Protocol for inducing epidermis-specific gene deletion and establishing a UVB-irradiated skin inflammation model.

IF 1.4 Q4 BIOCHEMICAL RESEARCH METHODS STAR Protocols Pub Date : 2025-06-20 Epub Date: 2025-03-16 DOI:10.1016/j.xpro.2025.103701
Ye Liu, George L Sen
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引用次数: 0

Abstract

When skin is exposed to ultraviolet B (UVB) radiation, damaged keratinocytes release double-stranded RNA to trigger an inflammatory response. Here, we present a protocol to induce epidermal-specific Zfp750 gene-deficient mice and establish a UVB-induced skin inflammation model. We detail procedures for detecting gene expressions in the epidermis by quantitative reverse-transcription PCR (RT-qPCR) and analyzing changes in skin immune cell subsets after UVB radiation using flow cytometry. For complete details on the use and execution of this protocol, please refer to Liu et al.1.

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诱导表皮特异性基因缺失和建立uvb辐照皮肤炎症模型的方案。
当皮肤暴露在紫外线B (UVB)辐射下时,受损的角质形成细胞会释放双链RNA,引发炎症反应。在这里,我们提出了一种方案来诱导表皮特异性Zfp750基因缺陷小鼠,并建立uvb诱导的皮肤炎症模型。我们详细介绍了通过定量反转录PCR (RT-qPCR)检测表皮基因表达的程序,并使用流式细胞术分析UVB辐射后皮肤免疫细胞亚群的变化。有关本协议使用和执行的完整细节,请参见Liu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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