Evidence map›Paper›PMID 27468423›Full record

ArticleNeurogenesis (Austin, Tex.)

Cholinergic Circuit Control of Postnatal Neurogenesis.

Brent Asrican, Patricia Paez-Gonzalez, Joshua Erb, Chay T Kuo

Abstract read
In one paragraph

Article in Neurogenesis (Austin, Tex.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. International journal of molecular sciences · 2020
    Article
  9. Article
  10. Article
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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

4 authors.

Brent AsricanDepartment of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA.
Patricia Paez-GonzalezDepartment of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA.
Joshua ErbDepartment of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA; Neurobiology Graduate Training Program, Duke University School of Medicine, Durham, NC 27710, USA.
Chay T KuoDepartment of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA; Neurobiology Graduate Training Program, Duke University School of Medicine, Durham, NC 27710, USA; Brumley Neonatal Perinatal Research Institute, Duke University School of Medicine, Durham, NC 27710, USA; Department of Neurobiology, Duke University School of Medicine, Durham, NC 27710, USA; Preston Robert Tisch Brain Tumor Center, Duke University School of Medicine, Durham, NC 27710, USA; Duke Institute for Brain Sciences, Duke University School of Medicine, Durham, NC 27710, USA.

Funding

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
NIMH NIH HHS R01 MH105416NINDS NIH HHS R01 NS078192
6 · The paper itself

Abstract

New neuron addition via continued neurogenesis in the postnatal/adult mammalian brain presents a distinct form of nervous system plasticity. During embryonic development, precise temporal and spatial patterns of neurogenesis are necessary to create the nervous system architecture. Similar between embryonic and postnatal stages, neurogenic proliferation is regulated by neural stem cell (NSC)-intrinsic mechanisms layered upon cues from their local microenvironmental niche. Following developmental assembly, it remains relatively unclear what may be the key driving forces that sustain continued production of neurons in the postnatal/adult brain. Recent experimental evidence suggests that patterned activity from specific neural circuits can also directly govern postnatal/adult neurogenesis. Here, we review experimental findings that revealed cholinergic modulation, and how patterns of neuronal activity and acetylcholine release may differentially or synergistically activate downstream signaling in NSCs. Higher-order excitatory and inhibitory inputs regulating cholinergic neuron firing, and their implications in neurogenesis control are also considered.

Identifiers

PMID27468423
PMCPMC4959609

What OpenQuestion holds

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Registered trials

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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.