Effects of non-enzymatic glycation on the micro- and nano-mechanics of articular cartilage

Journal Article (2018)
Author(s)

P. Rahnamay Moshtagh (TU Delft - Biomaterials & Tissue Biomechanics, University Medical Center Utrecht)

N. Korthagen (University Medical Center Utrecht, Universiteit Utrecht)

M. H.P. van Rijen (University Medical Center Utrecht)

R.M. Castelein (University Medical Center Utrecht)

Amir A. A. Zadpoor (TU Delft - Biomaterials & Tissue Biomechanics)

H.H. Weinans (University Medical Center Utrecht, TU Delft - Biomaterials & Tissue Biomechanics)

Research Group
Biomaterials & Tissue Biomechanics
DOI related publication
https://doi.org/10.1016/j.jmbbm.2017.09.035
More Info
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Publication Year
2018
Language
English
Research Group
Biomaterials & Tissue Biomechanics
Volume number
77
Pages (from-to)
551-556

Abstract

The mechanical properties of articular cartilage depend on the quality of its matrix, which consists of collagens and glycosaminoglycans (GAGs). The accumulation of advanced glycation end products (AGEs) can greatly affect
the mechanics of cartilage. In the current study, we simulated the accumulation of AGEs by using L-threose to cross-link collagen molecules in the cartilage matrix (in vitro). The resulting changes in the mechanical properties (stiffness) of cartilage are then measured both at the micrometer-scale (using micro-indenter) and nanometer-scale (using indentation-type atomic force microscopy). Non-enzymatic cross-linking within the cartilage matrix was confirmed by the browning of L-threose-treated samples. We observed > 3 times increase in the
micro-scale stiffness and up to 12-fold increase in the nano-scale stiffness of the glycated cartilage in the peak pertaining to the collagen fibers, which is caused by cartilage network embrittlement. At the molecular level, we found that besides the collagen component, the glycation process also influenced the GAG macromolecules.
Comparing cartilage samples before and after L-threose treatment revealed that artificially induced-AGEs also
decelerate in vitro degradation (likely via matrix metalloproteinases), observed at both micro- and nano-scales.
The combined observations suggest that non-enzymatic glycation may play multiple roles in mechanochemical
functioning of articular cartilage

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