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MHC class I chain-related protein A and B (MICA and MICB) are predominantly expressed intracellularly in tumour and normal tissue.
Ghadially, Hormas; Brown, Lee; Lloyd, Chris; Lewis, Leeanne; Lewis, Arthur; Dillon, Janette; Sainson, Richard; Jovanovic, Jelena; Tigue, Natalie J; Bannister, David; Bamber, Lisa; Valge-Archer, Viia; Wilkinson, Robert W.
Afiliação
  • Ghadially H; MedImmune Ltd., Granta Park, Cambridge CB21 6GH, UK.
  • Brown L; MedImmune Ltd., Granta Park, Cambridge CB21 6GH, UK.
  • Lloyd C; MedImmune Ltd., Granta Park, Cambridge CB21 6GH, UK.
  • Lewis L; MedImmune Ltd., Granta Park, Cambridge CB21 6GH, UK.
  • Lewis A; MedImmune Ltd., Granta Park, Cambridge CB21 6GH, UK.
  • Dillon J; MedImmune Ltd., Granta Park, Cambridge CB21 6GH, UK.
  • Sainson R; MedImmune Ltd., Granta Park, Cambridge CB21 6GH, UK.
  • Jovanovic J; MedImmune Ltd., Granta Park, Cambridge CB21 6GH, UK.
  • Tigue NJ; MedImmune Ltd., Granta Park, Cambridge CB21 6GH, UK.
  • Bannister D; MedImmune Ltd., Granta Park, Cambridge CB21 6GH, UK.
  • Bamber L; MedImmune Ltd., Granta Park, Cambridge CB21 6GH, UK.
  • Valge-Archer V; AstraZeneca, Chesterford Research Park, Little Chesterford CB10 1XL, UK.
  • Wilkinson RW; MedImmune Ltd., Granta Park, Cambridge CB21 6GH, UK.
Br J Cancer ; 116(9): 1208-1217, 2017 Apr 25.
Article em En | MEDLINE | ID: mdl-28334733
ABSTRACT

BACKGROUND:

Major histocompatibility complex (MHC) class I chain-related protein A (MICA) and MHC class I chain-related protein B (MICB) are polymorphic proteins that are induced upon stress, damage or transformation of cells which act as a 'kill me' signal through the natural-killer group 2, member D receptor expressed on cytotoxic lymphocytes. MICA/B are not thought to be constitutively expressed by healthy normal cells but expression has been reported for most tumour types. However, it is not clear how much of this protein is expressed on the cell surface.

METHODS:

Using a novel, well-characterised antibody and both standard and confocal microscopy, we systematically profiled MICA/B expression in multiple human tumour and normal tissue.

RESULTS:

High expression of MICA/B was detected in the majority of tumour tissues from multiple indications. Importantly, MICA/B proteins were predominantly localised intracellularly with only occasional evidence of cell membrane localisation. MICA/B expression was also demonstrated in most normal tissue epithelia and predominantly localised intracellularly. Crucially, we did not observe qualitative differences in cell surface expression between tumour and MICA/B expressing normal epithelia.

CONCLUSIONS:

This demonstrates for the first time that MICA/B is more broadly expressed in normal tissue and that expression is mainly intracellular with only a small fraction appearing on the cell surface of some epithelia and tumour cells.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Antígenos de Histocompatibilidade Classe I / Neoplasias Tipo de estudo: Qualitative_research Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Antígenos de Histocompatibilidade Classe I / Neoplasias Tipo de estudo: Qualitative_research Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article