Human Toll-like receptor 2 mediates monocyte activation by Listeria monocytogenes, but not by group B streptococci or lipopolysaccharide

被引:251
作者
Flo, TH
Halaas, O
Lien, E
Ryan, L
Teti, G
Golenbock, DT
Sundan, A
Espevik, T [1 ]
机构
[1] Norwegian Univ Sci & Technol, Inst Canc Res & Mol Biol, N-7489 Trondheim, Norway
[2] Univ Messina, Fac Med & Chirurg, Inst Microbiol, Messina, Italy
[3] Boston Univ, Sch Med, Boston, MA 02118 USA
[4] Boston Med Ctr, Maxwell Finland Lab Infect Dis, Dept Med, Boston, MA 02118 USA
关键词
D O I
10.4049/jimmunol.164.4.2064
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human Toll like receptor (TLR) 2 has been implicated as a signaling receptor for LPS from Gram-negative bacteria and cell wall components from Gram-positive organisms, In this study, we investigated whether TLR2 can signal cell activation by the heat-killed group B streptococci type III (GBS) and Listeria monocytogenes (HKLM), HKLM, but not GBS, showed a time- and dose-dependent activation of Chinese hamster ovary cells transfected with human TLR2, as measured by translocation of NF-kappa B and induction of IL-6 production, A mAb recognizing a TLR2-associated epitope (TL2.1) was generated that inhibited IL-6 production from Chinese hamster ovary-TLR2 cells stimulated with HKLM or LPS, The TL2.1 mAb reduced HKLM-induced TNF production from human monocytes by 60%, whereas a CD14 mAb (3C10) reduced the TNF production by 30%, However, coadministrating TL2.1 and 3C10 inhibited the TNF response by 80%, In contrast to this, anti-CD14 blocked LPS induced TNF production from monocytes, whereas anti-TLR2 showed no inhibition. Neither TL2.1 nor 3C10 affected GBS-induced TNF production. These results show that TLR2 can function as a signaling receptor for HKLM, possibly together with CD14, but that TLR2 is unlikely to be involved in cell activation by GBS, Furthermore, although LPS can activate transfected cell lines through TLR2, this receptor does not seem to be the main transducer of LPS activation of human monocytes, Thus, our data demonstrate the ability of TLR2 to distinguish between different pathogens. The Journal of Immunology, 2000, 164: 2064-2069.
引用
收藏
页码:2064 / 2069
页数:6
相关论文
共 42 条
  • [1] PRODUCTION OF HYBRIDOMA GROWTH-FACTOR BY HUMAN-MONOCYTES
    AARDEN, LA
    DEGROOT, ER
    SCHAAP, OL
    LANSDORP, PM
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1987, 17 (10) : 1411 - 1416
  • [2] THE PATHOGENESIS OF SEPSIS
    BONE, RC
    [J]. ANNALS OF INTERNAL MEDICINE, 1991, 115 (06) : 457 - 469
  • [3] GRAM-POSITIVE ORGANISMS AND SEPSIS
    BONE, RC
    [J]. ARCHIVES OF INTERNAL MEDICINE, 1994, 154 (01) : 26 - 34
  • [4] BOYERT SM, 1988, SCIENCE, V239, P497
  • [5] Host defense mechanisms triggered by microbial lipoproteins through toll-like receptors
    Brightbill, HD
    Libraty, DH
    Krutzik, SR
    Yang, RB
    Belisle, JT
    Bleharski, JR
    Maitland, M
    Norgard, MV
    Plevy, SE
    Smale, ST
    Brennan, PJ
    Bloom, BR
    Godowski, PJ
    Modlin, RL
    [J]. SCIENCE, 1999, 285 (5428) : 732 - 736
  • [6] Cloning and characterization of two Toll/interleukin-1 receptor-like genes TIL3 and TIL4: Evidence for a multi-gene receptor family in humans
    Chaudhary, PM
    Ferguson, C
    Nguyen, V
    Nguyen, O
    Massa, HF
    Eby, M
    Jasmin, A
    Trask, BJ
    Hood, L
    Nelson, PS
    [J]. BLOOD, 1998, 91 (11) : 4020 - 4027
  • [7] Toll-like receptor-4 mediates lipopolysaccharide-induced signal transduction
    Chow, JC
    Young, DW
    Golenbock, DT
    Christ, WJ
    Gusovsky, F
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (16) : 10689 - 10692
  • [8] Lipoteichoic acid preparations of grain-positive bacteria induce interleukin-12 through a CD14-dependent pathway
    Cleveland, MG
    Gorham, JD
    Murphy, TL
    Tuomanen, E
    Murphy, KM
    [J]. INFECTION AND IMMUNITY, 1996, 64 (06) : 1906 - 1912
  • [9] Binding of bacterial peptidoglycan to CD14
    Dziarski, R
    Tapping, RI
    Tobias, PS
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (15) : 8680 - 8690
  • [10] LPS-binding proteins and receptors
    Fenton, MJ
    Golenbock, DT
    [J]. JOURNAL OF LEUKOCYTE BIOLOGY, 1998, 64 (01) : 25 - 32