Neuroregeneration and Stem Cell Programs, Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA; Adrienne Helis Malvin Medical Research Foundation, New Orleans, LA 70130-2685, USA.
Department of Pharmacology and Molecular Sciences and SJ Yan and HJ Mao Laboratory of Chemical Biology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Cell. 2022 May 26;185(11):1943-1959.e21. doi: 10.1016/j.cell.2022.04.020. Epub 2022 May 10.
Parthanatos-associated apoptosis-inducing factor (AIF) nuclease (PAAN), also known as macrophage migration inhibitor factor (MIF), is a member of the PD-D/E(X)K nucleases that acts as a final executioner in parthanatos. PAAN's role in Parkinson's disease (PD) and whether it is amenable to chemical inhibition is not known. Here, we show that neurodegeneration induced by pathologic α-synuclein (α-syn) occurs via PAAN/MIF nuclease activity. Genetic depletion of PAAN/MIF and a mutant lacking nuclease activity prevent the loss of dopaminergic neurons and behavioral deficits in the α-syn preformed fibril (PFF) mouse model of sporadic PD. Compound screening led to the identification of PAANIB-1, a brain-penetrant PAAN/MIF nuclease inhibitor that prevents neurodegeneration induced by α-syn PFF, AAV-α-syn overexpression, or MPTP intoxication in vivo. Our findings could have broad relevance in human pathologies where parthanatos plays a role in the development of cell death inhibitors targeting the druggable PAAN/MIF nuclease.
与细胞凋亡相关的调亡诱导因子(AIF)核酸酶(PAAN),也称为巨噬细胞移动抑制因子(MIF),是 PD-D/E(X)K 核酸酶家族的成员,在细胞调亡中充当最终执行者。PAAN 在帕金森病(PD)中的作用及其是否可被化学抑制尚不清楚。在这里,我们表明病理性α-突触核蛋白(α-syn)诱导的神经退行性变是通过 PAAN/MIF 核酸酶活性发生的。PAAN/MIF 的基因缺失和缺乏核酸酶活性的突变可防止α-syn 预形成纤维(PFF)帕金森病散发性小鼠模型中多巴胺能神经元的丧失和行为缺陷。化合物筛选导致发现了 PAANIB-1,这是一种可穿透大脑的 PAAN/MIF 核酸酶抑制剂,可预防α-syn PFF、AAV-α-syn 过表达或 MPTP 中毒诱导的神经退行性变。我们的发现可能与细胞调亡在细胞死亡抑制剂的发展中起作用的人类病理学具有广泛的相关性,这些抑制剂可针对可药物治疗的 PAAN/MIF 核酸酶。