Boulton M, Foreman D, Williams G, McLeod D
University Department of Ophthalmology, Manchester Royal Eye Hospital.
Br J Ophthalmol. 1998 May;82(5):561-8. doi: 10.1136/bjo.82.5.561.
To determine the staining pattern of vascular endothelial growth factor (VEGF) at different stages of diabetic retinopathy (including post-laser photocoagulation) and to compare staining in excised fibrovascular and fibrocellular (non-diabetic) preretinal membranes.
Immunohistochemical localisation of VEGF, using antibodies raised against VEGF165 and VEGF121,165,189, was carried out on specimens of normal human retina (n = 15), diabetic retinas ((a) with no overt retinopathy (n = 19), (b) with intraretinal vascular abnormalities but no proliferative retinopathy (n = 6), (c) with active proliferative retinopathy (n = 6), (d) with no residual proliferative retinopathy after photocoagulation therapy (n = 15)), excised diabetic fibrovascular membranes (n = 19), and non-diabetic fibrocellular membranes (n = 7). The degree and pattern of immunostaining was recorded.
In general, VEGF was absent from the majority of normal retinas. VEGF staining was apparent in most diabetic tissues but the staining pattern was dependent on both the specificity of the antibody used and the category of tissue. Staining with the VEGF165 antibody was generally confined to endothelial cells adn perivascular regions while the VEGF121,165,189 antibody was also associated with extravascular components of the inner retina. Intensity of immunostaining of diabetic eyes was dependent on the severity of retinopathy being least in diabetics with no overt retinopathy and greatest in retinas with proliferative retinopathy. Interestingly, the intensity of immunostaining in diabetic retinas which had undergone laser surgery for proliferative retinopathy was reduced to basal levels. Moderate to intense immunostaining was observed in all fibrovascular and fibrocellular membranes examined.
This study supports a circumstantial role for VEGF in the pathogenesis of both the preclinical and proliferative stages of diabetic retinopathy.
确定血管内皮生长因子(VEGF)在糖尿病视网膜病变不同阶段(包括激光光凝术后)的染色模式,并比较切除的纤维血管性和纤维细胞性(非糖尿病性)视网膜前膜中的染色情况。
使用针对VEGF165以及VEGF121、165、189产生的抗体,对正常人视网膜标本(n = 15)、糖尿病视网膜标本((a)无明显视网膜病变,n = 19;(b)有视网膜内血管异常但无增殖性视网膜病变,n = 6;(c)有活动性增殖性视网膜病变,n = 6;(d)激光光凝治疗后无残留增殖性视网膜病变,n = 15)、切除的糖尿病纤维血管膜(n = 19)和非糖尿病纤维细胞性膜(n = 7)进行VEGF的免疫组织化学定位。记录免疫染色的程度和模式。
一般来说,大多数正常视网膜中不存在VEGF。VEGF染色在大多数糖尿病组织中明显,但染色模式取决于所用抗体的特异性和组织类别。用VEGF165抗体染色通常局限于内皮细胞和血管周围区域,而VEGF121、165、189抗体还与视网膜内层的血管外成分有关。糖尿病眼免疫染色的强度取决于视网膜病变的严重程度,在无明显视网膜病变的糖尿病患者中最低,在有增殖性视网膜病变的视网膜中最高。有趣的是,接受增殖性视网膜病变激光手术的糖尿病视网膜中的免疫染色强度降低到了基础水平。在所有检查的纤维血管性和纤维细胞性膜中均观察到中度至强烈的免疫染色。
本研究支持VEGF在糖尿病视网膜病变临床前期和增殖期发病机制中起间接作用。