缺氧作为组织形成的刺激:在微手术血管化的组织工程构造中,有机生成的概念是微手术血管化的组织
Ahmad Eweida1, Elli Sandberg2, Oliver Ritthaler2
1Department of Hand, Plastic and Reconstructive Surgery, Burn Center, BG Trauma Center Ludwigshafen, University of Heidelberg, Ludwig-Guttmann-Str. 13, 67071, Ludwigshafen, Germany; Department of Head, Neck and Endocrine Surgery, Faculty of Medicine, University of Alexandria, Alkhartoum Square, 5372066, Alexandria, Egypt.
概括
带有动脉静脉循环 (AVL) 的组织工程结构促进了放射治疗后的再生. 在AVL结构中的缺氧激活HIF1-SDF1轴,增强原生细胞招募和骨质分化,改善骨再生.
科学领域:
- 生物材料科学 生物材料科学
- 再生医学是一种再生医学.
- 组织工程是组织工程.
背景情况:
- 轴向血管化对于再生大型,临床相关的组织结构至关重要.
- 动脉静脉循环 (AVL) 已经在各种模型中证明了在骨再生中的多功能性.
- 之前的研究表明,AVL在辐射后血管化组织结构方面具有能力.
研究的目的:
- 调查缺氧和HIF1-SDF1轴在辐射后AVL介导组织再生中的作用.
- 分析氧诱导因子1 (HIF1) 和 stromal-derived factor 1 (SDF1) 在被辐射的AVL骨结构中的表达.
- 评估辐射对这些结构中的骨质基因表达的影响.
主要方法:
- 在易斯老鼠骨结构中对HIF1和SDF1表达的免疫光分析.
- 骨质生成区分基因的实时PCR分析 (原-1,RUNX,性酸酶,骨).
- 在植入后2周和5周,用9Gy或15Gy对建筑物的局部辐射.
主要成果:
- 与对照组相比,在15Gy照射后2周观察到HIF1和SDF1的增强表达.
- 在5周内,骨质原生标志物的升调,包括原-1,性酸酶和骨质菌素.
- 在照射和AVL植入后,组织分化标志物的显著增强.
结论:
- 在AVL结构中的缺氧,加上高SDF1表达,促进组织分化.
- 这项研究支持这样一个假设,即HIF1-SDF1轴在被辐射的AVL骨结构中调节再生.
- 这种缺氧驱动的组织生成过程与器官生成相似,为再生策略提供了洞察力.
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