Chintala Shravan K, Wang Nan, Diskin Shiri, Mattox Cynthia, Kagemann Larry, Fini M Elizabeth, Schuman Joel S
Eye Research Institute, Oakland University, 40g Dodge Hall, Rochester, MI, USA.
Exp Eye Res. 2005 Oct;81(4):429-36. doi: 10.1016/j.exer.2005.03.001.
The goal of glaucoma filtering surgery is to create a low resistance pathway for aqueous outflow. The result is a blister or 'bleb' on the conjunctiva, from which fluid drains into the vasculature. Filtering surgery results may be compromised if blebs develop leaks, a problem that surfaces more frequently when antimetabolites are used to control the wound healing response. We investigated the role of tissue remodelling enzymes of the Matrix metalloproteinase (MMP) family in the development of bleb leaks. Our design was a case series. We enrolled glaucoma patients with leaking blebs, glaucoma patients with overhanging blebs and normal eyes. Leaking bleb tissues (n=11) and bleb leak fluid were collected from patients undergoing bleb revision surgery. Overhanging bleb tissues (from non-leaking blebs, n=3), normal conjunctiva (n=8), and aqueous humour (n=4) were collected for comparison. Samples were analysed for MMP content and proteinase activity by the methods of zymography, western blotting, immunohistochemistry, and in situ zymography. Our main outcome measures were presence and activity of MMP in sample. Zymography revealed the presence of a high molecular weight caseinase and a 92-kDa gelatinase of a size appropriate for the proenzyme form of gelatinase B (gelB; MMP-9), in extracts from leaking bleb tissue, but not in bleb leak fluid or aqueous humour samples. In contrast, a 65-kDa gelatinase of a size appropriate for gelatinase A (MMP-2) proenzyme was observed in all samples. All proteinases disappeared when 10mm EDTA was added to the development buffer, consistent with their identity as MMPs. Western blotting and immunohistochemical analyses confirmed the identity of the 92kDa proteinase as gelB, and further revealed its absence from extracts of overhanging bleb tissue and normal conjunctiva. In situ zymography demonstrated strong gelatinolytic activity in leaking bleb tissue, but not overhanging bleb tissue or normal conjunctiva. MMP-g may be involved in the mechanism of formation of bleb leaks. Precise description of the cascade of events leading to bleb leakage may allow the design of therapeutic interventions to prevent, stabilize or reverse bleb leakage.
青光眼滤过手术的目的是为房水流出创建一条低阻力通道。结果是在结膜上形成一个水泡或“滤疱”,房水从这里排入脉管系统。如果滤疱出现渗漏,滤过手术的效果可能会受到影响,当使用抗代谢药物来控制伤口愈合反应时,这个问题会更频繁地出现。我们研究了基质金属蛋白酶(MMP)家族的组织重塑酶在滤疱渗漏形成中的作用。我们的设计是一个病例系列研究。我们纳入了滤疱渗漏的青光眼患者、滤疱悬垂的青光眼患者和正常眼睛。从接受滤疱修复手术的患者中收集渗漏滤疱组织(n = 11)和滤疱渗漏液。收集滤疱悬垂组织(来自无渗漏滤疱,n = 3)、正常结膜(n = 8)和房水(n = 4)用于比较。通过酶谱法、蛋白质印迹法、免疫组织化学法和原位酶谱法分析样本中的MMP含量和蛋白酶活性。我们的主要观察指标是样本中MMP的存在和活性。酶谱法显示,在渗漏滤疱组织提取物中存在一种高分子量酪蛋白酶和一种92 kDa的明胶酶,其大小与明胶酶B(gelB;MMP - 9)的酶原形式相符,但在滤疱渗漏液或房水样本中未检测到。相反,在所有样本中均观察到一种65 kDa的明胶酶,其大小与明胶酶A(MMP - 2)酶原相符。当在显影缓冲液中加入10 mM EDTA时,所有蛋白酶均消失,这与其作为MMP的身份一致。蛋白质印迹法和免疫组织化学分析证实92 kDa蛋白酶为gelB,并进一步显示在滤疱悬垂组织和正常结膜提取物中不存在该蛋白酶。原位酶谱法显示渗漏滤疱组织中有强烈的明胶溶解活性,但滤疱悬垂组织或正常结膜中没有。MMP - g可能参与了滤疱渗漏的形成机制。对导致滤疱渗漏的一系列事件的精确描述可能有助于设计预防、稳定或逆转滤疱渗漏的治疗干预措施。