GPR39 protects against corticosterone-induced neuronal injury in hippocampal cells through the CREB-BDNF signaling pathway.


Journal

Journal of affective disorders
ISSN: 1573-2517
Titre abrégé: J Affect Disord
Pays: Netherlands
ID NLM: 7906073

Informations de publication

Date de publication:
01 07 2020
Historique:
received: 17 05 2019
revised: 11 02 2020
accepted: 29 03 2020
entrez: 20 6 2020
pubmed: 20 6 2020
medline: 16 2 2021
Statut: ppublish

Résumé

The release of zinc from glutamatergic terminals in the hippocampal CA3 region can activate postsynaptic GPR39 receptors and regulate cognition and depression. However, the role and mechanism of GPR39 in the stress-induced depression is still poorly understood. In this study, hippocampal cells (HT-22) were treated with corticosterone (CORT). Then the effects of stress on the activity, mitochondrial function and apoptosis of HT-22 cells were observed. The effects of GPR39 on CORT-induced stress injury were analyzed by both siRNA and agonist (TC-G-1008). Compared with the 500 nM CORT group, the cell viability, apoptosis, mitochondrial membrane potential, and expression levels of BCL-2, CREB and BDNF mRNA were significantly decreased in the GPR39 siRNA+500 nM CORT group, while the expression levels of caspase3, caspase9, AIF and BAX mRNA were significantly increased in the GPR39 siRNA+500 nM CORT group. Compared with the 1 μM CORTgroup, the cell viability, apoptosis, mitochondrial membrane potential, and expression levels of BCL-2, CREB and BDNF were significantly increased in the GPR39 agonist+1 μΜ CORT group, while the expression levels of caspase3, caspase9, AIF and BAX mRNA were significantly decreased in the GPR39 siRNA+500 nM CORT group. Compared with the control group, the mRNA and protein levels of GPR39, CREB and BDNF were significantly increased, and the mRNA and protein levels of CREB and BDNF were significantly decreased after 50 μM zinc sulfate treatment for 6 h. GPR39 may play a neuroprotective role in CORT-induced cell injury via the improvement of CREB-BDNF expression, by inhibiting pro-apoptotic proteins and by upregulating anti-apoptotic proteins.

Sections du résumé

BACKGROUND
The release of zinc from glutamatergic terminals in the hippocampal CA3 region can activate postsynaptic GPR39 receptors and regulate cognition and depression. However, the role and mechanism of GPR39 in the stress-induced depression is still poorly understood.
METHODS
In this study, hippocampal cells (HT-22) were treated with corticosterone (CORT). Then the effects of stress on the activity, mitochondrial function and apoptosis of HT-22 cells were observed. The effects of GPR39 on CORT-induced stress injury were analyzed by both siRNA and agonist (TC-G-1008).
RESULTS
Compared with the 500 nM CORT group, the cell viability, apoptosis, mitochondrial membrane potential, and expression levels of BCL-2, CREB and BDNF mRNA were significantly decreased in the GPR39 siRNA+500 nM CORT group, while the expression levels of caspase3, caspase9, AIF and BAX mRNA were significantly increased in the GPR39 siRNA+500 nM CORT group. Compared with the 1 μM CORTgroup, the cell viability, apoptosis, mitochondrial membrane potential, and expression levels of BCL-2, CREB and BDNF were significantly increased in the GPR39 agonist+1 μΜ CORT group, while the expression levels of caspase3, caspase9, AIF and BAX mRNA were significantly decreased in the GPR39 siRNA+500 nM CORT group. Compared with the control group, the mRNA and protein levels of GPR39, CREB and BDNF were significantly increased, and the mRNA and protein levels of CREB and BDNF were significantly decreased after 50 μM zinc sulfate treatment for 6 h.
CONCLUSIONS
GPR39 may play a neuroprotective role in CORT-induced cell injury via the improvement of CREB-BDNF expression, by inhibiting pro-apoptotic proteins and by upregulating anti-apoptotic proteins.

Identifiants

pubmed: 32553391
pii: S0165-0327(19)31265-0
doi: 10.1016/j.jad.2020.03.137
pii:
doi:

Substances chimiques

Brain-Derived Neurotrophic Factor 0
Cyclic AMP Response Element-Binding Protein 0
GPR39 protein, human 0
Receptors, G-Protein-Coupled 0
Corticosterone W980KJ009P

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

474-484

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no conflict of interest.

Auteurs

Fengfeng Mo (F)

Department of Nutrition and Food Hygiene, Faculty of Naval Medicine, Second Military Medical University, 800 Xiangyin Rd, 200433 Shanghai, China.

Yuxiao Tang (Y)

Department of Nutrition and Food Hygiene, Faculty of Naval Medicine, Second Military Medical University, 800 Xiangyin Rd, 200433 Shanghai, China.

Peng Du (P)

Institute of Aviation Medicine, 28 Fucheng Rd, 100142 Beijing, China.

Zhilei Shen (Z)

Department of Nutrition and Food Hygiene, Faculty of Naval Medicine, Second Military Medical University, 800 Xiangyin Rd, 200433 Shanghai, China.

Jianxin Yang (J)

Department of Nutrition and Food Hygiene, Faculty of Naval Medicine, Second Military Medical University, 800 Xiangyin Rd, 200433 Shanghai, China.

Mengyu Cai (M)

Department of Nutrition and Food Hygiene, Faculty of Naval Medicine, Second Military Medical University, 800 Xiangyin Rd, 200433 Shanghai, China.

Yinyin Zhang (Y)

Department of Nutrition and Food Hygiene, Faculty of Naval Medicine, Second Military Medical University, 800 Xiangyin Rd, 200433 Shanghai, China.

Hongxia Li (H)

Department of Nutrition and Food Hygiene, Faculty of Naval Medicine, Second Military Medical University, 800 Xiangyin Rd, 200433 Shanghai, China. Electronic address: Hongxialove617@126.com.

Hui Shen (H)

Department of Nutrition and Food Hygiene, Faculty of Naval Medicine, Second Military Medical University, 800 Xiangyin Rd, 200433 Shanghai, China. Electronic address: shenhuicn@126.com.

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Classifications MeSH