PLK2破坏自噬通量,促进SNCA/α-突触核蛋白病理。

Chuang Zhang, Zhanpeng Huang, Xinyue Huang, Yanni Ma, Yifan Cao, Zhixiong Zhang, Rui Wang, Haigang Ren, Longtai Zheng, Chun-Feng Liu, Guanghui Wang
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引用次数: 0

摘要

SNCA/α-突触核蛋白(synuclein, α)的聚集和传递是帕金森病(PD)的标志性病理。PLK2 (polo样激酶2)是一种进化上保守的丝氨酸/苏氨酸激酶,在所有家族成员的大脑中含量更高,在PD中高表达,与SNCA沉积有关。然而,除了其磷酸化SNCA的作用外,PLK2在PD中的作用以及引发神经退行性变的机制尚不清楚。在这里,我们发现PLK2独立于S129调节SNCA病理。PLK2的过表达促进了SNCA预形成纤维(PFF)诱导的野生型SNCA和突变型SNCAS129A的聚集。PLK2的遗传或药理抑制可减轻SNCA沉积和神经毒性。从机制上讲,PLK2通过阻断巨噬/自噬通量阻碍SNCA聚集物的清除,从而加剧了SNCA病理的增殖。我们进一步发现PLK2磷酸化DCTN1的S1098, DCTN1是一种控制细胞器运动的蛋白质,导致自噬体-溶酶体融合受损。此外,基因抑制PLK2可减轻体内SNCA聚集和运动功能障碍。我们的研究结果表明,PLK2负性调节自噬,促进SNCA病理,提示PLK2在PD中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PLK2 disrupts autophagic flux to promote SNCA/α-synuclein pathology.

The aggregation and transmission of SNCA/α-synuclein (synuclein, alpha) is a hallmark pathology of Parkinson disease (PD). PLK2 (polo like kinase 2) is an evolutionarily conserved serine/threonine kinase that is more abundant in the brains of all family members, is highly expressed in PD, and is linked to SNCA deposition. However, in addition to its role in phosphorylating SNCA, the role of PLK2 in PD and the mechanisms involved in triggering neurodegeneration remain unclear. Here, we found that PLK2 regulated SNCA pathology independently of S129. Overexpression of PLK2 promoted SNCA preformed fibril (PFF)-induced aggregation of wild-type SNCA and mutant SNCAS129A. Genetic or pharmacological inhibition of PLK2 attenuated SNCA deposition and neurotoxicity. Mechanistically, PLK2 exacerbated the propagation of SNCA pathology by impeding the clearance of SNCA aggregates by blocking macroautophagic/autophagic flux. We further showed that PLK2 phosphorylated S1098 of DCTN1 (dynactin 1), a protein that controls the movement of organelles, leading to impaired autophagosome-lysosome fusion. Furthermore, genetic suppression of PLK2 alleviated SNCA aggregation and motor dysfunction in vivo. Our findings suggest that PLK2 negatively regulates autophagy, promoting SNCA pathology, suggesting a role for PLK2 in PD.Abbreviation: AD: Alzheimer disease; AMPK: AMP-activated protein kinase; CASP3: caspase 3; DCTN1: dynactin 1; LBs: lewy bodies; LDH: lactate dehydrogenase; LAMP1: lysosomal associated membrane protein 1; MAP1LC3/LC3: microtubule associated protein 1 light chain 3; MAP2: microtubule associated protein 2; MTOR: mechanistic target of rapamycin kinase; NH4Cl: ammonium chloride; p-SNCA: phosphorylation of SNCA at S129; PD: Parkinson disease; PFF: preformed fibril; PI: propidium iodide; PLK2: polo like kinase 2; PRKAA/AMPK: protein kinase AMP-activated catalytic subunit alpha; shRNA: short hairpin RNA; SNCA: synuclein, alpha; SQSTM1/p62: sequestosome 1; TH: tyrosine hydroxylase; TX: Triton X-100; ULK1: unc-51 like autophagy activating kinase 1.

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