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Quantitative phase imaging characterization of tumor-associated blood vessel formation on a chip

机译:芯片上肿瘤相关血管形成的定量相位成像特征

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Angiogenesis, the formation of new blood vessels from existing ones, is a biological process that has an essential role in solid tumor growth, development, and progression. Recent advances in Lab-on-a-Chip technology has created an opportunity for scientists to observe endothelial cell(EC)behaviors during the dynamic process of angiogenesis using a simple and economical in vitro platform that recapitulates in vivo blood vessel formation. Here, we use quantitative phase imaging(QPI)microscopy to continuously and non-invasively characterize the dynamic process of tumor cell-induced angiogenic sprout formation on a microfluidic chip. The live tumor cell-induced angiogenic sprouts are generated by multicellular endothelial sprouting into 3 dimensional(3D)Matrigel using human umbilical vein endothelial cells(HUVECs). By using QPI, we quantitatively measure a panel of cellular morphological and behavioral parameters of each individual EC participating in this sprouting. In this proof-of-principle study, we demonstrate that QPI is a powerful tool that can provide real-time quantitative analysis of biological processes in in vitro 3D biomimetic devices, which, in turn, can improve our understanding of the biology underlying functional tissue engineering.
机译:血管生成,来自现有血管的新血管的形成是一种生物过程,具有在实体肿瘤生长,发育和进展中具有重要作用。实验室技术的最新进展为科学家们创造了一种机会,在使用简单且经济的体外平台中,在血管生成的动态过程中观察内皮细胞(EC)行为的机会,这些血管形成概括。这里,我们使用定量相位成像(QPI)显微镜以连续和非侵入性地表征在微流体芯片上的肿瘤细胞诱导的血管生成芽形成的动态过程。使用人的脐静脉内皮细胞(HUVEC),通过多细胞内皮芽为3尺寸(3D)基质胶产生活肿瘤细胞诱导的血管生成豆芽。通过使用QPI,我们定量测量参与这一发芽的每个欧共体的细胞形态学和行为参数的小组。在这种原则上的研究中,我们证明了QPI是一种强大的工具,可以提供对体外3D仿生装置中的生物过程的实时定量分析,这反过来可以改善我们对潜在功能组织的生物学的理解工程。

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