帕金
品脱1
粒体自噬
生物
脱磷
自噬
细胞生物学
发病机制
泛素
蛋白磷酸酶2
癌症研究
遗传学
磷酸化
免疫学
疾病
细胞凋亡
基因
磷酸酶
帕金森病
病理
医学
作者
Ningning Li,Hongyu Hou,Dan Su,Bin Yang,Ruiqing Ni,Guoqiang Ma,Shan Sun,Qilian Ma,Qiang Peng,Siqian Chen,Kin Yip Tam,Hongfeng Wang,Zheng Ying
出处
期刊:Autophagy
[Informa]
日期:2025-10-08
卷期号:: 1-13
标识
DOI:10.1080/15548627.2025.2572528
摘要
Atg8-family proteins are autophagosome-associated proteins and play important roles in macroautophagy/autophagy, a conserved process for degrading defective or excessive cellular components. Post-translational modifications of mammalian Atg8-family proteins, including phosphorylation, regulate multiple steps in the autophagic process. In this context, several Atg8-family protein-associated kinases have been found to regulate autophagy, yet the phosphatases in the dephosphorylation of Atg8-family proteins remain unknown. Here, we report that the heterotrimeric PPP2/PP2A (protein phosphatase 2) is a novel regulator in modulating LC3B dephosphorylation. Mechanistically, we find that PPP2-mediated LC3B dephosphorylation reduces the interaction between LC3B and the mitophagy receptor OPTN, thereby impeding the mitochondrial recruitment of phagophores during PINK1-PRKN/Parkin-mediated mitophagy. Interestingly, we find that overexpression of the β2 isoform of PPP2R2B (protein phosphatase 2 regulatory subunit Bbeta; PPP2R2Bβ2), which mimics the spinocerebellar ataxia type 12 (SCA12) pathological condition, harms neuronal survival by enhancing PPP2-mediated LC3B dephosphorylation and reducing mitochondrial recruitment of phagophores upon mitochondrial damage. Importantly, pharmacological induction of mitophagy by the small molecule compound deferiprone (DFP) relieves PPP2R2Bβ2-mediated neuronal toxicity. Overall, our results not only uncover a mechanism by which protein dephosphorylation negatively regulates mitophagy but also provide insights into the pathogenesis of PPP2R2Bβ2-mediated SCA12.Abbreviations: AO: antimycin A and oligomycin A; DFP: deferiprone; EGFP: enhanced green fluorescent protein; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; MAP1LC3B/LC3B: microtubule associated protein 1 light chain 3 beta; OPTN: optineurin; PINK1: PTEN induced kinase 1; PLA: proximity ligation assay; PPP2: protein phosphatase 2; PPP2CA: protein phosphatase 2 catalytic subunit alpha; PPP2CB: protein phosphatase 2 catalytic subunit beta; PPP2R2Bβ2: protein phosphatase 2 regulatory subunit B beta 2; PRKN/Parkin: parkin RBR E3 ubiquitin protein ligase; SCA12: spinocerebellar ataxia type 12; WT: wild type.
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