Gullapalli Vamsi K, Sugino Ilene K, Van Patten Yancy, Shah Sumit, Zarbin Marco A
Institute of Ophthalmology and Visual Science, University of Medicine and Dentistry of New Jersey-New Jersey Medical School, Newark, New Jersey, USA.
Trans Am Ophthalmol Soc. 2004;102:123-37; discussion 137-8.
To determine whether cultured fetal human retinal pigment epithelium (RPE) cells can attach and differentiate on submacular Bruch's membrane from donors over age 55.
Differential debridements of Bruch's membrane were performed to expose three different surfaces: the RPE basement membrane, the superficial inner collagenous layer (ICL) directly below the RPE basement membrane, and the deeper ICL. Approximately 3,146 cells/mm2 were seeded onto these Bruch's membrane explants and cultured for 1 or 7 days. Explants were bisected and examined histologically or analyzed with scanning electron microscopy. Nuclear density counts were performed on stained sections. Morphology and cell density were compared to those of cells seeded onto bovine corneal endothelial cell-extracellular matrix (BCE-ECM).
Compared to cells seeded onto BCE-ECM at similar density, cell coverage and cellular morphology were poor at both time points. Unlike cells on BCE-ECM, cell density remained the same or decreased with time. In general, cell morphology on all surfaces worsened by day 7 compared to day 1. Although cells were more pigmented on RPE basement membrane and deep ICL at day 7, poor cellular morphology indicated the remaining cells were not well differentiated. An explant from a donor with large soft drusen showed the poorest resurfacing at day 7 in organ culture.
These data indicate that aged submacular human Bruch's membrane does not support transplanted RPE survival and differentiation. The formation of localized RPE defects, cell death, and worsening cellular morphology on aged Bruch's membrane suggest that modification of Bruch's membrane may be necessary in patients with age-related macular degeneration receiving RPE transplants to prevent graft failure.
确定培养的人胎儿视网膜色素上皮(RPE)细胞能否在55岁以上供体的黄斑下 Bruch 膜上附着并分化。
对 Bruch 膜进行差异性清创,以暴露三种不同的表面:RPE 基底膜、RPE 基底膜正下方的浅表内胶原层(ICL)以及更深层的 ICL。将约3146个细胞/mm²接种到这些 Bruch 膜外植体上,并培养1天或7天。将外植体一分为二,进行组织学检查或用扫描电子显微镜分析。对染色切片进行核密度计数。将形态和细胞密度与接种到牛角膜内皮细胞 - 细胞外基质(BCE - ECM)上的细胞进行比较。
与以相似密度接种到 BCE - ECM 上的细胞相比,在两个时间点,细胞覆盖率和细胞形态均较差。与 BCE - ECM 上的细胞不同,细胞密度随时间保持不变或降低。一般来说,与第1天相比,到第7天所有表面上的细胞形态都变差。尽管在第7天时,RPE 基底膜和深层 ICL 上的细胞色素沉着更多,但较差的细胞形态表明剩余细胞未得到良好分化。来自有大的软性玻璃膜疣供体的外植体在器官培养第7天时表面修复最差。
这些数据表明,老化的黄斑下人 Bruch 膜不支持移植的 RPE 存活和分化。老化的 Bruch 膜上局部 RPE 缺陷的形成、细胞死亡以及细胞形态的恶化表明,在接受 RPE 移植的年龄相关性黄斑变性患者中,可能有必要对 Bruch 膜进行改良以防止移植物失败。