TY - JOUR
T1 - Magnetization transfer imaging provides a quantitative measure of chondrogenic differentiation and tissue development
AU - Li, Weiguo
AU - Hong, Liu
AU - Hu, Liping
AU - Magin, Richard L.
PY - 2010/12/1
Y1 - 2010/12/1
N2 - The goal of the present investigation was to test whether quantitative magnetization transfer imaging can be used as a noninvasive evaluation method for engineered cartilage. In this work, we used magnetic resonance imaging (MRI) to monitor the chondrogenesis of stem-cell-based engineered tissue over a 3-week period by measuring on a pixel-by-pixel basis the relaxation times (T1 and T2), the apparent diffusion coefficient, and the magnetization transfer parameters: bound proton fraction and cross-relaxation rate (k). Tissue-engineered constructs for generating cartilage were created by seeding mesenchymal stem cells in a gelatin sponge. Every 7 days, tissue samples were analyzed using MRI, histological, and biochemical methods. The MRI measurements were verified by histological analysis, and the imaging data were correlated with biochemical analysis of the developing cartilage matrix for glycosaminoglycan content. The MRI analysis for bound proton fraction and k showed a statistically significant increase that was correlated with the increase of glycosaminoglycan (R=0.96 and 0.87, respectively, p<0.05), whereas T1, T2, and apparent diffusion coefficient results did not show any significant changes over the 3-week measurement period.
AB - The goal of the present investigation was to test whether quantitative magnetization transfer imaging can be used as a noninvasive evaluation method for engineered cartilage. In this work, we used magnetic resonance imaging (MRI) to monitor the chondrogenesis of stem-cell-based engineered tissue over a 3-week period by measuring on a pixel-by-pixel basis the relaxation times (T1 and T2), the apparent diffusion coefficient, and the magnetization transfer parameters: bound proton fraction and cross-relaxation rate (k). Tissue-engineered constructs for generating cartilage were created by seeding mesenchymal stem cells in a gelatin sponge. Every 7 days, tissue samples were analyzed using MRI, histological, and biochemical methods. The MRI measurements were verified by histological analysis, and the imaging data were correlated with biochemical analysis of the developing cartilage matrix for glycosaminoglycan content. The MRI analysis for bound proton fraction and k showed a statistically significant increase that was correlated with the increase of glycosaminoglycan (R=0.96 and 0.87, respectively, p<0.05), whereas T1, T2, and apparent diffusion coefficient results did not show any significant changes over the 3-week measurement period.
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U2 - 10.1089/ten.tec.2009.0777
DO - 10.1089/ten.tec.2009.0777
M3 - Article
C2 - 20373975
AN - SCOPUS:78649675863
SN - 1937-3384
VL - 16
SP - 1407
EP - 1415
JO - Tissue Engineering - Part C: Methods
JF - Tissue Engineering - Part C: Methods
IS - 6
ER -