Extracellular vesicles in neurodegenerative disease - pathogenesis to biomarkers

被引:304
|
作者
Thompson, Alexander G. [1 ]
Gray, Elizabeth [1 ]
Heman-Ackah, Sabrina M. [2 ]
Mager, Imre [2 ]
Talbot, Kevin [1 ]
El Andaloussi, Samir [2 ,3 ]
Wood, Matthew J. [2 ]
Turner, Martin R. [1 ]
机构
[1] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Clin Neurosci, Level 6,West Wing, Oxford OX3 9DU, England
[2] Univ Oxford, Dept Physiol Anat & Genet, Le Gros Clark Bldg,S Parks Rd, Oxford OX1 3QX, England
[3] Karolinska Inst, Dept Lab Med, SE-17177 Stockholm, Sweden
基金
英国医学研究理事会;
关键词
FRONTOTEMPORAL LOBAR DEGENERATION; AMYOTROPHIC-LATERAL-SCLEROSIS; AMYLOID PRECURSOR PROTEIN; PAIRED HELICAL FILAMENTS; ALPHA-SYNUCLEIN; CEREBROSPINAL-FLUID; ALZHEIMERS-DISEASE; PARKINSONS-DISEASE; SUPEROXIDE-DISMUTASE; EXOSOME SECRETION;
D O I
10.1038/nrneurol.2016.68
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
To develop effective disease-modifying therapies for neurodegenerative diseases, reliable markers of diagnosis, disease activity and progression are a research priority. The fact that neurodegenerative pathology is primarily associated with distinct subsets of cells in discrete areas of the CNS makes the identification of relevant biomarker molecules a challenge. The trafficking of macromolecules from the CNS to the cerebrospinal fluid and blood, mediated by extracellular vesicles (EVs), presents a promising source of CNS-specific biomarkers. EVs are released by almost all cell types and carry a cargo of protein and nucleic acid that varies according to the cell of origin. EV output changes with cell status and reflects intracellular events, so surface marker expression can be used to identify the cell type from which EVs originate. EVs could, therefore, provide an enriched pool of information about core neuropathogenic, cell-specific processes. This Review examines the current knowledge of the biology and function of EVs, discusses the evidence for their involvement in the pathogenesis of neurodegenerative diseases, and considers their potential as biomarkers of disease.
引用
收藏
页码:346 / 357
页数:12
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