Department of Neurohumoral Regulations, Institute of Physiology, Academy of Science of the Czech Republic, Prague, Czech Republic; and.
Am J Physiol Gastrointest Liver Physiol. 2014 Feb 15;306(4):G346-56. doi: 10.1152/ajpgi.00340.2013. Epub 2013 Dec 12.
Colonic morphology and function change significantly during ontogenesis. In mammals, many colonic physiological functions are temporally controlled by the circadian clock in the colon, which is entrained by the central circadian clock in the suprachiasmatic nuclei (SCN). The aim of this present study was to ascertain when and how the circadian clock in the colon develops during the perinatal period and whether maternal cues and/or the developing pup SCN may influence the ontogenesis of the colonic clock. Daily profiles of clock genes Per1, Per2, Cry1, Cry2, Rev-erbα, Bmal1, and Clock expression in the colon underwent significant modifications since embryonic day 20 (E20) through postnatal days (P) 2, 10, 20, and 30 via changes in the mutual phasing among the individual clock gene expression rhythms, their relative phasing to the light-dark regime, and their amplitudes. An adult-like state was achieved around P20. The foster study revealed that during the prenatal period, the maternal circadian phase may partially modulate development of the colonic clock. Postnatally, the absence and/or presence of rhythmic maternal care affected the phasing of the clock gene expression profiles in pups at P10 and P20. A reversal in the colonic clock phase between P10 and P20 occurred in the absence of rhythmic signals from the pup SCN. The data demonstrate ontogenetic maturation of the colonic clock and stress the importance of prenatal and postnatal maternal rhythmic signals for its development. These data may contribute to the understanding of colonic function-related diseases in newborn children.
结肠形态和功能在个体发育过程中发生显著变化。在哺乳动物中,许多结肠的生理功能受结肠生物钟的时间控制,而结肠生物钟受视交叉上核(SCN)中的中枢生物钟所调节。本研究旨在确定结肠生物钟在围生期何时以及如何发育,以及母体线索和/或发育中的幼鼠 SCN 是否可能影响结肠生物钟的发生。从胚胎第 20 天(E20)到出生后第 2、10、20 和 30 天,结肠中时钟基因 Per1、Per2、Cry1、Cry2、Rev-erbα、Bmal1 和 Clock 的表达的日常节律发生了显著变化,这是通过个体时钟基因表达节律之间的相互相位变化、它们相对于光-暗周期的相对相位以及它们的幅度来实现的。大约在 P20 时达到了类似成人的状态。寄养研究表明,在产前阶段,母体生物钟相位可能部分调节结肠时钟的发育。出生后,节律性母体护理的缺失和/或存在会影响 10 天和 20 天龄幼鼠时钟基因表达谱的相位。在没有来自幼鼠 SCN 的节律信号的情况下,结肠时钟相位在 P10 和 P20 之间发生反转。这些数据表明结肠时钟的个体发育成熟,并强调了产前和产后母体节律信号对其发育的重要性。这些数据可能有助于理解新生儿中与结肠功能相关的疾病。