Evidence map›Paper›PMID 23834718›Full record

ArticleAging cell2013

Notch1 signaling modulates neuronal progenitor activity in the subventricular zone in response to aging and focal ischemia.

Fen Sun, XiaoOu Mao, Lin Xie, Meiping Ding, Bei Shao, Kunlin Jin

Abstract read
In one paragraph

Article in Aging cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing 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

41 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Astragalus Flavone Induces Proliferation and Differentiation of Neural Stem Cells in a Cerebral Infarction Model.Medical science monitor : international medical journal of experimental and clinical research · 2022
    Article
  12. Review
  13. Hypothalamic inflammation in metabolic disorders and aging.Cellular and molecular life sciences : CMLS · 2021
    Review
  14. Article
  15. ESC-sEVs Rejuvenate Aging Hippocampal NSCs by Transferring SMADs to Regulate the MYT1-Egln3-Sirt1 Axis.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Article
  16. Article
  17. Article
  18. Article
  19. 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.

Fen SunDepartment of Neurology, Second Affiliated Hospital, School of Medicine, Zhejiang University, No. 88, Jiefang Road, Hangzhou, Zhejiang, 310009, China; Department of Pharmacology & Neuroscience, Institute for Aging and Alzheimer's Disease Research, University of North Texas Health Science Center, 3500 Camp Bowie Boulevard, Fort Worth, TX, 76107, USA.
XiaoOu Mao
Lin Xie
Meiping Ding
Bei Shao
Kunlin Jin

Funding

Aging and NeurogenesisR01AG021980 · NIA · UNIVERSITY OF NORTH TEXAS HLTH SCI CTR · PI JIN, KUNLIN · 2003 to 2014
$3.9M
Functional contribution of neural stem cells in strokeR01NS057186 · NINDS · BUCK INSTITUTE FOR RESEARCH ON AGING · PI JIN, KUNLIN · 2009 to 2010
$970k
NIA NIH HHS AG21980NIA NIH HHS R01 AG021980NINDS NIH HHS NS057186NINDS NIH HHS R01 NS057186
6 · The paper itself

Abstract

Neurogenesis diminishes with aging and ischemia-induced neurogenesis also occurs, but reduced in aged brain. Currently, the cellular and molecular pathways mediating these effects remain largely unknown. Our previous study has shown that Notch1 signaling regulates neurogenesis in subventricular zone (SVZ) of young adult brain after focal ischemia, but whether a similar effect occurs in aged normal and ischemic animals is unknown. Here, we used normal and ischemic aged rat brains to investigate whether Notch1 signaling was involved in the reduction of neurogenesis in response to aging and modulates neurogenesis in aged brains after focal ischemia. By Western blot, we found that Notch1 and Jagged1 expression in the SVZ of aged brain was significantly reduced compared with young adult brain. Consistently, the activated form of Notch1 (Notch intracellular domain; NICD) expression was also declined. Immunohistochemistry confirmed that expression and activation of Notch1 signaling in the SVZ of aged brain were reduced. Double or triple immunostaining showed that that Notch1 was mainly expressed in doublecortin (DCX)-positive cells, whereas Jagged1 was predominantly expressed in astroglial cells in the SVZ of normal aged rat brain. In addition, disruption or activation of Notch1 signaling altered the number of proliferating cells labeled by bromodeoxyuridine (BrdU) and DCX in the SVZ of aged brain. Moreover, ischemia-induced cell proliferation in the SVZ of aged brain was enhanced by activating the Notch1 pathway and was suppressed by inhibiting the Notch1 signaling. Reduced infarct volume and improved motor deficits were also observed in Notch1 activator-treated aged ischemic rats. Our data suggest that Notch1 signaling modulates the SVZ neurogenesis in aged brain in normal and ischemic conditions.

Indexed as

Signal TransductionAgingAnimalsBehavior, AnimalBrain IschemiaCalcium-Binding ProteinsCell ProliferationCerebral InfarctionCerebral VentriclesDoublecortin ProteinIntercellular Signaling Peptides and ProteinsJagged-1 ProteinMaleMembrane ProteinsNeural Stem CellsProtein Structure, TertiaryCalcium-Binding ProteinsDcx protein, ratDoublecortin ProteinIntercellular Signaling Peptides and ProteinsJag1 protein, ratJagged-1 ProteinMembrane ProteinsReceptors, NotchSerrate-Jagged Proteinsaged rat brainfocal cerebral ischemianeurogenesisNotch1 signaling pathway

Identifiers

PMID23834718
PMCPMC3838489

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.