Evidence map›Paper›PMID 40296211›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2025

The Function and Regulation of celsr1a in Skeletal Age-associated Homeostasis and Repair in Zebrafish.

Joao Castro, Kira Fagerstrom, Stephen Treaster, Jeffrey Duryea, Julia Charles, Matthew P Harris

Abstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Joao CastroDepartment of Orthopedic Surgery, Boston Children's Hospital, Boston, Massachusetts, USA.
Kira FagerstromDepartment of Orthopedic Surgery, Boston Children's Hospital, Boston, Massachusetts, USA.ORCID 0009-0001-1060-8963
Stephen TreasterDepartment of Orthopedic Surgery, Boston Children's Hospital, Boston, Massachusetts, USA.
Jeffrey DuryeaDepartment of Radiology, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Julia CharlesDepartment of Orthopedic Surgery, Brigham and Women's Hospital, Boston, Massachusetts, USA.ORCID 0000-0002-5875-314X
Matthew P HarrisDepartment of Orthopedic Surgery, Boston Children's Hospital, Boston, Massachusetts, USA.

Funding

Patterning the Vertebrate Dentition Through Replacement and RepairR01DE019637 · NIDCR · GEORGIA INSTITUTE OF TECHNOLOGY · PI STREELMAN, JEFFERY TODD · 2010 to 2022
$4.5M
Identifying determinants of rapid structural and/or clinical progression in knee osteoarthritis by quantitative assessment of structural features on radiographsR01AR080742 · NIAMS · UNIVERSITY OF ARIZONA · PI JEFFREY W DURYEA, C KENT KWOH · 2022 to 2026
$3.7M
Talking Back: leveraging dysfunctional osteoclasts to identify novel pathways of osteoclast-osteoblast communicationR21AR077768 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI CHARLES, JULIA F · 2021 to 2022
$456k
NIAMS NIH HHS R01AR080742NIAMS NIH HHS R21 AR077768NIAMS NIH HHS R21AR077768NIDCR NIH HHS R01DE019637
6 · The paper itself

Abstract

The decrease of tissue resiliency with aging is due, in part, to changes in the retention of stem cell/progenitor populations that act to restore and maintain tissue quality with age or injury. In mice, the Celsr1 gene has been identified as a regulator of quiescent stem cells, while in zebrafish, celsr1a mutants demonstrate an essential function in maintaining adult stem cell populations within the highly proliferative tissues of the gut and skin. Here, we investigate the role of celsr1a as a regulator of adult skeletal stem cells and mediator of skeletal homeostasis and repair. We find that celsr1a is essential for maintenance of bone mineral density and volume in adult zebrafish. Using an enhancer screen to identify tissue/cell-specific regulators of celsr1a, we identified enhancers active in specific tissues that reflect the normal expression of celsr1a. We characterized C1a-A an enhancer that is active within stem/progenitor cells of diverse tissues. Consistent with this role, C1a-A marks specific cells in mature skeletal structures of the zebrafish, residing on the endosteal surface of zebrafish vertebrae and fin long-bones. These cells are limited in number and contribute to osteocyte populations within the bony matrix. Using a novel long bone fracture assay in adult zebrafish, we find that celsr1a positive skeletal cells respond to damage and that celsr1a function is essential for fracture healing. Our investigation details an unexpected role of cels1a in skeletal repair and quality with age and highlights a new regulator of stem cell activity in the skeleton.

Indexed as

AgingBone and BonesHomeostasisZebrafish ProteinsAnimalsBone DensityZebrafishZebrafish ProteinsBone repairEnhancer regulationResponse to injuryStem-cell population

Identifiers

PMID40296211
PMCPMC12302133

What Socratic holds

Textmetadata
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 Socratic graph.