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J Immunol Methods ; 301(1-2): 53-65, 2005 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-15936768

RESUMO

The recently identified IL-6 family member cardiotrophin-like cytokine (also named novel neurotrophin-1 or B cell stimulating factor-3) forms a secreted complex with cytokine-like factor-1 which binds and activates the tripartite ciliary neurotrophic factor receptor. The striking differences between the phenotype of mice in which either the ciliary neurotrophic factor or its receptor are inactivated suggest that the cardiotrophin-like cytokine/cytokine-like factor-1 complex could be the developmentally important ciliary neurotrophic factor receptor ligand. Cardiotrophin-like cytokine is also produced in the immune system and has been reported to activate B cells in vivo and in vitro. B cells do not express the ciliary neurotrophic factor receptor suggesting the existence of an alternative receptor. We produced the cardiotrophin-like cytokine/cytokine-like factor-1 complex tagged with a Bir A biotin ligase AviTag peptide substrate. This cytokine could be efficiently biotinylated in vitro with Bir A. It was subsequently validated as a sensitive tool for ciliary neurotrophic factor receptor detection by flow cytometry and for magnetic-activated cell sorting. It was also shown to allow the detection of a specific receptor by activated B cells. Whereas binding to cells expressing the ciliary neurotrophic factor receptor could be prevented by competition with ciliary neurotrophic factor, binding to B cells was not. The biotinylated cardiotrophin-like cytokine/cytokine-like factor-1 complex therefore represents a new reagent to study ciliary neurotrophic factor and cardiotrophin-like cytokine receptor expression and for the identification of the putative cardiotrophin-like cytokine B cell receptor. It further validates the use of biotin ligase catalysed biotinylation for the detection of cytokine receptors.


Assuntos
Carbono-Nitrogênio Ligases/metabolismo , Células/imunologia , Células/metabolismo , Citocinas/metabolismo , Proteínas de Escherichia coli/metabolismo , Regulação da Expressão Gênica , Receptores de Citocinas/metabolismo , Proteínas Repressoras/metabolismo , Fatores de Transcrição/metabolismo , Animais , Avidina/metabolismo , Linfócitos B/efeitos dos fármacos , Linfócitos B/metabolismo , Carbono-Nitrogênio Ligases/química , Células/efeitos dos fármacos , Células Cultivadas , Citocinas/química , Epitopos/imunologia , Escherichia coli , Proteínas de Escherichia coli/química , Feminino , Humanos , Camundongos , Ligação Proteica , Receptor do Fator Neutrófico Ciliar/metabolismo , Receptores de Citocinas/imunologia , Proteínas Repressoras/química , Baço/efeitos dos fármacos , Baço/metabolismo , Fatores de Transcrição/química
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