Lactoferrin: a modulator of immune and inflammatory responses

被引:300
作者
Legrand, D
Elass, E
Carpentier, M
Mazurier, J
机构
[1] Univ Sci & Technol Lille, Unite Glycobiol Struct & Fonct, F-59655 Villeneuve Dascq, France
[2] Univ Sci & Technol Lille, UMR 8576, CNRS, Inst Fed Rech N118, F-59655 Villeneuve Dascq, France
关键词
lactoferrin; inflammation; immunity; ROS; Th1;
D O I
10.1007/s00018-005-5370-2
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 of the transferrin family. Abundant expression and secretion of lactoferrin, in particular in milk and fluids of the digestive tract, are related to its implication in the first line of host defense. Lactoferrin is also a prominent component of the secondary granules of neutrophils (PMNs) and is released in infected tissues and blood during the inflammatory process. In addition to its direct antimicrobial properties, the abilities of lactoferrin to regulate the immune response and to protect against infection and septic shock have been described in numerous in vitro and in vivo studies. Although the cellular and molecular mechanisms that account for the modulation of the inflammatory and immune responses by lactoferrin are not yet totally elucidated, many are now established. At the cellular level, lactoferrin modulates the migration, maturation and function of immune cells. At the molecular level and in addition to iron binding, interactions of lactoferrin with a plethora of compounds, either soluble or membrane molecules, account for its modulatory properties. This paper reviews our current understanding of the cellular and molecular mechanisms that explain the regulatory properties of lactoferrin in host defence.
引用
收藏
页码:2549 / 2559
页数:11
相关论文
共 124 条
[1]   Expression of lactoferrin on human granulocytes: Analysis with polyclonal and monoclonal antibodies [J].
Afeltra, A ;
Caccavo, D ;
Ferri, GM ;
Addessi, MA ;
DeRosa, FG ;
Amoroso, A ;
Bonomo, L .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 1997, 109 (02) :279-285
[2]   APOLACTOFERRIN STRUCTURE DEMONSTRATES LIGAND-INDUCED CONFORMATIONAL CHANGE IN TRANSFERRINS [J].
ANDERSON, BF ;
BAKER, HM ;
NORRIS, GE ;
RUMBALL, SV ;
BAKER, EN .
NATURE, 1990, 344 (6268) :784-787
[3]   STRUCTURE OF HUMAN LACTOFERRIN AT 3.2-A RESOLUTION [J].
ANDERSON, BF ;
BAKER, HM ;
DODSON, EJ ;
NORRIS, GE ;
RUMBALL, SV ;
WATERS, JM ;
BAKER, EN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (07) :1769-1773
[4]   Septic shock [J].
Annane, D ;
Bellissant, E ;
Cavaillon, JM .
LANCET, 2005, 365 (9453) :63-78
[5]   LACTOFERRIN IS A LIPID A-BINDING PROTEIN [J].
APPELMELK, BJ ;
AN, YQ ;
GEERTS, M ;
THIJS, BG ;
DEBOER, HA ;
MACLAREN, D ;
DEGRAAFF, J ;
NUIJENS, JH .
INFECTION AND IMMUNITY, 1994, 62 (06) :2628-2632
[6]   Effects of lactoferrin on IL-6 production by peritoneal and alveolar cells in cyclophosphamide-treated mice [J].
Artym, J ;
Zimecki, M ;
Kruzel, ML .
JOURNAL OF CHEMOTHERAPY, 2004, 16 (02) :187-192
[7]   Reconstitution of the cellular immune response by lactoferrin in cyclophosphamide-treated mice is correlated with renewal of T cell compartment [J].
Artym, J ;
Zimecki, M ;
Kruzel, ML .
IMMUNOBIOLOGY, 2003, 207 (03) :197-205
[8]   Orally administered lactoferrin restores humoral immune response in immunocompromised mice [J].
Artyrn, J ;
Zimecki, M ;
Paprocka, M ;
Kruzel, ML .
IMMUNOLOGY LETTERS, 2003, 89 (01) :9-15
[9]   Cellular internalization of lactoferrin in intestinal epithelial cells [J].
Ashida, K ;
Sasaki, H ;
Suzuki, YA ;
Lönnerdal, B .
BIOMETALS, 2004, 17 (03) :311-315
[10]   Dealing with iron: Common structural principles in proteins that transport iron and heme [J].
Baker, HM ;
Anderson, BF ;
Baker, EN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3579-3583