Regulatory roles for CD14 and phosphatidylinositol in the signaling via toll-like receptor 4-MD-2

被引:133
作者
Akashi, S
Ogata, H
Kirikae, F
Kirikae, T
Kawasaki, K
Nishijima, M
Shimazu, R
Nagai, Y
Fukudome, K
Kimoto, M
Miyake, K [1 ]
机构
[1] Saga Med Sch, Dept Immunol, Saga 8498501, Japan
[2] Int Med Ctr Japan, Res Inst, Dept Infect Dis & Trop Med, Tokyo, Japan
[3] Natl Inst Infect Dis, Dept Biochem & Cell Biol, Tokyo, Japan
关键词
D O I
10.1006/bbrc.2000.2089
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
The complex consisting of Toll-like receptor 4 (TLR4) and associated MD-2 signals the presence of lipopolysaccharide (LPS) when it is expressed in cell lines. We here show that normal human mononuclear cells express TLR4 and signal LPS via TLR4. CD14 is a molecule that binds to LPS and facilitates its signaling. Little is known, however, about the relationship of CD14 with TLR4-MD-2. We show that CD14 helps TLR4-MD-2 to sense and signal the presence of LPS. CD14 has also been implicated in recognition of apoptotic cells, which leads to phagocytosis without activation. Membrane phospholipids such as phosphatidylserine (PS) or phosphatidylinositol (PtdIns) are thought to serve as the ligands for CD14 in apoptotic cells. We find that PtdIns acts as an LPS antagonist in the signaling via TLR4-MD-2. TLR4-MD-2 seems to discriminate LPS from phospholipids. The signaling via TLR4-MD-2 is thus regulated by CD14 and phospholipid such as PtdIns. (C) 2000 Academic Press.
引用
收藏
页码:172 / 177
页数:6
相关论文
共 36 条
[1]   Serum amyloid P component controls chromatin degradation and prevents antinuclear autoimmunity [J].
Bickerstaff, MCM ;
Botto, M ;
Hutchinson, WL ;
Herbert, J ;
Tennent, GA ;
Bybee, A ;
Mitchell, DA ;
Cook, HT ;
Butler, PJG ;
Walport, MJ ;
Pepys, MB .
NATURE MEDICINE, 1999, 5 (06) :694-697
[2]   Homozygous C1q deficiency causes glomerulonephritis associated with multiple apoptotic bodies [J].
Botto, M ;
Dell'Agnola, C ;
Bygrave, AE ;
Thompson, EM ;
Cook, HT ;
Petry, F ;
Loos, M ;
Pandolfi, PP ;
Walport, MJ .
NATURE GENETICS, 1998, 19 (01) :56-59
[3]   AUTOANTIGENS TARGETED IN SYSTEMIC LUPUS-ERYTHEMATOSUS ARE CLUSTERED IN 2 POPULATIONS OF SURFACE-STRUCTURES ON APOPTOTIC KERATINOCYTES [J].
CASCIOLAROSEN, LA ;
ANHALT, G ;
ROSEN, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (04) :1317-1330
[4]   Human CD14 mediates recognition and phagocytosis of apoptotic cells [J].
Devitt, A ;
Moffatt, OD ;
Raykundalia, C ;
Capra, JD ;
Simmons, DL ;
Gregory, CD .
NATURE, 1998, 392 (6675) :505-509
[5]   SEPTIC SHOCK - PATHOGENESIS [J].
GLAUSER, MP ;
ZANETTI, G ;
BAUMGARTNER, JD ;
COHEN, J .
LANCET, 1991, 338 (8769) :732-736
[6]   Induction of anticardiolipin antibody and/or lupus anticoagulant in rabbits by immunization with lipoteichoic acid, lipopolysaccharide and lipid A [J].
Gotoh, M ;
Matsuda, J .
LUPUS, 1996, 5 (06) :593-597
[7]  
HARAKUGE S, 1990, J BIOL CHEM, V265, P6606
[8]   Functional effects of anticardiolipin antibodies [J].
Harris, EN ;
Pierangeli, SS .
LUPUS, 1996, 5 (05) :372-377
[9]  
Hoshino K, 1999, J IMMUNOL, V162, P3749
[10]   Human Toll-like receptor 2 confers responsiveness to bacterial lipopolysaccharide [J].
Kirschning, CJ ;
Wesche, H ;
Ayres, TM ;
Rothe, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (11) :2091-2097