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Extra-platelet low-molecular-mass thiols mediate the inhibitory action of S-nitrosoalbumin on human platelet aggregation via S-transnitrosylation of the platelet surface
Nitrosylation of sulfhydryl (SH) groups of cysteine (Cys) moieties is an important post-translational modification (PTM), often on a par with phosphorylation. S-Nitrosoalbumin (ALB-Cys(34)SNO; SNALB) in plasma and S-nitrosohemoglobin (Hb-Cys(β93)SNO; HbSNO) in red blood cells are considered the most...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Vienna
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8107154/ https://www.ncbi.nlm.nih.gov/pubmed/33586042 http://dx.doi.org/10.1007/s00726-021-02950-8 |
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author | Tsikas, Dimitrios |
author_facet | Tsikas, Dimitrios |
author_sort | Tsikas, Dimitrios |
collection | PubMed |
description | Nitrosylation of sulfhydryl (SH) groups of cysteine (Cys) moieties is an important post-translational modification (PTM), often on a par with phosphorylation. S-Nitrosoalbumin (ALB-Cys(34)SNO; SNALB) in plasma and S-nitrosohemoglobin (Hb-Cys(β93)SNO; HbSNO) in red blood cells are considered the most abundant high-molecular-mass pools of nitric oxide (NO) bioactivity in the human circulation. SNALB per se is not an NO donor. Yet, it acts as a vasodilator and an inhibitor of platelet aggregation. SNALB can be formed by nitrosation of the sole reduced Cys group of albumin (Cys(34)) by nitrosating species such as nitrous acid (HONO) and nitrous anhydride (N(2)O(3)), two unstable intermediates of NO autoxidation. SNALB can also be formed by the transfer (S-transnitrosylation) of the nitrosyl group (NO(+)) of a low-molecular-mass (LMM) S-nitrosothiol (RSNO) to ALB-Cys(34)SH. In the present study, the effects of LMM thiols on the inhibitory potential of ALB-Cys(34)SNO on human washed platelets were investigated. ALB-Cys(34)SNO was prepared by reacting n-butylnitrite with albumin after selective extraction from plasma of a healthy donor on HiTrapBlue Sepharose cartridges. ALB-Cys(34)SNO was used in platelet aggregation measurements after extended purification on HiTrapBlue Sepharose and enrichment by ultrafiltration (cutoff, 20 kDa). All tested LMM cysteinyl thiols (R-CysSH) including l-cysteine and L-homocysteine (at 10 µM) were found to mediate the collagen-induced (1 µg/mL) aggregation of human washed platelets by SNALB (range, 0–10 µM) by cGMP-dependent and cGMP-independent mechanisms. The LMM thiols themselves did not affect platelet aggregation. It is assumed that the underlying mechanism involves S-transnitrosylation of SH groups of the platelet surface by LMM RSNO formed through the reaction of SNALB with the thiols: ALB-Cys(34)SNO + R-CysSH ↔ ALB-Cys(34)SH + R-CysSNO. Such S-transnitrosylation reactions may be accompanied by release of NO finally resulting in cGMP-dependent and cGMP-independent mechanisms. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00726-021-02950-8. |
format | Online Article Text |
id | pubmed-8107154 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-81071542021-05-24 Extra-platelet low-molecular-mass thiols mediate the inhibitory action of S-nitrosoalbumin on human platelet aggregation via S-transnitrosylation of the platelet surface Tsikas, Dimitrios Amino Acids Original Article Nitrosylation of sulfhydryl (SH) groups of cysteine (Cys) moieties is an important post-translational modification (PTM), often on a par with phosphorylation. S-Nitrosoalbumin (ALB-Cys(34)SNO; SNALB) in plasma and S-nitrosohemoglobin (Hb-Cys(β93)SNO; HbSNO) in red blood cells are considered the most abundant high-molecular-mass pools of nitric oxide (NO) bioactivity in the human circulation. SNALB per se is not an NO donor. Yet, it acts as a vasodilator and an inhibitor of platelet aggregation. SNALB can be formed by nitrosation of the sole reduced Cys group of albumin (Cys(34)) by nitrosating species such as nitrous acid (HONO) and nitrous anhydride (N(2)O(3)), two unstable intermediates of NO autoxidation. SNALB can also be formed by the transfer (S-transnitrosylation) of the nitrosyl group (NO(+)) of a low-molecular-mass (LMM) S-nitrosothiol (RSNO) to ALB-Cys(34)SH. In the present study, the effects of LMM thiols on the inhibitory potential of ALB-Cys(34)SNO on human washed platelets were investigated. ALB-Cys(34)SNO was prepared by reacting n-butylnitrite with albumin after selective extraction from plasma of a healthy donor on HiTrapBlue Sepharose cartridges. ALB-Cys(34)SNO was used in platelet aggregation measurements after extended purification on HiTrapBlue Sepharose and enrichment by ultrafiltration (cutoff, 20 kDa). All tested LMM cysteinyl thiols (R-CysSH) including l-cysteine and L-homocysteine (at 10 µM) were found to mediate the collagen-induced (1 µg/mL) aggregation of human washed platelets by SNALB (range, 0–10 µM) by cGMP-dependent and cGMP-independent mechanisms. The LMM thiols themselves did not affect platelet aggregation. It is assumed that the underlying mechanism involves S-transnitrosylation of SH groups of the platelet surface by LMM RSNO formed through the reaction of SNALB with the thiols: ALB-Cys(34)SNO + R-CysSH ↔ ALB-Cys(34)SH + R-CysSNO. Such S-transnitrosylation reactions may be accompanied by release of NO finally resulting in cGMP-dependent and cGMP-independent mechanisms. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00726-021-02950-8. Springer Vienna 2021-02-14 2021 /pmc/articles/PMC8107154/ /pubmed/33586042 http://dx.doi.org/10.1007/s00726-021-02950-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Tsikas, Dimitrios Extra-platelet low-molecular-mass thiols mediate the inhibitory action of S-nitrosoalbumin on human platelet aggregation via S-transnitrosylation of the platelet surface |
title | Extra-platelet low-molecular-mass thiols mediate the inhibitory action of S-nitrosoalbumin on human platelet aggregation via S-transnitrosylation of the platelet surface |
title_full | Extra-platelet low-molecular-mass thiols mediate the inhibitory action of S-nitrosoalbumin on human platelet aggregation via S-transnitrosylation of the platelet surface |
title_fullStr | Extra-platelet low-molecular-mass thiols mediate the inhibitory action of S-nitrosoalbumin on human platelet aggregation via S-transnitrosylation of the platelet surface |
title_full_unstemmed | Extra-platelet low-molecular-mass thiols mediate the inhibitory action of S-nitrosoalbumin on human platelet aggregation via S-transnitrosylation of the platelet surface |
title_short | Extra-platelet low-molecular-mass thiols mediate the inhibitory action of S-nitrosoalbumin on human platelet aggregation via S-transnitrosylation of the platelet surface |
title_sort | extra-platelet low-molecular-mass thiols mediate the inhibitory action of s-nitrosoalbumin on human platelet aggregation via s-transnitrosylation of the platelet surface |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8107154/ https://www.ncbi.nlm.nih.gov/pubmed/33586042 http://dx.doi.org/10.1007/s00726-021-02950-8 |
work_keys_str_mv | AT tsikasdimitrios extraplateletlowmolecularmassthiolsmediatetheinhibitoryactionofsnitrosoalbuminonhumanplateletaggregationviastransnitrosylationoftheplateletsurface |