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APP17肽对紫外线照射的皮肤成纤维细胞MMP-1和TIMP-1 mRNA表达的影响 被引量:2

The effects of APP17-mer peptide on the expression of MMP-1 and TIMP-1 in cultured human skin fibroblasts irradiated with ultraviolet
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摘要 目的:探讨β-淀粉样前体蛋白17肽(APP17肽)对紫外线照射后人皮肤成纤维细胞增殖及MMP-1和TIMP-1mRNA表达的影响。方法:在培养的人皮肤成纤维细胞中加入不同浓度的APP17肽,并用UV照射培养的人皮肤成纤维细胞。MTT法检测细胞活性,应用RT-PCR方法检测不同剂量APP17肽及UV照射后细胞中MMP-1mRNA和TIMP-1mRNA的表达情况。结果:APP17肽可增加非照射及UV照射后成纤维细胞的活性(P<0.05)。RT-PCR结果显示,6J/cm2UVA+36mJ/cm2UVB照射后MMP-1mRNA的表达增加1.78倍(P<0.01),TIMP-1mRNA的表达增加1.13倍(P<0.05)。APP17肽可在一定水平抑制MMP-1mRNA的表达,并诱导TIMP-1mRNA的表达(P<0.05)。结论:APP17肽可抑制体外培养的成纤维细胞的胶原降解,并可抑制UV诱导的胶原降解。 Objective: To determine the effects of β - amyloid precursor protein 17 - met peptide (APP17) on the proliferation and MMP- 1 mRNA and TIMP- 1 mRNA expressions in cultured fibroblasts after ultraviolet irradiation. Methods: Human skin fibroblasts were cultured in a series of concentrations of APP 17 - mer peptide (0,20, 40,80 μmol/L, respectively) and irradiated by a single exposure to ultraviolet. The activities of fibroblasts were detected by the assay of MTr. The expressions of MMP- 1 and TIMP- 1 were analyzed by real - time quantitative RT - PCR in APP17 treated and 9 J/cm^2 UVA + 54 mJ/cm^2 UVB irradiated fibroblasts. Results: After treatment with APP17, the activities of fibroblasts increased in both unirradiated and UV - irradiated skin ( P 〈 0.05). A single exposure of fibroblasts to 6 J/cm^2 UVA + 36 mJ/cm^2 UVB irradiation resulted in a 1.78 - fold up - regulation of MMP- 1 mRNA and a 1.13 - fold up - regulation of TIMP - 1 mRNA compared with unirradiated control ( P 〈 0.01, P 〈 0.05 respectively). 40 μmol/L and 80 μmol/L APP17 decreased the expression of MMP - 1 mRNA ( P 〈0.05, P 〈 0.01 respectively) and increased the expression of TIMP - 1 mRNA (P 〈 0.05). Conclusion: APP17 can inhibit collagen degradation in unirradiated and irradiated fibroblasts with ultraviolet.
出处 《中国麻风皮肤病杂志》 2007年第9期759-762,共4页 China Journal of Leprosy and Skin Diseases
关键词 APP17肽 成纤维细胞 实时定量RT-PCR β- amyloid precursor protein 17 - met peptide fibroblasts real - time quantitative RT- PCR
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