Emergence of exosomal miRNAs as a diagnostic biomarker for Alzheimer's disease

被引:101
作者
Van Giau, Vo [1 ]
An, Seong Soo A. [1 ]
机构
[1] Gachon Univ, Gachon Med Res Inst, Dept Bionano Technol, Songnam, South Korea
关键词
miRNAs; Biomarkers; Alzheimer's disease; Diagnostic; Nanovesicles; CELL-DERIVED EXOSOMES; HUMAN URINARY EXOSOMES; COMPLEX CLASS-II; MICRORNA EXPRESSION; NEURODEGENERATIVE DISEASES; TRANSFERRIN RECEPTOR; CEREBROSPINAL-FLUID; PREFRONTAL CORTEX; MESSENGER-RNAS; CSF BIOMARKERS;
D O I
10.1016/j.jns.2015.12.005
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Alzheimer's disease (AD) is the most common progressive degenerative disorder, and is characterized by memory loss and cognitive decline. It is a complex disorder with both environmental and genetic components. Current diagnosis of AD is based primarily on the analysis of the patient's cognitive function using imaging techniques and the biochemical analyses of bodily fluids. Efforts have been made to develop not only an effective therapeutic, but also a diagnostic capable of identifying AD before the onset of irreversible neurological damage. The molecular content of exosomes is a fingerprint of the releasing cell type and its status. A significant body of literature has demonstrated that molecular constituents of exosomes, especially exosomal proteins and microRNAs (miRNAs), hold great promise as novel biomarkers for clinical diagnosis. In addition, expression profiling of miRNAs found in nanovesicles has revealed diagnostic potential in neurodegenerative diseases. Currently, exosomal miRNAs within biological fluids are known as good disease-related markers, and have emerged as a powerful tool for solving many difficulties in both the diagnosis and treatment of AD patients. In this review, we reviewed recent advances in the research of exosomal biomarkers as well as exosomal miRNAs, summarized of actively used approaches to identifying potential miRNA biomarkers through mouse models and their potential application in clinical diagnostics in AD. We also supply a comprehensive overview of the formation, function, and isolation of exosomes. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:141 / 152
页数:12
相关论文
共 152 条
[1]   Exosomes with major histocompatibility complex class II and co-stimulatory molecules are present in human BAL fluid [J].
Admyre, C ;
Grunewald, J ;
Thyberg, J ;
Gripenbäck, S ;
Tornling, G ;
Eklund, A ;
Scheynius, A ;
Gabrielsson, S .
EUROPEAN RESPIRATORY JOURNAL, 2003, 22 (04) :578-583
[2]   Exosomes with immune modulatory features are present in human breast milk [J].
Admyre, Charlotte ;
Johansson, Sara M. ;
Qazi, Khaleda Rahman ;
Filen, Jan-Jonas ;
Lahesmaa, Riitta ;
Norman, Mikael ;
Neve, Etienne P. A. ;
Scheynius, Annika ;
Gabrielsson, Susanne .
JOURNAL OF IMMUNOLOGY, 2007, 179 (03) :1969-1978
[3]   Mouse neuroblastoma cells release prion infectivity associated with exosomal vesicles [J].
Alais, Sandrine ;
Simoes, Sabrina ;
Baas, Dominique ;
Lehmann, Sylvain ;
Raposo, Graca ;
Darlix, Jean Luc ;
Leblanc, Pascal .
BIOLOGY OF THE CELL, 2008, 100 (10) :603-615
[4]   LRRK2 regulates autophagic activity and localizes to specific membrane microdomains in a novel human genomic reporter cellular model [J].
Alegre-Abarrategui, Javier ;
Christian, Helen ;
Lufino, Michele M. P. ;
Mutihac, Ruxandra ;
Venda, Lara Lourenco ;
Ansorge, Olaf ;
Wade-Martins, Richard .
HUMAN MOLECULAR GENETICS, 2009, 18 (21) :4022-4034
[5]  
Alexandrov Peter N, 2012, Int J Biochem Mol Biol, V3, P365
[6]   Comparison of protein, microRNA, and mRNA yields using different methods of urinary exosome isolation for the discovery of kidney disease biomarkers [J].
Alvarez, M. Lucrecia ;
Khosroheidari, Mahdieh ;
Ravi, Rupesh Kanchi ;
DiStefano, Johanna K. .
KIDNEY INTERNATIONAL, 2012, 82 (09) :1024-1032
[7]   Lysosomal dysfunction increases exosome-mediated alpha-synuclein release and transmission [J].
Alvarez-Erviti, Lydia ;
Seow, Yiqi ;
Schapira, Anthony H. ;
Gardiner, Chris ;
Sargent, Ian L. ;
Wood, Matthew J. A. ;
Cooper, J. Mark .
NEUROBIOLOGY OF DISEASE, 2011, 42 (03) :360-367
[8]   Are there multiple pathways in the pathogenesis of Huntington's disease? [J].
Aronin, N ;
Kim, M ;
Laforet, G ;
DiFiglia, M .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1999, 354 (1386) :995-1003
[9]   Exosomes: vehicles for the transfer of toxic proteins associated with neurodegenerative diseases? [J].
Bellingham, Shayne A. ;
Guo, Belinda B. ;
Coleman, Bradley M. ;
Hill, Andrew F. .
FRONTIERS IN PHYSIOLOGY, 2012, 3
[10]   Increased nnicroRNA-34c abundance in Alzheimer's disease circulating blood plasma [J].
Bhatnagar, Shephali ;
Chertkow, Howard ;
Schipper, Hyman M. ;
Yuan, Zongfei ;
Shetty, Vikranth ;
Jenkins, Samantha ;
Jones, Timothy ;
Wang, Eugenia .
FRONTIERS IN MOLECULAR NEUROSCIENCE, 2014, 7