Podskochy A, Fagerholm P
St. Eriks Eye Hospital, Polhemsgatan 50, S-112 82 Stockholm, Sweden.
Acta Ophthalmol Scand. 2001 Dec;79(6):603-8. doi: 10.1034/j.1600-0420.2001.790611.x.
To evaluate hyaluronan (HA) production and level of apoptosis of corneal cells after repeated UVR exposures.
Fifteen albino rabbit corneas were exposed to 310 nm UVR at a dose that causes biomicroscopically significant keratitis (0.47 J/cm2). Nine rabbits received a single dose of UVR. Six rabbits were irradiated 3 times at 7-day intervals. Rabbits exposed to the single dose of UVR, were sacrificed 24 hours, 7 and 14 days after irradiation. Rabbits exposed to the repeated doses of UVR, were sacrificed 24 hours and 14 days after the last irradiation. The corneal tissue specimens were processed for histological analysis using specific staining for HA, and the TdT-dUTP terminal nick-end labeling (TUNEL) assay.
Corneas exposed to a single UVR dose showed extensive positive TUNEL staining 24 hours after exposure. Almost all basal epithelial cells, keratocytes throughout the entire thickness of the stroma, and endothelial cells were TUNEL-positive. No HA was found 24 hours after exposure. Extracellular HA staining of high intensity was found at day 7 throughout the entire central stroma, except the anterior one-fourth. At day 14 only a faint HA staining was detected in the posterior stroma, close to Descemet's membrane. Corneas exposed to repeated UVR doses showed at 24 hours positive TUNEL staining only in epithelial cells and in very few stromal cells. The majority of stromal cells and endothelial cells were unaffected. At the same time HA staining of very high intensity was found both at 24 hours and day 14, and it was evenly distributed throughout the entire thickness of the stroma.
Repeated UVR exposures lead to increased production and accumulation of HA in the corneal stroma. The repopulated keratocytes are much more resistant to apoptosis than the native ones. HA accumulation may be a sign of long-term changes in the cornea.
评估反复紫外线辐射(UVR)暴露后角膜细胞的透明质酸(HA)产生情况及凋亡水平。
15只白化兔角膜接受波长310 nm的UVR照射,剂量为引起生物显微镜下显著角膜炎的剂量(0.47 J/cm²)。9只兔子接受单次UVR照射。6只兔子每隔7天照射3次。接受单次UVR照射的兔子在照射后24小时、7天和14天处死。接受反复UVR照射的兔子在最后一次照射后24小时和14天处死。对角膜组织标本进行处理,采用HA特异性染色及TdT-dUTP末端脱氧核苷酸转移酶介导的缺口末端标记(TUNEL)法进行组织学分析。
接受单次UVR照射的角膜在照射后24小时显示广泛的TUNEL阳性染色。几乎所有基底上皮细胞、整个基质厚度的角膜细胞以及内皮细胞均为TUNEL阳性。照射后24小时未发现HA。在第7天,除前四分之一外,整个中央基质均发现高强度的细胞外HA染色。在第14天,仅在靠近后弹力层的基质后部检测到微弱的HA染色。接受反复UVR照射的角膜在24小时时仅上皮细胞和极少数基质细胞显示TUNEL阳性染色。大多数基质细胞和内皮细胞未受影响。同时,在24小时和第14天均发现非常高强度的HA染色,且均匀分布于整个基质厚度。
反复UVR暴露导致角膜基质中HA产生增加和积聚。重新增殖的角膜细胞比原始角膜细胞对凋亡更具抗性。HA积聚可能是角膜长期变化的一个迹象。