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首页> 外文期刊>Investigative ophthalmology & visual science >Keratan sulfate and chondroitin/dermatan sulfate in maximally recovered hypocellular stromal interface scars of postmortem human LASIK corneas.
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Keratan sulfate and chondroitin/dermatan sulfate in maximally recovered hypocellular stromal interface scars of postmortem human LASIK corneas.

机译:死后人类LASIK角膜最大程度恢复的细胞间质界面瘢痕中的硫酸角质素和软骨素/硫酸皮肤素。

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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)-beta-1,3-Gal (MSD2) and disulfated Gal (6S)-beta-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 DeltaUA-beta-1,3-GalNAc(6S) (Deltadi-6S) CS/DS disaccharides from the LASIK interface scar was significantly higher than normal corneal stroma, whereas concentrations of DeltaUA-beta-1,3-GalNAc(4S) (Deltadi-4S) and nonsulfated Deltadi-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.
机译:目的:分析人死后LASIK角膜与正常对照角膜相比,非硫酸化和硫酸化硫酸角质素(KS)和软骨素/硫酸皮肤素(CS / DS)二糖的数量和分布。方法:通过激光捕获显微切割术(LCM)收集人LASIK角膜中央和中央下丘脑下细胞原始基质界面疤痕以及正常对照角膜类似区域的角膜基质组织样品,然后用特异性糖苷酶消化。消化液通过电喷雾串联质谱法(ESI-MS / MS)直接分析。结果:LASIK界面疤痕中单硫酸化的GlcNAc(6S)-β-1,3-Gal(MSD2)和二硫化的Gal(6S)-β-1,4-GlcNAc(6S)(DSD)KS二糖的浓度均显着低于正常对照组的角膜基质。与正常对照组相比,LASIK界面疤痕中非硫酸化(NSD)KS二糖的浓度没有发现显着差异。 LASIK界面瘢痕中DeltaUA-β-1,3-GalNAc(6S)(Deltadi-6S)CS / DS二糖的浓度显着高于正常角膜基质,而DeltaUA-beta-1,3-GalNAc( 4S)(Deltadi-4S)和未硫酸化的Deltadi-0S CS / DS二糖与正常角膜无明显差异。结论:LCM和ESI-MS / MS显示,LASIK界面瘢痕中KS和CS / DS二糖的分布与正常角膜基质组织中的显着不同。

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