The role of toll-like receptors (TLRs) in bacteria-induced maturation of murine dendritic cells (DCs) - Peptidoglycan and lipoteichoic acid are inducers of DC maturation and require TLR2

被引:236
作者
Michelsen, KS
Aicher, A
Mohaupt, M
Hartung, T
Dimmeler, S
Kirschning, CJ
Schumann, RR
机构
[1] Humboldt Univ, Univ Med Ctr Charite, Inst Mikrobiol & Hyg, D-10117 Berlin, Germany
[2] Univ Frankfurt, Zentrum Inneren Med, D-60590 Frankfurt, Germany
[3] Max Delbruck Ctr Mol Med, D-13125 Berlin, Germany
[4] Univ Konstanz, Dept Biochem Pharmacol, D-78457 Constance, Germany
[5] Tech Univ Munich, Inst Med Microbiol Immunol & Hyg, D-81675 Munich, Germany
关键词
D O I
10.1074/jbc.M011615200
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
Toll-like receptors (TLRs) have been found to be key elements in pathogen recognition by the host immune system. Dendritic cells (DCs) are crucial for both innate immune responses and initiation of acquired immunity, Here we focus on the potential involvement of TLR ligand interaction in DC maturation. TLR2 knockout mice and mice carrying a TLR4 mutation (C3H/HeJ) were investigated for DC maturation induced by peptidoglycan (PGN), lipopolysaccharide (LPS), or lipoteichoic acids (LTAs), All stimuli induced maturation of murine bone marrow-derived DCs in control mice. TLR2(-/-) mice lacked maturation upon stimulation with PGN, as assessed by expression of major histocompatibility complex class II, CD86, cytokine, and chemokine production, fluorescein isothiocyanate-dextran uptake, and mixed lymphocyte reactions, while being completely responsive to LPS. A similar lack of maturation was observed in C3H/HeJ mice upon stimulation with LPS, DC maturation induced by LTAs from two different types of bacteria was severely impaired in TLR2(-/-), whereas C3H/HeJ mice responded to LTAs in a manner similar to wild-type mice, We demonstrate that DC maturation is induced by stimuli from Gram-positive microorganisms, such as PGN and LTA, with similar efficiency as by LPS, Finally, we provide evidence that TLR2 and TLR4 interaction with the appropriate ligand is essential for bacteria-induced maturation of DCs.
引用
收藏
页码:25680 / 25686
页数:7
相关论文
共 34 条
[11]  
Mahnke K, 1997, ADV EXP MED BIOL, V417, P145
[12]   The biology of Toll-like receptors [J].
Means, TK ;
Golenbock, DT ;
Fenton, MJ .
CYTOKINE & GROWTH FACTOR REVIEWS, 2000, 11 (03) :219-232
[13]  
Means TK, 1999, J IMMUNOL, V163, P6748
[14]   A human homologue of the Drosophila Toll protein signals activation of adaptive immunity [J].
Medzhitov, R ;
PrestonHurlburt, P ;
Janeway, CA .
NATURE, 1997, 388 (6640) :394-397
[15]   Advances in immunology: Innate immunity. [J].
Medzhitov, R ;
Janeway, CJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (05) :338-344
[16]  
MORRISON DC, 1975, J BIOL CHEM, V250, P2911
[17]   Differential expression and regulation of toll-like receptors (TLR) in human leukocytes: Selective expression of TLR3 in dendritic cells [J].
Muzio, M ;
Bosisio, D ;
Polentarutti, N ;
D'amico, G ;
Stoppacciaro, A ;
Mancinelli, R ;
van't Veer, C ;
Penton-Rol, G ;
Ruco, LP ;
Allavena, P ;
Mantovani, A .
JOURNAL OF IMMUNOLOGY, 2000, 164 (11) :5998-6004
[18]   SECRETORY PRODUCTS OF MACROPHAGES [J].
NATHAN, CF .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 79 (02) :319-326
[19]   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
[20]   CD14 IS A PATTERN-RECOGNITION RECEPTOR [J].
PUGIN, J ;
HEUMANN, D ;
TOMASZ, A ;
KRAVCHENKO, VV ;
AKAMATSU, Y ;
NISHIJIMA, M ;
GLAUSER, MP ;
TOBIAS, PS ;
ULEVITCH, RJ .
IMMUNITY, 1994, 1 (06) :509-516