Therapeutic role of long non-coding RNA TCONS_00019174 in depressive disorders is dependent on Wnt/β-catenin signaling pathway
Abstract
Chronic stress is one of the major causes that lead to major depressive disorder (MDD), which is a prevalent mood disorder worldwide. Lots of MDD patients could not benefit from available medication due to the complex etiology of MDD. Recently, long non-coding RNAs (lncRNAs), molecular switches of downstream genes expression, have been reported to be involved in the pathogenesis of MDD. LncRNA TCONS_00019174 has been implicated in MDD risk and antidepressant effects, However, the effect of lncRNA TCONS_00019174 on antidepressant responses has not been investigated. This study is designed to determine whether altered expression of lncRNA TCONS_00019174 contributes to the depression-like behaviors associated with chronic stress. We found that mice exposed to chronic ultra-mild stress (CUMS) displayed apparent depression-like behaviors and decreased expression of lncRNA TCONS_00019174 in hippocampus. Both changed behaviors and lncRNA TCONS_00019174 expression level were rescued by chronic treatment of imipramine (IMI). Viral-mediated lncRNA TCONS_00019174 overexpression in hippocampal neurons improved behaviors of mice exposed to CUMS. Further, we found lncRNA TCONS_00019174 overexpression upregulated phosphorylated-GSK3β (p-GSK3β) protein and β-catenin in the hippocampus. These findings suggest that lncRNA TCONS_00019174 exerts antidepressant-like effect in mice by activating Wnt/β-catenin pathway, proposing that lncRNAs may serve as a potential therapeutic target for MDD in the clinical application.
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In MDD patients, lncRNA TCONS 00019174 levels were lower, and phosphorylated-GSK3 and -catenin was higher in the hippocampus, potentially causing neuronal damage.
“In MDD patients, LncRNA TCONS 00019174 levels were lower, and phosphorylated-GSK3 and -catenin was higher in the hippocampus, potentially causing neuronal damage.313”
From Epigenetic regulation in major depression and other stress-related disorders: molecular mechanisms, clinical relevance and therapeutic potential (2023) · cites this paper as [313]
Viral-mediated overexpression of lncRNA TCONS 00019174 aggravated depression status in a depressed mice model, indicating that lncRNA TCONS 00019174 may be linked to the pathogenesis of depression.
“viral-mediated overexpression of lncRNA TCONS 00019174 aggravated depression status in depressed mice model, indicating that lncRNA TCONS 00019174 may be linked to the pathogenesis of depression.313”
From Epigenetic regulation in major depression and other stress-related disorders: molecular mechanisms, clinical relevance and therapeutic potential (2023) · cites this paper as [313]
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References 43 · Cited by 26
- Authors
- Ni, X., Liao, Y., Li, L., Zhang, X., & Wu, Z.
- Affiliations
- Shenzhen Second People's Hospital (CN)
- Shenzhen Traditional Chinese Medicine Hospital (CN)
- Shenzhen Institute of Geriatrics, Shenzhen, Guangdong, 518037, P.R. China
- Corresponding author
- Wu, Zhengzhi
- Venue
- Journal of Integrative Neuroscience
- Publisher
- SAGE Publications
- Published
- 2018-03-06
- Volume
- 17
- Issue
- 2
- Pages
- 203-215
- ISSN
- 0219-6352 (ISSN-L)
- 1757-448X
- OpenAlex
- W4248769523
- Cited by
- 26
- References
- 43
- Citations by year
- 2024: 3 · 2023: 3 · 2022: 2 · 2021: 2 · 2020: 10 · 2019: 3 · 2018: 3
- FWCI
- 3.06
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Integrative Neuroscience (publishedVersion)
- Funders
- National Institutes of Health
- Topics
- Health Sciences › Medicine › Pharmacology › Treatment of Major Depression
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer-related molecular mechanisms research
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Keywords
- major depressive disorder, chronic unpredictable mild stress, depression-like behavior, Wnt/β-catenin signaling, GSK3β phosphorylation, β-catenin, hippocampus, imipramine, antidepressant response, viral overexpression, therapeutic target
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