细胞外小泡
共域化
淀粉样前体蛋白
淀粉样前体蛋白分泌酶
ADAM10型
α分泌酶
细胞外
化学
阿尔茨海默病
早老素
细胞生物学
神经科学
生物化学
生物
医学
疾病
病理
酶
去整合素
金属蛋白酶
作者
Hyo Yong Kim,Junseok Lee,Audrey Qian,You‐Ren Ji,Ryan Zhang,Qixin Hu,Christopher Kazu Williams,Han‐Yu Chuang,Matthew Smalley,Yaya Xu,Liang Gao,Mary Catherine Mayo,Ting Zhang,Edwin M. Posadas,Zaldy S. Tan,Harry V. Vinters,Keith Vossel,Shino Magaki,Yazhen Zhu,Hsian‐Rong Tseng
标识
DOI:10.1002/advs.202415289
摘要
Abstract Alzheimer's disease (AD), the most prevalent type of dementia, is characterized by a biological process that begins with the development of AD neuropathologic change (ADNPC) while individuals remain asymptomatic. A key molecular hallmark of ADNPC is the accumulation of amyloid‐β plaques. β‐secretase plays a critical role in the upstream pathological cleavage of amyloid precursor protein (APP), producing amyloid‐β peptides that are prone to misfolding, ultimately contributing to plaque formation. Neuronal extracellular vesicles (NEVs) in the blood transport β‐secretase and preserve its activity, allowing for noninvasive profiling of β‐secretase activity for detecting early onset of ADNPC. In this study, a novel approach is approached for noninvasive assessment of β‐secretase activity in AD patients using an NEV β‐secretase activity assay. This assay identifies NEVs exhibiting colocalization of NEV markers with AD‐associated β‐secretase, generating a β‐secretase activity profile for each patient. The NEV β‐secretase activity assay represents a significant advancement in leveraging the diagnostic potential of NEVs, offering a noninvasive, quantitative method for reliably assessing β‐secretase activity to detect the early onset of ADNPC.
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