Miller B, Miller H, Patterson R, Ryan S J
Arch Ophthalmol. 1986 Feb;104(2):281-5. doi: 10.1001/archopht.1986.01050140139037.
Cellular activity at the vitreoretinal interface after full-thickness retinal wounds was studied in rabbit eyes, using light and electron microscopy. Glial cell extensions grew initially on the retinal surface around the wound site. This brief period of glial proliferation was associated with the posttraumatic inflammatory response and, more specifically, with phagocytic monocyte accumulation at the vitreoretinal interface. Once the inflammation subsided, this abortive attempt to grow membranes on the retinal surface stopped and true epiretinal membranes did not develop. Our observations suggest that intraocular inflammation and macrophage response determine the extent of healing and scarring on an injured retinal surface, and thus may play a key role in the pathogenesis of epiretinal membranes.
利用光学显微镜和电子显微镜,对兔眼全层视网膜损伤后玻璃体视网膜界面的细胞活性进行了研究。胶质细胞突起最初在伤口部位周围的视网膜表面生长。这段短暂的胶质细胞增殖期与创伤后炎症反应有关,更具体地说,与玻璃体视网膜界面处吞噬性单核细胞的积聚有关。一旦炎症消退,这种在视网膜表面生长膜的失败尝试就会停止,真正的视网膜前膜不会形成。我们的观察结果表明,眼内炎症和巨噬细胞反应决定了受损视网膜表面的愈合和瘢痕形成程度,因此可能在视网膜前膜的发病机制中起关键作用。