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Nanoparticle-mediated Zn delivery impacts neural protein phosphatase activity
André Nadais1, Carolina Castro1, Inês Martins2
1Department of Medical Sciences, University of Aveiro, 3810-193, Aveiro, Portugal; Neurosciences and Signalling Group, Institute of Biomedicine (iBiMED), 3810-193, Aveiro, Portugal.
Biomaterials Advances
|January 7, 2026
Summary
Zinc oxide nanoparticles (ZnO NP) reduce protein aggregation in brain cells but may worsen Alzheimer
Area of Science:
- Neuroscience
- Materials Science
- Biochemistry
Background:
- Nanoparticles (NPs) are increasingly researched for medical diagnosis and treatment.
- Zinc oxide nanoparticles (ZnO NP) show varied effects on brain health, with some studies suggesting neuroprotection and others indicating neurotoxicity.
- Previous research indicated beneficial effects of zinc (Zn) cations in Alzheimer's disease (AD) models.
Purpose of the Study:
- To investigate the impact of ZnO NP on protein aggregation.
- To explore the influence of ZnO NP on protein phosphorylation in Alzheimer's disease (AD) pathology.
- To evaluate ZnO NP as a potential delivery system for zinc (Zn) in neurological applications.
Main Methods:
- Cultured neuronal cells were used to assess the effects of ZnO NP.
- Protein aggregation levels were measured in response to ZnO NP treatment.
- Protein phosphorylation events, including those related to tau and amyloid precursor protein (APP), were analyzed.
Main Results:
- ZnO NP treatment led to a reduction in protein aggregation within neuronal cells.
- However, ZnO NP decreased the activity of protein phosphatases PP1 and PP2A.
- This phosphatase inhibition potentially increased the phosphorylation of tau and APP, hallmarks of AD.
Conclusions:
- While ZnO NP may reduce protein aggregation, they can induce detrimental molecular changes relevant to AD.
- The use of NPs as a zinc (Zn) delivery system presents a dual-edged effect on cellular processes.
- A comprehensive approach is necessary to understand the multifaceted impacts of NPs in biological systems.

