LBP, CD14, TLR4 and the murine innate immune response to a peritoneal Salmonella infection

被引:41
作者
Bernheiden, M
Heinrich, JM
Minigo, G
Schütt, C
Stelter, F
Freeman, M
Golenbock, D
Jack, RS [1 ]
机构
[1] Univ Klinikum Greifswald, Inst Immunol & Transfus Med, D-17489 Greifswald, Germany
[2] Massachusetts Gen Hosp, Boston, MA 02114 USA
[3] Boston Univ, Sch Med, Boston, MA 02118 USA
来源
JOURNAL OF ENDOTOXIN RESEARCH | 2001年 / 7卷 / 06期
关键词
D O I
10.1179/096805101101533061
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
In mice, defense against an intraperitoneal Salmonella infection depends on a vigorous innate immune response, Mutations which lead to an inadequate early response to the pathogen thus identify genes involved in innate immunity. The best studied host resistance factor, NRAMP-1, is an endosomal membrane protein whose loss leads to an inability of the animals to hold the infection in check. However, innate defense against Salmonella is not restricted to mechanisms which directly attack the pathogen within macrophages. Here we have examined the contribution of the LBP, CD14 and TLR4 gene products to innate defense against Salmonella. To this end, we have generated mice which carry a wild-type allele of NRAMP-1, but which are deficient for the LBP, CD14 or TLR4 genes. Loss of any of these genes leads to a susceptibility to Salmonella as dramatic as that seen in animals lacking functional NRAMP-1 protein. This indicates that LBP, CD14 and TLR4 are all critical elements required in the proper induction of this innate defense system.
引用
收藏
页码:447 / 450
页数:4
相关论文
共 10 条
[1]
Natural resistance to infection with intracellular pathogens: The Nramp1 protein is recruited to the membrane of the phagosome [J].
Gruenheid, S ;
Pinner, E ;
Desjardins, M ;
Gros, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (04) :717-730
[2]
Natural resistance to intracellular infections: Natural resistance-associated macrophage protein 1 (NRAMP1) functions as a pH-dependent manganese transporter at the phagosomal membrane [J].
Jabado, N ;
Jankowski, A ;
Dougaparsad, S ;
Picard, V ;
Grinstein, S ;
Gros, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (09) :1237-1247
[3]
Lipopolysaccharide-binding protein is required to combat a murine Gram-negative bacterial infection [J].
Jack, RS ;
Fan, XL ;
Bernheiden, M ;
Rune, G ;
Ehlers, M ;
Weber, A ;
Kirsch, G ;
Mentel, R ;
Furll, B ;
Freudenberg, M ;
Schmitz, G ;
Stelter, F ;
Schutt, C .
NATURE, 1997, 389 (6652) :742-745
[4]
KAUFMANN SHE, 1998, FUNDAMENTAL IMMUNOLO, P1335
[5]
The Nramp1 antimicrobial resistance gene segregates independently of resistance to virulent Mycobacterium tuberculosis [J].
Medina, E ;
Rogerson, BJ ;
North, RJ .
IMMUNOLOGY, 1996, 88 (04) :479-481
[6]
Divergent response to LPS and bacteria in CD14-deficient murine macrophages [J].
Moore, KJ ;
Andersson, LP ;
Ingalls, RR ;
Monks, BG ;
Li, R ;
Arnaout, MA ;
Golenbock, DT ;
Freeman, MW .
JOURNAL OF IMMUNOLOGY, 2000, 165 (08) :4272-4280
[7]
Defective LPS signaling in C3H/HeJ and C57BL/10ScCr mice:: Mutations in Tlr4 gene [J].
Poltorak, A ;
He, XL ;
Smirnova, I ;
Liu, MY ;
Van Huffel, C ;
Du, X ;
Birdwell, D ;
Alejos, E ;
Silva, M ;
Galanos, C ;
Freudenberg, M ;
Ricciardi-Castagnoli, P ;
Layton, B ;
Beutler, B .
SCIENCE, 1998, 282 (5396) :2085-2088
[8]
NATURAL-RESISTANCE TO INFECTION WITH INTRACELLULAR PARASITES - ISOLATION OF A CANDIDATE FOR BCG [J].
VIDAL, SM ;
MALO, D ;
VOGAN, K ;
SKAMENE, E ;
GROS, P .
CELL, 1993, 73 (03) :469-485
[9]
SOLUBLE CD14 ACTS AS A SHUTTLE IN THE NEUTRALIZATION OF LIPOPOLYSACCHARIDE (LPS) BY LPS-BINDING PROTEIN AND RECONSTITUTED HIGH-DENSITY-LIPOPROTEIN [J].
WURFEL, MM ;
HAILMAN, E ;
WRIGHT, SD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (05) :1743-1754
[10]
Yu B, 1996, J BIOL CHEM, V271, P4100