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在具有内置柱阵列的微流控通道中对哺乳动物细胞进行灌注培养。

Perfusion culture of mammalian cells in a microfluidic channel with a built-in pillar array.

作者信息

Zhang Chi

机构信息

Division of Nanobiotechnology, AlbaNova University Centre, Royal Institute of Technology, Stockholm, Sweden.

出版信息

Methods Mol Biol. 2012;853:83-94. doi: 10.1007/978-1-61779-567-1_8.

Abstract

In vitro culture of mammalian cells is fundamental to various biological studies such as single cell analysis, pathological research, and drug/therapy development. However, there are limitations with the current in vitro cell culture methods. Cells tend to lose their specific functions due to the lack of a cellular microenvironment when they are maintained under standard culture conditions. Microscale devices can be a novel tool to reestablish a cellular microenvironment for culturing mammalian cells in vitro and maintaining their differentiated functions. Different microscale cell culture techniques have been developed to suit different biological applications. This chapter describes a method to trap and culture mammalian cells in a microfluidic channel with a built-in pillar array.

摘要

哺乳动物细胞的体外培养是单细胞分析、病理研究以及药物/疗法开发等各种生物学研究的基础。然而,当前的体外细胞培养方法存在局限性。当细胞在标准培养条件下维持培养时,由于缺乏细胞微环境,它们往往会失去其特定功能。微尺度装置可以成为一种新型工具,用于在体外重建细胞微环境以培养哺乳动物细胞并维持其分化功能。已开发出不同的微尺度细胞培养技术以适应不同的生物学应用。本章描述了一种将哺乳动物细胞捕获并培养在具有内置柱阵列的微流控通道中的方法。

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