Bioenergetic relevance of hydrogen sulfide and the interplay between gasotransmitters at human cystathionine β-synthase

Biochim Biophys Acta. 2016 Aug;1857(8):1127-1138. doi: 10.1016/j.bbabio.2016.03.030. Epub 2016 Mar 31.

Abstract

Merely considered as a toxic gas in the past, hydrogen sulfide (H2S) is currently viewed as the third 'gasotransmitter' in addition to nitric oxide (NO) and carbon monoxide (CO), playing a key signalling role in human (patho)physiology. H2S can either act as a substrate or, similarly to CO and NO, an inhibitor of mitochondrial respiration, in the latter case by targeting cytochrome c oxidase (CcOX). The impact of H(2)S on mitochondrial energy metabolism crucially depends on the bioavailability of this gaseous molecule and its interplay with the other two gasotransmitters. The H(2)S-producing human enzyme cystathionine β-synthase (CBS), sustaining cellular bioenergetics in colorectal cancer cells, plays a role in the interplay between gasotransmitters. The enzyme was indeed recently shown to be negatively modulated by physiological concentrations of CO and NO, particularly in the presence of its allosteric activator S-adenosyl-l-methionine (AdoMet). These newly discovered regulatory mechanisms are herein reviewed. This article is part of a Special Issue entitled 'EBEC 2016: 19th European Bioenergetics Conference, Riva del Garda, Italy, July 2-6, 2016', edited by Prof. Paolo Bernardi.

Keywords: Cystathionine β-synthase; Cytochrome c oxidase; Gasotransmitters; Heme chemistry; Mitochondrial respiration; Sulfide metabolism.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Carbon Monoxide / metabolism
  • Colonic Neoplasms / genetics
  • Colonic Neoplasms / metabolism*
  • Colonic Neoplasms / pathology
  • Cystathionine beta-Synthase / chemistry
  • Cystathionine beta-Synthase / genetics
  • Cystathionine beta-Synthase / metabolism*
  • Electron Transport Complex IV / genetics
  • Electron Transport Complex IV / metabolism
  • Gasotransmitters / metabolism*
  • Gene Expression
  • Glutathione / metabolism
  • Humans
  • Hydrogen Sulfide / metabolism*
  • Kinetics
  • Mitochondria / metabolism*
  • Mitochondria / pathology
  • Models, Molecular
  • Nitric Oxide / metabolism
  • Oxidative Phosphorylation
  • S-Adenosylmethionine / metabolism
  • Signal Transduction

Substances

  • Gasotransmitters
  • Nitric Oxide
  • S-Adenosylmethionine
  • Carbon Monoxide
  • Electron Transport Complex IV
  • Cystathionine beta-Synthase
  • Glutathione
  • Hydrogen Sulfide