Evidence map›Paper›PMID 29618286›Full record

ReviewAnnual review of neuroscience2018

Neuronal Activity-Dependent Control of Postnatal Neurogenesis and Gliogenesis.

Ragnhildur T Káradóttir, Chay T Kuo

Abstract readReview
In one paragraph

Review in Annual review of neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
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

21 citing papers in PubMed.

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  15. Metabolic tuning of inhibition regulates hippocampal neurogenesis in the adult brain.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  16. Review
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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

2 authors.

Ragnhildur T KáradóttirWellcome Trust - Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Cambridge CB2 1QR, United Kingdom; email: rk385@cam.ac.uk.
Chay T KuoDepartments of Cell Biology and Neurobiology, Duke University School of Medicine, Durham, North Carolina 27710, USA; email: chay.kuo@duke.edu.

Funding

Women's Cancer Research ProgramP30CA014236 · NCI · DUKE UNIVERSITY · PI JOHN N. NORTON · 1985 to 2026
$174.8M
Neural Circuit Control of Postnatal Quiescent Neural Stem Cell ActivationR01MH105416 · NIMH · DUKE UNIVERSITY · PI YIN, HENRY · 2015 to 2024
$4.6M
Molecular control of ependymal cell plasticity and its contribution to new neuron production in the mammalian brainR01NS078192 · NINDS · DUKE UNIVERSITY · PI KUO, CHAY TITUS · 2012 to 2020
$3.1M
MOLECULAR AND CELLULAR CONTROL OF INJURY-INDUCED ASTROGENESISR01NS096096 · NINDS · DUKE UNIVERSITY · PI DENEEN, BENJAMIN · 2017 to 2021
$2.6M
Medical Research Council MC_PC_12009Medical Research Council MC_PC_15042NCI NIH HHS P30 CA014236NIMH NIH HHS R01 MH105416NINDS NIH HHS R01 NS078192NINDS NIH HHS R01 NS096096
6 · The paper itself

Abstract

The addition of new neurons and oligodendroglia in the postnatal and adult mammalian brain presents distinct forms of gray and white matter plasticity. Substantial effort has been devoted to understanding the cellular and molecular mechanisms controlling postnatal neurogenesis and gliogenesis, revealing important parallels to principles governing the embryonic stages. While during central nervous system development, scripted temporal and spatial patterns of neural and glial progenitor proliferation and differentiation are necessary to create the nervous system architecture, it remains unclear what driving forces maintain and sustain postnatal neural stem cell (NSC) and oligodendrocyte progenitor cell (OPC) production of new neurons and glia. In recent years, neuronal activity has been identified as an important modulator of these processes. Using the distinct properties of neurotransmitter ionotropic and metabotropic channels to signal downstream cellular events, NSCs and OPCs share common features in their readout of neuronal activity patterns. Here we review the current evidence for neuronal activity-dependent control of NSC/OPC proliferation and differentiation in the postnatal brain, highlight some potential mechanisms used by the two progenitor populations, and discuss future studies that might advance these research areas further.

Indexed as

NeurogenesisAnimalsBrainCell DifferentiationCell ProliferationHumansNeural Stem CellsNeurogliaNeuronsNeurotransmitter AgentsOligodendrocyte Precursor CellsNeurotransmitter Agentsneural stem cellneurotransmitter signalingoligodendrocyte progenitor celloligodendrogenesispostnatal neurogenesisprogenitor proliferation

Identifiers

PMID29618286
PMCPMC6324739

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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.