RESUMO
The potential for gene therapy to be an effective treatment for cystic fibrosis has been hampered by the limited gene transfer efficiency of current vectors. We have shown that recombinant Sendai virus (SeV) is highly efficient in mediating gene transfer to differentiated airway epithelial cells, because of its capacity to overcome the intra- and extracellular barriers known to limit gene delivery. Here, we have identified a novel method to allow the cystic fibrosis transmembrane conductance regulator (CFTR) cDNA sequence to be inserted within SeV (SeV-CFTR). Following in vitro transduction with SeV-CFTR, a chloride-selective current was observed using whole-cell and single-channel patch-clamp techniques. SeV-CFTR administration to the nasal epithelium of cystic fibrosis (CF) mice (Cftr(G551D) and Cftr(tm1Unc)TgN(FABPCFTR)#Jaw mice) led to partial correction of the CF chloride transport defect. In addition, when compared to a SeV control vector, a higher degree of inflammation and epithelial damage was found in the nasal epithelium of mice treated with SeV-CFTR. Second-generation transmission-incompetent F-deleted SeV-CFTR led to similar correction of the CF chloride transport defect in vivo as first-generation transmission-competent vectors. Further modifications to the vector or the host may make it easier to translate these studies into clinical trials of cystic fibrosis.
Assuntos
Regulador de Condutância Transmembrana em Fibrose Cística/genética , Fibrose Cística/terapia , Terapia Genética/métodos , Vetores Genéticos/administração & dosagem , Vírus Sendai/genética , Aerossóis , Animais , Cloretos/metabolismo , Regulador de Condutância Transmembrana em Fibrose Cística/metabolismo , Células Epiteliais/metabolismo , Células Epiteliais/virologia , Feminino , Expressão Gênica , Engenharia Genética , Vetores Genéticos/genética , Iodetos/metabolismo , Canais Iônicos/metabolismo , Pulmão , Masculino , Camundongos , Camundongos Knockout , Mutação , Técnicas de Patch-Clamp , Transdução Genética/métodosRESUMO
Systemic sclerosis (SSc) is a connective tissue disease of unknown aetiology characterized by fibrosis of the skin and internal organs, vascular abnormalities and humoral autoimmunity. Strong T-cell-dependent autoantibody and HLA associations are found in SSc subsets. The co-stimulatory molecule, CD86, expressed by antigen-presenting cells, plays a crucial role in priming naïve lymphocytes. We hypothesized that SSc, or one of the disease subsets, could be associated with single-nucleotide polymorphisms of the CD86 gene. Using sequence specific primer-polymerase chain reaction (SSP-PCR) methodology, we assessed four CD86 polymorphisms in 221 patients with SSc and 227 healthy control subjects from the UK. Haplotypes were constructed by inference and confirmed using PHASE algorithm. We found a strong association between SSc and a specific haplotype (haplotype 5), which was more prevalent in patients than in controls (29% vs 15%, OR = 2.3, chi(2) = 12, P = 0.0005). This association could be attributed to the novel -3479 promoter polymorphism; a significant difference was observed in the distribution of the CD86 -3479 G allele in patients with SSc compared to controls (43.7% vs. 32.4%, OR = 1.7, chi(2) = 12.1, P = 0.0005). TRANSFAC analyses suggest that the CD86-3479T allele contains putative GATA and TBP sites, whereas G allele does not. We assessed the relative DNA protein-binding activity of the -3479 polymorphism in vitro using electromobility gel shift assays (EMSA), which showed that the -3479G allele has less binding affinity compared to the T allele for nuclear proteins. These findings highlight the importance of co-stimulatory pathways in SSc pathogenesis.
Assuntos
Alelos , Antígeno B7-2/genética , Predisposição Genética para Doença , Polimorfismo de Nucleotídeo Único/genética , Elementos de Resposta/genética , Escleroderma Sistêmico/genética , Algoritmos , Antígeno B7-2/biossíntese , Antígeno B7-2/imunologia , Sítios de Ligação/genética , Sítios de Ligação/imunologia , Proteínas de Ligação a DNA/genética , Proteínas de Ligação a DNA/imunologia , Proteínas de Ligação a DNA/metabolismo , Ensaio de Desvio de Mobilidade Eletroforética , Feminino , Haplótipos , Humanos , Masculino , Polimorfismo de Nucleotídeo Único/imunologia , Ligação Proteica/genética , Ligação Proteica/imunologia , Elementos de Resposta/imunologia , Escleroderma Sistêmico/imunologia , Escleroderma Sistêmico/metabolismo , Transdução de Sinais/genética , Transdução de Sinais/imunologia , Software , Reino UnidoRESUMO
Much of the morbidity and mortality seen in cystic fibrosis (CF) is related to chronic infection of the respiratory tract with Pseudomonas aeruginosa. Some studies have attributed the strong relationship between CF and Pseudomonas colonization to the presence of increased numbers of specific cell-surface receptors, although other work suggests that this relates to the presence of mucus. Several groups are now assessing the use of gene transfer as a novel form of treatment for CF. We have examined whether P. aeruginosa binding to freshly obtained CF respiratory epithelial cells is increased, and have studied the effects of transfer of the CF transmembrane conductance regulator (CFTR) gene on this attachment. Binding of P. aeruginosa to noncultured nasal epithelial cells from both CF patients (n = 31) and healthy controls (n = 15) was studied with scanning electron microscopy. Binding was also assessed for CF cells following transfection with CFTR/liposome complexes. Epifluorescence microscopy was used to assess the effects of gene transfer on chloride fluxes. Adherence of P. aeruginosa directly to the cell surface of CF airway epithelium was significantly (P < 0.001) increased over that in non-CF controls. Liposome-mediated CFTR gene transfer resulted in a significant (P < 0.01) reduction in the numbers of bacteria bound to ciliated epithelial cells. Fluorescence microscopy confirmed correction of the basic chloride defect. Thus, in CF, the absence of normal CFTR results in increased binding of P. aeruginosa to respiratory epithelial cells. This abnormality can be corrected in vitro by restoration of CFTR function. This has important implications both for the pathogenesis of CF and for the future application and assessment of gene therapy for this disease.
Assuntos
Aderência Bacteriana/fisiologia , Regulador de Condutância Transmembrana em Fibrose Cística/genética , Técnicas de Transferência de Genes , Pseudomonas aeruginosa/metabolismo , Conchas Nasais/citologia , Cloretos/metabolismo , Fibrose Cística/genética , Fibrose Cística/microbiologia , Regulador de Condutância Transmembrana em Fibrose Cística/metabolismo , Células Epiteliais , Humanos , Processamento de Imagem Assistida por Computador , Lipossomos/química , Microscopia Eletrônica de Varredura , Microscopia de Fluorescência , Pseudomonas aeruginosa/ultraestrutura , Conchas Nasais/microbiologia , Conchas Nasais/ultraestruturaRESUMO
A number of recent observations suggest a link between airway Cl-transport and asthma. We have previously described the properties of a voltage- and Ca2+ -dependent chloride channel present in airway epithelium. We now show that agents able to prevent indirectly induced bronchoconstriction (sodium cromoglycate, nedocromil sodium, and furosemide) reduce either the single-channel conductance or the open probability of this channel. The effects of these agents and the Ca2+ dependence of the channel are localized to the same surface, and we show that the channel possesses a specific divalent cation binding site, which responds to concentrations of Ca2+ found on the airway mucosal surface. No alteration of the single-channel properties of this channel were seen in cystic fibrosis epithelium. These data suggest a mechanism by which structurally diverse agents may influence asthma.
Assuntos
Antiasmáticos/farmacologia , Canais de Cloreto/efeitos dos fármacos , Canais de Cloreto/fisiologia , Pulmão/fisiologia , Animais , Cálcio/farmacologia , Linhagem Celular , Cromolina Sódica/farmacologia , Fibrose Cística/fisiopatologia , Condutividade Elétrica , Epitélio/efeitos dos fármacos , Epitélio/fisiologia , Furosemida/farmacologia , Humanos , Pulmão/efeitos dos fármacos , Nedocromil/farmacologia , Ratos , OvinosRESUMO
Functional assessment of the efficacy of CFTR gene transfer protocols in humans has previously involved measurement of in vivo potential difference. We have studied whether freshly obtained airway epithelial cells may provide suitable tissue for studies of in vivo gene transfer using fluorescent digital imaging microscopy. Nasal epithelial cells from non-cystic fibrosis subjects (n = 6) and from cystic fibrosis (CF) patients (delta F508: delta F508, n = 5) were obtained by brushing and loaded with 6-methoxy-N-(3-sulfopropyl)quinolinium (SPQ). Addition of the cAMP-agonists forskolin (20 microM) and 3-isobutyl-1-methylxanthine (IBMX, 100 microM) produced an increased efflux of iodide from the cells which was significantly (P < 0.05) greater in non-CF than in CF cells. Efflux following addition of the calcium ionophore, ionomycin (100 microM) was similar in both non-CF and CF cells. Liposome-mediated transfection of CF nasal epithelial cells in vitro with CFTR-cDNA restored the cAMP-stimulated efflux to non-CF values. Bronchial epithelial cells from non-CF subjects showed responses to forskolin and ionomycin that were not different to those in non-CF nasal epithelia. These data demonstrate that the assay provides a useful method for assessing correction of abnormal ion transport in non-cultured CF epithelium and is likely to provide a further assay for assessment of in vivo gene transfer efficiency in protocols of gene therapy for CF.
Assuntos
Brônquios/metabolismo , Cloretos/metabolismo , Regulador de Condutância Transmembrana em Fibrose Cística/genética , Fibrose Cística/metabolismo , Mucosa Nasal/metabolismo , Adulto , Idoso , Brônquios/citologia , Brônquios/patologia , Células Cultivadas , Cloretos/análise , Colforsina/farmacologia , Fibrose Cística/patologia , Fibrose Cística/terapia , Regulador de Condutância Transmembrana em Fibrose Cística/biossíntese , Epitélio/efeitos dos fármacos , Epitélio/metabolismo , Epitélio/patologia , Corantes Fluorescentes , Terapia Genética , Humanos , Ionomicina/farmacologia , Cinética , Pessoa de Meia-Idade , Mucosa Nasal/citologia , Mucosa Nasal/patologia , Compostos de Quinolínio , Valores de Referência , Transfecção , Conchas NasaisRESUMO
Phase one clinical trials for gene therapy of cystic fibrosis are in progress using either liposomes or adenoviral vectors for CFTR gene transfer to epithelial cells in the airways. In addition to electrophysiological measurements, expression of vector CFTR is usually assessed by RT-PCR. We have developed a CFTR-expression vector, pCFAS, that simplifies the distinction of transgene-derived CFTR mRNA from endogenous mRNA. Two point mutations were introduced into CFTR cDNA which eliminated a SphI restriction site and created a new, unique AgeI restriction site. Neither mutation altered the predicted amino acid sequence of the protein. Restriction digestion of RT-PCR products from cells transfected with pCFAS allowed the differentiation of transgene and endogenous CFTR transcripts. To verify function of the mutated CFTR, the plasmid was transferred into freshly obtained nasal epithelial cells from CF patients ex vivo using cationic liposomes. Fluorescence microscopy using the halide-sensitive fluorophore SPQ demonstrated restoration of cAMP-mediated Cl- secretion. This plasmid will be useful for CFTR gene transfer studies in vitro and in vivo.
Assuntos
Regulador de Condutância Transmembrana em Fibrose Cística/genética , Técnicas de Transferência de Genes , Vetores Genéticos , Mutagênese , Sequência de Bases , Linhagem Celular , Cloretos/metabolismo , Colforsina/farmacologia , Fibrose Cística/metabolismo , DNA Complementar , Humanos , Ionomicina/farmacologia , Dados de Sequência Molecular , Mucosa Nasal/efeitos dos fármacos , Mucosa Nasal/metabolismo , Transcrição GênicaRESUMO
Two important issues that can be addressed by animal models are disease pathogenesis and the testing of new treatments, including gene therapy. How closely these models mimic the relevant disorder in humans will determine their usefulness. This study examines how closely the characteristic bioelectric features of cystic fibrosis (CF) are reproduced in the airways and intestinal tract of the exon 10 insertional mutant mouse (cf/cf). In agreement with CF subjects these cf/cf mutant mice demonstrate the following: 1) reduced adenosine 3',5'-cyclic monophosphate-related chloride secretion throughout the respiratory and intestinal tracts both in vivo and in vitro, 2) calcium-related chloride secretion that is preserved in the airways but reduced in the intestine, and 3) a more negative nasal potential difference and increased amiloride response compared with wild-type animals, likely to relate to increased sodium absorption. In contrast to humans, sodium absorption is not increased in the small intestine and is reduced in the trachea of the cf/cf mice. We conclude that the majority of the salient electrophysiological features of CF required for studies of pathogenesis or testing of new treatments are present in these cf/cf mice.
Assuntos
Fibrose Cística/genética , Fibrose Cística/fisiopatologia , Elementos de DNA Transponíveis , Éxons , Animais , Cálcio/fisiologia , Cloretos/metabolismo , AMP Cíclico/fisiologia , Eletrofisiologia , Humanos , Intestino Grosso/fisiopatologia , Intestino Delgado/fisiopatologia , Camundongos , Camundongos Mutantes , Cavidade Nasal/fisiopatologia , Valores de Referência , Traqueia/fisiopatologiaRESUMO
The effect of osmotic stress on Cl- permeability in human squamous lung carcinoma epithelial (S1) cells was investigated using a macroscopic 125I efflux assay. Hypotonic challenge of monolayers led to a significant (P < 0.01) dose-related increase in efflux from pre-loaded cells, returning to pre-activation rates within 10 min. A similar magnitude of response could be produced by challenge with an isotonic low chloride-containing solution. Neither 100 mM dideoxy-forskolin nor 100 mM verapamil inhibited the increase in Cl- secretion after hypotonic challenge, whereas 100 mM DIDS inhibited volume-activated Cl- secretion by 55%. Both Northern and Western blot analysis confirmed the absence of MDR1 mRNA and P-glycoprotein in the S1 cells. We conclude that these cells have a volume-regulated Cl- secretory pathway that is independent of the ABC transporter, P-glycoprotein.
Assuntos
Ácido 4,4'-Di-Isotiocianoestilbeno-2,2'-Dissulfônico/farmacologia , Carcinoma de Células Escamosas/metabolismo , Cloretos/metabolismo , Colforsina/análogos & derivados , Neoplasias Pulmonares/metabolismo , Verapamil/farmacologia , Membro 1 da Subfamília B de Cassetes de Ligação de ATP/genética , Northern Blotting , Western Blotting , Tamanho Celular , Colforsina/farmacologia , Humanos , Concentração Osmolar , Células Tumorais CultivadasRESUMO
We report gene transfer to the Edinburgh insertional mutant mouse (cf/cf), delivering CFTR cDNA-liposome complexes into the airways by nebulization. We show full restoration of cAMP related chloride responses in some animals and demonstrate, in the same tissues, human CFTR cDNA expression. Overall, a range of correction was seen with restoration of about 50% of the deficit between wild type mice and untreated cf/cf controls. We report modest correction in the intestinal tract following direct instillation and provide initial encouraging safety data for both the respiratory and intestinal tract following the liposome mediated gene delivery. The non-viral nature and potentially lower immunogenicity of DNA-liposomes suggest that this may offer a therapeutic alternative to adenoviral therapies.
Assuntos
Fibrose Cística/terapia , Terapia Genética , Proteínas de Membrana/genética , Animais , Sequência de Bases , Transporte Biológico/genética , Fibrose Cística/genética , Regulador de Condutância Transmembrana em Fibrose Cística , DNA Complementar , Genes Reporter , Humanos , Intestinos , Íons , Lipossomos , Camundongos , Camundongos Mutantes , Dados de Sequência Molecular , Nebulizadores e Vaporizadores , OligodesoxirribonucleotídeosRESUMO
A detailed methodology is presented of two reconstitution protocols for the (Ca(2+)-Mg2+)-ATPase from rabbit skeletal muscle, using the detergent potassium cholate. Method A was shown to produce fully fragmented membranes of definable lipid to protein ratios, which were unable to take up calcium upon hydrolysis of ATP. This protocol was shown to produce a homologous population of membranes with respect to their lipid and protein composition at lipid to protein ratios up to 900:1 (mol/mol). Method B produced vesicles only of high lipid to protein ratios (3000:1), which have the ability to accumulate calcium on addition of ATP. Calcium accumulation and ATP hydrolysis for the ATPase reconstituted into different fatty acyl chain length phospholipids were also studied.
Assuntos
ATPase de Ca(2+) e Mg(2+)/isolamento & purificação , ATPases Transportadoras de Cálcio/isolamento & purificação , Retículo Sarcoplasmático/enzimologia , Animais , Ácidos e Sais Biliares , ATPase de Ca(2+) e Mg(2+)/química , ATPase de Ca(2+) e Mg(2+)/metabolismo , Cálcio/metabolismo , ATPases Transportadoras de Cálcio/química , ATPases Transportadoras de Cálcio/metabolismo , Detergentes , Feminino , Cinética , Lipídeos/análise , Métodos , Proteínas Musculares/análise , CoelhosRESUMO
m-Maleimidobenzoyl-N-hydroxysuccinimide ester (MBS) was used to cross-link the protein components of rabbit skeletal muscle sarcoplasmic reticulum. Analysis of cross-linked material by SDS-polyacrylamide gel electrophoresis showed that both the (Ca(2+)-Mg2+)-ATPase and the 53 kDa glycoprotein could be cross-linked, since the amount of protein at the locations on the gel corresponding to uncross-linked material was reduced in the presence of 1.0 mM MBS. Cross-linked products of 130 kDa, 200-260 kDa and approx. 300 kDa were identified. Probing the cross-linked products with monoclonal antibodies against ATPase, 53 kDa glycoprotein and calsequestrin revealed no cross-linked products containing the ATPase and either calsequestrin or the 53 kDa glycoprotein over the range of molecular weights examined here. Possible interactions between the ATPase and calsequestrin or the 53 kDa glycoprotein were also investigated by studying the ATPase activity for the purified ATPase and for the ATPase in sarcoplasmic reticulum vesicles made permeable to Ca2+ with A23187. Effects of Ca2+ and ATP on the two systems were indistinguishable, providing no evidence for a major modulatory role of calsequestrin or the 53 kDa glycoprotein on the ATPase.
Assuntos
Cálcio/metabolismo , Reagentes de Ligações Cruzadas , Glicoproteínas de Membrana/metabolismo , Retículo Sarcoplasmático/metabolismo , Trifosfato de Adenosina/farmacologia , Animais , Anticorpos Monoclonais , Transporte Biológico , Western Blotting , ATPase de Ca(2+) e Mg(2+)/metabolismo , Calcimicina/farmacologia , Cálcio/farmacologia , ATPases Transportadoras de Cálcio/metabolismo , Calsequestrina/metabolismo , Eletroforese em Gel de Poliacrilamida/métodos , Cinética , Glicoproteínas de Membrana/imunologia , Proteínas/análise , Coelhos , Retículo Sarcoplasmático/efeitos dos fármacos , SuccinimidasRESUMO
Oat and rye plants were treated with either tetcyclacis (an experimental plant growth regulator), nuarimol (a fungicide) or gamma-ketotriazole (an experimental herbicide). These treatments reduced shoot growth and changed the lipid composition of the shoot plasma membranes. In oat, both tetcyclacis and nuarimol treatments increased plasma membrane cholesterol and increased the phosphatidylethanolamine/phosphatidylcholine (PE/PC) ratio, whereas gamma-ketotriazole treatment reduced cholesterol and the PE/PC ratio. In rye, all treatments reduced the PE/PC ratio. Generally, the sterol/phospholipid ratio was less in oat than in rye but the cholesterol/phospholipid ratio was greater. With all treatments in oat and rye, increases were observed in unsaturation of the phospholipid acyl chains. The fluidity of membranes was measured by steady-state fluorescence polarisation of the probe diphenylhexatriene; oat membranes were more fluid than rye. Membrane fluidity was greater in plasma membranes from plants treated with the xenobiotics than the controls. The results are discussed in the context of the effect of plasma membrane lipid composition on membrane fluidity, and it is concluded that there appears to be no overall simple relationship between membrane lipid composition and fluidity that holds for all treatments in both species.
Assuntos
Grão Comestível/metabolismo , Metabolismo dos Lipídeos , Fluidez de Membrana/efeitos dos fármacos , Secale/metabolismo , Esteróis/biossíntese , Xenobióticos/farmacologia , Membrana Celular/química , Difenilexatrieno , Fungicidas Industriais/farmacologia , Herbicidas/farmacologia , Fosfolipídeos/metabolismo , Reguladores de Crescimento de Plantas/farmacologia , Proteínas de Plantas/metabolismo , Pirimidinas/farmacologia , Espectrometria de Fluorescência , Triazóis/farmacologiaAssuntos
Anticorpos Monoclonais , Proteínas Musculares/imunologia , Retículo Sarcoplasmático/imunologia , Animais , ATPase de Ca(2+) e Mg(2+)/imunologia , ATPase de Ca(2+) e Mg(2+)/isolamento & purificação , ATPases Transportadoras de Cálcio/imunologia , ATPases Transportadoras de Cálcio/isolamento & purificação , Calsequestrina/imunologia , Calsequestrina/isolamento & purificação , Reagentes de Ligações Cruzadas , Glicoproteínas/imunologia , Glicoproteínas/isolamento & purificação , Peso Molecular , Proteínas Musculares/isolamento & purificaçãoRESUMO
Experiments were performed in which two batches of sarcoplasmic reticulum were isolated from rabbit hind leg muscle, one in the presence of dithiothreitol, the other in the absence of reducing agent. A comparative study was made of some of the properties of the two preparations, in particular, the Arrhenius behavior of the Ca2+-ATPase. The Ca2+-ATPase isolated in the absence of dithiothreitol is thermally unstable with the result that a triphasic Arrhenius plot was obtained. This triphasic behavior is largely the consequence of an uncoupling of the hydrolytic machinery from the calcium pump. In contrast, the sarcoplasmic reticulum preparation obtained in the presence of dithiothreitol is thermally stable and yields a linear Arrhenius plot. The difference in the Arrhenius behavior shown by the two preparations was abolished when the measurements of Ca2+-ATPase activity were made in the presence of the calcium ionophore, A23187.
Assuntos
ATPases Transportadoras de Cálcio/metabolismo , Cálcio/metabolismo , Canais Iônicos/metabolismo , Retículo Sarcoplasmático/enzimologia , Animais , Fenômenos Biomecânicos , Calcimicina/farmacologia , Ditiotreitol/farmacologia , Estabilidade de Medicamentos , Membro Posterior , Temperatura Alta , Matemática , Coelhos , Retículo Sarcoplasmático/metabolismoRESUMO
The effect of palmitic and oleic acids on Ca2+-ATPase activity in coupled preparations of sarcoplasmic reticulum isolated from rabbit hind leg muscle have been compared with their effects on vesicles uncoupled with Ca2+ ionophore, A23187. Palmitate at 2 microM X mg protein-1 has no significant effect on enzyme activity and does not uncouple catalytic activity from calcium accumulation within the vesicles. Oleic acid at 1 microM X mg protein-1 uncouples the vesicles, whereas 2 microM X mg protein-1 completely inhibits Ca2+-ATPase activity. Fluorescence anisotropy of diphenylhexatriene is not significantly altered by palmitate, but a large transient increase in motion of the probe is observed with addition of oleic acid. The effects of oleic acid on enzyme activity are not mediated via an effect on the bulk properties of the hydrophobic domain of the membrane lipids.