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Matrix metalloproteinase in acral and non-acrai vitiligo

机译:血症中的基质金属蛋白酶和非acraIAI白癜风

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摘要

Repigmentation in vitiligo requires activation, proliferation, and migration of the melanoblasts and melanocytes into the depigmented epidermis. Cell migration involves modifications of the architecture of cells which requires activation of enzymes that are involved in ECM degradation such as matrix metalloproteinases (MMPs). The significant reduction in their expression in vitiliginous skin has been previously demonstrated and thereby incriminated to share in reducing the migration of melanocytes and their precursors. Phototherapy in the form of narrow band UVB and photoche-motherapy (PUVA) are still considered the pillar in the treatment of vitiligo. Among a vast array of effects that could account for their efficacy, it has been demonstrated that UVA can lead to increased expression of MMPs which could aid in the process of repigmentation of vitiliginous lesions. In the current work, we aimed at detection of the differences between acral and non-acral vitiligo skin as regards the expression of three members of the MMP family; MMP1, MMP2, and MMP9, and how would they change after PUVA therapy.
机译:白癜风中的复杂需要将黑素细胞和黑素细胞的活化,增殖和迁移到沉淀的表皮中。细胞迁移涉及需要激活参与ECM降解的酶如基质金属蛋白酶(MMPS)的细胞架构的修饰。预先证明了它们在紫外线皮肤中表达的显着降低,从而令人报入以减少黑素细胞及其前体的迁移。窄带UVB和光学母乳(PUVA)形式的光疗仍然认为是维生素治疗的柱。在可能考虑其疗效的大量效果中,已经证明UVA可以导致MMP的表达增加,这有助于复发性病变的过程。在目前的工作中,我们旨在检测患有MMP家族的三个成员的表达的患者和非腺体白癜风皮肤的差异; MMP1,MMP2和MMP9,以及在PUVA治疗后如何改变。

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