Department of Neurology, Washington University School of Medicine, St. Louis, MO, USA.
Hope Center for Neurological Disorders, Washington University School of Medicine, St. Louis, MO, USA.
Nat Neurosci. 2019 Aug;22(8):1217-1222. doi: 10.1038/s41593-019-0433-0. Epub 2019 Jun 24.
Variants in the triggering receptor expressed on myeloid cells 2 (TREM2) have been associated with increased risk for sporadic, late-onset Alzheimer's disease. Here we show that germline knockout of Trem2 or the TREM2 variant reduces microgliosis around amyloid-β plaques and facilitates the seeding and spreading of neuritic plaque tau aggregates. These findings demonstrate a key role for TREM2 and microglia in limiting the development of peri-plaque tau pathologies.
髓系细胞触发受体 2(TREM2)的变异与散发性、晚发性阿尔茨海默病的风险增加有关。在这里,我们表明 Trem2 或 TREM2 变体的种系敲除可减少淀粉样蛋白-β斑块周围的小胶质细胞增生,并促进神经原纤维斑块 tau 聚集物的播种和扩散。这些发现表明 TREM2 和小胶质细胞在限制斑块周围 tau 病变的发展中起着关键作用。