5 results on '"Ian M C, Martin"'
Search Results
2. Unique Roles for Streptococcus pneumoniae Phosphodiesterase 2 in Cyclic di-AMP Catabolism and Macrophage Responses
- Author
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Alicia K. Wooten, Anukul T. Shenoy, Emad I. Arafa, Hisashi Akiyama, Ian M. C. Martin, Matthew R. Jones, Lee J. Quinton, Suryaram Gummuluru, Guangchun Bai, and Joseph P. Mizgerd
- Subjects
cyclic di-AMP ,innate immunity ,interferon-β ,macrophages ,pneumococcus ,pneumonia ,Immunologic diseases. Allergy ,RC581-607 - Abstract
Cyclic di-AMP (c-di-AMP) is an important signaling molecule for pneumococci, and as a uniquely prokaryotic product it can be recognized by mammalian cells as a danger signal that triggers innate immunity. Roles of c-di-AMP in directing host responses during pneumococcal infection are only beginning to be defined. We hypothesized that pneumococci with defective c-di-AMP catabolism due to phosphodiesterase deletions could illuminate roles of c-di-AMP in mediating host responses to pneumococcal infection. Pneumococci deficient in phosphodiesterase 2 (Pde2) stimulated a rapid induction of interferon β (IFNβ) expression that was exaggerated in comparison to that induced by wild type (WT) bacteria or bacteria deficient in phosphodiesterase 1. This IFNβ burst was elicited in mouse and human macrophage-like cell lines as well as in primary alveolar macrophages collected from mice with pneumococcal pneumonia. Macrophage hyperactivation by Pde2-deficient pneumococci led to rapid cell death. STING and cGAS were essential for the excessive IFNβ induction, which also required phagocytosis of bacteria and triggered the phosphorylation of IRF3 and IRF7 transcription factors. The select effects of Pde2 deletion were products of a unique role of this enzyme in c-di-AMP catabolism when pneumococci were grown on solid substrate conditions designed to enhance virulence. Because pneumococci with elevated c-di-AMP drive aberrant innate immune responses from macrophages involving hyperactivation of STING, excessive IFNβ expression, and rapid cytotoxicity, we surmise that c-di-AMP is pivotal for directing innate immunity and host-pathogen interactions during pneumococcal pneumonia.
- Published
- 2020
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3. Neutrophil Extracellular Traps as an Exacerbating Factor in Bacterial Pneumonia
- Author
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Nathan L. Sanders, Ian M. C. Martin, Arjun Sharma, Matthew R. Jones, Lee J. Quinton, Markus Bosmann, and Joseph P. Mizgerd
- Subjects
Histones ,Inflammation ,Host Response and Inflammation ,Mice ,Infectious Diseases ,Neutrophils ,Immunology ,Pneumonia, Bacterial ,Animals ,Parasitology ,Extracellular Traps ,Microbiology - Abstract
Neutrophils are capable of extruding neutrophil extracellular traps (NETs), a network of granule proteins and chromatin material, upon activation. NETs provide defense against extracellular microbes, but histones in NETs can also induce cytotoxicity and activate inflammatory responses. The relevance of NETs to bacterial pneumonias is beginning to be defined. In the present study, we found that the extracellular concentration of citrullinated histone H3, a component of NETs, was elevated in bronchoalveolar lavage fluid recovered from mice with diverse bacterial pneumonias and correlated with neutrophil infiltration and cell death in the lungs as well as levels of H4. Because the histone H4 component of NETs is sufficient to stimulate inflammation, we tested its effects in the air spaces of the lungs. Recombinant histone H4 in the noninflamed lung produced only modest effects, but in the setting of neutrophilic inflammation, H4 substantially increased pulmonary neutrophils, NETs, necrosis, and edema. However, blockade of histone H4 with a monoclonal antibody during pneumonia did not significantly alter measures of lung damage. Taken together, these results implicate NETs and extracellular histone H4 in exacerbating the lung injury resulting from bacterial pneumonia.
- Published
- 2022
4. Unique Roles for
- Author
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Alicia K, Wooten, Anukul T, Shenoy, Emad I, Arafa, Hisashi, Akiyama, Ian M C, Martin, Matthew R, Jones, Lee J, Quinton, Suryaram, Gummuluru, Guangchun, Bai, and Joseph P, Mizgerd
- Subjects
Macrophages ,Immunology ,cyclic di-AMP ,Pneumonia, Pneumococcal ,Cyclic Nucleotide Phosphodiesterases, Type 2 ,Immunity, Innate ,Mice, Inbred C57BL ,Mice ,RAW 264.7 Cells ,Streptococcus pneumoniae ,Bacterial Proteins ,interferon-β ,Host-Pathogen Interactions ,Animals ,Humans ,pneumonia ,innate immunity ,pneumococcus ,Dinucleoside Phosphates ,Original Research ,STING - Abstract
Cyclic di-AMP (c-di-AMP) is an important signaling molecule for pneumococci, and as a uniquely prokaryotic product it can be recognized by mammalian cells as a danger signal that triggers innate immunity. Roles of c-di-AMP in directing host responses during pneumococcal infection are only beginning to be defined. We hypothesized that pneumococci with defective c-di-AMP catabolism due to phosphodiesterase deletions could illuminate roles of c-di-AMP in mediating host responses to pneumococcal infection. Pneumococci deficient in phosphodiesterase 2 (Pde2) stimulated a rapid induction of interferon β (IFNβ) expression that was exaggerated in comparison to that induced by wild type (WT) bacteria or bacteria deficient in phosphodiesterase 1. This IFNβ burst was elicited in mouse and human macrophage-like cell lines as well as in primary alveolar macrophages collected from mice with pneumococcal pneumonia. Macrophage hyperactivation by Pde2-deficient pneumococci led to rapid cell death. STING and cGAS were essential for the excessive IFNβ induction, which also required phagocytosis of bacteria and triggered the phosphorylation of IRF3 and IRF7 transcription factors. The select effects of Pde2 deletion were products of a unique role of this enzyme in c-di-AMP catabolism when pneumococci were grown on solid substrate conditions designed to enhance virulence. Because pneumococci with elevated c-di-AMP drive aberrant innate immune responses from macrophages involving hyperactivation of STING, excessive IFNβ expression, and rapid cytotoxicity, we surmise that c-di-AMP is pivotal for directing innate immunity and host-pathogen interactions during pneumococcal pneumonia.
- Published
- 2019
5. Lung CD4
- Author
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Anukul T, Shenoy, Gregory A, Wasserman, Emad I, Arafa, Alicia K, Wooten, Nicole M S, Smith, Ian M C, Martin, Matthew R, Jones, Lee J, Quinton, and Joseph P, Mizgerd
- Subjects
Chemokine CXCL5 ,Neutrophils ,Mice, Transgenic ,Cell Communication ,Respiratory Mucosa ,Article ,Mice ,resident memory T cell ,IL-17A ,Animals ,Humans ,pneumonia ,Lung ,respiratory system ,Pneumonia, Pneumococcal ,lung epithelial cells ,Immunity, Innate ,CD4+ T cells ,Mice, Inbred C57BL ,Streptococcus pneumoniae ,Gene Expression Regulation ,Immune System Diseases ,Airway Remodeling ,Th17 Cells ,Immunologic Memory ,Leukocyte Disorders - Abstract
Previous pneumococcal experience establishes lung-resident IL-17A-producing CD4+ memory TRM cells that accelerate neutrophil recruitment against heterotypic pneumococci. Herein, we unravel a novel crosstalk between CD4+ TRM cells and lung epithelial cells underlying this protective immunity. Depletion of CD4+ cells in pneumococcus-experienced mice diminished CXCL5 (but not CXCL1 or CXCL2) and downstream neutrophil accumulation in the lungs. Epithelial cells from experienced lungs exhibited elevated mRNA for CXCL5 but not other epithelial products like GM-CSF or CCL20, suggesting a skewing by CD4+ TRM cells. Genome-wide expression analyses revealed a significant remodeling of the epithelial transcriptome of infected lungs due to infection history, ~80% of which was CD4+ cell-dependent. The CD4+ TRM cell product IL-17A stabilized CXCL5 but not GM-CSF or CCL20 mRNA in cultured lung epithelial cells, implicating post-transcriptional regulation as a mechanism for altered epithelial responses. These results suggest that epithelial cells in experienced lungs are effectively different owing to their communication with TRM cells. Our study highlights the role of tissue resident adaptive immune cells in fine-tuning epithelial functions to hasten innate immune responses and optimize defense in experienced lungs, a concept which may apply broadly to mucosal immunology.
- Published
- 2019
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