Wang F, Xu X, Zhang X, Yan Y
Department of Ophthalmology, Shanghai First People's Hospital, Shanghai 200080, China.
Zhonghua Yan Ke Za Zhi. 2000 Sep;36(5):369-71, 24.
To investigate the ultrastructural distribution of platelet-derived growth factor (PDGF), transforming growth factor beta(1) (TGF-beta(1)) and their receptors in epiretinal membranes (ERM) and discuss the clinical significance of the distribution.
25 membrane specimens were surgically removed by vitrectomy from 9 patients with rhegmatogenous retinal detachment. Double-staining techniques of immunoelectromicroscopy for eight antibodies (PDGF, TGF-beta(1), PDGF receptor subunits alpha and beta, TGF-beta subunits I and II, type I and III collagen) were used in these specimens as previously designed.
PDGF and TGF-beta(1) staining appeared to be stronger on early (< 2 months) and late (> 6 months) stage membranes than that of middle (2 - 6 months) stage of membranes, and the immunostaining intensity inverted with the degree of proliferative vitreoretinopathy (PVR). We found that the gold particles of PDGF and TGF-beta(1) tended to get together with that of type I and III collagen. In addition, the stainings of four growth factor receptors were frequently positive in a type of epithelial-like cells with rich cytoplasm components, and also the gold particles of PDGF and TGF-beta(1) were found around these cells.
A concentration change of PDGF and TGF-beta(1) exists in development of ERM throughout. The epithelial-like cells are of a type of active cells, and autocrine and paracrine activity may be involved in ERM pathogenesis. PDGF and TGF-beta(1) influence the contractile activity of ERM.
研究血小板衍生生长因子(PDGF)、转化生长因子β1(TGF-β1)及其受体在视网膜前膜(ERM)中的超微结构分布,并探讨其分布的临床意义。
通过玻璃体切除术从9例孔源性视网膜脱离患者中手术切除25个膜标本。如先前设计的那样,在这些标本中使用针对8种抗体(PDGF、TGF-β1、PDGF受体亚基α和β、TGF-β亚基I和II、I型和III型胶原)的免疫电镜双染技术。
PDGF和TGF-β1染色在早期(<2个月)和晚期(>6个月)的膜上似乎比中期(2 - 6个月)的膜更强,且免疫染色强度与增殖性玻璃体视网膜病变(PVR)程度呈相反关系。我们发现PDGF和TGF-β1的金颗粒倾向于与I型和III型胶原的金颗粒聚集在一起。此外,四种生长因子受体的染色在一种细胞质成分丰富的上皮样细胞中经常呈阳性,并且在这些细胞周围也发现了PDGF和TGF-β1的金颗粒。
在ERM的整个发展过程中存在PDGF和TGF-β1的浓度变化。上皮样细胞是一种活跃细胞,自分泌和旁分泌活动可能参与ERM的发病机制。PDGF和TGF-β1影响ERM的收缩活性。