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1From the Division of Biology, Kansas State University, Manhattan, Kansas; the 3Department of Ophthalmology, Emory University, Atlanta, Georgia; the 4Department of Ophthalmology, Ruprecht-Karls-University, Heidelberg, Germany; and the 5Central Research Laboratories, Seikagaku Corp., Higashiyamato-shi, Japan.
PURPOSE. To analyze the amounts and distributions of nonsulfated and sulfated keratan sulfate (KS) and chondroitin/dermatan sulfate (CS/DS) disaccharides in the interface wound of human postmortem LASIK corneas in comparison with normal control corneas.
METHODS. Corneal stromal tissue samples from central and paracentral hypocellular primitive stromal interface scars of human LASIK corneas and from similar regions of normal control corneas were collected by laser capture microdissection (LCM) and subsequently were digested with specific glycosidase enzymes. Digests were directly analyzed by electrospray ionization tandem mass spectrometry (ESI-MS/MS).
RESULTS. Concentrations of both monosulfated GlcNAc(6S)-ß-1,3-Gal (MSD2) and disulfated Gal (6S)-ß-1,4-GlcNAc(6S) (DSD) KS disaccharides from the LASIK interface scars were significantly lower than in normal control corneal stromas. No significant difference was found for the concentration of nonsulfated (NSD) KS disaccharides in LASIK interface scars compared with normal controls. The concentration of
UA-ß-1,3-GalNAc(6S) (
di-6S) CS/DS disaccharides from the LASIK interface scar was significantly higher than normal corneal stroma, whereas concentrations of
UA-ß-1,3-GalNAc(4S) (
di-4S) and nonsulfated
di-0S CS/DS disaccharides demonstrated no significant differences from normal corneas.
CONCLUSIONS. The profiles of KS and CS/DS disaccharides in LASIK interface scars are significantly different from those in normal cornea stromal tissue, as revealed by LCM and ESI-MS/MS.
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