PMCCPMCCPMCC

Search tips
Search criteria 

Advanced

 
Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
 
J Immunol. Author manuscript; available in PMC 2017 May 1.
Published in final edited form as:
PMCID: PMC4868647
NIHMSID: NIHMS766374

TLR10 is a Negative Regulator of Both MyD88-Dependent and Independent TLR Signaling

Abstract

Toll-like receptors are central components of the innate immune system which, upon recognition of bacterial, fungal or viral components, activate intracellular signals that lead to protective inflammatory responses. Among the ten-member human TLR family, TLR10 is the only remaining orphan receptor without a known ligand or signaling function. Murine TLR10 is a disrupted pseudogene, which precludes investigation using classic gene knock-out approaches. We report here that TLR10 suppressed the production of an array of cytokines in stably transfected human myelomonocytic U937 cells in response to other TLR agonists. This broad TLR suppressive activity affects both MyD88 and TRIF-mediated signaling pathways upstream of IκB and MAPK activation. Compared to non-transgenic littermate controls, monocytes of TLR10 transgenic mice exhibited blunted IL-6 production following ex vivo blood stimulation with other TLR agonists. After intraperitoneal injection of LPS, lower levels of TNFα, IL-6 and Type 1 IFN was measured in the serum of TLR10 transgenic mice, compared to non-transgenic mice, but did not affect mouse survival in an LPS-induced septic shock model. Finally, treatment of human mononuclear cells with a monoclonal anti-TLR10 antibody suppressed pro-inflammatory cytokines released by LPS stimulation. These results demonstrate that TLR10 functions as a broad negative regulator of TLR signaling and suggests TLR10 may have a role in controlling immune responses in vivo.

INTRODUCTION

Toll-like receptors are type 1 transmembrane receptors that are part of a broad class of innate immune receptors known as pattern-recognition receptors. TLRs serve as the first line of defense against infectious pathogens by initiating protective inflammatory responses following the direct sensing of bacterial, fungal or viral components. Recognition of a cognate microbial ligand by the extracellular leucine-rich repeat domain of each TLR leads to receptor dimerization (1). This event dimerizes two C-terminal TIR-domains which provide a scaffold for the recruitment of other cytosolic TIR-domain containing adaptor molecules that propagate intracellular signaling (2, 3).

Humans possess 10 TLR family members, numbered 1 through 10, subsets of which are expressed in leukocytes and various tissue cells (4, 5). TLRs 1, 2, 4, 5 and 6 traffic to the plasma membrane, sense microbial and fungal cell wall components and stimulate the production of classic proinflammatory molecules. TLRs 3, 7, 8 and 9 are located in endosomal compartments, sense viral and bacterial nucleic acids and are best known for their ability to stimulate the production of Type 1 IFNs (3). Almost all TLRs utilize the TIR-domain containing adaptor MyD88 which upon recruitment to dimerized TLRs at the plasma membrane induce the activation of NF-κB and other transcription factors that promote expression of classic pro-inflammatory cytokines (6). TRIF is utilized by both TLR3 and endosomal TLR4 and, in a MyD88-independent manner, drives the expression of Type 1 IFN production through activation of the transcription factor interferon response factor 3 (IRF3) (3).

To date, we have a fairly clear understanding of the ligand recognition, signaling and biological functions of human TLRs 1 through 9. In contrast, TLR10 is the only remaining orphan human TLR without a confirmed ligand, signaling pathway or biological function. The TLR10 gene was first cloned in 2001 and various studies has revealed strong transcriptional expression in the lymphoid tissues including the spleen, lymph node, thymus and tonsils. TLR10 is expressed among a number of leukocyte subtypes and perhaps most prominently by B cells (4, 5). A major obstacle toward defining a function for TLR10 is that several retroviral insertion elements have rendered TLR10 a pseudogene in mice thus precluding a classic knockout mouse model (7). Although TLR10 is disrupted in mice, every other mammal sequenced to date contains an undisrupted TLR10 gene including numerous primate species, domestic animals and a variety of rodents (8, 9).

TLR10 is most homologous to TLR1 and TLR6 which both cooperate with TLR2 to mediate inflammatory responses to a variety of microbial lipids including bacterial lipoproteins (8, 9). Previously, we have shown that TLR10 is capable of binding the TLR2/1 ligand PAM3CSK4 in cooperation with TLR2. The resulting dimer is able to recruit MyD88 although no TLR-associated events including the transcriptional activation of NF-κB, IL-8 and IFN-β promoters has been detected (10). Sequence analysis has revealed that the TIR domain of TLR10 is less conserved and has a calculated rate of evolutionary change that is higher than that of any other TLR (8). This suggests that TLR10 may have a unique function among the TLR family.

To assess the function of human TLR10 we have generated stably transfected monocytic cells lines, a transgenic mouse model as well as biologically active monoclonal antibodies to the TLR10 receptor. Collectively, our findings support the idea that TLR10 is an anti-inflammatory receptor. Importantly, we also show that the TLR10-mediated suppression broadly effects both MyD88 and TRIF-dependent signaling pathways making TLR10 a potential global suppressor of TLR signaling.

Materials and methods

Reagents

Antibodies specific for phospho p38 (clone D3F9), phospho-JNK (clone 81E11), phospho-ERK (clone D13.14.4E), IκBα (clone 44D4) and β-actin (clone 13E5) were from Cell Signaling Technologies (Beverly, MA). Anti-FLAG antibody (clone M2) are from Sigma-Aldrich (St. Louis, MO). FITC conjugated CD11b (clone 3A33) were from Abcam (Cambridge, MA). Directly conjugated antibodies to Ly6G (clone 1A8) and IL-6 (clone MP5-20F3) were from BioLegend (San Diego, CA). The synthetic triacylated lipopeptide Pam3CSK4 was purchased from Alexis Biochemicals (San Diego, CA), LPS from E. coli strain K235 and pI:C were from Sigma-Aldrich. Monoclonal antibodies against the extracellular domain of recombinant human TLR10 were produced in-house. One clone, 3C10C5, is commercially available. The antibody clone used in this study is 5C2C5. The isotype control used was MOPC-21, a murine IgG1 with no known specificity.

Plasmid Constructs

Expression constructs for TLR10, TLR1, TLR1-10, TLR10-1, CD4-TLR10, CD4-TLR1, MyD88, TRIF, IL-8 promoter driven luciferase, IFN-β promoter driven luciferase, and Renilla-luciferase transfection control are previously described (Guan et al., 2010). The pMX-IRES-Puro expression vector, used for the production of retrovirus, was purchased from Cell Biolabs (San Diego, CA). This vector was then modified to include a preprotrypsin leader sequence and a FLAG linker region into which the coding region of TLR10 was sub-cloned to generate pMX-FLAG-TLR10. The CMV-FLAG-TLR10 plasmid, used in the generation of TLR10 transgenic mice, was constructed by inserting the TLR10 coding sequence lacking the endogenous signal peptide into pFLAG-CMV vector (Sigma-Aldrich).

Development of Stable Cell Lines

The NIH3T3 amphoteric packaging line was plated in 10cm dishes and transfected with either pMX-FLAG-TLR10 or the empty pMX-FLAG vector using FuGene 6 according to manufacturer’s instructions (Roche, Indianapolis, IN). Forty-eight hours after transfection, viral supernatants were cleared of cell debris and applied to parental U937 cells during log phase growth. Twenty-four hours after viral transduction, virus was removed and stably transduced cells were selected in media containing 2 μg/ml Puromycin (Sigma-Aldrich). Batch derived cells were expanded and surface expression of the FLAG epitope was verified.

Cell Culture and TLR Stimulation

Human cell lines were cultured in RPMI medium supplemented with 10% FBS, 2mM L-Glutamine, 100 IU/ml Penicillin, and 100 μg/ml Streptomycin. Stably transduced U937 cells were kept under selection in the presence of 2 μg/ml Puromycin (Sigma-Aldrich). To investigate cytokine production, cells were plated at 5×104 cells per well in 96-well plates and differentiated with PMA at 100 ng/ml for 48 hours. Cells were then washed and allowed to rest in fresh media for 24 hours. Media was replaced before cells were stimulated with either 50ng/ml PAM3CSK4, 50 μg/ml pI:C, or 50 ng/ml LPS. Cells were stimulated overnight with the indicated agonist and cell-free supernatants were collected for cytokine analysis.

Transient Transfection Assays

HEK293T cells were transfected in 12-well plates using FuGene 6 with vectors encoding either MyD88 or TRIF constructs (20 ng/ml), TLR vectors (100 ng/ml), either IL-8 or IFN-β luciferase reporter (150 ng/ml) and Renilla luciferase as a transfection control (50 ng/ml). Luciferase readings were obtained using the Dual-Luciferase Assay Kit (Promega, Madison, WI) according to the manufacturer’s instructions.

Real-time PCR Analysis

U937 cell lines were plated at 2×106 cells/mL and differentiated for 48 hours in 100 ng/ml PMA. Media was changed and cells were allowed to rest for 24 hours before stimulation with 100 ng/ml PAM3CSK4 for 4 hours. After stimulation, cells were harvested and RNA was isolated using the RNeasy kit (Qiagen, Hilden, Germany). RNA quality was assessed by spectrophotometry and agarose gel electrophoresis. Specific mRNA transcripts were quantified using the SABiosciences TLR pathway qPCR Array (Qiagen), according to manufacturer’s instructions. The array includes analysis of 84 genes involved in TLR signaling plus five housekeeping genes for normalization as well as controls for genomic DNA contamination, RNA quality, and general PCR performance.

Analysis of MAPK Signaling and NFκB Activation

Vector control and TLR10-expressing U937 cells were stimulated with either 50 ng/ml PAM3CSK4, 50 μg/ml pI:C or 50 ng/ml LPS for the indicated time periods. Cell lysates were prepared from 1×107 cells in RIPA lysis buffer (150mM NaCl, 50mM Tris-HCl PH8.0, 1% NP-40, 1mM EDTA) supplemented with the Halt protease and phosphatase inhibitor cocktail (Thermo Scientific, Rockford, IL). Equal amounts of protein lysate were loaded on SDS-PAGE gels, transferred to PVDF membranes and blotted using specific antibodies (Cell Signaling Technologies, Beverly, MA).

Development of TLR10 Transgenic Mice

CMV-FLAG-TLR10 plasmid (Guan et al., 2010) was digested with Spe1 and Stu1 and 2μg of the purified linearized CMV-FLAG-TLR10 double stranded DNA was injected into C57BL/6 (Harlan Laboratories) fertilized oocytes. Early embryos were then transferred into Swiss Webster pseudo pregnant fosters to generate transgenic founders. Pups were weaned and genotyped using a primer set specific to the 5′ end of the transgene: Forward 5′-ACA AAG ACG ATG ACG ACA AGC-3′ and Reverse 5′-AAT AGA ACC GAT GTC TTA GC-3′. A second primer set was specific to the 3′ end of the transgene: Forward 5′-ACT TTG TCC AGA ATG AGT GG-3′ and Reverse 5′-TAT TAG GAC AAG GCT GGT GG-3′. All transgenic mice were generated by the Transgenic Mouse Core Facility at University of Illinois Urbana-Champaign under an approved IACUC protocol.

Southern Blot Analysis

Mouse tail genomic DNA was isolated through proteinase K treatment and phenol:chloroform:isoamylalcohol (25:24:1) purification. A total of 5 μg of genomic DNA was digested with Sac1 and separated on a 1% agarose gel. DNA was blotted onto Immobilon-Ny+ membrane (Millipore Inc.), washed with 6 x SSC buffer and then cross-linked using a UV Stratalinker (Agilent technologies). Hybridization was carried out at 65°C with a biotin-labeled 3′-transgene fragment containing the hGH polyA sequence of the CMV-FLAG-TLR10 vector as described by the manufacturer (South2North, Thermo Scientific). Transgene copy number was estimated from copy number standards containing varying amounts of unlabeled probe DNA.

Tissue RNA Extraction and RT-PCR

Approximately 100 mg of mouse tissue was homogenized in 1 ml Trizol (Ambion Inc.) reagent using a Dounce homogenizer (Wilmad lab glass). RNA was then purified with PureLinkTM RNA purification kit (Ambion Inc.) and used to generate 1st strand cDNA with SuperScript III reverse transcriptase (Invitrogen Inc.). PCR was carried out using the forward primer 5′-ACA AAG ACG ATG ACG ACA AGC-3′ and the reverse primer 5′-AAT AGA ACC GAT GTC TTA GC-3′.

Western Blotting of TLR10

Mouse tissue was ground with a Dounce homogenizer in 1 ml RIPA lysis buffer containing protease and phosphatase inhibitors. Cell homogenate was then incubated on ice for 2 hours followed by centrifugation at top speed for 15 minutes at 4°C. Total protein was separated on a 7% SDS-PAGE gel, blotted onto PVDF membrane (GE Healthcare) and probed with HRP conjugated anti-FLAG antibody (clone M2).

Mouse Whole Blood Stimulation and Intracellular IL-6 Staining

Mouse whole blood was collected from the lateral tail vein of age and gender matched non-transgenic and transgenic mice. 50 μL of whole blood was mixed with an equal volume of RPMI medium containing either 500 ng/ml PAM3CSK4, 100 μg/ml pI:C or 200 ng/ml LPS and incubated at 37°C with gentle agitation overnight. Centrifuged supernatants were assessed for cytokines by standard ELISA. For intracellular IL-6 staining, 100 μl mouse whole blood was stimulated with 500 ng/ml LPS in the presence of Brefeldin A for 6 hours. Red blood cells were lysed with ACK buffer and peripheral blood leukocytes were stained with anti-mouse CD11b and Ly6G antibodies. Permeabilized cells were stained with directly conjugated anti-mouse IL-6 antibody or isotype control antibody.

Intraperitoneal injection and shock assay

Age and gender matched non-transgenic and transgenic mice (8–10 week old) were injected intraperitoneally with a high dose of LPS, 0111:B4 (20–25mg/kg). Tail blood was collected at 1 and 4 hours post injection and serum was prepared and assayed for cytokines as above. In the shock assay, injected mice were monitored for survival for up to 7 days.

Cytokine assays

Human IL-6 and IL-8 as well as mouse IL-6 and TNFα were analyzed by paired-antibody ELISA according to manufacturer’s instructions (Invitrogen, Grand Island, NY). Type 1 IFN was detected using an ISRE-L929 reporter cell line bioassay (a kind gift from Dr. Bruce Beutler, UT Southwestern). Briefly, ISRE-L929 cells were plated at 2×104 cells per well in a 96-well format. Cell culture media was replaced 24 hours later with cell-free supernatant from either stimulated U937 cells or mouse serum. ISRE-L929 cells were incubated for another 6 hours and luciferase activity was detected in cell lysates using a luciferase reporter assay system (Promega).

Human Mononuclear Cell Stimulation

Primary human mononuclear cells were obtained from venous blood of consenting healthy adult volunteers under an approved IRB protocol. Blood was mixed 1:1 in Leukocyte Isolation Buffer (1X PBS, 2 mM EDTA, 2% FBS) before centrifuging over a Ficoll gradient (1.077g/L) at 1100xg for 15 min with no brake. The resulting buffy coat was washed twice in cell culture media before plating 100 μL of ~2–5×104 cells in a 96 well plate. Cells were allowed to pre-incubate in the presence of either an isotype control (clone MOPC-21) or anti-TLR10 antibody (clone 5C2C5) before stimulation with LPS (10ng/mL). After 24h, cell-free supernatants were collected and assayed by ELISA.

Statistical analysis

All data were analyzed with two-tailed Student’s t test unless otherwise indicated.

RESULTS

TLR10 is a Suppressor of TLR2/1-Induced Responses

To examine the biologic function of TLR10, we stably expressed the receptor in U937 cells, a human myelomonocytic line which we found lacks detectable endogenous TLR10 expression (Fig. 1A). Using MMLV retrovirus, a N-terminally tagged FLAG-TLR10 construct was stably transduced into U937 cells and TLR10 expression was confirmed by both RT-PCR and flow cytometry using an anti-FLAG antibody (Fig. 1, A and B). The stably transduced cell line exhibited no differences in cell growth or viability compared to either the parental or empty vector (MMLV) control lines (unpublished observation). To explore potential signaling outputs of TLR10, we compared the CMV and TLR10 cell lines for the expression of 84 genes known to be targets of TLR signaling following stimulation with the TLR2/1 lipopeptide agonist PAM3CSK4. Compared to CMV-U937 cells, the RNA message for 11 genes had lower PAM3CSK4 induction levels in TLR10-U937 cells. These genes included those encoding the pro-inflammatory cytokines TNFα, IL-1α, IL-6 and IFN-β. These genes also included the anti-inflammatory cytokine IL-10 which was also suppressed in TLR10-U937 cells compared to control CMV-U937 cells (Supplemental Table I). Supernatants from cells stimulated with varying concentrations of PAM3CSK4 confirmed that TLR10-U937 cells secreted significantly lower levels of both IL-6 and TNFα (data not shown). These data suggest that TLR10 mediates an anti-inflammatory function in U937 cells stimulated with TLR2/1 lipopeptide agonist.

Fig. 1
Stable TLR10 expression in U937 cells suppresses TLR-induced cytokine production

TLR10 Inhibits TLR-Induced Inflammatory Responses

To examine the specificity of TLR10 suppression, we stimulated the U937 cell lines with TLR agonists in addition to those for TLR2/1 (PAM3CSK4), including TLR2/6 (MALP-2), TLR3 (pI:C) and TLR4 (LPS). Compared to CMV-U937 cells, TLR10-U937 cells secreted significantly less IL-6 in response to all the TLR agonists tested (Fig. 1C). The secretion of Type 1 IFNs following stimulation with the TLR3 agonist pI:C (Fig. 1D) was also marked decreased in TLR10-U937 cells. The cell lines had indiscernible differences in IL-6 production in response to IFN-β as well as indiscernible differences in Type 1 IFN production in response to TNFα. Taken together these results support the idea that TLR10 broadly inhibits production of both IL-6 and IFN-β induced by a variety of TLRs but not the production of these cytokines induced through other signaling pathways.

TLR10 Suppresses IκBα Degradation and the Phosphorylation of MAPKs

To gain insight into the mechanism of TLR10-mediated suppression we analyzed the effect of TLR10 on various canonical TLR signaling pathways including the activation of NF-κB and various MAP kinases. As shown in Fig. 2, PAM3CSK4, pI:C and LPS each triggered IκBα degradation within 30 minutes of TLR stimulation in vector control cells. However, degradation of IκBα was consistently inhibited in TLR10-expressing cells, suggesting that TLR10 suppresses NF- κB signaling upstream of IκBα degradation. TLR10-U937 cells also exhibited reduced ERK, JNK, and p38 phosphorylation levels compared to vector control cells following stimulation with TLR agonists PAM3CSK4, pI:C or LPS. Taken together, these results indicate that TLR10 acts as a broad suppressor of TLR-induced pro-inflammatory signaling including NF-κB and MAP kinase signaling pathways.

Fig. 2
TLR10 suppresses phosphorylation of MAPKs and degradation of IκB

TLR10 Suppresses MyD88 and TRIF Signaling

The ability of TLR10 to broadly suppress responses from a variety of TLRs suggests that this receptor inhibits MyD88-dependent signaling. To assess this we examined the effect of TLR10 on HEK293T cells expressing MyD88. As expected, the overexpression of MyD88 in HEK293T cells resulted in strong constitutive induction of an IL-8 promoter-driven luciferase reporter (Fig. 3A). Consistent with its suppressive role, co-expression of TLR10 resulted in an 8-fold reduction of MyD88-induced IL-8 luciferase activity. In contrast, co-expression of TLR1, the closest homologue of TLR10, had no measureable effect.

Fig. 3
TLR10 suppresses both MyD88 and TRIF signaling

The inhibitory effect on TLR3-induced IFN-β production strongly suggests that TLR10 also suppresses MyD88-independent signaling mediated by the TLR adaptor TRIF. To assess this we examined the effect of TLR10 on HEK293T cells expressing TRIF which induces constitutive activation of IRF3 thereby driving Type 1 IFN production. The overexpression of TLR10 resulted in a marked reduction of Type 1 IFN production, as measured by a bioassay, while co-expression of TLR1 had no measureable effect (Fig. 3B). Importantly, TLR10 suppression of both MyD88 and TRIF-mediated pathways is dose-dependent (Supplemental Fig. 1). The data together suggest that TLR10 acts as a negative regulator of pro-inflammatory TLR signaling, targeting both MyD88 and TRIF-dependent TLR signaling.

To assess the roles of the extracellular LRR domain and the intracellular TIR domain of TLR10 in suppression we generated chimeric receptors between TLR1 and TLR10. Interestingly, neither the construct containing the extracellular domain of TLR1 and the intracellular domain of TLR10 (TLR1-10) or the reverse chimeric receptor (TLR10-1) were able to suppress MyD88-dependent or TRIF-dependent activation demonstrating that both domains of TLR10 are required for its suppressive function (Fig. 3, A and B). To assess the role of receptor dimerization, we replaced the extracellular domain of TLR10 with that of CD4; an approach that has been shown to cause constitutive TIR domain-mediated signaling since CD4 naturally forms dimers. Similar to full length TLR10, CD4-TLR10 inhibited both MyD88 and TRIF-dependent signaling. In contrast, CD4-TLR1 had no effect on either MyD88 or TRIF signaling (Fig. 3, C and D). Cellular expression of all the chimeric receptors was confirmed by flow cytometry (Supplemental Fig. 2). Taken together, these data suggest that TLR10 functions as a homodimer to suppress both MyD88 and TRIF-dependent TLR signaling.

Development of TLR10 transgenic mice

To explore the potential function of TLR10 in vivo, we developed a transgenic mouse in which an N-terminally FLAG-tagged human TLR10 is constitutively expressed behind a strong viral promoter. Thirty-two pups were derived from oocyte injection of the vector and then screened for the transgene with 14 PCR positive founders further analyzed by southern blot (Fig. 4A). A founder with an intermediate copy number of the transgene and broad tissue expression was selected from among the 14 candidates for further analysis (Fig. 4B). TLR10 expression levels were highest in the spleen with confirmed expression in blood leukocytes (Fig. 4C).

Fig. 4
Generation of a TLR10 transgenic mouse under a constitutive CMV promoter

Founder mice showed no overt developmental abnormalities and reproduced at expected mendelian ratios. However, two founders which exhibited the highest level of TLR10 expression across a variety of tissues developed lethal urethral tract infections in the first two months of life. Necroscopy revealed a high concentration of Gram-positive bacteria including Staphylococcus aureus as well as species of Enterococcus in the urine (unpublished observation). These observations suggest that high levels of TLR10 expression in mice may suppress the immune system allowing for the opportunistic overgrowth of commensal bacteria.

TLR10 Transgenic Mice Exhibit Reduced TLR-Induced Responses

To determine the effect of TLR10 expression on murine blood leukocytes we examined IL-6 production following ex vivo stimulation of whole blood with different TLR agonists. Production of IL-6 in whole blood of TLR10 transgenic mice was significantly lower than that of non-transgenic control mice in response to PAM3CSK4, pI:C and LPS (Fig. 5A). The reduced cytokine production is not due to any significant differences in the numbers of peripheral blood monocytes or neutrophils (Supplemental Fig. 3). To identify the cell type(s) that are targeted by TLR10-mediated suppression, we stimulated mouse peripheral blood ex vivo with LPS and measured intracellular IL-6 by flow cytometry. Monocytes (CD11b+, Ly6G), but not neutrophils (CD11b+, Ly6G+), were shown to have suppressed IL-6 production in response to LPS stimulation compared to equivalent cells from non-transgenic control mice (Fig. 5, B and C). These data confirm our previous findings in human myelomonocytic cell lines and suggest that even in a murine background human TLR10 maintains its function as an inhibitor of pro-inflammatory cytokine production.

Fig. 5
Blood monocytes of TLR10 transgenic mice exhibit suppressed cytokine production in response to TLR agonists

TLR10 Suppresses in vivo Response to LPS

To assess the role of TLR10 in vivo, we measured blood cytokine levels in mice following intraperitoneal injection with a sub-lethal dose of LPS. The induction of IL-6, TNFα and Type 1 IFNs were all reduced in the TLR10 transgenic mice compared to the non-transgenic littermate control mice (Fig. 6A). To determine if TLR10 can protect mice from LPS-induced septic shock, we monitored survival following intraperitoneal injection of mice with a high, almost uniformly fatal, dose of LPS. However, no significant difference in either mortality or time-to-death was observed between TLR10 transgenic and non-transgenic mice (Fig. 6B). These data show that TLR10 is able to suppress a broad array of TLR responses in both MyD88 and TRIF-dependent manners but is not capable of protecting mice from LPS-induced septic shock in vivo.

Fig. 6
TLR10 transgenic mice exhibit suppressed responses to injected LPS but are not protected in a model of septic shock

Endogenous TLR10 Suppresses Human Mononuclear Cell Activation

To assess the effect of TLR10 engagement on pro-inflammatory responses, we incubated human mononuclear cells isolated from the peripheral blood of healthy donors with either an anti-TLR10 antibody or a non-specific isotype matched control antibody. These cells were then stimulated overnight with the TLR4 agonist LPS. Compared to an isotype control antibody, the anti-TLR10 antibody suppressed the secretion of both IL-6 and TNFα from the mononuclear cells of two independent donors (Fig. 7). This data shows that antibody engagement of endogenous human TLR10 in primary human cells suppresses inflammatory responses mediated by MyD88.

Fig. 7
Anti-TLR10 antibody inhibits TLR-induced activation of peripheral blood mononuclear cells

DISCUSSION

Previously we have shown that the TLR10, either alone or with TLR2, fails to activate pro-inflammatory responses typically associated with this family of receptors (10). In this paper, results stemming from a variety of experimental approaches support the idea that TLR10 functions as a broad suppressor of other TLRs with inhibitory activity toward both MyD88 and TRIF-dependent signaling. We believe that, as a suppressor, TLR10 functions as a homodimer as evidenced by the fact that replacement of the extracellular domain of TLR10 with CD4, but not the extracellular domain of TLR1, results in a receptor that retains full suppressive function. Consistent with this notion is the observation that the crystal structure of the TLR10 TIR domain was solved as a symmetric homodimer (11). Additionally, using gel filtration chromatography, we have found that the TLR10 extracellular domain purifies as a homodimer (data not shown). Together, these observations suggest that the extracellular and TIR domains of TLR10 contribute to homodimerization and that this event can be driven by either overexpression, in cell lines or mice, or through engagement of the endogenous receptor with a divalent monoclonal antibody.

Among members of the TLR family, TLR10 is most homologous to TLRs 1 and 6 with highest homology observed within the signaling TIR domain (9). In the crystal structure of the TLR10 TIR domain a portion of the BB loop forms part of the dimer interface but much of the loop is exposed and available to interact with TIR domain adaptor molecules such as MyD88 and TRIF (11). In this context, there are notable differences in key residues of the BB loop that mediate intracellular signaling which include a two amino acid insertion just before the BB loop as well as amino acid changes within residues of the BB loop itself. Whether these difference are responsible for the suppressive activity of TLR10 remains to be investigated.

In support of our studies, another report published last year revealed TLR10 as an anti-inflammatory receptor that suppresses TLR2-mediated inflammatory responses in both human mononuclear cells and in a transgenic mouse model (12). In that study TLR10 was shown to suppress the release of a number of pro-inflammatory cytokines in response to the TLR2 agonists PAM3CSK4 as well as whole Borrelia burgdorferi. In support of this, genetic polymorphisms in TLR10 have been shown to associate with variability of responses to bacterial lipopeptide (13). A number of possible mechanisms for suppression are proposed including possible competition for ligand and/or co-receptors as well as the induction of anti-inflammatory cytokine expression. This study extends the suppressive function of TLR10 to that of other TLR family members as well as to both MyD88 and TRIF-dependent signaling pathways. Our analysis of signaling pathways indicate that TLR10 acts proximally in the signaling cascade through a currently undefined mechanism.

Two other studies have proposed an opposite, pro-inflammatory, function for TLR10. One study showed that siRNA-mediated knock down of endogenous TLR10 in HT-29 colonic epithelial cells blunted inflammatory responses to Listeria monocytogenes (14). Another study, showed that knock down of TLR10 in the THP-1 myelomonocytic cell line inhibited cellular responses to the H1N1 and H5N1 flu virus strains (15). Interestingly, both studies revealed fairly broad effects on pro-inflammatory cytokine and Type 1 IFN production that were dependent on infection of cells with live pathogens but not with heat-killed pathogens. Since both these organisms replicate in the cytoplasm, this suggests that intracellular forms of TLR10 may have a pro-inflammatory function following recognition of a PAMP associated with virulence (16). In the study of flu virus, transfection studies suggested that TLR10 responds to viral ribonuclear protein complexes (15). Although these findings contrast our own and others (12), it is noteworthy that we have engaged endogenous TLR10 at the cell surface where it may possess an opposing signaling function.

The finding that TLR10 is a negative regulator among members of the TLR family is perhaps not surprising (17). Even within the closely related IL-1 receptor family, whose members have TIR domains and utilize MyD88 to propagate signaling, are two inhibitory receptors known as ST2 (18) and SIGIRR (19). The transmembrane receptor ST2 has been shown to suppress NF-κB activation mediated by TLR2, TLR4 and TLR9 but not TLR3 by sequestering the adaptor proteins MyD88 and MAL. SIGIRR has been shown to inhibit MyD88-dependent signaling through its interactions with TRAF6 (TNF receptor-associated factor 6) and IRAK (Interleukin-1 receptor-associated kinase 1) (19). Thus, there is precedence for regulatory or inhibitory function among members of the TLR/IL-1 receptor superfamily.

The biologic function of TLR10 may not be truly understood until a natural ligand has been discovered. Nevertheless, since sustained TLR signaling is an underlying feature of a wide variety of chronic inflammatory conditions including many autoimmune diseases and cancers (13), the characterization of TLR10 as a broadly acting suppressor of TLR activation has far reaching therapeutic implications.

Supplementary Material

Acknowledgments

This work was supported by the NIAID of the NIH; grant 1R01-AI097639

We would like to thank the Flow Cytometry Facility and the Transgenic Mouse Facility; both of the Roy J. Carver Biotechnology Center at the University of Illinois Urbana-Champaign, for expert technical support. We’d also like to thank Dr. Bruce Beutler (UT Southwestern, Dallas, TX) for providing the ISRE-L929 reporter cell line.

Abbreviations

TIR
Toll/Interleukin Receptor
MyD88
Myeloid Differentiation Factor 88
TRIF
TIR-domain-containing adaptor-inducing interferon-β
PAM3CSK4
N-Palmitoyl-S-[2,3-bis(palmitoyloxy)-(2RS)- propyl]-[R]-cysteinyl-[S]-seryl-([S]-lysine)4
pI:C
polyinosinic:polycytidylic acid

Footnotes

Authorship Contributions

S.J. & X.L contributed equally to this manuscript. S.J., X.L., R.I.T designed the study; S.J., X.L. and N.J.H performed the research; S.J., X.L and N.J.H analyzed the data; and S.J., X.L., N.J.H and R.I.T. wrote the paper.

References

1. Kawai Taro, Akira Shizuo. The Role of Pattern-Recognition Receptors in Innate Immunity: Update on Toll-like Receptors. Nature Immunology. 2010;11(5):373–384. [PubMed]
2. Kawasaki Takumi, Kawai Taro. Toll-like Receptor Signaling Pathways. Frontiers in Immunology. 2014;5:461. [PMC free article] [PubMed]
3. Gay Nicholas J, Symmons Martyn F, Gangloff Monique, Bryant Clare E. Assembly and Localization of Toll-like Receptor Signalling Complexes. Nature Reviews. Immunology. 2014;14(8):546–558. [PubMed]
4. Chuang T, Ulevitch RJ. Identification of hTLR10: A Novel Human Toll-like Receptor Preferentially Expressed in Immune Cells. Biochimica Et Biophysica Acta. 2001;1518(1–2):157–161. [PubMed]
5. Hornung Veit, Rothenfusser Simon, Britsch Stefanie, Krug Anne, Jahdörfer Bernd, Giese Thomas, Endres Stefan, Hartmann Gunther. Quantitative Expression of Toll-like Receptor 1-10 mRNA in Cellular Subsets of Human Peripheral Blood Mononuclear Cells and Sensitivity to CpG Oligodeoxynucleotides. Journal of Immunology. 2002;168(9):4531–4537. [PubMed]
6. Lin Su-Chang, Lo Yu-Chih, Wu Hao. Helical Assembly in the MyD88-IRAK4-IRAK2 Complex in TLR/IL-1R Signalling. Nature. 2010;465(7300):885–890. [PMC free article] [PubMed]
7. Hasan Uzma, Chaffois Claire, Gaillard Claude, Saulnier Virginie, Merck Estelle, Tancredi Sandra, Guiet Chantal, et al. Human TLR10 Is a Functional Receptor, Expressed by B Cells and Plasmacytoid Dendritic Cells, Which Activates Gene Transcription through MyD88. Journal of Immunology. 2005;174(5):2942–2950. [PubMed]
8. Mikami Tomoko, Miyashita Hiroki, Takatsuka Shintaro, Kuroki Yoshio, Matsushima Norio. Molecular Evolution of Vertebrate Toll-like Receptors: Evolutionary Rate Difference between Their Leucine-Rich Repeats and Their TIR Domains. Gene. 2012;503(2):235–243. [PubMed]
9. Roach Jared C, Glusman Gustavo, Rowen Lee, Kaur Amardeep, Purcell Maureen K, Smith Kelly D, Hood Leroy E, Aderem Alan. The Evolution of Vertebrate Toll-like Receptors. Proceedings of the National Academy of Sciences of the United States of America. 2005;102(27):9577–9582. [PubMed]
10. Guan Yue, Ranoa Diana Rose E, Jiang Song, Mutha Sarita K, Li Xinyan, Baudry Jerome, Tapping Richard I. Human TLRs 10 and 1 Share Common Mechanisms of Innate Immune Sensing but Not Signaling. Journal of Immunology. 2010;184(9):5094–5103. [PubMed]
11. Nyman Tomas, Stenmark Pål, Flodin Susanne, Johansson Ida, Hammarström Martin, Nordlund Pär. The Crystal Structure of the Human Toll-like Receptor 10 Cytoplasmic Domain Reveals a Putative Signaling Dimer. The Journal of Biological Chemistry. 2008;283(18):11861–11865. [PubMed]
12. Oosting Marije, Cheng Shih-Chin, Bolscher Judith M, Vestering-Stenger Rachel, Plantinga Theo S, Verschueren Ineke C, Arts Peer, et al. Human TLR10 Is an Anti-Inflammatory Pattern-Recognition Receptor. Proceedings of the National Academy of Sciences of the United States of America. 2014;111(42):E4478–4484. [PubMed]
13. Mikacenic C, Reiner AP, Holden TD, Nickerson DA, Wurfel MM. Variation in the TLR10/TLR1/TLR6 Locus Is the Major Genetic Determinant of Interindividual Difference in TLR1/2-Mediated Responses. Genes and Immunity. 2013;14(1):52–57. [PMC free article] [PubMed]
14. Regan Tim, Nally Ken, Carmody Ruaidhri, Houston Aileen, Shanahan Fergus, Macsharry John, Brint Elizabeth. Identification of TLR10 as a Key Mediator of the Inflammatory Response to Listeria Monocytogenes in Intestinal Epithelial Cells and Macrophages. Journal of Immunology. 2013;191(12):6084–6092. [PubMed]
15. Lee Suki MY, Kok Kin-Hang, Jaume Martial, Cheung Timothy KW, Yip Tsz-Fung, Lai Jimmy CC, Guan Yi, Webster Robert G, Jin Dong-Yan, Malik Peiris JS. Toll-like Receptor 10 Is Involved in Induction of Innate Immune Responses to Influenza Virus Infection. Proceedings of the National Academy of Sciences of the United States of America. 2014;111(10):3793–3798. [PubMed]
16. Mourao-Sa Diego, Roy Soumit, Magarian Blander J. Vita-PAMPs: Signatures of Microbial Viability. Advances in Experimental Medicine and Biology. 2013;785:1–8. [PubMed]
17. Kondo Takeshi, Kawai Taro, Akira Shizuo. Dissecting Negative Regulation of Toll-like Receptor Signaling. Trends in Immunology. 2012;33(9):449–458. [PubMed]
18. Brint Elizabeth K, Xu Damo, Liu Haiying, Dunne Aisling, McKenzie Andrew NJ, O’Neill Luke AJ, Liew Foo Y. ST2 Is an Inhibitor of Interleukin 1 Receptor and Toll-like Receptor 4 Signaling and Maintains Endotoxin Tolerance. Nature Immunology. 2004;5(4):373–379. [PubMed]
19. Wald David, Qin Jinzhong, Zhao Zhendong, Qian Youcun, Naramura Mayumi, Tian Liping, Towne Jennifer, Sims John E, Stark George R, Li Xiaoxia. SIGIRR, a Negative Regulator of Toll-like Receptor-Interleukin 1 Receptor Signaling. Nature Immunology. 2003;4(9):920–927. [PubMed]