4.5 Article

Atomic force microscopy to investigate spatial patterns of response to interleukin-1beta in engineered cartilage tissue elasticity

Journal

JOURNAL OF BIOMECHANICS
Volume 47, Issue 9, Pages 2157-2164

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.jbiomech.2013.10.056

Keywords

Chondrocyte differentiation; Tissue engineering; Inflammation; Mechanical properties; Atomic force microscopy

Funding

  1. European Union (Project OPHIS) [FP7-NMP-2009-SMALL-3-246373]

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Atomic force microscopy (AFM) has been proposed as a tool to evaluate the structural and mechanical properties of cartilage tissue. Here, we aimed at assessing whether AFM can be employed to quantify spatially resolved elastic response of tissue engineered cartilage (TEC) to short exposure to IL-1 beta, thus mimicking the initially inflammatory implantation site. TEC generated by 14 days of pellet-culture of expanded human chondrocytes was left untreated (ctr) or exposed to IL-1 beta for 3 days. TEC pellets were then cut in halves that were glued on a Petri dish. Profiles of elasticity were obtained by sampling with a nanometer sized, pyramidal indenting tip, with 200 gm step resolution, the freshly exposed surfaces along selected directions. Replicate TECs were analyzed biochemically and histologically. GAG contents and elasticity of pellets decreased (1.4- and 2.6-fold, respectively, p < 0.05) following IL-1 beta stimulation. Tissue quality was evaluated by scoring histological pictures taken at 200 mu m intervals, using the Bern-score grading system. At each distance, scores of ctr TEC were higher than those IL-1 beta treated, with the largest differences between the two groups observed in the central regions. Consistent with the histological results, elasticity of IL-1 beta-treated TEC was lower than in ctr pellets (up to 3.4-fold at 200 pm from the center). IL-1 beta treated but not ctr TEC was intensely stained for MMP-13 and DIPEN (cryptic fragment of aggrecan) especially in the central regions. The findings indicate the potential of AFM to investigate structure/function relationships in TEC and to perform tests aimed at predicting the functionality of TEC upon implantation. (C) 2013 Elsevier Ltd. All rights reserved.

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