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Receptor for advanced glycation end products is overexpressed in psoriatic plaques independent of disease severity
被引:2
|作者:
Ozgor, Ozkay
[1
]
Akoglu, Gulsen
[2
]
Sungu, Nuran
[3
]
Karaismailoglu, Eda
[4
]
Aktas, Akin
[2
]
机构:
[1] Kastamonu Univ, Ankara Ataturk Training & Res Hosp, Dept Dermatol, Sch Med, Kastamonu, Turkey
[2] Kastamonu Univ, Ankara Ataturk Training & Res Hosp, Dept Dermatovenereol, Sch Med, Kastamonu, Turkey
[3] Kastamonu Univ, Ankara Ataturk Training & Res Hosp, Sch Med, Dept Pathol, Kastamonu, Turkey
[4] Kastamonu Univ, Sch Med, Dept Biostat, Kastamonu, Turkey
关键词:
Immunohistochemistry;
pathogenesis;
psoriasis;
receptor for advanced glycation end products;
FACTOR-KAPPA-B;
TRANSCRIPTION FACTOR;
RAGE;
SKIN;
INFLAMMATION;
EXPRESSION;
PATHWAY;
D O I:
10.4103/ijdvl.IJDVL_718_16
中图分类号:
R75 [皮肤病学与性病学];
学科分类号:
100206 ;
摘要:
Background: Enhanced expression and excitation of the receptor for advanced glycation end products is considered to play a role in the regulation of many pro-inflammatory genes involved in the pathogenesis of psoriasis. Aim: We investigated the expression of receptor for advanced glycation end product in various cell types, in lesional and peri-lesional skin of patients with psoriasis, and its correlation with disease severity. Methods: Paraffin-embedded punch biopsy tissue taken from psoriatic plaques and peri-lesional normal appearing skin tissue of twenty patients with psoriasis, and normal skin samples of eleven healthy participants, were enrolled in the study. The sections were stained immunohistochemically with anti-receptor for advanced glycation end product antibody. The intensity of receptor for advanced glycation end product expression was assessed semi-quantitatively on epidermal cells, microvascular endothelium, dermal fibroblasts and inflammatory cells. They were graded as follows: 0 (no staining), 1 (weak), 2 (moderate) and 3 (strong) intensity. Results: Receptor for advanced glycation end product expression on epidermis, microvascular endothelium, inflammatory cells and fibroblasts in the psoriatic plaques was more intense than perilesional and normal tissue (all P < 0.05). It did not correlate with disease severity. Limitations: The main limitation of our study is that this was a semi-quantitative assessment, detected immunohistochemically in skin biopsies. Conclusion: Receptor for advanced glycation end product expression may have an important role in psoriasis pathogenesis, independent of disease severity.
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页码:556 / 560
页数:5
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