Department of Ophthalmology, Medical and Health Science Center, University of Debrecen, Hungary.
Acta Ophthalmol. 2011 Feb;89(1):e30-4. doi: 10.1111/j.1755-3768.2010.02047.x. Epub 2010 Nov 23.
Failure of retinal pigment epithelial (RPE) cells and macrophages to engulf different dying cells in the retina may result in accumulation of debris and development of age-related macular degeneration (AMD). The dynamics and influence of different treatments on this clearance process can be studied in vitro using human ARPE-19 cells and macrophages as phagocytes modelling dry and wet type of AMD, respectively.
Death through extracellular matrix detachment using polyHEMA-coated surfaces (anoikis) and UV irradiation (apoptosis) was induced in ARPE-19 cells. Two-coloured phagocytic assays were performed to quantify the amount of dying cells phagocytes engulfed (flow cytometry) and for visualization (fluorescent and scanning electron microscopy). The effect of phosphatidylserine inhibition with recombinant annexin-V and glucocorticoid (triamcinolone) treatment on the phagocytic process was tested.
The clearance of anoikic and apoptotic cells by nondying ARPE-19 cells over 8 hr of co-incubation increased over time (at 8 hr, over 53% and 35% of the phagocytes contained engulfed dying cells, respectively). The human macrophages engulfed the anoikic and apoptotic ARPE-19 cells with seven and four times lower capacity, respectively. Phosphatidylserine appearance on the dying cells did not affect, but triamcinolone treatment enhanced the phagocytosis of the dying cells by macrophages.
ARPE-19 cells are more efficient in clearing anoikic than UV-induced apoptotic cells. Macrophages are less efficient in the clearance process than ARPE-19 cells. The present model can be used for studying both dry and wet type of AMD in vitro and for testing different pharmacological aspects affecting this disease.
视网膜色素上皮 (RPE) 细胞和巨噬细胞不能吞噬视网膜中不同的死亡细胞,可能导致碎片堆积和年龄相关性黄斑变性 (AMD) 的发生。使用人 ARPE-19 细胞和巨噬细胞作为吞噬细胞,分别模拟干性和湿性 AMD 类型,可以在体外研究不同治疗方法对这种清除过程的影响。
通过用聚己内酯 (polyHEMA) 涂层表面(细胞失巢凋亡)和紫外线照射(细胞凋亡)诱导 ARPE-19 细胞死亡。进行双色吞噬实验,通过流式细胞术定量检测吞噬细胞吞噬死亡细胞的数量(流式细胞术),并通过荧光和扫描电子显微镜进行可视化观察。通过重组 annexin-V 和糖皮质激素(曲安奈德)抑制磷脂酰丝氨酸处理,测试吞噬过程的影响。
在共孵育 8 小时内,非死亡 ARPE-19 细胞对失巢凋亡和凋亡细胞的清除随着时间的推移而增加(在 8 小时时,分别有超过 53%和 35%的吞噬细胞含有吞噬的死亡细胞)。人巨噬细胞吞噬失巢凋亡和凋亡 ARPE-19 细胞的能力分别低 7 倍和 4 倍。凋亡细胞上出现的磷脂酰丝氨酸不会影响,但曲安奈德处理增强了巨噬细胞对死亡细胞的吞噬作用。
ARPE-19 细胞清除失巢凋亡细胞比清除紫外线诱导的凋亡细胞更有效。巨噬细胞在清除过程中的效率比 ARPE-19 细胞低。该模型可用于体外研究干性和湿性 AMD 两种类型,并测试影响这种疾病的不同药理学方面。