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exRNA Atlas Analysis Reveals Distinct Extracellular RNA Cargo Types and Their Carriers Present across Human Biofluids.

Authors :
Murillo OD
Thistlethwaite W
Rozowsky J
Subramanian SL
Lucero R
Shah N
Jackson AR
Srinivasan S
Chung A
Laurent CD
Kitchen RR
Galeev T
Warrell J
Diao JA
Welsh JA
Hanspers K
Riutta A
Burgstaller-Muehlbacher S
Shah RV
Yeri A
Jenkins LM
Ahsen ME
Cordon-Cardo C
Dogra N
Gifford SM
Smith JT
Stolovitzky G
Tewari AK
Wunsch BH
Yadav KK
Danielson KM
Filant J
Moeller C
Nejad P
Paul A
Simonson B
Wong DK
Zhang X
Balaj L
Gandhi R
Sood AK
Alexander RP
Wang L
Wu C
Wong DTW
Galas DJ
Van Keuren-Jensen K
Patel T
Jones JC
Das S
Cheung KH
Pico AR
Su AI
Raffai RL
Laurent LC
Roth ME
Gerstein MB
Milosavljevic A
Source :
Cell [Cell] 2019 Apr 04; Vol. 177 (2), pp. 463-477.e15.
Publication Year :
2019

Abstract

To develop a map of cell-cell communication mediated by extracellular RNA (exRNA), the NIH Extracellular RNA Communication Consortium created the exRNA Atlas resource (https://exrna-atlas.org). The Atlas version 4P1 hosts 5,309 exRNA-seq and exRNA qPCR profiles from 19 studies and a suite of analysis and visualization tools. To analyze variation between profiles, we apply computational deconvolution. The analysis leads to a model with six exRNA cargo types (CT1, CT2, CT3A, CT3B, CT3C, CT4), each detectable in multiple biofluids (serum, plasma, CSF, saliva, urine). Five of the cargo types associate with known vesicular and non-vesicular (lipoprotein and ribonucleoprotein) exRNA carriers. To validate utility of this model, we re-analyze an exercise response study by deconvolution to identify physiologically relevant response pathways that were not detected previously. To enable wide application of this model, as part of the exRNA Atlas resource, we provide tools for deconvolution and analysis of user-provided case-control studies.<br /> (Copyright © 2019 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1097-4172
Volume :
177
Issue :
2
Database :
MEDLINE
Journal :
Cell
Publication Type :
Academic Journal
Accession number :
30951672
Full Text :
https://doi.org/10.1016/j.cell.2019.02.018