Evidence map›Paper›PMID 23613892›Full record

ArticlePloS one2013

Effect of age and cytoskeletal elements on the indentation-dependent mechanical properties of chondrocytes.

Nadeen O Chahine, Craig Blanchette, Cynthia B Thomas, Jeffrey Lu, Dominik Haudenschild, Gabriela G Loots

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. The cellular mechanobiology of aging: from biology to mechanics.Annals of the New York Academy of Sciences · 2021
    Review
  6. Article
  7. Article
  8. Proteome Alterations in Equine Osteochondrotic Chondrocytes.International journal of molecular sciences · 2019
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. High-Throughput Assessment of Cellular Mechanical Properties.Annual review of biomedical engineering · 2015
    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

6 authors at 4 institutions in 1 country.

Nadeen O ChahineThe Feinstein Institute for Medical Research, Hofstra North Shore LIJ School of Medicine, Manhasset, New York, United States of America.
Craig Blanchette
Cynthia B Thomas
Jeffrey Lu
Dominik Haudenschild
Gabriela G Loots
Lawrence Livermore National Laboratory · USUniversity of California Davis Medical Center · USFeinstein Institute for Medical Research · USUniversity of California, Merced · US

Funding

Identification of Mechanoresponsive Promoter Elements in ChondrogenesisR03AR061038 · NIAMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HAUDENSCHILD, DOMINIK R · 2011 to 2013
$227k
NIAMS NIH HHS AR061038NIAMS NIH HHS R03 AR061038
6 · The paper itself

Abstract

Articular cartilage chondrocytes are responsible for the synthesis, maintenance, and turnover of the extracellular matrix, metabolic processes that contribute to the mechanical properties of these cells. Here, we systematically evaluated the effect of age and cytoskeletal disruptors on the mechanical properties of chondrocytes as a function of deformation. We quantified the indentation-dependent mechanical properties of chondrocytes isolated from neonatal (1-day), adult (5-year) and geriatric (12-year) bovine knees using atomic force microscopy (AFM). We also measured the contribution of the actin and intermediate filaments to the indentation-dependent mechanical properties of chondrocytes. By integrating AFM with confocal fluorescent microscopy, we monitored cytoskeletal and biomechanical deformation in transgenic cells (GFP-vimentin and mCherry-actin) under compression. We found that the elastic modulus of chondrocytes in all age groups decreased with increased indentation (15-2000 nm). The elastic modulus of adult chondrocytes was significantly greater than neonatal cells at indentations greater than 500 nm. Viscoelastic moduli (instantaneous and equilibrium) were comparable in all age groups examined; however, the intrinsic viscosity was lower in geriatric chondrocytes than neonatal. Disrupting the actin or the intermediate filament structures altered the mechanical properties of chondrocytes by decreasing the elastic modulus and viscoelastic properties, resulting in a dramatic loss of indentation-dependent response with treatment. Actin and vimentin cytoskeletal structures were monitored using confocal fluorescent microscopy in transgenic cells treated with disruptors, and both treatments had a profound disruptive effect on the actin filaments. Here we show that disrupting the structure of intermediate filaments indirectly altered the configuration of the actin cytoskeleton. These findings underscore the importance of the cytoskeletal elements in the overall mechanical response of chondrocytes, indicating that intermediate filament integrity is key to the non-linear elastic properties of chondrocytes. This study improves our understanding of the mechanical properties of articular cartilage at the single cell level.

Indexed as

AgingAnimalsCartilage, ArticularCattleChondrocytesCytoskeletonElastic ModulusMicroscopy, Atomic ForceStress, Mechanical

Identifiers

PMID23613892
PMCPMC3628340
OpenAlexW2091458234

What OpenQuestion holds

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LicenceCC0
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.