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人Thy-1(CD 90)与整合素αvβ3(CD51/CD61)的相互作用:介导黑色素瘤细胞黏附于活化内皮细胞的重要机制。

Interaction of human Thy-1 (CD 90) with the integrin alphavbeta3 (CD51/CD61): an important mechanism mediating melanoma cell adhesion to activated endothelium.

作者信息

Saalbach Anja, Wetzel Anne, Haustein Uwe-Frithjof, Sticherling Michael, Simon Jan C, Anderegg Ulf

机构信息

Saxon Academy of Science, D-04107 Leipzig, Germany.

出版信息

Oncogene. 2005 Jul 7;24(29):4710-20. doi: 10.1038/sj.onc.1208559.

Abstract

The expression of the alphavbeta3 integrin (CD51/CD61) on human melanoma cells has been shown to be associated most closely with tumor progression and metastases formation in melanoma. Here, we demonstrated a specific interaction of the alphavbeta3 integrin on melanoma cells with the human Thy-1, an inducible cell adhesion molecule expressed on the cell surface of activated endothelial cells (EC). The interaction was shown by the binding of purified Thy-1 protein to alpha(V)beta(3) transfected cells, to alphavbeta3-expressing melanoma cells and to purified alpha(V)beta(3) integrin. Moreover, melanoma cells adhere specifically to Thy-1 transfectants via alphavbeta3 on melanoma cells showing the functional relevance of this interaction for cell adhesion. Finally, the importance of the alphavbeta3/Thy-1 interaction for the adhesion of melanoma cells to the activated endothelium was confirmed under static and flow conditions by the inhibition of melanoma cell adhesion to and transmigration across activated EC by blocking the alphavbeta3/Thy-1 interaction. In conclusion, we have identified a new pair of adhesion molecules Thy-1 and alphavbeta3 mediating the interaction of melanoma cells and activated EC. These data explain at least in part the high tumorigenicity of alphavbeta3-expressing melanoma cells and the association of alphavbeta3-positive melanoma cells with a high risk of metastasis and poor prognosis.

摘要

已证明人黑色素瘤细胞上的αvβ3整合素(CD51/CD61)表达与黑色素瘤的肿瘤进展和转移形成密切相关。在此,我们证明了黑色素瘤细胞上的αvβ3整合素与人类Thy-1存在特异性相互作用,Thy-1是一种在活化内皮细胞(EC)细胞表面表达的可诱导细胞粘附分子。通过纯化的Thy-1蛋白与α(V)β(3)转染细胞、表达αvβ3的黑色素瘤细胞以及纯化的α(V)β(3)整合素的结合,证实了这种相互作用。此外,黑色素瘤细胞通过黑色素瘤细胞上的αvβ3特异性粘附于Thy-1转染细胞,表明这种相互作用对细胞粘附具有功能相关性。最后,通过阻断αvβ3/Thy-1相互作用抑制黑色素瘤细胞对活化内皮细胞的粘附和跨膜迁移,在静态和流动条件下证实了αvβ3/Thy-1相互作用对黑色素瘤细胞与活化内皮细胞粘附的重要性。总之,我们鉴定出了一对新的粘附分子Thy-1和αvβ3,它们介导黑色素瘤细胞与活化内皮细胞的相互作用。这些数据至少部分解释了表达αvβ3的黑色素瘤细胞的高致瘤性以及αvβ3阳性黑色素瘤细胞与高转移风险和不良预后的关联。

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