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1.
Biol. Res ; 54: 13-13, 2021. tab
Artículo en Inglés | LILACS | ID: biblio-1505806

RESUMEN

BACKGROUND: Helicobacter pylori is detected by pathogen recognition receptors including toll-like receptors (TLR) and nucleotide-binding oligomerization domain (NOD)-like receptors, eliciting an innate immune response against this bacteria. The aim of this study was to assess if polymorphisms of TLR2, TLR4, TLR5, NOD1 and NOD2 genes are associated with gastric cancer, in particular in individuals infected with H. pylori. RESULTS: A case-control study of 297 gastric cancer patients and 300 controls was performed to assess the association of 17 polymorphisms. Analyses performed under the allele model did not find association with gastric cancer. However, NOD1 rs2075820 (p.E266K) showed association with intestinal-type gastric cancer among H. pylori infected subjects (OR = 2.69, 95% CI 1.41-5.13, p = 0.0026). The association was not statistically significant in diffuse-type gastric cancer cases (OR = 1.26, 95% CI 0.63-2.52, p = 0.51). When the analyses were performed in patients carrying H. pylori strains harboring the cag pathogenicity island (cagPAI), we noticed significant association with NOD1 rs2075820 (OR = 4.90, 95% CI 1.80-3.36, p = 0.0019), in particular for intestinal-type gastric cancer cases (OR = 7.16, 95% CI 2.40-21.33, p = 4.1 × 10- 4) but not among diffuse-type gastric cancer cases (OR = 3.39, 95% CI 1.13-0.10, p = 0.03). CONCLUSIONS: NOD1 rs2075820 increases the risk of intestinal-type gastric cancer among individuals infected with H. pylori, particularly in those harboring the cagPAI.


Asunto(s)
Humanos , Neoplasias Gástricas/genética , Infecciones por Helicobacter/genética , Proteína Adaptadora de Señalización NOD1/genética , Estudios de Casos y Controles , Helicobacter pylori , Islas Genómicas
2.
Protein & Cell ; (12): 55-66, 2017.
Artículo en Inglés | WPRIM | ID: wpr-757357

RESUMEN

The innate immune system is critical for clearing infection, and is tightly regulated to avert excessive tissue damage. Nod1/2-Rip2 signaling, which is essential for initiating the innate immune response to bacterial infection and ER stress, is subject to many regulatory mechanisms. In this study, we found that LRRK2, encoded by a gene implicated in Crohn's disease, leprosy and familial Parkinson's disease, modulates the strength of Nod1/2-Rip2 signaling by enhancing Rip2 phosphorylation. LRRK2 deficiency markedly reduces cytokine production in macrophages upon Nod2 activation by muramyl dipeptide (MDP), Nod1 activation by D-gamma-Glu-meso-diaminopimelic acid (iE-DAP) or ER stress. Our biochemical study shows that the presence of LRRK2 is necessary for optimal phosphorylation of Rip2 upon Nod2 activation. Therefore, this study reveals that LRRK2 is a new positive regulator of Rip2 and promotes inflammatory cytokine induction through the Nod1/2-Rip2 pathway.


Asunto(s)
Animales , Humanos , Ratones , Citocinas , Genética , Alergia e Inmunología , Células HEK293 , Inmunidad Innata , Genética , Inflamación , Genética , Alergia e Inmunología , Proteína 2 Quinasa Serina-Treonina Rica en Repeticiones de Leucina , Genética , Alergia e Inmunología , Ratones Noqueados , Proteína Adaptadora de Señalización NOD1 , Genética , Alergia e Inmunología , Proteína Adaptadora de Señalización NOD2 , Genética , Alergia e Inmunología , Fosforilación , Genética , Alergia e Inmunología , Proteína Serina-Treonina Quinasa 2 de Interacción con Receptor , Genética , Alergia e Inmunología , Proteína Serina-Treonina Quinasas de Interacción con Receptores , Genética , Alergia e Inmunología , Transducción de Señal , Genética , Alergia e Inmunología
3.
Rev. bras. enferm ; 68(2): 253-260, Mar-Apr/2015. tab
Artículo en Portugués | LILACS, BDENF | ID: lil-752516

RESUMEN

RESUMO Objetivo: construir e validar um instrumento para monitorar a qualidade dos registros de enfermagem no Programa de Assistência Domiciliar (PAD) em um hospital universitário. Método: estudo metodológico envolvendo a elaboração de um manual e submetido à validação de conteúdo por seis juízes sob consenso ≥ 80%. A coleta ocorreu em 2012 por meio de questionário contendo: evolução de enfermagem, diagnóstico e prescrição de enfermagem e normas para os registros da equipe de enfermagem preconizadas pelo Conselho Regional de Enfermagem-SP e pela instituição. Os itens do manual foram julgados de acordo com as variáveis - relevância, pertinência, clareza e simplicidade. Resultados: das 39 proposições 100% atingiram consenso ≥ 80% em relevância, pertinência e clareza; 92,3% em simplicidade. Os itens sono/repouso, mobilidade e checagem nas atividades prescritas não atingiram consenso mínimo favorável, sendo aprimorados pelas sugestões dos juízes. Conclusão: acreditamos que o instrumento possibilitará a melhoria dos processos de trabalho no PAD. .


RESUMEN Objetivo: construir y validar un instrumento para monitorear la calidad del registros de enfermería en Programa de Atención Domiciliaria (PAD) de un Hospital Universitario. Metodo: estudio metodológico. Fue construido un manual y sometió a validación de contenido por seis jueces bajo el consenso ≥80%. La recogida currió en 2012, con un cuestionario que contiene: evolución de enfermería, diagnóstico y prescripción de enfermería y normas para los registros del personal de enfermaria estabelecidas por Consejo Regional de Enfermería-SP y por la institución. Los artículos del manual fueran juzgadso conforme las variables relevancia, pertinencia, claridad y sencillez. Resultados: de las 39 proposiciones 100% alcanzó consenso ≥ 80% en la relevancia, pertinencia y claridad; 92,3% en la simplicidad. Los itens sueño/resto, movilidad y verificar las actividades prescritas no alcanzó consenso favorable, siendo mejoradas por las sugerencias de los jueces. Conclusión: creemos que el instrumento permitirá la mejora de los procesos de trabajo en PAD. .


ABSTRACT Objective: to build and validate an instrument aimed at monitoring the quality of nursing records in the Home Care Program (HCP) of a university hospital. Method: methodological study involving the elaboration of a manual, whose content was later submitted to six experts for validation, reaching a ≥ 80% consensus. The data collection process was carried out in 2012 by means of a questionnaire comprised of the following issues: nursing evolution, nursing diagnosis, and nursing prescription, and standards for the nursing team recommended by the Regional Nursing Council of São Paulo and by the assessed institution. Manual items were judged according to the following variables: relevance, pertinence, clarity and simplicity. Results: of the 39 propositions, 100% achieved ≥ 80% agreement in the relevance, pertinence and clarity variables; 92.3% in the simplicity variable. Sleep/rest, Mobility and Check-out variables did not reach a favorable minimum consensus in the prescribed activities and were improved following suggestions from the experts. Conclusion: we believe that the instrument will enable the improvement of the HCP’s work process. .


Asunto(s)
Humanos , Actinas/metabolismo , Cofilina 1/metabolismo , Disentería Bacilar/microbiología , Proteína Adaptadora de Señalización NOD1/metabolismo , Fosfoproteínas Fosfatasas/metabolismo , Shigella flexneri/fisiología , Actinas/química , Western Blotting , Células Cultivadas , Cofilina 1/genética , Ensayo de Inmunoadsorción Enzimática , Técnica del Anticuerpo Fluorescente Indirecta , Regulación de la Expresión Génica , Células HeLa , Ensayos Analíticos de Alto Rendimiento , Técnicas para Inmunoenzimas , Inmunoprecipitación , Inflamación , Mediadores de Inflamación/metabolismo , FN-kappa B/genética , FN-kappa B/metabolismo , Proteína Adaptadora de Señalización NOD1/antagonistas & inhibidores , Proteína Adaptadora de Señalización NOD1/genética , Fosforilación , Fosfoproteínas Fosfatasas/genética , Reacción en Cadena en Tiempo Real de la Polimerasa , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , ARN Mensajero/genética , ARN Interferente Pequeño/genética , Transducción de Señal
4.
Journal of Clinical Otorhinolaryngology Head and Neck Surgery ; (24): 1323-1328, 2015.
Artículo en Chino | WPRIM | ID: wpr-749177

RESUMEN

OBJECTIVE@#To explore role of Nods (nucleotide-binding oligomerization domain Nod Like receptors) kind of pattern recognition receptors (PRR) in patients with allergic rhinitis.@*METHOD@#The mRNA and protein of Nod1, Nod2 of Nalp3 were analyzed in the turbinate mucosa of patients with allergic rhinitis, nasal septum deviation (NSD) nasal mucosa of patients and nasal polyp mucosa with Real-Time RT-PCR, Western blot and immunohistochemistry respectively, and Nod1 expression changes was explored in PBMC with wad explored Western-blot and then the level of IL-4, IL-6, IL-10, IFN-γ were detected in serum of AR after desensitization treatment.@*RESULT@#These Nods like receptors, mainly found in nasal mucosa epithelial cells, glandular epithelium and inflammatory cells (e. g. plasma cells, eosinophils), were expressed in the nasal mucosa tissues. In AR group, Nod1 (mRNA and protein) expression were lower than NSD group (P0.05.@*CONCLUSION@#Nod1, Nod2 and Nalp3 expression were seen in the two groups,and the Nod1 expression in allergic rhinitis group was lower than other two groups, while, the Nalp3 was higher than other two groups. It showed Nod1, Nalp3 may be involved in the pathogenesis of allergic rhinitis. Expression of Nod1 in PBMC reduced after sublingual desensitization treatment. Besides, the change of Nod1 was negatively correlated with the change of IL-10 in PBMC. So,it seemed that Nod1 may regulate IL-10 changes and be involved in sublingual desensitization therapy.


Asunto(s)
Humanos , Proteínas Portadoras , Metabolismo , Interferón gamma , Sangre , Interleucina-10 , Sangre , Interleucina-4 , Sangre , Interleucina-6 , Sangre , Leucocitos Mononucleares , Metabolismo , Proteína con Dominio Pirina 3 de la Familia NLR , Mucosa Nasal , Metabolismo , Pólipos Nasales , Metabolismo , Proteína Adaptadora de Señalización NOD1 , Metabolismo , Proteína Adaptadora de Señalización NOD2 , Metabolismo , Receptores de Reconocimiento de Patrones , Metabolismo , Rinitis Alérgica , Metabolismo , Cornetes Nasales , Metabolismo
5.
Gut and Liver ; : 358-369, 2015.
Artículo en Inglés | WPRIM | ID: wpr-203890

RESUMEN

BACKGROUND/AIMS: The cytosolic host protein nucleotide binding oligomerization domain 1 (Nod1) has emerged as a key pathogen recognition molecule for innate immune responses in epithelial cells. The purpose of the study was to elucidate the mechanism by which Helicobacter pylori infection leads to transepithelial neutrophil migration in a Nod1-mediated manner. METHODS: Human epithelial cell lines AGS and Caco-2 were grown and infected with H. pylori. Interleukin (IL)-8 mRNA expression and IL-8 secretion were assessed, and nuclear factor kappaB (NF-kappaB) activation was determined. Stable transfections of AGS and Caco-2 cells with dominant negative Nod1 were generated. Neutrophil migration across the monolayer was quantified. RESULTS: Cytotoxin-associated gene pathogenicity island (cagPAI)(+) H. pylori infection upregulated IL-8 mRNA expression and IL-8 secretion in AGS and Caco-2 cells compared with controls. NF-kappaB activation, IL-8 mRNA expression and IL-8 secretion by cagPAI knockdown strains were reduced compared with those infected with the wild-type strain. NF-kappaB activation, IL-8 mRNA expression and IL-8 secretion in dominant-negative (DN)-Nod1 stably transfected cells were reduced compared with the controls. The transepithelial migration of neutrophils in DN-Nod1 stably transfected cells was reduced compared with that in controls. CONCLUSIONS: Signaling through Nod1 plays an essential role in neutrophil migration induced by the upregulated NF-kappaB activation and IL-8 expression in H. pylori-infected human epithelial cells.


Asunto(s)
Humanos , Células Madre Adultas/fisiología , Células CACO-2 , Línea Celular , Células Epiteliales/metabolismo , Expresión Génica , Islas Genómicas , Infecciones por Helicobacter/genética , Helicobacter pylori , Interleucina-8/genética , FN-kappa B/metabolismo , Neutrófilos/fisiología , Proteína Adaptadora de Señalización NOD1/fisiología , ARN Mensajero/metabolismo , Transducción de Señal , Migración Transendotelial y Transepitelial/fisiología , Regulación hacia Arriba
6.
Invest. clín ; 55(1): 61-81, mar. 2014. ilus
Artículo en Español | LILACS | ID: lil-746286

RESUMEN

Las células del sistema inmunitario (SI) son capaces de reconocer una gran variedad de microorganismos, a través de los receptores que se encuentran expresados y distribuidos a lo largo de su arquitectura celular. La interacción entre los patrones moleculares asociados a microorganismos o a daño (PMAM o PMAD) y los receptores reconocedores de patrones (RRP) presentes en las células del hospedero es un evento crítico que implica procesos intracelulares de señalización que finalizan en la expresión de mediadores tanto proinflamatorios como antivirales. Por consiguiente, de la integridad de estos receptores dependerá el buen funcionamiento de los distintos mecanismos de transducción de señal desde las membranas celulares al citoplasma y por ende, de la respuesta que el SI desencadene contra los patógenos entre ellos los agentes virales. De allí que, en esta revisión se discutirá el papel de los receptores tipo toll (TLRs) y receptores para dominios de oligomerización para la unión a nucleótidos (NLRs) en las infecciones virales, tomando como evidencia los estudios en humanos y ratones que a la fecha se conocen.


The immune system (IS) cells are capable of recognizing a wide variety of microorganisms, through receptors that are expressed and distributed throughout the cell architecture. The interaction between the pathogen-associated molecular patterns or damage-associated molecular patterns (PAMPs or DAMPs) and pattern recognition receptors (PRR), present in host cells, is a critical event that involves intracellular signaling processes that end up in the expression of both, proinflammatory and antiviral mediators. Accordingly, the proper functioning of the different mechanisms of signal transduction from the cell membrane to the cytoplasm will depend on the integrity of these receptors (PRR); and therefore, the IS response triggered against pathogens including viral agents. Hence, in this review we discuss the role of toll-like receptors (TLRs) and nucleotide-binding oligomerization domain receptors (NLRs) in viral infections, using as evidence the studies in humans and mice known to date.


Asunto(s)
Animales , Humanos , Ratones , Proteínas Adaptadoras de Señalización CARD/fisiología , Interacciones Huésped-Patógeno/inmunología , /fisiología , Receptores Toll-Like/fisiología , Virosis/inmunología , Proteínas Portadoras/fisiología , Citocinas/biosíntesis , Citocinas/genética , Evolución Molecular , Predicción , Inmunidad Innata , Modelos Inmunológicos , Familia de Multigenes , Proteína Adaptadora de Señalización NOD1/fisiología , Estructura Terciaria de Proteína , Transducción de Señal , Receptores Toll-Like/química , Receptores Toll-Like/clasificación
7.
Chinese Journal of Stomatology ; (12): 464-469, 2014.
Artículo en Chino | WPRIM | ID: wpr-260799

RESUMEN

<p><b>OBJECTIVE</b>To examine the expression of nucleotide-binding oligomerization domain 1 (NOD1), nuclear factor-kappa B (NF-κB) and human beta-defensins in candidal albicans leukoplakia and to investigate the effect of candida albicans infection on key proteins in NOD1 signaling pathway and the expression of human beta-defensin.</p><p><b>METHODS</b>Forty cases of oral leukoplakia samples were collected and stained by hematoxylin-eosin staining, periodic acid-Schiff staining, silver staining and immunohistochemical methods. Nineteen samples were positive with these four methods and judged as candidal albicans leukoplakia, and the other twenty- one samples judged as leukoplakia without candidal albicans infection. Western blotting was used to detect the expressions of NOD1 and NF-κB in these forty samples. In addition, the immunohistochemical method was adopted to investigate the relationship between NOD1, NF-κB, human beta-defensin 1, 2, 3 expressions and candida albicans.</p><p><b>RESULTS</b>The positive rate of candida albicans in oral leukoplakia was 48% (19/40). The expressions of NOD1 and NF-κB in the candida albicans leukoplakia were lower than that in leukoplakia without candida albicans infection. The mean optical density value of NOD1, NF-κB, human beta-defensin 1, 2, 3 in candidal albicans leukoplakia were 0.25 ± 0.01, 0.30 ± 0.02, 0.35 ± 0.02, 0.42 ± 0.03, 0.36 ± 0.02 respectively, which were significantly lower than that in leukoplakia without candida albicans infection (0.31 ± 0.02, 0.47 ± 0.03, 0.42 ± 0.02, 0.53 ± 0.04, 0.47 ± 0.03) (P < 0.05).</p><p><b>CONCLUSIONS</b>By inhibiting the NOD1 signaling pathway, candida albicans infection may reduce the expression level of human beta-defensin 1, 2, 3 in oral leukoplakia.</p>


Asunto(s)
Humanos , Western Blotting , Candida albicans , Candidiasis , Metabolismo , Leucoplasia Bucal , Metabolismo , FN-kappa B , Proteína Adaptadora de Señalización NOD1 , Nucleótidos , Transducción de Señal , beta-Defensinas
8.
Journal of Clinical Otorhinolaryngology Head and Neck Surgery ; (24): 393-396, 2013.
Artículo en Chino | WPRIM | ID: wpr-749518

RESUMEN

OBJECTIVE@#To investigate the expression of NOD1 and NOD2 in the nasal mucosa of healthy individuals and allergic rhinitis(AR), and explored the regulation of glucocorticoids on them.@*METHOD@#RT-PCR and immunohistochemistry were used to detect the expression of NOD1 and NOD2 in nasal mucosa from healthy control and AR. Nasal explant culture was used to explore the effect of glucocorticoids on NOD1 and NOD2 expression.@*RESULT@#NOD1 and NOD2 mRNA expression level was significantly increased in AR compared with control. Immunohistochemical staining demonstrated that NOD1 and NOD2 were mainly expressed by epithelial cells and some unknown cells in lamina propria and there were significantly more positive staining cells were observed in AR tissue when compared with control. Glucocorticoids down-regulated NOD1 and NOD2 expression in AR.@*CONCLUSION@#NOD1 and NOD2 as two PRRs may take part in the pathogenesis of AR, glucocorticoids may play a therapeutical role on allergic rhinitis through down-regulated the expression of NOD1 and NOD2.


Asunto(s)
Adulto , Femenino , Humanos , Masculino , Persona de Mediana Edad , Adulto Joven , Estudios de Casos y Controles , Regulación de la Expresión Génica , Glucocorticoides , Farmacología , Mucosa Nasal , Metabolismo , Proteína Adaptadora de Señalización NOD1 , Metabolismo , Proteína Adaptadora de Señalización NOD2 , Metabolismo , Rinitis Alérgica , Rinitis Alérgica Perenne , Metabolismo
9.
Chinese Medical Sciences Journal ; (4): 211-217, 2013.
Artículo en Inglés | WPRIM | ID: wpr-243188

RESUMEN

<p><b>OBJECTIVE</b>To investigate the potential role of nucleotide-binding oligomerization domain 1 (NOD1), a component of the innate immune system, in mediating lipid-induced insulin resistance in adipocytes.</p><p><b>METHODS</b>Adipocytes from Toll-like receptor 4 deficiency mice were used for stimulation experiments. The effect of oleate/palmitate mixture on nuclear factor-κB (NF-κB) activation was analyzed by reporter plasmid assay. The release of proinflammatory chemokine/cytokines production was determined by using real-time PCR. Insulin-stimulated glucose uptake was measured by 2-deoxy-D-[3H] glucose uptake assay. Chemokine/cytokine expression and glucose uptake in adipocytes transfected with small interfering RNA (siRNA) targeting NOD1 upon fatty acids treatment were analyzed.</p><p><b>RESULTS</b>Oleate/palmitate mixture activated the NF-κB pathway and induced interleukin-6, tumor necrosis factor-α, and monocyte chemoattractant protein-1 mRNA expressions in adipocytes from mice deficient in Toll-like receptor 4, and these effects were blocked by siRNA targeting NOD1. Furthermore, saturated fatty acids decreased the ability of insulin-stimulated glucose uptake. Importantly, siRNA targeting NOD1 partially reversed saturated fatty acid-induced suppression of insulin-induced glucose uptake.</p><p><b>CONCLUSION</b>NOD1 might play an important role in saturated fatty acid-induced insulin resistance in adipocytes, suggesting a mechanism by which reduced NOD1 activity confers beneficial effects on insulin action.</p>


Asunto(s)
Animales , Masculino , Ratones , Adipocitos , Metabolismo , Ácidos Grasos , Farmacología , Resistencia a la Insulina , Ratones Endogámicos C57BL , FN-kappa B , Fisiología , Proteína Adaptadora de Señalización NOD1 , Fisiología , Transducción de Señal , Receptor Toll-Like 4 , Fisiología
10.
Journal of Clinical Otorhinolaryngology Head and Neck Surgery ; (24): 1118-1122, 2013.
Artículo en Chino | WPRIM | ID: wpr-747194

RESUMEN

OBJECTIVE@#To investigate the expression and role of a new pattern-recognition receptors (PRR), nucleotide binding oligomerization domain (Nod) like receptors (NLRs), in the patients with nasal polyps and nasal septum normal control group.@*METHOD@#The expressions of Nod1, Nod2 and Nalp3 mRNA and protein were explored with real-time RT-PCR, Western-Blot and immunohistochemistry respectively.@*RESULT@#The protein levels of Nod1, Nod2 and Nalp3 were expressed in nasal polyp and the control, but the expression of Nod1 and Nalp3 in nasal polyps were higher than those in control. No significant difference of Nod2 was seen between the two groups. And then, there was no significant difference of Nod1, Nod2, Nalp3 mRNA between two groups with Real-time RT-PCR.@*CONCLUSION@#The expression of Nod1 and Nalp3 are increased in nasal polyp tissues and maybe a etiological factors in the formation of nasal polyps.


Asunto(s)
Adulto , Femenino , Humanos , Masculino , Persona de Mediana Edad , Proteínas Portadoras , Metabolismo , Estudios de Casos y Controles , Proteína con Dominio Pirina 3 de la Familia NLR , Pólipos Nasales , Metabolismo , Patología , Proteína Adaptadora de Señalización NOD1 , Metabolismo , Proteína Adaptadora de Señalización NOD2 , Metabolismo , Receptores de Reconocimiento de Patrones , Metabolismo
11.
Chinese Medical Sciences Journal ; (4): 147-152, 2012.
Artículo en Inglés | WPRIM | ID: wpr-243247

RESUMEN

<p><b>OBJECTIVE</b>To investigate the effects of stimulant for nucleotide-binding oligomerization domain 1 (NOD1) on secretion of proinflammatory chemokine ÷ cytokines and insulin-dependent glucose uptake in human differentiated adipocytes.</p><p><b>METHODS</b>Adipose tissues were obtained from patients undergoing liposuction. Stromal vascular cells were extracted and differentiated into adipocytes.A specific ligand for NOD1, was administered to human adipocytes in culture. Nuclear factor-κB transcriptional activity and proinflammatory chemokine ÷ cytokines production were determined by reporter plasmid assay and enzyme-linked immunosorbent assay, respectively.Insulin-stimulated glucose uptake was measured by 2-deoxy-D-[³H] glucose uptake assay. Furthermore, chemokine ÷ cytokine secretion and glucose uptake in adipocytes transfected with small interfering RNA (siRNA) targeting NOD1 upon stimulation of NOD1 ligand were analyzed.</p><p><b>RESULTS</b>Nuclear factor-κB transcriptional activity and monocyte chemoattractant protein-1 (MCP-1), interleukin (IL)-6, and IL-8 secretion in human adipocytes were markedly increased stimulated with NOD1 ligand (all P<0.01).Insulin-induced glucose uptake was decreased upon the activation of NOD1 (P<0.05).NOD1 gene silencing by siRNA reduced NOD1 ligand-induced MCP-1,IL-6, and IL-8 release and increased insulin-induced glucose uptake (all P<0.05).</p><p><b>CONCLUSION</b>NOD1 activation in adipocytes might be implicated in the onset of insulin resistance.</p>


Asunto(s)
Adulto , Femenino , Humanos , Persona de Mediana Edad , Adipocitos , Metabolismo , Células Cultivadas , Citocinas , Glucosa , Metabolismo , Inflamación , Resistencia a la Insulina , Ligandos , FN-kappa B , Fisiología , Proteína Adaptadora de Señalización NOD1 , Fisiología
12.
Biomedical and Environmental Sciences ; (12): 350-356, 2010.
Artículo en Inglés | WPRIM | ID: wpr-306918

RESUMEN

<p><b>OBJECTIVE</b>To explore the immune stimulation effect of recombinant E.coli LLO/OVA on mice bone marrow-derived dendritic cells (BMDCs) and T lymphocytes in vitro.</p><p><b>METHODS</b>After BMDCs stimulated by E.coli LLO/OVA, their Toll-like receptor (TLR) and nucleotide-binding oligomerization domain (NOD) receptor signalling pathway were examined by superarray hybridization; and the priming effect of the vaccine activated BMDCs on CD4(+)T and CD8(+)T was determined by [3H]thymidine uptake and ELISA, the tumor cytotoxic effect of activated CD8(+)T cells was determined by cytotoxic assay.</p><p><b>RESULTS</b>After BMDCs were activated by E. coli LLO/OVA via TLR4, NOD1 receptor and NF-κB signalling pathway, the expression of their surface molecules including MHC class I, MHC class II, CD40, CD80 and CD86 significantly up-regulated; the secretion of IL-12 and IFN-γ increased also. The mature BMDCs stimulated the allergic CD4(+)T and CD8(+)T cells proliferation and their IL-2 and IFN-γ secretion, and the activated CD8(+)T cells effectively killed B16-OVA melanoma cells and RMA-S/OVA lymphoma cells in vitro.</p><p><b>CONCLUSION</b>E.coli LLO/OVA is effective in inducing BMDCs maturation via activating TLR4 and NOD1 receptor signalling pathway and promoting specific anti-tumor T cell immunity in vitro.</p>


Asunto(s)
Animales , Femenino , Ratones , Antígenos de Neoplasias , Genética , Farmacología , Toxinas Bacterianas , Genética , Farmacología , Vacunas contra el Cáncer , Genética , Farmacología , Línea Celular Tumoral , Proliferación Celular , Supervivencia Celular , Alergia e Inmunología , Técnicas de Cocultivo , Citocinas , Alergia e Inmunología , Secreciones Corporales , Células Dendríticas , Biología Celular , Alergia e Inmunología , Metabolismo , Ensayo de Inmunoadsorción Enzimática , Escherichia coli , Genética , Metabolismo , Citometría de Flujo , Proteínas de Choque Térmico , Genética , Farmacología , Proteínas Hemolisinas , Genética , Farmacología , Inmunidad Innata , Ratones Endogámicos C57BL , Proteína Adaptadora de Señalización NOD1 , Genética , Fisiología , Ovalbúmina , Genética , Farmacología , Proteínas Recombinantes de Fusión , Genética , Farmacología , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Linfocitos T Citotóxicos , Alergia e Inmunología , Receptor Toll-Like 4 , Genética , Fisiología
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