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A New E-Series Resolvin: RvE4 Stereochemistry and Function in Efferocytosis of Inflammation-Resolution

The resolution of the acute inflammatory response is governed by phagocytes actively clearing apoptotic cells and pathogens. Biosynthesis of the specialized pro-resolving mediators (SPMs) is pivotal in the resolution of inflammation via their roles in innate immune cells. Resolvin E4 (RvE4: 5S,15S-d...

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Autores principales: Libreros, Stephania, Shay, Ashley E., Nshimiyimana, Robert, Fichtner, David, Martin, Michael J., Wourms, Nicholas, Serhan, Charles N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7902526/
https://www.ncbi.nlm.nih.gov/pubmed/33643307
http://dx.doi.org/10.3389/fimmu.2020.631319
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author Libreros, Stephania
Shay, Ashley E.
Nshimiyimana, Robert
Fichtner, David
Martin, Michael J.
Wourms, Nicholas
Serhan, Charles N.
author_facet Libreros, Stephania
Shay, Ashley E.
Nshimiyimana, Robert
Fichtner, David
Martin, Michael J.
Wourms, Nicholas
Serhan, Charles N.
author_sort Libreros, Stephania
collection PubMed
description The resolution of the acute inflammatory response is governed by phagocytes actively clearing apoptotic cells and pathogens. Biosynthesis of the specialized pro-resolving mediators (SPMs) is pivotal in the resolution of inflammation via their roles in innate immune cells. Resolvin E4 (RvE4: 5S,15S-dihydroxy-eicosapentaenoic acid) is a newly uncovered member of the E-series resolvins biosynthesized from eicosapentaenoic acid (EPA) recently elucidated in physiologic hypoxia. This new resolvin was termed RvE4 given its ability to increase efferocytosis of apoptotic cells by macrophages. Herein, we report on the total organic synthesis of RvE4 confirming its unique structure, complete stereochemistry assignment and function. This synthetic RvE4 matched the physical properties of biogenic RvE4 material, i.e. ultra-violet (UV) absorbance, chromatographic behavior, and tandem mass spectrometry (MS(2)) fragmentation, as well as bioactivity. We confirmed RvE4 potent responses with human M2 macrophage efferocytosis of human apoptotic neutrophils and senescent red blood cells. Together, these results provide direct evidence for the assignment of the complete stereochemistry of RvE4 as 5S,15S-dihydroxy-6E,8Z,11Z,13E,17Z-eicosapentaenoic acid and its bioactions in human phagocyte response.
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spelling pubmed-79025262021-02-25 A New E-Series Resolvin: RvE4 Stereochemistry and Function in Efferocytosis of Inflammation-Resolution Libreros, Stephania Shay, Ashley E. Nshimiyimana, Robert Fichtner, David Martin, Michael J. Wourms, Nicholas Serhan, Charles N. Front Immunol Immunology The resolution of the acute inflammatory response is governed by phagocytes actively clearing apoptotic cells and pathogens. Biosynthesis of the specialized pro-resolving mediators (SPMs) is pivotal in the resolution of inflammation via their roles in innate immune cells. Resolvin E4 (RvE4: 5S,15S-dihydroxy-eicosapentaenoic acid) is a newly uncovered member of the E-series resolvins biosynthesized from eicosapentaenoic acid (EPA) recently elucidated in physiologic hypoxia. This new resolvin was termed RvE4 given its ability to increase efferocytosis of apoptotic cells by macrophages. Herein, we report on the total organic synthesis of RvE4 confirming its unique structure, complete stereochemistry assignment and function. This synthetic RvE4 matched the physical properties of biogenic RvE4 material, i.e. ultra-violet (UV) absorbance, chromatographic behavior, and tandem mass spectrometry (MS(2)) fragmentation, as well as bioactivity. We confirmed RvE4 potent responses with human M2 macrophage efferocytosis of human apoptotic neutrophils and senescent red blood cells. Together, these results provide direct evidence for the assignment of the complete stereochemistry of RvE4 as 5S,15S-dihydroxy-6E,8Z,11Z,13E,17Z-eicosapentaenoic acid and its bioactions in human phagocyte response. Frontiers Media S.A. 2021-02-10 /pmc/articles/PMC7902526/ /pubmed/33643307 http://dx.doi.org/10.3389/fimmu.2020.631319 Text en Copyright © 2021 Libreros, Shay, Nshimiyimana, Fichtner, Martin, Wourms and Serhan http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Libreros, Stephania
Shay, Ashley E.
Nshimiyimana, Robert
Fichtner, David
Martin, Michael J.
Wourms, Nicholas
Serhan, Charles N.
A New E-Series Resolvin: RvE4 Stereochemistry and Function in Efferocytosis of Inflammation-Resolution
title A New E-Series Resolvin: RvE4 Stereochemistry and Function in Efferocytosis of Inflammation-Resolution
title_full A New E-Series Resolvin: RvE4 Stereochemistry and Function in Efferocytosis of Inflammation-Resolution
title_fullStr A New E-Series Resolvin: RvE4 Stereochemistry and Function in Efferocytosis of Inflammation-Resolution
title_full_unstemmed A New E-Series Resolvin: RvE4 Stereochemistry and Function in Efferocytosis of Inflammation-Resolution
title_short A New E-Series Resolvin: RvE4 Stereochemistry and Function in Efferocytosis of Inflammation-Resolution
title_sort new e-series resolvin: rve4 stereochemistry and function in efferocytosis of inflammation-resolution
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7902526/
https://www.ncbi.nlm.nih.gov/pubmed/33643307
http://dx.doi.org/10.3389/fimmu.2020.631319
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