Christopher Hunter, Zhang Jianglin, Oladejo Sarah Olanrewaju, Sharma Samskrathi Aravinda, Kuang Zheng
Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA, United States.
Front Epigenet Epigenom. 2024;2. doi: 10.3389/freae.2024.1496999. Epub 2024 Nov 27.
Circadian rhythms play an essential role in the regulation of intestinal absorption and barrier function. Tight junctions, including claudins, are fundamental components of the intestinal epithelial barrier. However, the regulatory mechanisms governing their diurnal expression remain poorly understood. Furthermore, the impact of circadian rhythms on intestinal permeability through claudin modulation has yet to be fully explored. Here we investigated the expression and the diurnal rhythms of claudin transcripts in the intestinal epithelium. We identified histone deacetylase 3 (HDAC3) as an epigenetic regulator that represses claudin expression and drives the diurnal rhythms via histone deacetylation. Loss of HDAC3 leads to increased intestinal permeability and dampened its diurnal rhythm. We further revealed that HDAC3 affects the basolateral localization of claudin-3. Together, our findings give insights into epigenetic modification in regulating tight junction and its diurnal rhythms, providing targets for therapeutic mediations in gastrointestinal disorders.
昼夜节律在肠道吸收和屏障功能的调节中起着至关重要的作用。紧密连接,包括闭合蛋白,是肠道上皮屏障的基本组成部分。然而,其昼夜表达的调控机制仍知之甚少。此外,昼夜节律通过调节闭合蛋白对肠道通透性的影响尚未得到充分研究。在这里,我们研究了肠道上皮中闭合蛋白转录本的表达及其昼夜节律。我们确定组蛋白去乙酰化酶3(HDAC3)是一种表观遗传调节因子,它通过组蛋白去乙酰化抑制闭合蛋白的表达并驱动昼夜节律。HDAC3的缺失导致肠道通透性增加并减弱其昼夜节律。我们进一步揭示,HDAC3影响闭合蛋白-3的基底外侧定位。总之,我们的研究结果为调节紧密连接及其昼夜节律的表观遗传修饰提供了见解,为胃肠道疾病的治疗干预提供了靶点。