Evidence map›Paper›PMID 36180273›Full record

ArticleBiointerphases2022

Interleukin 1β and lipopolysaccharides induction dictate chondrocyte morphological properties and reduce cellular roughness and adhesion energy comparatively.

Alia H Mallah, Mahmoud Amr, Arda Gozen, Juana Mendenhall, Bernard J Van-Wie, Nehal I Abu-Lail

Open access · greenAbstract read
In one paragraph

Article in Biointerphases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Alia H MallahDepartment of Biomedical Engineering and Chemical Engineering, The University of Texas at San Antonio (UTSA), San Antonio, Texas 78249.ORCID 0000-0001-9555-5583
Mahmoud AmrDepartment of Biomedical Engineering and Chemical Engineering, The University of Texas at San Antonio (UTSA), San Antonio, Texas 78249.ORCID 0000-0002-8555-8497
Arda GozenSchool of Mechanical and Materials Engineering, Washington State University, Pullman, Washington 99164.ORCID 0000-0002-2680-2269
Juana MendenhallDepartment of Chemistry, Morehouse College, Atlanta, Georgia 30314.
Bernard J Van-WieGene and Linda Voiland School of Chemical Engineering and Bioengineering, Washington State University, Pullman, Washington 99164.ORCID 0000-0001-7382-9715
Nehal I Abu-LailDepartment of Biomedical Engineering and Chemical Engineering, The University of Texas at San Antonio (UTSA), San Antonio, Texas 78249.ORCID 0000-0002-2319-2450
The University of Texas at San Antonio · US

Funding

TRAINING IN BIOTECHNOLOGY: EMPHASIS ON PROTEIN CHEMISTRYT32GM008336 · NIGMS · WASHINGTON STATE UNIVERSITY · PI CALL, DOUGLAS R. · 1989 to 2023
$8.9M
NIGMS NIH HHS T32 GM008336
6 · The paper itself

Abstract

Osteoarthritis (OA) is a whole joint disease marked by the degradation of the articular cartilage (AC) tissue, chronic inflammation, and bone remodeling. Upon AC's injury, proinflammatory mediators including interleukin 1β (IL1β) and lipopolysaccharides (LPS) play major roles in the onset and progression of OA. The objective of this study was to mechanistically detect and compare the effects of IL1β and LPS, separately, on the morphological and nanomechanical properties of bovine chondrocytes. Cells were seeded overnight in a full serum medium and the next day divided into three main groups: A negative control (NC) of a reduced serum medium and 10 ng/ml IL1ß or 10 ng/ml LPS-modified media. Cells were induced for 24 h. Nanomechanical properties (elastic modulus and adhesion energy) and roughness were quantified using atomic force microscopy. Nitric oxide, prostaglandin 2 (PGE2), and matrix metalloproteinases 3 (MMP3) contents; viability of cells; and extracellular matrix components were quantified. Our data revealed that viability of the cells was not affected by inflammatory induction and IL1ß induction increased PGE2. Elastic moduli of cells were similar among IL1β and NC while LPS significantly decreased the elasticity compared to NC. IL1ß induction resulted in least cellular roughness while LPS induction resulted in least adhesion energy compared to NC. Our images suggest that IL1ß and LPS inflammation affect cellular morphology with cytoskeleton rearrangements and the presence of stress fibers. Finally, our results suggest that the two investigated inflammatory mediators modulated chondrocytes' immediate responses to inflammation in variable ways.

Indexed as

ChondrocytesOsteoarthritisAnimalsCattleCells, CulturedDinoprostoneInflammationInterleukin-1betaLipopolysaccharidesMatrix Metalloproteinase 3Nitric OxideDinoprostoneInterleukin-1betaLipopolysaccharidesMatrix Metalloproteinase 3Nitric Oxide

Identifiers

PMID36180273
PMCPMC9526521
OpenAlexW4298149256

What OpenQuestion 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 OpenQuestion graph.