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1.
J Dent Res ; 90(7): 874-9, 2011 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-21471326

RESUMO

UNLABELLED: The cytolethal distending toxin (Cdt), expressed by the periodontal pathogen Aggregatibacter actinomycetemcomitans, inhibits the proliferation of cultured epithelial cells by arresting the cell cycle. The gingival epithelium is an early line of defense against microbial assault. When damaged, bacteria collectively gain entry into underlying connective tissue where microbial products can affect infiltrating inflammatory cells, leading to the destruction of the attachment apparatus. Histological evaluation of rat and healthy human gingival tissue exposed ex vivo to the Cdt for 36 and 18 hours, respectively, revealed extensive detachment of the keratinized outer layer and distention of spinous and basal cells in the oral epithelium. Treated human tissue also exhibited disruption of rete pegs and dissolution of cell junctions. Cells in the connective tissue appeared unaffected. Primary gingival epithelial cells, but not gingival fibroblasts, isolated from the same healthy human tissue were cell-cycle-arrested when treated with the toxin. These findings provide new evidence that the Cdt severely damages the oral epithelium, ex vivo, by specifically targeting epithelial cells, in situ. The Cdt shows preferential targeting of the epithelium as opposed to connective tissue in animal and human gingival explant models. ABBREVIATIONS: cytolethal distending toxin (Cdt), connective tissue (CT), 4',6-diamidino-2-phenylindole (DAPI), human gingival epithelial cells (HGEC), human gingival explants (HGX), human gingival fibroblasts (HGF), junctional epithelium (JE), oral epithelium (OE), rete pegs (RP), sulcular epithelium (SE).


Assuntos
Aggregatibacter actinomycetemcomitans/química , Toxinas Bacterianas/toxicidade , Células Epiteliais/efeitos dos fármacos , Gengiva/efeitos dos fármacos , Mucosa Bucal/efeitos dos fármacos , Adulto , Animais , Ciclo Celular/efeitos dos fármacos , Células Cultivadas , Gengiva/citologia , Humanos , Mucosa Bucal/citologia , Ratos , Ratos Sprague-Dawley , Proteínas Recombinantes , Técnicas de Cultura de Tecidos
2.
J Dent Res ; 90(5): 638-45, 2011 May.
Artigo em Inglês | MEDLINE | ID: mdl-21220361

RESUMO

UNLABELLED: Resistance to treatment and the appearance of secondary tumors in head and neck squamous cell carcinomas (HNSCC) have been attributed to the presence of cells with stem-cell-like properties in the basal layer of the epithelium at the site of the lesion. In this study, we tested the hypothesis that these putative cancer stem cells (CSC) in HNSCC could be specifically targeted and inhibited. We found that 9 of 10 head and neck tumor biopsies contained a subpopulation of cells that expressed CD133, an unusual surface-exposed membrane-spanning glycoprotein associated with CSC. A genetically modified cytolethal distending toxin (Cdt), from the periodontal pathogen Aggregatibacter actinomycetemcomitans, was conjugated to an anti-human CD133 monoclonal antibody (MAb). The Cdt-MAb complex preferentially inhibited the proliferation of CD133(+) cells in cultures of established cell lines derived from HNSCC. Inhibition of the CD133(+) cells was rate- and dose-dependent. Saturation kinetics indicated that the response to the Cdt-MAb complex was specific. Healthy primary gingival epithelial cells that are native targets of the wild-type Cdt were not affected. Analysis of these data provides a foundation for the future development of new therapies to target CSC in the early treatment of HNSCC. ABBREVIATIONS: Cdt, cytolethal distending toxin; CSC, cancer stem cells; HNSCC, head and neck squamous cell carcinoma; MAb, monoclonal antibody.


Assuntos
Antígenos CD/biossíntese , Toxinas Bacterianas/farmacologia , Carcinoma de Células Escamosas/patologia , Regulação Neoplásica da Expressão Gênica , Glicoproteínas/biossíntese , Terapia de Alvo Molecular , Neoplasias Bucais/patologia , Células-Tronco Neoplásicas/efeitos dos fármacos , Antígeno AC133 , Aggregatibacter actinomycetemcomitans/fisiologia , Animais , Anticorpos Monoclonais , Toxinas Bacterianas/genética , Carcinoma de Células Escamosas/tratamento farmacológico , Carcinoma de Células Escamosas/genética , Linhagem Celular Tumoral , Proliferação de Células/efeitos dos fármacos , Humanos , Imunotoxinas/genética , Imunotoxinas/farmacologia , Camundongos , Neoplasias Bucais/tratamento farmacológico , Neoplasias Bucais/genética , Mutagênese Sítio-Dirigida , Células-Tronco Neoplásicas/metabolismo , Peptídeos
3.
Oral Microbiol Immunol ; 24(2): 116-23, 2009 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-19239638

RESUMO

INTRODUCTION: Cytolethal distending toxin (Cdt) is potentially one of several virulence factors of Aggregatibacter actinomycetemcomitans, the prime etiological agent of localized aggressive periodontitis (LAP). Little is known regarding the Cdt-specific antibody response in humans. The current study is a quantitative and qualitative evaluation of the toxin-specific antibody response in a cohort of LAP patients and age-, race- and sex-matched controls. METHODS: Ninety-five subjects provided a total of 692 serum samples. Sera were analysed by enzyme-linked immunosorbent assays to determine the titers of antibody against the intact Cdt holotoxin as well as the individual subunit proteins (CdtA, CdtB, and CdtC). Neutralization of growth inhibition mediated by Cdt was evaluated in a modified colony-forming assay using Chinese hamster ovary cells. RESULTS: Fourteen of the 95 subjects exhibited significant serum Cdt-binding activity. There were no differences in the percentages of seropositive individuals or in the mean antibody titers between the control and LAP groups. Binding activity was detected against each of the three Cdt subunit proteins in all of the positive samples. Neutralization of Cdt-mediated growth inhibition was detected in samples from all of the seropositive subjects (range 20-75%). CONCLUSIONS: Cdt, a recently identified A. actinomycetemcomitans virulence factor, is capable of inducing a neutralizing antibody response indicating that the toxin is produced during natural infection of humans. The failure of a vast majority (20 of 23) of the LAP subjects to mount a significant anti-Cdt response may in part explain their relative susceptibility to the disease.


Assuntos
Infecções por Actinobacillus/imunologia , Aggregatibacter actinomycetemcomitans/imunologia , Periodontite Agressiva/imunologia , Periodontite Agressiva/microbiologia , Toxinas Bacterianas/imunologia , Adolescente , Adulto , Aggregatibacter actinomycetemcomitans/patogenicidade , Animais , Anticorpos Antibacterianos/sangue , Anticorpos Antibacterianos/imunologia , Reações Antígeno-Anticorpo , Células CHO , Estudos de Casos e Controles , Ciclo Celular/imunologia , Criança , Cricetinae , Cricetulus , Feminino , Humanos , Masculino , Mutagênicos , Subunidades Proteicas/imunologia , Proteínas Recombinantes/imunologia , Fatores de Virulência/imunologia , Adulto Jovem
4.
Acta Neurobiol Exp (Wars) ; 60(2): 175-86, 2000.
Artigo em Inglês | MEDLINE | ID: mdl-10909173

RESUMO

The NADPH-diaphorase (as a neuronal NO-synthase) reactivity in the medullary structures of the respiratory rhythm (RR) generator and the role of NO in the regulation of respiratory activity in the phrenic nerve of artificially superfused semi-isolated medulla-spinal cord preparations were investigated in newborn rats. NADPH-diaphorase positive neurons were found in all nuclei of both dorsal and ventral respiratory groups of neurons. The maximal density of stained cells was present within the rostral part of the ventrolateral medulla (VLM), in the region of the lateral paragigantocellular reticular nucleus. It was found that endogenous NO mediates the mechanism of tonic inhibitory control of the RR frequency located in the rostral VLM under normal and hypoxic conditions, and appears to be involved in generation of the basic RR by the more caudal structures of VLM. It was shown that NO biosynthesis mediates the effect of NMDA receptors activation on the RR.


Assuntos
Animais Recém-Nascidos/fisiologia , Bulbo/metabolismo , Óxido Nítrico/metabolismo , Mecânica Respiratória/fisiologia , Animais , Hipóxia/metabolismo , Técnicas In Vitro , Bulbo/citologia , NADPH Desidrogenase/metabolismo , Neurônios/enzimologia , Óxido Nítrico Sintase/metabolismo , Óxido Nítrico Sintase Tipo I , Ratos , Ratos Wistar
8.
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