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TGF-ß in tolerance, development and regulation of immunity.
Johnston, Chris J C; Smyth, Danielle J; Dresser, David W; Maizels, Rick M.
Afiliação
  • Johnston CJ; Institute of Immunology and Infection Research, University of Edinburgh, UK.
  • Smyth DJ; Institute of Immunology and Infection Research, University of Edinburgh, UK.
  • Dresser DW; Institute of Immunology and Infection Research, University of Edinburgh, UK.
  • Maizels RM; Institute of Immunology and Infection Research, University of Edinburgh, UK. Electronic address: r.maizels@ed.ac.uk.
Cell Immunol ; 299: 14-22, 2016 Jan.
Article em En | MEDLINE | ID: mdl-26617281
The TGF-ß superfamily is an ancient metazoan protein class which cuts across cell and tissue differentiation, developmental biology and immunology. Its many members are regulated at multiple levels from intricate control of gene transcription, post-translational processing and activation, and signaling through overlapping receptor structures and downstream intracellular messengers. We have been interested in TGF-ß homologues firstly as key players in the induction of immunological tolerance, the topic so closely associated with Ray Owen. Secondly, our interests in how parasites may manipulate the immune system of their host has also brought us to study the TGF-ß pathway in infections with longlived, essentially tolerogenic, helminth parasites. Finally, within the spectrum of mammalian TGF-ß proteins is an exquisitely tightly-regulated gene, anti-Müllerian hormone (AMH), whose role in sex determination underpins the phenotype of freemartin calves that formed the focus of Ray's seminal work on immunological tolerance.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Fator de Crescimento Transformador beta / Tolerância Imunológica Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Cell Immunol Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Fator de Crescimento Transformador beta / Tolerância Imunológica Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Cell Immunol Ano de publicação: 2016 Tipo de documento: Article