miRNA in Circulating Microvesicles as Biomarkers for Age-Related Cognitive Decline

被引:67
作者
Rani, Asha [1 ]
O'Shea, Andrew [2 ,3 ]
Ianov, Lara [1 ,4 ]
Cohen, Ronald A. [2 ,3 ]
Woods, Adam J. [1 ,2 ,3 ]
Foster, Thomas C. [1 ,4 ]
机构
[1] Univ Florida, Dept Neurosci, McKnight Brain Inst, Gainesville, FL 32610 USA
[2] Univ Florida, Dept Clin & Hlth Psychol, Gainesville, FL USA
[3] Univ Florida, McKnight Brain Inst, Ctr Cognit Aging & Memory, Gainesville, FL USA
[4] Univ Florida, Genet Inst, Genet & Genom Program, Gainesville, FL 32610 USA
关键词
exosome; microRNA; biomarker; normal aging; Alzheimer's disease; CELL-FREE MICRORNA; ALZHEIMERS-DISEASE; CLINICAL-RELEVANCE; MEMORY; BRAIN; MECHANISMS; EXPRESSION; SERUM; VALIDATION; SIGNATURE;
D O I
10.3389/fnagi.2017.00323
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Community dwelling older individuals from the North Florida region were examined for health status and a comprehensive neuropsychological battery, including the Montreal Cognitive Assessment (MoCA), was performed on each participant. A subpopulation (58 females and 39 males) met the criteria for age (60-89) and no evidence of mild cognitive impairment, with a MoCA score >= 23. Despite the stringent criteria for participation, MoCA scores were negatively correlated within the limited age range. Extracellular microvesicles were isolated from the plasma and samples were found to be positive for the exosome marker CD63, with an enrichment of particles within the size range for exosomes. miRNA was extracted and examined using next generation sequencing with a stringent criterion (average of >= 10 counts per million reads) resulting in 117 miRNA for subsequent analysis. Characterization of expression confirmed pervious work concerning the relative abundance and overall pattern of expression of miRNA in plasma. Correlation analysis indicated that most of the miRNAs (74 miRNAs) were positively correlated with age (p < 0.01). Multiple regression was employed to identify the relationship of miRNA expression and MoCA score, accounting for age. MoCA scores were negatively correlated with 13 miRNAs. The pattern of expression for cognition-related miRNA did not match that previously described for Alzheimer's disease. Enrichment analysis was employed to identify miRNA-gene interactions to reveal possible links to brain function.
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页数:10
相关论文
共 65 条
[1]   Characterizing cognitive aging in humans with links to animal models [J].
Alexander, Gene E. ;
Ryan, Lee ;
Bowers, Dawn ;
Foster, Thomas C. ;
Bizon, Jennifer L. ;
Geldmacher, David S. ;
Glisky, Elizabeth L. .
FRONTIERS IN AGING NEUROSCIENCE, 2012, 4
[2]   Delivery of siRNA to the mouse brain by systemic injection of targeted exosomes [J].
Alvarez-Erviti, Lydia ;
Seow, Yiqi ;
Yin, HaiFang ;
Betts, Corinne ;
Lakhal, Samira ;
Wood, Matthew J. A. .
NATURE BIOTECHNOLOGY, 2011, 29 (04) :341-U179
[3]  
Barrientos RM, 2010, AGING DIS, V1, P212
[4]   Assessing sample and miRNA profile quality in serum and plasma or other biofluids [J].
Blondal, Thorarinn ;
Nielsen, Soren Jensby ;
Baker, Adam ;
Andreasen, Ditte ;
Mouritzen, Peter ;
Teilum, Maria Wrang ;
Dahlsveen, Ina K. .
METHODS, 2013, 59 (01) :S1-S6
[5]   Brain plasticity and motor practice in cognitive aging [J].
Cai, Liuyang ;
Chan, John S. Y. ;
Yan, Jin H. ;
Peng, Kaiping .
FRONTIERS IN AGING NEUROSCIENCE, 2014, 6
[6]   Prognostic serum miRNA biomarkers associated with Alzheimer's disease shows concordance with neuropsychological and neuroimaging assessment [J].
Cheng, L. ;
Doecke, J. D. ;
Sharples, R. A. ;
Villemagne, V. L. ;
Fowler, C. J. ;
Rembach, A. ;
Martins, R. N. ;
Rowe, C. C. ;
Macaulay, S. L. ;
Masters, C. L. ;
Hill, A. F. .
MOLECULAR PSYCHIATRY, 2015, 20 (10) :1188-1196
[7]   Exosomes provide a protective and enriched source of miRNA for biomarker profiling compared to intracellular and cell-free blood [J].
Cheng, Lesley ;
Sharples, Robyn A. ;
Scicluna, Benjamin J. ;
Hill, Andrew F. .
JOURNAL OF EXTRACELLULAR VESICLES, 2014, 3 (01)
[8]   Plasma miR-34a-5p and miR-545-3p as Early Biomarkers of Alzheimer's Disease: Potential and Limitations [J].
Cosin-Tomas, Marta ;
Antonell, Anna ;
Llado, Albert ;
Alcolea, Daniel ;
Fortea, Juan ;
Ezquerra, Mario ;
Lleo, Albert ;
Jose Marti, Maria ;
Pallas, Merce ;
Sanchez-Valle, Raquel ;
Luis Molinuevo, Jose ;
Sanfeliu, Coral ;
Kaliman, Perla .
MOLECULAR NEUROBIOLOGY, 2017, 54 (07) :5550-5562
[9]   Session III: Mechanisms of Age-Related Cognitive Change and Targets for Intervention: Inflammatory, Oxidative, and Metabolic Processes [J].
Craft, Suzanne ;
Foster, Thomas C. ;
Landfield, Philip W. ;
Maier, Steven F. ;
Resnick, Susan M. ;
Yaffe, Kristine .
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 2012, 67 (07) :754-759
[10]   Influence of age on the correlations of hematological and biochemical variables with the stability of erythrocyte membrane in relation to sodium dodecyl sulfate [J].
de Freitas, Mariana V. ;
Marquez-Bernardes, Liandra F. ;
de Arvelos, Leticia R. ;
Paraiso, Lara F. ;
Gonalves e Oliveira, Ana Flavia M. ;
Mascarenhas Netto, Rita de C. ;
Neto, Morun Bernardino ;
Garrote-Filho, Mario S. ;
de Souza, Paulo Cesar A. ;
Penha-Silva, Nilson .
HEMATOLOGY, 2014, 19 (07) :424-430