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Signature profile of cyclooxygenase-independent F2 series prostaglandins in C. elegans and their role in sperm motility
We previously discovered that Caenorhabditis elegans synthesizes Cox-independent F-series prostaglandins (PGs). To delineate the Cox-independent prostaglandin pathways and evaluate their role in sperm motility in C. elegans, we developed a novel biochemical method for the rapid production of F-serie...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6692340/ https://www.ncbi.nlm.nih.gov/pubmed/31409838 http://dx.doi.org/10.1038/s41598-019-48062-y |
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author | Tiwary, Ekta Hu, Muhan Miller, Michael A. Prasain, Jeevan K. |
author_facet | Tiwary, Ekta Hu, Muhan Miller, Michael A. Prasain, Jeevan K. |
author_sort | Tiwary, Ekta |
collection | PubMed |
description | We previously discovered that Caenorhabditis elegans synthesizes Cox-independent F-series prostaglandins (PGs). To delineate the Cox-independent prostaglandin pathways and evaluate their role in sperm motility in C. elegans, we developed a novel biochemical method for the rapid production of F-series PGs using arachidonic acid as the substrate and worm lysate as source of enzyme(s). Among the four F2-series PGs produced in the reaction, three of them were identified as 8-isoPGF2α, 5iPF2 VI, and PGF2α based on their retention times and MS/MS spectral comparison with standards using LC-MS/MS. PG production was not markedly affected by specific antioxidants, or Cox, Lox, and Cyp inhibitors, suggesting that these PGs are formed through a novel, biologically regulated mechanism in C. elegans. This study also assessed the ability of 8-isoPGF2α, 5iPF2 VI, PGF2α, and a mixture containing these PGs in a 0.5/0.08/1 ratio that reflects their synthetic composition to modulate sperm motility in fat-2 mutants. PGF2α and the PG mixture at 25 μM concentration significantly stimulated sperm velocity by 28% and 38%, whereas 8-isoPGF2α and 5iPF2 VI reduced the velocity by 21% and 30%, respectively, compared to vehicle control. These results indicate that the sperm motility effects of PGs are structure- and composition-dependent in C. elegans. |
format | Online Article Text |
id | pubmed-6692340 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66923402019-08-19 Signature profile of cyclooxygenase-independent F2 series prostaglandins in C. elegans and their role in sperm motility Tiwary, Ekta Hu, Muhan Miller, Michael A. Prasain, Jeevan K. Sci Rep Article We previously discovered that Caenorhabditis elegans synthesizes Cox-independent F-series prostaglandins (PGs). To delineate the Cox-independent prostaglandin pathways and evaluate their role in sperm motility in C. elegans, we developed a novel biochemical method for the rapid production of F-series PGs using arachidonic acid as the substrate and worm lysate as source of enzyme(s). Among the four F2-series PGs produced in the reaction, three of them were identified as 8-isoPGF2α, 5iPF2 VI, and PGF2α based on their retention times and MS/MS spectral comparison with standards using LC-MS/MS. PG production was not markedly affected by specific antioxidants, or Cox, Lox, and Cyp inhibitors, suggesting that these PGs are formed through a novel, biologically regulated mechanism in C. elegans. This study also assessed the ability of 8-isoPGF2α, 5iPF2 VI, PGF2α, and a mixture containing these PGs in a 0.5/0.08/1 ratio that reflects their synthetic composition to modulate sperm motility in fat-2 mutants. PGF2α and the PG mixture at 25 μM concentration significantly stimulated sperm velocity by 28% and 38%, whereas 8-isoPGF2α and 5iPF2 VI reduced the velocity by 21% and 30%, respectively, compared to vehicle control. These results indicate that the sperm motility effects of PGs are structure- and composition-dependent in C. elegans. Nature Publishing Group UK 2019-08-13 /pmc/articles/PMC6692340/ /pubmed/31409838 http://dx.doi.org/10.1038/s41598-019-48062-y Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Tiwary, Ekta Hu, Muhan Miller, Michael A. Prasain, Jeevan K. Signature profile of cyclooxygenase-independent F2 series prostaglandins in C. elegans and their role in sperm motility |
title | Signature profile of cyclooxygenase-independent F2 series prostaglandins in C. elegans and their role in sperm motility |
title_full | Signature profile of cyclooxygenase-independent F2 series prostaglandins in C. elegans and their role in sperm motility |
title_fullStr | Signature profile of cyclooxygenase-independent F2 series prostaglandins in C. elegans and their role in sperm motility |
title_full_unstemmed | Signature profile of cyclooxygenase-independent F2 series prostaglandins in C. elegans and their role in sperm motility |
title_short | Signature profile of cyclooxygenase-independent F2 series prostaglandins in C. elegans and their role in sperm motility |
title_sort | signature profile of cyclooxygenase-independent f2 series prostaglandins in c. elegans and their role in sperm motility |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6692340/ https://www.ncbi.nlm.nih.gov/pubmed/31409838 http://dx.doi.org/10.1038/s41598-019-48062-y |
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