Evidence map›Paper›PMID 30451865›Full record

ArticleScientific reports2018

Hydrostatic pressure-generated reactive oxygen species induce osteoarthritic conditions in cartilage pellet cultures.

Bernhard Rieder, Anna M Weihs, Adelheid Weidinger, Dorota Szwarc, Sylvia Nürnberger, Heinz Redl, Dominik Rünzler, Carina Huber-Gries, Andreas H Teuschl

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed, 34 citations in OpenAlex.

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  13. Chondrocytes In Vitro Systems Allowing Study of OA.International journal of molecular sciences · 2022
    Review
  14. Remodeling Osteoarthritic Articular Cartilage under Hypoxic Conditions.International journal of molecular sciences · 2022
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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

9 authors at 2 institutions in 1 country.

Bernhard RiederDepartment Life Science Engineering, University of Applied Sciences Technikum Wien, 1200, Vienna, Austria.ORCID http://orcid.org/0000-0001-8961-2801
Anna M WeihsDepartment Life Science Engineering, University of Applied Sciences Technikum Wien, 1200, Vienna, Austria.
Adelheid WeidingerLudwig Boltzmann Institute for Experimental and Clinical Traumatology, AUVA Research Center, 1200, Vienna, Austria.
Dorota SzwarcDepartment Life Science Engineering, University of Applied Sciences Technikum Wien, 1200, Vienna, Austria.
Sylvia NürnbergerLudwig Boltzmann Institute for Experimental and Clinical Traumatology, AUVA Research Center, 1200, Vienna, Austria.ORCID http://orcid.org/0000-0002-5175-5118
Heinz RedlLudwig Boltzmann Institute for Experimental and Clinical Traumatology, AUVA Research Center, 1200, Vienna, Austria.ORCID http://orcid.org/0000-0003-1654-462X
Dominik RünzlerDepartment Life Science Engineering, University of Applied Sciences Technikum Wien, 1200, Vienna, Austria.
Carina Huber-GriesDepartment Life Science Engineering, University of Applied Sciences Technikum Wien, 1200, Vienna, Austria.
Andreas H TeuschlDepartment Life Science Engineering, University of Applied Sciences Technikum Wien, 1200, Vienna, Austria. teuschl@technikum-wien.at.
University of Applied Sciences Technikum Wien · ATLudwig Boltzmann Institute for Traumatology, The Research Center in Cooperation with AUVA · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoarthritis (OA) is one of the most common causes of disability and represents a major socio-economic burden. Despite intensive research, the molecular mechanisms responsible for the initiation and progression of OA remain inconclusive. In recent years experimental findings revealed elevated levels of reactive oxygen species (ROS) as a major factor contributing to the onset and progression of OA. Hence, we designed a hydrostatic pressure bioreactor system that is capable of stimulating cartilage cell cultures with elevated ROS levels. Increased ROS levels in the media did not only lead to an inhibition of glycosaminoglycans and collagen II formation but also to a reduction of already formed glycosaminoglycans and collagen II in chondrogenic mesenchymal stem cell pellet cultures. These effects were associated with the elevated activity of matrix metalloproteinases as well as the increased expression of several inflammatory cytokines. ROS activated different signaling pathways including PI3K/Akt and MAPK/ERK which are known to be involved in OA initiation and progression. Utilizing the presented bioreactor system, an OA in vitro model based on the generation of ROS was developed that enables the further investigation of ROS effects on cartilage degradation but can also be used as a versatile tool for anti-oxidative drug testing.

Indexed as

ChondrogenesisCartilage, ArticularCells, CulturedHumansHydrostatic PressureMesenchymal Stem CellsOsteoarthritisReactive Oxygen SpeciesSignal TransductionReactive Oxygen Species

Identifiers

PMID30451865
PMCPMC6242959
OpenAlexW2900673052

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.