I.R.C.C.S. Neuromed, 86077 Pozzilli, Italy.
Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt University Medical Center, Nashville, TN 37232-0697, USA.
Neuropharmacology. 2018 Jan;128:301-313. doi: 10.1016/j.neuropharm.2017.10.026. Epub 2017 Oct 25.
mGlu5 receptors are involved in mechanisms of activity-dependent synaptic plasticity, and are targeted by drugs developed for the treatment of CNS disorders. We report that mGlu3 receptors, which are traditionally linked to the control of neurotransmitter release, support mGlu5 receptor signaling in neurons and largely contribute to the robust mGlu5 receptor-mediated polyphosphoinositide hydrolysis in the early postnatal life. In cortical pyramidal neurons, mGlu3 receptor activation potentiated mGlu5 receptor-mediated somatic Ca mobilization, and mGlu3 receptor-mediated long-term depression in the prefrontal cortex required the endogenous activation of mGlu5 receptors. The interaction between mGlu3 and mGlu5 receptors was also relevant to mechanisms of neuronal toxicity, with mGlu3 receptors shaping the influence of mGlu5 receptors on excitotoxic neuronal death. These findings shed new light into the complex role played by mGlu receptors in physiology and pathology, and suggest reconsideration of some of the current dogmas in the mGlu receptor field.
mGlu5 受体参与活动依赖性突触可塑性的机制,并且是为治疗中枢神经系统疾病而开发的药物的作用靶点。我们报告称,mGlu3 受体传统上与神经递质释放的控制有关,但其在神经元中支持 mGlu5 受体信号转导,并在很大程度上促成了新生后期强大的 mGlu5 受体介导的多磷酸肌醇水解。在皮质锥体神经元中,mGlu3 受体的激活增强了 mGlu5 受体介导的体细胞 Ca2+动员,并且前额叶皮层中 mGlu3 受体介导的长时程抑制需要内源性激活 mGlu5 受体。mGlu3 和 mGlu5 受体之间的相互作用也与神经元毒性的机制有关,mGlu3 受体影响 mGlu5 受体对兴奋性神经元死亡的影响。这些发现为 mGlu 受体在生理学和病理学中所起的复杂作用提供了新的认识,并提示需要重新考虑 mGlu 受体领域中的一些当前定论。