The histamine‐synthesizing enzyme histidine decarboxylase is upregulated by keratinocytes in atopic skin. (30th September 2014)
- Record Type:
- Journal Article
- Title:
- The histamine‐synthesizing enzyme histidine decarboxylase is upregulated by keratinocytes in atopic skin. (30th September 2014)
- Main Title:
- The histamine‐synthesizing enzyme histidine decarboxylase is upregulated by keratinocytes in atopic skin
- Authors:
- Gutowska‐Owsiak, D.
Greenwald, L.
Watson, C.
Selvakumar, T.A.
Wang, X.
Ogg, G.S. - Abstract:
- <abstract abstract-type="main" id="bjd13199-abs-0001"> <title>Summary</title> <sec id="bjd13199-sec-0001" sec-type="section"> <title>Background</title> <p>Histamine is an abundant mediator accumulating in the skin of atopic patients, where it is thought to be derived from immune cells. While keratinocytes express histidine decarboxylase (HDC), levels of the enzyme in normal or diseased epidermis and factors that influence its expression in human keratinocytes are not known.</p> </sec> <sec id="bjd13199-sec-0002" sec-type="section"> <title>Objectives</title> <p>To assess levels of HDC in inflammatory skin diseases and factors influencing its expression.</p> </sec> <sec id="bjd13199-sec-0003" sec-type="section"> <title>Methods</title> <p>Normal and filaggrin‐insufficient human keratinocytes, organotypic epidermal models and skin samples were investigated for the expression of HDC. The effect of cytokines, bacterial and allergen stimuli exposure and functional changes in differentiation were evaluated <italic>in vitro</italic>.</p> </sec> <sec id="bjd13199-sec-0004" sec-type="section"> <title>Results</title> <p>We detected abundant expression of the HDC protein in all models studied; expression was increased in atopic skin samples. Filaggrin‐insufficient keratinocytes maintained HDC levels, but exposure of keratinocytes to thymic stromal lymphopoietin, tumour necrosis factor‐α, lipopolysaccharide (LPS) and house dust mite (HDM) extract increased HDC expression <italic>in<abstract abstract-type="main" id="bjd13199-abs-0001"> <title>Summary</title> <sec id="bjd13199-sec-0001" sec-type="section"> <title>Background</title> <p>Histamine is an abundant mediator accumulating in the skin of atopic patients, where it is thought to be derived from immune cells. While keratinocytes express histidine decarboxylase (HDC), levels of the enzyme in normal or diseased epidermis and factors that influence its expression in human keratinocytes are not known.</p> </sec> <sec id="bjd13199-sec-0002" sec-type="section"> <title>Objectives</title> <p>To assess levels of HDC in inflammatory skin diseases and factors influencing its expression.</p> </sec> <sec id="bjd13199-sec-0003" sec-type="section"> <title>Methods</title> <p>Normal and filaggrin‐insufficient human keratinocytes, organotypic epidermal models and skin samples were investigated for the expression of HDC. The effect of cytokines, bacterial and allergen stimuli exposure and functional changes in differentiation were evaluated <italic>in vitro</italic>.</p> </sec> <sec id="bjd13199-sec-0004" sec-type="section"> <title>Results</title> <p>We detected abundant expression of the HDC protein in all models studied; expression was increased in atopic skin samples. Filaggrin‐insufficient keratinocytes maintained HDC levels, but exposure of keratinocytes to thymic stromal lymphopoietin, tumour necrosis factor‐α, lipopolysaccharide (LPS) and house dust mite (HDM) extract increased HDC expression <italic>in vitro</italic>. Furthermore, filaggrin expression in cultured keratinocytes increased following histamine depletion.</p> </sec> <sec id="bjd13199-sec-0005" sec-type="section"> <title>Conclusions</title> <p>Keratinocytes express abundant HDC protein, and the levels increase in atopic skin. LPS, HDM and cytokines, which are implicated in allergic inflammation, promote the expression of the enzyme and upregulate histamine levels in keratinocytes. Actively produced histamine influences keratinocyte differentiation, suggesting functional relevance of the axis to atopic dermatitis. The findings therefore identify a new point of therapeutic intervention.</p> </sec> </abstract> … (more)
- Is Part Of:
- British journal of dermatology. Volume 171:Number 4(2014:Oct.)
- Journal:
- British journal of dermatology
- Issue:
- Volume 171:Number 4(2014:Oct.)
- Issue Display:
- Volume 171, Issue 4 (2014)
- Year:
- 2014
- Volume:
- 171
- Issue:
- 4
- Issue Sort Value:
- 2014-0171-0004-0000
- Page Start:
- 771
- Page End:
- 778
- Publication Date:
- 2014-09-30
- Subjects:
- Dermatology -- Periodicals
Skin -- Diseases -- Periodicals
616.5 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2133 ↗
https://academic.oup.com/bjd ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/bjd.13199 ↗
- Languages:
- English
- ISSNs:
- 0007-0963
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2307.400000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3788.xml