IRCCS, San Martino General Hospital, Ophthalmology Unit, Genoa, Italy.
Department of Experimental Medicine (DIMES), University of Genoa, Genoa, Italy.
ALTEX. 2020;37(2):265-274. doi: 10.14573/altex.1909262. Epub 2020 Jan 27.
Glaucoma is the second leading cause of blindness worldwide. Currently, glaucoma treatments aim to lower intraocular pressure by decreasing aqueous humor production or increasing aqueous humor outflow through pharmacological approaches or trabeculectomy. The lack of an effective cure requires new therapeutic strategies. We compared the biological responses of a three-dimensional trabecular meshwork model with or without perfusion bioreactor technology to better understand the early molecular changes induced by prolonged oxidative stress conditions induced by repeated daily peroxide exposure. We used standard 3D cultures of trabecular meshwork cells in Matrigel cultured under either static and dynamic conditions for one week. We studied changes in F-actin expression and organization in the cells, cellular metabolic activity, proinflammatory gene expression, expression of pro- and anti-apoptotic proteins, PARP-1 cleavage, and NFκB activation in the model. We demonstrate that the dynamic conditions improve the adaptive behavior of 3D trabecular meshwork cultures to chronic oxidative stress via offsetting pathway activation.
青光眼是全球第二大致盲原因。目前,青光眼的治疗方法旨在通过药理学方法或小梁切除术降低房水产生或增加房水流出,从而降低眼内压。由于缺乏有效的治疗方法,需要新的治疗策略。我们比较了有或没有灌注生物反应器技术的三维小梁网模型的生物学反应,以更好地了解反复每日过氧化物暴露引起的长期氧化应激条件下诱导的早期分子变化。我们使用标准的基质胶三维小梁网细胞培养物,在静态和动态条件下培养一周。我们研究了细胞中 F-肌动蛋白表达和组织的变化、细胞代谢活性、促炎基因表达、促凋亡和抗凋亡蛋白的表达、PARP-1 切割和 NFκB 激活在模型中的变化。我们证明,动态条件通过抵消途径激活改善了 3D 小梁网培养物对慢性氧化应激的适应性行为。