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首页> 外文期刊>British journal of ophthalmology >Verteporfin photodynamic therapy induced apoptosis in choroidal neovascular membranes.
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Verteporfin photodynamic therapy induced apoptosis in choroidal neovascular membranes.

机译:Verteporfin光动力疗法可诱导脉络膜新生血管膜细胞凋亡。

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AIM: To evaluate the impact of verteporfin photodynamic therapy (PDT) on the induction of apoptosis in choroidal neovascular membranes (CNV) secondary to age related macular degeneration. METHODS: Retrospective review of 22 surgically excised CNV. 12 of these patients had been treated with PDT 3-146 days previously. Apoptotic cells were detected with the TUNEL technique and compared to the expression of CD34 (endothelial cells, EC), CD105 (activated endothelial cells), Ki-67 (proliferation marker), and cytokeratin18 (retinal pigment epithelial cells, RPE). RESULTS: CNV excised 3 days after PDT were characterised both by collapsed and patent vessels. The EC displayed a statistical significant positive TUNEL reaction when compared to the remaining treated CNV (p < 0.001) and untreated CNV (P = 0.002). The proliferative activity was reduced. CNV excised 1-5 months after PDT displayed a patent vascularisation and high proliferative activity. All membranes either treated or untreated disclosed only sporadicTUNEL positive cells within the stroma and the RPE. CONCLUSIONS: Verteporfin PDT leads to selective and effective damage of EC within CNV. Both patent and occluded vessels were lined by apoptotic EC. This finding and the increased expression of proliferation marker at later time points suggest that revascularisation after PDT is caused by angiogenesis rather than recanalisation.
机译:目的:评估维替泊芬光动力疗法(PDT)对继发于年龄相关性黄斑变性的脉络膜新生血管膜(CNV)诱导凋亡的影响。方法:回顾性分析22例经手术切除的CNV。这些患者中有12位在3-146天之前接受过PDT治疗。使用TUNEL技术检测凋亡细胞,并将其与CD34(内皮细胞,EC),CD105(活化的内皮细胞),Ki-67(增殖标记)和细胞角蛋白18(视网膜色素上皮细胞,RPE)的表达进行比较。结果:PDT 3天后切除的CNV均以血管塌陷和专利血管为特征。与剩余的CNV(p <0.001)和未处理的CNV(P = 0.002)相比,EC显示出统计上显着的TUNEL阳性反应。增殖活性降低。 PDT在显示专利血管化和高增殖活性后的1-5个月切除了CNV。所有处理过的膜或未处理过的膜仅披露了基质和RPE内的散发TUNEL阳性细胞。结论:Verteporfin PDT导致CNV中EC的选择性和有效损伤。专利性血管和闭塞性血管均由凋亡性EC衬里。这一发现和增殖标志物在以后的时间点表达的增加表明,PDT后的血运重建是由血管生成而不是再血管化引起的。

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