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Detection of changes in mitochondrial hydrogen sulfide in vivo in the fish model Poecilia mexicana (Poeciliidae).

Published version
Peer-reviewed

Type

Article

Change log

Authors

Lau, Gigi Y 
Barts, Nicholas 
Hartley, Richard C 
Tobler, Michael 
Richards, Jeffrey G 

Abstract

In this paper, we outline the use of a mitochondria-targeted ratiometric mass spectrometry probe, MitoA, to detect in vivo changes in mitochondrial hydrogen sulfide (H2S) in Poecilia mexicana (family Poeciliidae). MitoA is introduced via intraperitoneal injection into the animal and is taken up by mitochondria, where it reacts with H2S to form the product MitoN. The MitoN/MitoA ratio can be used to assess relative changes in the amounts of mitochondrial H2S produced over time. We describe the use of MitoA in the fish species P. mexicana to illustrate the steps for adopting the use of MitoA in a new organism, including extraction and purification of MitoA and MitoN from tissues followed by tandem mass spectrometry. In this proof-of-concept study we exposed H2S tolerant P. mexicana to 59 µM free H2S for 5 h, which resulted in increased MitoN/MitoA in brain and gills, but not in liver or muscle, demonstrating increased mitochondrial H2S levels in select tissues following whole-animal H2S exposure. This is the first time that accumulation of H2S has been observed in vivo during whole-animal exposure to free H2S using MitoA. This article has an associated First Person interview with the first author of the paper.

Description

Keywords

Fish, Hydrogen sulfide, Mass spectrometry probe, MitoA, Mitochondria

Journal Title

Biology Open

Conference Name

Journal ISSN

2046-6390
2046-6390

Volume Title

8

Publisher

Company of Biologists
Sponsorship
Medical Research Council (MC_UU_00015/3)
Medical Research Council (MC_U105663142)
Wellcome Trust (110159/Z/15/Z)
This work was supported by grants from the National Science Foundation (IOS-1557860), the U.S. Army Research Office (W911NF-15-1-0175) and the Defense University Research Instrumentation Program of the U.S. Office of Naval Research (W911NF-16-1-0225) to M.T.; by a Natural Sciences and Engineering Research Council (NSERC) of Canada Discovery Grant to J.G.R.; and by the Medical Research Council UK (MC_U105663142) and a Wellcome Trust Investigator award (110159/Z/15/Z) to M.P.M. G.Y.L. was supported by a NSERC Canada Graduate Scholarship.