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题名: Triflavin, an Arg-Gly-Asp-Containing Peptide, Inhibits Human Cervical Carcinoma (HeLa) Cell-Substratum Adhesion Through an RGD-Dependent Mechanism
作者: 許準榕;林昭信;彭惠琴;黃德富
SHEU, JOEN-RONG;LIN, CHAO-HSINE;PENG, HUI-CHIN;HUANG, TUR-FU
贡献者: 動物中心
日期: 1994
上传时间: 2009-01-19T02:41:32Z
摘要:   Triflavin, an Arg-Gly-Asp-cintaining peptide, inhibits human cervical carcinoma (HeLa) cell-substratum adhesion through an RGD-dependent mechanism. PEPTIDES 15(8) 1391-1398 , 1994.-Triflavin, 1 7.5-kDa cysteine- rich polypeptide purified from Trimeresurus flavoviridis snake venom, belongs to a family of RGD-containing peptides, termed disintegrins , that have been isolated from the venoms of various vipers and shown to be potent inhibitors of platelet aggregation. The interaction of tumor cells with extracellular matrices such as fibronectin, vitronectin, and collagen has been shown to be mediated through a family of cell surface receptors that specifically recognize an arginie-glycine- aspartic acid (RGD) sequence within each adhesive protein. In this study, we show that triflavin dose-dependently inhibited adhesion of human cerical carcinoma ( HeLa) cells to extracellular matrices (ECMs; i.e., fibronectin, fibrinogen , and vitronectin). On the other hand, triflavin exerted a limited inhibitory effect on cell adhesion to laminin and collagen (type I and IV) . On a molar basis, triflavin is approximately 800 times more potent than Gly- Arg-Gly-Asp-Ser (GRGDS) at inhibiting cell adhesion. When immobilized on plate, triflavin significantly promoted HeLa cell adhesion, and this attachment was inhibited by GRGDS. Furthermore, FITC-conjugated triflavin bound to cells in a saturable manner and its binding was inhibited by GRGDS. In addition, triflavin did not affect [3H]thymidine uptade of HeLa cells during 1 3-day incubation. These results suggest that triflavin probably binds to integrin receptors expressed on HeLa cell surface via its RGD sequence within its molecule, thereby inhibiting the adhesion of extracellular matrices to HeLa cells.#0844#
關聯: PEPTIDES v.15 n.8 pp.1391-1398
显示于类别:[實驗動物中心] 期刊論文

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