ATP1A3 as a target for isolating neuron-specific extracellular vesicles from human brain and biofluids.

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作者： Yang,You ^[1] ; Zhengrong,Zhang ^[2] ; Nadia,Sultana ^[1] ; Maria,Ericsson ^[3] ; Yuka A,Martens ^[4] ; Min,Sun ^[5] ; Takahisa,Kanekiyo ^[1] ; Seiko,Ikezu ^[6] ; Scott A,Shaffer ^[1] ; Tsuneya,Ikezu ^[1]

作者单位： Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA. ^[1] Department of Pharmacology and Experimental Therapeutics, Boston University School of Medicine, Boston, MA, USA. ^[2] Department of Biochemistry and Molecular Biotechnology, University of Massachusetts Chan Medical School, Worcester, MA, USA. ^[3] Mass Spectrometry Facility, University of Massachusetts Chan Medical School, Shrewsbury, MA USA. ^[4] Department of Cell Biology, Harvard Medical School, Boston, MA, USA. ^[5] Nanoview Biosciences, Boston, MA, USA School, Boston, MA, USA. ^[6]

主题词人类(Humans);蛋白质组学(Proteomics);脑(Brain);阿尔茨海默病(Alzheimer Disease);神经细胞黏附分子类(Neural Cell Adhesion Molecules);神经元(Neurons);钠钾交换ATP酶(Sodium-Potassium-Exchanging ATPase)

DOI 10.1126/sciadv.adi3647

PMID 37713494

发布时间 2024-02-23

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Science advances

2023年9卷37期

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ATP1A3 as a target for isolating neuron-specific extracellular vesicles from human brain and biofluids.

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ATP1A3 as a target for isolating neuron-specific extracellular vesicles from human brain and biofluids.

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