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联合阻断 VEGFR-2 和 VEGFR-3 可抑制早期和中期的炎症性淋巴管生成。

Combined blockade of VEGFR-2 and VEGFR-3 inhibits inflammatory lymphangiogenesis in early and middle stages.

机构信息

Center of Eye Disease and Development, Program in Vision Science, and School of Optometry, University of California, Berkeley, CA 94720, USA.

出版信息

Invest Ophthalmol Vis Sci. 2011 Apr 20;52(5):2593-7. doi: 10.1167/iovs.10-6408.

Abstract

PURPOSE

Lymphangiogenesis (LG) accompanies many corneal diseases after inflammatory, infectious, or chemical insults and is a primary mediator of transplant rejection. The purpose of this study was to investigate whether there is a time window for therapeutic intervention of corneal LG and whether a combined blockade of VEGFR-2 and VEGFR-3 effectively suppresses early-, middle-, or late-stage LG.

METHODS

Corneal inflammatory neovascularization was induced by a standard suture placement model in mice. Neutralizing antibodies against VEGFR-3 and/or VEGFR-2 were administrated systemically with the treatment started at postoperative day 0, day 7, or day 14. Whole mount corneas were sampled for immunofluorescence microscopic studies using LYVE-1 (a lymphatic marker) antibodies. Digital images were analyzed by software.

RESULTS

Both VEGFR-3 and VEGFR-2 were involved in corneal suture-induced inflammatory LG. Their combined blockade led to a significant inhibition of both early- and middle-stage LG while demonstrating no effect on late-stage LG.

CONCLUSIONS

Corneal inflammatory LG has a discrete time window for intervention therapy. Although it is important to start the treatment as soon as possible, interventions initiated in the middle of the LG process are still effective. These novel findings will shed some light on our understanding of inflammatory LG and the development of new therapeutic protocols for LG-related diseases at different stages.

摘要

目的

淋巴管生成(LG)伴随着许多角膜疾病,如炎症、感染或化学刺激后,并作为移植排斥的主要介质。本研究旨在探讨是否存在治疗性干预角膜 LG 的时间窗,以及联合阻断 VEGFR-2 和 VEGFR-3 是否能有效抑制早期、中期或晚期 LG。

方法

通过在小鼠中标准缝线放置模型诱导角膜炎症性新生血管形成。在术后第 0、7 或 14 天开始全身性给予针对 VEGFR-3 和/或 VEGFR-2 的中和抗体。使用 LYVE-1(淋巴管标记物)抗体对整个角膜进行免疫荧光显微镜研究的标本采样。通过软件对数字图像进行分析。

结果

VEGFR-3 和 VEGFR-2 均参与了角膜缝线诱导的炎症性 LG。它们的联合阻断导致早期和中期 LG 显著抑制,而对晚期 LG 无影响。

结论

角膜炎症性 LG 具有干预治疗的离散时间窗。尽管尽早开始治疗很重要,但在 LG 过程的中期开始干预仍然有效。这些新发现将为我们理解炎症性 LG 以及在不同阶段为 LG 相关疾病开发新的治疗方案提供一些启示。

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Invest Ophthalmol Vis Sci. 2011 Jan 21;52(1):334-8. doi: 10.1167/iovs.10-5404. Print 2011 Jan.
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Invest Ophthalmol Vis Sci. 2010 May;51(5):2436-40. doi: 10.1167/iovs.09-4505. Epub 2009 Dec 17.
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The lymphatic system in health and disease.健康与疾病中的淋巴系统。
Lymphat Res Biol. 2008;6(3-4):109-22. doi: 10.1089/lrb.2008.1008.
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