Department of Pediatrics, Guizhou Medical University, The Affiliated Hospital of Guizhou Medical University, Guiyang 550004, China.
Cell Mol Biol (Noisy-le-grand). 2024 Jun 5;70(6):66-72. doi: 10.14715/cmb/2024.70.6.11.
This study aimed to investigate the mechanism of the effect of TREM2 on cognitive function in autistic mice. TREM2 overexpression and knockdown viruses were given to autism spectrum disorder (ASD) mice and BV2 microglia cell line. To assess cognitive performance, all groups of mice took part in the open field, new object recognition, Morris water maze, and three-box social experiments. Double immunofluorescence labeling demonstrated co-localization of LC3II and NeuN. Proteins from the PI3K/Akt/mTOR pathway were identified. In vivo, behavior studies revealed that TREM2 could successfully improve ASD mice's social interaction and cognitive performance. Besides, we discovered that TREM2 could increase autophagy in ASD mice. In vitro, overexpressing TREM2 reduced the expression of PI3K/AKT/mTOR pathway proteins, whereas knocking down TREM2 increased the expression of PI3K/AKT/mTOR pathway proteins. In conclusion, TREM2 could inhibit PI3K/Akt/mTOR signaling pathway, enhance autophagy, and improve the social communication ability and cognitive function of ASD mice.
本研究旨在探讨 TREM2 对自闭症小鼠认知功能影响的作用机制。给予自闭症谱系障碍(ASD)小鼠和 BV2 小胶质细胞系过表达和敲低 TREM2 的病毒。为了评估认知表现,所有小鼠组均参加了旷场、新物体识别、Morris 水迷宫和三箱社交实验。双免疫荧光标记显示 LC3II 和 NeuN 共定位。鉴定了 PI3K/Akt/mTOR 通路的蛋白。在体内,行为研究表明 TREM2 可以成功改善 ASD 小鼠的社交互动和认知表现。此外,我们发现 TREM2 可以增加 ASD 小鼠的自噬。在体外,过表达 TREM2 降低了 PI3K/AKT/mTOR 通路蛋白的表达,而敲低 TREM2 增加了 PI3K/AKT/mTOR 通路蛋白的表达。总之,TREM2 可以抑制 PI3K/Akt/mTOR 信号通路,增强自噬,改善 ASD 小鼠的社交沟通能力和认知功能。