Department of Molecular & Integrative Physiology, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Compr Physiol. 2013 Apr;3(2):917-40. doi: 10.1002/cphy.c120017.
In mammals, circadian rhythms function to coordinate a diverse panel of physiological processes with environmental conditions such as food and light. As the driving force for circadian rhythmicity, the molecular clock is a self-sustained transcription-translational feedback loop system consisting of transcription factors, epigenetic modulators, kinases/phosphatases, and ubiquitin E3 ligases. The molecular clock exists not only in the suprachiasmatic nuclei of the hypothalamus but also in the peripheral tissues to regulate cellular and physiological function in a tissue-specific manner. The circadian clock system in the liver plays important roles in regulating metabolism and energy homeostasis. Clock gene mutant animals display impaired glucose and lipid metabolism and are susceptible to diet-induced obesity and metabolic dysfunction, providing strong evidence for the connection between the circadian clock and metabolic homeostasis. Circadian-controlled hepatic metabolism is partially achieved by controlling the expression and/or activity of key metabolic enzymes, transcription factors, signaling molecules, and transporters. Reciprocally, intracellular metabolites modulate the molecular clock activity in response to the energy status. Although still at the early stage, circadian clock dysfunction has been implicated in common chronic liver diseases. Circadian dysregulation of lipid metabolism, detoxification, reactive oxygen species (ROS) production, and cell-cycle control might contribute to the onset and progression of liver steatosis, fibrosis, and even carcinogenesis. In summary, these findings call for a comprehensive study of the function and mechanisms of hepatic circadian clock to gain better understanding of liver physiology and diseases.
在哺乳动物中,昼夜节律的功能是将各种生理过程与环境条件(如食物和光)协调起来。作为昼夜节律的驱动力,分子钟是一个自我维持的转录-翻译反馈环系统,由转录因子、表观遗传调节剂、激酶/磷酸酶和泛素 E3 连接酶组成。分子钟不仅存在于下丘脑的视交叉上核,也存在于外周组织中,以组织特异性的方式调节细胞和生理功能。肝脏中的生物钟系统在调节代谢和能量稳态方面起着重要作用。时钟基因突变动物表现出葡萄糖和脂质代谢受损,容易发生饮食诱导的肥胖和代谢功能障碍,为生物钟与代谢稳态之间的联系提供了有力证据。昼夜节律控制的肝脏代谢部分通过控制关键代谢酶、转录因子、信号分子和转运体的表达和/或活性来实现。反过来,细胞内代谢物也会根据能量状态调节分子钟的活性。尽管仍处于早期阶段,但昼夜节律紊乱已被认为与常见的慢性肝病有关。脂质代谢、解毒、活性氧(ROS)产生和细胞周期控制的昼夜节律失调可能导致肝脂肪变性、纤维化,甚至癌变的发生和发展。总之,这些发现呼吁对肝脏生物钟的功能和机制进行全面研究,以更好地理解肝脏生理学和疾病。