Liu Yashuang, Li Siyu, Wang Kexin, Wang Yiwen, Wang Yange, Zhang Chenxu, Wu Hao, Wang Gang, Qin Fangyuan, Song Zongming, Tao Ye
Department of Ophthalmology, People's Hospital of Zhengzhou University, Henan Provincial People's Hospital, Henan Eye Institute, Henan Eye Hospital, Zhengzhou, 450003, China.
Department of Ophthalmology, People's Hospital of Zhengzhou University, Henan Provincial People's Hospital, Henan Eye Institute, Henan Eye Hospital, Zhengzhou, 450003, China.
Free Radic Biol Med. 2025 Sep;237:176-194. doi: 10.1016/j.freeradbiomed.2025.05.414. Epub 2025 May 23.
Retinal degeneration (RD) is a class of polygenic blind eye disease characterized by photoreceptors loss and dysfunction of retinal pigment epithelium. Thus far, there is no effective treatment to save the declining vision in RD patients. Animal models are highly precious tools for studying the pathological mechanisms of RD, and for screening potential therapeutics. AUY922 is a heat shock protein 90 inhibitor that exhibits potent anti-cancer effects. However, it causes adverse ocular reactions such as reduced visual acuity and night blindness. This study intends to explore the pathological mechanism underlying the AUY922 induced RD. In vitro study, AUY922 induced cytotoxic effects on the 661W cells, which are ascribed to endoplasmic reticulum (ER) stress and oxidative damages. ER stress inhibitor 4-PBA alleviated 661W cells apoptosis and oxidative stress. Subsequently, AUY922 was delivered into the vitreous cavity of mouse and induced selective photoreceptor death and visual impairments. Overactivation of neuroglial and retinal remodeling occurred during the degenerative process. Moreover, enhanced CHOP expression was tied to profound disturbances in redox homeostasis, which readied photoreceptors for apoptosis. The underlying mechanism should be attributed to the activation of the PERK-eIF2α-ATF4-CHOP pathway. AUY922 can compensate for the high toxicity and instability of traditional inducers in RD modeling. These results not only enrich our understanding of the toxicology of AUY922 but also provide clues for establishing reliable RD models.
视网膜变性(RD)是一类多基因致盲眼病,其特征为光感受器丧失和视网膜色素上皮功能障碍。迄今为止,尚无有效的治疗方法来挽救RD患者逐渐下降的视力。动物模型是研究RD病理机制和筛选潜在治疗方法的极为珍贵的工具。AUY922是一种热休克蛋白90抑制剂,具有强大的抗癌作用。然而,它会引起不良眼部反应,如视力下降和夜盲。本研究旨在探讨AUY922诱导RD的病理机制。在体外研究中,AUY922对661W细胞具有细胞毒性作用,这归因于内质网(ER)应激和氧化损伤。ER应激抑制剂4-PBA减轻了661W细胞的凋亡和氧化应激。随后,将AUY922注入小鼠玻璃体腔,诱导选择性光感受器死亡和视力损害。在退变过程中发生了神经胶质细胞过度激活和视网膜重塑。此外,CHOP表达增强与氧化还原稳态的严重紊乱有关,这使光感受器易于发生凋亡。其潜在机制应归因于PERK-eIF2α-ATF4-CHOP通路的激活。AUY922可以弥补传统诱导剂在RD建模中的高毒性和不稳定性。这些结果不仅丰富了我们对AUY922毒理学的认识,也为建立可靠的RD模型提供了线索。