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Sultana, Nadia

0000-0001-8627-101X

Mayo Clinic

University of Massachusetts Chan Medical School

Citations 1

ATP1A3 as a target for isolating neuron-specific extracellular vesicles from human brain and biofluids
You, Yang , Zhang, Zhengrong , Sultana, Nadia , Ericsson, Maria , Martens, Yuka A. , Sun, Min , Kanekiyo, Takahisa , Ikezu, Seiko , Shaffer, Scott A. , Ikezu, Tsuneya , Ikezu, Tsuneya , Yang, You , Shaffer, Scott , Sultana, Nadia

Science Advances | September 15, 2023 | Volume: 9 | Issue: 37 | Pages: No page available

10.1126/sciadv.adi3647 Get It

Neuron-derived extracellular vesicles (NDEVs) are potential biomarkers of neurological diseases although their reliable molecular target is not well established. Here, we demonstrate that ATPase Na + /K + transporting subunit alpha 3 (ATP1A3) is abundantly expressed in extracellular vesicles (EVs) isolated from induced human neuron, brain, cerebrospinal fluid, and plasma in comparison with the presumed NDEV markers NCAM1 and L1CAM by using super-resolution microscopy and biochemical assessments. Proteomic analysis of immunoprecipitated ATP1A3 + brain-derived EVs shows higher enrichment of synaptic markers and cargo proteins relevant to Alzheimer’s disease (AD) compared to NCAM1 + or LICAM + EVs. Single particle analysis shows the elevated amyloid-β positivity in ATP1A3 + EVs from AD plasma, providing better diagnostic prediction of AD over other plasma biomarkers. Thus, ATP1A3 is a reliable target to isolate NDEV from biofluids for diagnostic research.