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1.
J Cyst Fibros ; 20(5): 779-784, 2021 09.
Article in English | MEDLINE | ID: mdl-33478894

ABSTRACT

BACKGROUND: Cystic fibrosis (CF) related diabetes (CFRD) is a common complication of CF. CFRD is associated with declining lung function even before its onset. Regular screening for CFRD using oral glucose tolerance test (OGTT) is recommended. Additionally, continuous glucose monitoring (CGM) has surfaced as a possible surveillance method, but evidence for its use and concordance with OGTT has not been established. METHODS: Children were prospectively recruited at CF center Lund to undergo both intermittent scan CGM (isCGM) and OGTT. Lung function was evaluated by spirometry and multiple breath washout. Demographic and clinical data were collected from the Swedish national CF registry. RESULTS: 32 patients participated in the study, yielding 28 pairs of isCGMs and OGTTs. The OGTTs showed that two patients met the criteria of CFRD, seven had impaired glucose tolerance (IGT) and indeterminate glycemia (INDET) was found in eleven cases. The isCGM percent of measurements >8mmol/L and the number of peaks per day >11 mmol/L have correlations with intermediate OGTT glucose time points, but not the 2hour glucose value. Patients with abnormal glucose tolerance (AGT) had lower lung function than those with normal glucose tolerance demonstrated by both FEV1% predicted and lung clearance index (LCI). CONCLUSION: Correlations can be found between isCGM and OGTT in regards to the latter's intermediate time points. LCI demonstrates as well as FEV1% of predicted, worse lung function in children and adolescents with abnormal glucose tolerance in CF.


Subject(s)
Blood Glucose Self-Monitoring/methods , Cystic Fibrosis/metabolism , Cystic Fibrosis/physiopathology , Glucose Intolerance/diagnosis , Glucose Intolerance/physiopathology , Glucose Tolerance Test/methods , Adolescent , Child , Female , Humans , Male , Prospective Studies , Respiratory Function Tests
2.
Leukemia ; 30(7): 1502-9, 2016 07.
Article in English | MEDLINE | ID: mdl-26984787

ABSTRACT

Chronic myeloid leukemia (CML) is characterized by expression of Bcr-abl, a tyrosine kinase oncogene. Clinical outcomes in CML were revolutionized by development of Bcr-abl-targeted tyrosine kinase inhibitors (TKIs), but CML is not cured by these agents. CML leukemia stem cells (LSCs) are relatively TKI insensitive and persist even in remission. LSC persistence results in relapse upon TKI discontinuation, or drug resistance or blast crisis (BC) during prolonged treatment. We hypothesize that increased expression of Fas-associated phosphatase 1 (Fap1) in CML contributes to LSC persistence and BC. As Fap1 substrates include Fas and glycogen synthase kinase-3ß (Gsk3ß), increased Fap1 activity in CML is anticipated to induce Fas resistance and stabilization of ß-catenin protein. Resistance to Fas-induced apoptosis may contribute to CML LSC persistence, and ß-catenin activity increases during BC. In the current study, we directly tested the role of Fap1 in CML LSC persistence using in an in vivo murine model. In TKI-treated mice, we found that inhibiting Fap1, using a tripeptide or small molecule, prevented TKI resistance, BC and relapse after TKI discontinuation; all events observed with TKI alone. In addition, Fap1 inhibition increased Fas sensitivity and decreased ß-catenin activity in CD34(+) bone marrow cells from human subjects with CML. Therapeutic Fap1 inhibition may permit TKI discontinuation and delay in progression in CML.


Subject(s)
Leukemia, Myelogenous, Chronic, BCR-ABL Positive/drug therapy , Protein Tyrosine Phosphatase, Non-Receptor Type 13/physiology , Animals , Apoptosis/drug effects , Blast Crisis/etiology , Blast Crisis/pathology , Drug Resistance, Neoplasm/drug effects , Humans , Mice , Neoplastic Stem Cells/pathology , PDZ Domains , Protein Binding/drug effects , Protein Kinase Inhibitors/administration & dosage , Protein Kinase Inhibitors/pharmacology , Protein Kinase Inhibitors/therapeutic use , Protein Tyrosine Phosphatase, Non-Receptor Type 13/antagonists & inhibitors , Protein Tyrosine Phosphatase, Non-Receptor Type 13/metabolism , Recurrence , fas Receptor/metabolism
3.
Oncogenesis ; 3: e135, 2014 Dec 22.
Article in English | MEDLINE | ID: mdl-25531430

ABSTRACT

Cdx and Hox proteins are homeodomain transcription factors that regulate hematopoiesis. Transcription of the HOX and CDX genes decreases during normal myelopoiesis, but is aberrantly sustained in leukemias with translocation or partial tandem duplication of the MLL1 gene. Cdx4 activates transcription of the HOXA9 and HOXA10 genes, and HoxA10 activates CDX4 transcription. The events that break this feedback loop, permitting a decreased Cdx4 expression during normal myelopoiesis, were previously undefined. In the current study, we find that HoxA9 represses CDX4 transcription in differentiating myeloid cells, antagonizing activation by HoxA10. We determine that tyrosine phosphorylation of HoxA10 impairs transcriptional activation of CDX4, but tyrosine phosphorylation of HoxA9 facilitates repression of this gene. As HoxA9 and HoxA10 are phosphorylated during myelopoiesis, this provides a mechanism for differentiation stage-specific Cdx4 expression. HoxA9 and HoxA10 are increased in cells expressing Mll-Ell, a leukemia-associated MLL1 fusion protein. We find that Mll-Ell induces a HoxA10-dependent increase in Cdx4 expression in myeloid progenitor cells. However, Cdx4 decreases in a HoxA9-dependent manner on exposure of Mll-Ell-expressing cells to differentiating cytokines. Leukemia-associated, constitutively active mutants of Shp2 block cytokine-induced tyrosine phosphorylation of HoxA9 and HoxA10. In comparison with myeloid progenitor cells that are expressing Mll-Ell alone, we find increased CDX4 transcription and Cdx4 expression in cells co-expressing Mll-Ell plus constitutively active Shp2. Increased Cdx4 expression is sustained on exposure of these cells to differentiating cytokines. Our results identify a mechanism for increased and sustained CDX4 transcription in leukemias co-overexpressing HoxA9 and HoxA10 in combination with constitutive activation of Shp2. This is clinically relevant, because MLL1 translocations and constitutive Shp2 activation co-exist in human myeloid leukemias.

4.
J Neuroendocrinol ; 24(6): 962-72, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22296042

ABSTRACT

The inhibin/activin family of proteins is known to have a broad distribution of synthesis and expression in many species, as well as a variety of functions in reproductive and other physiological systems. Yet, our knowledge regarding the production and function of inhibin and activin in the central nervous system is relatively limited, especially in humans. The present study aimed to explore the distribution of inhibin/activin protein subunits and receptors in the adult human brain. The human hypothalamus and surrounding basal forebrain was examined using post-mortem tissues from 29 adults. Immunocytochemical studies were conducted with antibodies directed against the inhibin/activin α, ßA, and ßB subunits, betaglycan and the activin type IIA and IIB receptors. An immunoassay was also utilised to measure dimeric inhibin A and B levels in tissue homogenates of the infundibulum of the hypothalamus. Robust ßA subunit immunoreactivity was present in the paraventricular, supraoptic, lateral hypothalamic, infundibular, dorsomedial and suprachiasmatic nuclei of the hypothalamus, in the basal ganglia, and in the nucleus basalis of Meynert. A similar staining distribution was noted for the ßB subunit, betaglycan and the type II receptor antibodies, whereas α subunit staining was not detected in any of the major anatomical regions of the human brain. Inhibin B immunoreactivity was present in all tissues, whereas inhibin A levels were below detectable limits. These studies show for the first time that the inhibin/activin protein subunits and receptors can be co-localised in the human brain, implicating potential, diverse neural functions.


Subject(s)
Activin Receptors, Type II/biosynthesis , Activin Receptors/biosynthesis , Activins/biosynthesis , Hypothalamus/metabolism , Inhibin-beta Subunits/biosynthesis , Inhibins/biosynthesis , Prosencephalon/metabolism , Receptors, Peptide/biosynthesis , Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Young Adult
5.
Clin Exp Allergy ; 33(3): 331-6, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12614447

ABSTRACT

BACKGROUND: Eosinophil peroxidase (EPO) is an eosinophilic basic protein, which leads to increased permeability and damage of bronchial epithelial cells in asthma. OBJECTIVE: As little is known about its local expression and release in humans the intracellular expression in lung and peripheral eosinophils and the concentrations of EPO in bronchoalveolar lavage (BAL) fluid and serum was investigated in patients with asthma. METHODS: Twelve mild atopic asthmatic and nine control subjects underwent segmental sham and allergen challenge. EPO concentrations in BAL fluid and serum were determined by immunoassay and flow cytometry was used to determine the intracellular expression of EPO in BAL-derived and peripheral eosinophils. RESULTS: In asthmatic patients a large increase in BAL eosinophils--total cells: median 9.5 x 10(6) (range: 0.5 to 455.0 x 10(6)); relative: 38% (1 to 91%)--was detectable 24 h following allergen challenge, but peripheral blood eosinophil counts did not change. Concentrations of EPO in BAL fluid increased from 1 microg/L (1.0 to 6.8 microg/L) to 42 microg/L (5.6 to 379.6 microg/L; P < 0.01) after allergen but not after saline challenge (1.5 microg/L; 1.0 to 21.9 microg/L), whereas in control subjects all measurements were below the detection limit. Serum concentrations of EPO increased slightly from 18.3 microg/L (3.0 to 56.8 microg/L) to 27 microg/L (3.8 to 133.9 microg/L; P < 0.05) 24 h after allergen challenge in asthmatic patients. Furthermore, the intracellular expression of EPO (measured as mean fluorescence intensity) was decreased in BAL eosinophils compared with blood eosinophils (mean fluorescence intensity 29 (7 to 71) vs. 48 (20 to 85); P < 0.01) after allergen challenge. CONCLUSION: The finding of increased EPO concentrations in the BAL fluid and decreased intracellular EPO expression in pulmonary eosinophils of asthmatic patients reflects the allergen-triggered release of EPO into the bronchial space.


Subject(s)
Asthma/enzymology , Bronchoalveolar Lavage Fluid/chemistry , Eosinophils/enzymology , Peroxidases/metabolism , Adult , Asthma/blood , Bronchial Provocation Tests/methods , Case-Control Studies , Eosinophil Peroxidase , Female , Forced Expiratory Volume , Humans , Leukocyte Count , Male , Skin Tests , Statistics, Nonparametric
6.
J Biol Chem ; 276(46): 42863-8, 2001 Nov 16.
Article in English | MEDLINE | ID: mdl-11551969

ABSTRACT

Laminin-5, the major extracellular matrix protein produced by mammary epithelial cells, is composed of three chains (designated alpha3A, beta3, and gamma2), each encoded by a separate gene. Laminin-5 is markedly down-regulated in breast cancer cells. Little is known about the regulation of laminin gene transcription in normal breast cells, nor about the mechanism underlying the down-regulation seen in cancer. In the present study, we cloned the promoter of the gene for the human laminin alpha3A chain (LAMA3A) and investigated its regulation in functionally normal MCF10A breast epithelial cells and several breast cancer cell lines. Using site-directed mutagenesis of promoter-reporter constructs in transient transfection assays in MCF10A cells, we find that two binding sites for Kruppel-like factor 4 (KLF4/GKLF/EZF) are required for expression driven by the LAMA3A promoter. Electrophoretic mobility shift assays reveal absence of KLF4 binding activity in extracts from T47D, MDA-MB 231, ZR75-1, MDA-MB 436, and MCF7 breast cancer cells. Transient transfection of a plasmid expressing KLF4 activates transcription from the LAMA3A promoter in breast cancer cells. A reporter vector containing duplicate KLF4-binding sites in its promoter is expressed at high levels in MCF10A cells but at negligible levels in breast cancer cells. Thus, KLF4 is required for LAMA3A expression and absence of laminin alpha3A in breast cancer cells appears, at least in part, attributable to the lack of KLF4 activity.


Subject(s)
Breast/metabolism , DNA-Binding Proteins/metabolism , DNA-Binding Proteins/physiology , Epithelial Cells/metabolism , Laminin/biosynthesis , Transcription Factors/metabolism , Transcription Factors/physiology , Binding Sites , Blotting, Western , Cell Line , Cell Nucleus/metabolism , Cloning, Molecular , Down-Regulation , Gene Expression Regulation , Genes, Reporter , Humans , Kruppel-Like Factor 4 , Kruppel-Like Transcription Factors , Models, Genetic , Molecular Sequence Data , Mutagenesis, Site-Directed , Plasmids/metabolism , Promoter Regions, Genetic , Protein Binding , Time Factors , Transcription Factor AP-1/metabolism , Transcription, Genetic , Transfection , Tumor Cells, Cultured
7.
J Biol Chem ; 276(41): 37868-78, 2001 Oct 12.
Article in English | MEDLINE | ID: mdl-11483597

ABSTRACT

The CYBB and NCF2 genes encode the phagocyte respiratory burst oxidase proteins, gp91PHOX and p67PHOX. Previously, we identified homologous CYBB and NCF2 cis elements that are necessary for lineage-specific transcription during late myeloid differentiation. We determined that these homologous cis elements are activated by PU.1, IRF1, interferon consensus sequence-binding protein (ICSBP), and the CREB-binding protein (CBP). Since expression of PU.1 and ICSBP is lineage-restricted, our investigations identified a mechanism of lineage-specific CYBB and NCF2 transcription. Since PU.1, IRF1, ICSBP, and CBP are expressed in undifferentiated myeloid cells, our investigations did not determine the mechanism of differentiation stage-specific CYBB and NCF2 transcription. In the current investigations, we determine that SHP1 protein-tyrosine phosphatase (SHP1-PTP) inhibits gp91PHOX and p67PHOX expression, in undifferentiated myeloid cell lines, by decreasing interaction of PU.1, IRF1, ICSBP, and CBP with the CYBB and NCF2 genes. We also determine that IRF1 and ICSBP are tyrosine-phosphorylated during interferon gamma differentiation of myeloid cell lines, and we identify IRF1 and ICSBP tyrosine residues that are necessary for CYBB and NCF2 transcription. Therefore, these investigations identify a novel mechanism by which SHP1-PTP antagonizes myeloid differentiation and determine that tyrosine phosphorylation of IRF1 and ICSPB mediates stage-specific transcriptional activation in differentiating myeloid cells.


Subject(s)
Membrane Glycoproteins/antagonists & inhibitors , Membrane Glycoproteins/genetics , NADPH Oxidases , Phosphoproteins/antagonists & inhibitors , Transcription Factors/antagonists & inhibitors , Base Sequence , DNA Primers , Gene Expression Regulation, Enzymologic , Humans , Membrane Glycoproteins/metabolism , Mutagenesis, Site-Directed , NADPH Oxidase 2 , Phosphoproteins/genetics , Phosphoproteins/metabolism , Phosphorylation , Protein Binding , RNA, Messenger/genetics , Transcription Factors/metabolism , Transcription, Genetic , U937 Cells
8.
Arch Biochem Biophys ; 387(1): 99-106, 2001 Mar 01.
Article in English | MEDLINE | ID: mdl-11368189

ABSTRACT

Bikunin is a Kunitz-type proteinase inhibitor, which is cross-linked to heavy chains via a chondroitin sulfate chain, forming inter-alpha-inhibitor and related molecules. Rat bikunin was produced by baculovirus-infected insect cells. The protein could be purified with a total yield of 20 mg/liter medium. Unlike naturally occuring bikunin the recombinant protein had no galactosaminoglycan chain. Endoglycosidase digestion also suggested that the recombinant form lacked N-linked oligosaccharides. Bikunin is translated as a part of a precursor, alpha1-microglobulin/bikunin, but the functional significance of the cotranslation is unknown. Our results indicate that the proteinase inhibitory function of bikunin is not regulated by the alpha1-microglobulin-part of the alpha1-microglobulin/bikunin precursor since recombinant bikunin had the same trypsin inhibitory activity as the recombinant precursor. Both free bikunin and the precursor were also functional as a substrate in an in vitro xylosylation system. This demonstrates that the alpha1-microglobulin-part is not necessary for the first step of galactosaminoglycan assembly.


Subject(s)
Membrane Glycoproteins/biosynthesis , Protein Precursors/metabolism , Recombinant Proteins/biosynthesis , Serine Proteinase Inhibitors/biosynthesis , Trypsin Inhibitor, Kunitz Soybean , Xylose/metabolism , Animals , Membrane Glycoproteins/genetics , Protein Precursors/genetics , Protein Processing, Post-Translational , Rats , Serine Proteinase Inhibitors/genetics , Trypsin/drug effects
9.
J Biol Chem ; 275(26): 20117-26, 2000 Jun 30.
Article in English | MEDLINE | ID: mdl-10766757

ABSTRACT

The DNA binding affinity of HoxA10 is increased by partnering with Pbx proteins. A consensus sequence for Pbx1-HoxA10 DNA binding has been derived, but genuine target genes have not been identified. We noted that the derived Pbx-HoxA10 DNA-binding consensus is similar to a repressor element in the CYBB promoter. The CYBB gene, which encodes the respiratory burst oxidase component gp91(phox), is expressed only in myeloid cells that have differentiated beyond the promyelocyte stage. In these studies, we demonstrate that interferon gamma (IFN-gamma)-induced differentiation of myeloid cell lines abolishes in vitro Pbx-HoxA10 binding to either the derived consensus or the similar CYBB sequence. We also demonstrate that HoxA10, overexpressed in myeloid cell lines, represses reporter gene expression from artificial promoter constructs with Pbx-HoxA10 binding sites. We determine that HoxA10 has endogenous repression domains that are not functionally altered by IFN-gamma treatment. However, IFN-gamma-induced differentiation of myeloid cell lines leads to HoxA10 tyrosine phosphorylation, which decreases in vitro DNA binding to Pbx-HoxA10 binding sites. Therefore, these investigations identify the CYBB gene as a potential target for HoxA10 and define repression of genes expressed in mature myeloid cells as a novel role for HoxA10 during myeloid differentiation.


Subject(s)
DNA-Binding Proteins/metabolism , DNA/metabolism , Homeodomain Proteins , Interferon-gamma/pharmacology , Leukemia, Myeloid/metabolism , NADPH Oxidases , Transcription, Genetic , Tyrosine/metabolism , Binding Sites , Blotting, Northern , Blotting, Western , Cell Differentiation/drug effects , DNA, Complementary/metabolism , DNA-Binding Proteins/genetics , Genes, Reporter , Homeobox A10 Proteins , Humans , Membrane Glycoproteins/metabolism , Mutagenesis, Site-Directed , NADPH Oxidase 2 , Oligonucleotides/metabolism , Phosphoproteins/metabolism , Phosphorylation , Plasmids , Precipitin Tests , Protein Binding , Transcription, Genetic/drug effects , Transfection , Tumor Cells, Cultured , U937 Cells
10.
Arch Biochem Biophys ; 383(2): 171-7, 2000 Nov 15.
Article in English | MEDLINE | ID: mdl-11185550

ABSTRACT

The biosynthesis of dermatan sulfate is a complex process that involves, inter alia, formation of L-iduronic acid residues by C5-epimerization of D-glucuronic acid residues already incorporated into the growing polymer. It has been shown previously that this reaction is promoted by the presence of the sulfate donor 3'-phosphoadenosine-5'-phosphosulfate. In the present investigation, the role of sulfation in the biosynthesis of L-iduronic acid-rich galactosaminoglycans was examined more closely by a study of the substrate specificities and kinetic properties of the sulfotransferases involved in dermatan sulfate biosynthesis. Comparison of the acceptor reactivities of oligosaccharides from chondroitin and dermatan, in an in vitro system containing microsomes from cultured human skin fibroblasts and 3'-phosphoadenosine-5'-phosphosulfate, showed that Km values for the dermatan fragments were substantially lower than those for their chondroitin counterparts. Calculation of Vmax values likewise showed that dermatan was the better substrate. Whereas dermatan incorporated [35S]sulfate exclusively at the C4 position of N-acetylgalactosamine residues, approximately equal amounts of radioactivity were found at the C4 and C6 positions in the labelled chondroitin. Under standard assay conditions, the 4-O-sulfation of dermatan proceeded about six times faster than the 4-O-sulfation of chondroitin. On the basis of these results, we propose that L-iduronic acids, formed in the course of the biosynthesis of dermatan sulfates, enhance sulfation of their adjacent N-acetylgalactosamine residues, and will thereby be locked in the L-ido configuration.


Subject(s)
Chondroitin/metabolism , Dermatan Sulfate/metabolism , Galactosamine/biosynthesis , Cells, Cultured , Chondroitin/chemistry , Chromatography, Affinity , Dermatan Sulfate/chemistry , Dose-Response Relationship, Drug , Fibroblasts/chemistry , Fibroblasts/metabolism , Galactosamine/chemistry , Hexuronic Acids/pharmacology , Humans , Hydrogen-Ion Concentration , Iduronic Acid/chemistry , Kinetics , Phosphoadenosine Phosphosulfate/metabolism , Protein Binding , Substrate Specificity , Sulfotransferases/chemistry , Time Factors
11.
J Immunol ; 163(11): 6095-105, 1999 Dec 01.
Article in English | MEDLINE | ID: mdl-10570299

ABSTRACT

Activation of the phagocyte respiratory burst oxidase requires interaction between the oxidase components p47phox, p67phox, p22phox, and gp91phox. IFN-gamma induces transcription of the genes encoding p67phox (the NCF2 gene) and gp91phox (the CYBB gene) during monocyte differentiation, and also in mature monocytes. In these studies, we identify an NCF2 cis element, necessary for IFN-gamma-induced p67phox expression, and determine that this element is activated by cooperation between the transcription factors PU.1, IFN regulatory factor 1 (IRF1), and the IFN consensus-binding protein (ICSBP). Previously, we identified a CYBB cis element, necessary for IFN-gamma-induced gp91phox expression, and also activated by this transcription factor combination. In these investigations, we determine that recruitment of a coactivator protein, CBP (the CREBbinding protein), to the CYBB or NCF2 promoter is the molecular mechanism of transcriptional activation by PU.1, IRF1, and ICSBP. Also, we determine that the multiprotein interaction of CBP with PU. 1, IRF1, and ICSBP requires either the CYBB- or NCF2--binding site. Because IFN-gamma induces simultaneous expression of p67phox and gp91phox, these investigations identify a molecular event that coordinates oxidase gene transcription during the inflammatory response. Also, these investigations identify CBP recruitment by cooperation between PU.1, IRF1, and ICSBP as a novel molecular mechanism for IFN-gamma-induced activation of myeloid genes that are involved in the system of host defense.


Subject(s)
Gene Expression Regulation, Enzymologic , Interferon-gamma/pharmacology , Membrane Glycoproteins/genetics , NADPH Oxidases/genetics , Phosphoproteins/genetics , Transcription Factors/metabolism , Base Sequence , Binding Sites , Bone Marrow/immunology , CREB-Binding Protein , DNA-Binding Proteins/metabolism , Humans , Interferon Regulatory Factor-1 , Interferon Regulatory Factors , Introns , Membrane Glycoproteins/biosynthesis , Molecular Sequence Data , NADPH Oxidase 2 , NADPH Oxidases/biosynthesis , Nuclear Proteins/metabolism , Phosphoproteins/biosynthesis , Phosphoproteins/metabolism , Protein Binding , Proto-Oncogene Proteins/metabolism , Repressor Proteins/metabolism , Response Elements , Trans-Activators/metabolism , Transcription, Genetic
12.
Clin Exp Allergy ; 29(11): 1507-15, 1999 Nov.
Article in English | MEDLINE | ID: mdl-10520079

ABSTRACT

BACKGROUND: Eosinophils are involved in the chronic inflammatory response in asthma and their basic proteins are thought to play a major pathophysiological role in this process. While serum levels of basic proteins have been used to monitor the ongoing allergic disease, little is known about the intracellular expression of these proteins in clinical situations. OBJECTIVE: The aim of the study was to determine the intracellular expression of eosinophil cationic protein (ECP) and eosinophil peroxidase (EPO) in asthmatic children and control subjects and relate it to serum levels of both proteins, lung function tests and immunoglobulin (Ig)E levels. METHODS: Serum ECP and EPO concentrations were determined by immunoassays in 13 asthmatic children (mean age: 9 +/- 1 years, mean FEV1: 92 +/- 10% predicted, geometric mean PC20 histamine 0.5 mg/mL) and 10 age-matched, healthy control subjects. A flow cytometric single cell assay was employed to detect intracellular ECP and EPO in peripheral blood eosinophils. RESULTS: While serum concentrations of both ECP (asthma: median 15.0 microg/L [range 3.6-57.7] vs control: 5.9 microg/L [2.7-9.1]; P = 0.02) and EPO (22.9 microg/L [5.2-82.5] vs 7. 2 microg/L [2.5-12.7]; P = 0.008) were significantly elevated in asthmatics, the intracellular expression of ECP and EPO (measured as mean fluorescence intensity) was decreased (EG1: 55.3 [17.7-120.8] vs 100.3 [46.5-264.4]; P = 0.01; EG2: 80.2 [24.1-135.3] vs 133.7 [32. 1-244.9]; P = 0.04 and EPO: 49.7 [23.1-155.8] vs 94.9 [28.8-115.2]; P = 0.03). In asthmatics there was a significant correlation of FEV1 with intracellular ECP and of bronchial hyperresponsiveness with serum EPO and ECP. Furthermore, total IgE levels were positively correlated with serum EPO only. CONCLUSION: We conclude that in asthmatics the intracellular content of ECP and EPO in peripheral eosinophils is reduced possibly due to degranulation. Epitope masking in activated eosinophils or a shift to early bone marrow-derived progenitors with less granule proteins are further possible explanations.


Subject(s)
Asthma/blood , Blood Proteins/metabolism , Eosinophils/metabolism , Peroxidases/metabolism , Ribonucleases , Asthma/immunology , Child , Eosinophil Granule Proteins , Eosinophil Peroxidase , Eosinophils/immunology , Female , Humans , Immunoglobulin E/blood , Male , Respiratory Function Tests
13.
J AOAC Int ; 82(4): 923-8, 1999.
Article in English | MEDLINE | ID: mdl-10490320

ABSTRACT

This paper presents results of a collaborative trial study (IUPAC project No. 650/93/97) involving 29 laboratories in 13 countries applying a method for detecting genetically modified organisms (GMOs) in food. The method is based on using the polymerase chain reaction to determine the 35S promotor and the NOS terminator for detection of GMOs. reference materials were produced that were derived from genetically modified soy beans and maize. Correct identification of samples containing 2% GMOs is achievable for both soy beans and maize. For samples containing 0.5% genetically modified soy beans, analysis of the 35S promotor resulted also in a 100% correct classification. However, 3 false-negative results (out of 105 samples analyzed) were reported for analysis of the NOS terminator, which is due to the lower sensitivity of this method. Because of the bigger genomic DNA of maize, the probability of encountering false-negative results for samples containing 0.5% GMOs is greater for maize than for soy beans. For blank samples (0% GMO), only 2 false-positive results for soy beans and one for maize were reported. These results appeared as very weak signals and were most probably due to contamination of laboratory equipment.


Subject(s)
Food Analysis , Genetic Engineering , Glycine max/genetics , Plants, Genetically Modified , Polymerase Chain Reaction , Zea mays/genetics , Agrobacterium tumefaciens/genetics , Caulimovirus/genetics , Electrophoresis, Polyacrylamide Gel , False Negative Reactions , False Positive Reactions , Promoter Regions, Genetic , Terminator Regions, Genetic
16.
J Chromatogr B Biomed Sci Appl ; 708(1-2): 195-200, 1998 Apr 24.
Article in English | MEDLINE | ID: mdl-9653962

ABSTRACT

Sameridine is a new candidate drug with both local anaesthetic and analgesic properties. The free concentration of sameridine in blood plasma was determined by coupled-column liquid chromatography. Following adjustment of the pH and the temperature of the plasma samples, the free fraction was prepared by ultrafiltration. The coupled-column liquid chromatographic system consisted of a reversed-phase column, a cation-exchange extraction column and a cation-exchange analytical column. Sameridine was detected by UV determination at 205 nm and the system showed high selectivity. The limit of quantification was 1 nM and the within-day precision was 4.6% (R.S.D., n = 10).


Subject(s)
Analgesics/blood , Anesthetics, Local/blood , Chromatography, Liquid/methods , Piperidines/blood , Humans , Proteins/metabolism , Ultrafiltration
17.
J Biol Chem ; 273(22): 13957-65, 1998 May 29.
Article in English | MEDLINE | ID: mdl-9593745

ABSTRACT

gp91(phox) is a subunit of the phagocyte respiratory burst oxidase catalytic unit. Transcription of CYBB, the gene encoding gp91(phox), is restricted to terminally differentiated phagocytic cells. An element in the proximal CYBB promoter binds a protein complex, referred to as hematopoiesis-associated factor (HAF1), that is necessary for interferon-gamma (IFNgamma)-induced gp91(phox) expression. In these investigations, we determined that HAF1 was a multiprotein complex, cross-immunoreactive with the transcription factors PU.1, interferon regulatory factor 1 (IRF-1), and interferon consensus sequence-binding protein (ICSBP). In electrophoretic mobility shift assay, the HAF1 complex was reconstituted by either in vitro translated PU.1 with IRF-1 or PU.1 with ICSBP, but not by IRF-1 with ICSBP. HAF1a, a slower mobility complex with the same binding site specificity as HAF1, was also investigated. Similar to the HAF1 complex, the HAF1a complex was cross-immunoreactive with PU. 1, IRF-1, and ICSBP. Unlike the HAF1 complex, reconstitution of the HAF1a complex required in vitro translated PU.1 with both IRF-1 and ICSBP. An artificial promoter construct containing the HAF1/HAF1a binding site was modestly activated in the myelomonocytic cell line U937 by co-transfection either with PU.1 and IRF-1 or with PU.1 and ICSBP, but it was strongly activated by co-transfection with PU.1, IRF-1, and ICSBP. This activation required serine 148-phosphorylated PU.1. These studies describe a novel mechanism for PU.1 transcriptional activation via interaction with both IRF-1 and ICSBP, a target gene for the interaction of IRF-1 with ICSBP, and a novel activation function for ICSBP as a component of a multiprotein complex.


Subject(s)
DNA-Binding Proteins/metabolism , Membrane Glycoproteins/metabolism , NADPH Oxidases , Phosphoproteins/metabolism , Proto-Oncogene Proteins/metabolism , Repressor Proteins/metabolism , Trans-Activators/metabolism , Humans , Interferon Regulatory Factor-1 , Interferon Regulatory Factors , Molecular Sequence Data , NADPH Oxidase 2 , Promoter Regions, Genetic , Protein Binding , Tumor Cells, Cultured
18.
Eur J Biochem ; 248(3): 767-74, 1997 Sep 15.
Article in English | MEDLINE | ID: mdl-9342228

ABSTRACT

Biosynthesis of decorin was investigated by incubating a rat fibroblast cell line with various radiolabelled protein and galactosaminoglycan precursors. The following cell-associated and distinct intermediates were isolated and identified: a pool of non-glycosylated core protein, two pools of decorin with incomplete chains, one with three sulphated disaccharide repeats and another with five or more sulphated disaccharide repeats, as well as decorin with mature chains. Results of pulse/chase experiments indicated that these pools represented discrete stages in chain growth. Treatment with brefeldin A, which blocks transport from the endoplasmic reticulum to the Golgi, resulted in accumulation of decorin with an incomplete chain containing six or seven largely unsulphated disaccharide repeats. During recovery from drug treatment, 4-sulfation reappeared earlier than 6-sulfation. The results suggest that the galactosaminoglycan assembly-line consists of separate multienzyme complexes that build only a limited section of the chain. Furthermore, brefeldin A causes segregation of compartments involved in separate stages of the assembly line. In an earlier report [Moses, J., Oldberg. A., Cheng, F. & Fransson, L.-A. (1997) Eur. J. Biochem. 248, 521-526] we took advantage of such segregation to identify and characterize a transient 2-phosphorylation of xylose in the linkage region.


Subject(s)
Polysaccharides/biosynthesis , Proteoglycans/biosynthesis , Amino Acid Sequence , Animals , Brefeldin A , Cell Line , Chromatography, Gel , Cyclopentanes/pharmacology , Decorin , Disaccharides/analysis , Disaccharides/metabolism , Extracellular Matrix Proteins , Fibroblasts , Methionine/metabolism , Molecular Sequence Data , Oligosaccharides/metabolism , Protein Precursors/metabolism , Protein Synthesis Inhibitors/pharmacology , Rats , Sulfates/metabolism , Sulfur Radioisotopes/metabolism
19.
J Biol Chem ; 272(14): 9344-55, 1997 Apr 04.
Article in English | MEDLINE | ID: mdl-9083071

ABSTRACT

The CYBB gene encodes gp91(phox), the heavy chain of the phagocyte-specific NADPH oxidase. CYBB is transcriptionally inactive until the promyelocyte stage of myelopoiesis, and in mature phagocytes, expression of gp91(phox) is further increased by interferon-gamma (IFN-gamma) and other inflammatory mediators. The CYBB promoter region contains several lineage-specific cis-elements involved in the IFN-gamma response. We screened a leukocyte cDNA expression library for proteins able to bind to one of these cis-elements (-214 to -262 base pairs) and identified TF1(phox), a protein with sequence-specific binding to the CYBB promoter. Electrophoretic mobility shift assay with nuclear proteins from a variety of cell lines demonstrated binding of a protein to the CYBB promoter that was cross-immunoreactive with TF1(phox). DNA binding of this protein was increased by IFN-gamma treatment in the myeloid cell line PLB985, but not in the non-myeloid cell line HeLa. Overexpression of recombinant TF1(phox) in PLB985 cells increased endogenous gp91(phox) message abundance, but did not lead to cellular differentiation. Overexpression of TF1(phox) in myeloid leukemia cell lines increased reporter gene expression from artificial promoter constructs containing CYBB promoter sequence. These data suggested that TF1(phox) increased expression of gp91(phox).


Subject(s)
DNA-Binding Proteins/chemistry , Leukemia, Myeloid/metabolism , Membrane Glycoproteins/biosynthesis , NADPH Oxidases/genetics , Base Sequence , Cell Differentiation , Electrophoresis, Polyacrylamide Gel , Genes, Reporter , HeLa Cells , Humans , Interferon-gamma/pharmacology , Leukemia, Myeloid/genetics , Molecular Sequence Data , NADPH Oxidase 2 , Promoter Regions, Genetic , Transfection
20.
J Immunol ; 157(6): 2418-29, 1996 Sep 15.
Article in English | MEDLINE | ID: mdl-8805641

ABSTRACT

The cytochrome b558 heavy chain (gp9l-phox) is expressed in terminally differentiated myelomonocytic cells. Three cis-elements located between -450 and -100 bp of the gp91-phox promoter are required for IFN-gamma induced transcription. Mutations that disrupt individual cis-elements incrementally decrease gp9l-phox promoter activity, and one of the two proximal elements must be present for an IFN-gamma response. The DNA-binding activities that interact with each of the cis-elements exhibit similar gel mobility and binding site specificity, although a consensus binding site common to the three elements is not apparent. An increased level of each DNA/protein complex is observed in myeloid cells following treatment with PMA, retinoic acid/dimethylformamide, or IFN-gamma, but not in similarly treated HeLa cells. The myeloid-specific increase in the intensity of each complex is delayed 12 to 24 h following IFN-gamma treatment, and the complexes are not immunoreactive with antisera directed against IFN-responsive factors such as IRF-1, IRF-2, IFN consensus sequence binding protein, Stat1, and IFN-stimulated gene factor-3 gamma, although IRF-2 is additionally detected as binding to the middle cis-element. These results reveal cis-elements and a DNA-binding factor(s) that participate in a common pathway in response to various stimuli that induce gp9l-phox transcription.


Subject(s)
DNA-Binding Proteins/genetics , DNA-Binding Proteins/physiology , Gene Expression Regulation/immunology , Interferon-gamma/pharmacology , Membrane Glycoproteins/genetics , NADPH Oxidases , Promoter Regions, Genetic/immunology , Transcription, Genetic/immunology , Base Sequence , Binding Sites/genetics , Binding Sites/immunology , DNA-Binding Proteins/metabolism , Humans , Interferon-gamma/genetics , Membrane Glycoproteins/immunology , Molecular Sequence Data , NADPH Oxidase 2 , Promoter Regions, Genetic/physiology , Transcription, Genetic/drug effects , Tumor Cells, Cultured
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