Department and Institute of Physiology, National Yang-Ming University, 155 Sec. 2, Linong Street, Taipei, 11221, Taiwan.
Department of Anesthesiology, Taipei Veterans General Hospital and National Yang-Ming University School of Medicine, Taipei, Taiwan.
Mol Neurobiol. 2019 Dec;56(12):8451-8474. doi: 10.1007/s12035-019-01669-8. Epub 2019 Jul 1.
Astrocytes play pivotal roles in regulating glutamate homeostasis at tripartite synapses. Inhibition of soluble epoxide hydrolase (sEHi) provides neuroprotection by blocking the degradation of 14,15-epoxyeicosatrienoic acid (14,15-EET), a lipid mediator whose synthesis can be activated downstream from group 1 metabotropic glutamate receptor (mGluR) signaling in astrocytes. However, it is unclear how sEHi regulates glutamate excitotoxicity. Here, we used three primary rat cortical culture systems, neuron-enriched (NE), astrocyte-enriched glia-neuron mix (GN), and purified astrocytes, to delineate the underlying mechanism by which sEHi and 14,15-EET attenuate excitotoxicity. We found that sEH inhibitor 12-(3-adamantan-1-yl-ureido)-dodecanoic acid (AUDA) and 14,15-EET both attenuated N-methyl-D-aspartate (NMDA)-induced neurite damage and cell death in GN, not NE, cortical cultures. The anti-excitotoxic effects of 14,15-EET and AUDA were both blocked by the group 1 mGluR5 antagonist 2-methyl-6-(phenylethynyl)pyridine (MPEP), as were their protective effects against NMDA-disrupted perineuronal astrocyte processes expressing glutamate transporter-1 (GLT-1) and subsequent glutamate uptake. Knockdown of sEH expression also attenuated NMDA neurotoxicity in mGluR5- and GLT-1-dependent manners. The 14,15-EET/AUDA-preserved astroglial integrity was confirmed in glutamate-stimulated primary astrocytes along with the reduction of the c-Jun N-terminal kinase 1 phosphorylation, in which the 14,15-EET effect is mGluR5-dependent. In vivo studies validated that sEHi and genetic deletion of sEH (Ephx2-KO) ameliorated excitotoxic kainic acid-induced seizure, memory impairment, and neuronal loss while preserving GLT-1-expressing perineuronal astrocytes in hippocampal CA3 subregions. These results suggest that 14,15-EET mediates mGluR5-dependent anti-excitotoxicity by protecting astrocytes to maintain glutamate homeostasis, which may account for the beneficial effect of sEH inhibition in excitotoxic brain injury and diseases.
星形胶质细胞在三突触中发挥调节谷氨酸稳态的关键作用。抑制可溶性环氧化物水解酶 (sEH) 通过阻断 14,15-环氧二十碳三烯酸 (14,15-EET) 的降解提供神经保护作用,14,15-EET 是一种脂质介质,其合成可以在星形胶质细胞中的组 1 代谢型谷氨酸受体 (mGluR) 信号下游激活。然而,sEH 如何调节谷氨酸兴奋性毒性尚不清楚。在这里,我们使用了三种原代大鼠皮质培养系统,神经元富集 (NE)、星形胶质细胞富集的神经胶质混合 (GN) 和纯化的星形胶质细胞,以描绘 sEH 和 14,15-EET 减轻兴奋性毒性的潜在机制。我们发现,sEH 抑制剂 12-(3-金刚烷-1-基-脲基)-十二烷酸 (AUDA) 和 14,15-EET 均减轻了 GN 而非 NE 皮质培养物中 N-甲基-D-天冬氨酸 (NMDA) 诱导的神经突损伤和细胞死亡。14,15-EET 和 AUDA 的抗兴奋毒性作用均被组 1 mGluR5 拮抗剂 2-甲基-6-(苯乙炔基)吡啶 (MPEP) 阻断,它们对 NMDA 破坏表达谷氨酸转运体-1 (GLT-1) 和随后谷氨酸摄取的周围神经胶质细胞过程的保护作用也被阻断。sEH 表达的敲低也以 mGluR5 和 GLT-1 依赖的方式减轻 NMDA 神经毒性。在谷氨酸刺激的原代星形胶质细胞中证实了 14,15-EET/AUDA 维持的星形胶质细胞完整性,并减少了 c-Jun N 末端激酶 1 磷酸化,其中 14,15-EET 作用依赖于 mGluR5。体内研究验证了 sEH 抑制 (Ephx2-KO) 和基因缺失减轻了兴奋性海人酸诱导的癫痫发作、记忆障碍和神经元丢失,同时保留了海马 CA3 亚区中表达 GLT-1 的周围神经胶质细胞。这些结果表明,14,15-EET 通过保护星形胶质细胞来维持谷氨酸稳态,从而介导 mGluR5 依赖性抗兴奋毒性,这可能是 sEH 抑制在兴奋性脑损伤和疾病中有益作用的原因。