Protocol to study the genomic profile of histone lactylation with CUT&RUN assay in tumor-associated macrophages.

IF 1.3 Q4 BIOCHEMICAL RESEARCH METHODS
Alessandra De Leo, Alessio Ugolini, Filippo Veglia
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引用次数: 0

Abstract

Lysine lactylation is a distinctive histone modification that plays a crucial role in epigenetic regulation and gene transcription. Here, we present a protocol for studying the genomic profile of histone lactylation with the CUT&RUN assay in tumor-associated macrophages. We describe steps for preparing live cells, gating strategies for isolating glucose transporter type 1 + (GLUT1+) monocyte-derived macrophages (MDMs) by fluorescence-activated cell sorting (FACS), binding lactyl-specific primary antibodies, and quantifying DNA using qPCR. This protocol is applicable to both tumor-derived and in-vitro-generated bone-marrow-derived macrophages. For complete details on the use and execution of this protocol, please refer to De Leo et al.1.

在肿瘤相关巨噬细胞中使用CUT&RUN试验研究组蛋白乳酸化的基因组图谱。
赖氨酸乳酸化是一种独特的组蛋白修饰,在表观遗传调控和基因转录中起着至关重要的作用。在这里,我们提出了一种方案,用于研究肿瘤相关巨噬细胞中组蛋白乳酸化的基因组图谱。我们描述了制备活细胞的步骤,通过荧光激活细胞分选(FACS)分离葡萄糖转运蛋白1+ (GLUT1+)单核细胞源性巨噬细胞(MDMs)的门控策略,结合乳酸特异性一抗,并使用qPCR定量DNA。该方案适用于肿瘤源性和体外生成的骨髓源性巨噬细胞。有关本协议使用和执行的完整细节,请参阅De Leo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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