The JI
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
QUICK SEARCH:   [advanced]


     
 

The Journal of Immunology, 2007, 179, 5811 -5818
Copyright © 2007 by The American Association of Immunologists, Inc.
This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Geisel, J.
Right arrow Articles by Frick, J.-S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Geisel, J.
Right arrow Articles by Frick, J.-S.

IL-6 and Maturation Govern TLR2 and TLR4 Induced TLR Agonist Tolerance and Cross-Tolerance in Dendritic Cells1

Julia Geisel*, Frauke Kahl*, Martina Müller*, Hermann Wagner{dagger}, Carsten J. Kirschning{dagger}, Ingo B. Autenrieth* and Julia-Stefanie Frick2,*

* Institute of Medical Microbiology and Hygiene, University of Tübingen, Tübingen, Germany; and {dagger} Institute of Medical Microbiology, Immunology, and Hygiene, Technical University of Munich, Munich, Germany


   Abstract
Top
 Abstract
Introduction
 Materials and Methods
 Results
 Discussion
 Disclosures
 References
 
Stimulation of naive mouse dendritic cells (DC) with LPS or Pam3CSK4 (P3C) induces production of TNF-{alpha} via TLR4- or TLR2-signaling. Although tolerance in macrophages has been studied in detail, we investigated the role of TLR agonist concentration and IL-6 for tolerance in DC. P3C- or LPS-primed DC were nonresponsive to P3C or LPS restimulation in terms of TNF-{alpha} but not IL-6 production. The mechanisms involved in tolerance were dependent on the concentration of the TLR ligand used for DC priming. DC primed with LPS or P3C at high concentrations developed a maturation dependent, IL-6 independent tolerance associated with inhibition of TLR signaling upstream of I{kappa}B as indicated by decreased I{kappa}B degradation. In contrast, priming of DC with LPS or P3C at low concentrations resulted in IL-6-dependent tolerance, which was abolished in IL-6 deficient DC, and was not accompanied by maturation of DC or by down-regulation of TLR2 or TLR4. In homotolerogenic DC primed with LPS or P3C at high concentrations, degradation of I{kappa}B upon restimulation with LPS or P3C was inhibited suggesting tolerance mechanism(s) upstream of I{kappa}B; in contrast, cross-tolerance in DC primed with LPS or P3C at low concentrations was not associated with reduced I{kappa}B degradation suggesting tolerance mechanisms downstream of I{kappa}B. Our data indicate that in naive DC TLR4- and TLR2-stimulation results in homo- and cross-tolerance; the mechanisms involved in tolerance depend on the concentration of the TLR agonist used for DC priming and are governed by IL-6 and maturation.


   Introduction
Top
 Abstract
 Introduction
Materials and Methods
 Results
 Discussion
 Disclosures
 References
 
Dendritic cells (DC)3 are among the first APCs encountering bacteria at mucosal surfaces and play an important role in maintenance of regular homeostasis in the intestine. LPS from the cell wall of Gram-negative bacteria is widely used for DC activation. Activation of DC with TLR agonists leads to activation of NF-{kappa}B and MAPK family members (1). Furthermore, cytokines and proinflammatory mediators that affect for instance T cell differentiation are produced rapidly. Stimulation of DC with TLR2 or TLR4 agonists results in different patterns of cytokine secretion. Stimulation with TLR4 promotes induction of IL-12(p70) and the chemokine IFN-{gamma} inducible protein-10, which are both associated with Th1 responses. In contrast, TLR2 stimulation failed to induce IL-12(p70) and inducible protein-10 secretion but resulted in production of IL-12(p40) homodimer and a rapid release of IL-10 (1, 2). Whereas TLR4 transduces enterobacterial LPS signals, TLR2 mediates nonenterobacterial such as Porphyromonas gingivalis (3) and Leptospira interrogans LPS signals (4). TLR1 has been implicated as TLR2 coreceptor and its coexpression increased a TLR4 independent response to Escherichia coli LPS and Neisseria meningitidis lipooligosaccharide (5).

Following the recognition of LPS by TLR4/MD-2/CD14 complex or P3C (N-palmitoyl-bis(palmitoyloxy)-propyl-cysteinyl-seryl-Lys4) by TLR2/TLR1/CD14 complex, the intracellular adaptor protein MyD88 binds to intracellular domains of most TLRs which recruits members of the IL-1 receptor-associated kinase (IRAK) family to the TLR/MyD88 complex (6). IRAK-1 phosphorylates itself and leaves the TLR/MyD88 complex to associate with the TNF receptor-associated factor 6. This leads to downstream activation of signaling pathways involving MAPKs and NF-{kappa}B (6). It is known that exposure to LPS both in vitro and in vivo can lead to a desensitization of immune cells to subsequent stimulation with LPS. This finding has been referred to as "endotoxin tolerance."

One of the main characteristics of LPS tolerance in vitro is a change in the pattern of inflammatory gene expression when responses to a single or two sequential LPS exposures are compared (7). Furthermore stimulation with TLR2 agonists leads to desensitization toward a subsequent TLR2 stimulus (8). In macrophages priming with a TLR2 stimulus reduces responsiveness to restimulation with LPS (9). In addition, in human promonocytic cells priming with LPS leads to cross-tolerance to TLR2 restimulation (10). These phenomena of cross-tolerance both have been reported to be associated with down-regulation of IRAK-1 (10, 11). However, a major effect accompanying tolerance via TLR4 might be induction of p50p50 homodimer formation (11, 12, 13, 14, 15). In contrast to p65, the p50 protein does not transactivate, but binds NF-{kappa}B recognition elements in gene promoters thus preventing expression of NF-{kappa}B driven genes such as TNF-{alpha} (16). Additionally, a role for suppressor of cytokine signaling 1 in LPS tolerance has been implicated (17, 18). Furthermore, IRAK-M has been reported to prevent dissociation of the IRAK-1/IRAK-4 complex thereby preventing formation of the IRAK-1/ TNF receptor-associated factor 6 complex and subsequent TLR signaling (19).

We have shown recently that treatment of DC with Bacteroides vulgatus- an anaerobe Gram-negative rod closely related to P. gingivalis phylogenetically and recognized via TLR2 mainly leads to a reduced responsiveness to restimulation with E. coli in bone-marrow-derived DC and differentiates DC toward a semimature status (20).

In this study, we investigated mechanisms underlying TLR2/4 induced DC tolerance toward restimulation with specific TLR agonists. Our main focus was on DC maturation and activation, as well as TLR2/4 surface expression and the role of IL-6 in the modulation of these processes. Our results implicate that TLR2 or TLR4 signals induce homo- and cross-tolerogenic DC. We observed that different mechanisms account for induction of tolerogenic DC; on the one hand, maturation processes and, on the other hand, an IL-6 dependent differentiation to a semimature tolerogenic DC phenotype.


   Materials and Methods
Top
 Abstract
 Introduction
 Materials and Methods
Results
 Discussion
 Disclosures
 References
 
Mice

C57Bl/6 x 129Sv, IL-6–/– (21), and TLR2/4–/– mice were obtained from own breeding. All mice were kept under SPF conditions. Male and female mice were sacrificed at 6–10 wk of age. Animal experiments were reviewed and approved by the responsible institutional review committee.

Abs and reagents

P3C was purchased from ECM microcollections and ultra pure LPS S. enterica serovar Minnesota from Calbiochem. The following Abs were used for flow cytometry: PE conjugated anti-mouse CD11c, clone HL3 and FITC conjugated anti-mouse CD40, clone HM 40–3, CD80, clone 16–10A1, CD86, clone GL1 and MHC class II clone 2G9; isotype control hamster IgG1{lambda} and hamster IgM{kappa}, hamster IgG2{kappa}, rat IgG2a{kappa} (BD Biosciences); anti-mouse TLR4, clone MTS 510 and anti-mouse TLR2, clone 6C2; isotype control rat IgG2a and rat IgG2b (eBioscience/NatuTec); anti I{kappa}B-{alpha} (Cell Signaling Technology) and anti-mouse beta-actin (Sigma-Aldrich); and secondary Ab anti-rabbit (Cell Signaling Technology) and rabbit anti-mouse IgG HRP (DakoCytomation) were used. Recombinant mouse IL-6 was purchased from R&D Systems.

Mouse DC isolation

Bone marrow cells were isolated and cultured as described previously (22) with minor modifications. Cells were harvested at day 8 and used to evaluate the effects of cellular challenge with LPS and P3C on cytokine release and expression of surface markers as described below.

Stimulation of isolated DC

DC were stimulated with LPS or P3C at different concentrations (1 ng/ml–1000 ng/ml). After 24 h, cell culture supernatant was harvested for analysis of cytokine expression and cells were used for flow cytometry of surface marker expression. For sequential stimulation cells were challenged with LPS or P3C at day 7 and restimulated with LPS or P3C at day 8. Twenty-four hours later, cell culture supernatants and cells were harvested.

Cytokine analysis by ELISA

For analysis of IL-6, IL-10, and TNF-{alpha} concentrations of cell culture supernatants commercially available ELISA kits (BD Biosciences) were used according to the manufacturer’s instructions.

Flow cytometry analysis

A total of 1 x 106 cells were incubated in 150 µl PBS containing fluorochrome conjugated Abs at a concentration of 0.7 ng/µl (anti-CD11c) and 1.7 ng/µl (anti-CD40, CD80, CD86, and MHC class II). TLR4 and TLR2 Abs were used at a concentration of 3.3 ng/µl after incubation in Fc-block ({alpha}-Fc{gamma}RIII/II CD16/CD32; BD Biosciences) containing 10% FCS. 30.000 cells were analyzed. A total of 7.5 ng propidiumiodide (Sigma-Aldrich) was added 1 min before FACS analyses to 150 µl samples.

I{kappa}B-{alpha} Western blot

A total of 2 x 106 DC were treated with P3C or LPS for 24 h and restimulated for another 15 min. After cells were washed in ice cold PBS the pellet was lysed by adding 75 µl SDS sample buffer (62.5 mM Tris-HCl (pH 6.8), 2% w/v SDS, 10% glycerol, 50 mM DTT, and 0.01% w/v bromphenol blue). Cells were sonicated for 10–15 s to shear DNA and reduce viscosity. Samples were heated to 95°C for 5 min and microcentrifuged for another 5 min. A 15-µl sample was loaded onto one lane of a 10% PAA gel. Proteins were transferred to nitrocellulose membrane after subjection to SDS-PAGE. The membrane was incubated in blocking buffer (1 x TBS and 0.1% Tween 20 with 5% nonfat dry milk) for 1 h at room temperature. Incubation with primary Ab overnight at 4°C was followed by incubation with HRP-conjugated secondary Ab for 1 h at room temperature. Proteins were detected by adding LumiGLO (Cell Signaling Technology) and exposure to x-ray film.

Statistical analysis

Statistical analysis was performed using Student’s t test. Values of p < 0.05 were considered significant. Error bars represent ± SEM.


   Results
Top
 Abstract
 Introduction
 Materials and Methods
 Results
Discussion
 Disclosures
 References
 
Pretreatment with LPS or P3C at high concentrations induces maturation dependent but IL-6 independent cross- and homo-tolerogenic DC

To quantify cytokine secretion of naive DC upon stimulation with TLR agonists, wild-type (Fig. 1, A–C) and IL-6–/– (Fig. 1, D–F) DC were stimulated with LPS or P3C at various concentrations and TNF-{alpha}, IL-6, and IL-10 production were determined in supernatants after 24 h. Stimulation with LPS or P3C resulted in dose dependent secretion of TNF-{alpha} and IL-6 which was enhanced upon LPS as compared with P3C stimulation. IL-10 was only detectable upon stimulation with LPS but not upon stimulation with P3C. Wild-type and IL-6–/– DC revealed similar cytokine secretion pattern (except for IL-6). (Fig. 1, A–F).


Figure 1
View larger version (19K):
[in this window]
[in a new window]

  		FIGURE 1. TNF-{alpha}, IL-6, and IL-10 secretion of DC upon stimulation with LPS or P3C. WT (A–C) and IL-6–/– (D–F) DC were stimulated with different concentrations of LPS or P3C (1 ng/ml - 1000 ng/ml) for 24 h. TNF-{alpha} (A and D), IL-6 (B and E), and IL-10 (C and F) levels in supernatants were determined by ELISA. The results are representative for at least three independent experiments. Each experiment was performed in triplicates; values represent the mean ± SD of triplicates.

 
We next addressed the question whether LPS or P3C may induce tolerance in DC. For this purpose, naive DC were stimulated with LPS or P3C at high concentrations (1000 ng/ml) for 24 h. Then, the culture medium was changed and primed DC were restimulated with 1000 ng/ml LPS or P3C. After the following 24 h TNF-{alpha}, IL-6, and IL-10 concentrations in culture supernatants were determined. Priming of DC with LPS resulted in a significantly decreased production of TNF-{alpha} upon restimulation with LPS or P3C. This nonresponsiveness was designated as homo- (LPS restimulation) or cross- (P3C restimulation) tolerance (Fig. 2A); comparable findings were obtained upon priming of DC at high concentrations of P3C (Fig. 2B). These results suggest that high concentrations of TLR2 or TLR4 agonists induce both LPS/P3C homo- and LPS/P3C cross-tolerant DC designated as LPShigh and P3Chigh tolerance, respectively.


Figure 2
View larger version (29K):
[in this window]
[in a new window]

  		FIGURE 2. Induction of homo- and cross-tolerance in WT DC. WT DC were pretreated with different concentrations (1 ng/ml or 1000 ng/ml) LPS (A and C) or P3C (B and D) for 24 h, the medium was changed and cells were restimulated with 1000 ng/ml LPS or P3C for another 24 h. TNF-{alpha} and IL-6 levels in the cell culture supernatants were determined by ELISA. The results are representative for at least three independent experiments. Each experiment was performed in triplicates, values represent the mean ± SD of triplicates (*, p < 0.05).

 
In contrast, IL-6 production was only inhibited in homo-tolerogenic DC primed with LPS but not in DC primed with P3C or cross-tolerogenic DC (Fig. 2, C and D) suggesting that different pathways control TLR2- and TLR4-induced TNF-{alpha} and IL-6 production and thus tolerance in terms of TNF-{alpha} and IL-6. Secretion of IL-10 from homo- but not from cross-tolerant DC primed at high concentrations of LPS was reduced, whereas secretion of IL-10 from cross- but not from homo-tolerant DC primed at high concentrations of P3C was unaltered (data not shown).

To investigate whether tolerance of primed DC upon restimulation with LPS or P3C is associated with maturation of DC, expression of activation and maturation markers was analyzed. For this purpose, naive DC were stimulated with LPS or P3C at high concentrations and expression of CD40, MHC class II, CD80, and CD86 was determined by flow cytometry 24 h later. The data demonstrate that priming of naive DC with LPS or P3C both led to enhanced expression of CD40 as well as MHC class II, CD80, and CD86 expression (Fig. 3), indicating maturation and activation of DC. Moreover, these data indicate that mature DC are tolerant to restimulation with LPS or P3C in terms of TNF-{alpha} but not in terms of IL-6 or IL-10.


Figure 3
View larger version (17K):
[in this window]
[in a new window]

  		FIGURE 3. CD40, CD80, CD86, and MHC class II expression of LPS or P3C treated DC. DC were stimulated with 1 ng/ml or 1000 ng/ml LPS or P3C for 24 h and analyzed by flow cytometry. Black lines represent the surface marker-specific staining, gray lines the isotype control. The results are representative for at least three independent experiments.

 
In macrophages, down-regulation of TLR has been described as a mechanism underlying LPS tolerance (23, 24). Therefore, we addressed whether down-regulation of TLR2 or TLR4 expression might also be involved in LPS/P3C tolerance in DC. To this end, naive DC were stimulated with LPS or P3C at low or high concentrations and surface expression of TLR2 and TLR4 was determined by flow cytometry 24 h later. The results demonstrate that stimulation of naive DC with P3C at low or high concentrations had no impact on surface expression of TLR4 (Fig. 4A) but led to a moderate up-regulation of TLR2 expression (Fig. 4B). In contrast, stimulation of DC with LPS at high concentrations led to a profound down-regulation of TLR4, whereas expression of TLR2 was increased (Fig. 4). Moreover, stimulation of DC with LPS at low concentrations did not significantly change expression of TLR4 or TLR2 (Fig. 4). As a control to assess Ab specificity, DC from TLR2–/– x TLR4–/– mice were used and revealed no significant immunostaining. These results suggest that down-regulation of TLRs in DC might be involved in LPShigh tolerance but not in LPSlow or P3C tolerance.


Figure 4
View larger version (16K):
[in this window]
[in a new window]

  		FIGURE 4. TLR2 and TLR4 surface expression in DC treated with LPS or P3C. Expression of TLR4 (A) and TLR2 (B) in WT DC treated with different concentrations (1 ng/ml or 1000 ng/ml) LPS or P3C for 24 h. As control TLR2/4–/– DC or isotype control (IT) were used. The results are representative for at least three independent experiments.

 
In previous studies, we observed an important role for IL-6 in tolerance of DC (20). Therefore, we investigated the role of IL-6 in tolerance induction by TLR4 and TLR2 stimulation. Naive DC were prepared from IL-6–/– mice (21) and stimulated as described above. Priming of DC from IL-6–/– mice with LPS at high concentration abolished responsiveness toward restimulation with LPS or P3C (Fig. 5A). Likewise, IL-6–/– DC primed with P3C at high concentration displayed unresponsiveness toward restimulation with P3C or LPS (Fig. 5B). To investigate whether LPShigh and P3Chigh tolerance of primed IL-6–/– DC is associated with maturation, expression of activation and maturation markers was analyzed by flow cytometry. The data depicted in Fig. 5C demonstrate that priming of naive IL-6–/– DC with LPS or P3C both led to enhanced expression of CD40 (Fig. 5C), as well as MHC class II, CD80, and CD86 expression (data not shown). These data indicate that in DC primed with LPS or P3C at high concentrations endogenous IL-6 is not required for LPShigh/P3Chigh homo- or cross-tolerance.


Figure 5
View larger version (26K):
[in this window]
[in a new window]

  		FIGURE 5. Homo- and cross-tolerance is partially IL-6 dependent. IL-6–/– DC were pretreated with different concentrations (1 ng/ml or 1000 ng/ml) LPS (A) or P3C (B) for 24 h, the medium was changed and cells were stimulated with 1000 ng/ml LPS or P3C for another 24 h. TNF-{alpha} levels in the supernatants were determined by ELISA. The results are representative for at least three independent experiments. Each experiment was performed in triplicates, values represent the mean ± SD of triplicates (*, p < 0.05). C, CD40 expression of LPS or P3C treated IL-6–/– DC. DC were stimulated with 1 ng/ml or 1000 ng/ml LPS or P3C for 24 h and analyzed by flow cytometry. Black lines represent the specific anti-CD40 staining, gray lines the isotype control. The results are representative for at least three independent experiments.

 
Degradation of I{kappa}B leads to subsequent activation and translocation of NF-{kappa}B (25). To analyze whether LPS or P3C tolerance in DC is associated with altered I{kappa}B degradation indicating NF-{kappa}B activation, DC were primed with LPS or P3C at high concentrations for 24 h and then restimulated for 15 min with LPS or P3C. DC were lysed and subjected to Western blot analyses for analysis of I{kappa}B expression. Stimulation of naive DC with LPS or P3C led to degradation of I{kappa}B after 15 min. After 24 h, I{kappa}B expression levels reached those in unstimulated cells (data not shown). In DC primed with LPS or P3C at high concentration, we observed a significantly reduced I{kappa}B degradation upon restimulation with LPS or P3C reflecting reduced NF-{kappa}B activation (Fig. 6). These data argue that LPShigh and P3Chigh cross- and homo-tolerance in DC is governed by mechanisms upstream of I{kappa}B.


Figure 6
View larger version (36K):
[in this window]
[in a new window]

  		FIGURE 6. I{kappa}B expression in DC upon stimulation with LPS or P3C. WT or IL-6–/– DC were pretreated with medium, LPS (A) or P3C (B) for 24 h. DC were stimulated for another 15 min with either 1000 ng/ml LPS, P3C, or medium. I{kappa}B-{alpha} expression was analyzed by Western blotting. Results shown are representative for at least three independent experiments.

 
Priming with LPS or P3C at low concentrations induces cross- and homo-tolerant DC dependent on IL-6 but independent of maturation

Because priming with LPS or P3C at high concentrations led to a DC tolerance phenotype associated with maturation, we next investigated whether maturation-independent tolerance mechanisms may exist in DC. For this purpose, DC were primed with LPS or P3C at low concentrations (1 ng/ml) as described above and restimulated with LPS or P3C (1000 ng/ml) 24 h later. Priming of DC with LPS or P3C at low concentrations induced cross- as well as homo-tolerant DC as implied from significantly reduced TNF-{alpha} secretion upon restimulation with LPS or P3C (Fig. 2, A and B). In contrast, the secretion of IL-6 upon restimulation with LPS or P3C was not altered in LPSlow- or P3Clow-tolerant DC (Fig. 2, C and D). However, the secretion of IL-10 was significantly impaired in DC primed with low concentrations of LPS or P3C (data not shown). These data demonstrate that LPSlow and P3Clow tolerance in DC is associated with reduced production of both TNF-{alpha} and IL-10. However, LPSlow and P3Clow tolerance only partially (~50–80%) attenuated TNF-{alpha} production as compared with total attenuation of TNF-{alpha} in LPShigh/P3Chigh tolerance.

Moreover, stimulation of naive DC with LPS or P3C at low concentrations did not induce significant DC maturation but induced a phenotype of semimature DC (20, 26) as indicated by only moderately increased expression of CD40, CD80, CD86, and lack of up-regulation of MHC class II (Fig. 3). Likewise, surface TLR2 and TLR4 expression was unaltered upon stimulation of naive wild-type DC (Fig. 4, A and B) or IL-6–/– DC (data not shown) with LPS or P3C at low concentrations. These data indicate that LPSlow/P3Clow tolerance in DC occurs independent of maturation processes and TLR2/TLR4 down-regulation.

Next, we addressed the role of IL-6 in homo- or cross-tolerance in DC primed with LPS or P3C at low concentrations. To this end, naive DC from IL-6–/– mice were primed with LPS or P3C and after 24 h restimulated with LPS or P3C as described above. Interestingly, treatment of IL-6–/– DC with P3C or LPS at low concentrations induced neither homo- nor cross-tolerance as indicated by an unaltered strong TNF-{alpha} response upon restimulation with LPS or P3C (Fig. 5, A and B). These data demonstrate that IL-6 is required for LPSlow/P3Clow homo- or cross-tolerance in DC.

To investigate whether this effect can be mimicked by priming of DC with IL-6, DC were incubated with rIL-6 for 24 h and then stimulated with LPS or P3C (1000 ng/ml) for another 24 h. We observed a significant reduction (~40–50%) of LPS (Fig. 7A) or P3C (Fig. 7B) induced TNF-{alpha} secretion from DC primed with IL-6 as compared with nonprimed DC. Priming of DC with rIL-10 did not change TNF-{alpha} secretion upon restimulation with LPS or P3C (data not shown). These data suggest that LPSlow/P3Clow tolerance of DC can be mimicked by IL-6 and suggest that this type of tolerance is mediated by an auto or paracrine IL-6 loop.


Figure 7
View larger version (15K):
[in this window]
[in a new window]

  		FIGURE 7. Treatment with rIL-6 mimics tolerance induction by LPS or P3C. WT DC were pretreated with 50 ng/ml recombinant murine IL-6 for 24 h and stimulated with 1000 ng/ml LPS (A) or P3C (B) for another 24 h. TNF-{alpha} levels in the supernatants were determined by ELISA. The results illustrated are representative for results of three independent experiments. Each experiment was performed in triplicates, values represent the mean ± SD of triplicates (*, p < 0.05).

 
To analyze whether priming of DC with LPS or P3C at low concentrations has a different impact on I{kappa}B degradation in wild-type and IL-6–/– DC, we performed Western blot analyzes as described above. Although I{kappa}B was not degraded in LPSlow primed DC restimulated with LPS (reflects LPSlow homo-tolerance), I{kappa}B was degradated in LPSlow primed IL-6–/– DC restimulated with LPS (no LPSlow homo-tolerance), suggesting that LPSlow homo-tolerance in DC is mediated by IL-6 and occurs upstream of I{kappa}B (Fig. 6A). Similar results were obtained in P3Clow homo-tolerance (Fig. 6B). Thus, we observed an inhibition of I{kappa}B degradation in homo-tolerogenic DC but not in cross-tolerogenic DC. Furthermore, inhibition of I{kappa}B degradation in homo-tolerogenic DC proved to be IL-6 dependent because it was not observed in IL-6–/– DC.


   Discussion
Top
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
Disclosures
 References
 
We examined the effect of priming DC with a bacterial cell wall component or a lipopeptide analog that are both recognized by distinct TLRs on their state of tolerance toward subsequent restimulation. We used P3C and LPS as agonists for TLR2 and TLR4, respectively (27, 28). Stimulation of naive DC with LPS or P3C resulted in a dose-dependent increase of TNF-{alpha} and IL-6 secretion and expression of activation surface markers such as CD40, CD80, CD86, and MHC class II (29, 30, 31, 32). As reported previously (33), stimulation via TLR4 was more efficient in inducing a cytokine response than activation via TLR2. In line with other studies, stimulation of DC with LPShigh led to a down-regulation of TLR4/MD2 expression (23, 34) indicating activation and maturation of DC, and a dose-dependent increase of TLR2 expression upon stimulation with LPS or P3C (11).

We demonstrated that stimulation of DC with P3C or LPS leads to induction of homo- as well as cross-tolerance as indicated by reduced TNF-{alpha} secretion in response to restimulation by any of the two TLR ligands. In dependency of the concentrations used for the priming of DC different phenomena were associated with induction of tolerance. The IL-6 independent homo- and cross-tolerance upon LPShigh or P3Chigh stimulation was associated with maturation of DC, and based upon inhibition of TLR signaling upstream of I{kappa}B (Fig. 8). In contrast, LPSlow and P3Clow primed homo- and cross-tolerance proved to be IL-6 dependent and was independent of maturation processes. LPSlow and P3Clow homo-tolerance rested upon inhibition of TLR signaling upstream of I{kappa}B, whereas LPSlow and P3Clow cross-tolerance was based on inhibition of TLR induced DC activation downstream of I{kappa}B (Fig. 8). Whereas inhibition of I{kappa}B degradation in combination with reduced TLR4 expression might be responsible for the LPShigh tolerance, we observed in homo- and cross-tolerant DC primed with P3C or LPS at high concentrations an inhibition of I{kappa}B degradation suggesting that irrespective of the TLR expression levels other such as reduced IRAK-1 (11) expression or up-regulation of IRAK-M (19) or suppressor of cytokine signaling (SOCS) 1 (35, 36) may contribute to the maturation dependent, IL-6 independent tolerance.


Figure 8
View larger version (14K):
[in this window]
[in a new window]

  		FIGURE 8. The chart illustrates the synopsis of the mechanism described within this study, that might contribute to tolerance induction in DC.

 
Treatment of macrophages with LPS/P3C induces homo-tolerance toward subsequent restimulation with LPS/P3C (8, 9, 10, 11, 37). It is discussed that repression of transcription and rapid degradation of proinflammatory cytokine mRNAs contribute to decreased proinflammatory cytokine production in LPS tolerant macrophages. Furthermore selective and specific disruption of certain TLR4 signaling components is likely to contribute to the altered LPS response in tolerant cells. It has been reported, that TLR4 levels decrease following LPS treatment in macrophages, suggesting that TLR4 down-regulation may disrupt TLR signaling (10, 37). Furthermore induction of RelB is thought to participate in endotoxin tolerance in macrophages by repressing proinflammatory gene expression (38). The P3C induced homo- tolerance in macrophages seems to be based on an ablation of IRAK 1 (11). Additionally treatment of macrophages with LPS induces cross-tolerance toward a subsequent TLR2 stimulus and closely correlates with down-regulation of IRAK1 protein levels and kinase activity (10). However other studies also report, that neither treatment with LPS nor P3C leads to induction of cross-tolerance in macrophages (8).

Previously, we reported on a major role of IL-6 in induction of tolerogenic DC upon stimulation with commensal bacteria (20). Stimulation of DC with E. coli induced TNF-{alpha}, IL-12 and IL-6 secretion and expression of activation-markers, whereas stimulation with B. vulgatus led only to secretion of IL-6 and DC were driven to a semimature state with low expression of activation-markers. Those semimature DC were nonresponsive to stimulation by E. coli in terms of maturation, TNF-{alpha} but not IL-6 production. The nonresponsiveness of B. vulgatus stimulated DC was abrogated by addition of anti-IL-6-mAb or mimicked with rIL-6 (20). In this study, we observed that treatment with P3C or LPS at low concentrations induced tolerogenic DC which depended on IL-6 but not on maturation or reduced expression of TLR. We assume consequently that by an autocrine as well as a paracrine loop IL-6 induces inhibition of TLR signaling because the effect was not observed in IL-6–/– DC. Vice versa, priming of DC with rIL-6 mimicked priming with LPS/P3C at low concentrations. Homo-tolerance was associated to inhibition of I{kappa}B degradation and IL-6 dependent, whereas cross-tolerance involved a different and currently unknown mechanism. IL-6 dependent cross-tolerance induced by LPSlow or P3Clow priming of DC did not inhibit degradation of I{kappa}B and suggested p50 homodimerization or induction of RelB as candidate-inhibitors of TNF-{alpha} secretion as reported in LPS tolerance in macrophages or human promonocyte cells respectively (11, 38). Moreover in keeping with our previous data obtained by stimulation of DC with B. vulgatus or E. coli and our present data, there is evidence that B. vulgatus, which is phylogenetically closely related to Porphyromonas gingivalis (8) primarily signals via TLR2 whereas E. coli signals via both, TLR2 and TLR4.

Recently it has been reported that DC primed with LPS or P3C and rested for 48 h showed an enhanced production of IL-10 and reduced IL-12p40 production upon TLR4 restimulation (34). In the primed DC highly activated ERK1/2 and TRAF3 inducing selective production of IL-10 appeared to compensate for reduced p38 MAPK phosphorylation, resulting in enhanced and reduced production of IL10 and IL-12p40, respectively (34). However, in our model LPSlow/P3Clow stimulation of naive DC did not induce significant IL-10 production arguing against an impact of IL-10 in LPSlow/P3Clow tolerance. Although naive DC stimulated with LPS at high concentrations produced high quantities of IL-10 which thus might contribute to the nonresponsiveness, priming of DC with rIL-10, however, did not result in a reduced responsiveness toward subsequent restimulation (data not shown).

Although BMDC closely resemble myeloid DC occurring in vivo, we cannot exclude that tolerance mechanisms in vivo may be different from what we observed for BMDC in vitro. Nevertheless, given that comparable mechanisms may operate in DC in vivo we would like to speculate that the mechanisms reported herein might contribute to the maintenance of intestinal homeostasis even though this hypothesis is highly speculative. In such a model scenario we propose that under physiologic conditions DC might be exposed to only a low stimulation of TLR. In fact, the physiologic gastrointestinal microbiota is separated from the intestinal DC by a thick mucus layer (39). This might lead to the induction of tolerogenic DC in dependency of IL-6, thereby, contributing to the perpetuation of intestinal homeostasis and tolerance of occasional stimulation via TLR2 or TLR4. In contrast, in a state of chronic disease the microbiota might overcome a reduced mucus layer (39), leading to activation and maturation of DC, which provide a proinflammatory cytokine response, trigger T cell proliferation and an inflammatory host reaction before shading off into a maturation dependent, IL-6 independent state of tolerance.

IL-6 is known to influence cell growth, differentiation and migration during immune response, hematopoiesis, and inflammation (40). IL-6 also affects the differentiation of myeloid lineages, including macrophages and DC (41, 42). In the presence of IL-6 the number of resting/immature DC in lymph nodes and spleen is increased, whereas the number of activated mature DC is decreased upon stimulation with LPS in vivo (43). IL-6 plays an important role in T cell differentiation (42) and promotes of Th2 polarized T cell differentiation (44). Second, IL-6 up-regulates the expression of suppressor of cytokine signaling (SOCS)1 in CD4+ cells which inhibits IFN-{gamma} signaling and thus Th1 differentiation (45). The presence of IL-6 may shift the Th1/Th2 balance toward Th2 (44). In keeping with these findings we hypothesize that in our model IL-6 triggered by low dose TLR priming induces semimature DC which inhibit the induction of proinflammatory Th1 responses. Therefore, it is tempting to speculate that IL-6, in the absence of TNF-{alpha} and IL-12(p70), can be considered as a modulatory rather than simply a proinflammatory cytokine. In contrast, IL-6 secreted from splenic DC upon TLR stimulation was an important factor of T cell activation by overcoming Tr mediated suppression of T cell proliferation (46). Production of IL-6 by DC in response to TLR ligation during stimulation appears to be critical for T cell activation, because it allows pathogen specific T cells to overcome the suppressive effect of CD4+CD25+ T cells (46). However, as splenic DCs include different subsets of DC we cannot exclude that our findings are limited to a system working with only myeloid DC. Furthermore, studies describe that in macrophages in absence of SOCS3 IL-6 induces an anti-inflammatory response, indicating that SOCS3 selectively blocks signaling by IL-6, thereby preventing its ability to inhibit LPS signaling (47). The important role of SOCS3 in tolerance is supported by another study reporting on the silencing of SOCS3 in DC by RNA interference. Silencing of SOCS3 led to induction of IDO and onset of tolerogenic properties in DC upon CD28-Ig treatment. The authors suggest that these effects appear to result from a combination of unopposed IFN-{gamma} signaling and the occurrence of IFN-{gamma} like actions by IL-6 (48). Together, the data provide evidence that IL-6 might play an ambiguous role in inflammatory diseases. Depending on the host status IL-6 may act as proinflammatory or anti-inflammatory cytokine promoting or inhibiting T cell priming and Th1 responses.

However, future studies will have to elucidate the mechanism contributing to IL-6 dependent DC tolerance and the relevance of IL-6 dependent tolerogenic DC for intestinal immune homeostasis and on disease in vivo.


   Disclosures
Top
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
 Disclosures
References
 
The authors have no financial conflict of interest.


   Footnotes
 
The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

1 This work was supported in part by grants from Deutsche Forschungsgemeinschaft and Interdisciplinary Center for Clinical Research (University of Tübingen, Tübingen, Germany). Back

2 Address correspondence and reprint requests to Dr. J.-S. Frick, Institute of Medical Microbiology and Hygiene, University of Tübingen, Elfriede-Aulhorn-Strasse 6, Tübingen, Germany. E-mail address: julia-stefanie.frick{at}med.uni-tuebingen.de Back

3 Abbreviations used in this paper: DC, dendritic cells; IRAK, IL-1 receptor-associated kinase; SOCS, suppressor of cytokine signaling. Back

Received for publication June 28, 2007. Accepted for publication August 23, 2007.


   References
Top
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
 Disclosures
 References
 

  1. Re, F., J. L. Strominger. 2001. Toll-like receptor 2 (TLR2) and TLR4 differentially activate human dendritic cells. J. Biol. Chem. 276: 37692-37699. [Abstract/Free Full Text]
  2. Re, F., J. L. Strominger. 2004. IL-10 released by concomitant TLR2 stimulation blocks the induction of a subset of Th1 cytokines that are specifically induced by TLR4 or TLR3 in human dendritic cells. J. Immunol. 173: 7548-7555. [Abstract/Free Full Text]
  3. Hirschfeld, M., J. J. Weis, V. Toshchakov, C. A. Salkowski, M. J. Cody, D. C. Ward, N. Qureshi, S. M. Michalek, S. N. Vogel. 2001. Signaling by toll-like receptor 2 and 4 agonists results in differential gene expression in murine macrophages. Infect. Immun. 69: 1477-1482. [Abstract/Free Full Text]
  4. Werts, C., R. I. Tapping, J. C. Mathison, T. H. Chuang, V. Kravchenko, I. Saint Girons, D. A. Haake, P. J. Godowski, F. Hayashi, A. Ozinsky, et al 2001. Leptospiral lipopolysaccharide activates cells through a TLR2-dependent mechanism. Nat. Immunol. 2: 346-352. [Medline]
  5. Wyllie, D. H., E. Kiss-Toth, A. Visintin, S. C. Smith, S. Boussouf, D. M. Segal, G. W. Duff, S. K. Dower. 2000. Evidence for an accessory protein function for toll-like receptor 1 in anti-bacterial responses. J. Immunol. 165: 7125-7132. [Abstract/Free Full Text]
  6. Medzhitov, R.. 2001. Toll-like receptors and innate immunity. Nat. Rev. Immunol. 1: 135-145. [Medline]
  7. Henricson, B. E., R. Neta, S. N. Vogel. 1991. An interleukin-1 receptor antagonist blocks lipopolysaccharide-induced colony-stimulating factor production and early endotoxin tolerance. Infect. Immun. 59: 1188-1191. [Abstract/Free Full Text]
  8. Dobrovolskaia, M. A., A. E. Medvedev, K. E. Thomas, N. Cuesta, V. Toshchakov, T. Ren, M. J. Cody, S. M. Michalek, N. R. Rice, S. N. Vogel. 2003. Induction of in vitro reprogramming by toll-like receptor (TLR)2 and TLR4 agonists in murine macrophages: effects of TLR "homotolerance" versus "heterotolerance" on NF-{kappa}B signaling pathway components. J. Immunol. 170: 508-519. [Abstract/Free Full Text]
  9. Sato, S., F. Nomura, T. Kawai, O. Takeuchi, P. F. Muhlradt, K. Takeda, S. Akira. 2000. Synergy and cross-tolerance between toll-like receptor (TLR) 2- and TLR4-mediated signaling pathways. J. Immunol. 165: 7096-7101. [Abstract/Free Full Text]
  10. Jacinto, R., T. Hartung, C. McCall, L. Li. 2002. Lipopolysaccharide- and lipoteichoic acid-induced tolerance and cross-tolerance: distinct alterations in IL-1 receptor-associated kinase. J. Immunol. 168: 6136-6141. [Abstract/Free Full Text]
  11. Siedlar, M., M. Frankenberger, E. Benkhart, T. Espevik, M. Quirling, K. Brand, M. Zembala, L. Ziegler-Heitbrock. 2004. Tolerance induced by the lipopeptide Pam3Cys is due to ablation of IL-1R-associated kinase-1. J. Immunol. 173: 2736-2745. [Abstract/Free Full Text]
  12. Goldring, C. E., S. Reveneau, D. Pinard, J. F. Jeannin. 1998. Hyporesponsiveness to lipopolysaccharide alters the composition of NF-{kappa}B binding to the regulatory regions of inducible nitric oxide synthase gene. Eur. J. Immunol. 28: 2960-2970. [Medline]
  13. Liu, H., P. Sidiropoulos, G. Song, L. J. Pagliari, M. J. Birrer, B. Stein, J. Anrather, R. M. Pope. 2000. TNF-{alpha} gene expression in macrophages: regulation by NF-{kappa}B is independent of c-Jun or C/EBP beta. J. Immunol. 164: 4277-4285. [Abstract/Free Full Text]
  14. Fujihara, M., S. Wakamoto, T. Ito, M. Muroi, T. Suzuki, H. Ikeda, K. Ikebuchi. 2000. Lipopolysaccharide-triggered desensitization of TNF-{alpha} mRNA expression involves lack of phosphorylation of I{kappa}B{alpha} in a murine macrophage-like cell line, P388D1. J. Leukocyte Biol. 68: 267-276. [Abstract/Free Full Text]
  15. Jin, L., D. P. Raymond, T. D. Crabtree, S. J. Pelletier, C. K. Rudy, T. L. Pruett, R. G. Sawyer. 2002. Preexposure of murine macrophages to CpG-containing oligonucleotides results in nuclear factor kappaB p50 homodimer-associated hyporesponsiveness. Surgery 132: 245-251. [Medline]
  16. Ziegler-Heitbrock, L.. 2001. The p50-homodimer mechanism in tolerance to LPS. J. Endotoxin Res. 7: 219-222. [Medline]
  17. Nakagawa, R., T. Naka, H. Tsutsui, M. Fujimoto, A. Kimura, T. Abe, E. Seki, S. Sato, O. Takeuchi, K. Takeda, et al 2002. SOCS-1 participates in negative regulation of LPS responses. Immunity 17: 677-687. [Medline]
  18. Kinjyo, I., T. Hanada, K. Inagaki-Ohara, H. Mori, D. Aki, M. Ohishi, H. Yoshida, M. Kubo, A. Yoshimura. 2002. SOCS1/JAB is a negative regulator of LPS-induced macrophage activation. Immunity 17: 583-591. [Medline]
  19. Akira, S., K. Takeda. 2004. Toll-like receptor signalling. Nat. Rev. Immunol. 4: 499-511. [Medline]
  20. Frick, J. S., N. Zahir, M. Muller, F. Kahl, O. Bechtold, M. B. Lutz, C. J. Kirschning, J. Reimann, B. Jilge, E. Bohn, I. B. Autenrieth. 2006. Colitogenic and non-colitogenic commensal bacteria differentially trigger DC maturation and Th cell polarization: an important role for IL-6. Eur. J. Immunol. 36: 1537-1547. [Medline]
  21. Kopf, M., H. Baumann, G. Freer, M. Freudenberg, M. Lamers, T. Kishimoto, R. Zinkernagel, H. Bluethmann, G. Kohler. 1994. Impaired immune and acute-phase responses in interleukin-6-deficient mice. Nature 368: 339-342. [Medline]
  22. Lutz, M. B., N. Kukutsch, A. L. Ogilvie, S. Rossner, F. Koch, N. Romani, G. Schuler. 1999. An advanced culture method for generating large quantities of highly pure dendritic cells from mouse bone marrow. J. Immunol. Methods 223: 77-92. [Medline]
  23. Nomura, F., S. Akashi, Y. Sakao, S. Sato, T. Kawai, M. Matsumoto, K. Nakanishi, M. Kimoto, K. Miyake, K. Takeda, S. Akira. 2000. Cutting edge: endotoxin tolerance in mouse peritoneal macrophages correlates with down-regulation of surface toll-like receptor 4 expression. J. Immunol. 164: 3476-3479. [Abstract/Free Full Text]
  24. Brint, E. K., D. Xu, H. Liu, A. Dunne, A. N. McKenzie, L. A. O’Neill, F. Y. Liew. 2004. ST2 is an inhibitor of interleukin 1 receptor and toll-like receptor 4 signaling and maintains endotoxin tolerance. Nat. Immunol. 5: 373-379. [Medline]
  25. Perkins, N. D.. 2007. Integrating cell-signalling pathways with NF-{kappa}B and IKK function. Nat. Rev. Mol. Cell Biol. 8: 49-62. [Medline]
  26. Hegde, S., J. Pahne, S. Smola-Hess. 2004. Novel immunosuppressive properties of interleukin-6 in dendritic cells: inhibition of NF-{kappa}B binding activity and CCR7 expression. FASEB J. 18: 1439-1441. [Abstract/Free Full Text]
  27. Takeuchi, O., S. Sato, T. Horiuchi, K. Hoshino, K. Takeda, Z. Dong, R. L. Modlin, S. Akira. 2002. Cutting edge: role of toll-like receptor 1 in mediating immune response to microbial lipoproteins. J. Immunol. 169: 10-14. [Abstract/Free Full Text]
  28. Poltorak, A., X. He, I. Smirnova, M. Y. Liu, C. Van Huffel, X. Du, D. Birdwell, E. Alejos, M. Silva, C. Galanos, et al 1998. Defective LPS signaling in C3H/HeJ and C57BL/10ScCr mice: mutations in Tlr4 gene. Science 282: 2085-2088. [Abstract/Free Full Text]
  29. Pulendran, B., K. Palucka, J. Banchereau. 2001. Sensing pathogens and tuning immune responses. Science 293: 253-256. [Abstract/Free Full Text]
  30. Taguchi, H., M. Takahashi, H. Yamaguchi, T. Osaki, A. Komatsu, Y. Fujioka, S. Kamiya. 2002. Experimental infection of germ-free mice with hyper-toxigenic enterohaemorrhagic Escherichia coli O157: H7, strain 6. J. Med. Microbiol. 51: 336-343. [Abstract/Free Full Text]
  31. Banchereau, J., R. M. Steinman. 1998. Dendritic cells and the control of immunity. Nature 392: 245-252. [Medline]
  32. Lanzavecchia, A., F. Sallusto. 2001. The instructive role of dendritic cells on T cell responses: lineages, plasticity and kinetics. Curr. Opin. Immunol. 13: 291-298. [Medline]
  33. Schmitz, F., J. Mages, A. Heit, R. Lang, H. Wagner. 2004. Transcriptional activation induced in macrophages by toll-like receptor (TLR) ligands: from expression profiling to a model of TLR signaling. Eur. J. Immunol. 34: 2863-2873. [Medline]
  34. Yanagawa, Y., K. Onoe. 2007. Enhanced IL-10 production by TLR4- and TLR2-primed dendritic cells upon TLR restimulation. J. Immunol. 178: 6173-6180. [Abstract/Free Full Text]
  35. Mahan, M. J., D. M. Heithoff, R. L. Sinsheimer, D. A. Low. 2000. Assessment of bacterial pathogenesis by analysis of gene expression in the host. Annu. Rev. Genet. 34: 139-164. [Medline]
  36. Rothwarf, D. M., M. Karin. 1999. The NF-{kappa}B activation pathway: a paradigm in information transfer from membrane to nucleus. Sci. STKE 1999: RE1[Medline]
  37. Lehner, M. D., S. Morath, K. S. Michelsen, R. R. Schumann, T. Hartung. 2001. Induction of cross-tolerance by lipopolysaccharide and highly purified lipoteichoic acid via different toll-like receptors independent of paracrine mediators. J. Immunol. 166: 5161-5167. [Abstract/Free Full Text]
  38. Yoza, B. K., J. Y. Hu, S. L. Cousart, L. M. Forrest, C. E. McCall. 2006. Induction of RelB participates in endotoxin tolerance. J. Immunol. 177: 4080-4085. [Abstract/Free Full Text]
  39. Swidsinski, A., J. Weber, V. Loening-Baucke, L. P. Hale, H. Lochs. 2005. Spatial organization and composition of the mucosal flora in patients with inflammatory bowel disease. J. Clin. Microbiol. 43: 3380-3389. [Abstract/Free Full Text]
  40. Hirano, T.. 1998. Interleukin 6 and its receptor: ten years later. Int. Rev. Immunol. 16: 249-284. [Medline]
  41. Chomarat, P., J. Banchereau, J. Davoust, A. K. Palucka. 2000. IL-6 switches the differentiation of monocytes from dendritic cells to macrophages. Nat. Immunol. 1: 510-514. [Medline]
  42. Murphy, K. M., W. Ouyang, J. D. Farrar, J. Yang, S. Ranganath, H. Asnagli, M. Afkarian, T. L. Murphy. 2000. Signaling and transcription in T helper development. Annu. Rev. Immunol. 18: 451-494. [Medline]
  43. Park, S. J., T. Nakagawa, H. Kitamura, T. Atsumi, H. Kamon, S. Sawa, D. Kamimura, N. Ueda, Y. Iwakura, K. Ishihara, et al 2004. IL-6 regulates in vivo dendritic cell differentiation through STAT3 activation. J. Immunol. 173: 3844-3854. [Abstract/Free Full Text]
  44. Diehl, S., M. Rincon. 2002. The two faces of IL-6 on Th1/Th2 differentiation. Mol. Immunol. 39: 531-536. [Medline]
  45. Diehl, S., J. Anguita, A. Hoffmeyer, T. Zapton, J. N. Ihle, E. Fikrig, M. Rincon. 2000. Inhibition of Th1 differentiation by IL-6 is mediated by SOCS1. Immunity 13: 805-815. [Medline]
  46. Pasare, C., R. Medzhitov. 2003. Toll pathway-dependent blockade of CD4+CD25+ T cell-mediated suppression by dendritic cells. Science 299: 1033-1036. [Abstract/Free Full Text]
  47. Yasukawa, H., M. Ohishi, H. Mori, M. Murakami, T. Chinen, D. Aki, T. Hanada, K. Takeda, S. Akira, M. Hoshijima, et al 2003. IL-6 induces an anti-inflammatory response in the absence of SOCS3 in macrophages. Nat. Immunol. 4: 551-556. [Medline]
  48. Orabona, C., M. L. Belladonna, C. Vacca, R. Bianchi, F. Fallarino, C. Volpi, S. Gizzi, M. C. Fioretti, U. Grohmann, P. Puccetti. 2005. Cutting edge: silencing suppressor of cytokine signaling 3 expression in dendritic cells turns CD28-Ig from immune adjuvant to suppressant. J. Immunol. 174: 6582-6586. [Abstract/Free Full Text]



This article has been cited by other articles:


Home page
 J. Biol. Chem.Home page
J. A. Fulcher, M. H. Chang, S. Wang, T. Almazan, S. T. Hashimi, A. U. Eriksson, X. Wen, M. Pang, L. G. Baum, R. R. Singh, et al.
Galectin-1 Co-clusters CD43/CD45 on Dendritic Cells and Induces Cell Activation and Migration through Syk and Protein Kinase C Signaling
J. Biol. Chem., September 25, 2009; 284(39): 26860 - 26870.
[Abstract] [Full Text] [PDF]

Home page
 Innate ImmunityHome page
B. W. Kramer, S. G. Kallapur, T. J. Moss, I. Nitsos, J. P. Newnham, and A. H. Jobe
Intra-amniotic LPS modulation of TLR signaling in lung and blood monocytes of fetal sheep
Innate Immunity, April 1, 2009; 15(2): 101 - 107.
[Abstract] [PDF]

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Geisel, J.
Right arrow Articles by Frick, J.-S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Geisel, J.
Right arrow Articles by Frick, J.-S.

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS