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A study on collagen constitute And affected factors in hypertrophic Scar at different age periods

机译:不同年龄段肥厚性瘢痕的胶原组成及影响因素研究

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Objective: To investigate the difference in ratio of collagen in hypertrophic scar (HS) at different age periods and its causes, in order to provide a theoretical base for its special clinical treatment. Method: The expression of type I, type III collagen, and transforming growth factor-beta1 (TGF-beta1) was measured immunohistochemically in different-age HS and normal skin (NS). All the quantities were analysed. Messenger RNA (mRNA) expressions of collagenase (MMP-1) and tissue inhibitor of metallo-proteinase (TIMP-1) were measured with the in situ hybridization technique. Results: 1. The ratio of type I/type III collagen and the quantification of type I collagen in HS increased compared with NS. The ratio of type I/type III collagen in the 1-19 years old HS group increased compared with the 20-50 years old group. 2. The expression of TGF-beta1 protein in HS was enhanced. The expression of TGF-beta1 in the 1-19 years old HS group significantly increased more than in the 20-50 years old group. 3. A significant increase of expression of TIMP-1 mRNA in HS was observed, but the expression of MMP-1 was lower both in HS and in NS. The expression of TIMP-1 mRNA and the expression of MMP-1 in the HS 1-19 years old group and the 20-50 years old group presented no difference. Conclusion: 1. The significant increase in TGF-beta1, which stimulates fibroblast to synthesize more type I collagen and enhances the ratio of type I/type III collagen, may be a cause of the higher incidence of scarring in the 1-19 years old group (children and teenagers). 2. The higher expression of TIMP-1 mRNA and the lower expression of MMP-1 mRNA are among the factors causing HS. Expressions of TIMP-1 and MMP-1 in HS have no direct relationship to age.
机译:目的:探讨不同年龄段增生性瘢痕(HS)中胶原蛋白比例的差异及其成因,为其特殊的临床治疗提供理论依据。方法:采用免疫组织化学方法在不同年龄的HS和正常皮肤(NS)中检测I型,III型胶原和转化生长因子β1(TGF-β1)的表达。分析了所有数量。采用原位杂交技术检测胶原酶(MMP-1)和金属蛋白酶组织抑制剂(TIMP-1)的信使RNA(mRNA)表达。结果:1.与NS相比,HS中I型/ III型胶原蛋白的比率和I型胶原蛋白的定量增加。与20-50岁组相比,HS组1-19岁的I型/ III型胶原蛋白的比例增加。 2. TGF-beta1蛋白在HS中表达增强。在1-19岁的HS组中,TGF-beta1的表达明显高于20-50岁的组。 3.观察到HS中TIMP-1 mRNA的表达显着增加,但HS和NS中MMP-1的表达均较低。 HS 1-19岁组和20-50岁组TIMP-1 mRNA和MMP-1的表达无差异。结论:1.TGF-β1的显着增加,刺激成纤维细胞合成更多的I型胶原蛋白并提高I / III型胶原蛋白的比例,可能是导致1-19岁瘢痕形成更高的原因。组(儿童和青少年)。 2. TIMP-1 mRNA的高表达和MMP-1 mRNA的低表达是引起HS的因素之一。 HS中TIMP-1和MMP-1的表达与年龄没有直接关系。

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