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体外肿瘤微血管生成模型的建立

Setting Up of the Tumor Angiogenesis Model in vitro

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【作者】 赵静苗俊英张尚立石梅

【Author】 ZHAO Jing 1, 2 MIAO Jun-ying 1, 2 ZHANG Shang-li 1, 2 SHI Mei 1, 2 (1 Institute of Developmental Biology, School of Life Science, Shandong University Jinan 250100, China) (2 Key laboratory of Experimental Teratology, Ministry of Education Jinan 250100, China)

【机构】 山东大学生命科学学院发育生物学研究所山东大学生命科学学院发育生物学研究所 济南250100山东大学实验畸形学教育部重点实验室济南250100济南250100山东大学实验畸形学教育部重点实验室

【摘要】 以体外微血管培养模型为基础,用鼠尾胶原包埋大鼠动脉环,并将包埋的动脉环转移到种有人肺癌A549细胞单层的培养皿中,用MCDB131无血清培养液对动脉环和肿瘤细胞进行共培养,从而建立肿瘤微血管体外生成模型。大鼠动脉环于培养后第3天从血管壁长出微血管芽,第6至10天长成微血管丛,两周后新生微血管开始萎缩;没有肿瘤细胞刺激的条件下,大鼠动脉环新生微血管数量明显减少。结果表明人肺癌A549细胞能够促进血管生成,体外大鼠动脉环肿瘤微血管培养模型操作简单、灵敏度高,适合研究肿瘤血管新生及其机制。

【Abstract】 Tumor angiogenesis model in vitro was set up by embedding the rat aortic rings in collegen and culturing them in serum-free MCDB 131 culture medium with or without lung cancer A549 cells. This model was based on the rat aortic ring model. In both control cultures and cultures supplemented with lung cancer A549 cells, most of the microvessels sprouted from the cut edges of the aortic rings. Microvessels usually appeared by the third day, at their maximal growth by days 6~10 and began to degenerate by the end of the second week, but cultures supplemented with lung cancer A549 cells could generate more microvessels than control. It concluded from current study that Lung cancer A549 cells could promote angiogenesis. The rat aortic ring model is simple and sensitive. It is a promising meathod to study angiogenesis and its mechanisms.

【基金】 教育部科研重点项目(104112);山东省自然科学基金(Z2002D05)
  • 【文献出处】 中国生物工程杂志 ,China Biotechnology , 编辑部邮箱 ,2006年03期
  • 【分类号】R73-3
  • 【被引频次】7
  • 【下载频次】396
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