Department of Ophthalmology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
State Key Laboratory of Brain and Cognitive Sciences, The University of Hong Kong, Hong Kong, China.
Int J Mol Sci. 2020 Jun 30;21(13):4658. doi: 10.3390/ijms21134658.
Age-related macular degeneration (AMD) is a sight-threatening disease with limited treatment options. We investigated whether amyloid β (Aβ) could cause pyroptosis and evaluated the effects of polysaccharides (LBP) on Aβ oligomers-induced retinal pigment epithelium 19 (ARPE-19) damage, which is an in vitro AMD model. Aβ oligomers verified by Western blot were added to ARPE-19 cells with or without 24 h LBP treatment. Aβ oligomers significantly decreased ARPE-19 cell viability with obvious morphological changes under light microscopy. SEM revealed swollen cells with a bubbling appearance and ruptured cell membrane, which are morphological characteristics of pyroptosis. ELISA results showed increased expression of IL-1β and IL-18, which are the final products of pyroptosis. LBP administration for 24 h had no toxic effects on ARPE-19 cells and improved cell viability and morphology while disrupting Aβ oligomerization in a dose-dependent manner. Furthermore, Aβ oligomers up-regulated the cellular immunoreactivity of pyroptosis markers including NOD-like receptors protein 3 (NLRP3), caspase-1, and membrane N-terminal cleavage product of GSDMD (GSDMD-N), which could be reversed by LBP treatment. Taken together, this study showed that LBP effectively protects the Aβ oligomers-induced pyroptotic ARPE-19 cell damages by its anti-Aβ oligomerization properties and its anti-pyroptotic effects.
年龄相关性黄斑变性(AMD)是一种致盲性疾病,治疗选择有限。我们研究了淀粉样蛋白β(Aβ)是否会引起细胞焦亡,并评估了多糖(LBP)对 Aβ寡聚体诱导的视网膜色素上皮 19(ARPE-19)损伤的作用,这是一种体外 AMD 模型。用 Western blot 验证的 Aβ寡聚体与用或不用 24 小时 LBP 处理的 ARPE-19 细胞一起孵育。Aβ寡聚体明显降低 ARPE-19 细胞活力,在光镜下观察到明显的形态变化。SEM 显示肿胀的细胞呈起泡状,细胞膜破裂,这是细胞焦亡的形态特征。ELISA 结果显示 IL-1β和 IL-18 的表达增加,这是细胞焦亡的终产物。LBP 给药 24 小时对 ARPE-19 细胞没有毒性作用,并且以剂量依赖的方式改善细胞活力和形态,同时破坏 Aβ 寡聚体。此外,Aβ寡聚体上调了细胞焦亡标志物的细胞免疫反应性,包括 NOD 样受体蛋白 3(NLRP3)、半胱氨酸天冬氨酸蛋白酶-1(caspase-1)和 GSDMD 的膜 N 端裂解产物(GSDMD-N),这可以通过 LBP 治疗来逆转。总之,这项研究表明,LBP 通过其抗 Aβ 寡聚体特性及其抗细胞焦亡作用,有效保护 Aβ 寡聚体诱导的 ARPE-19 细胞焦亡损伤。