State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China.
University of Chinese Academy of Sciences, Beijing 100049, China.
Int J Mol Sci. 2024 Jan 18;25(2):1160. doi: 10.3390/ijms25021160.
Synapse loss is one of the most critical features in Alzheimer's disease (AD) and correlates with cognitive decline. Astrocytes mediate synapse elimination through multiple EGF-like domains 10 (MEGF10) pathways in the developing and adult brain to build the precise neural connectivity. However, whether and how astrocytes mediate synapse loss in AD remains unknown. We here find that the phagocytic receptor MEGF10 of astrocytes is significantly increased in vivo and in vitro, which results in excessive engulfment of synapses by astrocytes in APP/PS1 mice. We also observe that the astrocytic lysosomal-associated membrane protein 1 (LAMP1) is significantly elevated, colocalized with the engulfed synaptic puncta in APP/PS1 mice, and astrocytic lysosomes contain more engulfed synaptic puncta in APP/PS1 mice relative to wild type mice. Together, our data provide evidence that astrocytes excessively engulf synapses in APP/PS1 mice, which is mediated by increased MEGF10 and activated lysosomes. The approach targeting synapse engulfment pathway in astrocytes would be a potent therapy for AD.
突触丧失是阿尔茨海默病(AD)的最关键特征之一,与认知能力下降相关。星形胶质细胞通过发育中和成年大脑中的多个表皮生长因子样结构域 10(MEGF10)途径来介导突触消除,以建立精确的神经连接。然而,星形胶质细胞是否以及如何在 AD 中介导突触丧失仍然未知。我们在这里发现,星形胶质细胞的吞噬受体 MEGF10 在体内和体外都显著增加,导致 APP/PS1 小鼠中的星形胶质细胞过度吞噬突触。我们还观察到星形胶质细胞溶酶体相关膜蛋白 1(LAMP1)显著升高,与 APP/PS1 小鼠中吞噬的突触点状结构共定位,并且 APP/PS1 小鼠中的星形胶质细胞溶酶体含有更多吞噬的突触点状结构。总之,我们的数据提供了证据,表明星形胶质细胞在 APP/PS1 小鼠中过度吞噬突触,这是由增加的 MEGF10 和激活的溶酶体介导的。靶向星形胶质细胞中突触吞噬途径的方法可能是 AD 的有效治疗方法。