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Molecular and histological studies of bladder wound healing in a rodent model

机译:分子和组织学的研究膀胱伤口愈合在啮齿动物模型

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Abstract The field of regenerative medicine encounters different challenges. The success of tissue‐engineered implants is dependent on proper wound healing. Today, the process of normal urinary bladder wound healing is poorly characterized. We aspired to explore and elucidate the natural response to injury in an in vivo model in order to further optimize tissue regeneration in future studies. In this study, we aimed to characterize histological and molecular changes during normal healing in a rat model by performing a standardized incisional wound followed by surgical closure. We used a rodent model (n = 40) to follow the healing process in the urinary bladder for 28?days. Surgical exposure of the bladder without incision (n = 40) was performed in controls. Histological characterization and western blot analyses of proteins was carried out using specific staining and markers for inflammation, proliferation, angiogenesis, and tissue maturation. For the molecular characterization of gene expression total RNA was collected for RT 2 ‐PCR in wound healing pathway arrays. Analysis of histology revealed distinct, but overlapping, phases of healing with a local inflammatory response (days 1‐8) simultaneous with a rapid formation of granulation tissue and proliferation (days 2‐8). We also identified significant changes in gene expression related to inflammation, proliferation, and extracellular matrix formation. Healing of an incisional wound in a rodent urinary bladder demonstrated that all the classical phases of wound healing: hemostasis, inflammation, proliferation followed by tissue maturation were present. Our data suggest that the bladder and the skin share similar molecular signaling during wound healing, although we noted differences in the duration of each phase compared to previous studies in rat skin. Further studies will address whether our findings can be extrapolated to the human bladder.
机译:抽象的再生医学领域的遇到不同的挑战。组织工程植入取决于适当的伤口愈合。膀胱伤口愈合不佳为特征。阐明了受伤的自然反应为了进一步优化组织活体模型在将来的研究中再生。旨在描述组织学和分子变化在正常治疗大鼠模型执行标准化的切口其次是手术关闭。模型(n = 40)遵循的愈合过程28岁的膀胱?天。暴露的膀胱无切口(n = 40)在执行控制。特征和免疫印迹分析蛋白质进行了使用特定的染色和炎症扩散,血管生成和组织成熟。基因表达的分子特征总RNA收集2 RT PCR在伤口治疗途径数组。显示不同,但重叠的阶段治疗局部炎症反应(天1 8)同时与一个快速形成肉芽组织和扩散(2天还是8)。我们还发现了重要基因的变化表达与炎症有关,增殖,细胞外基质形成。啮齿动物膀胱证明所有的伤口愈合的古典阶段:止血,炎症、增生组织紧随其后成熟。膀胱和皮肤分子相似信号在伤口愈合过程中,尽管我们说每个阶段持续时间的差异而先前的研究在大鼠皮肤。研究将解决我们的发现是否可以外推到人的膀胱。

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