Evidence map›Paper›PMID 41126299›Full record

ArticleTranslational neurodegeneration2025

SIK2-mediated phosphorylation of GABARAPL2 facilitates autophagosome-lysosome fusion and rescues neurodegeneration in an Alzheimer's disease model.

Xiaoman Dai, Ziling Ye, Chen Wang, Yufei Huang, Yun Chen, Tianqing Han, Weijie Gao, Xin Wu, Jing Zhang, Xiaochun Chen

Abstract read
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Article in Translational neurodegeneration, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Xiaoman Dai *Department of Neurology and Geriatrics, Fujian Institute of Geriatrics, Fujian Medical University Union Hospital, Fuzhou, 350001, China.ORCID http://orcid.org/0000-0003-3409-5936
Ziling Ye *Fujian Key Laboratory of Molecular Neurology and Institute of Neuroscience, School of Basic Medical Sciences, Fujian Medical University, Fuzhou, 350001, China.
Chen Wang *Department of Neurology and Geriatrics, Fujian Institute of Geriatrics, Fujian Medical University Union Hospital, Fuzhou, 350001, China.
Yufei HuangFujian Key Laboratory of Molecular Neurology and Institute of Neuroscience, School of Basic Medical Sciences, Fujian Medical University, Fuzhou, 350001, China.
Yun ChenFujian Key Laboratory of Molecular Neurology and Institute of Neuroscience, School of Basic Medical Sciences, Fujian Medical University, Fuzhou, 350001, China.
Tianqing HanFujian Key Laboratory of Molecular Neurology and Institute of Neuroscience, School of Basic Medical Sciences, Fujian Medical University, Fuzhou, 350001, China.
Weijie GaoFujian Key Laboratory of Molecular Neurology and Institute of Neuroscience, School of Basic Medical Sciences, Fujian Medical University, Fuzhou, 350001, China.
Xin WuFujian Key Laboratory of Molecular Neurology and Institute of Neuroscience, School of Basic Medical Sciences, Fujian Medical University, Fuzhou, 350001, China.
Jing ZhangDepartment of Neurology and Geriatrics, Fujian Institute of Geriatrics, Fujian Medical University Union Hospital, Fuzhou, 350001, China. drzj@163.com.
Xiaochun ChenDepartment of Neurology and Geriatrics, Fujian Institute of Geriatrics, Fujian Medical University Union Hospital, Fuzhou, 350001, China. chenxc998@fjmu.edu.cn.

Funding

Excellent Young Scholars Cultivation Project of Fujian Medical University Union Hospital 2022XH032Joint Funds for the Innovation of Science and Technology,Fujian province 2024Y9236National Natural Science Foundation 82101481National Natural Science Foundation U21A20362National Natural Science Foundation U22A20298National Science and Technology Innovation 2030 Major Projects 2022ZD0211600
6 · The paper itself

Abstract

backgroundDefective autophagic flux is implicated in Alzheimer's disease (AD), but the molecular mechanisms underlying this process are not fully understood. Salt-inducible kinase 2 (SIK2) is associated with autophagic function. However, its specific involvement in autophagic flux regulation and AD pathogenesis remains unclear.

methodsWe evaluated hippocampal SIK2 expression and its age-related changes in postmortem AD patients and 5 × FAD mice by bioinformatics analysis, immunofluorescence, qPCR, and Western blotting. To investigate the functional role of SIK2, we employed adeno-associated virus-mediated SIK2 knockdown and overexpression in combination with behavioral tests (Morris water maze), electrophysiological recordings (long-term potentiation, LTP), and ultrastructural analysis (electron microscopy) to evaluate cognitive function and synaptic plasticity. Autophagic flux was measured using LC3B/p62 turnover assays, mRFP-GFP-LC3 tandem fluorescence assay, and transmission electron microscopy. Mechanistic insights were gained through co-immunoprecipitation assay, GST-pull down assay, phosphoproteomics, and site-directed mutagenesis. Additionally, phosphorylation-mimetic (S72E) and non-phosphorylatable (S72A) mutants of GABA type A receptor-associated protein-like 2 (GABARAPL2) were intrahippocampally delivered to 5 × FAD mice to explore their effects.

resultsOur study identified SIK2 as a critical regulator that is progressively downregulated in hippocampal neurons of AD patients and 5 × FAD mice, correlating with spatial memory deficits. Reducing SIK2 levels exacerbates cognitive impairment and amyloid-β (Aβ) plaque burden in mice, whereas restoring SIK2 levels mitigates these deficits, restores LTP amplitude, reverses synaptic ultrastructural pathology, and reduces Aβ deposition. Mechanistically, SIK2 enhances autophagic flux by phosphorylating GABARAPL2 at Ser72, a modification essential for autophagosome-lysosome fusion. Remarkably, hippocampal delivery of the phosphorylation-mimetic GABARAPL2-S72E mutant replicated the beneficial effects of SIK2, alleviating Aβ pathology and synaptic dysfunction in 5 × FAD mice. In contrast, the non-phosphorylatable S72A mutant failed to show any protective effects.

conclusionsThese findings establish the SIK2-GABARAPL2 axis as a novel signaling cascade governing autophagic flux through lysosomal fusion competence. Dysfunction in this axis contributes to Aβ deposition in AD, offering new insights into the pathogenic mechanisms underlying autophagosome-lysosome fusion in AD and highlighting its potential as a therapeutic target.

Indexed as

Adaptor Proteins, Signal TransducingAlzheimer DiseaseAutophagosomesLysosomesMicrotubule-Associated ProteinsProtein Serine-Threonine KinasesAgedAnimalsAutophagyDisease Models, AnimalFemaleHippocampusHumansMaleMiceMice, Inbred C57BLAdaptor Proteins, Signal TransducingMicrotubule-Associated ProteinsProtein Serine-Threonine KinasesAlzheimer's diseaseAutophagic fluxAutophagosome–lysosome fusionGABARAPL2NeurodegenerationSalt-inducible kinase 2

Identifiers

PMID41126299
PMCPMC12548284

What Socratic holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.