Plantner J J, Smine A, Quinn T A
Department of Ophthalmology, Case Western Reserve University, Cleveland, OH 44106-5068, USA.
Curr Eye Res. 1998 Feb;17(2):132-40. doi: 10.1076/ceyr.17.2.132.5610.
We wished to establish which matrix metalloproteinases (MMPs) and metalloproteinase inhibitors (TIMPs) were present in human interphotoreceptor matrix (IPM) and vitreous.
IPM and vitreous were obtained from postmortem human eyebank eyes. Western immunoblots were probed with antibodies against human MMPs and TIMPs. Assays specific for elastase activity were also performed.
Immunoblot analysis indicated the presence of MMP-1 (interstitial collagenase), MMP-2 and MMP-9 (gelatinases A and B), MMP-3 (stromelysin-1) and TIMP-1, -2 and -3 in both IPM and vitreous. MMP-7 (matrilysin) and MMP-12 (metalloelastase) were not found in either IPM or vitreous.
This is the first demonstration of the MMPs and TIMPs in human IPM and of the TIMPs in human vitreous. While these enzymes are most likely involved in normal turnover within the extracellular matrices that surround the neural retina, they may also play a role in a number of retinal diseases, particularly proliferative diabetic retinopathy and age-related macular degeneration.
我们希望确定人类光感受器间基质(IPM)和玻璃体中存在哪些基质金属蛋白酶(MMPs)和金属蛋白酶抑制剂(TIMPs)。
从死后人类眼库的眼睛中获取IPM和玻璃体。用抗人类MMPs和TIMPs的抗体进行蛋白质免疫印迹分析。还进行了弹性蛋白酶活性特异性检测。
免疫印迹分析表明,IPM和玻璃体中均存在MMP-1(间质胶原酶)、MMP-2和MMP-9(明胶酶A和B)、MMP-3(基质溶解素-1)以及TIMP-1、-2和-3。在IPM或玻璃体中均未发现MMP-7(基质溶素)和MMP-12(金属弹性蛋白酶)。
这是首次在人类IPM中证实MMPs的存在,以及在人类玻璃体中证实TIMPs的存在。虽然这些酶很可能参与神经视网膜周围细胞外基质的正常更新,但它们也可能在多种视网膜疾病中起作用,特别是增殖性糖尿病视网膜病变和年龄相关性黄斑变性。