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首页> 外文期刊>Wound repair and regeneration: official publication of the Wound Healing Society [and] the European Tissue Repair Society >Time course of the angiogenic response during normotrophic and hypertrophic scar formation in humans.
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Time course of the angiogenic response during normotrophic and hypertrophic scar formation in humans.

机译:血管生成反应的时间进程normotrophic肥厚性疤痕形成人类。

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Previous research suggests that in hypertrophic scars (HSs), an excess of microvessels is present compared with normotrophic scars (NSs). The aim of our study was to quantify vascular densities in HSs and normotrophic scars and to provide an insight into the kinetics of changes in the expression of angiogenic factors in time during wound healing and HS formation. Human presternal wound healing after cardiothoracic surgery through a sternotomy incision was investigated in a standardized manner. Skin biopsies were collected at consecutive time points, i.e., during surgery and 2, 4, 6, 12, and 52 weeks postoperatively. The expression levels of angiopoietin-1, angiopoietin-2, Tie-2, vascular endothelial growth factor, and urokinase-type plasminogen activator were measured by real-time reverse transcription-polymerase chain reaction. Quantification of angiogenesis and cellular localization of the proteins of interest were based on immunohistochemical analysis. Microvessel densities were higher in the HSs compared with the normotrophic scars 12 weeks (p=0.017) and 52 weeks (p=0.030) postoperatively. Angiopoietin-1 expression was lower in the hypertrophic group (p<0.001), which, together with a nonsignificant increase of angiopoietin-2 expression, represented a considerable decrease in the angiopoietin-1/angiopoietin-2 ratio in the hypertrophic group 4 weeks (p=0.053), 12 weeks (p<0.001), and 52 weeks (p<0.001) postoperatively. The expression of urokinase-type plasminogen activator was up-regulated during HS formation (p=0.008). Vascular endothelial growth factor expression was not significantly different when comparing both groups. In summary, the differential expression of angiopoietin-1, angiopoietin-2, and urokinase-type plasminogen activator in time is associated with an increased vascular density in HSs compared with normotrophic scars.
机译:先前的研究表明,在肥厚性疤痕(HSs),过多的微血管相比之下,normotrophic疤痕(NSs)。我们的研究旨在量化血管密度在高速钢和normotrophic伤痕和提供一个洞察的动力学变化血管生成因子的表达中伤口愈合和HS的形成。心胸手术后伤口愈合通过胸骨切开术切口了一个标准化的方式。在连续采集时间点,即在手术和2、4、6、12和52周术后。而,angiopoietin-2 Tie-2,血管内皮生长因子和urokinase-type纤溶酶原激活物被实时测量逆转录-聚合酶链反应。血管生成和细胞的量化定位感兴趣的蛋白质基于免疫组织化学分析。在高速钢微脉管密度更高相比normotrophic伤疤12周(p = 0.017)和术后52周(p = 0.030)。而较低的表达式肥厚性组(p < 0.001),而在一起angiopoietin-2无意义的增加表情,代表了一个相当大的减少而/ angiopoietin-2比率肥厚性组4周(p = 0.053), 12周(p < 0.001), 52周(p < 0.001)术后。纤溶酶原激活物在海关被上调形成(p = 0.008)。因子的表达没有明显不同当比较两组。而微分表达式,angiopoietin-2, urokinase-type纤溶酶原。物激活时间增加血管密度在高速钢相比normotrophic伤疤。

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