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Novel role for the innate immune receptor toll-like receptor 4 (TLR4) in the regulation of the wnt signaling pathway and photoreceptor apoptosis

机译:先天免疫受体toll样受体4(TLR4)在wnt信号通路和光感受器凋亡的调节中的新作用

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摘要

Recent evidence has implicated innate immunity in regulating neuronal survival in the brain during stroke and other neurodegenerations. Photoreceptors are specialized light-detecting neurons in the retina that are essential for vision. In this study, we investigated the role of the innate immunity receptor TLR4 in photoreceptors. TLR4 activation by lipopolysaccharide (LPS) significantly reduced the survival of cultured mouse photoreceptors exposed to oxidative stress. With respect to mechanism, TLR4 suppressed Wnt signaling, decreased phosphorylation and activation of the Wnt receptor LRP6, and blocked the protective effect of the Wnt3a ligand. Paradoxically, TLR4 activation prior to oxidative injury protected photoreceptors, in a phenomenon known as preconditioning. Expression of TNFα and its receptors TNFR1 and TNFR2 decreased during preconditioning, and preconditioning was mimicked by TNFα antagonists, but was independent of Wnt signaling. Therefore, TLR4 is a novel regulator of photoreceptor survival that acts through the Wnt and TNFα pathways. © 2012 Yi et al.
机译:最近的证据表明,先天性免疫可调节中风和其他神经退行性变期间大脑的神经元存活。感光器是视网膜中专门的光检测神经元,对视觉至关重要。在这项研究中,我们调查了先天免疫受体TLR4在感光细胞中的作用。脂多糖(LPS)激活TLR4大大降低了暴露于氧化应激的培养小鼠感光细胞的存活率。关于机制,TLR4抑制Wnt信号传导,减少Wnt受体LRP6的磷酸化和激活,并阻断Wnt3a配体的保护作用。矛盾的是,氧化损伤之前的TLR4活化保护了感光体,这种现象被称为预处理。在预处理过程中,TNFα及其受体TNFR1和TNFR2的表达下降,并且TNFα拮抗剂模拟了预处理,但与Wnt信号无关。因此,TLR4是一种通过Wnt和TNFα途径发挥作用的新型感光受体调节剂。 ©2012 Yi等。

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