Evidence map›Paper›PMID 23410025›Full record

ArticleTissue engineering. Part A2013

Effects of serum and compressive loading on the cartilage matrix synthesis and spatiotemporal deposition around chondrocytes in 3D culture.

Peihui Wu, Elizabeth DeLassus, Debabrata Patra, Weiming Liao, Linda J Sandell

Abstract read
In one paragraph

Article in Tissue engineering. Part A, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Effect of interface mechanical discontinuities on scaffold-cartilage integration.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2019
    Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
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

5 authors.

Peihui WuDepartment of Orthopaedic Surgery, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Elizabeth DeLassus
Debabrata Patra
Weiming Liao
Linda J Sandell

Funding

The Role of the Osteoblast Secretome in Bone FormationP30AR057235 · NIAMS · WASHINGTON UNIVERSITY · PI SILVA, MATTHEW J · 2009 to 2018
$5.7M
FUNCTION AND REGULATION OF CD/RAPR01AR045550 · NIAMS · WASHINGTON UNIVERSITY · PI SANDELL, LINDA J · 1998 to 2013
$4.1M
NIAMS NIH HHS 5R01AR045550-14NIAMS NIH HHS P30AR057235
6 · The paper itself

Abstract

The aim of this study was to investigate the effects of serum and compressive dynamic loading on the cartilaginous matrix spatiotemporal distribution around chondrocytes in vitro. Murine chondrocytes suspended in agarose were cultured in serum-free media or in varying concentrations of serum with or without compressive dynamic loading. Gene expression was assayed by quantitative polymerase chain reaction. Immunohistochemistry was performed for type II collagen and type VI collagen, aggrecan, or cartilage oligomeric matrix protein (COMP) to study the effect of serum and dynamic loading on the spatiotemporal distribution of cartilage matrix components. Chondrocytes in serum-free culture exhibited negligible differences in type II collagen, aggrecan, and COMP mRNA expression levels over 15 days of cultivation. However, higher serum concentrations decreased matrix gene expression. Expression of the matrix metalloproteinases (MMP)-3 and MMP-13 mRNA increased over time in serum-free or reduced serum levels, but was significantly suppressed in 10% fetal bovine serum (FBS). Compressive loading significantly stimulated MMP-3 expression on days 7 and 15. Immunohistochemical analysis demonstrated that maximum pericellular matrix deposition was achieved in 10% FBS culture in the absence of compressive loading. The pericellular distribution of type II and VI collagens, aggrecan, and COMP proteins tended to be more co-localized in the pericellular region from day 9 to day 21; compressive loading helped promote this co-localization of matrix proteins. The results of this study suggest that the quantity, quality, and spatial distribution of cartilaginous matrix can be altered by serum concentrations and compressive loading.

Indexed as

AnimalsCartilageChondrocytesCollagen Type IICollagen Type VICulture Media, Serum-FreeExtracellular Matrix ProteinsGlycoproteinsImmunohistochemistryMatrilin ProteinsMatrix Metalloproteinase 13Matrix Metalloproteinase 3MiceMice, Inbred C57BLReal-Time Polymerase Chain ReactionCollagen Type IICollagen Type VICulture Media, Serum-FreeExtracellular Matrix ProteinsGlycoproteinsMatn1 protein, mouseMatrilin ProteinsMatrix Metalloproteinase 13Matrix Metalloproteinase 3

Identifiers

PMID23410025
PMCPMC3609636

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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.