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Hypoxia and hypoxia-inducible factor in the burn wound.

机译:缺氧和低氧诱导因子在燃烧伤口。

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摘要

The importance of hypoxia-inducible factor (HIF) in promoting angiogenesis and vasculogenesis during wound healing has been demonstrated. It is widely accepted that HIF activity can be promoted by many factors, including hypoxia in the wound or cytokines from inflammatory cells infiltrating the wound. However, there has not been a systematic exploration of the relationship between HIF activity and hypoxia in the burn wound. The location of the hypoxic tissue has not been clearly delineated. The time course of the appearance of hypoxia and the increased activity of HIF and appearance of HIF's downstream transcription products has not been described. The aim of this study was to utilize pimonidazole, a specific tissue hypoxia marker, to characterize the spatial and temporal course of hypoxia in a murine burn model and correlate this with the appearance of HIF-1alpha and its important angiogenic and vasculogenic transcription products vascular endothelial growth factor and SDF-1. Hypoxia was found in the healing margin of burn wounds beginning at 48 hours after burn and peaking at day 3 after burn. On sequential sections of the same tissue block, positive staining of HIF-1alpha, SDF-1, and vascular endothelial growth factor all occurred at the leading margin of the healing area and peaked at day 3, as did hypoxia. Immunohistochemical analysis was used to explore the characteristics of the hypoxic region of the wound. The localization of hypoxia was found to be related to cell growth and migration, but not to proliferation or inflammatory infiltration.
机译:低氧诱导因子(HIF)的重要性在促进血管生成和血管生成在伤口愈合。人们普遍认为,低氧诱导因子活动可以提升由许多因素,包括缺氧的伤口或者从炎症细胞浸润细胞因子伤口。系统探索的关系低氧诱导因子之间的活动和缺氧燃烧伤口。轮廓清晰。缺氧和增加的活动低氧诱导因子和外观的低氧诱导因子的下游转录的产品没有被描述。本研究的目的是利用这种特定的组织缺氧标记,的空间和时间在小鼠缺氧燃烧模型和关联这与HIF-1alpha和它的外观重要的血管生成和vasculogenic转录产品血管内皮生长因子和SDF-1。在48烧伤伤口愈合的开始小时后燃烧,燃烧后第三天达到顶峰。顺序相同的区域组织块,积极的染色HIF-1alpha SDF-1,血管内皮生长因子都发生在治疗区域的边缘在第三天达到高峰,缺氧一样。免疫组织化学分析被用来探索的缺氧区域的特点伤口。与细胞生长和迁移,但不是扩散或炎性浸润。

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