The effects of epithelial viability on stromal keratocyte apoptosis in porcine corneas stored in Optisol-GS

被引:9
作者
Chang, SW
Wang, YH
Pang, JHS
机构
[1] Far Eastern Mem Hosp, Dept Ophthalmol, Taipei 220, Taiwan
[2] Natl Taiwan Univ Hosp, Dept Ophthalmol, Taipei, Taiwan
[3] Taipei Med Univ, Dept Ophthalmol, Taipei, Taiwan
[4] Jen Thh Jr Coll Med Nursing & Management, Miaoli, Taiwan
[5] China Med Univ, Grad Inst Pharmaceut Chem, Taichung, Taiwan
[6] Chagn Gung Univ, Grad Inst Clin Med Sci, Tao Yuan, Taiwan
关键词
corneal epithelium; keratocyte; apoptosis; programmed cell death; preservation; cornea; viability; ligation-mediated polymerase chain reaction;
D O I
10.1097/01.ico.0000160970.58330.09
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: To investigate the effect of corneal epithelium on the viability of corneal stromal keratocytes in Optisol-GS. Methods: After sterilization, corneoscleral buttons were excised and stored in Ciptisol-GS for various time periods. Group 1 corneas (n = 40) underwent mechanical corneal epithelial debridement before storage while group 2 corneas (n = 40) were stored with intact epithelium. Changes in corneal thickness, keratocyte density, and keratocyte apoptosis were investigated immediately, at 4 hours, and on days 1, 21 31 5, 7, and 14 in the preservation medium. The differences between group 1 and 2 corneas were analyzed. Results: Corneal thickness increased significantly in the second week of preservation in both groups, though more substantially in group 1. Significant corneal epithelial apoptosis was noticed in the first week in group 2 corneas. Corneal stromal keratocyte density decreased with prolonged preservation time. DNA laddering was detected by ligation-mediated polymerase chain reaction throughout the experiment periods in both groups, but the increase of keratocyte apoptosis was more significant after 5 days of preservation, especially in group 1. Conclusions: Stromal keratocytes underwent apoptosis in Optisol-GS. The absence of corneal epithelium during preservation further increased the stromal keratocyte apoptosis.
引用
收藏
页码:78 / 84
页数:7
相关论文
共 40 条
[1]  
Albon J, 2000, INVEST OPHTH VIS SCI, V41, P2887
[2]   Loss of corneal Langerhans cells during storage in organ culture medium, Optisol and McCarey-Kaufman medium [J].
Ardjomand, N ;
Berghold, A ;
Reich, ME .
EYE, 1998, 12 (1) :134-138
[3]  
Armitage WJ, 1997, INVEST OPHTH VIS SCI, V38, P16
[4]   Benzalkonium chloride and gentamicin cause a leak in corneal epithelial cell membrane [J].
Chang, SW ;
Chi, RF ;
Wu, CC ;
Su, MJ .
EXPERIMENTAL EYE RESEARCH, 2000, 71 (01) :3-10
[5]  
CHOU L, 1994, OPHTHALMIC SURG LAS, V25, P700
[6]  
Gao JP, 1997, CORNEA, V16, P200
[7]   Fluorescence microscopy and three-dimensional imaging of the porcine corneal keratocyte network [J].
Hahnel, C ;
Somodi, S ;
Slowik, C ;
Weiss, DG ;
Guthoff, RF .
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 1997, 235 (12) :773-779
[8]   The keratocyte network of human cornea: A three-dimensional study using confocal laser scanning fluorescence microscopy [J].
Hahnel, C ;
Somodi, S ;
Weiss, DG ;
Guthoff, RF .
CORNEA, 2000, 19 (02) :185-193
[9]   Comparative observations on corneas, with special reference to Bowman's layer and Descemet's membrane in mammals and amphibians [J].
Hayashi, S ;
Osawa, T ;
Tohyama, K .
JOURNAL OF MORPHOLOGY, 2002, 254 (03) :247-258
[10]  
Imbert D, 1997, CORNEA, V16, P666