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接受准分子原位角膜磨镶术(LASIK)的人角膜植片的蛋白聚糖合成

Proteoglycan synthesis by human corneal explants submitted to laser in situ keratomileusis (LASIK).

作者信息

Martins Suy Anne Reboucas, Campos Mauro Q, Vidal Benedicto C, Berto Alessandra G A, Aguiar Jair A K, Michelacci Yara M

机构信息

Departamento de Oftalmologia, Universidade Federal de São Paulo, Escola Paulista de Medicina, São Paulo, Brazil.

出版信息

Mol Vis. 2007 Feb 1;13:142-50.

Abstract

PURPOSE

To evaluate the acute effects of laser in situ keratomileusis (LASIK) upon the synthesis of proteoglycans (PGs) and collagen fibril organization in human corneal explants.

METHODS

Human corneas that had been rejected for transplants were obtained at Banco de Olhos of Hospital São Paulo. For each eye pair, one cornea was submitted to refractive surgery, and the other was used as its matched control. After surgery, the corneas were excised from the eyes and immediately placed in a Ham F-12 nutrient mixture containing (35)S-sulfate for the metabolic labeling of PGs. After 24 h incubation, PGs were extracted and identified by a combination of agarose gel electrophoresis and enzymatic degradation with protease and specific glycosaminoglycan lyases. Histopathological and birefringence analysis were performed in fixed tissue slices.

RESULTS

A marked decrease in (35)S-sulfate incorporation in PGs was observed in corneal explants that received LASIK, especially concerning dermatan sulfate-PGs, with keratan sulfate- and heparan sulfate-PG synthesis reduced to a lower degree. Only low molecular weight PGs were present in the corneas, both before and 24 h after LASIK. No sign of wound healing processes were observed, but a marked change in corneal birefringence was seen following LASIK treatment.

CONCLUSIONS

Laser application led to decreased PG biosynthesis in human corneal explants, with marked changes in the collagen fibril organization, as revealed by changes in the tissue birefringence.

摘要

目的

评估准分子原位角膜磨镶术(LASIK)对人角膜植片中蛋白聚糖(PGs)合成及胶原纤维组织的急性影响。

方法

在圣保罗医院眼库获取被拒绝用于移植的人角膜。对于每对眼睛,一只角膜接受屈光手术,另一只作为配对对照。术后,将角膜从眼中取出,立即置于含有(35)S - 硫酸盐的Ham F - 12营养混合物中,用于PGs的代谢标记。孵育24小时后,提取PGs,并通过琼脂糖凝胶电泳结合蛋白酶和特异性糖胺聚糖裂解酶的酶解进行鉴定。对固定组织切片进行组织病理学和双折射分析。

结果

接受LASIK的角膜植片中观察到PGs中(35)S - 硫酸盐掺入明显减少,尤其是硫酸皮肤素 - PGs,硫酸角质素和硫酸乙酰肝素 - PGs合成减少程度较低。LASIK术前和术后24小时角膜中均仅存在低分子量PGs。未观察到伤口愈合过程的迹象,但LASIK治疗后角膜双折射有明显变化。

结论

激光应用导致人角膜植片中PG生物合成减少,胶原纤维组织发生明显变化,这通过组织双折射的变化得以揭示。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fbf/2533033/8f56b6932c42/mv-v13-142-f1.jpg

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