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The suprachiasmatic nucleus (SCN) is the primary circadian pacemaker in mammals. Individual SCN neurons in dispersed culture can generate independent circadian oscillations of clock gene expression and neuronal firing. However, SCN rhythmicity depends on sufficient membrane depolarization and levels of intracellular calcium and cAMP. In the intact SCN, cellular oscillations are synchronized and reinforced by rhythmic synaptic input from other cells, resulting in a reproducible topographic pattern of distinct phases and amplitudes specified by SCN circuit organization. The SCN network synchronizes its component cellular oscillators, reinforces their oscillations, responds to light input by altering their phase distribution, increases their robustness to genetic perturbations, and enhances their precision. Thus, even though individual SCN neurons can be cell-autonomous circadian oscillators, neuronal network properties are integral to normal function of the SCN.
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Figure 3 Video: A movie of circadian rhythms of PER2::LUC bioluminescence recorded from mouse SCN neurons in dispersed culture over a period of two weeks, showing that the cells oscillate independently. Bioluminescence intensity of one cell highlighted near the center of the image is plotted below. Download movie file (MOV) Figure 5 Video: A movie of circadian rhythms of PER2::LUC bioluminescence recorded from mouse SCN neurons in a cultured slice over a period of seven days, showing that the cells oscillate with the same periods and similar phases, in a complex spatiotemporal pattern. This is a coronal slice of the ventral hypothalamus, including the bright bioluminescent left and right SCN, the third ventricle between them, and the optic chiasm below. Download movie file (MOV)