Evidence map›Paper›PMID 34129185›Full record

ArticleIn vitro cellular & developmental biology. Animal2021

Enhanced matrix production by cocultivated human stem cells and chondrocytes under concurrent mechanical strain.

Haneen A Abusharkh, Alia H Mallah, Mahmoud M Amr, Juana Mendenhall, Bulent A Gozen, Edwin M Tingstad, Nehal I Abu-Lail, Bernard J Van Wie

Open access · greenAbstract read
In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2021. 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 30% 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, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
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 1 country.

Haneen A AbusharkhVoiland School of Chemical Engineering and Bioengineering, Washington State University, 1505 NE Stadium Way, Pullman, WA, 99164-6515, USA.
Alia H MallahDepartment of Biomedical Engineering and Chemical Engineering, The University of Texas at San Antonio, San Antonio, TX, 78249, USA.
Mahmoud M AmrDepartment of Biomedical Engineering and Chemical Engineering, The University of Texas at San Antonio, San Antonio, TX, 78249, USA.
Juana MendenhallDepartment of Chemistry, Morehouse College, Atlanta, GA, 30314, USA.
Bulent A GozenSchool of Mechanical and Materials Engineering, Washington State University, Pullman, WA, 99164-2920, USA.
Edwin M TingstadInland Orthopedic Surgery and Sports Medicine Clinic, Pullman, WA, 99163, USA.
Nehal I Abu-LailDepartment of Biomedical Engineering and Chemical Engineering, The University of Texas at San Antonio, San Antonio, TX, 78249, USA.
Bernard J Van WieVoiland School of Chemical Engineering and Bioengineering, Washington State University, 1505 NE Stadium Way, Pullman, WA, 99164-6515, USA. bvanwie@wsu.edu.ORCID http://orcid.org/0000-0001-7382-9715
The University of Texas at San Antonio · USWashington State University · USAnderson Orthopaedic Clinic · USMorehouse College · US

Funding

TRAINING IN BIOTECHNOLOGY: EMPHASIS ON PROTEIN CHEMISTRYT32GM008336 · NIGMS · WASHINGTON STATE UNIVERSITY · PI CALL, DOUGLAS R. · 1989 to 2023
$8.9M
Division of Chemical, Bioengineering, Environmental, and Transport Systems 1606226NIGMS NIH HHS GM008336-31NIGMS NIH HHS T32 GM008336
6 · The paper itself

Abstract

Conventional treatments of osteoarthritis have failed to re-build functional articular cartilage. Tissue engineering clinical treatments for osteoarthritis, including autologous chondrocyte implantation, provides an alternative approach by injecting a cell suspension to fill lesions within the cartilage in osteoarthritic knees. The success of chondrocyte implantation relies on the availability of chondrogenic cell lines, and their resilience to high mechanical loading. We hypothesize we can reduce the numbers of human articular chondrocytes necessary for a treatment by supplementing cultures with human adipose-derived stem cells, in which stem cells will have protective and stimulatory effects on mixed cultures when exposed to high mechanical loads, and in which coculture will enhance production of requisite extracellular matrix proteins over those produced by stretched chondrocytes alone. In this work, adipose-derived stem cells and articular chondrocytes were cultured separately or cocultivated at ratios of 3:1, 1:1, and 1:3 in static plates or under excessive cyclic tensile strain of 10% and results were compared to culturing of both cell types alone with and without cyclic strain. Results indicate 75% of chondrocytes in engineered articular cartilage can be replaced with stem cells with enhanced collagen over all culture conditions and glycosaminoglycan content over stretched cultures of chondrocytes. This can be done without observing adverse effects on cell viability. Collagen and glycosaminoglycan secretion, when compared to chondrocyte alone under 10% strain, was enhanced 6.1- and 2-fold, respectively, by chondrocytes cocultivated with stem cells at a ratio of 1:3.

Indexed as

Coculture TechniquesAdipocytesAdipose TissueCartilage, ArticularCell DifferentiationChondrocytesExtracellular MatrixExtracellular Matrix ProteinsHumansMesenchymal Stem CellsOsteoarthritisStem CellsStress, MechanicalTissue EngineeringTissue ScaffoldsExtracellular Matrix ProteinsArticular cartilageChondrocytesCoculture techniquesCyclic tensile strainMesenchymal stem cellsTissue engineering

Identifiers

PMID34129185
PMCPMC8380185
OpenAlexW3170682283

What OpenQuestion holds

Textmetadata
LicenceTDM
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.