Non-Coding RNA in Salivary Extracellular Vesicles: A New Frontier in Sjögren’s Syndrome Diagnostics?

Author:

Cross Tanya1,Haug Kari Bente Foss2ORCID,Brusletto Berit Sletbakk2ORCID,Ommundsen Stine Kamilla1,Trøseid Anne-Marie Siebke2ORCID,Aspelin Trude2ORCID,Olstad Ole Kristoffer2,Aass Hans Christian Dalsbotten2,Galtung Hilde Kanli3,Utheim Tor Paaske1345678,Jensen Janicke Liaaen9ORCID,Øvstebø Reidun2ORCID

Affiliation:

1. The Regenerative Medicine Unit, Department of Medical Biochemistry, Oslo University Hospital, Ullevål, 0450 Oslo, Norway

2. The Blood Cell Research Group, Department of Medical Biochemistry, Oslo University Hospital, Ullevål, 0450 Oslo, Norway

3. Institute of Oral Biology, Faculty of Dentistry, University of Oslo, 0372 Oslo, Norway

4. Department of Plastic and Reconstructive Surgery, Oslo University Hospital, 0372 Oslo, Norway

5. Department of Ophthalmology, Oslo University Hospital, 0450 Oslo, Norway

6. Department of Ophthalmology, Sørlandet Hospital Arendal, 4838 Arendal, Norway

7. Department of Ophthalmology, Vestre Viken Hospital Trust, 3004 Drammen, Norway

8. The Norwegian Dry Eye Clinic, 0369 Oslo, Norway

9. Department of Oral Surgery and Oral Medicine, Faculty of Dentistry, University of Oslo, 0455 Oslo, Norway

Abstract

Sjögren’s syndrome is an autoimmune rheumatic disease characterized by inflammation of the salivary and lacrimal glands, often manifesting as dry mouth and dry eyes. To simplify diagnostics of primary Sjögren’s syndrome (pSS), a non-invasive marker is needed. The aim of the study was to compare the RNA content of salivary extracellular vesicles (EVs) between patients with pSS and healthy controls using microarray technology. Stimulated whole saliva was collected from 11 pSS patients and 11 age-matched controls. EV-RNA was isolated from the saliva samples using a Qiagen exoRNeasy Midi Kit and analyzed using Affymetrix Clariom D™ microarrays. A one-way ANOVA test was used to compare the mean signal values of each transcript between the two groups. A total of 9307 transcripts, coding and non-coding RNA, were detected in all samples. Of these transcripts, 1475 showed statistically significant differential abundance between the pSS and the control groups, generating two distinct EV-RNA patterns. In particular, tRNAs were downregulated in pSS patients, with the transcript tRNA-Ile-AAT-2-1 showing a 2-fold difference, and a promise as a potential biomarker candidate. This study therein demonstrates the potential for using salivary EV-RNA in pSS diagnostics.

Funder

Regenerative Medicine Unit and The Blood Cell Research Group of the Department of Medical Biochemistry, Oslo University Hospital

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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