Open AccessY‐RNA subtype ratios in plasma extracellular vesicles are cell type‐ specific and are candidate biomarkers for inflammatory diseases
Author(s) -
Driedonks Tom A.P.,
Mol Sanne,
Bruin Sanne,
Peters AnnaLinda,
Zhang Xiaogang,
Lindenbergh Marthe F.S.,
Beuger Boukje M.,
Stalborch AnneMarieke D.,
Spaan Thom,
Jong Esther C.,
Vries Erhard,
Margadant Coert,
Bruggen Robin,
Vlaar Alexander P.J.,
Groot Kormelink Tom,
Nolte‘T Hoen Esther N.M.
Publication year - 2020
Publication title -
journal of extracellular vesicles
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.94
H-Index - 68
ISSN - 2001-3078
DOI - 10.1080/20013078.2020.1764213
Subject(s) - rna , microrna , microvesicles , small rna , immune system , non coding rna , cell , extracellular vesicle , extracellular , biology , ribonucleoprotein , messenger rna , inflammation , gene expression , microbiology and biotechnology , gene , biochemistry , immunology
Major efforts are made to characterize the presence of microRNA (miRNA) and messenger RNA in blood plasma to discover novel disease‐associated biomarkers. MiRNAs in plasma are associated to several types of macromolecular structures, including extracellular vesicles (EV), lipoprotein particles (LPP) and ribonucleoprotein particles (RNP). RNAs in these complexes are recovered at variable efficiency by commonly used EV‐ and RNA isolation methods, which causes biases and inconsistencies in miRNA quantitation. Besides miRNAs, various other non‐coding RNA species are contained in EV and present within the pool of plasma extracellular RNA. Members of the Y‐RNA family have been detected in EV from various cell types and are among the most abundant non‐coding RNA types in plasma. We previously showed that shuttling of full‐length Y‐RNA into EV released by immune cells is modulated by microbial stimulation. This indicated that Y‐RNAs could contribute to the functional properties of EV in immune cell communication and that EV‐associated Y‐RNAs could have biomarker potential in immune‐related diseases. Here, we investigated which macromolecular structures in plasma contain full length Y‐RNA and whether the levels of three Y‐RNA subtypes in plasma (Y1, Y3 and Y4) change during systemic inflammation. Our data indicate that the majority of full length Y‐RNA in plasma is stably associated to EV. Moreover, we discovered that EV from different blood‐related cell types contain cell‐type‐specific Y‐RNA subtype ratios. Using a human model for systemic inflammation, we show that the neutrophil‐specific Y4/Y3 ratios and PBMC‐specific Y3/Y1 ratios were significantly altered after induction of inflammation. The plasma Y‐RNA ratios strongly correlated with the number and type of immune cells during systemic inflammation. Cell‐type‐specific “Y‐RNA signatures” in plasma EV can be determined without prior enrichment for EV, and may be further explored as simple and fast test for diagnosis of inflammatory responses or other immune‐related diseases.