Stevens Susan L, Ciesielski Thomas M P, Marsh Brenda J, Yang Tao, Homen Delfina S, Boule Jo-Lynn, Lessov Nikola S, Simon Roger P, Stenzel-Poore Mary P
Department of Molecular Microbiology and Immunology, Oregon Health & Science University, Portland, Oregon 97239, USA.
J Cereb Blood Flow Metab. 2008 May;28(5):1040-7. doi: 10.1038/sj.jcbfm.9600606. Epub 2008 Jan 9.
Preconditioning with lipopolysaccharide (LPS), a toll-like receptor 4 (TLR4) ligand, provides neuroprotection against subsequent cerebral ischemic brain injury, through a tumor necrosis factor (TNF)alpha-dependent process. Here, we report the first evidence that another TLR, TLR9, can induce neuroprotection. We show that the TLR9 ligand CpG oligodeoxynucleotide (ODN) can serve as a potent preconditioning stimulus and provide protection against ischemic brain injury. Our studies show that systemic administration of CpG ODN 1826 in advance of brain ischemia (middle cerebral artery occlusion (MCAO)) reduces ischemic damage up to 60% in a dose- and time-dependent manner. We also offer evidence that CpG ODN preconditioning can provide direct protection to cells of the central nervous system, as we have found marked neuroprotection in modeled ischemia in vitro. Finally, we show that CpG preconditioning significantly increases serum TNFalpha levels before MCAO and that TNFalpha is required for subsequent reduction in damage, as mice lacking TNFalpha are not protected against ischemic injury by CpG preconditioning. Our studies show that preconditioning with a TLR9 ligand induces neuroprotection against ischemic injury through a mechanism that shares common elements with LPS preconditioning via TLR4.
用脂多糖(LPS)(一种Toll样受体4(TLR4)配体)进行预处理,可通过肿瘤坏死因子(TNF)α依赖性过程,为后续的脑缺血性脑损伤提供神经保护作用。在此,我们首次报告了另一种Toll样受体TLR9可诱导神经保护作用的证据。我们发现,TLR9配体CpG寡脱氧核苷酸(ODN)可作为一种有效的预处理刺激物,并为缺血性脑损伤提供保护。我们的研究表明,在脑缺血(大脑中动脉闭塞(MCAO))之前全身给予CpG ODN 1826,可剂量和时间依赖性地将缺血损伤降低多达60%。我们还提供证据表明,CpG ODN预处理可为中枢神经系统细胞提供直接保护,因为我们在体外模拟缺血中发现了显著的神经保护作用。最后,我们表明,CpG预处理在MCAO前显著提高血清TNFα水平,且后续损伤的减轻需要TNFα,因为缺乏TNFα的小鼠不能通过CpG预处理免受缺血性损伤。我们的研究表明,用TLR9配体进行预处理可通过一种与经由TLR4的LPS预处理具有共同要素的机制,诱导对缺血性损伤的神经保护作用。