOCS3 expression was increased in monocytes and SOCS1 in lymphocytes along with increased plasma levels of IL-6 and tumor necrosis factor-alpha (TNFalpha) in chronic kidney disease patients. While monocyte SOCS3 correlated with glomerular filtration rate, urea and diastolic blood pressure, lymphocyte SOCS1 correlated with TNFalpha, pulse wave velocity and systolic blood pressure. IL-6 stimulation of whole blood caused expression of different SOCS genes in monocytes and lymphocytes. Increased expression of SOCS3 in monocytes versus SOCS1 in lymphocytes coincided with elevated plasma levels of IL-6 and TNFalpha, suggesting that these cell types process the uremic milieu differently. This could reflect cell-specific responses to inflammation, as supported by our ex vivo study. Moreover, increased SOCS expression in peripheral blood mononuclear cells correlated with decreased renal function. Since chronic kidney disease predisposes to cardiovascular disease, we speculate that increased SOCS expression in peripheral blood mononuclear cells could be a new marker of cardiovascular disease in chronic kidney disease patients.

摘要

炎症作为一种独立的心血管疾病风险因素,在慢性肾脏病患者中很常见。细胞因子信号转导抑制因子(SOCS)由多种细胞中的细胞因子诱导产生,并调节炎症反应。我们推测,在慢性肾脏病中,外周血单核细胞中SOCS的表达会增加,且与炎症和肾功能相关。我们还检测了SOCS表达与心血管疾病生物标志物及风险因素之间的相关性。体外实验检测了单核细胞和淋巴细胞对白细胞介素-6(IL-6)的反应是否存在差异。从慢性肾脏病患者(n = 9)和对照组(n = 11)的外周血中分离出单核细胞和淋巴细胞。在另外三名健康受试者中,细胞分离前将全血与IL-6一起孵育。通过实时定量PCR评估SOCS表达。检测血浆细胞因子以及脉搏波速度。慢性肾脏病患者的单核细胞中SOCS3表达增加,淋巴细胞中SOCS1表达增加,同时血浆中IL-6和肿瘤坏死因子-α(TNFα)水平升高。单核细胞SOCS3与肾小球滤过率、尿素和舒张压相关,而淋巴细胞SOCS1与TNFα、脉搏波速度和收缩压相关。IL-6刺激全血导致单核细胞和淋巴细胞中不同SOCS基因的表达。与淋巴细胞中的SOCS1相比,单核细胞中SOCS3表达增加与血浆中IL-6和TNFα水平升高一致,表明这些细胞类型对尿毒症环境的处理方式不同。正如我们的体外研究所支持的,这可能反映了细胞对炎症的特异性反应。此外,外周血单核细胞中SOCS表达增加与肾功能下降相关。由于慢性肾脏病易引发心血管疾病,我们推测外周血单核细胞中SOCS表达增加可能是慢性肾脏病患者心血管疾病的一个新标志物。

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