Inhibition of vitronectin-mediated haptotaxis and haptoinvasion of MG-63 cells by domain 5 (D5H) of human high-molecular-weight kininogen and identification of a minimal amino acid sequence

被引:17
作者
Kamiyama, F
Maeda, T
Yamane, T
Li, YH
Ogukubo, O
Otsuka, T
Ueyama, H
Takahashi, S
Ohkubo, I [1 ]
Matsui, N
机构
[1] Shiga Univ Med Sci, Dept Med Biochem, Otsu, Shiga 5202192, Japan
[2] Nagoya City Univ, Sch Med, Dept Orthoped, Mizuho Ku, Nagoya, Aichi 4678601, Japan
[3] Kyoto Womens Univ, Fac House Econ, Higashiyama Ku, Kyoto 6068501, Japan
关键词
high-molecular-weight kininogen; domain 5 (D5(H)); haptotaxis; haptoinvasion;
D O I
10.1006/bbrc.2001.5864
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
We found that human kinin-free high-molecular-weight kininogen (kf-HK) significantly inhibited vitronectin-mediated migration (haptotaxis) and invasive potentiation (haptoinvasion) of osteosarcoma (MG-63) cells but that HH, LK, the common heavy chain of RK and LK, and the light chain (D6(H)) of HK had no inhibitory effect. Recombinant GST-D5(H) (histidine-rich region of RK) obtained from Escherichia coli. (BL21) also inhibited both haptotaxis and haptoinvasion to about 30% of the control level in a dose-dependent manner. These findings suggest that a specific region of D5(H) is responsible for the inhibition of cell haptotaxis and haptoinvasion. Among the seven synthetic peptides covering D5(H), peptide H(479)KHGHGHGKHKNKGK(493) (P-5) inhibited both haptotaxis and haptoinvasion in a dose-dependent manner, suggesting that P-5 could possibly be utilized to prevent primary and secondary metastases of tumor cells. (C) 2001 Academic Press.
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页码:975 / 980
页数:6
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