Evidence map›Paper›PMID 37894787›Full record

ArticleInternational journal of molecular sciences2023

Endotenon-Derived Type II Tendon Stem Cells Have Enhanced Proliferative and Tenogenic Potential.

Marta Clerici, Vera Citro, Amy L Byrne, Tina P Dale, Aldo R Boccaccini, Giovanna Della Porta, Nicola Maffulli, Nicholas R Forsyth

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. 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
2.4field-weighted citation impact, top 11% 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

2 citing papers in PubMed, 10 citations in OpenAlex.

  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

8 authors at 4 institutions in 3 countries.

Marta ClericiSchool of Pharmacy and Bioengineering, Keele University, Stoke-on-Trent ST4 7QB, UK.ORCID 0009-0009-8579-5271
Vera CitroSchool of Pharmacy and Bioengineering, Keele University, Stoke-on-Trent ST4 7QB, UK.
Amy L ByrneSchool of Pharmacy and Bioengineering, Keele University, Stoke-on-Trent ST4 7QB, UK.
Tina P DaleSchool of Pharmacy and Bioengineering, Keele University, Stoke-on-Trent ST4 7QB, UK.ORCID 0000-0001-9461-8220
Aldo R BoccacciniInstitute for Biomaterials, Department of Materials Science and Engineering, Friedrich-Alexander-University of Erlangen-Nürnberg, 91058 Erlangen, Germany.ORCID 0000-0002-7377-2955
Giovanna Della PortaDepartment of Medicine, Surgery and Dentistry, University of Salerno, Via S. Allende, 84081 Baronissi, Italy.ORCID 0000-0002-1426-0159
Nicola MaffulliSchool of Pharmacy and Bioengineering, Keele University, Stoke-on-Trent ST4 7QB, UK.ORCID 0000-0002-5327-3702
Nicholas R ForsythSchool of Pharmacy and Bioengineering, Keele University, Stoke-on-Trent ST4 7QB, UK.ORCID 0000-0001-5156-4824
University of Salerno · ITFriedrich-Alexander-Universität Erlangen-Nürnberg · DEKeele University · GBUniversity of Aberdeen · GB

Funding

Engineering and Physical Sciences Research Council (EPSRC) Centre for Doctoral Training in Regenerative Medicine EP/L015072/1European Union's Horizon 2020 Research and Innovation Program under the Marie Skłodowska-Curie grant agreement 955685
6 · The paper itself

Abstract

Tendon injuries caused by overuse or age-related deterioration are frequent. Incomplete knowledge of somatic tendon cell biology and their progenitors has hindered interventions for the effective repair of injured tendons. Here, we sought to compare and contrast distinct tendon-derived cell populations: type I and II tendon stem cells (TSCs) and tenocytes (TNCs). Porcine type I and II TSCs were isolated via the enzymatic digestion of distinct membranes (paratenon and endotenon, respectively), while tenocytes were isolated through an explant method. Resultant cell populations were characterized by morphology, differentiation, molecular, flow cytometry, and immunofluorescence analysis. Cells were isolated, cultured, and evaluated in two alternate oxygen concentrations (physiological (2%) and air (21%)) to determine the role of oxygen in cell biology determination within this relatively avascular tissue. The different cell populations demonstrated distinct proliferative potential, morphology, and transcript levels (both for tenogenic and stem cell markers). In contrast, all tendon-derived cell populations displayed multipotent differentiation potential and immunophenotypes (positive for CD90 and CD44). Type II TSCs emerged as the most promising tendon-derived cell population for expansion, given their enhanced proliferative potential, multipotency, and maintenance of a tenogenic profile at early and late passage. Moreover, in all cases, physoxia promoted the enhanced proliferation and maintenance of a tenogenic profile. These observations help shed light on the biological mechanisms of tendon cells, with the potential to aid in the development of novel therapeutic approaches for tendon disorders.

Indexed as

Tendon InjuriesTendonsAnimalsCell DifferentiationOxygenStem CellsSwineOxygentendinopathiestendon regenerationtenogenic markersTNCsTSCs

Identifiers

PMID37894787
PMCPMC10606148
OpenAlexW4387573821

What Socratic 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 Socratic graph.