Hinton D R, He S, Lopez P F
Department of Pathology, University of Southern California School of Medicine, Los Angeles 90033, USA.
Arch Ophthalmol. 1998 Feb;116(2):203-9. doi: 10.1001/archopht.116.2.203.
Choroidal neovascular membranes (CNVMs) in age-related macular degeneration show progressive histologic changes from active, cellular, highly vascularized membranes to inactive paucicellular scars. The purpose of this study was to determine whether apoptosis was involved in the evolution of these changes, what cell types are involved, and whether there was an association with the Fas antigen (Fas or CD95) and Fas ligand (FasL).
Serial frozen sections from 10 surgically excised CNVMs were stained by the TUNEL (terminal deoxynucleotidyl transferase-mediated biotin-deoxyuridine 5-triphosphate nick-end labeling) method for detection of DNA strand breaks and by propidium iodide staining for morphologic detection of apoptosis. Immunoperoxidase staining was used for detection of Fas, FasL, and cell-type specific antigens.
Highly vascularized membranes contained cells with TUNEL-positive nuclei, particularly in the regions of neovascularization, while fibrotic membranes showed few, if any, TUNEL-positive cells. Many of the TUNEL-positive cells were stromal retinal pigment epithelial cells, although smaller numbers were identified as endothelial cells and macrophages. Confocal microscopy of propidium idoide-stained sections confirmed the presence of apoptotic nuclei. The extent of Fas antigen expression correlated with extent of apoptosis. FasL expression was found in all specimens but was most intense in the highly vascularized membranes.
Highly vascularized CNVMs related to age-related macular degeneration show apoptosis in stromal retinal pigment epithelial cells, endothelial cells, and occasional macrophages. Apoptosis is associated with prominent Fas and FasL expression.
年龄相关性黄斑变性中的脉络膜新生血管膜(CNVMs)显示出从活跃的、细胞丰富的、高度血管化的膜到不活跃的少细胞瘢痕的渐进性组织学变化。本研究的目的是确定凋亡是否参与这些变化的演变、涉及哪些细胞类型,以及是否与Fas抗原(Fas或CD95)和Fas配体(FasL)有关。
对10个手术切除的CNVMs的连续冰冻切片采用TUNEL(末端脱氧核苷酸转移酶介导的生物素-脱氧尿苷5-三磷酸缺口末端标记)法检测DNA链断裂,并用碘化丙啶染色进行凋亡的形态学检测。免疫过氧化物酶染色用于检测Fas、FasL和细胞类型特异性抗原。
高度血管化的膜含有TUNEL阳性核的细胞,特别是在新生血管形成区域,而纤维化膜显示很少(如果有的话)TUNEL阳性细胞。许多TUNEL阳性细胞是视网膜色素上皮基质细胞,尽管较少数量被鉴定为内皮细胞和巨噬细胞。碘化丙啶染色切片的共聚焦显微镜检查证实了凋亡核的存在。Fas抗原表达程度与凋亡程度相关。在所有标本中均发现FasL表达,但在高度血管化的膜中最为强烈。
与年龄相关性黄斑变性相关的高度血管化CNVMs在视网膜色素上皮基质细胞、内皮细胞和偶尔出现的巨噬细胞中显示凋亡。凋亡与显著的Fas和FasL表达相关。