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Structure of the TCR expressed on a gastritogenic T cell clone, II-6, and frequent appearance of similar clonotypes in mice bearing autoimmune gastritis.
Katakai, T; Agata, Y; Shimizu, A; Ohshima, C; Nishio, A; Inaba, M; Kasakura, S; Mori, K J; Masuda, T.
Afiliação
  • Katakai T; Institute for Immunology, Faculty of Medicine, Kyoto University, Japan.
Int Immunol ; 9(12): 1849-55, 1997 Dec.
Article em En | MEDLINE | ID: mdl-9466312
ABSTRACT
A parietal cell-specific Th1 clone, II-6, which was established from a BALB/c mouse bearing post-thymectomy autoimmune gastritis (AIG), recognizes a peptide of the alpha subunit (alpha891-905) of H+/K+-ATPase and induces gastritis in nu/nu BALB/c mice by adoptive cell transfer. In the present study, the primary structure of the TCR of II-6 was determined as Valpha10-Jalpha c5a-Calpha and Vbeta14-Jbeta2.3-Cbeta2 by cDNA cloning. Using PCR with specific primers, we defined the use of this II-6 TCR in nu/nu mice with transferred II-6 cells and in mice that spontaneously developed AIG by thymectomy on day 3 after birth (d3-Tx). II-6 TCR mRNAs were detected in the gastric mucosa of all of the nu/nu mice, suggesting that II-6 cells indeed home to the gastric mucosa and thereby were directly involved in the destruction of target parietal cells. TCR beta chain mRNAs encoding CDR3 region sequences almost identical with that of II-6 were also found in the gastric mucosa in 43% (six of 14 mice tested) of the d3-Tx AIG mice at 4-12 weeks old by nested RT-PCR. Such a frequent appearance of similar clonotypes in independent individuals suggests that T cells bearing II-6-like TCR including the II-6 itself might be directly involved in, although not essential for, the pathogenesis of AIG in 3d-Tx mice.
Assuntos
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Base de dados: MEDLINE Assunto principal: Doenças Autoimunes / Linfócitos T / Receptores de Antígenos de Linfócitos T alfa-beta / Gastrite Idioma: En Ano de publicação: 1997 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Doenças Autoimunes / Linfócitos T / Receptores de Antígenos de Linfócitos T alfa-beta / Gastrite Idioma: En Ano de publicação: 1997 Tipo de documento: Article