Biological clocks and incremental growth line formation in dentine.

Bmal1 biological rhythm circadian rhythm clock gene dental development enamel incremental feature subdaily rhythm suprachiasmatic nucleus ultradian rhythm

Journal

Journal of anatomy
ISSN: 1469-7580
Titre abrégé: J Anat
Pays: England
ID NLM: 0137162

Informations de publication

Date de publication:
08 2020
Historique:
received: 06 02 2020
revised: 12 03 2020
accepted: 16 03 2020
pubmed: 9 4 2020
medline: 2 4 2021
entrez: 9 4 2020
Statut: ppublish

Résumé

Dentine- and enamel-forming cells secrete matrix in consistent rhythmic phases, resulting in the formation of successive microscopic growth lines inside tooth crowns and roots. Experimental studies of various mammals have proven that these lines are laid down in subdaily, daily (circadian), and multidaily rhythms, but it is less clear how these rhythms are initiated and maintained. In 2001, researchers reported that lesioning the so-called master biological clock, the suprachiasmatic nucleus (SCN), halted daily line formation in rat dentine, whereas subdaily lines persisted. More recently, a key clock gene (Bmal1) expressed in the SCN in a circadian manner was also found to be active in dentine- and enamel- secretory cells. To probe these potential neurological and local mechanisms for the production of rhythmic lines in teeth, we reexamined the role of the SCN in growth line formation in Wistar rats and investigated the presence of daily lines in Bmal1 knockout mice (Bmal1

Identifiants

pubmed: 32266720
doi: 10.1111/joa.13198
pmc: PMC7369199
doi:

Substances chimiques

ARNTL Transcription Factors 0
Bmal1 protein, mouse 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

367-378

Subventions

Organisme : Howard Hughes Medical Institute
Pays : United States

Informations de copyright

© 2020 Anatomical Society.

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Auteurs

Amanda M Papakyrikos (AM)

Department of Anthropology, Wellesley College, Wellesley, MA, USA.
Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA, USA.

Manish Arora (M)

Department of Environmental Medicine and Public Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Christine Austin (C)

Department of Environmental Medicine and Public Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Julia C Boughner (JC)

Department of Anatomy, Physiology and Pharmacology, College of Medicine, University of Saskatchewan, Saskatoon, SK, Canada.

Terence D Capellini (TD)

Department of Human Evolutionary Biology, Harvard University, Cambridge, MA, USA.

Heather L Dingwall (HL)

Department of Human Evolutionary Biology, Harvard University, Cambridge, MA, USA.

Quentin Greba (Q)

Department of Anatomy, Physiology and Pharmacology, College of Medicine, University of Saskatchewan, Saskatoon, SK, Canada.

John G Howland (JG)

Department of Anatomy, Physiology and Pharmacology, College of Medicine, University of Saskatchewan, Saskatoon, SK, Canada.

Akiko Kato (A)

Department of Human Evolutionary Biology, Harvard University, Cambridge, MA, USA.
Department of Oral Anatomy, School of Dentistry, Aichi Gakuin University, Nagoya, Japan.

Xiu-Ping Wang (XP)

Department of Developmental Biology, Harvard School of Dental Medicine, Boston, MA, USA.

Tanya M Smith (TM)

Department of Human Evolutionary Biology, Harvard University, Cambridge, MA, USA.
Australian Research Centre for Human Evolution, Griffith University, Nathan, Qld, Australia.
Griffith Centre for Social and Cultural Research, Griffith University, Nathan, Qld, Australia.

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