Department of Neuroimmunology, Research Institute of Environmental Medicine, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8601, Japan.
Brain Res. 2010 Mar 31;1322:8-23. doi: 10.1016/j.brainres.2010.01.083. Epub 2010 Feb 6.
Microglia are intrinsic immune cells in the central nervous system and play key roles in the pathogenesis of various central nervous system disorders. Microglia have been shown to attack damaged neurons by secreting a variety of neurotoxic factors including inflammatory cytokines, reactive oxygen species and glutamate. On the other hand, they can produce neurotrophic factors (NTFs) which support neuronal survival and growth. However, the precise mechanism that regulates microglial NTF production is not fully understood, and the relation between glutamate and NTFs remains unclear. In the present study, we show that glutamate significantly induces microglial NTF production by the activation of N-methyl-d-aspartate (NMDA) receptors, group III metabotropic glutamate receptors, and glutamate transporters. Activation of NMDA receptors and group III metabotropic glutamate receptors induces intracellular Ca(2+) release from the endoplasmic reticulum. Further, stimulation of glutamate transporters leads to influx of extracellular Ca(2+) in a Na(+)-dependent manner. This intracellular Ca(2+) elevation activates the protein kinase C pathway which induces microglial NTF expression and production. These results suggest that microglia play a neuroprotective role during the excitotoxic state in neurodegenerative diseases.
小胶质细胞是中枢神经系统中的固有免疫细胞,在各种中枢神经系统疾病的发病机制中发挥关键作用。小胶质细胞通过分泌多种神经毒性因子,包括炎症细胞因子、活性氧和谷氨酸,攻击受损神经元。另一方面,它们可以产生神经营养因子(NTFs),支持神经元的存活和生长。然而,调节小胶质细胞 NTF 产生的确切机制尚不完全清楚,谷氨酸和 NTFs 之间的关系仍不清楚。在本研究中,我们表明,谷氨酸通过 N-甲基-D-天冬氨酸(NMDA)受体、III 组代谢型谷氨酸受体和谷氨酸转运体的激活,显著诱导小胶质细胞 NTF 的产生。NMDA 受体和 III 组代谢型谷氨酸受体的激活从内质网中释放细胞内 Ca(2+)。此外,谷氨酸转运体的刺激以 Na(+)-依赖性方式导致细胞外 Ca(2+)内流。这种细胞内 Ca(2+)升高激活蛋白激酶 C 途径,诱导小胶质细胞 NTF 的表达和产生。这些结果表明,小胶质细胞在神经退行性疾病的兴奋毒性状态中发挥神经保护作用。