Evidence map›Paper›PMID 19591192›Full record

ArticleBiotechnology and bioengineering2009

Shear stress magnitude and duration modulates matrix composition and tensile mechanical properties in engineered cartilaginous tissue.

Christopher V Gemmiti, Robert E Guldberg

Abstract read
In one paragraph

Article in Biotechnology and bioengineering, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. The functionality and translatability of neocartilage constructs are improved with the combination of fluid-induced shear stress and bioactive factors.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  6. Review
  7. Review
  8. A Novel Bioreactor System Capable of Simulating theTissue engineering. Part C, Methods · 2020
    Article
  9. Article
  10. Review
  11. Review
  12. Utilizing the Foreign Body Response to Grow Tissue Engineered Blood Vessels in Vivo.Journal of cardiovascular translational research · 2017
    Review
  13. Article
  14. Review
  15. Article
  16. Mechanical regulation of skeletal development.Current osteoporosis reports · 2013
    Review
  17. Article
  18. Article
  19. Physical stimulation of chondrogenic cells in vitro: a review.Clinical orthopaedics and related research · 2011
    Review
  20. 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

2 authors.

Christopher V GemmitiCoulter Department of Biomedical Engineering, Georgia Institute of Technology, Emory School of Medicine, Atlanta, Georgia, USA.
Robert E Guldberg

Funding

Engineering Joint Scaffolds for Function/RegenerationR01DE013608 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HOLLISTER, SCOTT J · 2001 to 2005
$3.9M
Analysis of Cartilage Morphology and sGAG Content via Contrast Enhanced Micro-CTR21AR053716 · NIAMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI GULDBERG, ROBERT E · 2006 to 2007
$352k
NIAMS NIH HHS R21 AR053716NIDCR NIH HHS DE 13608NIDCR NIH HHS R01 DE013608
6 · The paper itself

Abstract

Cartilage tissue-engineering strategies aim to produce a functional extracellular matrix similar to that of the native tissue. However, none of the myriad approaches taken have successfully generated a construct possessing the structure, composition, and mechanical properties of healthy articular cartilage. One possible approach to modulating the matrix composition and mechanical properties of engineered tissues is through the use of bioreactor-driven mechanical stimulation. In this study, we hypothesized that exposing scaffold-free cartilaginous tissue constructs to 7 days of continuous shear stress at 0.001 or 0.1 Pa would increase collagen deposition and tensile mechanical properties compared to that of static controls. Histologically, type II collagen staining was evident in all construct groups, while a surface layer of type I collagen increased in thickness with increasing shear stress magnitude. The areal fraction of type I collagen was higher in the 0.1-Pa group (25.2 +/- 2.2%) than either the 0.001-Pa (13.6 +/- 3.8%) or the static (7.9 +/- 1.5%) group. Type II collagen content, as assessed by ELISA, was also higher in the 0.1-Pa group (7.5 +/- 2.1%) compared to the 0.001-Pa (3.0 +/- 2.25%) or static groups (3.7 +/- 3.2%). Temporal gene expression analysis showed a flow-induced increase in type I and type II collagen expression within 24 h of exposure. Interestingly, while the 0.1-Pa group showed higher collagen content, this group retained less sulfated glycosaminoglycans in the matrix over time in bioreactor culture. Increases in both tensile Young's modulus and ultimate strength were observed with increasing shear stress, yielding constructs possessing a modulus of nearly 5 MPa and strength of 1.3 MPa. This study demonstrates that shear stress is a potent modulator of both the amount and type of synthesized extracellular matrix constituents in engineered cartilaginous tissue with corresponding effects on mechanical function.

Indexed as

Stress, MechanicalTensile StrengthAnimalsAnimals, NewbornCartilageCattleChondrocytesExtracellular MatrixTissue Engineering

Identifiers

PMID19591192
PMCPMC2753758

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Registered trials

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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.