Evidence map›Paper›PMID 25521289›Full record

ArticlePLoS genetics2014

Notch signaling mediates the age-associated decrease in adhesion of germline stem cells to the niche.

Chen-Yuan Tseng, Shih-Han Kao, Chih-Ling Wan, Yueh Cho, Shu-Yun Tung, Hwei-Jan Hsu

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 19% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Roles of the Notch Signaling Pathway in Ovarian Functioning.Reproductive sciences (Thousand Oaks, Calif.) · 2021
    Pooled it
  2. Article
  3. Article
  4. Article
  5. The Memory Gene,Biomolecules · 2025
    Article
  6. Review
  7. Article
  8. Article
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  12. Open biology · 2019
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  13. Article
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  15. Review
  16. Article
  17. Article
  18. Loss ofeLife · 2017
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Chen-Yuan TsengInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan; Graduate Institute of Life Sciences, National Defense Medical Center, Taipei, Taiwan.
Shih-Han KaoInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Chih-Ling WanInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Yueh ChoInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Shu-Yun TungGenomic Core Facility, Institute of Molecular Biology, Academia Sinica, Taipei, Taiwan.
Hwei-Jan HsuInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Institute of Cellular and Organismic Biology, Academia Sinica · TWInstitute of Molecular Biology, Academia Sinica · TWNational Defense Medical Center · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stem cells have an innate ability to occupy their stem cell niche, which in turn, is optimized to house stem cells. Organ aging is associated with reduced stem cell occupancy in the niche, but the mechanisms involved are poorly understood. Here, we report that Notch signaling is increased with age in Drosophila female germline stem cells (GSCs), and this results in their removal from the niche. Clonal analysis revealed that GSCs with low levels of Notch signaling exhibit increased adhesiveness to the niche, thereby out-competing their neighbors with higher levels of Notch; adhesiveness is altered through regulation of E-cadherin expression. Experimental enhancement of Notch signaling in GSCs hastens their age-dependent loss from the niche, and such loss is at least partially mediated by Sex lethal. However, disruption of Notch signaling in GSCs does not delay GSC loss during aging, and nor does it affect BMP signaling, which promotes self-renewal of GSCs. Finally, we show that in contrast to GSCs, Notch activation in the niche (which maintains niche integrity, and thus mediates GSC retention) is reduced with age, indicating that Notch signaling regulates GSC niche occupancy both intrinsically and extrinsically. Our findings expose a novel role of Notch signaling in controlling GSC-niche adhesion in response to aging, and are also of relevance to metastatic cancer cells, in which Notch signaling suppresses cell adhesion.

Indexed as

Cell AdhesionStem Cell NicheAgingAnimalsBone Morphogenetic ProteinsCdh1 ProteinsCell ProliferationDrosophila melanogasterDrosophila ProteinsFemaleReceptors, NotchRNA-Binding ProteinsSignal TransductionStem CellsBone Morphogenetic ProteinsCdh1 ProteinsDrosophila Proteinsfzr protein, DrosophilaN protein, DrosophilaReceptors, NotchRNA-Binding ProteinsSxl protein, Drosophila

Identifiers

PMID25521289
PMCPMC4270478
OpenAlexW2022392473

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.