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1.
JCI Insight ; 9(4)2024 Jan 16.
Article in English | MEDLINE | ID: mdl-38227369

ABSTRACT

Hypercapnia, elevation of the partial pressure of CO2 in blood and tissues, is a risk factor for mortality in patients with severe acute and chronic lung diseases. We previously showed that hypercapnia inhibits multiple macrophage and neutrophil antimicrobial functions and that elevated CO2 increases the mortality of bacterial and viral pneumonia in mice. Here, we show that normoxic hypercapnia downregulates innate immune and antiviral gene programs in alveolar macrophages (AMØs). We also show that zinc finger homeobox 3 (Zfhx3) - a mammalian ortholog of zfh2, which mediates hypercapnic immune suppression in Drosophila - is expressed in mouse and human macrophages. Deletion of Zfhx3 in the myeloid lineage blocked the suppressive effect of hypercapnia on immune gene expression in AMØs and decreased viral replication, inflammatory lung injury, and mortality in hypercapnic mice infected with influenza A virus. To our knowledge, our results establish Zfhx3 as the first known mammalian mediator of CO2 effects on immune gene expression and lay the basis for future studies to identify therapeutic targets to interrupt hypercapnic immunosuppression in patients with advanced lung disease.


Subject(s)
Influenza A virus , Lung Diseases , Animals , Humans , Mice , Carbon Dioxide/pharmacology , Drosophila , Homeodomain Proteins/genetics , Hypercapnia , Lung , Macrophages , Mammals
2.
bioRxiv ; 2023 Mar 01.
Article in English | MEDLINE | ID: mdl-36909510

ABSTRACT

Hypercapnia, elevation of the partial pressure of CO 2 in blood and tissues, is a risk factor for mortality in patients with severe acute and chronic lung diseases. We previously showed that hypercapnia inhibits multiple macrophage and neutrophil antimicrobial functions, and that elevated CO 2 increases the mortality of bacterial and viral pneumonia in mice. Here, we show that normoxic hypercapnia downregulates innate immune and antiviral gene programs in alveolar macrophages (AMØs). We also show that zinc finger homeobox 3 (Zfhx3), mammalian ortholog of zfh2, which mediates hypercapnic immune suppression in Drosophila , is expressed in mouse and human MØs. Deletion of Zfhx3 in the myeloid lineage blocked the suppressive effect of hypercapnia on immune gene expression in AMØs and decreased viral replication, inflammatory lung injury and mortality in hypercapnic mice infected with influenza A virus. Our results establish Zfhx3 as the first known mammalian mediator of CO 2 effects on immune gene expression and lay the basis for future studies to identify therapeutic targets to interrupt hypercapnic immunosuppression in patients with advanced lung diseases.

3.
Curr Biol ; 31(23): R1517-R1520, 2021 12 06.
Article in English | MEDLINE | ID: mdl-34875239

ABSTRACT

A new study reveals that the Drosophila tracheal system is disassembled during pupation via ecdysone-dependent remodeling of the extracellular matrix, which then signals through the Hippo-Yorkie/YAP network to induce apoptosis.


Subject(s)
Drosophila Proteins , Animals , Drosophila , Drosophila Proteins/genetics , Nuclear Proteins , Protein Serine-Threonine Kinases/genetics , Trans-Activators
4.
Interface Focus ; 11(2): 20200039, 2021 Apr 06.
Article in English | MEDLINE | ID: mdl-33633835

ABSTRACT

Hypercapnia, the elevation of CO2 in blood and tissues, commonly occurs in severe acute and chronic respiratory diseases and is associated with increased risk of death. Recent studies have shown that hypercapnia inhibits expression of select innate immune genes and suppresses host defence against bacterial and viral pneumonia in mice. In the current study, we evaluated the effect of culture under conditions of hypercapnia (20% CO2) versus normocapnia (5% CO2), both with normoxia, on global gene transcription in human THP-1 and mouse RAW 264.7 macrophages stimulated with lipopolysaccharide (LPS). We found that hypercapnia selectively downregulated transcription of LPS-induced genes associated with innate immunity, antiviral response, type I interferon signalling, cytokine signalling and other inflammatory pathways in both human and mouse macrophages. Simultaneously, hypercapnia increased expression of LPS-downregulated genes associated with mitosis, DNA replication and DNA repair. These CO2-induced changes in macrophage gene expression help explain hypercapnic suppression of antibacterial and antiviral host defence in mice and reveal a mechanism that may underlie, at least in part, the high mortality of patients with severe lung disease and hypercapnia.

5.
Fly (Austin) ; 14(1-4): 34-48, 2020.
Article in English | MEDLINE | ID: mdl-33016195

ABSTRACT

Genome editing via homology-directed repair (HDR) has made possible precise and deliberate modifications to gene sequences. CRISPR/Cas9-mediated HDR is the simplest means to carry this out. However, technical challenges remain to improve efficiency and broaden applicability to any genetic background of Drosophila melanogaster as well as to other Drosophila species. To address these issues, we developed a two-stage marker-assisted strategy in which embryos are injected with RNPs and pre-screened using T7EI. Using sgRNA in complex with recombinant Cas9 protein, we assayed each sgRNA for genome-cutting efficiency. We then conducted HDR using sgRNAs that efficiently cut target genes and the application of a transformation marker that generates RNAi against eyes absent. This allows for screening based on eye morphology rather than colour. These new tools can be used to make a single change or a series of allelic substitutions in a region of interest, or to create additional genetic tools such as balancer chromosomes.


Subject(s)
CRISPR-Associated Protein 9/metabolism , Drosophila melanogaster/genetics , Gene Editing/methods , RNA, Guide, Kinetoplastida/metabolism , Ribonucleoproteins/metabolism , Animals , Chromosomes , Drosophila melanogaster/embryology , RNA, Guide, Kinetoplastida/genetics , Ribonucleoproteins/genetics
6.
J Immunol ; 205(2): 489-501, 2020 07 15.
Article in English | MEDLINE | ID: mdl-32540997

ABSTRACT

Hypercapnia (HC), elevation of the partial pressure of CO2 in blood and tissues, is a risk factor for mortality in patients with severe acute and chronic lung diseases. We previously showed that HC inhibits multiple macrophage and neutrophil antimicrobial functions and increases the mortality of bacterial pneumonia in mice. In this study, we show that normoxic HC increases viral replication, lung injury, and mortality in mice infected with influenza A virus (IAV). Elevated CO2 increased IAV replication and inhibited antiviral gene and protein expression in macrophages in vivo and in vitro. HC potentiated IAV-induced activation of Akt, whereas specific pharmacologic inhibition or short hairpin RNA knockdown of Akt1 in alveolar macrophages blocked HC's effects on IAV growth and the macrophage antiviral response. Our findings suggest that targeting Akt1 or the downstream pathways through which elevated CO2 signals could enhance macrophage antiviral host defense and improve clinical outcomes in hypercapnic patients with advanced lung disease.


Subject(s)
Hypercapnia/immunology , Influenza A virus/physiology , Influenza, Human/immunology , Lung/pathology , Macrophages/immunology , Oncogene Protein v-akt/metabolism , Orthomyxoviridae Infections/immunology , Animals , Cells, Cultured , Gene Expression Regulation , Humans , Immunity, Cellular , Immunosuppression Therapy , Lung/virology , Macrophage Activation , Mice , Mice, Inbred C57BL , Signal Transduction , Virus Replication
7.
Sci Rep ; 9(1): 18251, 2019 12 03.
Article in English | MEDLINE | ID: mdl-31796806

ABSTRACT

Carbon dioxide (CO2) is sensed by cells and can trigger signals to modify gene expression in different tissues leading to changes in organismal functions. Despite accumulating evidence that several pathways in various organisms are responsive to CO2 elevation (hypercapnia), it has yet to be elucidated how hypercapnia activates genes and signaling pathways, or whether they interact, are integrated, or are conserved across species. Here, we performed a large-scale transcriptomic study to explore the interaction/integration/conservation of hypercapnia-induced genomic responses in mammals (mice and humans) as well as invertebrates (Caenorhabditis elegans and Drosophila melanogaster). We found that hypercapnia activated genes that regulate Wnt signaling in mouse lungs and skeletal muscles in vivo and in several cell lines of different tissue origin. Hypercapnia-responsive Wnt pathway homologues were similarly observed in secondary analysis of available transcriptomic datasets of hypercapnia in a human bronchial cell line, flies and nematodes. Our data suggest the evolutionarily conserved role of high CO2 in regulating Wnt pathway genes.


Subject(s)
Caenorhabditis elegans/metabolism , Carbon Dioxide/pharmacology , Drosophila melanogaster/metabolism , Wnt Signaling Pathway/drug effects , Animals , Bronchi/cytology , Bronchi/metabolism , Caenorhabditis elegans/drug effects , Cell Line , Drosophila melanogaster/drug effects , Gene Expression Profiling , Humans , Hypercapnia/metabolism , Male , Mice , Mice, Inbred C57BL , Real-Time Polymerase Chain Reaction , Tissue Array Analysis
8.
Development ; 146(12)2019 05 16.
Article in English | MEDLINE | ID: mdl-30967427

ABSTRACT

Biological tubes are essential for animal survival, and their functions are dependent on tube shape. Analyzing the contributions of cell shape and organization to the morphogenesis of small tubes has been hampered by the limitations of existing programs in quantifying cell geometry on highly curved tubular surfaces and calculating tube-specific parameters. We therefore developed QuBiT (Quantitative Tool for Biological Tubes) and used it to analyze morphogenesis of the embryonic Drosophila trachea (airway). In the main tube, we find previously unknown anterior-to-posterior (A-P) gradients of cell apical orientation and aspect ratio, and periodicity in the organization of apical cell surfaces. Inferred cell intercalation during development dampens an A-P gradient of the number of cells per cross-section of the tube, but does not change the patterns of cell connectivity. Computationally 'unrolling' the apical surface of wild-type trachea and the hindgut reveals previously unrecognized spatial patterns of the apical marker Uninflatable and a non-redundant role for the Na+/K+ ATPase in apical marker organization. These unexpected findings demonstrate the importance of a computational tool for analyzing small diameter biological tubes.


Subject(s)
Drosophila/embryology , Epithelium/embryology , Gene Expression Profiling , Gene Expression Regulation, Developmental , Trachea/embryology , Adenosine Triphosphate/chemistry , Animals , Body Patterning , CRISPR-Cas Systems , Cell Lineage , Computational Biology/instrumentation , Crosses, Genetic , Drosophila Proteins/metabolism , Membrane Proteins/metabolism , Models, Biological , Sodium-Potassium-Exchanging ATPase/metabolism
9.
Nat Commun ; 10(1): 1031, 2019 03 04.
Article in English | MEDLINE | ID: mdl-30833576

ABSTRACT

Although well known for its role in apoptosis, the executioner caspase DrICE has a non-apoptotic function that is required for elongation of the epithelial tubes of the Drosophila tracheal system. Here, we show that DrICE acts downstream of the Hippo Network to regulate endocytic trafficking of at least four cell polarity, cell junction and apical extracellular matrix proteins involved in tracheal tube size control: Crumbs, Uninflatable, Kune-Kune and Serpentine. We further show that tracheal cells are competent to undergo apoptosis, even though developmentally-regulated DrICE function rarely kills tracheal cells. Our results reveal a developmental role for caspases, a pool of DrICE that co-localizes with Clathrin, and a mechanism by which the Hippo Network controls endocytic trafficking. Given reports of in vitro regulation of endocytosis by mammalian caspases during apoptosis, we propose that caspase-mediated regulation of endocytic trafficking is an evolutionarily conserved function of caspases that can be deployed during morphogenesis.


Subject(s)
Caspase 3/metabolism , Caspases/metabolism , Drosophila Proteins/metabolism , Drosophila melanogaster/growth & development , Morphogenesis/physiology , Protein Transport/physiology , Trachea/growth & development , Animals , Apoptosis , Caspases/genetics , Drosophila Proteins/genetics , Drosophila melanogaster/embryology , Endocytosis/physiology , Gene Expression Regulation, Developmental/physiology , Inhibitor of Apoptosis Proteins , Intercellular Junctions , Intracellular Signaling Peptides and Proteins/metabolism , Male , Point Mutation , Protein Serine-Threonine Kinases/metabolism , Trachea/pathology
10.
Sci Rep ; 8(1): 13508, 2018 09 10.
Article in English | MEDLINE | ID: mdl-30202079

ABSTRACT

Hypercapnia, the elevation of CO2 in blood and tissues, commonly occurs in severe acute and chronic respiratory diseases, and is associated with increased risk of mortality. Recent studies have shown that hypercapnia adversely affects innate immunity, host defense, lung edema clearance and cell proliferation. Airway epithelial dysfunction is a feature of advanced lung disease, but the effect of hypercapnia on airway epithelium is unknown. Thus, in the current study we examined the effect of normoxic hypercapnia (20% CO2 for 24 h) vs normocapnia (5% CO2), on global gene expression in differentiated normal human airway epithelial cells. Gene expression was assessed on Affymetrix microarrays, and subjected to gene ontology analysis for biological process and cluster-network representation. We found that hypercapnia downregulated the expression of 183 genes and upregulated 126. Among these, major gene clusters linked to immune responses and nucleosome assembly were largely downregulated, while lipid metabolism genes were largely upregulated. The overwhelming majority of these genes were not previously known to be regulated by CO2. These changes in gene expression indicate the potential for hypercapnia to impact bronchial epithelial cell function in ways that may contribute to poor clinical outcomes in patients with severe acute or advanced chronic lung diseases.


Subject(s)
Carbon Dioxide/toxicity , Gene Expression Regulation/drug effects , Hypercapnia/complications , Lung Diseases/pathology , Respiratory Mucosa/drug effects , Bronchi/cytology , Bronchi/drug effects , Bronchi/immunology , Bronchi/pathology , Carbon Dioxide/blood , Cell Differentiation , Cells, Cultured , Chronic Disease , Epithelial Cells/drug effects , Epithelial Cells/immunology , Epithelial Cells/metabolism , Epithelial Cells/pathology , Gene Expression Profiling , Humans , Hypercapnia/blood , Immunity, Innate/drug effects , Immunity, Innate/genetics , Lipid Metabolism/drug effects , Lipid Metabolism/genetics , Lung Diseases/etiology , Nucleosomes/drug effects , Nucleosomes/metabolism , Respiratory Mucosa/cytology , Respiratory Mucosa/immunology , Respiratory Mucosa/pathology , Sarcoglycanopathies
11.
PLoS One ; 12(6): e0178590, 2017.
Article in English | MEDLINE | ID: mdl-28570602

ABSTRACT

Changes in the distribution of nucleosomes along the genome influence chromatin structure and impact gene expression by modulating the accessibility of DNA to transcriptional machinery. However, the role of genome-wide nucleosome positioning in gene expression and in maintaining differentiated cell states remains poorly understood. Drosophila melanogaster cell lines represent distinct tissue types and exhibit cell-type specific gene expression profiles. They thus could provide a useful tool for investigating cell-type specific nucleosome organization of an organism's genome. To evaluate this possibility, we compared genome-wide nucleosome positioning and occupancy in five different Drosophila tissue-specific cell lines, and in reconstituted chromatin, and then tested for correlations between nucleosome positioning, transcription factor binding motifs, and gene expression. Nucleosomes in all cell lines were positioned in accordance with previously known DNA-nucleosome interactions, with helically repeating A/T di-nucleotide pairs arranged within nucleosomal DNAs and AT-rich pentamers generally excluded from nucleosomal DNA. Nucleosome organization in all cell lines differed markedly from in vitro reconstituted chromatin, with highly expressed genes showing strong nucleosome organization around transcriptional start sites. Importantly, comparative analysis identified genomic regions that exhibited cell line-specific nucleosome enrichment or depletion. Further analysis of these regions identified 91 out of 16,384 possible heptamer sequences that showed differential nucleosomal occupation between cell lines, and 49 of the heptamers matched one or more known transcription factor binding sites. These results demonstrate that there is differential nucleosome positioning between these Drosophila cell lines and therefore identify a system that could be used to investigate the functional significance of differential nucleosomal positioning in cell type specification.


Subject(s)
Drosophila melanogaster/cytology , Nucleosomes , Animals , Binding Sites , DNA/metabolism , Nucleosomes/metabolism , Transcription Factors/metabolism
12.
J Immunol ; 196(2): 655-667, 2016 Jan 15.
Article in English | MEDLINE | ID: mdl-26643480

ABSTRACT

Hypercapnia, elevated partial pressure of CO2 in blood and tissue, develops in many patients with chronic severe obstructive pulmonary disease and other advanced lung disorders. Patients with advanced disease frequently develop bacterial lung infections, and hypercapnia is a risk factor for mortality in such individuals. We previously demonstrated that hypercapnia suppresses induction of NF-κB-regulated innate immune response genes required for host defense in human, mouse, and Drosophila cells, and it increases mortality from bacterial infections in both mice and Drosophila. However, the molecular mediators of hypercapnic immune suppression are undefined. In this study, we report a genome-wide RNA interference screen in Drosophila S2* cells stimulated with bacterial peptidoglycan. The screen identified 16 genes with human orthologs whose knockdown reduced hypercapnic suppression of the gene encoding the antimicrobial peptide Diptericin (Dipt), but did not increase Dipt mRNA levels in air. In vivo tests of one of the strongest screen hits, zinc finger homeodomain 2 (Zfh2; mammalian orthologs ZFHX3/ATBF1 and ZFHX4), demonstrate that reducing zfh2 function using a mutation or RNA interference improves survival of flies exposed to elevated CO2 and infected with Staphylococcus aureus. Tissue-specific knockdown of zfh2 in the fat body, the major immune and metabolic organ of the fly, mitigates hypercapnia-induced reductions in Dipt and other antimicrobial peptides and improves resistance of CO2-exposed flies to infection. Zfh2 mutations also partially rescue hypercapnia-induced delays in egg hatching, suggesting that Zfh2's role in mediating responses to hypercapnia extends beyond the immune system. Taken together, to our knowledge, these results identify Zfh2 as the first in vivo mediator of hypercapnic immune suppression.


Subject(s)
DNA-Binding Proteins/immunology , Drosophila Proteins/immunology , Hypercapnia/immunology , Staphylococcal Infections/complications , Animals , Blotting, Western , Disease Models, Animal , Drosophila , Gene Knockdown Techniques , Hypercapnia/microbiology , Immunity, Innate/immunology , RNA Interference , Staphylococcal Infections/immunology , Staphylococcus aureus
13.
J Biomol Screen ; 21(4): 363-71, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26701099

ABSTRACT

Patients with severe lung disease may develop hypercapnia, elevation of the levels of CO2 in the lungs and blood, which is associated with increased risk of death, often from infection. To identify compounds that ameliorate the adverse effects of hypercapnia, we performed a focused screen of 8832 compounds using a CO2-responsive luciferase reporter in Drosophila S2* cells. We found that evoxine, a plant alkaloid, counteracts the CO2-induced transcriptional suppression of antimicrobial peptides in S2* cells. Strikingly, evoxine also inhibits hypercapnic suppression of interleukin-6 and the chemokine CCL2 expression in human THP-1 macrophages. Evoxine's effects are selective, since it does not prevent hypercapnic inhibition of phagocytosis by THP-1 cells or CO2-induced activation of AMPK in rat ATII pulmonary epithelial cells. The results suggest that hypercapnia suppresses innate immune gene expression by definable pathways that are evolutionarily conserved and demonstrate for the first time that specific CO2 effects can be targeted pharmacologically.


Subject(s)
Alkaloids/pharmacology , Carbon Dioxide/antagonists & inhibitors , Epithelial Cells/drug effects , High-Throughput Screening Assays , Macrophages/drug effects , Animals , Antimicrobial Cationic Peptides/agonists , Antimicrobial Cationic Peptides/antagonists & inhibitors , Antimicrobial Cationic Peptides/genetics , Antimicrobial Cationic Peptides/immunology , Carbon Dioxide/toxicity , Cell Line , Chemokine CCL2/genetics , Chemokine CCL2/immunology , Drosophila melanogaster/cytology , Drosophila melanogaster/immunology , Epithelial Cells/cytology , Epithelial Cells/immunology , Gene Expression , Genes, Reporter , Humans , Hypercapnia/prevention & control , Interleukin-6/genetics , Interleukin-6/immunology , Luciferases/genetics , Luciferases/metabolism , Macrophages/cytology , Macrophages/immunology
15.
J Immunol ; 194(11): 5388-96, 2015 Jun 01.
Article in English | MEDLINE | ID: mdl-25895534

ABSTRACT

Hypercapnia, the elevation of CO2 in blood and tissue, commonly develops in patients with advanced lung disease and severe pulmonary infections, and it is associated with high mortality. We previously reported that hypercapnia alters expression of host defense genes, inhibits phagocytosis, and increases the mortality of Pseudomonas pneumonia in mice. However, the effect of hypercapnia on autophagy, a conserved process by which cells sequester and degrade proteins and damaged organelles that also plays a key role in antimicrobial host defense and pathogen clearance, has not previously been examined. In the present study we show that hypercapnia inhibits autophagy induced by starvation, rapamycin, LPS, heat-killed bacteria, and live bacteria in the human macrophage. Inhibition of autophagy by elevated CO2 was not attributable to acidosis. Hypercapnia also reduced macrophage killing of Pseudomonas aeruginosa. Moreover, elevated CO2 induced the expression of Bcl-2 and Bcl-xL, antiapoptotic factors that negatively regulate autophagy by blocking Beclin 1, an essential component of the autophagy initiation complex. Furthermore, small interfering RNA targeting Bcl-2 and Bcl-xL and the small molecule Z36, which blocks Bcl-2 and Bcl-xL binding to Beclin 1, prevented hypercapnic inhibition of autophagy and bacterial killing. These results suggest that targeting the Bcl-2/Bcl-xL-Beclin 1 interaction may hold promise for ameliorating hypercapnia-induced immunosuppression and improving resistance to infection in patients with advanced lung disease and hypercapnia.


Subject(s)
Autophagy/immunology , Hypercapnia/immunology , Macrophages, Alveolar/immunology , Proto-Oncogene Proteins c-bcl-2/genetics , bcl-X Protein/genetics , Acidosis , Animals , Apoptosis Regulatory Proteins/antagonists & inhibitors , Autophagy/drug effects , Beclin-1 , Carbon Dioxide/blood , Carbon Dioxide/pharmacology , Cell Line , Humans , Hypercapnia/blood , Indoles/pharmacology , Lipopolysaccharides , Lung Diseases/pathology , Macrophages, Alveolar/microbiology , Membrane Proteins/antagonists & inhibitors , Mice , Phagocytosis/drug effects , Protein Binding/drug effects , Proto-Oncogene Proteins c-bcl-2/biosynthesis , Pseudomonas aeruginosa/immunology , RNA Interference , RNA, Small Interfering , Sirolimus/pharmacology , bcl-X Protein/biosynthesis
16.
PLoS One ; 9(7): e101609, 2014.
Article in English | MEDLINE | ID: mdl-25036253

ABSTRACT

Precise control of epithelial tube size is critical for organ function, yet the molecular mechanisms remain poorly understood. Here, we examine the roles of cell growth and a highly conserved organ growth regulatory pathway in controlling the dimensions of the Drosophila tracheal (airway) system, a well-characterized system for investigating epithelial tube morphogenesis. We find that tracheal tube-size is regulated in unexpected ways by the transcription factor Yorkie (Yki, homolog of mammalian YAP and TAZ) and the Salvador/Warts/Hippo (SWH) kinase pathway. Yki activity typically promotes cell division, inhibits apoptosis, and can promote cell growth. However, reducing Yki activity in developing embryos increases rather than decreases the length of the major tracheal tubes, the dorsal trunks (DTs). Similarly, reduction of Hippo pathway activity, which antagonizes Yki, shortens tracheal DTs. yki mutations do not alter DT cell volume or cell number, indicating that Yki and the Hippo pathway regulate cell shape and apical surface area, but not volume. Yki does not appear to act through known tracheal pathways of apical extracellular matrix, septate junctions (SJs), basolateral or tubular polarity. Instead, the Hippo pathway and Yki appear to act downstream or in parallel to SJs because a double mutant combination of an upstream Hippo pathway activator, kibra, and the SJ component sinu have the short tracheal phenotype of a kibra mutant. We demonstrate that the critical target of Yki in tube size control is Drosophila Inhibitor of Apoptosis 1 (DIAP1), which in turn antagonizes the Drosophila effector caspase, Ice. Strikingly, there is no change in tracheal cell number in DIAP1 or Ice mutants, thus epithelial tube size regulation defines new non-apoptotic roles for Yki, DIAP1 and Ice.


Subject(s)
Drosophila Proteins/metabolism , Drosophila melanogaster/embryology , Drosophila melanogaster/metabolism , Inhibitor of Apoptosis Proteins/metabolism , Nuclear Proteins/metabolism , Trans-Activators/metabolism , Animals , Caspases/metabolism , Cell Shape , Drosophila Proteins/genetics , Drosophila melanogaster/genetics , Epithelium/embryology , Epithelium/metabolism , Intracellular Signaling Peptides and Proteins/metabolism , Mutation , Nuclear Proteins/genetics , Organogenesis , Protein Serine-Threonine Kinases/metabolism , Proto-Oncogene Proteins pp60(c-src)/metabolism , Trachea/cytology , Trachea/embryology , Trans-Activators/genetics , YAP-Signaling Proteins
17.
Development ; 140(14): 2851-5, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23821032

ABSTRACT

Metazoans require epithelial and endothelial tubes to transport liquids and gasses throughout their bodies. Although biological tubes may look relatively similar at first glance, there are multiple and distinct mechanisms by which tubes form and even more regulatory events driving the cell shape changes that produce tubes of specific dimensions. An overview of the current understanding of the molecular processes and physical forces involved in tubulogenesis is presented in this review and the accompanying poster.


Subject(s)
Endothelial Cells/cytology , Epithelial Cells/cytology , Morphogenesis , Animals , Blood Vessels/cytology , Blood Vessels/embryology , Exocrine Glands/cytology , Exocrine Glands/growth & development , Humans , Kidney Tubules/cytology , Kidney Tubules/growth & development , Lung/cytology , Lung/growth & development
18.
Am J Respir Cell Mol Biol ; 49(5): 821-8, 2013 Nov.
Article in English | MEDLINE | ID: mdl-23777386

ABSTRACT

Hypercapnia, an elevation of the level of carbon dioxide (CO2) in blood and tissues, is a marker of poor prognosis in chronic obstructive pulmonary disease and other pulmonary disorders. We previously reported that hypercapnia inhibits the expression of TNF and IL-6 and phagocytosis in macrophages in vitro. In the present study, we determined the effects of normoxic hypercapnia (10% CO2, 21% O2, and 69% N2) on outcomes of Pseudomonas aeruginosa pneumonia in BALB/c mice and on pulmonary neutrophil function. We found that the mortality of P. aeruginosa pneumonia was increased in 10% CO2-exposed compared with air-exposed mice. Hypercapnia increased pneumonia mortality similarly in mice with acute and chronic respiratory acidosis, indicating an effect unrelated to the degree of acidosis. Exposure to 10% CO2 increased the burden of P. aeruginosa in the lungs, spleen, and liver, but did not alter lung injury attributable to pneumonia. Hypercapnia did not reduce pulmonary neutrophil recruitment during infection, but alveolar neutrophils from 10% CO2-exposed mice phagocytosed fewer bacteria and produced less H2O2 than neutrophils from air-exposed mice. Secretion of IL-6 and TNF in the lungs of 10% CO2-exposed mice was decreased 7 hours, but not 15 hours, after the onset of pneumonia, indicating that hypercapnia inhibited the early cytokine response to infection. The increase in pneumonia mortality caused by elevated CO2 was reversible when hypercapnic mice were returned to breathing air before or immediately after infection. These results suggest that hypercapnia may increase the susceptibility to and/or worsen the outcome of lung infections in patients with severe lung disease.


Subject(s)
Hypercapnia/complications , Lung/immunology , Neutrophils/immunology , Pneumonia, Bacterial/complications , Pseudomonas aeruginosa/pathogenicity , Acidosis, Respiratory/immunology , Acidosis, Respiratory/microbiology , Animals , Bacterial Load , Disease Models, Animal , Female , HL-60 Cells , Humans , Hypercapnia/immunology , Hypercapnia/pathology , Inflammation Mediators/metabolism , Interleukin-6/metabolism , Lung/microbiology , Lung/pathology , Mice , Mice, Inbred BALB C , Neutrophils/microbiology , Phagocytosis , Pneumonia, Bacterial/immunology , Pneumonia, Bacterial/microbiology , Pneumonia, Bacterial/pathology , Reactive Oxygen Species/metabolism , Time Factors , Tumor Necrosis Factor-alpha/metabolism
19.
PLoS One ; 7(10): e46696, 2012.
Article in English | MEDLINE | ID: mdl-23056407

ABSTRACT

Elevated CO(2) levels (hypercapnia) occur in patients with respiratory diseases and impair alveolar epithelial integrity, in part, by inhibiting Na,K-ATPase function. Here, we examined the role of c-Jun N-terminal kinase (JNK) in CO(2) signaling in mammalian alveolar epithelial cells as well as in diptera, nematodes and rodent lungs. In alveolar epithelial cells, elevated CO(2) levels rapidly induced activation of JNK leading to downregulation of Na,K-ATPase and alveolar epithelial dysfunction. Hypercapnia-induced activation of JNK required AMP-activated protein kinase (AMPK) and protein kinase C-ζ leading to subsequent phosphorylation of JNK at Ser-129. Importantly, elevated CO(2) levels also caused a rapid and prominent activation of JNK in Drosophila S2 cells and in C. elegans. Paralleling the results with mammalian epithelial cells, RNAi against Drosophila JNK fully prevented CO(2)-induced downregulation of Na,K-ATPase in Drosophila S2 cells. The importance and specificity of JNK CO(2) signaling was additionally demonstrated by the ability of mutations in the C. elegans JNK homologs, jnk-1 and kgb-2 to partially rescue the hypercapnia-induced fertility defects but not the pharyngeal pumping defects. Together, these data provide evidence that deleterious effects of hypercapnia are mediated by JNK which plays an evolutionary conserved, specific role in CO(2) signaling in mammals, diptera and nematodes.


Subject(s)
Carbon Dioxide/toxicity , Epithelial Cells/drug effects , Epithelial Cells/enzymology , JNK Mitogen-Activated Protein Kinases/metabolism , Pulmonary Alveoli/cytology , Animals , Burkitt Lymphoma , Caenorhabditis elegans , Drosophila , Enzyme Activation/drug effects , Epithelial Cells/metabolism , Evolution, Molecular , Humans , JNK Mitogen-Activated Protein Kinases/genetics , Phosphorylation/drug effects , Protein Kinase C/metabolism , Rats , Sodium-Potassium-Exchanging ATPase/genetics , Sodium-Potassium-Exchanging ATPase/metabolism
20.
Nat Cell Biol ; 14(5): 518-25, 2012 Mar 25.
Article in English | MEDLINE | ID: mdl-22446737

ABSTRACT

Networks of epithelial and endothelial tubes are essential for the function of organs such as the lung, kidney and vascular system. The sizes and shapes of these tubes are highly regulated to match their individual functions. Defects in tube size can cause debilitating diseases such as polycystic kidney disease and ischaemia. It is therefore critical to understand how tube dimensions are regulated. Here we identify the tyrosine kinase Src as an instructive regulator of epithelial-tube length in the Drosophila tracheal system. Loss-of-function Src42 mutations shorten tracheal tubes, whereas Src42 overexpression elongates them. Surprisingly, Src42 acts distinctly from known tube-size pathways and regulates both the amount of apical surface growth and, with the conserved formin dDaam, the direction of growth. Quantitative three-dimensional image analysis reveals that Src42- and dDaam-mutant tracheal cells expand more in the circumferential than the axial dimension, resulting in tubes that are shorter in length-but larger in diameter-than wild-type tubes. Thus, Src42 and dDaam control tube dimensions by regulating the direction of anisotropic growth, a mechanism that has not previously been described.


Subject(s)
Drosophila/growth & development , Epithelium/growth & development , src-Family Kinases/metabolism , Animals
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