Cell Signalling Laboratory, Department of Neuroinflammation, Institute of Neurology, University College London, London WC1N 1PJ, UK.
Neurosci Lett. 2011 Nov 14;505(2):140-5. doi: 10.1016/j.neulet.2011.10.007. Epub 2011 Oct 8.
Microglial activation and blood brain barrier dysfunction are significant hallmarks in an array of neurodegenerative disorders. A leaky blood brain barrier potentially allows infiltration of blood-borne proteins into the CNS parenchyma, and previous studies have shown that the blood borne protein fibrinogen (FG) can activate microglia to produce a neurotoxic phenotype. Here we show that FG-mediated neurotoxicity and ERK1/2 phosphorylation in neuronal cultures is significantly attenuated by activation of metabotropic glutamate receptor 5 (mGluR5) but not mGluR2. Furthermore, FG-mediated microglial activation was down-regulated by direct mGluR5 activation on these cells but not by mGluR2, suggesting that targeting microglial mGluR5 provides neuronal protection against blood protein-triggered innate inflammatory responses.
小胶质细胞激活和血脑屏障功能障碍是多种神经退行性疾病的重要标志。血脑屏障的渗漏可能使血液来源的蛋白质渗透到中枢神经系统实质中,先前的研究表明,血液来源的蛋白质纤维蛋白原(FG)可以激活小胶质细胞产生神经毒性表型。在这里,我们表明,在神经元培养物中,FG 介导的神经毒性和 ERK1/2 磷酸化通过代谢型谷氨酸受体 5(mGluR5)的激活而显著减弱,但不是通过 mGluR2。此外,FG 介导的小胶质细胞激活通过这些细胞上的直接 mGluR5 激活下调,但不是通过 mGluR2,这表明针对小胶质细胞 mGluR5 可提供神经元保护,防止血液蛋白引发的固有炎症反应。