Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, ON K1H 8M5, Canada.
Brain and Mind Research Institute, University of Ottawa, Ottawa, ON K1H 8M5, Canada.
Proc Natl Acad Sci U S A. 2018 May 29;115(22):E5164-E5173. doi: 10.1073/pnas.1718946115. Epub 2018 May 14.
Leucine-rich repeat kinase 2 () has been implicated in both familial and sporadic Parkinson's disease (PD), yet its pathogenic role remains unclear. A previous screen in identified Scar/WAVE (Wiskott-Aldrich syndrome protein-family verproline) proteins as potential genetic interactors of Here, we provide evidence that LRRK2 modulates the phagocytic response of myeloid cells via specific modulation of the actin-cytoskeletal regulator, WAVE2. We demonstrate that macrophages and microglia from PD patients and mice display a WAVE2-mediated increase in phagocytic response, respectively. Lrrk2 loss results in the opposite effect. LRRK2 binds and phosphorylates Wave2 at Thr470, stabilizing and preventing its proteasomal degradation. Finally, we show that Wave2 also mediates Lrrk2G2019S-induced dopaminergic neuronal death in both macrophage-midbrain cocultures and in vivo. Taken together, a LRRK2-WAVE2 pathway, which modulates the phagocytic response in mice and human leukocytes, may define an important role for altered immune function in PD.
富含亮氨酸重复激酶 2 (LRRK2) 既与家族性帕金森病 (PD) 有关,也与散发性 PD 有关,但它的致病作用仍不清楚。之前的一项研究在 中发现 Scar/WAVE (Wiskott-Aldrich 综合征蛋白家族脯氨酰肽) 蛋白可能是 LRRK2 的潜在遗传相互作用因子。在这里,我们提供的证据表明,LRRK2 通过对肌动蛋白细胞骨架调节因子 WAVE2 的特异性调节,调节髓样细胞的吞噬反应。我们证明,来自 PD 患者和小鼠的巨噬细胞和小胶质细胞分别显示出 WAVE2 介导的吞噬反应增加。Lrrk2 缺失则产生相反的效果。LRRK2 结合并磷酸化 Wave2 的 Thr470,稳定并防止其蛋白酶体降解。最后,我们表明 Wave2 还介导了 Lrrk2G2019S 在巨噬细胞-中脑共培养物和体内诱导的多巴胺能神经元死亡。总之,LRRK2-WAVE2 通路调节了小鼠和人白细胞的吞噬反应,这可能表明免疫功能改变在 PD 中的重要作用。