Tribble James R, Kastanaki Elizabeth, Uslular A Berşan, Rutigliani Carola, Enz Tim J, Williams Pete A
Department of Clinical Neuroscience, Division of Eye and Vision, St. Erik Eye Hospital, Karolinska Institutet, Stockholm, Sweden.
Front Cell Dev Biol. 2022 May 12;10:903436. doi: 10.3389/fcell.2022.903436. eCollection 2022.
Neuroinflammation is a critical and targetable pathogenic component of neurodegenerative diseases, including glaucoma, the leading cause of irreversible blindness. Valproic acid has previously been demonstrated to reduce neuroinflammation and is neuroprotective in a number of experimental settings. To determine whether valproic acid can limit retinal neuroinflammation and protect retinal neurons we used an retina explant (axotomy) model to isolate resident glial responses from blood-derived monocytes. Neuroinflammatory status was defined using high resolution confocal imaging with 3D morphological reconstruction and cytokine protein arrays. Valproic acid significantly reduced microglia and astrocyte morphological changes, consistent with a reduction in pro-inflammatory phenotypes. Cytokine profiling demonstrated that valproic acid significantly attenuated or prevented expression of pro-inflammatory cytokines in injured retina. This identifies that the retinal explant model as a useful tool to explore resident neuroinflammation in a rapid timescale whilst maintaining a complex system of cell interactions and valproic acid as a useful drug to further explore anti-neuroinflammatory strategies in retinal disease.
神经炎症是神经退行性疾病(包括青光眼,不可逆性失明的主要原因)的一个关键且可靶向的致病成分。先前已证明丙戊酸可减轻神经炎症,并在多种实验环境中具有神经保护作用。为了确定丙戊酸是否能限制视网膜神经炎症并保护视网膜神经元,我们使用了视网膜外植体(轴突切断)模型,以将驻留神经胶质反应与血液来源的单核细胞分离。使用高分辨率共聚焦成像和三维形态重建以及细胞因子蛋白阵列来定义神经炎症状态。丙戊酸显著减少了小胶质细胞和星形胶质细胞的形态变化,这与促炎表型的减少一致。细胞因子分析表明,丙戊酸显著减弱或阻止了损伤视网膜中促炎细胞因子的表达。这表明视网膜外植体模型是在快速时间尺度上探索驻留神经炎症的有用工具,同时维持复杂的细胞相互作用系统,且丙戊酸是进一步探索视网膜疾病抗神经炎症策略的有用药物。