Transcriptional Profiling of Monocytes Deficient in Nuclear Orphan Receptors NR4A2 and NR4A3 Reveals Distinct Signalling Roles Related to Antigen Presentation and Viral Response

The nuclear receptor sub-family 4 group A (NR4A) family are early response genes that encode proteins that are activated in several tissues/cells in response to a variety of stressors. The NR4A family comprises NR4A1, NR4A2 and NR4A3 of which NR4A2 and NR4A3 are under researched and less understood,...

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Main Authors: David E. Phelan, Masahiko Shigemura, Sarah Aldhafiri, Catarina Mota, Thomas J. Hall, Jacob I. Sznajder, Evelyn P. Murphy, Daniel Crean, Eoin P. Cummins
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-06-01
Series:Frontiers in Immunology
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Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2021.676644/full
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author David E. Phelan
David E. Phelan
Masahiko Shigemura
Sarah Aldhafiri
Sarah Aldhafiri
Catarina Mota
Catarina Mota
Thomas J. Hall
Jacob I. Sznajder
Evelyn P. Murphy
Daniel Crean
Daniel Crean
Eoin P. Cummins
Eoin P. Cummins
author_facet David E. Phelan
David E. Phelan
Masahiko Shigemura
Sarah Aldhafiri
Sarah Aldhafiri
Catarina Mota
Catarina Mota
Thomas J. Hall
Jacob I. Sznajder
Evelyn P. Murphy
Daniel Crean
Daniel Crean
Eoin P. Cummins
Eoin P. Cummins
author_sort David E. Phelan
collection DOAJ
description The nuclear receptor sub-family 4 group A (NR4A) family are early response genes that encode proteins that are activated in several tissues/cells in response to a variety of stressors. The NR4A family comprises NR4A1, NR4A2 and NR4A3 of which NR4A2 and NR4A3 are under researched and less understood, particularly in the context of immune cells. NR4A expression is associated with multiple diseases e.g. arthritis and atherosclerosis and the development of NR4A-targetting molecules as therapeutics is a current focus in this research field. Here, we use a combination of RNA-sequencing coupled with strategic bioinformatic analysis to investigate the down-stream effects of NR4A2 and NR4A3 in monocytes and dissect their common and distinct signalling roles. Our data reveals that NR4A2 and NR4A3 depletion has a robust and broad-reaching effect on transcription in both the unstimulated state and in the presence of LPS. Interestingly, many of the genes affected were present in both the unstimulated and stimulated states revealing a previously unappreciated role for the NR4As in unstimulated cells. Strategic clustering and bioinformatic analysis identified both distinct and common transcriptional roles for NR4A2 and NR4A3 in monocytes. NR4A2 notably was linked by both bioinformatic clustering analysis and transcription factor interactome analysis to pathways associated with antigen presentation and regulation of MHC genes. NR4A3 in contrast was more closely linked to pathways associated with viral response. Functional studies further support our data analysis pointing towards preferential/selective roles for NR4A2 in the regulation of antigen processing with common roles for NR4A2 and NR4A3 evident with respect to cell migration. Taken together this study provides novel mechanistic insights into the role of the enigmatic nuclear receptors NR4A2 and NR4A3 in monocytes.
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spelling doaj.art-5f6313cef0a746c58a9dc45ec6c10ed82022-12-21T20:38:18ZengFrontiers Media S.A.Frontiers in Immunology1664-32242021-06-011210.3389/fimmu.2021.676644676644Transcriptional Profiling of Monocytes Deficient in Nuclear Orphan Receptors NR4A2 and NR4A3 Reveals Distinct Signalling Roles Related to Antigen Presentation and Viral ResponseDavid E. Phelan0David E. Phelan1Masahiko Shigemura2Sarah Aldhafiri3Sarah Aldhafiri4Catarina Mota5Catarina Mota6Thomas J. Hall7Jacob I. Sznajder8Evelyn P. Murphy9Daniel Crean10Daniel Crean11Eoin P. Cummins12Eoin P. Cummins13School of Medicine, University College Dublin, Dublin, IrelandConway Institute of Biomolecular and Biomedical Research, University College Dublin, Dublin, IrelandDivision of Pulmonary and Critical Care Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, United StatesConway Institute of Biomolecular and Biomedical Research, University College Dublin, Dublin, IrelandAnimal Genomics Laboratory, School of Veterinary Medicine, University College Dublin, Dublin, IrelandSchool of Medicine, University College Dublin, Dublin, IrelandConway Institute of Biomolecular and Biomedical Research, University College Dublin, Dublin, IrelandSchool of Agriculture and Food Science, University College Dublin, Dublin, IrelandDivision of Pulmonary and Critical Care Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, United StatesSchool of Medicine, University of Limerick, Limerick, IrelandConway Institute of Biomolecular and Biomedical Research, University College Dublin, Dublin, IrelandAnimal Genomics Laboratory, School of Veterinary Medicine, University College Dublin, Dublin, IrelandSchool of Medicine, University College Dublin, Dublin, IrelandConway Institute of Biomolecular and Biomedical Research, University College Dublin, Dublin, IrelandThe nuclear receptor sub-family 4 group A (NR4A) family are early response genes that encode proteins that are activated in several tissues/cells in response to a variety of stressors. The NR4A family comprises NR4A1, NR4A2 and NR4A3 of which NR4A2 and NR4A3 are under researched and less understood, particularly in the context of immune cells. NR4A expression is associated with multiple diseases e.g. arthritis and atherosclerosis and the development of NR4A-targetting molecules as therapeutics is a current focus in this research field. Here, we use a combination of RNA-sequencing coupled with strategic bioinformatic analysis to investigate the down-stream effects of NR4A2 and NR4A3 in monocytes and dissect their common and distinct signalling roles. Our data reveals that NR4A2 and NR4A3 depletion has a robust and broad-reaching effect on transcription in both the unstimulated state and in the presence of LPS. Interestingly, many of the genes affected were present in both the unstimulated and stimulated states revealing a previously unappreciated role for the NR4As in unstimulated cells. Strategic clustering and bioinformatic analysis identified both distinct and common transcriptional roles for NR4A2 and NR4A3 in monocytes. NR4A2 notably was linked by both bioinformatic clustering analysis and transcription factor interactome analysis to pathways associated with antigen presentation and regulation of MHC genes. NR4A3 in contrast was more closely linked to pathways associated with viral response. Functional studies further support our data analysis pointing towards preferential/selective roles for NR4A2 in the regulation of antigen processing with common roles for NR4A2 and NR4A3 evident with respect to cell migration. Taken together this study provides novel mechanistic insights into the role of the enigmatic nuclear receptors NR4A2 and NR4A3 in monocytes.https://www.frontiersin.org/articles/10.3389/fimmu.2021.676644/fullNR4ANR4A2NR4A3nuclear orphan receptornuclear receptormonocytes
spellingShingle David E. Phelan
David E. Phelan
Masahiko Shigemura
Sarah Aldhafiri
Sarah Aldhafiri
Catarina Mota
Catarina Mota
Thomas J. Hall
Jacob I. Sznajder
Evelyn P. Murphy
Daniel Crean
Daniel Crean
Eoin P. Cummins
Eoin P. Cummins
Transcriptional Profiling of Monocytes Deficient in Nuclear Orphan Receptors NR4A2 and NR4A3 Reveals Distinct Signalling Roles Related to Antigen Presentation and Viral Response
Frontiers in Immunology
NR4A
NR4A2
NR4A3
nuclear orphan receptor
nuclear receptor
monocytes
title Transcriptional Profiling of Monocytes Deficient in Nuclear Orphan Receptors NR4A2 and NR4A3 Reveals Distinct Signalling Roles Related to Antigen Presentation and Viral Response
title_full Transcriptional Profiling of Monocytes Deficient in Nuclear Orphan Receptors NR4A2 and NR4A3 Reveals Distinct Signalling Roles Related to Antigen Presentation and Viral Response
title_fullStr Transcriptional Profiling of Monocytes Deficient in Nuclear Orphan Receptors NR4A2 and NR4A3 Reveals Distinct Signalling Roles Related to Antigen Presentation and Viral Response
title_full_unstemmed Transcriptional Profiling of Monocytes Deficient in Nuclear Orphan Receptors NR4A2 and NR4A3 Reveals Distinct Signalling Roles Related to Antigen Presentation and Viral Response
title_short Transcriptional Profiling of Monocytes Deficient in Nuclear Orphan Receptors NR4A2 and NR4A3 Reveals Distinct Signalling Roles Related to Antigen Presentation and Viral Response
title_sort transcriptional profiling of monocytes deficient in nuclear orphan receptors nr4a2 and nr4a3 reveals distinct signalling roles related to antigen presentation and viral response
topic NR4A
NR4A2
NR4A3
nuclear orphan receptor
nuclear receptor
monocytes
url https://www.frontiersin.org/articles/10.3389/fimmu.2021.676644/full
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