褐色脂肪组织
HDAC3型
表观基因组
激活剂(遗传学)
组蛋白脱乙酰基酶
生物
西妥因1
内分泌学
内科学
细胞生物学
医学
组蛋白
脂肪组织
遗传学
下调和上调
DNA甲基化
基因
基因表达
作者
Shin‐ichi Inoue,Matthew J. Emmett,Hee‐Woong Lim,Mohit Midha,Hannah J. Richter,Isaac J. Celwyn,Rashid Mehmood,Maria Chondronikola,Samuel Klein,Amy K. Hauck,Mitchell A. Lazar
出处
期刊:Cell Metabolism
[Elsevier]
日期:2024-06-17
卷期号:36 (8): 1764-1778.e9
被引量:2
标识
DOI:10.1016/j.cmet.2024.05.011
摘要
Deficiency of the epigenome modulator histone deacetylase 3 (HDAC3) in brown adipose tissue (BAT) impairs the ability of mice to survive in near-freezing temperatures. Here, we report that short-term exposure to mild cold temperature (STEMCT: 15°C for 24 h) averted lethal hypothermia of mice lacking HDAC3 in BAT (HDAC3 BAT KO) exposed to 4°C. STEMCT restored the induction of the thermogenic coactivator PGC-1α along with UCP1 at 22°C, which is greatly impaired in HDAC3-deficient BAT, and deletion of either UCP1 or PGC-1α prevented the protective effect of STEMCT. Remarkably, this protection lasted for up to 7 days. Transcriptional activator C/EBPβ was induced by short-term cold exposure in mouse and human BAT and, uniquely, remained high for 7 days following STEMCT. Adeno-associated virus-mediated knockdown of BAT C/EBPβ in HDAC3 BAT KO mice erased the persistent memory of STEMCT, revealing the existence of a C/EBPβ-dependent and HDAC3-independent cold-adaptive epigenomic memory.
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