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作 者:蒋孟军[1] 杨敏[1] 周尧远[1] 张荣军[1] 曹国宪[1] 蔡刚明[1] 王广基[1]
机构地区:[1]江苏省原子医学研究所核医学国家重点实验室,江苏无锡214063
出 处:《细胞与分子免疫学杂志》2006年第1期88-91,共4页Chinese Journal of Cellular and Molecular Immunology
基 金:江苏省自然基金资助项目(No.BK2004025)
摘 要:目的探讨23-羟基桦木酸(23-HBA)对体外血管生成的抑制作用。方法采用磺酰罗丹明B(SRB)法测定23-HBA对人毛细血管内皮细胞(HMEC)增殖、迁移和小管形成的影响;用免疫组化染色法检测HMEC中CD31表达的变化。结果23-HBA体外可明显抑制HMEC增殖(IC50为40.44mg/L)、迁移和小管的形成,且呈明显的剂量依赖性。23-HBA的浓度为10mg/L时,HMEC中CD31的表达明显降低。结论23-HBA体外具有明显抑制血管生成的作用,有可能成为有效的血管生成抑制剂。AIM: To study the inhibitory effect of 23- HBA on angiogenesis in vitro. METHODS : The effect of 23- hydroxy butulinic acid (23-HBA) on the in vitro proliferation of human microcapillary endothelial cells (HMECs) was examined by sulfonylrhodamine B (SRB) assay. The effect of 23-HBA on endothelial cell migration, and tubule formation on Matrigel was also observed. The CD31 expression in HMECs was dectected by immunohistochemical staining. RESULTS: The proliferation of HMECs was inhibited significantly by 23-HBA with IC50 being 40.44 mg/L. 23-HBA inhibited endothelial cell migration and tubule formation in a dose-dependent manner. The expression of CD31 in HMECs was reduced after treatment with 10 mg/L 23-HBA. CONCLUSION: 23-HBA can inhibit angiogenesis in vitro, which would become a promising antiangiogenic drug.
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