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Long non-coding RNA uc.80- overexpression promotes M2 polarization of microglias to ameliorate depression in rats
Xun-Hu Gu1, Li-Jun Xu1, Li-Li Zheng2
1Department of Neurology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China.
Abstract:
Microglia polarization is associated with the pathogenesis of depression. A previous study shows that long non-coding RNA uc.80- is down-regulated in the hippocampus of depressed rats. Thus, this article aims to investigate the role of uc.80- in microglia polarization in depression. We first established depression model rats by chronic unpredictable mild stress (CUMS) regiment. We found that hippocampus of depressed rats exhibited an increase of M1 microglias and a decrease of M2 microglias. uc.80- was down-regulated in hippocampus of depressed rats. Furthermore, the detection of behaviouristics of depressed rats showed that uc.80- overexpression alleviated depression of rats. In addition, uc.80- overexpression promoted M2 polarization of microglias in vivo and in vitro. uc.80- overexpression led to a decrease in apoptosis of hippocampal neurons in vivo and in vitro. In conclusion, our study confirms that lncRNA uc.80- overexpression ameliorates depression in rats by promoting M2 polarization of microglias. Thus, our work suggests that uc.80- may be a target gene for depression treatment.
Insights
Long non-coding RNA uc.80- overexpression alleviates depression in rats by promoting beneficial M2 microglia polarization. This suggests uc.80- as a potential therapeutic target for depression treatment.
Area of Science:
- Neuroscience
- Molecular Biology
- Genetics
Background:
- Microglia polarization plays a role in depression pathogenesis.
- Long non-coding RNA uc.80- is downregulated in the hippocampus of depressed rats.
Purpose of the Study:
- To investigate the role of uc.80- in microglia polarization in depression.
- To explore uc.80- as a potential therapeutic target for depression.
Main Methods:
- Established a rat model of depression using chronic unpredictable mild stress (CUMS).
- Analyzed microglia polarization (M1/M2) and uc.80- expression in rat hippocampi.
- Assessed behavioral changes and hippocampal neuron apoptosis in response to uc.80- overexpression in vivo and in vitro.
Main Results:
- Depressed rats showed increased M1 and decreased M2 microglia in the hippocampus.
- uc.80- was significantly downregulated in depressed rat hippocampi.
- uc.80- overexpression alleviated depressive behaviors, promoted M2 microglia polarization, and reduced hippocampal neuron apoptosis.
Conclusions:
- lncRNA uc.80- overexpression ameliorates depression in rats.
- This effect is mediated by promoting M2 microglia polarization.
- uc.80- represents a potential therapeutic target for depression.
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