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Cell surface expression of MR1B, a splice variant of the MHC class I-related molecule MR1, revealed with antibodies.
Yamaguchi, Hisateru; Tsukamoto, Kentaro; Hashimoto, Keiichiro.
Afiliação
  • Yamaguchi H; Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi 470-1192, Japan.
  • Tsukamoto K; Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi 470-1192, Japan.
  • Hashimoto K; Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi 470-1192, Japan. Electronic address: keihashi@fujita-hu.ac.jp.
Biochem Biophys Res Commun ; 443(2): 422-7, 2014 Jan 10.
Article em En | MEDLINE | ID: mdl-24309098
ABSTRACT
The major histocompatibility complex (MHC) class I-related molecule, MR1, is highly conserved in mammals and can present bacteria-derived vitamin B metabolites to mucosal-associated invariant T (MAIT) cells, possibly having important defense function in the microbial infection. MR1B is a splice variant of MR1 and possesses an intriguing domain structure with only two extracellular domains resembling some NKG2D ligand molecules. Thus far, cell surface expression of MR1B could not be analyzed with flow cytometry due to a lack of appropriate antibodies reactive with MR1B. Here we clarified the expression of MR1B recombinant protein on the cell surface of the transfected cells by flow cytometry analyses using the antiserum against MR1. Consistently, MR1B tagged with FLAG peptide at the N-terminus also could be detected with anti-FLAG monoclonal antibodies. Our result showed that MR1B can be recognized on the cell surface by macromolecules such as antibodies, indicating its potential of interaction with certain receptor(s). We discuss possibility of interaction of MR1B and/or the full-length MR1 with some receptor(s) other than αß T cell receptor (TCR) of MAIT cells based on the highly conserved characteristic residues of the ligand-binding domains of MR1 and its MAIT cells αßTCR footprints.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imunoensaio / Antígenos de Histocompatibilidade Classe I / Membrana Celular / Anticorpos Monoclonais Limite: Humans Idioma: En Revista: Biochem Biophys Res Commun Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imunoensaio / Antígenos de Histocompatibilidade Classe I / Membrana Celular / Anticorpos Monoclonais Limite: Humans Idioma: En Revista: Biochem Biophys Res Commun Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Japão