Division of Endocrinology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Branch of the National Clinical Research Center for Metabolic Disease, Wuhan, China.
Division of Endocrinology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Methods Mol Biol. 2022;2455:149-161. doi: 10.1007/978-1-0716-2128-8_13.
Non-alcoholic steatohepatitis (NASH) is an advanced form of non-alcoholic fatty liver disease characterized by hepatosteatosis, liver cell injury, and inflammation. The pathogenesis of NASH involves dysregulated transcription of genes involved in critical processes in the liver, including metabolic homeostasis and inflammation. Chromatin immunoprecipitation (ChIP) utilizes antibody-mediated immunoprecipitation followed by the detection of associated DNA fragments via real-time PCR or high-throughput sequencing to quantitatively profile the interactions of proteins of interest with functional chromatin elements. Here, we present a detailed protocol to study the interactions of DNA and chromatin-associated proteins (e.g., transcription factors, co-activators, co-repressors, and chromatin modifiers) and modified histones (e.g., acetylated and methylated) in isolated primary mouse hepatocytes and mouse liver. The application of these methods can enable the identification of molecular mechanisms that underpin dysregulated hepatic processes in NASH.
非酒精性脂肪性肝炎(NASH)是一种非酒精性脂肪性肝病的晚期形式,其特征为肝脂肪变性、肝细胞损伤和炎症。NASH 的发病机制涉及涉及肝脏关键过程的基因转录失调,包括代谢稳态和炎症。染色质免疫沉淀(ChIP)利用抗体介导的免疫沉淀,然后通过实时 PCR 或高通量测序检测相关的 DNA 片段,以定量分析与功能染色质元件相互作用的靶蛋白。在这里,我们提供了一个详细的方案,用于研究分离的原代小鼠肝细胞和小鼠肝脏中 DNA 和染色质相关蛋白(例如转录因子、共激活因子、共抑制因子和染色质修饰因子)以及修饰组蛋白(例如乙酰化和甲基化)的相互作用。这些方法的应用可以确定 NASH 中失调的肝过程的分子机制。