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Induction of PYPAF1 during in vitro maturation of mouse mast cells.
Kikuchi-Yanoshita, Rei; Taketomi, Yoshitaka; Koga, Kumiko; Sugiki, Toshihiko; Atsumi, Yohei; Saito, Takanori; Ishii, Shin-Ichi; Hisada, Masato; Suzuki-Nishimura, Tamiko; Uchida, Masaatsu K; Moon, Tae-Chul; Chang, Hyeun-Wook; Sawada, Masatsugu; Inagaki, Naoki; Nagai, Hiroichi; Murakami, Makoto; Kudo, Ichiro.
Afiliação
  • Kikuchi-Yanoshita R; Department of Health Chemistry, School of Pharmaceutical Sciences, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142-8555.
J Biochem ; 134(5): 699-709, 2003 Nov.
Article em En | MEDLINE | ID: mdl-14688236
ABSTRACT
Coculture of mouse bone marrow-derived immature mast cells (BMMC) with Swiss 3T3 fibroblasts in the presence of stem cell factor (SCF) promotes morphological and functional maturation toward a connective tissue mast cell (CTMC)-like phenotype, which is accompanied by increased expression of several unique genes. Here we report the molecular identification of one of them, mast cell maturation-associated inducible gene (MMIG)-1. The MMIG-1 cDNA encodes a 117-kDa cytosolic protein that comprises an N-terminal PYRIN domain, a central nucleotide-binding domain, and nine C-terminal leucine-rich repeats. MMIG-1 shows >85% sequence similarity to human cryopyrin/PYPAF1, a causal gene for familial cold urticaria and Muckle-Wells syndrome. MMIG-1 was distributed in the cytosol of CTMC-like differentiated BMMC. MMIG-1 underwent alternative splicing in the leucine-rich repeats and each variant was induced differently in BMMC during coculture. Moreover, its expression was increased in the ears of mice with experimental atopic dermatitis. Thus, MMIG-1, a likely mouse PYPAF1 ortholog, may play a role in mast cell-directed inflammatory diseases.
Assuntos
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Base de dados: MEDLINE Assunto principal: Proteínas de Transporte / Diferenciação Celular / Regulação da Expressão Gênica / Mastócitos Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2003 Tipo de documento: Article
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Base de dados: MEDLINE Assunto principal: Proteínas de Transporte / Diferenciação Celular / Regulação da Expressão Gênica / Mastócitos Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2003 Tipo de documento: Article