Copper-induced vascular endothelial growth factor expression and wound healing

被引:408
作者
Sen, CK [1 ]
Khanna, S [1 ]
Venojarvi, M [1 ]
Trikha, P [1 ]
Ellison, EC [1 ]
Hunt, TK [1 ]
Roy, S [1 ]
机构
[1] Ohio State Univ, Med Ctr, Dept Surg, Davis Heart & Lung Res Inst 512,Lab Mol Med, Columbus, OH 43210 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2002年 / 282卷 / 05期
关键词
redox; oxidant; skin; angiogenesis; repair;
D O I
10.1152/ajpheart.01015.2001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
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.
引用
收藏
页码:H1821 / H1827
页数:7
相关论文
共 43 条
[1]  
ALESSANDRI G, 1983, CANCER RES, V43, P1790
[2]   OXYGEN-DEPENDENT MICROBIAL KILLING BY PHAGOCYTES .1. [J].
BABIOR, BM .
NEW ENGLAND JOURNAL OF MEDICINE, 1978, 298 (12) :659-668
[3]  
Bancroft J.D., 1990, THEORY PRACTICE HIST, V3rd
[4]   AN UNUSUAL SKIN EXPOSURE TO COPPER - CLINICAL AND PHARMACOKINETIC EVALUATION [J].
BENTUR, Y ;
KOREN, G ;
MCGUIGAN, M ;
SPIELBERG, SP .
JOURNAL OF TOXICOLOGY-CLINICAL TOXICOLOGY, 1988, 26 (5-6) :371-380
[5]   MAP kinases and hypoxia in the control of VEGF expression [J].
Berra, E ;
Pagès, G ;
Pouysségur, J .
CANCER AND METASTASIS REVIEWS, 2000, 19 (1-2) :139-145
[6]  
Blancher C, 2001, CANCER RES, V61, P7349
[7]   NORMAL KERATINIZATION IN A SPONTANEOUSLY IMMORTALIZED ANEUPLOID HUMAN KERATINOCYTE CELL-LINE [J].
BOUKAMP, P ;
PETRUSSEVSKA, RT ;
BREITKREUTZ, D ;
HORNUNG, J ;
MARKHAM, A ;
FUSENIG, NE .
JOURNAL OF CELL BIOLOGY, 1988, 106 (03) :761-771
[8]   Activator-protein-1 binding potentiates the hypoxia-inducible factor-1-mediated hypoxia-induced transcriptional activation of vascular-endothelial growth factor expression in C6 glioma cells [J].
Damert, A ;
Ikeda, E ;
Risau, W .
BIOCHEMICAL JOURNAL, 1997, 327 :419-423
[9]   Kinases involved in MSP/RON signaling [J].
Danilkovitch, A ;
Leonard, EJ .
JOURNAL OF LEUKOCYTE BIOLOGY, 1999, 65 (03) :345-348
[10]   A redox-triggered Ras-effector interaction -: Recruitment of phosphatidylinositol 5′-kinase to Ras by redox stress [J].
Deora, AA ;
Win, T ;
Vanhaesebroeck, B ;
Lander, HM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (45) :29923-29928