Effects of human lactoferrin on NK cell cytotoxicity against haematopoietic and epithelial tumour cells

被引:102
作者
Damiens, E [1 ]
Mazurier, J [1 ]
El Yazidi, I [1 ]
Masson, M [1 ]
Duthille, I [1 ]
Spik, G [1 ]
Boilly-Marer, Y [1 ]
机构
[1] Univ Sci & Technol Lille, Chim Biol Lab, CNRS, UMR 111, F-59655 Villeneuve Dascq, France
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 1998年 / 1402卷 / 03期
关键词
lactoferrin; NK cell; cytotoxicity; tumor cell;
D O I
10.1016/S0167-4889(98)00013-5
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
Lactoferrin is an iron-binding glycoprotein implicated in particular in the control of immune functions and cell proliferation. We have investigated its involvement, at inflammatory concentrations, in cancer progression. We report that lactoferrin has a significant effect on natural killer (NK) cell cytotoxicity against haematopoietic and breast epithelial cell lines. Lactoferrin increases cytolysis at a low concentration (10 mu g/ml) while at a high concentration (100 mu g/ml) it modulates cytolysis depending on the target cell phenotype. By pre-treatment of either NK cells or target cells with lactoferrin, we have demonstrated that the lactoferrin effect is due both to a modulation of NK cell cytotoxicity and the target cell sensitivity to lysis. Lactoferrin binds to 91% of the naturally heterogeneous CD56(dim/bright) NK cell population and increases the NK cell cytotoxic activity at low concentrations. High concentrations of lactoferrin seem to be toxic for the CD56(bright) NK cells and decrease NK cell cytotoxicity. Lactoferrin also exerts an effect on target cells depending on the cell phenotype. It does not modify the susceptibility to lysis of haematopoietic cells such as Jurkat and K-562 cells, but does significantly increase that of the breast and colon epithelial cells. We have also demonstrated that lactoferrin inhibits epithelial cell proliferation by blocking the cell cycle progression. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:277 / 287
页数:11
相关论文
共 30 条
[1]  
AMOURIC M, 1984, IN VITRO CELL DEV B, V20, P543
[2]   STIMULATORY EFFECT OF HUMAN LACTOFERRIN ON DNA-SYNTHESIS IN BALB/C 3T3 CELLS [J].
AZUMA, N ;
MORI, H ;
KAMINOGAWA, S ;
YAMAUCHI, K .
AGRICULTURAL AND BIOLOGICAL CHEMISTRY, 1989, 53 (01) :31-35
[3]  
BEZAULT J, 1994, CANCER RES, V54, P2310
[4]   RETRACTED: OLIGOSACCHARIDE LIGANDS FOR NKR-P1 PROTEIN ACTIVATE NK CELLS AND CYTOTOXICITY (Retracted article. See vol. 500, pg. 492, 2013) [J].
BEZOUSKA, K ;
YUEN, CT ;
OBRIEN, J ;
CHILDS, RA ;
CHAI, WG ;
LAWSON, AM ;
DRBAL, K ;
FISEROVA, A ;
POSPISIL, M ;
FEIZI, T .
NATURE, 1994, 372 (6502) :150-157
[5]  
Bi BY, 1996, EUR J CELL BIOL, V69, P288
[6]  
BI BY, 1994, EUR J CELL BIOL, V65, P164
[7]  
BOYUM A, 1968, SCAND J CLIN LAB INV, VS 21, P77
[8]   ISOLATION OF A LACTOFERRIN CDNA CLONE AND ITS EXPRESSION IN HUMAN BREAST-CANCER [J].
CAMPBELL, T ;
SKILTON, RA ;
COOMBES, RC ;
SHOUSHA, S ;
GRAHAM, MD ;
LUQMANI, YA .
BRITISH JOURNAL OF CANCER, 1992, 65 (01) :19-26
[9]   EFFECT OF TRANSFERRIN, LACTOFERRIN AND CHELATED IRON ON HUMAN LYMPHOCYTES-T [J].
DJEHA, A ;
BROCK, JH .
BRITISH JOURNAL OF HAEMATOLOGY, 1992, 80 (02) :235-241
[10]   LACTOFERRIN BINDING-SITES AND NUCLEAR-LOCALIZATION IN K562(S) CELLS [J].
GARRE, C ;
BIANCHISCARRA, G ;
SIRITO, M ;
MUSSO, M ;
RAVAZZOLO, R .
JOURNAL OF CELLULAR PHYSIOLOGY, 1992, 153 (03) :477-482