在宿主新陈代谢中,肠道微生物通过3基因素脱酶调节白天节律
Zheng Kuang1, Yuhao Wang1, Yun Li1
1Department of Immunology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
概括
在小鼠中,肠道微生物通过基因脱酶3 (HDAC3) 编程白天代谢节奏. 这种机制影响营养吸收,脂质吸收和肥胖,整合微生物和昼夜信号.
科学领域:
- 代谢调节
- 微生物组与宿主之间的相互作用
- 时间生物学
背景情况:
- 昼夜节律对哺乳动物的新陈代谢至关重要,
- 肠道微生物在宿主代谢节奏的编程中的作用是一个新兴的研究领域.
研究的目的:
- 研究基因脱乙酶3 (HDAC3) 调解肠道微生物群对小鼠日常代谢节律的影响.
- 阐明HDAC3集成微生物和昼夜线索以调节宿主代谢的分子机制.
主要方法:
- 在小鼠小肠中分析HDAC3的表达和定位.
- 染色体免疫沉以评估HDAC3对目标基因的招募.
- 测量基因乙化,基因表达,营养摄取和脂质吸收.
主要成果:
- 肠道微生物群诱导上皮细胞HDAC3表达,该表达以节奏方式与染色体结合.
- HDAC3驱动着日间动的基因乙化,代谢基因表达和营养吸收.
- 调节节律性*Cd36*转录,脂质吸收和饮食引起的肥胖.
结论:
- HDAC3是肠道微生物群编程昼间代谢节律的关键调解器.
- HDAC3集成微生物和昼夜信号来控制宿主代谢过程,包括脂质代谢和吸收.
- 针对HDAC3介导的途径可以为与饮食和微生物群相关的代谢障碍提供新的策略.
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