Protocol for generating a pericyte reporter zebrafish line Ki(pdgfrb-P2A-GAL4-VP16) using a CRISPR-Cas9-mediated knockin technique.

IF 1.3 Q4 BIOCHEMICAL RESEARCH METHODS
STAR Protocols Pub Date : 2025-03-21 Epub Date: 2024-12-13 DOI:10.1016/j.xpro.2024.103490
Huaxing Zi, Xiaolan Peng, Jiulin Du, Jia Li
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引用次数: 0

Abstract

Pericytes, the mural cells that envelop small blood vessels, play crucial roles in the formation of the blood-brain barrier (BBB). Here, we present a protocol for generating a pericyte reporter zebrafish line Ki(pdgfrb-P2A-GAL4-VP16) using a CRISPR-Cas9-mediated knockin technique. We describe steps for identifying efficient single guide RNA (sgRNA), constructing donor plasmid, and generating and maintaining the knockin line. We then detail procedures for in vivo imaging of brain pericytes. This protocol is adaptable for creating other knockin lines for specific cell labeling. For complete details on the use and execution of this protocol, please refer to Zi et al.1.

使用crispr - cas9介导的敲入技术生成斑马鱼周细胞报告细胞系Ki(pdgfrb-P2A-GAL4-VP16)的方案。
周细胞是包裹小血管的壁细胞,在血脑屏障(BBB)的形成中起着至关重要的作用。在这里,我们提出了一种使用crispr - cas9介导的敲入技术生成斑马鱼周细胞报告细胞系Ki(pdgfrb-P2A-GAL4-VP16)的方案。我们描述了识别有效的单导RNA (sgRNA),构建供体质粒,以及产生和维持敲蛋白线的步骤。然后,我们详细说明了脑周细胞的体内成像程序。该协议适用于创建用于特定细胞标记的其他敲蛋白系。有关本协议使用和执行的完整细节,请参阅Zi等人1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
STAR Protocols
STAR Protocols Biochemistry, Genetics and Molecular Biology-General Biochemistry, Genetics and Molecular Biology
CiteScore
2.00
自引率
0.00%
发文量
789
审稿时长
10 weeks
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