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1.
Inflamm Res ; 58(4): 204-9, 2009 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-19169648

RESUMEN

OBJECTIVE: Mice selected for a strong (AIRmax) or weak (AIRmin) acute inflammatory response present different susceptibilities to bacterial infections, autoimmune diseases and carcinogenesis. Variations in these phenotypes have been also detected in AIRmax and AIRmin mice rendered homozygous for Slc11a1 resistant (R) and susceptible (S) alleles. Our aim was to investigate if the phenotypic differences observed in these mice was related to the complement system. MATERIAL: AIRmax and AIRmin mice and AIRmax and AIRmin groups homozygous for the resistance (R) or susceptibility (S) alleles of the solute carrier family 11a1 member (Slc11a1) gene, formerly designated Nramp-1. METHODS AND RESULTS: While no difference in complement activity was detected in sera from AIRmax and AIRmin strains, all sera from AIRmax Slc11a1 resistant mice (AIRmax(RR)) presented no complement-dependent hemolytic activity. Furthermore, C5 was not found in their sera by immunodiffusion and, polymerase chain reaction and DNA sequencing of its gene demonstrated that AIRmax(RR) mice are homozygous for the C5 deficient (D) mutation previously described in A/J. Therefore, the C5D allele was fixed in homozygosis in AIRmax(RR) line. CONCLUSIONS: The AIRmax(RR) line is a new experimental mouse model in which a strong inflammatory response can be triggered in vivo in the absence of C5.


Asunto(s)
Complemento C5 , Inflamación/genética , Ratones Endogámicos , Animales , Proteínas de Transporte de Catión/genética , Proteínas de Transporte de Catión/inmunología , Activación de Complemento , Complemento C5/genética , Complemento C5/inmunología , Vía Alternativa del Complemento/inmunología , Femenino , Predisposición Genética a la Enfermedad , Hemólisis , Inflamación/inmunología , Masculino , Ratones , Ratones Endogámicos/genética , Ratones Endogámicos/inmunología
2.
Scand J Immunol ; 68(4): 445-55, 2008 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-18782275

RESUMEN

We identified a 4-year-old Brazilian boy from a family of Japanese descent and history of consanguinity, who suffered from severe recurrent pneumonia. He carries factor H (FH) deficiency associated with reduced levels of component C9 and low serum levels of C3 and factor B. His mother also presented low levels of these proteins and factor I, while his father and sister had only lower levels of FH. Western blot assays confirmed the complete absence of FH and FHL-1 polypeptides in this patient. Sequencing of the proband's FH cDNA revealed a homozygous G453A substitution, encoding an Arg(127)His change. His mother, father and sister are heterozygous for this substitution. Despite the absence of FH in the plasma, this protein was detected in the patient's fibroblasts, suggesting that Arg(127) may be important for FH secretion. Low concentrations of C9 were detected in the proband serum but no mutations in the patient's C9 gene or promoter have been identified, suggesting that this is a consequence of uncontrolled complement activation and high C9 consumption.


Asunto(s)
Trastornos de la Coagulación Sanguínea Heredados/sangre , Trastornos de la Coagulación Sanguínea Heredados/genética , Complemento C9/análisis , Factor H de Complemento/deficiencia , Factor H de Complemento/genética , Secuencia de Bases , Trastornos de la Coagulación Sanguínea Heredados/fisiopatología , Western Blotting , Preescolar , Activación de Complemento/fisiología , Proteínas Inactivadoras del Complemento C3b , Complemento C9/genética , Proteínas del Sistema Complemento/análisis , Consanguinidad , Ensayo de Inmunoadsorción Enzimática , Femenino , Fibroblastos/metabolismo , Humanos , Masculino , Microscopía Confocal , Mutación , Linaje , Neumonía/etiología , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa
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