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Erythroid Differentiation Regulator 1 as a Regulator of Neuronal GSH Synthesis.
Bhadhprasit, Wattanaporn; Kinoshita, Chisato; Matsumura, Nobuko; Aoyama, Koji.
Afiliación
  • Bhadhprasit W; Department of Pharmacology, Teikyo University School of Medicine, Tokyo 173-8605, Japan.
  • Kinoshita C; Department of Pharmacology, Teikyo University School of Medicine, Tokyo 173-8605, Japan.
  • Matsumura N; Department of Pharmacology, Teikyo University School of Medicine, Tokyo 173-8605, Japan.
  • Aoyama K; Department of Pharmacology, Teikyo University School of Medicine, Tokyo 173-8605, Japan.
Antioxidants (Basel) ; 13(7)2024 Jun 26.
Article en En | MEDLINE | ID: mdl-39061840
ABSTRACT
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 in vitro 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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Antioxidants (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Antioxidants (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Japón