Evidence map›Paper›PMID 37904343›Full record

ArticleCNS neuroscience & therapeutics2024

Survivin enhances hippocampal neurogenesis and cognitive function in Alzheimer's disease mouse model.

Yeongae Lee, Yeon-Joo Ju, Min Sung Gee, Seung Ho Jeon, Namkwon Kim, Taeyoung Koo, Jong Kil Lee

Open access · goldAbstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. lncRNA ENSRNOT00000087717 mediated differentiation of satellite glial cells derived from dorsal root ganglion via AKT1.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2025
    Article
  6. ERRα and ERRγ coordinate expression of genes associated with Alzheimer's disease, inhibitingProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  7. Article
  8. 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

7 authors at 1 institution in 1 country.

Yeongae LeeCollege of Pharmacy, Kyung Hee University, Seoul, Korea.ORCID 0000-0003-3521-8440
Yeon-Joo JuCollege of Pharmacy, Kyung Hee University, Seoul, Korea.
Min Sung GeeCollege of Pharmacy, Kyung Hee University, Seoul, Korea.
Seung Ho JeonCollege of Pharmacy, Kyung Hee University, Seoul, Korea.
Namkwon KimCollege of Pharmacy, Kyung Hee University, Seoul, Korea.
Taeyoung KooCollege of Pharmacy, Kyung Hee University, Seoul, Korea.
Jong Kil LeeCollege of Pharmacy, Kyung Hee University, Seoul, Korea.
Kyung Hee University · KR

Funding

National Research Foundation of Korea (NRF) grant funded by the Korea government 2021R1F1A1045522National Research Foundation of Korea (NRF) grant funded by the Korea government 2022R1A2C1013352National Research Foundation of Korea (NRF) grant funded by the Korea government RS-2023-00262386
6 · The paper itself

Abstract

aimsCognitive impairment is associated with reduced hippocampal neurogenesis; however, the causes of decreased hippocampal neurogenesis remain highly controversial. Here, we investigated the role of survivin in the modulation of hippocampal neurogenesis in AD.

methodsTo investigate the effect of survivin on neurogenesis in neural stem cells (NSCs), we treated mouse embryonic NSCs with a survivin inhibitor (YM155) and adeno-associated viral survivin (AAV-Survivin). To explore the potential role of survivin expression in AD, AAV9-Survivin or AAV9-GFP were injected into the dentate gyrus (DG) of hippocampus of 7-month-old wild-type and 5XFAD mice. Cognitive function was measured by the Y maze and Morris water maze. Neurogenesis was investigated by BrdU staining, immature, and mature neuron markers.

resultsOur results indicate that suppression of survivin expression resulted in decreased neurogenesis. Conversely, overexpression of survivin using AAV-Survivin restored neurogenesis in NSCs that had been suppressed by YM155 treatment. Furthermore, the expression level of survivin decreased in the 9-month-old 5XFAD compared with that in wild-type mice. AAV-Survivin-mediated overexpression of survivin in the DG in 5XFAD mice enhanced neurogenesis and cognitive function.

conclusionHippocampal neurogenesis can be enhanced by survivin overexpression, suggesting that survivin could serve as a promising therapeutic target for the treatment of AD.

Indexed as

Alzheimer DiseaseSurvivinAnimalsCognitionDisease Models, AnimalHippocampusMiceMice, TransgenicNeurogenesisSurvivin5XFAD mouseAlzheimer's diseaseneurogenesisproneural genessurvivin

Identifiers

PMID37904343
PMCPMC11017468
OpenAlexW4388035232

What OpenQuestion holds

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LicenceCC BY
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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.