Evidence map›Paper›PMID 27707966›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2016

Neuregulin-Dependent Regulation of Fast-Spiking Interneuron Excitability Controls the Timing of the Critical Period.

Yu Gu, Trinh Tran, Sachiko Murase, Andrew Borrell, Alfredo Kirkwood, Elizabeth M Quinlan

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

51 citing papers in PubMed, 1 synthesis or guideline pooled it, 77 citations in OpenAlex.

  1. Pooled it
  2. Investigating hierarchical critical periods in human neurodevelopment.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Review
  3. Article
  4. Article
  5. The Richness of Vision in the Mammalian Brain: Neural Codes for Visual Perception and Behavior in Three Dimensions.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Review
  6. Connectivity, Computation, and Plasticity of the Early Visual System.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. In vivo whole-cortex marker of excitation-inhibition ratio indexes cortical maturation and cognitive ability in youth.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  13. Article
  14. Article
  15. Article
  16. Article
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  18. Article
  19. Psychedelics and Neural Plasticity: Therapeutic Implications.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Yu GuNeuroscience and Cognitive Science Program, Department of Biology, University of Maryland, College Park, Maryland 20742, and.
Trinh TranMind/Brain Institute, Johns Hopkins University, Baltimore, Maryland 21218.
Sachiko MuraseNeuroscience and Cognitive Science Program, Department of Biology, University of Maryland, College Park, Maryland 20742, and.
Andrew BorrellNeuroscience and Cognitive Science Program, Department of Biology, University of Maryland, College Park, Maryland 20742, and.ORCID 0000-0002-2986-9573
Alfredo KirkwoodMind/Brain Institute, Johns Hopkins University, Baltimore, Maryland 21218 equinlan@umd.edu kirkwood@jhu.edu.
Elizabeth M QuinlanNeuroscience and Cognitive Science Program, Department of Biology, University of Maryland, College Park, Maryland 20742, and equinlan@umd.edu kirkwood@jhu.edu.
University of Maryland, College Park · USJohns Hopkins University · US

Funding

TRANSCRIPTIONAL MECHANISMS OF HIPPOCAMPAL AGINGP01AG009973 · NIA · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI JAMES J KNIERIM · 1991 to 2026
$52.4M
Synaptic Plasticity in Young versus Aged Visual CortexR01EY016431 · NEI · UNIV OF MARYLAND, COLLEGE PARK · PI Elizabeth Mary Quinlan · 2006 to 2026
$5.9M
Reversible activation on critical plasticity in visual cortexR01EY025922 · NEI · UNIV OF MARYLAND, COLLEGE PARK · PI KIRKWOOD, ALFREDO, MURASE, SACHIKO · 2015 to 2024
$3.6M
NEI NIH HHS R01 EY016431NEI NIH HHS R01 EY025922NIA NIH HHS P01 AG009973
6 · The paper itself

Abstract

Maturation of excitatory drive onto fast-spiking interneurons (FS INs) in the visual cortex has been implicated in the control of the timing of the critical period for ocular dominance plasticity. However, the mechanisms that regulate the strength of these synapses over cortical development are not understood. Here we use a mouse model to show that neuregulin (NRG) and the receptor tyrosine kinase erbB4 regulate the timing of the critical period. NRG1 enhanced the strength of excitatory synapses onto FS INs, which inhibited ocular dominance plasticity during the critical period but rescued plasticity in transgenics with hypoexcitable FS INs. Blocking the effects of endogenous neuregulin via inhibition of erbBs rescued ocular dominance plasticity in postcritical period adults, allowing recovery from amblyopia induced by chronic monocular deprivation. Thus, the strength of excitation onto FS INs is a key determinant of critical period plasticity and is maintained at high levels by NRG-erbB4 signaling to constrain plasticity in adulthood. SIGNIFICANCE STATEMENT: Despite decades of experimentation, the mechanisms by which critical periods of enhanced synaptic plasticity are initiated and terminated are not completely understood. Here we show that neuregulin (NRG) and the receptor tyrosine kinase erbB4 determine critical period timing by controlling the strength of excitatory synapses onto FS INs. NRG1 enhanced excitatory drive onto fast spiking interneurons, which inhibited ocular dominance plasticity in juveniles but rescued plasticity in transgenics with hypoexcitable FS INs. Blocking the effects of endogenous neuregulin via inhibition of erbBs rescued ocular dominance plasticity in adults, allowing recovery from amblyopia induced by chronic monocular deprivation. Thus, in contrast to prevailing views of the termination of the critical period, active maintenance of strong excitation onto FS INs constrains plasticity in adults.

Indexed as

Critical Period, PsychologicalAmblyopiaAnimalsDominance, OcularFemaleInterneuronsMaleMiceMice, Inbred C57BLMice, KnockoutNeuregulin-1Neuronal PlasticityReceptor, ErbB-4Recovery of FunctionSynapsesVision, MonocularErbb4 protein, mouseNeuregulin-1Nrg1 protein, mouseReceptor, ErbB-4critical periodfast-spiking interneuronsneuregulinocular dominance plasticityparvalbumin

Identifiers

PMID27707966
PMCPMC5050326
OpenAlexW2527757248

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.