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Evaluation of the expression of P-selectin, ICAM-1, and TNF-alpha in bacteria-free lesional skin of atopic dogs with low-to-mild inflammation
被引:8
|作者:
de Mora, F.
de la Fuente, C.
Jasmin, R.
Gatto, H.
Marco, A.
Ferrer, L.
Fondati, A.
Fondevila, D.
Torres, R.
机构:
[1] Univ Autonoma Barcelona, Dept Farmacol, E-08193 Barcelona, Spain
[2] Autonomous Univ Barcelona, Dept Anim Pathol, E-08193 Barcelona, Spain
[3] Virbac SA, Carros, France
关键词:
adhesion molecules;
atopic dermatitis;
cytokines;
inflammation;
D O I:
10.1016/j.vetimm.2006.11.004
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Canine atopic dermatitis (AD) is a pruritic skin condition that shares many clinical and pathophysiological features with its human counterpart. A major therapeutic challenge of AD is the control of the skin inflammatory process. A detailed knowledge of the pro-inflammatory molecules involved in cell recruitment in AD would allow for a better control of the disease. We thus have studied the protein expression of P-selectin, ICAM-I and TNF-alpha in the lesional and non-lesional skin of atopic dogs that had been treated for bacterial infections. Despite a low-to-mild inflammatory process, P-selectin protein was clearly upregulated in the lesional skin areas when compared with non-lesional skin (four-fold average increase). This P-selectin upregulation was accompanied by signs of functional changes such as increased cell margination, and membrane-associated protein expression. Although the expression of ICAM-1 and TNF-alpha was not enhanced in the lesional versus the non-lesional skin, there was a trend towards a correlated upregulation of both molecules. Further studies will help elucidate the significance of the substantial overexpression of P-selectin in canine AD, in particular in a scenario where bacterial antigens are not contributing as proinflammatory stimuli. (c) 2006 Elsevier B.V. All rights reserved.
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页码:223 / 229
页数:7
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