The platelet transcriptome and proteome in Alzheimer's disease and aging: an exploratory cross-sectional study

被引:3
|
作者
de Sousa, Diana M. Bessa [1 ,2 ]
Poupardin, Rodolphe [2 ,3 ]
Villeda, Saul A. [4 ]
Schroer, Adam B. [4 ]
Froehlich, Thomas [5 ]
Frey, Vanessa [2 ,6 ]
Staffen, Wolfgang [6 ]
Mrowetz, Heike [1 ,2 ]
Altendorfer, Barbara [1 ,2 ]
Unger, Michael S. [1 ,2 ]
Iglseder, Bernhard [6 ]
Paulweber, Bernhard [7 ]
Trinka, Eugen [6 ,8 ,9 ,10 ]
Cadamuro, Janne [11 ]
Drerup, Martin
Schallmoser, Katharina [2 ]
Aigner, Ludwig [1 ,2 ]
Kniewallner, Kathrin M. [1 ,2 ]
机构
[1] Paracelsus Med Univ, Inst Mol Regenerat Med, Salzburg, Austria
[2] Paracelsus Med Univ, Spinal Cord Injury & Tissue Regenerat Ctr Salzburg, Salzburg, Austria
[3] Paracelsus Med Univ, Expt & Clin Cell Therapy Inst, Salzburg, Austria
[4] Univ Calif San Francisco, Dept Anat, San Francisco, CA USA
[5] Ludwig Maximilian Univ Munich, Gene Ctr, Lab Funct Genome Anal LAFUGA, Munich, Germany
[6] Paracelsus Med Univ, Dept Neurol, Christian Doppler Clin, Salzburg, Austria
[7] Paracelsus Med Univ, St Johanns Univ Hosp, Dept Internal Med, Salzburg, Austria
[8] UMIT Univ Hlth Sci Med Informat & Technol, Dept Publ Hlth, Hlth Serv Res & Hlth Technol Assessment, Hall In Tirol, Austria
[9] Paracelsus Med Univ, Christian Doppler Univ Hosp, Neurosci Inst, Salzburg, Austria
[10] Ctr Cognit Neurosci Salzburg, Salzburg, Austria
[11] Univ Hosp SALK, Dept Lab Med, Salzburg, Austria
关键词
Alzheimer's disease; aging; platelets; proteomics; transcriptomics; MILD COGNITIVE IMPAIRMENT; MOUSE MODELS; ACTIVATION; AUTOPHAGY; IMMUNOPROTEASOME; BLOOD; EXPRESSION; RECEPTORS; INCREASE; DEMENTIA;
D O I
10.3389/fmolb.2023.1196083
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: Alzheimer's disease (AD) and aging are associated with platelet hyperactivity. However, the mechanisms underlying abnormal platelet function in AD and aging are yet poorly understood.Methods: To explore the molecular profile of AD and aged platelets, we investigated platelet activation (i.e., CD62P expression), proteome and transcriptome in AD patients, non-demented elderly, and young individuals as controls.Results: AD, aged and young individuals showed similar levels of platelet activation based on CD62P expression. However, AD and aged individuals had a proteomic signature suggestive of increased platelet activation compared with young controls. Transcriptomic profiling suggested the dysregulation of proteolytic machinery involved in regulating platelet function, particularly the ubiquitin-proteasome system in AD and autophagy in aging. The functional implication of these transcriptomic alterations remains unclear and requires further investigation.Discussion: Our data strengthen the evidence of enhanced platelet activation in aging and provide a first glimpse of the platelet transcriptomic changes occurring in AD.
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页数:16
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