Role of nuclear factor of activated T cells 2 (NFATc2) in allergic asthma
Background We recently described increased NFATc1, IRF4, and NIP45 messenger RNA (mRNA) expression in peripheral blood mononuclear cells (PBMCs) of asthmatic children and adults with multiple allergies. Objective NFATc2 has been described to associate with IRF4 to induce interleukin‐4, and to be inh...
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Published in | Immunity, Inflammation and Disease Vol. 8; no. 4; pp. 704 - 712 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
John Wiley & Sons, Inc
01.12.2020
John Wiley and Sons Inc Wiley |
Subjects | |
Online Access | Get full text |
ISSN | 2050-4527 2050-4527 |
DOI | 10.1002/iid3.360 |
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Abstract | Background
We recently described increased NFATc1, IRF4, and NIP45 messenger RNA (mRNA) expression in peripheral blood mononuclear cells (PBMCs) of asthmatic children and adults with multiple allergies.
Objective
NFATc2 has been described to associate with IRF4 to induce interleukin‐4, and to be inhibited by T‐bet. Here, we analyzed the role of NFATc2 in asthmatic children and adults.
Methods
PBMCs were isolated from the blood of control of asthmatics subjects. Some PBMCs were analyzed untreated and some cultured with and without phytohemagglutinin. Then, RNA was extracted from the cells and cytokines were measured in the supernatants via enzyme‐linked immunosorbent assay or multiplex analysis. RNA was then reverse‐transcribed and NFATc1, NFATC2, IRF4, and T‐bet mRNA were analyzed by real‐time polymerase chain reaction. In addition, in peripheral blood cells, NFATc2 expression was analyzed, in a population of asthmatic children and adults from the Asthma BRIDGE study.
Results
In addition to NFATc1 and NIP45, also NFATc2 was found upregulated in PBMCs and peripheral blood cells from asthmatic children and adults with allergic asthma. Moreover, NFATc1 directly correlated with lymphocytes number whereas NFATc2 correlated with peripheral eosinophilia in asthma.
Conclusions
In addition to NFATc1 and NIP45, NFATc2 was found upregulated in asthma. Moreover, NFATc1 mRNA correlated with lymphocytes both in control and asthma, and NFATC1 and NFATc2 mRNA showed a direct correlation with eosinophils in controls but not in asthma, indicating that NFATc1 is associated with lymphocytes and not eosinophils in asthma.
Clinical Significance
Targeting NFATc2 in T lymphocytes might ameliorate the allergic phenotype in asthmatic subjects.
In addition to NFATc1 and NIP45, NFATc2 was found upregulated in asthma. Moreover, NFATc1 messenger RNA (mRNA) correlated with lymphocytes both in control and asthma. NFATc2 mRNA showed a direct correlation with eosinophils both in controls and asthma, indicating that NFATc1 is associated with lymphocytes and not eosinophils in asthma. |
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AbstractList | We recently described increased NFATc1, IRF4, and NIP45 messenger RNA (mRNA) expression in peripheral blood mononuclear cells (PBMCs) of asthmatic children and adults with multiple allergies.
NFATc2 has been described to associate with IRF4 to induce interleukin-4, and to be inhibited by T-bet. Here, we analyzed the role of NFATc2 in asthmatic children and adults.
PBMCs were isolated from the blood of control of asthmatics subjects. Some PBMCs were analyzed untreated and some cultured with and without phytohemagglutinin. Then, RNA was extracted from the cells and cytokines were measured in the supernatants via enzyme-linked immunosorbent assay or multiplex analysis. RNA was then reverse-transcribed and NFATc1, NFATC2, IRF4, and T-bet mRNA were analyzed by real-time polymerase chain reaction. In addition, in peripheral blood cells, NFATc2 expression was analyzed, in a population of asthmatic children and adults from the Asthma BRIDGE study.
In addition to NFATc1 and NIP45, also NFATc2 was found upregulated in PBMCs and peripheral blood cells from asthmatic children and adults with allergic asthma. Moreover, NFATc1 directly correlated with lymphocytes number whereas NFATc2 correlated with peripheral eosinophilia in asthma.
In addition to NFATc1 and NIP45, NFATc2 was found upregulated in asthma. Moreover, NFATc1 mRNA correlated with lymphocytes both in control and asthma, and NFATC1 and NFATc2 mRNA showed a direct correlation with eosinophils in controls but not in asthma, indicating that NFATc1 is associated with lymphocytes and not eosinophils in asthma.
Targeting NFATc2 in T lymphocytes might ameliorate the allergic phenotype in asthmatic subjects. In addition to NFATc1 and NIP45, NFATc2 was found upregulated in asthma. Moreover, NFATc1 messenger RNA (mRNA) correlated with lymphocytes both in control and asthma. NFATc2 mRNA showed a direct correlation with eosinophils both in controls and asthma, indicating that NFATc1 is associated with lymphocytes and not eosinophils in asthma. Abstract Background We recently described increased NFATc1, IRF4, and NIP45 messenger RNA (mRNA) expression in peripheral blood mononuclear cells (PBMCs) of asthmatic children and adults with multiple allergies. Objective NFATc2 has been described to associate with IRF4 to induce interleukin‐4, and to be inhibited by T‐bet. Here, we analyzed the role of NFATc2 in asthmatic children and adults. Methods PBMCs were isolated from the blood of control of asthmatics subjects. Some PBMCs were analyzed untreated and some cultured with and without phytohemagglutinin. Then, RNA was extracted from the cells and cytokines were measured in the supernatants via enzyme‐linked immunosorbent assay or multiplex analysis. RNA was then reverse‐transcribed and NFATc1, NFATC2, IRF4, and T‐bet mRNA were analyzed by real‐time polymerase chain reaction. In addition, in peripheral blood cells, NFATc2 expression was analyzed, in a population of asthmatic children and adults from the Asthma BRIDGE study. Results In addition to NFATc1 and NIP45, also NFATc2 was found upregulated in PBMCs and peripheral blood cells from asthmatic children and adults with allergic asthma. Moreover, NFATc1 directly correlated with lymphocytes number whereas NFATc2 correlated with peripheral eosinophilia in asthma. Conclusions In addition to NFATc1 and NIP45, NFATc2 was found upregulated in asthma. Moreover, NFATc1 mRNA correlated with lymphocytes both in control and asthma, and NFATC1 and NFATc2 mRNA showed a direct correlation with eosinophils in controls but not in asthma, indicating that NFATc1 is associated with lymphocytes and not eosinophils in asthma. Clinical Significance Targeting NFATc2 in T lymphocytes might ameliorate the allergic phenotype in asthmatic subjects. BackgroundWe recently described increased NFATc1, IRF4, and NIP45 messenger RNA (mRNA) expression in peripheral blood mononuclear cells (PBMCs) of asthmatic children and adults with multiple allergies.ObjectiveNFATc2 has been described to associate with IRF4 to induce interleukin‐4, and to be inhibited by T‐bet. Here, we analyzed the role of NFATc2 in asthmatic children and adults.MethodsPBMCs were isolated from the blood of control of asthmatics subjects. Some PBMCs were analyzed untreated and some cultured with and without phytohemagglutinin. Then, RNA was extracted from the cells and cytokines were measured in the supernatants via enzyme‐linked immunosorbent assay or multiplex analysis. RNA was then reverse‐transcribed and NFATc1, NFATC2, IRF4, and T‐bet mRNA were analyzed by real‐time polymerase chain reaction. In addition, in peripheral blood cells, NFATc2 expression was analyzed, in a population of asthmatic children and adults from the Asthma BRIDGE study.ResultsIn addition to NFATc1 and NIP45, also NFATc2 was found upregulated in PBMCs and peripheral blood cells from asthmatic children and adults with allergic asthma. Moreover, NFATc1 directly correlated with lymphocytes number whereas NFATc2 correlated with peripheral eosinophilia in asthma.ConclusionsIn addition to NFATc1 and NIP45, NFATc2 was found upregulated in asthma. Moreover, NFATc1 mRNA correlated with lymphocytes both in control and asthma, and NFATC1 and NFATc2 mRNA showed a direct correlation with eosinophils in controls but not in asthma, indicating that NFATc1 is associated with lymphocytes and not eosinophils in asthma.Clinical SignificanceTargeting NFATc2 in T lymphocytes might ameliorate the allergic phenotype in asthmatic subjects. Background We recently described increased NFATc1, IRF4, and NIP45 messenger RNA (mRNA) expression in peripheral blood mononuclear cells (PBMCs) of asthmatic children and adults with multiple allergies. Objective NFATc2 has been described to associate with IRF4 to induce interleukin‐4, and to be inhibited by T‐bet. Here, we analyzed the role of NFATc2 in asthmatic children and adults. Methods PBMCs were isolated from the blood of control of asthmatics subjects. Some PBMCs were analyzed untreated and some cultured with and without phytohemagglutinin. Then, RNA was extracted from the cells and cytokines were measured in the supernatants via enzyme‐linked immunosorbent assay or multiplex analysis. RNA was then reverse‐transcribed and NFATc1, NFATC2, IRF4, and T‐bet mRNA were analyzed by real‐time polymerase chain reaction. In addition, in peripheral blood cells, NFATc2 expression was analyzed, in a population of asthmatic children and adults from the Asthma BRIDGE study. Results In addition to NFATc1 and NIP45, also NFATc2 was found upregulated in PBMCs and peripheral blood cells from asthmatic children and adults with allergic asthma. Moreover, NFATc1 directly correlated with lymphocytes number whereas NFATc2 correlated with peripheral eosinophilia in asthma. Conclusions In addition to NFATc1 and NIP45, NFATc2 was found upregulated in asthma. Moreover, NFATc1 mRNA correlated with lymphocytes both in control and asthma, and NFATC1 and NFATc2 mRNA showed a direct correlation with eosinophils in controls but not in asthma, indicating that NFATc1 is associated with lymphocytes and not eosinophils in asthma. Clinical Significance Targeting NFATc2 in T lymphocytes might ameliorate the allergic phenotype in asthmatic subjects. In addition to NFATc1 and NIP45, NFATc2 was found upregulated in asthma. Moreover, NFATc1 messenger RNA (mRNA) correlated with lymphocytes both in control and asthma. NFATc2 mRNA showed a direct correlation with eosinophils both in controls and asthma, indicating that NFATc1 is associated with lymphocytes and not eosinophils in asthma. We recently described increased NFATc1, IRF4, and NIP45 messenger RNA (mRNA) expression in peripheral blood mononuclear cells (PBMCs) of asthmatic children and adults with multiple allergies.BACKGROUNDWe recently described increased NFATc1, IRF4, and NIP45 messenger RNA (mRNA) expression in peripheral blood mononuclear cells (PBMCs) of asthmatic children and adults with multiple allergies.NFATc2 has been described to associate with IRF4 to induce interleukin-4, and to be inhibited by T-bet. Here, we analyzed the role of NFATc2 in asthmatic children and adults.OBJECTIVENFATc2 has been described to associate with IRF4 to induce interleukin-4, and to be inhibited by T-bet. Here, we analyzed the role of NFATc2 in asthmatic children and adults.PBMCs were isolated from the blood of control of asthmatics subjects. Some PBMCs were analyzed untreated and some cultured with and without phytohemagglutinin. Then, RNA was extracted from the cells and cytokines were measured in the supernatants via enzyme-linked immunosorbent assay or multiplex analysis. RNA was then reverse-transcribed and NFATc1, NFATC2, IRF4, and T-bet mRNA were analyzed by real-time polymerase chain reaction. In addition, in peripheral blood cells, NFATc2 expression was analyzed, in a population of asthmatic children and adults from the Asthma BRIDGE study.METHODSPBMCs were isolated from the blood of control of asthmatics subjects. Some PBMCs were analyzed untreated and some cultured with and without phytohemagglutinin. Then, RNA was extracted from the cells and cytokines were measured in the supernatants via enzyme-linked immunosorbent assay or multiplex analysis. RNA was then reverse-transcribed and NFATc1, NFATC2, IRF4, and T-bet mRNA were analyzed by real-time polymerase chain reaction. In addition, in peripheral blood cells, NFATc2 expression was analyzed, in a population of asthmatic children and adults from the Asthma BRIDGE study.In addition to NFATc1 and NIP45, also NFATc2 was found upregulated in PBMCs and peripheral blood cells from asthmatic children and adults with allergic asthma. Moreover, NFATc1 directly correlated with lymphocytes number whereas NFATc2 correlated with peripheral eosinophilia in asthma.RESULTSIn addition to NFATc1 and NIP45, also NFATc2 was found upregulated in PBMCs and peripheral blood cells from asthmatic children and adults with allergic asthma. Moreover, NFATc1 directly correlated with lymphocytes number whereas NFATc2 correlated with peripheral eosinophilia in asthma.In addition to NFATc1 and NIP45, NFATc2 was found upregulated in asthma. Moreover, NFATc1 mRNA correlated with lymphocytes both in control and asthma, and NFATC1 and NFATc2 mRNA showed a direct correlation with eosinophils in controls but not in asthma, indicating that NFATc1 is associated with lymphocytes and not eosinophils in asthma.CONCLUSIONSIn addition to NFATc1 and NIP45, NFATc2 was found upregulated in asthma. Moreover, NFATc1 mRNA correlated with lymphocytes both in control and asthma, and NFATC1 and NFATc2 mRNA showed a direct correlation with eosinophils in controls but not in asthma, indicating that NFATc1 is associated with lymphocytes and not eosinophils in asthma.Targeting NFATc2 in T lymphocytes might ameliorate the allergic phenotype in asthmatic subjects.CLINICAL SIGNIFICANCETargeting NFATc2 in T lymphocytes might ameliorate the allergic phenotype in asthmatic subjects. |
Author | Akdis, Mubeccel Finotto, Susetta Kiefer, Alexander Mirzakhani, Hooman Papadopoulos, Nikolaos G. Raby, Benjamin A. Weiss, Scott T. Zimmermann, Theodor Stanic, Barbara Xepapadaki, Paraskevi Jakobi, Marielena Rauh, Manfred |
AuthorAffiliation | 2 Department of Allergy and Pneumology, Children's Hospital, Universitätsklinikum Erlangen Friedrich‐Alexander‐Universität (FAU) Erlangen‐Nürnberg Erlangen Germany 6 Centre for Respiratory Medicine and Allergy University of Manchester UK 5 Swiss Institute of Allergy and Asthma Research (SIAF) University of Zurich Davos Wolfgang Switzerland 3 Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital Harvard Medical School Boston Massachusetts USA 4 Department of Allergy, 2nd Pediatric Clinic National and Kapodistrian University of Athens Athens Greece 1 Department of Molecular Pneumology, Universitätsklinikum Erlangen Friedrich‐Alexander‐Universität Erlangen‐Nürnberg Erlangen Germany |
AuthorAffiliation_xml | – name: 4 Department of Allergy, 2nd Pediatric Clinic National and Kapodistrian University of Athens Athens Greece – name: 2 Department of Allergy and Pneumology, Children's Hospital, Universitätsklinikum Erlangen Friedrich‐Alexander‐Universität (FAU) Erlangen‐Nürnberg Erlangen Germany – name: 6 Centre for Respiratory Medicine and Allergy University of Manchester UK – name: 1 Department of Molecular Pneumology, Universitätsklinikum Erlangen Friedrich‐Alexander‐Universität Erlangen‐Nürnberg Erlangen Germany – name: 3 Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital Harvard Medical School Boston Massachusetts USA – name: 5 Swiss Institute of Allergy and Asthma Research (SIAF) University of Zurich Davos Wolfgang Switzerland |
Author_xml | – sequence: 1 givenname: Marielena surname: Jakobi fullname: Jakobi, Marielena organization: Friedrich‐Alexander‐Universität Erlangen‐Nürnberg – sequence: 2 givenname: Alexander surname: Kiefer fullname: Kiefer, Alexander organization: Friedrich‐Alexander‐Universität (FAU) Erlangen‐Nürnberg – sequence: 3 givenname: Hooman orcidid: 0000-0002-2290-4436 surname: Mirzakhani fullname: Mirzakhani, Hooman organization: Harvard Medical School – sequence: 4 givenname: Manfred surname: Rauh fullname: Rauh, Manfred organization: Harvard Medical School – sequence: 5 givenname: Theodor surname: Zimmermann fullname: Zimmermann, Theodor organization: Harvard Medical School – sequence: 6 givenname: Paraskevi surname: Xepapadaki fullname: Xepapadaki, Paraskevi organization: National and Kapodistrian University of Athens – sequence: 7 givenname: Barbara surname: Stanic fullname: Stanic, Barbara organization: University of Zurich – sequence: 8 givenname: Mubeccel surname: Akdis fullname: Akdis, Mubeccel organization: University of Zurich – sequence: 9 givenname: Nikolaos G. orcidid: 0000-0002-4448-3468 surname: Papadopoulos fullname: Papadopoulos, Nikolaos G. organization: University of Manchester – sequence: 10 givenname: Benjamin A. surname: Raby fullname: Raby, Benjamin A. organization: Harvard Medical School – sequence: 11 givenname: Scott T. surname: Weiss fullname: Weiss, Scott T. organization: Harvard Medical School – sequence: 12 givenname: Susetta orcidid: 0000-0001-7623-7977 surname: Finotto fullname: Finotto, Susetta email: susetta.finotto@uk-erlangen.de organization: Friedrich‐Alexander‐Universität Erlangen‐Nürnberg |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33079489$$D View this record in MEDLINE/PubMed |
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Keywords | animals T cells allergy processes human eosinophils cells |
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Notes | The present work was performed in fulfillment of the requirements for obtaining the degree “Dr. med.” for Marielena Jakobi. Marielena Jakobi, Alexander Kiefer, and Hooman Mirzakhani contributed equally to this work. Correction added after online publication on 28 October 2020: “Affiliation of Barbara Stanic was changed from Musculoskeletal Infection, AO Research Institute Davos, Davos Platz, Switzerland to Swiss Institute of Allergy and Asthma Research (SIAF), University of Zurich, Davos Wolfgang, Switzerland” ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
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We recently described increased NFATc1, IRF4, and NIP45 messenger RNA (mRNA) expression in peripheral blood mononuclear cells (PBMCs) of asthmatic... We recently described increased NFATc1, IRF4, and NIP45 messenger RNA (mRNA) expression in peripheral blood mononuclear cells (PBMCs) of asthmatic children and... BackgroundWe recently described increased NFATc1, IRF4, and NIP45 messenger RNA (mRNA) expression in peripheral blood mononuclear cells (PBMCs) of asthmatic... In addition to NFATc1 and NIP45, NFATc2 was found upregulated in asthma. Moreover, NFATc1 messenger RNA (mRNA) correlated with lymphocytes both in control and... Abstract Background We recently described increased NFATc1, IRF4, and NIP45 messenger RNA (mRNA) expression in peripheral blood mononuclear cells (PBMCs) of... |
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SubjectTerms | Age Allergens Allergies allergy processes animals Asthma Blood Cell culture Clinical trials Collaboration Data collection Eosinophils eosinophils cells Families & family life Gene expression human Humans Laboratories Leukocytes, Mononuclear Lymphocytes NFATC Transcription Factors - metabolism Original Research Pediatrics Preschool children Spirometry T cells T-Lymphocytes Transcription factors Transplants & implants |
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Title | Role of nuclear factor of activated T cells 2 (NFATc2) in allergic asthma |
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