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Filaggrin-stratified transcriptomic analysis of pediatric skin identifies mechanistic pathways in patients with atopic dermatitis.
Cole, Christian; Kroboth, Karin; Schurch, Nicholas J; Sandilands, Aileen; Sherstnev, Alexander; O'Regan, Grainne M; Watson, Rosemarie M; McLean, W H Irwin; Barton, Geoffrey J; Irvine, Alan D; Brown, Sara J.
Afiliación
  • Cole C; Division of Computational Biology, College of Life Sciences, University of Dundee, Dundee, United Kingdom.
  • Kroboth K; Centre for Dermatology and Genetic Medicine, Division of Molecular Medicine, Colleges of Life Sciences and Medicine, Dentistry & Nursing, University of Dundee, Dundee, United Kingdom.
  • Schurch NJ; Division of Computational Biology, College of Life Sciences, University of Dundee, Dundee, United Kingdom.
  • Sandilands A; Centre for Dermatology and Genetic Medicine, Division of Molecular Medicine, Colleges of Life Sciences and Medicine, Dentistry & Nursing, University of Dundee, Dundee, United Kingdom.
  • Sherstnev A; Division of Computational Biology, College of Life Sciences, University of Dundee, Dundee, United Kingdom.
  • O'Regan GM; Department of Dermatology, Our Lady's Children's Hospital, Crumlin, Dublin, Ireland.
  • Watson RM; Department of Dermatology, Our Lady's Children's Hospital, Crumlin, Dublin, Ireland.
  • McLean WH; Centre for Dermatology and Genetic Medicine, Division of Molecular Medicine, Colleges of Life Sciences and Medicine, Dentistry & Nursing, University of Dundee, Dundee, United Kingdom.
  • Barton GJ; Division of Computational Biology, College of Life Sciences, University of Dundee, Dundee, United Kingdom. Electronic address: g.j.barton@dundee.ac.uk.
  • Irvine AD; Department of Dermatology, Our Lady's Children's Hospital, Crumlin, Dublin, Ireland; National Children's Research Centre, Our Lady's Children's Hospital, Crumlin, Dublin, Ireland; Clinical Medicine, Trinity College Dublin, Dublin, Ireland. Electronic address: irvinea@tcd.ie.
  • Brown SJ; Centre for Dermatology and Genetic Medicine, Division of Molecular Medicine, Colleges of Life Sciences and Medicine, Dentistry & Nursing, University of Dundee, Dundee, United Kingdom; National Children's Research Centre, Our Lady's Children's Hospital, Crumlin, Dublin, Ireland. Electronic addres
J Allergy Clin Immunol ; 134(1): 82-91, 2014 Jul.
Article en En | MEDLINE | ID: mdl-24880632
ABSTRACT

BACKGROUND:

Atopic dermatitis (AD; eczema) is characterized by a widespread abnormality in cutaneous barrier function and propensity to inflammation. Filaggrin is a multifunctional protein and plays a key role in skin barrier formation. Loss-of-function mutations in the gene encoding filaggrin (FLG) are a highly significant risk factor for atopic disease, but the molecular mechanisms leading to dermatitis remain unclear.

OBJECTIVE:

We sought to interrogate tissue-specific variations in the expressed genome in the skin of children with AD and to investigate underlying pathomechanisms in atopic skin.

METHODS:

We applied single-molecule direct RNA sequencing to analyze the whole transcriptome using minimal tissue samples. Uninvolved skin biopsy specimens from 26 pediatric patients with AD were compared with site-matched samples from 10 nonatopic teenage control subjects. Cases and control subjects were screened for FLG genotype to stratify the data set.

RESULTS:

Two thousand four hundred thirty differentially expressed genes (false discovery rate, P < .05) were identified, of which 211 were significantly upregulated and 490 downregulated by greater than 2-fold. Gene ontology terms for "extracellular space" and "defense response" were enriched, whereas "lipid metabolic processes" were downregulated. The subset of FLG wild-type cases showed dysregulation of genes involved with lipid metabolism, whereas filaggrin haploinsufficiency affected global gene expression and was characterized by a type 1 interferon-mediated stress response.

CONCLUSION:

These analyses demonstrate the importance of extracellular space and lipid metabolism in atopic skin pathology independent of FLG genotype, whereas an aberrant defense response is seen in subjects with FLG mutations. Genotype stratification of the large data set has facilitated functional interpretation and might guide future therapy development.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Piel / Transcripción Genética / Dermatitis Atópica / Proteínas de Filamentos Intermediarios Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Allergy Clin Immunol Año: 2014 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Piel / Transcripción Genética / Dermatitis Atópica / Proteínas de Filamentos Intermediarios Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Allergy Clin Immunol Año: 2014 Tipo del documento: Article