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Analysis of innate immune signal transduction with autocatalytic expression vectors.
Guan, Hongtao; Kiss-Toth, Endre; Dower, Steven K.
Afiliação
  • Guan H; Section of Infection and Immunity, Division of Genomic Medicine, The University of Sheffield, Royal Hallamshire Hospital, Sheffield, UK. h.guan@sheffield.ac.uk
J Immunol Methods ; 330(1-2): 96-108, 2008 Jan 31.
Article em En | MEDLINE | ID: mdl-18155720
ABSTRACT
Signalling pathways modulated by the family of IL-1/TLR receptors are central to innate immune responses. Novel components playing key regulatory roles in these pathways continue to be isolated. Here we describe the use of autocatalytic vectors for identifying critical components of these signalling pathways. The method was tested with a vector system where cDNA clones are expressed as EGFP fusion proteins, or in an IRES containing mRNA, combined with a transcription reporter. These constructs are placed under the control of an inducible promoter, responsive to activation of TIR receptors such as IL-1RI or TLR-4. cDNAs which activate the promoter will, when transcribed, form a positive feedback loop. We introduced TIR signalling pathway components into both types of vectors. The components tested regulated reporter (EGFP/luciferase) expression in both cases. Our data suggest that this type of system is capable of selective identification of components from signal transduction pathways once the promoter of a relevant inducible gene is identified from, for example, micro-array experiments.
Assuntos
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Base de dados: MEDLINE Assunto principal: Transdução de Sinais / Receptores de Interleucina-1 / Genes Reporter / Fator de Transcrição RelA / Interleucina-1beta / Vetores Genéticos / Imunidade Inata Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2008 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Transdução de Sinais / Receptores de Interleucina-1 / Genes Reporter / Fator de Transcrição RelA / Interleucina-1beta / Vetores Genéticos / Imunidade Inata Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2008 Tipo de documento: Article