Evidence map›Paper›PMID 37268650›Full record

ArticleInternational journal of oral science2023

Primary cilia support cartilage regeneration after injury.

Dike Tao, Lei Zhang, Yunpeng Ding, Na Tang, Xiaoqiao Xu, Gongchen Li, Pingping Niu, Rui Yue, Xiaogang Wang, Yidong Shen and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of oral science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Ciliary-Mediated Mechanotransduction in Skeletal Development and Diseases.Results and problems in cell differentiation · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. Article
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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

11 authors at 4 institutions in 1 country.

Dike TaoDepartment of Implantology, School & Hospital of Stomatology, Tongji University, Shanghai, China.
Lei ZhangDepartment of Implantology, School & Hospital of Stomatology, Tongji University, Shanghai, China.
Yunpeng DingDepartment of Implantology, School & Hospital of Stomatology, Tongji University, Shanghai, China.
Na TangState Key Laboratory of Cell Biology, Shanghai Institute of Biochemistry and Cell Biology, Center for Excellence in Molecular Cell Science, Chinese Academy of Sciences, Shanghai, China.
Xiaoqiao XuDepartment of Implantology, School & Hospital of Stomatology, Tongji University, Shanghai, China.
Gongchen LiShanghai Engineering Research Center of Tooth Restoration and Regeneration, Shanghai, China.
Pingping NiuDepartment of Implantology, School & Hospital of Stomatology, Tongji University, Shanghai, China.
Rui YueInstitute for Regenerative Medicine, Shanghai East Hospital, Frontier Science Center for Stem Cell Research, Shanghai Key Laboratory of Signaling and Disease Research, School of Life Sciences and Technology, Tongji University, Shanghai, China.ORCID 0000-0002-3401-369X
Xiaogang WangKey Laboratory of Big Data-Based Precision Medicine, School of Engineering Medicine, Beihang University, Beijing, China.ORCID 0000-0001-9798-834X
Yidong ShenState Key Laboratory of Cell Biology, Shanghai Institute of Biochemistry and Cell Biology, Center for Excellence in Molecular Cell Science, Chinese Academy of Sciences, Shanghai, China.
Yao SunDepartment of Implantology, School & Hospital of Stomatology, Tongji University, Shanghai, China. yaosun@tongji.edu.cn.ORCID 0000-0002-4323-0506
Tongji University · CNChinese Academy of Sciences · CNBeihang University · CNShanghai East Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In growing children, growth plate cartilage has limited self-repair ability upon fracture injury always leading to limb growth arrest. Interestingly, one type of fracture injuries within the growth plate achieve amazing self-healing, however, the mechanism is unclear. Using this type of fracture mouse model, we discovered the activation of Hedgehog (Hh) signaling in the injured growth plate, which could activate chondrocytes in growth plate and promote cartilage repair. Primary cilia are the central transduction mediator of Hh signaling. Notably, ciliary Hh-Smo-Gli signaling pathways were enriched in the growth plate during development. Moreover, chondrocytes in resting and proliferating zone were dynamically ciliated during growth plate repair. Furthermore, conditional deletion of the ciliary core gene Ift140 in cartilage disrupted cilia-mediated Hh signaling in growth plate. More importantly, activating ciliary Hh signaling by Smoothened agonist (SAG) significantly accelerated growth plate repair after injury. In sum, primary cilia mediate Hh signaling induced the activation of stem/progenitor chondrocytes and growth plate repair after fracture injury.

Indexed as

Hedgehog ProteinsReceptors, G-Protein-CoupledAnimalsCartilageCiliaMiceRegenerationHedgehog ProteinsReceptors, G-Protein-Coupled

Identifiers

PMID37268650
PMCPMC10238430
OpenAlexW4379197083

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.