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Impaired Biomechanical Properties of Diabetic SkinImplications in Pathogenesis of Diabetic Wound Complications

机译:糖尿病皮肤并发症在糖尿病伤口并发症发病机制中的生物力学特性受损。

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Diabetic skin is known to have deficient wound healing properties, but little is known of its intrinsic biomechanical properties. We hypothesize that diabetic skin possesses inferior biomechanical properties at baseline, rendering it more prone to injury. Skin from diabetic and nondiabetic mice and humans underwent biomechanical testing. Real-time PCR was performed for genes integral to collagen synthesis and degradation. MMP-2 and MMP-9, and TIMP-1 protein levels were assessed by ELISA and zymography. Collagen I and III content was assessed using Western blot analysis. At baseline, both murine and human diabetic skin was biomechanically inferior compared to nondiabetic skin, with decreased maximum stress and decreased modulus (P < 0.001 and < 0.05, respectively). Surprisingly, the expression of genes involved in collagen synthesis were significantly up-regulated, and genes involved in collagen degradation were significantly down-regulated in murine diabetic skin (P < 0.01). In addition, MMP-2 and MMP-9/TIMP-1 protein ratios were significantly lower in murine diabetic skin (P < 0.05). Collagen I levels and I:III ratios were lower in diabetic skin (P < 0.05). These findings suggest that the predisposition of diabetics to wounds may be the result of impaired tissue integrity at baseline, and are due, in part, to a defect in the regulation of collagen protein synthesis at the post-transcriptional level.
机译:已知糖尿病皮肤具有不足的伤口愈合特性,但对其固有的生物力学特性知之甚少。我们假设糖尿病皮肤在基线时具有较差的生物力学特性,使其更容易受伤。来自糖尿病和非糖尿病小鼠以及人类的皮肤进行了生物力学测试。对胶原合成和降解必不可少的基因进行了实时PCR。通过ELISA和酶谱法评估MMP-2和MMP-9以及TIMP-1蛋白水平。使用蛋白质印迹分析评估胶原蛋白I和III的含量。在基线时,与非糖尿病皮肤相比,鼠和人糖尿病皮肤在生物力学上均较差,最大应力降低且模量降低(分别为P <0.001和<0.05)。出乎意料的是,鼠类糖尿病皮肤中胶原合成相关基因的表达显着上调,而胶原降解相关基因的表达显着下调(P <0.01)。此外,鼠糖尿病皮肤中的MMP-2和MMP-9 / TIMP-1蛋白比率显着降低(P <0.05)。糖尿病皮肤中的胶原蛋白I水平和I:III比值较低(P <0.05)。这些发现表明,糖尿病患者易患伤口可能是基线时组织完整性受损的结果,部分归因于转录后水平胶原蛋白合成调控的缺陷。

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