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Biology subjects

Matsu-ura, T.

Publications and source records attributed to Matsu-ura, T..

2 recordsLinked to original sources

Circadian clock regulates intestinal epithelial cell differentiation via NOTCH/Hes1 oscillations

The circadian clock regulates diverse cellular processes, including intestinal epithelial cell (IEC) proliferation. However, mechanisms regulating clock-dependent IEC differentiation remain unknown. We performed a time course RNA-Seq using the mouse small intestine and identified NOTCH signaling, a key mechanism regulating IEC differentiation, as one of the pathways under the control of circadian rhythms. Using mouse enteroids, we discovered that a NOTCH reporter, Hes1-luciferase, exhibits both ultradian or circadian oscillations depending on the stemness of mouse enteroids. Furthermore, single-cell analysis of Hes1-mCherry revealed that the period of Hes1 oscillations varies widely, but circadian rhythms modulate the number of Hes1-mCherry+ cells in the population. Finally, we show that Paneth cell numbers fluctuate over the circadian cycle, suggesting that circadian clock-regulated Hes1 drives the circadian dynamics of IEC composition. Our study provides a deeper insight into circadian regulation of IEC differentiation, which will be critical for applications of chronotherapies for digestive diseases.

molecular biology↗

Circadian clock-gated cell renewal controls time-dependent changes in taste sensitivity

Circadian regulation of the cell cycle progression produces a diurnal supply of newborn cells to replace the ones that were lost in the organs and tissues. Here we analyzed time-dependent changes in the cell types in the mouse tongue epithelium. We observed circadian regulated alternate oscillations of the stem/progenitor cell maker genes and the differentiated cell marker genes expressions in mouse tongue epithelial organoids. The cell cycle progression was regulated time-dependent manner in the tongue organoids and mice tongue. Single-cell RNA sequencing revealed time-dependent population changes of the stem/progenitor cells and the differentiated cells in mice tongues. Remarkably, we observed time-dependent type II taste cell population changes, resulting in time-dependent taste sensitivity changes. We also found the same population changes in mice intestines and uteruses, suggesting the contributions of the diurnal supply of newborn cells to the time-dependent physiological controls in the broad types of organs and tissues.

cell biology↗