Evidence map›Paper›PMID 37108698›Full record

ArticleInternational journal of molecular sciences2023

Differential Effects of Hypoxia versus Hyperoxia or Physoxia on Phenotype and Energy Metabolism in Human Chondrocytes from Osteoarthritic Compared to Macroscopically Normal Cartilage.

Lekha Jain, Scott M Bolam, A Paul Monk, Jacob T Munro, Even Chen, Jade Tamatea, Nicola Dalbeth, Raewyn C Poulsen

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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. 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 1 institution in 1 country.

Lekha JainDepartment of Pharmacology and Clinical Pharmacology, University of Auckland, Auckland 1023, New Zealand.
Scott M BolamDepartment of Surgery, University of Auckland, Auckland 1023, New Zealand.
A Paul MonkAuckland Bioengineering Institute, University of Auckland, Auckland 1010, New Zealand.
Jacob T MunroDepartment of Surgery, University of Auckland, Auckland 1023, New Zealand.
Even ChenDepartment of Pharmacology and Clinical Pharmacology, University of Auckland, Auckland 1023, New Zealand.
Jade TamateaTe Kupenga Hauora Māori, University of Auckland, Auckland 1010, New Zealand.
Nicola DalbethDepartment of Medicine, University of Auckland, Auckland 1023, New Zealand.
Raewyn C PoulsenDepartment of Pharmacology and Clinical Pharmacology, University of Auckland, Auckland 1023, New Zealand.ORCID 0000-0002-3788-6410
University of Auckland · NZ

Funding

Health Research Council of New Zealand 20/199
6 · The paper itself

Abstract

Chondrocyte phenotype and energy metabolism are altered in osteoarthritis (OA). However, most studies characterising the change in human chondrocyte behaviour in OA have been conducted in supraphysiological oxygen concentrations. The purpose of this study was to compare phenotype and energy metabolism in chondrocytes from macroscopically normal (MN) and OA cartilage maintained in 18.9% (standard tissue culture), 6% (equivalent to superficial zone of cartilage in vivo) or 1% oxygen (equivalent to deep zone of cartilage in vivo). MMP13 production was higher in chondrocytes from OA compared to MN cartilage in hyperoxia and physoxia but not hypoxia. Hypoxia promoted SOX9, COL2A1 and ACAN protein expression in chondrocytes from MN but not OA cartilage. OA chondrocytes used higher levels of glycolysis regardless of oxygen availability. These results show that differences in phenotype and energy metabolism between chondrocytes from OA and MN cartilage differ depending on oxygen availability. OA chondrocytes show elevated synthesis of cartilage-catabolising enzymes and chondrocytes from MN cartilage show reduced cartilage anabolism in oxygenated conditions. This is relevant as a recent study has shown that oxygen levels are elevated in OA cartilage in vivo. Our findings may indicate that this elevated cartilage oxygenation may promote cartilage loss in OA.

Indexed as

Cartilage, ArticularHyperoxiaOsteoarthritisCells, CulturedChondrocytesEnergy MetabolismHumansHypoxiaOxygenPhenotypeOxygenaggrecanchondrocyteglycolysishypoxiaMMP13osteoarthritisoxidative phosphorylationphysoxiaSOX9type II collagen

Identifiers

PMID37108698
PMCPMC10142591
OpenAlexW4366550112

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.