Critical period regulation across multiple timescales.


Journal

Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876

Informations de publication

Date de publication:
22 09 2020
Historique:
pubmed: 7 6 2020
medline: 11 11 2020
entrez: 7 6 2020
Statut: ppublish

Résumé

Brain plasticity is dynamically regulated across the life span, peaking during windows of early life. Typically assessed in the physiological range of milliseconds (real time), these trajectories are also influenced on the longer timescales of developmental time (nurture) and evolutionary time (nature), which shape neural architectures that support plasticity. Properly sequenced critical periods of circuit refinement build up complex cognitive functions, such as language, from more primary modalities. Here, we consider recent progress in the biological basis of critical periods as a unifying rubric for understanding plasticity across multiple timescales. Notably, the maturation of parvalbumin-positive (PV) inhibitory neurons is pivotal. These fast-spiking cells generate gamma oscillations associated with critical period plasticity, are sensitive to circadian gene manipulation, emerge at different rates across brain regions, acquire perineuronal nets with age, and may be influenced by epigenetic factors over generations. These features provide further novel insight into the impact of early adversity and neurodevelopmental risk factors for mental disorders.

Identifiants

pubmed: 32503914
pii: 1820836117
doi: 10.1073/pnas.1820836117
pmc: PMC7519216
doi:

Substances chimiques

Parvalbumins 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

23242-23251

Subventions

Organisme : NIMH NIH HHS
ID : P50 MH094271
Pays : United States

Déclaration de conflit d'intérêts

The authors declare no competing interest.

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Auteurs

Rebecca K Reh (RK)

Department of Psychology, University of British Columbia, Vancouver, BC V6T 1Z4, Canada.

Brian G Dias (BG)

Division of Behavioral Neuroscience and Psychiatric Disorders, Yerkes National Primate Research Center, Atlanta, GA 30322.
Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA 30329.

Charles A Nelson (CA)

Boston Children's Hospital, Harvard Medical School, Boston, MA 02115.
Graduate School of Education, Harvard University, Cambridge, MA 02138.

Daniela Kaufer (D)

Helen Wills Neuroscience Institute, University of California, Berkeley, CA 94720.
Department of Integrative Biology, University of California, Berkeley, CA 94720.

Janet F Werker (JF)

Department of Psychology, University of British Columbia, Vancouver, BC V6T 1Z4, Canada.

Bryan Kolb (B)

Department of Neuroscience, University of Lethbridge, Lethbridge, AB T1K 3M4, Canada.

Joel D Levine (JD)

Department of Biology, University of Toronto at Mississauga, Mississauga, ON L5L 1C6, Canada.

Takao K Hensch (TK)

Boston Children's Hospital, Harvard Medical School, Boston, MA 02115; hensch@mcb.harvard.edu.
Center for Brain Science, Department of Molecular Cellular Biology, Harvard University, Cambridge, MA 02138.
International Research Center for Neurointelligence, University of Tokyo Institutes for Advanced Study, Tokyo 113-0033, Japan.

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