Department of Ophthalmology, People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530021, Guangxi, People's Republic of China.
Department of Ophthalmology, Renmin Hospital of Wuhan University, Wuhan, 430060, Hubei, China.
J Mol Histol. 2020 Feb;51(1):89-97. doi: 10.1007/s10735-020-09860-1. Epub 2020 Feb 17.
To examine the expression of P53-induced protein with a death domain (PIDD) at retina in animal model of optic nerve crush (ONC) and to investigate the role of PIDD in retinal glial activation and NF-κB activation induced by optic nerve damage, ONC animal model was established in Sprague-Dawley rats. PIDD has three isoforms (Isof); Western blot was performed to examine the expression of PIDD (Isof-1, Isof-2, and Isof-3, respectively) in retina at different time points after ONC. Retinal glial activation is closely associated with retinal neuronal death and is monitored by the expression of GFAP+ glial cells and IBA1+ microglia, then activated microglia leads to inflammatory cytokine production. NF-kB activation in glial cells also can promote neuronal death. In our study, the role of PIDD in retinal glial activation and NF-kB activation was investigated with PIDD inhibition selectively. PIDD expression (Isof-1 and Isof-3) was dramatically increased, and peaked at 3 days after ONC, while Isof-2 did not show any difference. In the ONC animal model, the number of GFAP+ glial cells and IBA1+ microglia in retinal layers was increased significantly, inflammatory cytokine production was upregulated, and NF-κB in glial cell was also activated. Moreover, those responses induced by optic nerve damage were attenuated with PIDD inhibition, which indicated that PIDD could regulate retinal glial activation, neuro-inflammation, and NF-κB activation. These results provided the direct demonstration that the PIDD (Isof-1and Isof-3) was overexpressed in retina after ONC, and PIDD may be involved in retinal neurodegenerative diseases by regulating retinal glial activation and NF-κB activation.
为了研究 P53 诱导的含有死亡结构域的蛋白(PIDD)在视神经挤压(ONC)动物模型中的视网膜表达,并探讨 PIDD 在视神经损伤诱导的视网膜胶质细胞激活和 NF-κB 激活中的作用,建立了 Sprague-Dawley 大鼠 ONC 动物模型。PIDD 有三种异构体(Isof);Western blot 用于检测不同时间点 ONC 后视网膜中 PIDD(Isof-1、Isof-2 和 Isof-3)的表达。视网膜胶质细胞的激活与视网膜神经元的死亡密切相关,通过 GFAP+胶质细胞和 IBA1+小胶质细胞的表达来监测,然后激活的小胶质细胞导致炎症细胞因子的产生。胶质细胞中 NF-kB 的激活也可以促进神经元的死亡。在我们的研究中,通过选择性抑制 PIDD 来研究 PIDD 在视网膜胶质细胞激活和 NF-kB 激活中的作用。PIDD 表达(Isof-1 和 Isof-3)显著增加,并在 ONC 后 3 天达到峰值,而 Isof-2 没有显示出任何差异。在 ONC 动物模型中,视网膜各层 GFAP+胶质细胞和 IBA1+小胶质细胞的数量明显增加,炎症细胞因子的产生上调,胶质细胞中的 NF-κB 也被激活。此外,用 PIDD 抑制可减轻视神经损伤引起的这些反应,这表明 PIDD 可通过调节视网膜胶质细胞激活、神经炎症和 NF-κB 激活来调节视网膜神经退行性疾病。这些结果提供了直接证据,表明 PIDD(Isof-1 和 Isof-3)在 ONC 后在视网膜中过度表达,并且 PIDD 可能通过调节视网膜胶质细胞激活和 NF-κB 激活参与视网膜神经退行性疾病。