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子痫前期患者血清可溶性 Gp130 和白细胞介素-6 水平升高,Gp130 和 SOCS-3 表达降低。

Elevated maternal soluble Gp130 and IL-6 levels and reduced Gp130 and SOCS-3 expressions in women complicated with preeclampsia.

机构信息

Department of Obstetrics and Gynecology, LSUHSC-Shreveport, Shreveport, LA 71130, USA.

出版信息

Hypertension. 2011 Feb;57(2):336-42. doi: 10.1161/HYPERTENSIONAHA.110.163360. Epub 2010 Dec 20.

Abstract

Increased inflammatory response plays a significant role in the vascular pathophysiology in preeclampsia. However, the mechanism for increased inflammatory response in preeclampsia is largely unknown. Interleukin (IL)-6 levels are elevated in women with preeclampsia. IL-6 and its receptors, IL-6R and glycoprotein (gp)130, play a critical role in mediating antiinflammatory response via induction of SOCS-3 (suppressor of cytokine signaling-3). However, IL-6 receptor levels and expressions have not been studied in preeclampsia. In this study, we measured IL-6 and its 2 soluble receptors, soluble IL-6R and soluble gp130, in maternal plasma from normal and preeclamptic pregnant women and found that not only IL-6 but also soluble gp130 levels were significantly higher in preeclamptic women than in normotensive pregnant controls. We further examined IL-6R, gp130, and SOCS-3 expressions in maternal vessels and leukocytes and found that gp130 and SOCS-3 expressions were downregulated in both vessel endothelium and leukocytes from preeclampsia. Different patterns for IL-6R and gp130 expressions were found. IL-6R expression was also downregulated in leukocytes from preeclampsia. Our results suggest that increased plasma soluble gp130/soluble IL-6R/IL-6 ratio and reduced membrane transsignaling gp130 expression could contribute to decreased SOCS-3 expression and subsequent reduction in SOCS-3 antiinflammatory activity in women with preeclampsia. Thus, reduced gp130 and SOCS-3 expressions may offer, at least in part, a plausible explanation of reduced antiinflammatory protection in the maternal vascular system in preeclampsia.

摘要

在子痫前期中,炎症反应的增强在血管病理生理学中起着重要作用。然而,子痫前期中炎症反应增强的机制在很大程度上尚不清楚。白细胞介素(IL)-6 水平在子痫前期妇女中升高。IL-6 及其受体 IL-6R 和糖蛋白(gp)130 通过诱导 SOCS-3(细胞因子信号转导抑制剂-3)在介导抗炎反应中发挥关键作用。然而,尚未研究过子痫前期中的 IL-6 受体水平和表达。在这项研究中,我们测量了正常和子痫前期孕妇的母血浆中的 IL-6 及其 2 种可溶性受体,可溶性 IL-6R 和可溶性 gp130,并发现不仅 IL-6,而且可溶性 gp130 水平在子痫前期妇女中均显著高于正常血压孕妇对照组。我们进一步检查了母血管和白细胞中的 IL-6R、gp130 和 SOCS-3 的表达,发现 gp130 和 SOCS-3 的表达在子痫前期的血管内皮细胞和白细胞中均下调。发现 IL-6R 和 gp130 的表达模式不同。子痫前期的白细胞中 IL-6R 的表达也下调。我们的结果表明,增加的血浆可溶性 gp130/可溶性 IL-6R/IL-6 比值和减少的膜转导 gp130 表达可能导致 SOCS-3 表达减少,随后 SOCS-3 抗炎活性降低,这可能与子痫前期妇女的抗炎保护作用降低有关。因此,gp130 和 SOCS-3 的表达减少至少部分解释了子痫前期母体血管系统抗炎保护作用的降低。

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