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Designing nanozymes for in vivo applications

The inhibition of ferritinophagy by the knockdown of NCOA4 or the blockage of autophagy prevents the accumulation of ferroptosis-associated cellular labile iron and ROS, as well as eventual ferroptotic cell death

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Controlled postmortem studies that carefully match PD cases to controls on key variables including age, post-mortem interval, and clinical cause of death are essential to isolate disease-specific vascular signatures from terminal systemic effects ( These cellular and molecular signatures align with in vivo observations of progressive BBB dysfunction, but uniquely highlight how newly formed or remodeled vessels may lack the structural integrity necessary to support neuronal health, but also highlight how confounding factors related to mode of death can impact BBB structure and should be accounted for in study designs

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