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本文引用的文献

1
Microglia and macrophages differ in their inflammatory profile after permanent brain ischemia.小胶质细胞和巨噬细胞在永久性脑缺血后的炎症特征上存在差异。
Exp Neurol. 2018 Mar;301(Pt B):120-132. doi: 10.1016/j.expneurol.2017.08.011. Epub 2017 Aug 24.
2
Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases.帕金森病与自身免疫性疾病之间的全基因组多效性
JAMA Neurol. 2017 Jul 1;74(7):780-792. doi: 10.1001/jamaneurol.2017.0469.
3
LRRK2(I2020T) functional genetic interactors that modify eye degeneration and dopaminergic cell loss in Drosophila.LRRK2(I2020T)的功能性基因相互作用因子,其可改善果蝇的眼部退化和多巴胺能细胞损失。
Hum Mol Genet. 2017 Apr 1;26(7):1247-1257. doi: 10.1093/hmg/ddx030.
4
LRRK2 and RAB7L1 coordinately regulate axonal morphology and lysosome integrity in diverse cellular contexts.LRRK2 和 RAB7L1 共同调节不同细胞环境中的轴突形态和溶酶体完整性。
Sci Rep. 2016 Jul 18;6:29945. doi: 10.1038/srep29945.
5
Sequential recruitment of Rab GTPases during early stages of phagocytosis.吞噬作用早期阶段Rab GTP酶的顺序募集。
Cell Logist. 2016 Jan 29;6(1):e1140615. doi: 10.1080/21592799.2016.1140615. eCollection 2016 Jan-Mar.
6
A Missense LRRK2 Variant Is a Risk Factor for Excessive Inflammatory Responses in Leprosy.一种错义LRRK2变体是麻风病中过度炎症反应的危险因素。
PLoS Negl Trop Dis. 2016 Feb 4;10(2):e0004412. doi: 10.1371/journal.pntd.0004412. eCollection 2016 Feb.
7
Phosphoproteomics reveals that Parkinson's disease kinase LRRK2 regulates a subset of Rab GTPases.磷酸化蛋白质组学研究表明,帕金森病激酶LRRK2调节Rab GTP酶的一个亚群。
Elife. 2016 Jan 29;5:e12813. doi: 10.7554/eLife.12813.
8
Endoplasmic reticulum-resident Rab8A GTPase is involved in phagocytosis in the protozoan parasite Entamoeba histolytica.内质网驻留的Rab8A GTP酶参与原生动物寄生虫溶组织内阿米巴的吞噬作用。
Cell Microbiol. 2016 Oct;18(10):1358-73. doi: 10.1111/cmi.12570. Epub 2016 Apr 4.
9
The G2019S LRRK2 mutation increases myeloid cell chemotactic responses and enhances LRRK2 binding to actin-regulatory proteins.G2019S LRRK2突变增加髓样细胞趋化反应并增强LRRK2与肌动蛋白调节蛋白的结合。
Hum Mol Genet. 2015 Aug 1;24(15):4250-67. doi: 10.1093/hmg/ddv157. Epub 2015 Apr 29.
10
An early endosome regulator, Rab5b, is an LRRK2 kinase substrate.一种早期内体调节剂Rab5b是LRRK2激酶的底物。
J Biochem. 2015 Jun;157(6):485-95. doi: 10.1093/jb/mvv005. Epub 2015 Jan 19.

LRRK2 通过稳定 WAVE2 复合物调节髓样细胞吞噬作用,在帕金森病中发生改变。

Regulation of myeloid cell phagocytosis by LRRK2 via WAVE2 complex stabilization is altered in Parkinson's disease.

机构信息

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.

出版信息

Proc Natl Acad Sci U S A. 2018 May 29;115(22):E5164-E5173. doi: 10.1073/pnas.1718946115. Epub 2018 May 14.

DOI:10.1073/pnas.1718946115
PMID:29760073
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5984500/
Abstract

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.

摘要

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。