Lipopolysaccharide heterogeneity: Innate host responses to bacterial modification of lipid A structure

被引:153
作者
Dixon, DR [1 ]
Darveau, RP [1 ]
机构
[1] Univ Washington, Hlth Sci Ctr, Dept Periodont, Seattle, WA 98195 USA
关键词
lipopolysaccharide (LPS); lipid A; CD14; TLR; innate immunity;
D O I
10.1177/154405910508400702
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
The innate host response system is composed of various mechanisms designed to detect and facilitate host responses to microbial components, such as lipopolysaccharides ( LPS). To enable this to occur, innate systems contain multiple pattern recognition receptors ( i. e., LBP, CD14, and TLRs), which identify certain features within bacterial LPS that are foreign to the host, as well as essential and uniquely specific for bacteria. Innate host identification of unique bacterial components or patterns, therefore, relies on the inability of bacteria to alter these essential or critical components dramatically. Historically, LPS have been viewed as essential outer- membrane molecules containing both a highly variable outer region ( O- segment) as well as a relatively conserved inner region ( lipid A). However, over the last decade, new evidence has emerged, revealing that increased natural diversity or heterogeneity within specific components of LPS, such as lipid A - resulting in minor to moderate changes in lipid A structure - can produce dramatic host responses. Therefore, examples of natural lipid A heterogeneity, and the mechanisms that control it, represent a novel approach in which bacteria modulate host responses and may thereby confer specific advantages to certain bacterial species under changing environmental host conditions.
引用
收藏
页码:584 / 595
页数:12
相关论文
共 123 条
[1]   Human MD-2 confers on mouse Toll-like receptor 4 species-specific lipopolysaccharide recognition [J].
Akashi, S ;
Nagai, Y ;
Ogata, H ;
Oikawa, M ;
Fukase, K ;
Kusumoto, S ;
Kawasaki, K ;
Nishijima, M ;
Hayashi, S ;
Kimoto, M ;
Miyake, K .
INTERNATIONAL IMMUNOLOGY, 2001, 13 (12) :1595-1599
[2]   Novel variation of lipid A structures in strains of different Yersinia species [J].
Aussel, L ;
Thérisod, H ;
Karibian, D ;
Perry, MB ;
Bruneteau, M ;
Caroff, M .
FEBS LETTERS, 2000, 465 (01) :87-92
[3]  
BAINBRIDGE BW, 2002, ANN PERIODONTOL, V7, P1
[4]   Crystal structure of human BPI and two bound phospholipids at 2.4 angstrom resolution [J].
Beamer, LJ ;
Carroll, SF ;
Eisenberg, D .
SCIENCE, 1997, 276 (5320) :1861-1864
[5]   Identification of Toll-like receptor 4 (Tlr4) as the sole conduit for LPS signal transduction: genetic and evolutionary studies [J].
Beutler, B ;
Du, X ;
Poltorak, A .
JOURNAL OF ENDOTOXIN RESEARCH, 2001, 7 (04) :277-280
[6]   Transfer of palmitate from phospholipids to lipid A in outer membranes of Gram-negative bacteria [J].
Bishop, RE ;
Gibbons, HS ;
Guina, T ;
Trent, MS ;
Miller, SI ;
Raetz, CRH .
EMBO JOURNAL, 2000, 19 (19) :5071-5080
[7]   New insights into endotoxin-induced activation of macrophages:: Involvement of a K+ channel in transmembrane signaling [J].
Blunck, R ;
Scheel, O ;
Müller, M ;
Brandenburg, K ;
Seitzer, U ;
Seydel, U .
JOURNAL OF IMMUNOLOGY, 2001, 166 (02) :1009-1015
[8]   LIPOPOLYSACCHARIDES FROM A SLIGHTLY VIRULENT-STRAIN OF YERSINIA-PESTIS [J].
BORDET, C ;
BRUNETEAU, M ;
MICHEL, G .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1977, 79 (02) :443-449
[9]   A nonsubstituted primary hydroxyl group in position 6' of free lipid A is required for binding of lipid A monoclonal antibodies [J].
Brade, L ;
Engel, R ;
Christ, WJ ;
Rietschel, ET .
INFECTION AND IMMUNITY, 1997, 65 (09) :3961-3965
[10]   Structure of bacterial lipopolysaccharides [J].
Caroff, M ;
Karibian, D .
CARBOHYDRATE RESEARCH, 2003, 338 (23) :2431-2447