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Bruton’s Tyrosine Kinase-Mediated Signaling in Myeloid Cells Is Required for Protective Innate Immunity During Pneumococcal Pneumonia

Bruton’s tyrosine kinase (Btk) is a cytoplasmic kinase expressed in B cells and myeloid cells. It is essential for B cell development and natural antibody-mediated host defense against bacteria in humans and mice, but little is known about the role of Btk in innate host defense in vivo. Previous stu...

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Autores principales: de Porto, Alexander P., Liu, Zhe, de Beer, Regina, Florquin, Sandrine, Roelofs, Joris J. T. H., de Boer, Onno J., den Haan, Joke M. M., Hendriks, Rudi W., van ‘t Veer, Cornelis, van der Poll, Tom, de Vos, Alex F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450579/
https://www.ncbi.nlm.nih.gov/pubmed/34552589
http://dx.doi.org/10.3389/fimmu.2021.723967
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author de Porto, Alexander P.
Liu, Zhe
de Beer, Regina
Florquin, Sandrine
Roelofs, Joris J. T. H.
de Boer, Onno J.
den Haan, Joke M. M.
Hendriks, Rudi W.
van ‘t Veer, Cornelis
van der Poll, Tom
de Vos, Alex F.
author_facet de Porto, Alexander P.
Liu, Zhe
de Beer, Regina
Florquin, Sandrine
Roelofs, Joris J. T. H.
de Boer, Onno J.
den Haan, Joke M. M.
Hendriks, Rudi W.
van ‘t Veer, Cornelis
van der Poll, Tom
de Vos, Alex F.
author_sort de Porto, Alexander P.
collection PubMed
description Bruton’s tyrosine kinase (Btk) is a cytoplasmic kinase expressed in B cells and myeloid cells. It is essential for B cell development and natural antibody-mediated host defense against bacteria in humans and mice, but little is known about the role of Btk in innate host defense in vivo. Previous studies have indicated that lack of (natural) antibodies is paramount for impaired host defense against Streptococcus (S.) pneumoniae in patients and mice with a deficiency in functional Btk. In the present study, we re-examined the role of Btk in B cells and myeloid cells during pneumococcal pneumonia and sepsis in mice. The antibacterial defense of Btk(-/-) mice was severely impaired during pneumococcal pneumosepsis and restoration of natural antibody production in Btk(-/-) mice by transgenic expression of Btk specifically in B cells did not suffice to protect against infection. Btk(-/-) mice with reinforced Btk expression in MhcII(+) cells, including B cells, dendritic cells and macrophages, showed improved antibacterial defense as compared to Btk(-/-) mice. Bacterial outgrowth in Lysmcre-Btk(fl)/Y mice was unaltered despite a reduced capacity of Btk-deficient alveolar macrophages to respond to pneumococci. Mrp8cre-Btk(fl)/Y mice with a neutrophil specific paucity in Btk expression, however, demonstrated impaired antibacterial defense. Neutrophils of Mrp8cre-Btk(fl)/Y mice displayed reduced release of granule content after pulmonary installation of lipoteichoic acid, a gram-positive bacterial cell wall component relevant for pneumococci. Moreover, Btk deficient neutrophils showed impaired degranulation and phagocytosis upon incubation with pneumococci ex vivo. Taken together, the results of our study indicate that besides regulating B cell-mediated immunity, Btk is critical for regulation of myeloid cell-mediated, and particularly neutrophil-mediated, innate host defense against S. pneumoniae in vivo.
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spelling pubmed-84505792021-09-21 Bruton’s Tyrosine Kinase-Mediated Signaling in Myeloid Cells Is Required for Protective Innate Immunity During Pneumococcal Pneumonia de Porto, Alexander P. Liu, Zhe de Beer, Regina Florquin, Sandrine Roelofs, Joris J. T. H. de Boer, Onno J. den Haan, Joke M. M. Hendriks, Rudi W. van ‘t Veer, Cornelis van der Poll, Tom de Vos, Alex F. Front Immunol Immunology Bruton’s tyrosine kinase (Btk) is a cytoplasmic kinase expressed in B cells and myeloid cells. It is essential for B cell development and natural antibody-mediated host defense against bacteria in humans and mice, but little is known about the role of Btk in innate host defense in vivo. Previous studies have indicated that lack of (natural) antibodies is paramount for impaired host defense against Streptococcus (S.) pneumoniae in patients and mice with a deficiency in functional Btk. In the present study, we re-examined the role of Btk in B cells and myeloid cells during pneumococcal pneumonia and sepsis in mice. The antibacterial defense of Btk(-/-) mice was severely impaired during pneumococcal pneumosepsis and restoration of natural antibody production in Btk(-/-) mice by transgenic expression of Btk specifically in B cells did not suffice to protect against infection. Btk(-/-) mice with reinforced Btk expression in MhcII(+) cells, including B cells, dendritic cells and macrophages, showed improved antibacterial defense as compared to Btk(-/-) mice. Bacterial outgrowth in Lysmcre-Btk(fl)/Y mice was unaltered despite a reduced capacity of Btk-deficient alveolar macrophages to respond to pneumococci. Mrp8cre-Btk(fl)/Y mice with a neutrophil specific paucity in Btk expression, however, demonstrated impaired antibacterial defense. Neutrophils of Mrp8cre-Btk(fl)/Y mice displayed reduced release of granule content after pulmonary installation of lipoteichoic acid, a gram-positive bacterial cell wall component relevant for pneumococci. Moreover, Btk deficient neutrophils showed impaired degranulation and phagocytosis upon incubation with pneumococci ex vivo. Taken together, the results of our study indicate that besides regulating B cell-mediated immunity, Btk is critical for regulation of myeloid cell-mediated, and particularly neutrophil-mediated, innate host defense against S. pneumoniae in vivo. Frontiers Media S.A. 2021-09-06 /pmc/articles/PMC8450579/ /pubmed/34552589 http://dx.doi.org/10.3389/fimmu.2021.723967 Text en Copyright © 2021 de Porto, Liu, de Beer, Florquin, Roelofs, de Boer, den Haan, Hendriks, van ‘t Veer, van der Poll and de Vos https://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
de Porto, Alexander P.
Liu, Zhe
de Beer, Regina
Florquin, Sandrine
Roelofs, Joris J. T. H.
de Boer, Onno J.
den Haan, Joke M. M.
Hendriks, Rudi W.
van ‘t Veer, Cornelis
van der Poll, Tom
de Vos, Alex F.
Bruton’s Tyrosine Kinase-Mediated Signaling in Myeloid Cells Is Required for Protective Innate Immunity During Pneumococcal Pneumonia
title Bruton’s Tyrosine Kinase-Mediated Signaling in Myeloid Cells Is Required for Protective Innate Immunity During Pneumococcal Pneumonia
title_full Bruton’s Tyrosine Kinase-Mediated Signaling in Myeloid Cells Is Required for Protective Innate Immunity During Pneumococcal Pneumonia
title_fullStr Bruton’s Tyrosine Kinase-Mediated Signaling in Myeloid Cells Is Required for Protective Innate Immunity During Pneumococcal Pneumonia
title_full_unstemmed Bruton’s Tyrosine Kinase-Mediated Signaling in Myeloid Cells Is Required for Protective Innate Immunity During Pneumococcal Pneumonia
title_short Bruton’s Tyrosine Kinase-Mediated Signaling in Myeloid Cells Is Required for Protective Innate Immunity During Pneumococcal Pneumonia
title_sort bruton’s tyrosine kinase-mediated signaling in myeloid cells is required for protective innate immunity during pneumococcal pneumonia
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450579/
https://www.ncbi.nlm.nih.gov/pubmed/34552589
http://dx.doi.org/10.3389/fimmu.2021.723967
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