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Extracellular vesicles are independent metabolic units with asparaginase activity

Authors :
Carlos Bastos
Tommaso Leonardi
Ana S. H. Costa
Nunzio Iraci
Maurizio Gelati
Joshua D. Bernstock
Stefano Pluchino
Chiara Cossetti
Harpreet K Saini
Edoardo Gaude
Anton J. Enright
Nuno Faria
Luigi Occhipinti
Angelo L. Vescovi
Christian Frezza
Luca Peruzzotti-Jametti
Iraci, N
Gaude, E
Leonardi, T
Costa, A
Cossetti, C
Peruzzotti Jametti, L
Bernstock, J
Saini, H
Gelati, M
Vescovi, A
Bastos, C
Faria, N
Occhipinti, L
Enright, A
Frezza, C
Pluchino, S
Iraci, Nunzio [0000-0003-2146-9329]
Peruzzotti-Jametti, Luca [0000-0002-9396-5607]
Bernstock, Joshua D [0000-0002-7814-3867]
Frezza, Christian [0000-0002-3293-7397]
Apollo - University of Cambridge Repository
Source :
Nature Chemical Biology. 13:951-955
Publication Year :
2017
Publisher :
Springer Science and Business Media LLC, 2017.

Abstract

Extracellular vesicles (EVs) are membrane particles involved in the exchange of a broad range of bioactive molecules between cells and the microenvironment. Although it has been shown that cells can traffic metabolic enzymes via EVs, much remains to be elucidated with regard to their intrinsic metabolic activity. Accordingly, herein we assessed the ability of neural stem/progenitor cell (NSC)-derived EVs to consume and produce metabolites. Our metabolomics and functional analyses both revealed that EVs harbor L-asparaginase activity, catalyzed by the enzyme asparaginase-like protein 1 (Asrgl1). Critically, we show that Asrgl1 activity is selective for asparagine and is devoid of glutaminase activity. We found that mouse and human NSC EVs traffic Asrgl1. Our results demonstrate, for the first time, that NSC EVs function as independent metabolic units that are able to modify the concentrations of critical nutrients, with the potential to affect the physiology of their microenvironment.

Details

ISSN :
15524469 and 15524450
Volume :
13
Database :
OpenAIRE
Journal :
Nature Chemical Biology
Accession number :
edsair.doi.dedup.....3cf55f8ec0117fe2399ff3f86cc9f9e0
Full Text :
https://doi.org/10.1038/nchembio.2422