نبذة مختصرة : This study investigated changes in collagen fibril architecture and the sulphation status of keratan sulphate (KS) glycosaminoglycan (GAG) epitopes from central to peripheral corneal regions. Freshly excised adult bovine corneal tissue was examined as a function of radial position from the centre of the cornea outwards. Corneal thickness, tissue hydration, hydroxyproline content, and the total amount of sulphated GAG were all measured. High and low-sulphated epitopes of keratan sulphate were studied by immunohistochemistry and quantified by ELISA. Chondroitin sulphate (CS) and dermatan sulphate (DS) distributions were observed by immunohistochemistry following specific enzyme digestions. Electron microscopy and X-ray fibre diffraction were used to ascertain collagen fibril architecture. The bovine cornea was 1021 ± 5.42 μm thick at its outer periphery, defined as 9–12 mm from the corneal centre, compared to 844 ± 8.10 μm at the centre. The outer periphery of the cornea was marginally, but not significantly, more hydrated than the centre (H = 4.3 vs. H = 3.7), and was more abundant in hydroxyproline (0.12 vs. 0.06 mg/mg dry weight of cornea). DMMB assays indicated no change in the total amount of sulphated GAG across the cornea. Immunohistochemistry revealed the presence of both high- and low-sulphated epitopes of KS, as well as DS, throughout the cornea, and CS only in the peripheral cornea before the limbus. Quantification by ELISA, disclosed that although both high- and low-sulphated KS remained constant throughout stromal depth at different radial positions, high-sulphated epitopes remained constant from the corneal centre to outer-periphery, whereas low-sulphated epitopes increased significantly. Both small angle X-ray diffraction and TEM analysis revealed that collagen fibril diameter remained relatively constant until the outer periphery was reached, after which fibrils became more widely spaced (from small angle x-ray diffraction analysis) and of larger diameter as they approached the sclera. ...
Relation: https://orca.cardiff.ac.uk/id/eprint/64500/2/Meek%202014%201-s2.0-S0945053X14000973-main.pdf; Ho, Leona T. Y., Harris, Anthony M., Tanioka, Hidetoshi, Yagi, Naoto, Kinoshita, Shigeru, Caterson, Bruce https://orca.cardiff.ac.uk/view/cardiffauthors/A071381D.html orcid:0000-0001-6016-0661 orcid:0000-0001-6016-0661, Quantock, Andrew James https://orca.cardiff.ac.uk/view/cardiffauthors/A0636159.html orcid:0000-0002-2484-3120 orcid:0000-0002-2484-3120, Young, Robert David orcid:0000-0002-8300-8002 orcid:0000-0002-8300-8002 and Meek, Keith Michael Andrew https://orca.cardiff.ac.uk/view/cardiffauthors/A032669F.html orcid:0000-0002-9948-7538 orcid:0000-0002-9948-7538 2014. A comparison of glycosaminoglycan distributions, keratan sulphate sulphation patterns and collagen fibril architecture from central to peripheral regions of the bovine cornea. Matrix Biology 38 , pp. 59-68. 10.1016/j.matbio.2014.06.004 https://doi.org/10.1016/j.matbio.2014.06.004 file https://orca.cardiff.ac.uk/id/eprint/64500/2/Meek%202014%201-s2.0-S0945053X14000973-main.pdf
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