Human Adult Astrocyte Extracellular Vesicle Transcriptomics Study Identifies Specific RNAs Which Are Preferentially Secreted as EV Luminal Cargo

Author:

Shanthi Keerthanaa Balasubramanian1ORCID,Fischer Daniel2,Sharma Abhishek1,Kiviniemi Antti1,Kaakinen Mika3,Vainio Seppo J.14ORCID,Bart Geneviève1ORCID

Affiliation:

1. FBMM, Disease Networks Research Unit, Laboratory of Developmental Biology, University of Oulu, 90014 Oulu, Finland

2. Applied Statistical Methods, Natural Resources Institute Finland (Luke), Myllytie 1, 31600 Jokioinen, Finland

3. Biocenter Oulu, University of Oulu, and Oulu Centre for Cell-Matrix Research, Faculty of Biochemistry and Molecular Medicine, 90014 Oulu, Finland

4. Kvantum Institute, Infotech Oulu, University of Oulu, 90014 Oulu, Finland

Abstract

Astrocytes are central nervous system (CNS)-restricted glial cells involved in synaptic function and CNS blood flow regulation. Astrocyte extracellular vesicles (EVs) participate in neuronal regulation. EVs carry RNAs, either surface-bound or luminal, which can be transferred to recipient cells. We characterized the secreted EVs and RNA cargo of human astrocytes derived from an adult brain. EVs were isolated by serial centrifugation and characterized with nanoparticle tracking analysis (NTA), Exoview, and immuno-transmission electron microscopy (TEM). RNA from cells, EVs, and proteinase K/RNase-treated EVs was analyzed by miRNA-seq. Human adult astrocyte EVs ranged in sizes from 50 to 200 nm, with CD81 as the main tetraspanin marker and larger EVs positive for integrin β1. Comparison of the RNA between the cells and EVs identified RNA preferentially secreted in the EVs. In the case of miRNAs, enrichment analysis of their mRNA targets indicates that they are good candidates for mediating EV effects on recipient cells. The most abundant cellular miRNAs were also abundant in EVs, and the majority of their mRNA targets were found to be downregulated in mRNA-seq data, but the enrichment analysis lacked neuronal specificity. Proteinase K/RNase treatment of EV-enriched preparations identified RNAs secreted independently of EVs. Comparing the distribution of cellular and secreted RNA identifies the RNAs involved in intercellular communication via EVs.

Funder

Horizon 2020

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

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