微质先天免疫受体TREM2通过过度的前皮层突触修剪参与恐惧记忆的形成
Le-le Zhang1,2,3, Peng Cheng1,2,3, Yuan-Qing Chu1,2,3
1National Medical Products Administration Key Laboratory for Research and Evaluation of Narcotic and Psychotropic Drugs, Xuzhou Medical University, Xuzhou, China.
Frontiers in immunology
|November 15, 2024
概括
过度的微质切割突触,由TREM2 (触发受体表达在骨髓细胞2) 调节,有助于恐惧记忆形成和与压力相关的疾病.
科学领域:
- 神经科学是一个神经科学.
- 细胞生物学 细胞生物学
- 精神病学是一个精神病学.
背景情况:
- 恐惧记忆的形成与PTSD等与压力相关的疾病有关.
- 在PTSD中观察到微质激活和突触缺陷.
- 在恐惧记忆中TREM2 (在骨髓细胞2表达的触发受体) 的作用尚不清楚.
研究的目的:
- 研究微质和TREM2在恐惧记忆形成中的作用.
- 了解连接微质活动,突触修剪和恐惧记忆的机制.
主要方法:
- 通过在雄性小鼠中使用脚冲击来建立一个恐惧记忆模型.
- 评估了微质突触修剪能力,使用西方涂抹,免疫光和Golgi-Cox染色.
- 在Trem2淘汰赛小鼠和通过siRNA注射中检查了TREM2的参与.
主要成果:
- 足部冲击诱导了恐惧记忆,增加了突触的微质吞,并激活了前极性谷氨基神经元.
- 抑制微质细胞或删除TREM2会减少突触修剪和恐惧记忆.
- 发现TREM2 (在骨髓细胞2上表达的触发受体) 能够调节微细胞化和突触修剪.
结论:
- 过度的TREM2介导的前临床皮质中的微质突触修剪与恐惧记忆的形成有关.
- 这个过程可能会导致与压力相关的异常行为和精神疾病.
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