Positive allosteric modulation of metabotropic glutamate receptor 5 down-regulates fibrinogen-activated microglia providing neuronal protection
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 …
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 …
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.
Elsevier