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H2S biosynthesis and catabolism: new insights from molecular studies

Rose, Peter; Moore, Philip K.; Zhu, Yi Zhun

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Authors

PETER ROSE Peter.Rose@nottingham.ac.uk
Assistant Professor

Philip K. Moore

Yi Zhun Zhu



Abstract

Hydrogen sulfide (H2S) has profound biological effects within living organisms and is now increasingly being considered alongside other gaseous signalling molecules, such as nitric oxide (NO) and carbon monoxide (CO). Conventional use of pharmacological and molecular approaches has spawned a rapidly growing research field that has identified H2S as playing a functional role in cell-signalling and post-translational modifications. Recently, a number of laboratories have reported the use of siRNA methodologies and genetic mouse models to mimic the loss of function of genes involved in the biosynthesis and degradation of H2S within tissues. Studies utilising these systems are revealing new insights into the biology of H2S within the cardiovascular system, inflammatory disease, and in cell signalling. In light of this work, the current review will describe recent advances in H2S research made possible by the use of molecular approaches and genetic mouse models with perturbed capacities to generate or detoxify physiological levels of H2S gas within tissues.

Citation

Rose, P., Moore, P. K., & Zhu, Y. Z. (2017). H2S biosynthesis and catabolism: new insights from molecular studies. Cellular and Molecular Life Sciences, 74(8), 1391-1412. https://doi.org/10.1007/s00018-016-2406-8

Journal Article Type Review
Acceptance Date Nov 1, 2016
Online Publication Date Nov 14, 2016
Publication Date 2017-04
Deposit Date Jun 5, 2017
Publicly Available Date Nov 24, 2023
Journal Cellular and Molecular Life Sciences
Print ISSN 1420-682X
Electronic ISSN 1420-9071
Publisher Springer Verlag
Peer Reviewed Peer Reviewed
Volume 74
Issue 8
Pages 1391-1412
DOI https://doi.org/10.1007/s00018-016-2406-8
Public URL https://nottingham-repository.worktribe.com/output/1121724
Publisher URL https://link.springer.com/article/10.1007/s00018-016-2406-8
Related Public URLs http://europepmc.org/abstract/med/27844098

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