血管生成
伤口愈合
血管内皮生长因子
细胞外基质
细胞生物学
癌症研究
血管内皮生长因子A
新生血管
化学
生物
免疫学
血管内皮生长因子受体
作者
Chandan K. Sen,Savita Khanna,Mika Venojärvi,Prashant Trikha,E. Christopher Ellison,Thomas K. Hunt,Sashwati Roy
出处
期刊:American Journal of Physiology-heart and Circulatory Physiology
[American Physical Society]
日期:2002-05-01
卷期号:282 (5): H1821-H1827
被引量:458
标识
DOI:10.1152/ajpheart.01015.2001
摘要
Angiogenesis plays a central role in wound healing. Among many known growth factors, vascular endothelial growth factor (VEGF) is believed to be the most prevalent, efficacious, and long-term signal that is known to stimulate angiogenesis in wounds. Whereas a direct role of copper to facilitate angiogenesis has been evident two decades ago, the specific targets of copper action remained unclear. This report presents first evidence showing that inducible VEGF expression is sensitive to copper and that the angiogenic potential of copper may be harnessed to accelerate dermal wound contraction and closure. At physiologically relevant concentrations, copper sulfate induced VEGF expression in primary as well as transformed human keratinocytes. Copper shared some of the pathways utilized by hypoxia to regulate VEGF expression. Topical copper sulfate accelerated closure of excisional murine dermal wound allowed to heal by secondary intention. Copper-sensitive pathways regulate key mediators of wound healing such as angiogenesis and extracellular matrix remodeling. Copper-based therapeutics represents a feasible approach to promote dermal wound healing.
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