Evidence map›Paper›PMID 24880216›Full record

ArticleNature neuroscience2014

Identification of distinct ChAT⁺ neurons and activity-dependent control of postnatal SVZ neurogenesis.

Patricia Paez-Gonzalez, Brent Asrican, Erica Rodriguez, Chay T Kuo

Open access · greenAbstract read
In one paragraph

Article in Nature neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed
6.9field-weighted citation impact, top 2% 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

81 citing papers in PubMed, 140 citations in OpenAlex.

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  16. Neural Signaling in Cancer.Annual review of neuroscience · 2022
    Review
  17. Review
  18. Melatonin signalling in Schwann cells during neuroregeneration.Frontiers in cell and developmental biology · 2022
    Review
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  20. Article

21 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Patricia Paez-Gonzalez1] Department of Cell Biology, Duke University School of Medicine, Durham, North Carolina, USA. [2].ORCID 0000000267863869
Brent Asrican1] Department of Cell Biology, Duke University School of Medicine, Durham, North Carolina, USA. [2].
Erica Rodriguez1] Neurobiology Graduate Training Program, Duke University School of Medicine, Durham, North Carolina, USA. [2].
Chay T Kuo1] Department of Cell Biology, Duke University School of Medicine, Durham, North Carolina, USA. [2] Neurobiology Graduate Training Program, Duke University School of Medicine, Durham, North Carolina, USA. [3] Brumley Neonatal Perinatal Research Institute, Department of Pediatrics, Duke University School of Medicine, Durham, North Carolina, USA. [4] Department of Neurobiology, Duke University School of Medicine, Durham, North Carolina, USA. [5] Preston Robert Tisch Brain Tumor Center, Duke University School of Medicine, Durham, North Carolina, USA. [6] Duke Institute for Brain Sciences, Duke University School of Medicine, Durham, North Carolina, USA.
Duke University · US

Funding

Women's Cancer Research ProgramP30CA014236 · NCI · DUKE UNIVERSITY · PI DONNA NIEDZWIECKI · 1985 to 2026
$174.8M
Basic Predoctoral Training in NeuroscienceT32GM008441 · NIGMS · DUKE UNIVERSITY · PI MCNAMARA, JAMES O. · 1992 to 2017
$4.4M
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
Discovering pathways regulating neurogenesis and brain remodeling after injuryDP2OD004453 · OD · DUKE UNIVERSITY · PI KUO, CHAY TITUS · 2008 to 2008
$2.3M
NCI NIH HHS P30 CA014236NIGMS NIH HHS T32 GM008441NIH HHS DP2 OD004453NINDS NIH HHS R01 NS078192NINDS NIH HHS R01NS078192
6 · The paper itself

Abstract

Postnatal and adult subventricular zone (SVZ) neurogenesis is believed to be primarily controlled by neural stem cell (NSC)-intrinsic mechanisms, interacting with extracellular and niche-driven cues. Although behavioral experiments and disease states have suggested possibilities for higher level inputs, it is unknown whether neural activity patterns from discrete circuits can directly regulate SVZ neurogenesis. We identified a previously unknown population of choline acetyltransferase (ChAT)(+) neurons residing in the rodent SVZ neurogenic niche. These neurons showed morphological and functional differences from neighboring striatal counterparts and released acetylcholine locally in an activity-dependent fashion. Optogenetic inhibition and stimulation of subependymal ChAT(+) neurons in vivo indicated that they were necessary and sufficient to control neurogenic proliferation. Furthermore, whole-cell recordings and biochemical experiments revealed direct SVZ NSC responses to local acetylcholine release, synergizing with fibroblast growth factor receptor activation to increase neuroblast production. These results reveal an unknown gateway connecting SVZ neurogenesis to neuronal activity-dependent control and suggest possibilities for modulating neuroregenerative capacities in health and disease.

Indexed as

AcetylcholineAnimalsBlotting, WesternCell ProliferationCells, CulturedCerebral VentriclesCholine O-AcetyltransferaseElectrophoresis, Polyacrylamide GelElectrophysiological PhenomenaImmunohistochemistryMiceMicroscopy, ElectronNeural Stem CellsNeurogenesisNeuroimagingNeuronsAcetylcholineCholine O-AcetyltransferaseReceptors, Fibroblast Growth Factor

Identifiers

PMID24880216
PMCPMC4122286
OpenAlexW1968911616

What OpenQuestion holds

Textmetadata
LicenceTDM
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.