Document Type

Article

Language

eng

Format of Original

23 p.

Publication Date

7-2016

Publisher

BioScientifica

Source Publication

Journal of Endocrinology

Source ISSN

0022-0795

Original Item ID

DOI: 10.1530/JOE-16-0054; PMID: 27154335; PubMed Central PMCID: PMC4938744

Abstract

The suprachiasmatic nucleus (SCN) of the anterior hypothalamus is the master circadian clock that coordinates daily rhythms in behavior and physiology in mammals. Like other hypothalamic nuclei, the SCN displays an impressive array of distinct cell types characterized by differences in neurotransmitter and neuropeptide expression. Individual SCN neurons and glia are able to display self-sustained circadian rhythms in cellular function that are regulated at the molecular level by a 24h transcriptional–translational feedback loop. Remarkably, SCN cells are able to harmonize with one another to sustain coherent rhythms at the tissue level. Mechanisms of cellular communication in the SCN network are not completely understood, but recent progress has provided insight into the functional roles of several SCN signaling factors. This review discusses SCN organization, how intercellular communication is critical for maintaining network function, and the signaling mechanisms that play a role in this process. Despite recent progress, our understanding of SCN circuitry and coupling is far from complete. Further work is needed to map SCN circuitry fully and define the signaling mechanisms that allow for collective timekeeping in the SCN network.

Comments

Accepted version. Journal of Endocrinology, Vol. 230, No. 1 (July 2016): R27-R49. DOI. © BioScientifica 2016. Used with permission.

Disclaimer: this is not the definitive version of record of this article.This manuscript has been accepted for publication in Journal of Endocrinology, but the version presented here has not yet been copy-edited, formatted or proofed. Consequently, Bioscientifica accepts no responsibility for any errors or omissions it may contain. The definitive version is now freely available at DOI. 2016

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