Bhadhprasit Wattanaporn, Kinoshita Chisato, Matsumura Nobuko, Aoyama Koji
Department of Pharmacology, Teikyo University School of Medicine, Tokyo 173-8605, Japan.
Antioxidants (Basel). 2024 Jun 26;13(7):771. doi: 10.3390/antiox13070771.
Erythroid differentiation regulator 1 (Erdr1) is a cytokine known to play important roles in cell survival under stressful conditions, maintenance of cellular growth homeostasis, and activation of the immune system. However, the impact of Erdr1 on neurons remains undefined. In this study, we present novel evidence that Erdr1 plays a role in regulating glutathione (GSH) synthesis via glutamate transporter-associated protein 3-18 (GTRAP3-18), an anchor protein in the endoplasmic reticulum that holds excitatory amino acid carrier 1 (EAAC1) in neurons. Both DNA microarray and quantitative real-time PCR analyses revealed an approximately 2-fold increase in Erdr1 levels in the hippocampus of GTRAP3-18-deficient mice compared to those of wild-type mice. Knockdown of Erdr1 resulted in a decrease in GTRAP3-18 levels, leading to an increase in EAAC1 expression and intracellular GSH levels, and subsequently, cytoprotective effects against oxidative stress. Our findings shed light on the regulatory mechanisms involving Erdr1, GTRAP3-18, EAAC1, and GSH in the context of neuronal defense against oxidative stress. Understanding the intricate interplay among these molecules may pave the way for the development of promising therapeutic strategies for neurodegenerative disorders.
红细胞分化调节因子1(Erdr1)是一种细胞因子,已知其在应激条件下的细胞存活、维持细胞生长稳态以及激活免疫系统中发挥重要作用。然而,Erdr1对神经元的影响仍不明确。在本研究中,我们提供了新的证据,表明Erdr1通过谷氨酸转运体相关蛋白3-18(GTRAP3-18)发挥调节谷胱甘肽(GSH)合成的作用,GTRAP3-18是内质网中的一种锚定蛋白,可在神经元中结合兴奋性氨基酸载体1(EAAC1)。DNA微阵列和定量实时PCR分析均显示,与野生型小鼠相比,GTRAP3-18缺陷型小鼠海马中Erdr1水平增加了约2倍。敲低Erdr1导致GTRAP3-18水平降低,进而导致EAAC1表达增加和细胞内GSH水平升高,随后产生针对氧化应激的细胞保护作用。我们的研究结果揭示了在神经元抵御氧化应激的背景下,涉及Erdr1、GTRAP3-18、EAAC1和GSH的调节机制。了解这些分子之间复杂的相互作用可能为神经退行性疾病开发有前景的治疗策略铺平道路。