首页> 美国卫生研究院文献>The British Journal of Ophthalmology >Intraocular production of a cytokine (CINC) responsible for neutrophil infiltration in endotoxin induced uveitis.
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Intraocular production of a cytokine (CINC) responsible for neutrophil infiltration in endotoxin induced uveitis.

机译:眼内产生细胞因子(CINC)导致内毒素诱导的葡萄膜炎中性粒细胞浸润。

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摘要

AIMS/BACKGROUND: The subcutaneous injection of bacterial endotoxin in Lewis rats produces an acute intraocular inflammation evolving over a 24 hour period. This endotoxin induced uveitis (EIU) is characterised by a biphasic protein exudation and a cellular infiltrate composed of macrophages and polymorphonuclear neutrophils (PMNs). This model was used to study the mechanism of cellular infiltration in ocular inflammation. METHODS: EIU was induced by a subcutaneous injection of lipopolysaccharide (LPS) (S typhimurium) at 350 micrograms/kg. The levels of cytokine induced neutrophil chemoattractant (CINC) were measured every 2 hours in the serum and in the aqueous humour by ELISA. The intraocular inflammation was quantified by protein measurement and leucocyte counting. RESULTS: The kinetics of CINC production in the systemic circulation showed a rapid rise, peaking 2 hours after LPS injection, followed by a progressive decline over the next 8 hours. In the eye, the CINC levels increased above the serum levels 10 hours after EIU induction corresponding to the time of cellular infiltration. When leucocyte entry in the eye was inhibited by 56% and 64% with an antiadhesion molecule antibody, there was only a slight reduction in the aqueous humour CINC levels of 9% and 16%, respectively, indicating that CINC was produced by ocular tissue cells. The specific effect of CINC in the eye was confirmed when a direct intraocular injection of 250 ng of purified CINC was followed by significant PMN infiltration, in the absence of protein exudation. CONCLUSION: The data indicate that the production of the CINC chemotactic factor by ocular tissue participates in the inflammatory reaction in EIU.
机译:目的/背景:在Lewis大鼠中皮下注射细菌内毒素会在24小时内产生急性眼内炎症。这种内毒素诱发的葡萄膜炎(EIU)的特征是双相蛋白渗出和由巨噬细胞和多形核中性粒细胞(PMN)组成的细胞浸润。该模型用于研究眼部炎症中细胞浸润的机制。方法:通过皮下注射脂多糖(LPS)(鼠伤寒沙门氏菌)350微克/公斤诱导EIU。每两小时在血清和房水中通过ELISA测量细胞因子诱导的中性粒细胞趋化剂(CINC)的水平。通过蛋白质测量和白细胞计数来量化眼内炎症。结果:系统性循环中CINC产生的动力学显示出快速上升,在LPS注射后2小时达到峰值,然后在接下来的8小时内逐渐下降。在眼睛中,对应于细胞浸润的时间,EIU诱导后10小时,CINC水平升高至高于血清水平。当抗粘附分子抗体抑制白细胞进入眼内56%和64%时,房水CINC的水平仅分别略微降低了9%和16%,这表明CINC是由眼组织细胞产生的。当直接眼内注射250 ng纯化的CINC,然后在无蛋白质渗出的情况下,PMN明显浸润,从而证实了CINC对眼睛的特异性作用。结论:数据表明眼组织产生CINC趋化因子参与了EIU的炎症反应。

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