短期冷暴露诱导棕色脂肪中持久的表观基因组记忆。
Short-term cold exposure induces persistent epigenomic memory in brown fat.
机构信息
Institute for Diabetes, Obesity, and Metabolism, and Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.
Institute for Diabetes, Obesity, and Metabolism, and Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA; Broad Institute of MIT and Harvard, Cambridge, MA, USA; Department of Medical Oncology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA; Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
出版信息
Cell Metab. 2024 Aug 6;36(8):1764-1778.e9. doi: 10.1016/j.cmet.2024.05.011. Epub 2024 Jun 17.
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.
表观基因组调节剂组蛋白去乙酰化酶 3(HDAC3)在棕色脂肪组织(BAT)中的缺乏会损害小鼠在接近冰点的温度下生存的能力。在这里,我们报告说,短期暴露于温和的冷温度(STEMCT:15°C 持续 24 小时)可以避免 BAT 中缺乏 HDAC3(HDAC3BATKO)的小鼠在 4°C 下发生致命性低体温。STEMCT 恢复了在 22°C 下诱导的解偶联蛋白 1(UCP1)和生热共激活因子 PGC-1α的诱导,这在 HDAC3 缺陷的 BAT 中受到严重损害,而 UCP1 或 PGC-1α 的缺失阻止了 STEMCT 的保护作用。值得注意的是,这种保护作用可持续长达 7 天。转录激活因子 C/EBPβ在小鼠和人类 BAT 中被短期冷暴露诱导,并且在 STEMCT 后独特地保持高水平长达 7 天。在 HDAC3BATKO 小鼠中,通过腺相关病毒介导的 BAT C/EBPβ 敲低消除了 STEMCT 的持久记忆,揭示了存在 C/EBPβ 依赖性和 HDAC3 独立性的冷适应表观基因组记忆。
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