外体
微泡
分泌物
转录组
细胞生物学
基因表达谱
刺激
疾病
类有机物
生物
计算生物学
化学
仿形(计算机编程)
医学
生物信息学
分泌蛋白
载脂蛋白E
凝集素
小RNA
基因
内型
生物标志物
作者
Jinhee Yoo,Youngjun Kim,Won Jong Yu,Seongmin Kim,Yongjae Jo,Hanjun Cho,Hyunsu Park,Luke P. Lee,Jong‐Chan Park,Inki Kim,Byullee Park
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2026-09-23
卷期号:12 (39): eaed3930-eaed3930
标识
DOI:10.1126/sciadv.aed3930
摘要
Exosomes offer a promising vehicle for noninvasive diagnosis of neurodegenerative diseases by carrying multiple biomarkers across the blood-brain barrier. However, traditional exosome analysis often misses subtle genotype-specific variations because of weak signals from a few exosomes, reliance on markers, and limited understanding of disease signatures. Here, we present a sound way to understand Alzheimer's disease through label-free surface-enhanced Raman scattering (SERS) profiling of cortical organoid-derived exosomes. Initially, we enhanced exosomal SERS signal levels by optimizing ultrasound parameters to increase exosome secretion from cortical organoids. Using this strategy, we distinguished apolipoprotein E genotype-dependent differences in intact exosomal fingerprints. Transcriptome analysis confirmed that ultrasound stimulation increased exosome secretion and up-regulated exosome-related genes functionally linked to Alzheimer's pathology. Ultrasound-based stimulation and label-free exosome profiling reveal genotype-specific pathologies, providing a precision-diagnostic framework for Alzheimer's disease.
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