H2S, Polysulfides, and Enzymes: Physiological and Pathological Aspects 2.0

A special issue of Biomolecules (ISSN 2218-273X). This special issue belongs to the section "Molecular Medicine".

Deadline for manuscript submissions: 31 July 2024 | Viewed by 3223

Special Issue Editors


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Guest Editor
Chair of Medical Biochemistry, Faculty of Medicine, Jagiellonian University Medical College, 31034 Kraków, Poland
Interests: biochemistry; medical biochemistry; tissue-specific expression and function of sulfurtransferases
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Guest Editor
Chair of Medical Biochemistry, Faculty of Medicine, Jagiellonian University Medical College, 31034 Kraków, Poland
Interests: biochemistry; anticancer research; amino acids; pharmacological reports

Special Issue Information

Dear Colleagues,

This Special Issue was organized with the intent of elucidating novel physiological and pathological functions of H2S and polysulfides and explaining the regulation of the pathways and enzymes involved in their biosynthesis. We expect this Issue to advance scientific knowledge regarding the exact functions of H2S and polysulfides and the general properties and regulation of the enzymes involved in their metabolism, including cystathionine β-synthase (EC 4.2.1.22, CBS), cystathionine γ-lyase (EC 4.4.1.1, CTH), thiosulfate sulfurtransferase (EC 2.8.1.1, rhodanese, TST), and 3-mercaptopyruvate sulfurtransferase (EC 2.8.1.2, MST). Five topics will be covered: the biosynthesis of H2S and polysulfides; biosynthetic enzymes, as well as their properties and regulation; H2S-releasing pharmaceuticals; the physiological role of H2S and polysulfides in, e.g., synaptic transmission, vascular tone, inflammation, angiogenesis; and their role in several pathological processes, e.g., healing of ulcers, neurological disorders, myocardial infarction, ischemia–reperfusion injury, heart failure, carcinogenesis, pulmonary, renal, and hepatic diseases, and diabetes. We encourage scientists studying H2S and polysulfides (mechanisms of biosynthesis, functions, and clinical usage) and related enzymes (structure, reaction mechanisms, and regulation of enzymatic activity) to contribute to this Special Issue. Research articles, clinical studies, and reviews are welcome. For authors interested in submitting a paper, please refer to the Biomolecules “Author Guidelines”.

Dr. Maria Wróbel
Dr. Halina Jurkowska
Guest Editors

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Keywords

  • H2S and polysulfide
  • H2S in inflammation
  • H2S in brain, heart, liver, kidney, and pulmonary diseases
  • H2S in cancer cells
  • H2S in the pathogenesis of diabetes
  • H2S and polysulfides biosynthetic enzymes
  • H2S precursors

Published Papers (2 papers)

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Research

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16 pages, 4551 KiB  
Article
Hypoxia-Induced Changes in L-Cysteine Metabolism and Antioxidative Processes in Melanoma Cells
by Leszek Rydz, Maria Wróbel, Klaudia Janik and Halina Jurkowska
Biomolecules 2023, 13(10), 1491; https://doi.org/10.3390/biom13101491 - 07 Oct 2023
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Abstract
This study was performed on human primary (WM115) and metastatic (WM266-4) melanoma cell lines developed from the same individual. The expression of proteins involved in L-cysteine metabolism (sulfurtransferases, and cystathionine β-synthase) and antioxidative processes (thioredoxin, thioredoxin reductase-1, glutathione peroxidase, superoxide dismutase 1) as [...] Read more.
This study was performed on human primary (WM115) and metastatic (WM266-4) melanoma cell lines developed from the same individual. The expression of proteins involved in L-cysteine metabolism (sulfurtransferases, and cystathionine β-synthase) and antioxidative processes (thioredoxin, thioredoxin reductase-1, glutathione peroxidase, superoxide dismutase 1) as well as the level of sufane sulfur, and cell proliferation under hypoxic conditions were investigated. Hypoxia in WM115 and WM266-4 cells was confirmed by induced expression of carbonic anhydrase IX and 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4 by the RT-PCR and Western blot methods. It was shown that, under hypoxic conditions the inhibition of WM115 and WM266-4 melanoma cell proliferation was associated with decreased expression of thioredoxin reductase-1 and cystathionine β-synthase. These two enzymes may be important therapeutic targets in the treatment of melanoma. Interestingly, it was also found that in normoxia the expression and activity of 3-mercaptopyruvate sulfurtransferase in metastatic WM266-4 melanoma cells was significantly higher than in primary melanoma WM115 cells. Full article
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Review

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20 pages, 2160 KiB  
Review
Hydrogen Sulfide (H2S)/Polysulfides (H2Sn) Signalling and TRPA1 Channels Modification on Sulfur Metabolism
by Hideo Kimura
Biomolecules 2024, 14(1), 129; https://doi.org/10.3390/biom14010129 - 19 Jan 2024
Viewed by 1163
Abstract
Hydrogen sulfide (H2S) and polysulfides (H2Sn, n ≥ 2) produced by enzymes play a role as signalling molecules regulating neurotransmission, vascular tone, cytoprotection, inflammation, oxygen sensing, and energy formation. H2Sn, which have additional [...] Read more.
Hydrogen sulfide (H2S) and polysulfides (H2Sn, n ≥ 2) produced by enzymes play a role as signalling molecules regulating neurotransmission, vascular tone, cytoprotection, inflammation, oxygen sensing, and energy formation. H2Sn, which have additional sulfur atoms to H2S, and other S-sulfurated molecules such as cysteine persulfide and S-sulfurated cysteine residues of proteins, are produced by enzymes including 3-mercaptopyruvate sulfurtransferase (3MST). H2Sn are also generated by the chemical interaction of H2S with NO, or to a lesser extent with H2O2. S-sulfuration (S-sulfhydration) has been proposed as a mode of action of H2S and H2Sn to regulate the activity of target molecules. Recently, we found that H2S/H2S2 regulate the release of neurotransmitters, such as GABA, glutamate, and D-serine, a co-agonist of N-methyl-D-aspartate (NMDA) receptors. H2S facilitates the induction of hippocampal long-term potentiation, a synaptic model of memory formation, by enhancing the activity of NMDA receptors, while H2S2 achieves this by activating transient receptor potential ankyrin 1 (TRPA1) channels in astrocytes, potentially leading to the activation of nearby neurons. The recent findings show the other aspects of TRPA1 channels—that is, the regulation of the levels of sulfur-containing molecules and their metabolizing enzymes. Disturbance of the signalling by H2S/H2Sn has been demonstrated to be involved in various diseases, including cognitive and psychiatric diseases. The physiological and pathophysiological roles of these molecules will be discussed. Full article
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