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本文引用的文献

1
Altered interleukin-6 receptor, IL-6R and gp130, production and expression and decreased SOCS-3 expression in placentas from women with pre-eclampsia.子痫前期女性胎盘白细胞介素-6受体(IL-6R)、糖蛋白130(gp130)的产生和表达发生改变,且细胞因子信号转导抑制因子3(SOCS-3)表达降低。
Placenta. 2008 Dec;29(12):1024-8. doi: 10.1016/j.placenta.2008.09.011. Epub 2008 Nov 5.
2
sIL-6R: more than an agonist?可溶性白细胞介素-6受体:仅是一种激动剂吗?
Immunol Cell Biol. 2008 Jan;86(1):87-91. doi: 10.1038/sj.icb.7100113. Epub 2007 Aug 28.
3
Apoptosis is a natural stimulus of IL6R shedding and contributes to the proinflammatory trans-signaling function of neutrophils.细胞凋亡是白细胞介素6受体脱落的自然刺激因素,并有助于中性粒细胞的促炎转信号传导功能。
Blood. 2007 Sep 15;110(6):1748-55. doi: 10.1182/blood-2007-01-067918. Epub 2007 Jun 13.
4
Preeclampsia, insulin signalling and immunological dysfunction: a fetal, maternal or placental disorder?子痫前期、胰岛素信号传导与免疫功能障碍:是胎儿、母体还是胎盘疾病?
J Reprod Immunol. 2007 Dec;76(1-2):78-84. doi: 10.1016/j.jri.2007.03.019. Epub 2007 May 29.
5
Increased leukocyte adhesion to vascular endothelium in preeclampsia is inhibited by antioxidants.子痫前期中白细胞与血管内皮细胞粘附增加的现象可被抗氧化剂抑制。
Am J Obstet Gynecol. 2007 Apr;196(4):400.e1-7; discussion 400.e7-8. doi: 10.1016/j.ajog.2006.12.023.
6
Activation of NF-kappaB and expression of COX-2 in association with neutrophil infiltration in systemic vascular tissue of women with preeclampsia.子痫前期女性全身血管组织中NF-κB的激活及COX-2的表达与中性粒细胞浸润的关系
Am J Obstet Gynecol. 2007 Jan;196(1):48.e1-8. doi: 10.1016/j.ajog.2006.08.038.
7
Shed membrane particles from preeclamptic women generate vascular wall inflammation and blunt vascular contractility.先兆子痫女性的脱落膜颗粒会引发血管壁炎症并削弱血管收缩能力。
Am J Pathol. 2006 Oct;169(4):1473-83. doi: 10.2353/ajpath.2006.051304.
8
Inflammation and pre-eclampsia.炎症与子痫前期。
Semin Fetal Neonatal Med. 2006 Oct;11(5):309-16. doi: 10.1016/j.siny.2006.04.001. Epub 2006 Jul 7.
9
Divergent mechanisms utilized by SOCS3 to mediate interleukin-10 inhibition of tumor necrosis factor alpha and nitric oxide production by macrophages.细胞因子信号转导抑制因子3(SOCS3)利用不同机制介导白细胞介素-10对巨噬细胞产生肿瘤坏死因子α和一氧化氮的抑制作用。
J Biol Chem. 2006 Mar 10;281(10):6316-24. doi: 10.1074/jbc.M508608200. Epub 2005 Dec 12.
10
IL-6 transsignaling: the in vivo consequences.白细胞介素-6转信号传导:体内后果
J Interferon Cytokine Res. 2005 May;25(5):241-53. doi: 10.1089/jir.2005.25.241.

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.

DOI:10.1161/HYPERTENSIONAHA.110.163360
PMID:21173340
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3062273/
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。