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Ontogeny of Circadian Rhythms and Synchrony in the Suprachiasmatic Nucleus.

Authors :
Carmona-Alcocer, Vania
Carmona-Alcocer, Vania
Abel, John H
Sun, Tao C
Petzold, Linda R
Doyle, Francis J
Simms, Carrie L
Herzog, Erik D
Carmona-Alcocer, Vania
Carmona-Alcocer, Vania
Abel, John H
Sun, Tao C
Petzold, Linda R
Doyle, Francis J
Simms, Carrie L
Herzog, Erik D
Source :
The Journal of neuroscience : the official journal of the Society for Neuroscience; vol 38, iss 6, 1326-1334; 0270-6474
Publication Year :
2018

Abstract

In mammals, the suprachiasmatic nucleus (SCN) of the hypothalamus coordinates daily rhythms including sleep-wake, hormone release, and gene expression. The cells of the SCN must synchronize to each other to drive these circadian rhythms in the rest of the body. The ontogeny of circadian cycling and intercellular coupling in the SCN remains poorly understood. Recent in vitro studies have recorded circadian rhythms from the whole embryonic SCN. Here, we tracked the onset and precision of rhythms in PERIOD2 (PER2), a clock protein, within the SCN isolated from embryonic and postnatal mice of undetermined sex. We found that a few SCN cells developed circadian periodicity in PER2 by 14.5 d after mating (E14.5) with no evidence for daily cycling on E13.5. On E15.5, the fraction of competent oscillators increased dramatically corresponding with stabilization of their circadian periods. The cells of the SCN harvested at E15.5 expressed sustained, synchronous daily rhythms. By postnatal day 2 (P2), SCN oscillators displayed the daily, dorsal-ventral phase wave in clock gene expression typical of the adult SCN. Strikingly, vasoactive intestinal polypeptide (VIP), a neuropeptide critical for synchrony in the adult SCN, and its receptor, VPAC2R, reached detectable levels after birth and after the onset of circadian synchrony. Antagonists of GABA or VIP signaling or action potentials did not disrupt circadian synchrony in the E15.5 SCN. We conclude that endogenous daily rhythms in the fetal SCN begin with few noisy oscillators on E14.5, followed by widespread oscillations that rapidly synchronize on E15.5 by an unknown mechanism.SIGNIFICANCE STATEMENT We recorded the onset of PER2 circadian oscillations during embryonic development in the mouse SCN. When isolated at E13.5, the anlagen of the SCN expresses high, arrhythmic PER2. In contrast, a few cells show noisy circadian rhythms in the isolated E14.5 SCN and most show reliable, self-sustained, synchronized rhythms in the E15.5

Details

Database :
OAIster
Journal :
The Journal of neuroscience : the official journal of the Society for Neuroscience; vol 38, iss 6, 1326-1334; 0270-6474
Notes :
application/pdf, The Journal of neuroscience : the official journal of the Society for Neuroscience vol 38, iss 6, 1326-1334 0270-6474
Publication Type :
Electronic Resource
Accession number :
edsoai.on1367419386
Document Type :
Electronic Resource