细胞分离和培养。

Sihui Zhang, Jeffrey R Kuhn
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引用次数: 36

摘要

细胞分离和培养是研究细胞功能的重要工具。在受控条件下生长的分离细胞可以被操纵和成像,其分辨率水平在整个动物甚至组织移植体中是不可能的。最近的进展已经允许大规模分离和培养秀丽隐杆线虫的胚胎和所有四个幼虫阶段的初级细胞。分离的细胞可用于单细胞分析,电生理学和高分辨率显微镜来测定细胞自主发育和行为。本章描述秀丽隐杆线虫胚胎和幼虫阶段细胞的分离和培养方法。我们的方案描述了从高密度NA22细菌板上生长的线虫中分离胚胎期和L1期细胞,以及从无菌液体培养的线虫中分离L2至L4期细胞。胚胎细胞和幼虫细胞均可在3小时内从线虫种群中分离出来,并可培养数天。附录中给出了无菌细胞培养技术的引物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cell isolation and culture.

Cell isolation and culture are essential tools for the study of cell function. Isolated cells grown under controlled conditions can be manipulated and imaged at a level of resolution that is not possible in whole animals or even tissue explants. Recent advances have allowed for large-scale isolation and culture of primary C. elegans cells from both embryos and all four larval stages. Isolated cells can be used for single-cell profiling, electrophysiology, and high-resolution microscopy to assay cell autonomous development and behavior. This chapter describes protocols for the isolation and culture of C. elegans embryonic and larval stage cells. Our protocols describe isolation of embryonic and L1 stage cells from nematodes grown on high-density NA22 bacterial plates and isolation of L2 through L4 stage cells from nematodes grown in axenic liquid culture. Both embryonic and larval cells can be isolated from nematode populations within 3 hours and can be cultured for several days. A primer on sterile cell culture techniques is given in the appendices.

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