Sun Yao-Hui, Sun Yuxin, Zhu Kan, Draper Bruce W, Zeng Qunli, Mogilner Alex, Zhao Min
Department of Dermatology, School of Medicine, University of California-Davis, Sacramento, CA, USA.
Department of Radiology and Biomedical Imaging, University of California-San Francisco, San Francisco, CA, USA.
Methods Mol Biol. 2016;1407:251-72. doi: 10.1007/978-1-4939-3480-5_19.
Recent studies have demonstrated distinctive motility and responses to extracellular cues of cells in isolation, cells collectively in groups, and cell fragments. Here we provide a protocol for generating cell sheets, isolated cells, and cell fragments of keratocytes from zebrafish scales. The protocol starts with a comprehensive fish preparation, followed by critical steps for scale processing and subsequent cell sheet generation, single cell isolation, and cell fragment induction, which can be accomplished in just 3 days including a 36-48 h incubation time. Compared to other approaches that usually produce single cells only or together with either fragments or cell groups, this facile and reliable methodology allows generation of all three motile forms simultaneously. With the powerful genetics in zebrafish our model system offers a useful tool for comparison of the mechanisms by which cell sheets, single cells, and cell fragments respond to extracellular stimuli.
最近的研究表明,分离的细胞、成组的集体细胞以及细胞碎片具有独特的运动能力和对细胞外信号的反应。在这里,我们提供了一种从斑马鱼鳞片生成角膜细胞片、分离细胞和细胞碎片的方案。该方案首先是全面的鱼类准备,然后是鳞片处理以及随后生成细胞片、单细胞分离和细胞碎片诱导的关键步骤,整个过程仅需3天即可完成,其中包括36 - 48小时的孵育时间。与其他通常仅产生单细胞或同时产生碎片或细胞团的方法相比,这种简便可靠的方法能够同时生成所有三种运动形式。利用斑马鱼强大的遗传学特性,我们的模型系统为比较细胞片、单细胞和细胞碎片对细胞外刺激的反应机制提供了一个有用的工具。