唑来膦酸钠抑制内皮细胞α β 3和α β 5整合素表面表达。

A Bellahcène, M Chaplet, K Bonjean, V Castronovo
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引用次数: 25

摘要

唑来膦酸钠在体内和体外均表现出抗血管生成的特性。整合素α β 3和α β 5参与血管生成。由于唑来膦酸钠抑制内皮细胞粘附,作者探索了它可能改变这些整合素在局灶粘附位点的募集的假设。人脐静脉内皮细胞(HUVECs)用唑来膦酸钠或甲羟戊酸途径中间体香叶醇和法尼醇(FOH)处理。流式细胞术和免疫荧光检测显示,唑来丙酮酸显著降低HUVEC细胞表面alphavbeta3和alphavbeta5的表达。这种抑制作用被GGOH逆转,而不被FOH逆转。用唑来膦酸钠和GGOH共处理的细胞能够通过alphavbeta3和alphavbeta5附着在玻璃体连接蛋白上,这被使用特异性功能阻断抗体所证实。作者表明唑来膦酸钠改变内皮细胞整合素介导的粘附。这种作用可能有助于先前证明的唑来膦酸钠的抗血管生成作用。这种作用机制是否也适用于转移性肿瘤细胞还在研究中。
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Zoledronate inhibits alphavbeta3 and alphavbeta5 integrin cell surface expression in endothelial cells.

Zoledronate exhibits antiangiogenic properties in vitro and in vivo. Integrins alphavbeta3 and alphavbeta5 are involved in angiogenesis. Because zoledronate inhibits endothelial cell adhesion, the authors explored the hypothesis that it could alter these integrins recruitment to focal adhesion sites. Human umbilical vein endothelial cells (HUVECs) were treated with zoledronate or with mevalonate pathway intermediates geranylgeraniol (GGOH) and farnesol (FOH). Zoledronate generated a significant decrease in alphavbeta3 and alphavbeta5 expression at HUVEC cell surface using flow cytometry and immunofluorescence. This inhibition was reversed by GGOH but not by FOH. Cells cotreated with zoledronate and GGOH were able to attach to vitronectin through alphavbeta3 and alphavbeta5, as confirmed by the use of specific function-blocking antibodies. The authors showed that zoledronate alters endothelial cell integrin-mediated adhesion. This effect is likely to contribute to the previously demonstrated antiangiogenic effect of zoledronate. Whether this mechanism of action also applies to metastatic tumor cells is under investigation.

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