Azar D T, Hahn T W, Jain S, Yeh Y C, Stetler-Stevensen W G
Wilmer Eye Institute, Johns Hopkins Hospital, Baltimore, Maryland 21287-9233, USA.
Cornea. 1996 Jan;15(1):18-24.
To determine the expression of matrix metalloproteinases (MMPs) in cornea following excimer laser keratectomy, two sets of experiments were performed. In the first experiment, disciform excimer keratectomy was performed on rat corneas. The central regenerating epithelium was harvested at 3-96 h postwounding. MMP levels were assayed in the regenerated central epithelium and the stroma using zymography and immunoblot assays. In the second set of experiments, deep excimer annular keratectomy was performed on rabbit corneas to induce intrastromal epithelial migration. The effect of beta-mercaptomethyl tripeptide, a synthetic inhibitor of metalloproteinase, on the presence and extent of intrastromal epithelial migration was determined. In experiment I, MMP-2 and MMP-9 were expressed in the epithelium of excimer-ablated rat corneas 6-24 h postwounding, but not in the debridement wounds and untreated controls. Only excimer-treated stroma showed MMP-9 activity. In experiment II, intrastromal epithelial migration was delayed by topical application of beta-mercaptomethyl tripeptide, a synthetic inhibitor of MMPs (p < 0.05). After excimer wounds, MMPs are expressed in corneal epithelium and stroma during wound closure. They may play an important role in wound healing after excimer laser keratectomy.
为了确定准分子激光角膜切削术后角膜中基质金属蛋白酶(MMPs)的表达情况,进行了两组实验。在第一个实验中,对大鼠角膜进行盘状准分子激光角膜切削术。在创伤后3至96小时采集中央再生上皮。使用酶谱法和免疫印迹法测定再生中央上皮和基质中的MMP水平。在第二组实验中,对兔角膜进行深层准分子环形角膜切削术以诱导基质内上皮迁移。测定金属蛋白酶的合成抑制剂β-巯基甲基三肽对基质内上皮迁移的存在和程度的影响。在实验I中,在创伤后6至24小时,MMP-2和MMP-9在准分子激光切削的大鼠角膜上皮中表达,但在清创伤口和未处理的对照中未表达。仅准分子激光处理的基质显示出MMP-9活性。在实验II中,局部应用MMPs的合成抑制剂β-巯基甲基三肽可延迟基质内上皮迁移(p<0.05)。准分子激光创伤后,在伤口愈合过程中MMPs在角膜上皮和基质中表达。它们可能在准分子激光角膜切削术后的伤口愈合中起重要作用。