Scutellarin promotes in vitro angiogenesis in human umbilical vein endothelial cells

被引:47
作者
Gao, Zhong-Xiu-Zi [1 ]
Huang, Da-Yong [2 ]
Li, Hai-Xia [1 ]
Zhang, Li-Na [1 ]
Lv, Yan-Hong [1 ]
Cui, Hai-Dong [1 ]
Zheng, Jin-Hua [1 ]
机构
[1] Harbin Med Coll, Basic Med Sci Coll, Dept Anat, Harbin, Peoples R China
[2] Harbin Med Coll, Clin Hosp 2, Dept Oncol, Harbin, Peoples R China
关键词
Scutellarin; Angiogenesis; Human umbilical vein endothelial cell; MMP-2; PECAM-1; PROTEIN-KINASE-C; MATRIX METALLOPROTEINASES; NEOVASCULARIZATION; INHIBITION; ACTIVATION; MIGRATION; DISEASE; CANCER; ALPHA; INFLAMMATION;
D O I
10.1016/j.bbrc.2010.08.034
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Angiogenesis is critical to a wide range of physiological and pathological processes. Scutellarin, a major flavonoid of a Chinese herbal medicine Erigeron breviscapus (Vant.) Hand. Mazz. has been shown to offer beneficial effects on cardiovascular and cerebrovascular functions. However, scutellarin's effects on angiogenesis and underlying mechanisms are not fully elucidated. Here, we studied angiogenic effects of scutellarin on human umbilical vein endothelial cells (HUVECs) in vitro. Scutellarin was found by MTT assay to induce proliferation of HUVECs. In scutellarin-treated HUVECs, a dramatic increase in migration was measured by wound healing assay; Transwell chamber assay found significantly more invading cells in scutellarin-treated groups. Scutellarin also promoted capillary-like tube formation in HUVECs on Matrigel, and significantly upregulated platelet endothelial cell adhesion molecule-1 at both mRNA and protein levels. Scutellarin's angiogenic mechanism was investigated in vitro by measuring expression of angiogenic factors associated with cell migration and invasion. Scutellarin strongly induced MMP-2 activation and mRNA expression in cultured HUVECs in a concentration-dependent manner. Taken together, these results suggest that scutellarin promotes angiogenesis and may form a basis for angiogenic therapy. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:151 / 156
页数:6
相关论文
共 30 条
[1]   Disruption of angiogenesis by PEX, a noncatalytic metalloproteinase fragment with integrin binding activity [J].
Brooks, PC ;
Silletti, S ;
von Schalscha, TL ;
Friedlander, M ;
Cheresh, DA .
CELL, 1998, 92 (03) :391-400
[2]   Angiogenesis in cancer and other diseases [J].
Carmeliet, P ;
Jain, RK .
NATURE, 2000, 407 (6801) :249-257
[3]   Angiogenesis in health and disease [J].
Carmeliet, P .
NATURE MEDICINE, 2003, 9 (06) :653-660
[4]   Changing the logic of therapeutic angiogenesis for ischemic disease [J].
Emanueli, C ;
Madeddu, P .
TRENDS IN MOLECULAR MEDICINE, 2005, 11 (05) :207-216
[5]   ANGIOGENESIS IN CANCER, VASCULAR, RHEUMATOID AND OTHER DISEASE [J].
FOLKMAN, J .
NATURE MEDICINE, 1995, 1 (01) :27-31
[6]   Blood vessel formation: What is its molecular basis? [J].
Folkman, J ;
DAmore, PA .
CELL, 1996, 87 (07) :1153-1155
[7]   Tissue engineering - Current challenges and expanding opportunities [J].
Griffith, LG ;
Naughton, G .
SCIENCE, 2002, 295 (5557) :1009-+
[8]   Protein kinase C and other diacylglycerol effectors in cancer [J].
Griner, Erin M. ;
Kazanietz, Marcelo G. .
NATURE REVIEWS CANCER, 2007, 7 (04) :281-294
[9]   Enhancement of migration by protein kinase C alpha and inhibition of proliferation and cell cycle progression by protein kinase C delta in capillary endothelial cells [J].
Harrington, EO ;
Loffler, J ;
Nelson, PR ;
Kent, KC ;
Simons, M ;
Ware, JA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (11) :7390-7397
[10]   Binding of active (57 kDa) membrane type 1-matrix metalloproteinase (MT1-MMP) to tissue inhibitor of metalloproteinase (TIMP)-2 regulates MT1-MMP processing and pro-MMP-2 activation [J].
Hernandez-Barrantes, S ;
Toth, M ;
Bernardo, MM ;
Yurkova, M ;
Gervasi, DC ;
Raz, Y ;
Sang, QXA ;
Fridman, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (16) :12080-12089