Downregulation of 14‐3‐3β and 14‐3‐3ζ in lesions of psoriasis vulgaris. (21st March 2013)
- Record Type:
- Journal Article
- Title:
- Downregulation of 14‐3‐3β and 14‐3‐3ζ in lesions of psoriasis vulgaris. (21st March 2013)
- Main Title:
- Downregulation of 14‐3‐3β and 14‐3‐3ζ in lesions of psoriasis vulgaris
- Authors:
- Man, X.
Zhang, X.
Tang, J.
Chen, Y.
Li, H.
Xu, B.
Pan, L. - Abstract:
- <abstract abstract-type="main" id="ced12014-abs-0001"> <title>Summary</title> <sec id="ced12014-sec-0001" sec-type="section"> <title>Background</title> <p>The 14‐3‐3 proteins are a family of conserved regulatory molecules expressed in all eukaryotic cells, which play essential roles in a wide range of vital regulatory processes, including differentiation, proliferation and transformation. In mammalian cells, seven 14‐3‐3 isoforms (β, γ, ε, η, θ/τ, σ and ζ) have been identified, and each of these seems to have distinct tissue localizations and isoform‐specific functions. 14‐3‐3β and 14‐3‐3ζ are two important members of the 14‐3‐3 family.</p> </sec> <sec id="ced12014-sec-0002" sec-type="section"> <title>Aim</title> <p>To explore the role of 14‐3‐3β and 14‐3‐3ζ in normal skin and psoriasis vulgaris (PV) skin.</p> </sec> <sec id="ced12014-sec-0003" sec-type="section"> <title>Methods</title> <p>Using immunohistochemistry and western blotting, we measured expression of 14‐3‐3β and 14‐3‐3ζ in 30 PV lesions and 15 normal skin samples. The average optical density (OD) of immunostaining and the relative grey scale of immunoblotting for 4‐3‐3β and 14‐3‐3ζ were analysed by the <italic>t</italic>‐test.</p> </sec> <sec id="ced12014-sec-0004" sec-type="section"> <title>Results</title> <p>The average OD of immunostaining for 14‐3‐3β and 14‐3‐3ζ was 0.17 ± 0.00 and 0.24 ± 0.01, respectively, in psoriatic lesions, which was significantly lower than in normal controls (0.22 ± 0.01 and<abstract abstract-type="main" id="ced12014-abs-0001"> <title>Summary</title> <sec id="ced12014-sec-0001" sec-type="section"> <title>Background</title> <p>The 14‐3‐3 proteins are a family of conserved regulatory molecules expressed in all eukaryotic cells, which play essential roles in a wide range of vital regulatory processes, including differentiation, proliferation and transformation. In mammalian cells, seven 14‐3‐3 isoforms (β, γ, ε, η, θ/τ, σ and ζ) have been identified, and each of these seems to have distinct tissue localizations and isoform‐specific functions. 14‐3‐3β and 14‐3‐3ζ are two important members of the 14‐3‐3 family.</p> </sec> <sec id="ced12014-sec-0002" sec-type="section"> <title>Aim</title> <p>To explore the role of 14‐3‐3β and 14‐3‐3ζ in normal skin and psoriasis vulgaris (PV) skin.</p> </sec> <sec id="ced12014-sec-0003" sec-type="section"> <title>Methods</title> <p>Using immunohistochemistry and western blotting, we measured expression of 14‐3‐3β and 14‐3‐3ζ in 30 PV lesions and 15 normal skin samples. The average optical density (OD) of immunostaining and the relative grey scale of immunoblotting for 4‐3‐3β and 14‐3‐3ζ were analysed by the <italic>t</italic>‐test.</p> </sec> <sec id="ced12014-sec-0004" sec-type="section"> <title>Results</title> <p>The average OD of immunostaining for 14‐3‐3β and 14‐3‐3ζ was 0.17 ± 0.00 and 0.24 ± 0.01, respectively, in psoriatic lesions, which was significantly lower than in normal controls (0.22 ± 0.01 and 0.37 ± 0.02, respectively; <italic>P </italic>&lt; 0.01 for both). There was also a significant difference in the relative grey scale of 14‐3‐3β and 14‐3‐3ζ (0.52 ± 0.03 and 1.44 ± 0.06, respectively) in psoriatic lesions compared with normal control tissue (3.32 ± 0.15 and 2.76 ± 0.11, respectively; <italic>P </italic>&lt; 0.01 for both).</p> </sec> <sec id="ced12014-sec-0005" sec-type="section"> <title>Conclusions</title> <p>Expression of 14‐3‐3β and 14‐3‐3ζ were lower in psoriatic lesions than in normal human skin tissue. We speculate that 14‐3‐3β and 14‐3‐3ζ may be involved in the regulation of normal skin function, thus decreased expression of 14‐3‐3β and 14‐3‐3ζ might precipitate the disturbance in proliferation and differentiation of keratinocytes seen in psoriasis.</p> </sec> </abstract> … (more)
- Is Part Of:
- Clinical and experimental dermatology. Volume 38:Number 4(2013)
- Journal:
- Clinical and experimental dermatology
- Issue:
- Volume 38:Number 4(2013)
- Issue Display:
- Volume 38, Issue 4 (2013)
- Year:
- 2013
- Volume:
- 38
- Issue:
- 4
- Issue Sort Value:
- 2013-0038-0004-0000
- Page Start:
- 390
- Page End:
- 395
- Publication Date:
- 2013-03-21
- Subjects:
- Skin -- Diseases -- Periodicals
616.5 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2230 ↗
https://academic.oup.com/ced/issue ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/ced.12014 ↗
- Languages:
- English
- ISSNs:
- 0307-6938
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.250000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3251.xml