Endothelial cells in inflammation and angiogenesis.

Zoltán Szekanecz, Alisa E Koch
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引用次数: 33

Abstract

Endothelial cells are involved in leukocyte extravasation underlying inflammation. A number of adhesion molecules play a role in leukocyte-endothelial interactions. New vessel formation, termed angiogenesis, is also crucial for leukocyte extravasation. The outcome of neovascularization is highly dependent on the balance or imbalance between angiogenic mediators and inhibitors. There have been several attempts to therapeutically interfere with the cellular and molecular mechanisms, such as leukocyte-endothelial cell adhesion and angiogenesis. Most studies have been performed using animal models of various types of inflammation, such as arthritis. In addition, a very limited number of human clinical trials gave promising results. In this review, authors summarize the most relevant information on adhesion molecules, as well as angiogenic and angiostatic agents. In addition, further perspectives of anti-adhesive and anti-angiogenic therapy are also discussed. Specific targeting of pathological endothelial function including adhesion and angiogenesis, may be useful for the future management of various inflammatory diseases.

炎症和血管生成中的内皮细胞。
内皮细胞参与炎症下白细胞外渗。许多粘附分子在白细胞-内皮相互作用中起作用。新血管形成,称为血管生成,也是白细胞外渗的关键。新生血管的结果高度依赖于血管生成介质和抑制剂之间的平衡或不平衡。已经有一些尝试通过治疗干预细胞和分子机制,如白细胞-内皮细胞粘附和血管生成。大多数研究都是用各种炎症的动物模型进行的,比如关节炎。此外,数量非常有限的人体临床试验给出了令人鼓舞的结果。本文就黏附分子、血管生成和血管抑制药物的相关研究进展进行综述。此外,本文还讨论了抗粘连和抗血管生成治疗的进一步前景。特异性靶向病理内皮功能,包括粘连和血管生成,可能对未来各种炎症性疾病的治疗有用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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