Immunohistochemical expression of matrix metalloproteinases in photodamaged skin by photodynamic therapy

被引:38
作者
Issa, M. C. Almeida [1 ]
Pineiro-Maceira, J. [1 ]
Farias, R. E. [2 ]
Pureza, M. [3 ]
Luiz, R. Raggio [1 ]
Manela-Azulay, M. [1 ]
机构
[1] Univ Fed Rio de Janeiro, Dept Dermatol, BR-24230001 Rio De Janeiro, Brazil
[2] Univ Fed Juiz de Fora, Dept Pathol, Rio De Janeiro, Brazil
[3] Univ Fed Fluminense, Dept Pathol, Rio De Janeiro, Brazil
关键词
immunohistochemistry; methyl aminolaevulinate; photodamaged skin; photodynamic therapy; DERMATOLOGY; FIBROBLASTS; AND-9;
D O I
10.1111/j.1365-2133.2009.09326.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100227 [皮肤病学];
摘要
Background Photodynamic therapy (PDT) has been described for photoageing treatment, but its mechanism of action is not clarified. Although PDT-induced matrix metalloproteinase (MMP) expression and collagen production have been studied in normal skin and in inflammatory disease, there is no report about the effect of PDT on the extracellular matrix in photodamaged skin. Objectives To evaluate skin remodelling induced by methyl aminolaevulinate (MAL)-PDT in photodamaged skin by histological and immunohistochemical studies. Methods Fourteen patients were treated with two sessions of MAL-PDT. The light source was a light-emitting diode (635 nm, 37 J cm(-2)). Skin biopsies were performed in all patients before and at 3 and 6 months after treatment. Immunohistochemical studies evaluated collagen types I and III, MMP-1, MMP-3, MMP-7, MMP-9, MMP-12 and tissue inhibitor of metalloproteinases-1. Results Global improvement in photodamaged skin was observed. A significant increase in expression of MMP-9 in the dermis was detected at 3 months after treatment (P = 0 002). Significant increases in the expression of collagen type I at 3 months (P = 0 002) and at 6 months after treatment (P = 0 001) were also observed. Conclusions Skin remodelling induced by MAL-PDT was demonstrated in photodamaged skin. Two sessions of MAL-PDT increases immunohistochemical expression of MMP-9 in the dermis at 3 months after treatment, and also of collagen type I.
引用
收藏
页码:647 / 653
页数:7
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