Evidence map›Paper›PMID 41803431›Full record

ArticleCommunications biology2026

Stem cells resume asymmetric division upon niche re-entry through reactivating the centrosome orientation checkpoint.

Muhammed Burak Bener, Autumn Twillie, Naiya Patel, Mayu Inaba

Abstract read
In one paragraph

Article in Communications biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

4 authors.

Muhammed Burak BenerDepartment of Cell Biology, University of Connecticut Health, Farmington, CT, 06030, USA.
Autumn TwillieDepartment of Cell Biology, University of Connecticut Health, Farmington, CT, 06030, USA.ORCID http://orcid.org/0009-0005-7904-8502
Naiya PatelDepartment of Cell Biology, University of Connecticut Health, Farmington, CT, 06030, USA.ORCID http://orcid.org/0009-0005-4501-3686
Mayu InabaDepartment of Cell Biology, University of Connecticut Health, Farmington, CT, 06030, USA. inaba@uchc.edu.ORCID http://orcid.org/0000-0002-8508-7461

Funding

Nanotube-mediated regulation of niche-stem cell signalingR35GM128678 · NIGMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI Mayu Inaba-Oguro · 2018 to 2026
$3.3M
NIGMS NIH HHS R35 GM128678U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R35GM128678
6 · The paper itself

Abstract

In Drosophila testis, germline stem cells (GSCs) typically divide asymmetrically, keeping one daughter cell within the niche for self-renewal and placing the other daughter cell outside the niche to undergo differentiation. This is the primary mechanism for maintaining a stable number of stem cells in the niche. However, it has been shown that small fraction of GSCs continuously leave the niche, necessitating an additional mechanism to compensate for this loss and maintain a constant number of GSCs. Dedifferentiation and symmetric renewal have been shown to replenish lost GSCs during regenerative and physiological conditions. However, it remains unknown whether dedifferentiated GSCs reacquire native GSC behaviors. Using long-term live imaging, we trace the cells following dedifferentiation and show that dedifferentiated GSCs appear to reacquire at least one aspect of native GSC behavior, the centrosome orientation checkpoint, a GSC-specific checkpoint mechanism that ensures oriented spindle to achieve asymmetric stem cell divisions. Our findings provide important insights into the robust mechanisms ensuring asymmetric division in the niche.

Indexed as

Asymmetric Cell DivisionCentrosomeDrosophila melanogasterStem Cell NicheStem CellsAnimalsDrosophilaDrosophila ProteinsMaleTestisDrosophila Proteins

Identifiers

PMID41803431
PMCPMC13100198

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.