突触后lncRNA Sera/Pkm2通路通过重塑mPFC的神经组合,协调从社会竞争到等级的转变。

IF 13 1区 生物学 Q1 CELL BIOLOGY Cell Discovery Pub Date : 2024-08-20 DOI:10.1038/s41421-024-00706-8
Ling-Shuang Zhu, Chuan Lai, Chao-Wen Zhou, Hui-Yang Chen, Zhi-Qiang Liu, Ziyuan Guo, Hengye Man, Hui-Yun Du, Youming Lu, Feng Hu, Zhiye Chen, Kai Shu, Ling-Qiang Zhu, Dan Liu
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引用次数: 0

摘要

个体在与同类的竞争性互动中不断取得成功会对其社会等级产生强烈影响。内侧前额叶皮层(mPFC)是介导社会竞争和等级制度的关键脑区。然而,mPFC神经集合的分子调控机制仍不清楚。在这里,我们证明了在前边缘皮层(PL)的兴奋性神经元中,lncRNA Sera重塑了Pkm Exon9和Exon10的利用,导致高度竞争性小鼠的Pkm1/2比率下降。通过使用 tet-on/off 系统,我们控制了 PL 兴奋神经元中 Pkm2 的表达,从而破坏或重建了正常的 Pkm1/2 比率。我们发现,通过磷酸化 GluA1 的 Ser845 位点,长期的 Pkm2 调节可诱导及时的竞争改变和滞后等级变化。综上所述,本研究发现了lncRNA Sera/Pkm2通路通过重塑mPFC中的神经组合,在社会竞争向等级过渡中的关键作用。
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Postsynaptic lncRNA Sera/Pkm2 pathway orchestrates the transition from social competition to rank by remodeling the neural ensemble in mPFC.

Individuals' continuous success in competitive interactions with conspecifics strongly affects their social hierarchy. Medial prefrontal cortex (mPFC) is the key brain region mediating both social competition and hierarchy. However, the molecular regulatory mechanisms underlying the neural ensemble in the mPFC remains unclear. Here, we demonstrate that in excitatory neurons of prelimbic cortex (PL), lncRNA Sera remodels the utilization of Pkm Exon9 and Exon10, resulting in a decrease in the Pkm1/2 ratio in highly competitive mice. By employing a tet-on/off system, we disrupt or rebuild the normal Pkm1/2 ratio by controlling the expression of Pkm2 in PL excitatory neurons. We find that long-term Pkm2 modulation induces timely competition alteration and hysteretic rank change, through phosphorylating the Ser845 site of GluA1. Together, this study uncovers a crucial role of lncRNA Sera/Pkm2 pathway in the transition of social competition to rank by remodeling neural ensemble in mPFC.

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来源期刊
Cell Discovery
Cell Discovery Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
24.20
自引率
0.60%
发文量
120
审稿时长
20 weeks
期刊介绍: Cell Discovery is a cutting-edge, open access journal published by Springer Nature in collaboration with the Center for Excellence in Molecular Cell Science, Chinese Academy of Sciences (CAS). Our aim is to provide a dynamic and accessible platform for scientists to showcase their exceptional original research. Cell Discovery covers a wide range of topics within the fields of molecular and cell biology. We eagerly publish results of great significance and that are of broad interest to the scientific community. With an international authorship and a focus on basic life sciences, our journal is a valued member of Springer Nature's prestigious Molecular Cell Biology journals. In summary, Cell Discovery offers a fresh approach to scholarly publishing, enabling scientists from around the world to share their exceptional findings in molecular and cell biology.
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