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    Sinusoidal hemangioma and intravascular papillary endothelial hyperplasia: Interrelated processes that share a histogenetic piecemeal angiogenic mechanism
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    Objective To establish the human hemangioma model in nude mice. Methods Human hemangioma endothelial cells cultured in vitro were injected hypodermically into nude mice(BALB/c nude mice). The volume of in the transplanted tumor was measured in 60 days. Samples were taken from survival tumor and stained immunohistochemically by CD31 and Ki-67 before subjected to histopathological examination. Results Hemangioma model were successfully established in nude mice and the original tumor histological characters were retained in the transplanted tumor. Conclusion Hemangioma model established in nude mice by hypodermically injection with human hemangioma endothelial cells retains all the biological characteristics of the human hemangioma and can be a good model for research on hemangioma.
    CD31
    Nude mouse
    Suspension culture
    Histopathological examination
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    Angiogenesis 为许多生理、病理学的过程是很重要的。然而, angiogenesis 的分子的机制是不清楚的。阐明 angiogenesis 并且到的分子的机制为 angiogenesis 依赖的疾病开发处理,建立是必要的一在 vitro angiogenesis 合适模型。在这研究,我们基于一台 microfluidic 设备在 vitro angiogenesis 模型创造了一篇小说。我们的模型提供一在里面为 endothelial 房间(EC ) 的象 vivo 一样微型环境文化和监视器到在他们在实时的微型环境的变化的 EC 的反应。为了为研究 angiogenesis, EC 增长上的 pro-angiogenic 因素的效果,迁居和像试管的结构形成评估这台 microfluidic 设备的潜力,被调查。我们的结果证明在 3D 矩阵的 EC 的增长率被 pro-angiogenic 因素显著地支持(随 59.12% 的增加) 。与 pro-angiogenic 因素坡度的刺激,方向性地从低集中移植进 Matrigel 到高集中并且因而的 EC 形成了多房间弦和像试管的结构。这些结果建议设备能为阐明提供一个合适的平台 angiogenesis 并且为为 angiogenesis 依赖的疾病屏蔽 pro-angiogenic 或 anti-angiogenic 药的机制。
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