Evidence map›Paper›PMID 32211405›Full record

ArticleFrontiers in cell and developmental biology2020

Epiphyseal Cartilage Formation Involves Differential Dynamics of Various Cellular Populations During Embryogenesis.

Yi Zhang, Karl Annusver, Kazunori Sunadome, Polina Kameneva, Steven Edwards, Guanghua Lei, Maria Kasper, Andrei S Chagin, Igor Adameyko, Meng Xie

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Distal femoral morphology as a risk factor for osteoarthritis.Anatomical record (Hoboken, N.J. : 2007) · 2026
    Article
  2. Article
  3. 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

10 authors at 4 institutions in 4 countries.

Yi ZhangDepartment of Orthopaedics, Xiangya Hospital, Central South University, Changsha, China.
Karl AnnusverDepartment of Biosciences and Nutrition, Karolinska Institutet, Huddinge, Sweden.
Kazunori SunadomeDepartment of Physiology and Pharmacology, Karolinska Institutet, Solna, Sweden.
Polina KamenevaDepartment of Physiology and Pharmacology, Karolinska Institutet, Solna, Sweden.
Steven EdwardsLight Sheet Microscopy Pilot Facility at SciLifeLab, KTH Royal Institute of Technology, Stockholm, Sweden.
Guanghua LeiDepartment of Orthopaedics, Xiangya Hospital, Central South University, Changsha, China.
Maria KasperDepartment of Biosciences and Nutrition, Karolinska Institutet, Huddinge, Sweden.
Andrei S ChaginDepartment of Physiology and Pharmacology, Karolinska Institutet, Solna, Sweden.
Igor AdameykoDepartment of Physiology and Pharmacology, Karolinska Institutet, Solna, Sweden.
Meng XieDepartment of Physiology and Pharmacology, Karolinska Institutet, Solna, Sweden.
Karolinska Institutet · SECentral South University · CNMedical University of Vienna · ATScience for Life Laboratory · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A joint connects two or more bones together to form a functional unit that allows different types of bending and movement. Little is known about how the opposing ends of the connected bones are developed. Here, applying various lineage tracing strategies we demonstrate that progenies of Gdf5-, Col2-, Prrx1-, and Gli1-positive cells contribute to the growing epiphyseal cartilage in a spatially asymmetrical manner. In addition, we reveal that cells in the cartilaginous anlagen are likely to be the major sources for epiphyseal cartilage. Moreover, Gli1-positive cells are found to proliferate along the skeletal edges toward the periarticular region of epiphyseal surface. Finally, a switch in the mechanism of growth from cell division to cell influx likely occurs in the epiphyseal cartilage when joint cavitation has completed. Altogether, our findings reveal an asymmetrical mechanism of growth that drives the formation of epiphyseal cartilage ends, which might implicate on how the articular surface of these skeletal elements acquires their unique and sophisticated shape during embryonic development.

Indexed as

asymmetricalcartilageclonal tracingdynamicsembryonic developmentjoint

Identifiers

PMID32211405
PMCPMC7066500
OpenAlexW3010143753

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.