Long-Chain Acyl-CoA Synthetase 1 Role in Sepsis and Immunity: Perspectives From a Parallel Review of Public Transcriptome Datasets and of the Literature

<p dir="ltr">A potential role for the long-chain acyl-CoA synthetase family member 1 (ACSL1) in the immunobiology of sepsis was explored during a hands-on training workshop. Participants first assessed the robustness of the potential gap in biomedical knowledge identified via an init...

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محفوظ في:
التفاصيل البيبلوغرافية
المؤلف الرئيسي: Jessica Roelands (7516439) (author)
مؤلفون آخرون: Mathieu Garand (4861942) (author), Emily Hinchcliff (7516442) (author), Ying Ma (123771) (author), Parin Shah (3848437) (author), Mohammed Toufiq (7251596) (author), Mohamed Alfaki (7516445) (author), Wouter Hendrickx (44559) (author), Sabri Boughorbel (846228) (author), Darawan Rinchai (742366) (author), Amir Jazaeri (6309530) (author), Davide Bedognetti (2632474) (author), Damien Chaussabel (26369) (author)
منشور في: 2019
الموضوعات:
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author Jessica Roelands (7516439)
author2 Mathieu Garand (4861942)
Emily Hinchcliff (7516442)
Ying Ma (123771)
Parin Shah (3848437)
Mohammed Toufiq (7251596)
Mohamed Alfaki (7516445)
Wouter Hendrickx (44559)
Sabri Boughorbel (846228)
Darawan Rinchai (742366)
Amir Jazaeri (6309530)
Davide Bedognetti (2632474)
Damien Chaussabel (26369)
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author_facet Jessica Roelands (7516439)
Mathieu Garand (4861942)
Emily Hinchcliff (7516442)
Ying Ma (123771)
Parin Shah (3848437)
Mohammed Toufiq (7251596)
Mohamed Alfaki (7516445)
Wouter Hendrickx (44559)
Sabri Boughorbel (846228)
Darawan Rinchai (742366)
Amir Jazaeri (6309530)
Davide Bedognetti (2632474)
Damien Chaussabel (26369)
author_role author
dc.creator.none.fl_str_mv Jessica Roelands (7516439)
Mathieu Garand (4861942)
Emily Hinchcliff (7516442)
Ying Ma (123771)
Parin Shah (3848437)
Mohammed Toufiq (7251596)
Mohamed Alfaki (7516445)
Wouter Hendrickx (44559)
Sabri Boughorbel (846228)
Darawan Rinchai (742366)
Amir Jazaeri (6309530)
Davide Bedognetti (2632474)
Damien Chaussabel (26369)
dc.date.none.fl_str_mv 2019-10-01T00:00:00Z
dc.identifier.none.fl_str_mv 10.3389/fimmu.2019.02410
dc.relation.none.fl_str_mv https://figshare.com/articles/journal_contribution/Long-Chain_Acyl-CoA_Synthetase_1_Role_in_Sepsis_and_Immunity_Perspectives_From_a_Parallel_Review_of_Public_Transcriptome_Datasets_and_of_the_Literature/26020474
dc.rights.none.fl_str_mv CC BY 4.0
info:eu-repo/semantics/openAccess
dc.subject.none.fl_str_mv Biomedical and clinical sciences
Clinical sciences
Immunology
Medical biochemistry and metabolomics
sepsis
neutrophils
OMICS data
long-chain acyl-CoA synthetase
lipid metabolism
dc.title.none.fl_str_mv Long-Chain Acyl-CoA Synthetase 1 Role in Sepsis and Immunity: Perspectives From a Parallel Review of Public Transcriptome Datasets and of the Literature
dc.type.none.fl_str_mv Text
Journal contribution
info:eu-repo/semantics/publishedVersion
text
contribution to journal
description <p dir="ltr">A potential role for the long-chain acyl-CoA synthetase family member 1 (ACSL1) in the immunobiology of sepsis was explored during a hands-on training workshop. Participants first assessed the robustness of the potential gap in biomedical knowledge identified via an initial screen of public transcriptome data and of the literature associated with ACSL1. Increase in ACSL1 transcript abundance during sepsis was confirmed in several independent datasets. Querying the ACSL1 literature also confirmed the absence of reports associating ACSL1 with sepsis. Inferences drawn from both the literature (via indirect associations) and public transcriptome data (via correlation) point to the likely participation of ACSL1 and ACSL4, another family member, in inflammasome activation in neutrophils during sepsis. Furthermore, available clinical data indicate that levels of ACSL1 and ACSL4 induction was significantly higher in fatal cases of sepsis. This denotes potential translational relevance and is consistent with involvement in pathways driving potentially deleterious systemic inflammation. Finally, while ACSL1 expression was induced in blood in vitro by a wide range of pathogen-derived factors as well as TNF, induction of ACSL4 appeared restricted to flagellated bacteria and pathogen-derived TLR5 agonists and IFNG. Taken together, this joint review of public literature and omics data records points to two members of the acyl-CoA synthetase family potentially playing a role in inflammasome activation in neutrophils. Translational relevance of these observations in the context of sepsis and other inflammatory conditions remain to be investigated.</p><h2>Other Information</h2><p dir="ltr">Published in: Frontiers in Immunology<br>License: <a href="https://creativecommons.org/licenses/by/4.0/" target="_blank">https://creativecommons.org/licenses/by/4.0/</a><br>See article on publisher's website: <a href="https://dx.doi.org/10.3389/fimmu.2019.02410" target="_blank">https://dx.doi.org/10.3389/fimmu.2019.02410</a></p>
eu_rights_str_mv openAccess
id Manara2_e06aff9428b9b49038bef397f6eb2982
identifier_str_mv 10.3389/fimmu.2019.02410
network_acronym_str Manara2
network_name_str Manara2
oai_identifier_str oai:figshare.com:article/26020474
publishDate 2019
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spelling Long-Chain Acyl-CoA Synthetase 1 Role in Sepsis and Immunity: Perspectives From a Parallel Review of Public Transcriptome Datasets and of the LiteratureJessica Roelands (7516439)Mathieu Garand (4861942)Emily Hinchcliff (7516442)Ying Ma (123771)Parin Shah (3848437)Mohammed Toufiq (7251596)Mohamed Alfaki (7516445)Wouter Hendrickx (44559)Sabri Boughorbel (846228)Darawan Rinchai (742366)Amir Jazaeri (6309530)Davide Bedognetti (2632474)Damien Chaussabel (26369)Biomedical and clinical sciencesClinical sciencesImmunologyMedical biochemistry and metabolomicssepsisneutrophilsOMICS datalong-chain acyl-CoA synthetaselipid metabolism<p dir="ltr">A potential role for the long-chain acyl-CoA synthetase family member 1 (ACSL1) in the immunobiology of sepsis was explored during a hands-on training workshop. Participants first assessed the robustness of the potential gap in biomedical knowledge identified via an initial screen of public transcriptome data and of the literature associated with ACSL1. Increase in ACSL1 transcript abundance during sepsis was confirmed in several independent datasets. Querying the ACSL1 literature also confirmed the absence of reports associating ACSL1 with sepsis. Inferences drawn from both the literature (via indirect associations) and public transcriptome data (via correlation) point to the likely participation of ACSL1 and ACSL4, another family member, in inflammasome activation in neutrophils during sepsis. Furthermore, available clinical data indicate that levels of ACSL1 and ACSL4 induction was significantly higher in fatal cases of sepsis. This denotes potential translational relevance and is consistent with involvement in pathways driving potentially deleterious systemic inflammation. Finally, while ACSL1 expression was induced in blood in vitro by a wide range of pathogen-derived factors as well as TNF, induction of ACSL4 appeared restricted to flagellated bacteria and pathogen-derived TLR5 agonists and IFNG. Taken together, this joint review of public literature and omics data records points to two members of the acyl-CoA synthetase family potentially playing a role in inflammasome activation in neutrophils. Translational relevance of these observations in the context of sepsis and other inflammatory conditions remain to be investigated.</p><h2>Other Information</h2><p dir="ltr">Published in: Frontiers in Immunology<br>License: <a href="https://creativecommons.org/licenses/by/4.0/" target="_blank">https://creativecommons.org/licenses/by/4.0/</a><br>See article on publisher's website: <a href="https://dx.doi.org/10.3389/fimmu.2019.02410" target="_blank">https://dx.doi.org/10.3389/fimmu.2019.02410</a></p>2019-10-01T00:00:00ZTextJournal contributioninfo:eu-repo/semantics/publishedVersiontextcontribution to journal10.3389/fimmu.2019.02410https://figshare.com/articles/journal_contribution/Long-Chain_Acyl-CoA_Synthetase_1_Role_in_Sepsis_and_Immunity_Perspectives_From_a_Parallel_Review_of_Public_Transcriptome_Datasets_and_of_the_Literature/26020474CC BY 4.0info:eu-repo/semantics/openAccessoai:figshare.com:article/260204742019-10-01T00:00:00Z
spellingShingle Long-Chain Acyl-CoA Synthetase 1 Role in Sepsis and Immunity: Perspectives From a Parallel Review of Public Transcriptome Datasets and of the Literature
Jessica Roelands (7516439)
Biomedical and clinical sciences
Clinical sciences
Immunology
Medical biochemistry and metabolomics
sepsis
neutrophils
OMICS data
long-chain acyl-CoA synthetase
lipid metabolism
status_str publishedVersion
title Long-Chain Acyl-CoA Synthetase 1 Role in Sepsis and Immunity: Perspectives From a Parallel Review of Public Transcriptome Datasets and of the Literature
title_full Long-Chain Acyl-CoA Synthetase 1 Role in Sepsis and Immunity: Perspectives From a Parallel Review of Public Transcriptome Datasets and of the Literature
title_fullStr Long-Chain Acyl-CoA Synthetase 1 Role in Sepsis and Immunity: Perspectives From a Parallel Review of Public Transcriptome Datasets and of the Literature
title_full_unstemmed Long-Chain Acyl-CoA Synthetase 1 Role in Sepsis and Immunity: Perspectives From a Parallel Review of Public Transcriptome Datasets and of the Literature
title_short Long-Chain Acyl-CoA Synthetase 1 Role in Sepsis and Immunity: Perspectives From a Parallel Review of Public Transcriptome Datasets and of the Literature
title_sort Long-Chain Acyl-CoA Synthetase 1 Role in Sepsis and Immunity: Perspectives From a Parallel Review of Public Transcriptome Datasets and of the Literature
topic Biomedical and clinical sciences
Clinical sciences
Immunology
Medical biochemistry and metabolomics
sepsis
neutrophils
OMICS data
long-chain acyl-CoA synthetase
lipid metabolism