Tezel Gülgün
Department of Ophthalmology & Visual Sciences, University of Louisville School of Medicine, Louisville, KY, USA.
Prog Brain Res. 2008;173:409-21. doi: 10.1016/S0079-6123(08)01128-X.
Growing evidence supports the role of tumor necrosis factor-alpha (TNF-alpha) as a mediator of neurodegeneration in glaucoma. Glial production of TNF-alpha is increased, and its death receptor is upregulated on retinal ganglion cells (RGCs) and optic nerve axons in glaucomatous eyes. This multifunctional cytokine can induce RGC death through receptor-mediated caspase activation, mitochondrial dysfunction, and oxidative stress. In addition to direct neurotoxicity, potential interplay of TNF-alpha signaling with other cellular events associated with glaucomatous neurodegeneration may also contribute to spreading neuronal damage by secondary degeneration. Opposing these cell death-promoting signals, binding of TNF receptors can also trigger the activation of survival signals. A critical balance between a variety of intracellular signaling pathways determines the predominant in vivo bioactivity of TNF-alpha as best exemplified by differential responses of RGCs and glia. This review focuses on the present evidence supporting the involvement of TNF-alpha signaling in glaucomatous neurodegeneration and possible treatment targets to provide neuroprotection.
越来越多的证据支持肿瘤坏死因子-α(TNF-α)在青光眼神经退行性变中作为介质的作用。在青光眼患者眼中,神经胶质细胞产生的TNF-α增加,其死亡受体在视网膜神经节细胞(RGCs)和视神经轴突上上调。这种多功能细胞因子可通过受体介导的半胱天冬酶激活、线粒体功能障碍和氧化应激诱导RGC死亡。除了直接的神经毒性外,TNF-α信号与青光眼神经退行性变相关的其他细胞事件之间的潜在相互作用也可能通过继发性变性导致神经元损伤扩散。与这些促进细胞死亡的信号相反,TNF受体的结合也可触发生存信号的激活。多种细胞内信号通路之间的关键平衡决定了TNF-α在体内的主要生物活性,RGCs和神经胶质细胞的不同反应就是最好的例证。本综述重点关注支持TNF-α信号参与青光眼神经退行性变的现有证据以及可能提供神经保护作用的治疗靶点。