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DNA methylation of the Tacr2 gene in a CUMS model of depression
Dan Xiang1, Jiawei Xiao1, Linyan Fu1
1Department of Psychiatry, Renmin Hospital of Wuhan University, Wuhan, 430060, PR China.
Abstract:
Tacr2, the gene encoding the NK2 receptor, belongs to G protein-coupled receptors. Accumulating evidence has indicated that the tachykinin receptors may contribute to the pathophysiology of depression. During the last decade, some studies have shown that Tacr2 activation is involved in the modulation of emotional processes. However, the extent, to which stress impacts Tacr2 expression remains unclear. The molecular mechanisms underlying depression also remain poorly understood. In this study, we subjected adult male Sprague Dawley (SD) rats to chronic unpredictable mild stress (CUMS) to induce a depression-like phenotype. We then measured the body weight and performed the sucrose preference test, forced swimming test (FST) and open field test to detect the effects of stress on anhedonia and activity. Western blotting and real-time PCR were used to study the protein and mRNA expression levels of Tacr2, respectively, in the hypothalamus. To explore DNA methylation of the Tacr2 gene, we used methylated DNA immunoprecipitation sequencing (MeDIP-seq). Additionally, we used the bisulfite sequencing PCR (BSP) to further verify the DNA methylation levels of the Tacr2 receptor gene in rats. We found that the CUMS-sensitive rats exhibited a decrease in body weight and sucrose preference, a decrease in the distance traveled, rearing frequency and velocity in the open field test, and an increase in immobility time in the FST. Compared with the expression in the control rats, Tacr2 protein and mRNA expression in the hypothalamus significantly increased in the CUMS-sensitive rats; however, the DNA methylation levels of the Tacr2 gene were significantly lower than in the control rats. In summary, according to our findings, the stress-induced increase in Tacr2 expression in the hypothalamus correlated with a specific decrease in DNA methylation of the Tacr2 gene. These results may enrich the understanding of the pathological processes of depression and provide insights into therapeutic approaches for its treatment.
Insights
Chronic unpredictable stress increases Tacr2 (NK2 receptor) expression in rat hypothalamus by reducing DNA methylation. This finding offers insights into depression mechanisms and potential treatments.
Area of Science:
- Neuroscience
- Molecular Biology
- Psychiatry
Background:
- Tachykinin receptors, including Tacr2 (NK2 receptor), are implicated in depression.
- The impact of stress on Tacr2 expression and its underlying mechanisms are not fully understood.
- Molecular mechanisms of depression require further elucidation.
Purpose of the Study:
- To investigate the effect of chronic unpredictable mild stress (CUMS) on Tacr2 expression in the rat hypothalamus.
- To explore the role of DNA methylation in stress-induced changes in Tacr2 expression.
- To correlate Tacr2 expression changes with depression-like behaviors.
Main Methods:
- Induction of depression-like phenotype in Sprague Dawley rats using CUMS.
- Behavioral tests: sucrose preference, forced swimming test (FST), open field test.
- Molecular analysis: Western blotting, real-time PCR, methylated DNA immunoprecipitation sequencing (MeDIP-seq), bisulfite sequencing PCR (BSP) for Tacr2 gene expression and DNA methylation in the hypothalamus.
Main Results:
- CUMS-induced depression-like rats showed decreased body weight, sucrose preference, and activity, with increased immobility in FST.
- Tacr2 protein and mRNA levels were significantly elevated in the hypothalamus of CUMS-sensitive rats compared to controls.
- DNA methylation levels of the Tacr2 gene were significantly lower in CUMS-sensitive rats.
Conclusions:
- Stress-induced depression in rats is associated with increased hypothalamic Tacr2 expression.
- Reduced DNA methylation of the Tacr2 gene correlates with increased Tacr2 expression under stress.
- These findings contribute to understanding depression pathophysiology and may inform therapeutic strategies targeting the tachykinin system.
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