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增生性玻璃体视网膜病变增生膜再塑型机制的研究

Mechanism of remodeling of proliferative membrane in proliferative vitreoretinopathy

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【作者】 朱丹赵明威黎晓新姜燕荣

【Author】 ZHU Dan, ZHAO Ming-wei, LI Xiao-xin, et al. Department of Ophthalmology, People′s Hospital, Beijing University, Beijing 100044, China

【机构】 北京大学人民医院眼科中心北京大学人民医院眼科中心 100044内蒙古医学院附属医院眼科100044

【摘要】 目的观察不同病程增生性玻璃体视网膜病变(PVR)增生膜中不同细胞成分、细胞外基质(ECM)、基质金属蛋白酶(MMPs)及其抑制剂(TIMPs)随病程变化的规律,探讨PVR增生膜的再塑型机制。方法病程2个月至8年的孔源性视网膜脱离伴PVR患者的增生膜手术标本16例,用免疫组织化学方法标记增生膜中视网膜色素上皮(RPE)细胞、胶质细胞等不同的细胞成分,纤维连接蛋白(FN)、层粘连蛋白(laminin)、~型胶原等不同ECM成分,以及MMPs(MMP2、MMP9)和TIMP1,分析不同病程PVR增生膜中各标记成分的变化以及与病程的相关性。结果随PVR病程延长,增生膜中RPE细胞、MMP2、FN表达逐渐减少(P=0.014,P=0.001,P=0.008),胶质细胞、、型胶原逐渐增多(P=0.022,P=0.001,P=0.008),层粘连蛋白和、型胶原均有表达,但不随病程变化。RPE细胞、MMP2、纤维连接蛋白的表达与病程呈负相关,胶质细胞、、型胶原的表达与病程呈正相关;MMP2与FN变化呈正相关。MMP9、TIMP1始终都有表达,但不随病程变化。结论在PVR增生膜形成和发展的过程中,增生膜中的RPE细胞、胶质细胞、FN、、型胶原、MMP2参与了PVR的再塑型过程。

【Abstract】 Objective To detect the variation rule of different cellular components, extracellular matrix, matrix-metalloproteinases (MMPs), and tissue inhibitors of metalloproteinases(TIMPs)in proliferative membranes in proliferative vitreoretinopathy (PVR) with different courses of disease, and to investigate the remodeling mechanism of PVR. Methods Sixteen surgically excised specimens of proliferative membranes from patients with rhegmatogenous retinal detachment combined with PVR with the course of disease of 2 months to 8 years were selected. The different cellular component of retinal pigment epithelial (RPE) cells and glial cells, component of extracellular matrix including fibronectin, laminin,and collagen types Ⅰ to Ⅳ, and matrix metalloproteinases (MMP2, MMP9) and TIMP1 in proliferative membrane were labeled by immunohistochemical method. The variation of those labeled components in proliferative membrane in PVR duration and the correlation between these components and the course of PVR were analyzed. Results As the duration of PVR increased,the expression of RPE cells, fibronectin and MMP2 decreased (P<0.05),while glial cells,collagen type Ⅰ and Ⅲ increased (P<0.05).The positive staining of laminin and collagen type Ⅱ and Ⅳ were found, but the association with PVR duration was not detected. A negative correlation between PVR duration and RPE cells, MMP2, and fibronectin respectively and a positive correlation between PVR duration and glial cells, collagen Ⅰ and Ⅲ respectively were detected. MMP2 positively related with variation of fibronectin. Positive staining of MMP9 and TIMP1 was recorded but did not change with the variation of the disease course. Conclusion During the formation and development of proliferative membrane in PVR, RPE cells, glial cells, fibronectin, collagen type Ⅰ and Ⅲ and MMP2 take part in the remodeling of proliferative membrane.

【基金】 教育部博士点基金资助项目(20011001068)
  • 【文献出处】 中华眼底病杂志 ,Chinese Journal of Ocular Fundus Diseases , 编辑部邮箱 ,2006年05期
  • 【分类号】R774.1
  • 【被引频次】8
  • 【下载频次】184
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