Small RNA Profiles of Brain Tissue-Derived Extracellular Vesicles in Alzheimer's Disease

被引:2
|
作者
Huang, Yiyao [1 ]
Driedonks, Tom A. P. [1 ]
Cheng, Lesley [2 ]
Turchinovich, Andrey [3 ,4 ]
Pletnikova, Olga [5 ,6 ]
Redding-Ochoa, Javier [5 ]
Troncoso, Juan C. [5 ,7 ]
Hill, Andrew F. [2 ,8 ]
Mahairaki, Vasiliki [9 ,10 ]
Zheng, Lei [11 ]
Witwer, Kenneth W. [1 ,9 ,10 ]
机构
[1] Johns Hopkins Univ, Dept Mol & Comparat Pathobiol, Sch Med, Baltimore, MD 21218 USA
[2] La Trobe Univ, La Trobe Inst Mol Sci, Dept Biochem & Chem, Bundoora, Vic, Australia
[3] German Canc Res Ctr, Div Canc Genome Res, Heidelberg, Germany
[4] Heidelberg Biolabs GmbH, Heidelberg, Germany
[5] Johns Hopkins Univ, Dept Pathol, Sch Med, Baltimore, MD USA
[6] SUNY Buffalo, Dept Pathol & Anat Sci, Jacobs Sch Med & Biomed Sci, Buffalo, NY USA
[7] Johns Hopkins Univ, Dept Neurol, Sch Med, Baltimore, MD USA
[8] Victoria Univ, Inst Hlth & Sport, Melbourne, Australia
[9] Johns Hopkins Univ, Dept Genet Med, Sch Med, Baltimore, MD USA
[10] Johns Hopkins Univ, Richman Family Precis Med Ctr Excellence Alzheime, Sch Med, Baltimore, MD USA
[11] Southern Med Univ, Nanfang Hosp, Dept Lab Med, Guangzhou, Guangdong, Peoples R China
基金
英国医学研究理事会; 美国国家卫生研究院;
关键词
Alzheimer's disease; brain; ectosomes; exosomes; extracellular vesicles; microvesicles; miRNAs; non-coding RNAs; RNA sequencing; tRNAs; MESSENGER-RNA; CELL; TAU; BIOMARKERS; INSIGHTS; PATHOGENESIS; AGGREGATION; MECHANISMS;
D O I
10.3233/JAD-230872
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Extracellular vesicles (EVs) and non-codingRNAs (ncRNAs) are emerging contributors to Alzheimer's disease (AD) pathophysiology. Differential abundance of ncRNAs carried by EVs may provide valuable insights into underlying disease mechanisms. Brain tissue-derived EVs (bdEVs) are particularly relevant, as they may offer valuable insights about the tissue of origin. However, there is limited research on diverse ncRNA species in bdEVs in AD. Objective: This study explored whether the non-coding RNA composition of EVs isolated from post-mortem brain tissue is related to AD pathogenesis. Methods: bdEVs from age-matched late-stage AD patients (n = 23) and controls (n = 10) that had been separated and characterized in our previous study were used for RNA extraction, small RNA sequencing, and qPCR verification. Results: Significant differences of non-coding RNAs between AD and controls were found, especially for miRNAs and tRNAs. AD pathology-related miRNA and tRNA differences of bdEVs partially matched expression differences in source brain tissues. AD pathology had a more prominent association than biological sex with bdEV miRNA and tRNA components in late-stage AD brains. Conclusions: Our study provides further evidence that EV non-coding RNAs from human brain tissue, including but not limited to miRNAs, may be altered and contribute to AD pathogenesis.
引用
收藏
页码:S235 / S248
页数:14
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