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本文引用的文献

1
Optineurin negatively regulates TNFalpha- induced NF-kappaB activation by competing with NEMO for ubiquitinated RIP.视神经病相关蛋白通过与线性泛素链组装复合物竞争泛素化受体相互作用蛋白,负向调控肿瘤坏死因子α诱导的核因子κB激活。
Curr Biol. 2007 Aug 21;17(16):1438-43. doi: 10.1016/j.cub.2007.07.041.
2
Disease gene candidates revealed by expression profiling of retinal ganglion cell development.通过视网膜神经节细胞发育的表达谱分析揭示的疾病基因候选物。
J Neurosci. 2007 Aug 8;27(32):8593-603. doi: 10.1523/JNEUROSCI.4488-06.2007.
3
A glaucoma-associated mutant of optineurin selectively induces death of retinal ganglion cells which is inhibited by antioxidants.一种与青光眼相关的视紫质神经元突变体选择性地诱导视网膜神经节细胞死亡,而抗氧化剂可抑制这种死亡。
Invest Ophthalmol Vis Sci. 2007 Apr;48(4):1607-14. doi: 10.1167/iovs.06-0834.
4
Mechanisms of immune system activation in glaucoma: oxidative stress-stimulated antigen presentation by the retina and optic nerve head glia.青光眼免疫系统激活机制:视网膜和视神经乳头神经胶质细胞的氧化应激刺激抗原呈递。
Invest Ophthalmol Vis Sci. 2007 Feb;48(2):705-14. doi: 10.1167/iovs.06-0810.
5
Tumor necrosis factor-alpha mediates oligodendrocyte death and delayed retinal ganglion cell loss in a mouse model of glaucoma.在青光眼小鼠模型中,肿瘤坏死因子-α介导少突胶质细胞死亡和视网膜神经节细胞延迟性丢失。
J Neurosci. 2006 Dec 6;26(49):12633-41. doi: 10.1523/JNEUROSCI.2801-06.2006.
6
Bid-independent mitochondrial activation in tumor necrosis factor alpha-induced apoptosis and liver injury.肿瘤坏死因子α诱导的细胞凋亡和肝损伤中不依赖Bid的线粒体激活
Mol Cell Biol. 2007 Jan;27(2):541-53. doi: 10.1128/MCB.01166-06. Epub 2006 Nov 13.
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Blocking soluble tumor necrosis factor signaling with dominant-negative tumor necrosis factor inhibitor attenuates loss of dopaminergic neurons in models of Parkinson's disease.用显性负性肿瘤坏死因子抑制剂阻断可溶性肿瘤坏死因子信号传导可减轻帕金森病模型中多巴胺能神经元的损失。
J Neurosci. 2006 Sep 13;26(37):9365-75. doi: 10.1523/JNEUROSCI.1504-06.2006.
8
Optineurin increases cell survival and translocates to the nucleus in a Rab8-dependent manner upon an apoptotic stimulus.在凋亡刺激下,视紫质神经元诱导蛋白(Optineurin)以Rab8依赖的方式增加细胞存活并转位至细胞核。
J Biol Chem. 2006 Jun 9;281(23):16147-56. doi: 10.1074/jbc.M601467200. Epub 2006 Mar 28.
9
TNF-alpha-induced optic nerve degeneration and nuclear factor-kappaB p65.肿瘤坏死因子-α诱导的视神经变性与核因子-κB p65
Invest Ophthalmol Vis Sci. 2006 Apr;47(4):1448-57. doi: 10.1167/iovs.05-0299.
10
TNFalpha-induced MMP-9 promotes macrophage recruitment into injured peripheral nerve.肿瘤坏死因子α诱导的基质金属蛋白酶-9促进巨噬细胞募集至损伤的周围神经。
Mol Cell Neurosci. 2006 Mar;31(3):407-15. doi: 10.1016/j.mcn.2005.10.011. Epub 2005 Nov 16.

青光眼性神经变性中的肿瘤坏死因子-α信号传导

TNF-alpha signaling in glaucomatous neurodegeneration.

作者信息

Tezel Gülgün

机构信息

Department of Ophthalmology & Visual Sciences, University of Louisville School of Medicine, Louisville, KY, USA.

出版信息

Prog Brain Res. 2008;173:409-21. doi: 10.1016/S0079-6123(08)01128-X.

DOI:10.1016/S0079-6123(08)01128-X
PMID:18929124
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3150483/
Abstract

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.

摘要

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。