Profiling blood serum extracellular vesicles in plaque psoriasis and psoriatic arthritis patients reveals potential disease biomarkers
Autor: | Freddy Lättekivi, Irina Guljavina, Getnet Midekessa, Janeli Viil, Paul R. Heath, Rikke Bæk, Malene Møller Jørgensen, Aneta Andronowska, Kulli Kingo, Alireza Fazeli |
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Jazyk: | angličtina |
Rok vydání: | 2022 |
Předmět: |
Serum
Male Serum/metabolism genetic structures Organic Chemistry Arthritis Psoriatic psoriatic arthritis circulating EVs miRNA biomarker surface proteome Extracellular Vesicles/metabolism General Medicine Prostate-Specific Antigen Catalysis Computer Science Applications Inorganic Chemistry Psoriasis/genetics Extracellular Vesicles MicroRNAs Psoriasis Humans MicroRNAs/metabolism Physical and Theoretical Chemistry Molecular Biology Spectroscopy Arthritis Psoriatic/diagnosis Biomarkers circulatory and respiratory physiology |
Zdroj: | International Journal of Molecular Sciences; Volume 23; Issue 7; Pages: 4005 Lättekivi, F, Guljavina, I, Midekessa, G, Viil, J, Heath, P R, Bæk, R, Jørgensen, M M, Andronowska, A, Kingo, K & Fazeli, A 2022, ' Profiling Blood Serum Extracellular Vesicles in Plaque Psoriasis and Psoriatic Arthritis Patients Reveals Potential Disease Biomarkers ', International Journal of Molecular Sciences, vol. 23, no. 7, 4005 . https://doi.org/10.3390/ijms23074005 |
ISSN: | 1422-0067 |
DOI: | 10.3390/ijms23074005 |
Popis: | Psoriasis vulgaris (PsV) and psoriatic arthritis (PsA) are inflammatory diseases with unresolved pathophysiological aspects. Extracellular vesicles (EVs) play an important role in intercellular communication. We compared the miRNA contents and surface proteome of the EVs in the blood serum of PsV and PsA patients to healthy controls. Size-exclusion chromatography was used to isolate EVs from the blood serum of 12 PsV patients, 12 PsA patients and 12 healthy control subjects. EV samples were characterized and RNA sequencing was used to identify differentially enriched EV-bound miRNAs. We found 212 differentially enriched EV-bound miRNAs present in both PsV and PsA groups—a total of 13 miRNAs at FDR ≤ 0.05. The predicted target genes of these miRNAs were significantly related to lesser known but potentially disease-relevant pathways. The EV array revealed that PsV patient EV samples were significantly enriched with CD9 EV-marker compared to controls. Analysis of EV-bound miRNAs suggests that signaling via EVs in the blood serum could play a role in the pathophysiological processes of PsV and PsA. EVs may be able to fill the void in clinically applicable diagnostic and prognostic biomarkers for PsV and PsA. |
Databáze: | OpenAIRE |
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