The Atypical Inhibitor of NF-κB, IκBζ, Controls Macrophage Interleukin-10 Expression*

Macrophages constitute a first line of pathogen defense by triggering a number of inflammatory responses and the secretion of various pro-inflammatory cytokines. Recently, we and others found that IκBζ, an atypical IκB family member and transcriptional coactivator of selected NF-κB target genes, is essential for macrophage expression of a subset of pro-inflammatory cytokines, such as IL-6, IL-12, and CCL2. Despite defective pro-inflammatory cytokine expression, however, IκBζ-deficient mice develop symptoms of chronic inflammation. To elucidate this discrepancy, we analyzed a regulatory role of IκBζ for the expression of anti-inflammatory cytokines and identified IκBζ as an essential activator of IL-10 expression. LPS-challenged peritoneal and bone marrow-derived macrophages from IκBζ-deficient mice revealed strongly decreased transcription and secretion of IL-10 compared with wild-type mice. Moreover, ectopic expression of IκBζ was sufficient to stimulate Il10 transcription. On the molecular level, IκBζ directly activated the Il10 promoter at a proximal κB site and was required for the transcription-enhancing trimethylation of histone 3 at lysine 4. Together, our findings show for the first time the IκBζ-dependent expression of an anti-inflammatory cytokine that is crucial in controlling immune responses.

Macrophages constitute a first line of pathogen defense by triggering a number of inflammatory responses and the secretion of various pro-inflammatory cytokines. Recently, we and others found that IB, an atypical IB family member and transcriptional coactivator of selected NF-B target genes, is essential for macrophage expression of a subset of pro-inflammatory cytokines, such as IL-6, IL-12, and CCL2. Despite defective proinflammatory cytokine expression, however, IB-deficient mice develop symptoms of chronic inflammation. To elucidate this discrepancy, we analyzed a regulatory role of IB for the expression of anti-inflammatory cytokines and identified IB as an essential activator of IL-10 expression. LPS-challenged peritoneal and bone marrow-derived macrophages from IBdeficient mice revealed strongly decreased transcription and secretion of IL-10 compared with wild-type mice. Moreover, ectopic expression of IB was sufficient to stimulate Il10 transcription. On the molecular level, IB directly activated the Il10 promoter at a proximal B site and was required for the transcription-enhancing trimethylation of histone 3 at lysine 4. Together, our findings show for the first time the IB-dependent expression of an anti-inflammatory cytokine that is crucial in controlling immune responses.
Macrophages constitute a heterogeneous group of phagocytes that fulfill pro-as well as anti-inflammatory responses (1,2). A pro-inflammatory response of innate immune cells is indispensable for host defense. However, dysregulation of innate immunity can result in severe damage of the affected host. Weak immune responses lead to prolonged infection and persistence of pathogens, whereas overshooting responses promote chronic inflammation and autoimmune disease (3). Therefore, tight control of defense mechanisms is essential for host protection against self-destructive, excessive, and undue immune responses.
For macrophages, two distinct states of polarization have been defined. Classically activated (M1-polarized) macrophages exert their pro-inflammatory role as effector cells in cell-mediated immune responses, whereas alternatively activated (M2-polarized) macrophages are involved in immunosuppression, wound healing, and tissue regeneration (4). In contrast to M1 macrophages, the M2 counterparts secrete high amounts of anti-inflammatory cytokines, including the crucial immunosuppressive cytokine IL-10, thereby guaranteeing a balanced immune response (5).
IL-10 can inhibit various macrophage functions, such as nitric oxide synthesis and pro-inflammatory cytokine production, as well as the expression of major histocompatibility complex proteins and co-stimulatory receptors (6,7). In contrast, the absence of IL-10 results in spontaneous development of inflammatory bowel disease and increased pathological alterations caused by uncontrolled responses to infectious pathogens (8,9). IL-10 may also act as a negative feedback regulator of chronic infectious diseases by inhibiting IL-6, IL-12, and TNF␣ secretion, thereby keeping immune responses in check and preventing tissue damage (9). Furthermore, the administration of exogenous IL-10 has been shown to ameliorate inflammatory and autoimmune diseases in several animal models (8).
An important regulator for the expression of cytokines and other immune regulators is the transcription factor NF-B. The NF-B family consists of five members that bind as homo-or heterodimers at B sites in the DNA of target genes (10). Depending on their transactivation activity, the NF-B subunits can be divided into two subgroups. RelA (p65), RelB, and c-Rel possess a C-terminal transcription activation domain, whereas p50 (Nfkb1) and p52 (Nfkb2) lack a transcription activation domain. Based on these structural differences, NF-B dimers containing at least one subunit with a transcription activation domain act as transcriptional activators, whereas p50/ p50 or p52/p52 homodimers are assumed to function as transcriptional repressors.
Because various stimuli activate the NF-B signaling pathway and a great diversity of target genes is regulated by NF-B, a precise control of NF-B activity is required to avoid misguided immune responses. In fact, NF-B activation is controlled by a series of cytosolic and nuclear regulatory events, in which IB proteins play a pivotal role (10,11). In unstimulated cells, NF-B is sequestered as an inactive complex bound to cytosolic IB proteins such as IB␣, IB␤, and IB⑀. Various stimuli cause the phosphorylation of cytosolic IBs, leading to their proteasomal degradation, which subsequently enables NF-B to translocate to the nucleus and activate target genes.
Despite the presence of high-affinity binding sites, only a fraction of NF-B target genes is generally activated in response to an inflammatory stimulus. It was suggested that NF-B target genes can be categorized in two groups based on their kinetics of induction and the requirement of protein synthesis (12,13). Although primary NF-B response genes are rapidly induced, the expression of secondary target genes is delayed and requires the prior synthesis of additional NF-B coregulators. A novel and emerging group of such NF-B coregulators are so-called atypical IB proteins, including Bcl-3, IB NS , IB, and IB (11,14). Atypical IBs differ markedly from classical cytosolic IBs because they are mostly inducibly expressed and localized in the nucleus. Moreover, atypical IBs do not exclusively act as inhibitors but can also activate the expression of secondary response genes.
The atypical IB protein IB has been recently implicated in differential NF-B target gene expression in macrophages (15,16) even though its physiological function remains largely unknown. The IB-encoding Nfkbiz gene is rapidly induced as a primary NF-B response gene by various inflammatory stimuli and, through association with the NF-B subunit p50, is thought to exert its transcription-enhancing activity on secondary response genes mainly at the level of chromatin remodeling (12,17,18).
Recently, we showed that in macrophages, expression of CCL2 strictly depends on the presence of IB and, consequently, that expression of CCL2 is abolished in macrophages from IB-deficient mice (15). Furthermore, several other proinflammatory gene products, including IL-6, IL12p40, IL-17, IFN␥, and GM-CSF, have been found to be regulated by IB (16, 19 -23). Intriguingly, however, despite impaired expression of these pro-inflammatory cytokines, Nfkbiz Ϫ/Ϫ mice display a pro-inflammatory phenotype characterized by periocular inflammation, inflammatory skin alterations, and an M1 hyperpolarized macrophage state (15,16,24,25). In view of the phenotype of Nfkbiz Ϫ/Ϫ mice, we therefore investigated a potential role of IB for the regulation of IL-10 as an essential anti-inflammatory cytokine. Interestingly, although expression of Il10 has been found previously to be inhibited by the atypical IB protein Bcl-3 (26,27), our results establish IB as a novel and essential transcriptional inducer of Il10 in macrophages. Our results therefore show for the first time that IB is not only a pro-inflammatory mediator but also controls the activation of anti-inflammatory gene products.

Experimental Procedures
Animals-Nfkbiz Ϫ/Ϫ and control C57BL/6 mice were used at 6 -8 weeks of age as described previously (23). Nfkbiz Ϫ/Ϫ mice were originally generated by injection of targeted AB2.2 ES cell (129 strain) clones into C57BL/6 murine blastocysts (24) and were backcrossed in a C57BL/6 background for more than 50 generations. Mouse work was performed in accordance with the German law guidelines of animal care as permitted by regional authorities (Regierungspräsidium Tübingen, application no. H6/12).

Culture of Peritoneal and Bone Marrow Macrophages-
Female C57BL/6 mice were euthanized by CO 2 asphyxiation. For isolation of peritoneal macrophages (PM⌽), 3 the abdominal skin was removed, a catheter (24-gauge) was inserted into the peritoneal cavity, and 10 ml of ice-cold PBS was injected. After massage of the peritoneum, peritoneal fluids were aspirated and centrifuged at 500 ϫ g for 10 min, and the resulting PM⌽ were resuspended in 2 ml of macrophage medium containing DMEM/Ham's F-12, 10% FCS, and MycoZapPlusCL antibiotics (Lonza, Basel, Switzerland). Cells were seeded in 96-well plates and cultured for 2 h under standard conditions (5% CO 2 , 37°C). Next, adherent PM⌽ were washed four times with culture medium to remove non-adherent cells. To generate bone marrow-derived macrophages (BMM⌽), the femur and tibia were separated at the knee joint and rinsed with PBS. Bone marrow cells were singularized (40-m cell strainer) and pelleted by centrifugation (500 ϫ g, 10 min). Cells were resuspended in macrophage medium supplemented with M-CSF (30 ng/ml, Immunotools, Friesoythe, Germany), seeded in tissue culture flasks (3 ϫ 10 6 cells/ml), and cultured under low-oxygen conditions (5% CO 2 , 5% O 2 ). After 7 days of differentiation, cells were washed with PBS, scraped off, and cultured at a density of 2 ϫ 10 5 cells/cm 2 under low-oxygen conditions.
Activation and Pro-inflammatory Stimulation of PM⌽ and BMM⌽-PM⌽ and BMM⌽ were cultured with murine IL-4 (100 ng/ml) or IFN␥ (25 ng/ml, both from Immunotools) for 24 h to induce alternative or classical macrophage activation. Pro-inflammatory stimulation was achieved by culturing cells for the indicated time in the presence of 1 g/ml LPS (Escherichia coli serotype O111:B4; Sigma-Aldrich, Taufkirchen, Germany). Recombinant murine IL-10 was obtained from Immunotools.
Transfections and Reporter Gene Assays-Raw264.7 or Raw264.7/TetOn-IB cells were transfected with appropriate amounts of plasmids using jetPEI transfection reagent according to the instructions of the manufacturer (Polyplus, Illkirch, France). Expression plasmids for Nfkb1 (p50) and IB have been described previously (15,17). For reporter gene assays, the following luciferase promoter constructs were used: pGL2basic-Il10 and truncation mutants (28), pGL3basic-Lcn2 (29), and pGL3basic-Il6 and pGL3basic-Elam1 (16). Cells were trypsinized 24 h after transfection. Cells and quanta from each transfection were reseeded in four separate culture vessels for differential treatments. To induce ectopic IB expression, Raw264.7/TetOn-IB cells were cultured in the presence of 2 g/ml doxycycline. After additional 16 h, doxycycline-treated and untreated cells were incubated with 1 g/ml LPS. Cells were harvested 48 h after transfection, and luciferase assays were performed with the Dual-Luciferase reporter assay system (Promega Corp., Madison, WI).
Quantitative RT-PCR-Whole cell RNA was isolated using the RNeasy mini kit (Qiagen, Hilden, Germany) and reversetranscribed (QuantiTect kit, Qiagen) according to the instructions of the manufacturer. Quantitative PCR (qPCR; Light-Cycler 480 II, Roche) was performed using SYBR Green/ROX qPCR Master Mix (Fermentas, Sankt Leon-Rot, Germany) as described in the two-step cycling protocol of the manufacturer (384-well plates, 10-l reaction). The following primer pairs were used:  TAT GAT GTC  TCG TTT-3Ј and 5Ј-TGC TTT TCC GTA TGT TGT GCT-3Ј; and Tnfa, 5Ј-CCT CAG CCT CTT CTC CTT CCT-3Ј and 5Ј-GGT GTG GGT GAG GAG CA-3Ј. Quantification of reverse-transcribed mRNA was performed using the second derivate maximum-based advanced relative quantification algorithm of the Roche LightCycler 480 software (V1.5).
Measurement of Cytokine Concentrations-Concentrations of cytokines in cell culture supernatants were measured using the mouse cytometric bead array system (mouse anti-IL-6, anti-IL-10, and anti-TNF␣) according to the instructions of the manufacturer (BD Biosciences). Before stimulation of cells in 96-well plates, the culture medium was exchanged with 200 l of fresh medium per well. In the case of BMM⌽, cytokine concentrations in culture supernatants were directly compared and expressed as cytokine amounts per volume. To avoid mousespecific differences in peritoneal cell counts, cytokine concentrations in supernatants of PM⌽ were normalized to the protein content of cell lysates. To this end, 50 l of 0.2 M NaOH was added to each well after aspiration of the supernatants, and protein concentrations in lysates were measured with the BCA protein assay (Thermo Scientific, Bonn, Germany).
Statistical Analysis-Values are expressed as mean Ϯ S.D. or S.E. for the indicated numbers of independent experiments. For statistical comparisons, hypotheses were tested using an unpaired Student's t test.

IB Is Essential for Il10 Expression in Mouse Embryonic
Fibroblasts and Peritoneal Macrophages-Although IB transcriptionally induces several pro-inflammatory genes in cells of the monocyte lineage, Nfkbiz Ϫ/Ϫ mice exhibit features of chronic inflammation. To explore this discrepancy, we focused our analyses on IL-10 as one of the major anti-inflammatory mediators. Initially, we examined the gene expression profile of wild-type and Nfkbiz Ϫ/Ϫ MEFs by quantitative RT-PCR (qRT-PCR). As expected, LPS-challenged Nfkbiz Ϫ/Ϫ MEFs showed reduced expression of the IB-dependent target gene Il6 (16) compared with wild-type MEFs (Fig. 1A). In contrast to Il6, expression of Tnfa, an IB-independent NF-B target gene (15,16), was readily induced by LPS in wild-type and even more strongly in Nfkbiz Ϫ/Ϫ MEFs. Intriguingly, analysis of Il10 expression revealed strongly diminished transcript levels in Nfkbiz Ϫ/Ϫ MEFs compared with wild-type MEFs (Fig. 1A).
Because IL-10 is predominantly expressed by macrophages, we performed additional experiments in PM⌽ from wild-type and Nfkbiz Ϫ/Ϫ mice. We initially assayed the expression of macrophage surface markers, such as F4/80, CD11b, CD11c, and Ly6G/C (supplemental Fig. 1), and classical macrophage functions, such as phagocytosis, migration, and oxidative burst (supplemental Fig. 2). These analyses did not reveal significant differences between the two genotypes, indicating that PM⌽ are a suitable experimental system. Because IFN␥-primed PM⌽ have been used previously in studies on IB-dependent gene regulation (15), we next analyzed the gene expression profiles of naïve and IFN␥-primed wild-type and Nfkbiz Ϫ/Ϫ PM⌽. In line with published data (15), expression of Il6 was only slightly different in naïve PM⌽ from both genotypes but strongly reduced in IFN␥-primed PM⌽ from Nfkbiz Ϫ/Ϫ mice compared with wild-type cells. The expression levels of Tnfa did not significantly differ in wild-type and Nfkbiz Ϫ/Ϫ PM⌽ (Fig. 1B). Importantly, compared with wild-type PM⌽, both naïve and IFN␥-primed PM⌽ from Nfkbiz Ϫ/Ϫ mice revealed strongly reduced mRNA levels of Il10 (Fig. 1C).

IB Deficiency Reduces IL-10 Secretion in Bone Marrow
Macrophages-Having shown that Il10 expression is diminished in Nfkbiz Ϫ/Ϫ MEFs and PM⌽, we further analyzed IL-10 mRNA and protein expression in BMM⌽. Again, cells were left untreated (naïve) or pretreated with IFN␥ before challenging with LPS. Gene expression analyses revealed comparable mRNA levels of Tnfa in naïve and IFN␥-primed BMM⌽, whereas IL6 expression was significantly reduced in the absence of IB (Fig. 2, A and B). In line with the previous experiments, expression of Il10 mRNA was strongly reduced in Nfkbiz Ϫ/Ϫ BMM⌽ compared with wild-type BMM⌽.
We further analyzed the kinetic of Il10 expression in BMM⌽ of both genotypes. LPS stimulation of wild-type BMM⌽ induced Il10 mRNA expression already after 4 h, with maximal expression 8 h after addition of LPS (Fig. 2C). This time-dependent expression is comparable with that of Il6 and Ccl2 (15), which have been shown to be secondary response genes in the NF-B signaling cascade. In line with the previous results, LPS-treated Nfkbiz Ϫ/Ϫ BMM⌽ showed only marginally increased Il10 mRNA expression even 8 h after stimulation. In a similar setup, we analyzed cytokine concentrations in supernatants from LPS-challenged BMM⌽. The amount of TNF␣ detected in supernatants from LPS-challenged wild-type and Nfkbiz Ϫ/Ϫ BMM⌽ was similar and served as a positive control (Fig. 2D). In line with the qRT-PCR analysis, the concentration of IL-10 increased in supernatants from LPS-challenged wild-type BMM⌽, reaching a maximum after 16 h, whereas, in supernatants from Nfkbiz Ϫ/Ϫ BMM⌽, only basal IL-10 levels were detected. TNF␣ levels were comparable in supernatants from BMM⌽ of both genotypes (Fig.  2E), whereas the amount of IL-6 was significantly reduced in Nfkbiz Ϫ/Ϫ BMM⌽ compared with wild-type cells (Fig. 2F). Thus, these data clearly indicate IB-dependent regula- IB-regulated IL-10 Expression Is Independent of Macrophage Polarization-The classical activation of macrophages induces M1 polarization, whereas alternative activation results in M2 polarization. Previous gene expression analysis revealed that the regulation of Il6 gene expression depends on the macrophage polarization state (15). Hence, we wondered whether IL-10 expression is also influenced by the polarization state. Therefore, we quantified the concentration of cytokines in supernatants from LPS-challenged naïve and M1-and M2-polarized BMM⌽. As a positive control, we analyzed the secretion of TNF␣, which was readily detectable in supernatants from naïve and classically (M1) and alternatively (M2) activated wild-type and Nfkbiz Ϫ/Ϫ BMM⌽ (Fig. 3, A-C). Interestingly, naïve Nfkbiz Ϫ/Ϫ macrophages secreted slightly more TNF␣ than wild-type BMM⌽ (Fig. 3A). The concentrations of both IL-6 and IL-10 were significantly decreased in Nfkbiz Ϫ/Ϫ BMM⌽ compared with wild-type BMM⌽ in case of all three polarization states (Fig. 3, A-C). Thus, expression of IL-10 is not affected by the macrophage polarization state.

IB Overexpression Induces Il10 Promoter Activity and Gene
Expression-Because our investigations so far relied on knockout systems, we additionally employed the macrophage-like cell line Raw264.7, which was genetically modified to enable inducible doxycycline-dependent IB expression. Treatment of the Raw264.7/TetOn-IB cells with doxycycline resulted in the robust expression of IB, which was further increased by stimulation with LPS (Fig. 4A).
We next investigated the impact of transgenic IB expression on the induction of various IB-independent and -dependent genes. Quantitative RT-PCR analyses confirmed a dosedependent induction of Nfkbiz transcription in Raw264.7/ TetOn-IB by doxycycline (Fig. 4B). The expression of the IB-independent NF-B target genes Nfkbia and Elam1 remained unaffected by doxycycline, whereas expression of the IB-dependent target genes Il6 and Lcn2 correlated with the concentration of doxycycline and the mRNA levels of Nfkbiz. Similar to Il6 and Lcn2, expression of Il10 was enhanced in the presence of doxycycline and induced Nfkbiz (Fig. 4B). Thus, expression of IB is sufficient for induction of Il10 expression.
We further analyzed whether IB directly activates the Il10 promoter. In a first set of experiments, we transfected Raw264.7/TetOn-IB cells with Elam1, Lcn2, Il6, and Il10 reporter gene constructs and analyzed whether doxycyclineinduced IB expression results in increased luciferase activity. No reporter activity was induced from the empty vector backbone and the IB-independent promoter of Elam1 (Fig. 4C). In contrast, IB expression clearly induced luciferase activity from the Il6 and the Lcn2 promoters, which are both regulated by IB (16,31). Importantly, doxycycline-induced expression of IB also strongly induced luciferase expression from the Il10 promoter construct (Fig. 4C).

IB Targets the Proximal Promoter Region of the Il10
Genomic Locus-Analysis of the Il10 promoter reveals two NF-B consensus sites that are located in distal (Ϫ1115 to Ϫ1106 bp) and proximal (Ϫ55 to Ϫ46 bp) promoter regions (Fig. 5A). Because these regions potentially serve as anchor points for IB-mediated transcription, we used reporter constructs containing various truncated versions of the Il10 promoter. Upon transfection of Raw264.7 cells, LPS induced a strong activation of the full-length Il10 promoter (Fig. 5B). Truncations of the Il10 promoter and deletion of the distal NF-B-binding site resulted only in a minor reduction of luciferase activity, indicating that the proximal NF-B site is important for Il10 promoter activation.
The recruitment of IB to promoter regions is dependent on the DNA-binding subunit p50. To verify that the proximal NF-B-binding site is responsible for IB-mediated Il10 induction, we co-transfected Raw264.7 cells with the reporter construct of the proximal Il10 promoter region (Ϫ158 to ϩ64 bp) together with expression vectors for IB and p50. The single transfection of Nfkbiz did not result in luciferase activity (Fig. 5C). Furthermore, consistent with an inhibitory role of p50 homodimers (10), the sole expression of p50 even reduced reporter gene activity. However, upon co-transfection of IB and p50, luciferase activity increased by 2-to 3-fold (Fig. 5C), indicating a direct activation of Il10 gene expression by the complex of IB and p50.
Active gene transcription is associated with open chromatin and trimethylation of histone H3 at lysine 4 (H3K4me 3 ) at promoter regions. We and others have previously shown that IB is required for formation of the transcription preinitiation complex and H3K4 trimethylation at targeted loci (15,19,32). To further substantiate a role of the proximal Il10 promoter for IB-mediated gene expression, we analyzed the degree of H3K4 trimethylation in the presence and absence of Nfkbiz. To this end, we employed qPCR-coupled ChIP analysis of the endogenous proximal Il10, Il6, and Tnfa promoter regions using an H3K4me 3 -specific antibody. Compared with unstimulated wild-type BMM⌽, LPS stimulation resulted in an ϳ20fold enrichment of H3K4 trimethylation at the proximal Il10 promoter (Fig. 5D). An even stronger enrichment was seen for the Il6 promoter, whereas H3K4 trimethylation of the proximal Tnfa promoter was barely affected. Importantly, compared with wild-type BMM⌽, no H3K4 trimethylation was detectable at the endogenous Il6 and Il10 promoters in IB-deficient cells (Fig. 5D). The transcription-associated H3K4 trimethylation at the Il10 promoter was exclusively observed in the presence of IB. Thus, we conclude that IB regulates IL-10 expression by directly binding to the proximal region of the Il10 promoter together with p50.
IL-10 Partially Reverses the M1 Phenotype of Nfkbiz Ϫ/Ϫ BMM⌽-Our previous gene expression analysis comparing IB-proficient and -deficient macrophages (GEO accession no. GSE43075, Ref. 15) revealed a strong up-regulation of several M1 markers in the absence of IB, which is consistent with the pro-inflammatory phenotype of Nfkbiz Ϫ/Ϫ mice. Examples for the preferential M1 polarization are the elevated mRNA expression of Stat1, Gbp4, and Cxcl9 as well as the increased expression and phosphorylation of Stat1 protein in LPS-stimulated Nfkbiz Ϫ/Ϫ BMM⌽ compared with the wild-type counterparts (Fig. 6, A and B).
To investigate a potential role of IL-10 in this M1 polarization, we incubated Nfkbiz Ϫ/Ϫ BMM⌽ in the presence of LPS and varying concentrations of IL-10 and examined the expression of the M1 markers Stat1 and Gbp4. Quantitative RT-PCR revealed a dose-dependent reduction of Stat1 and Gbp4 expression by exogenous IL-10 (Fig. 6C), whereas Cxcl9 expression remained largely unaffected (data not shown). Importantly, when Nfkbiz Ϫ/Ϫ BMM⌽ were incubated with IL-10-proficient supernatants from LPS-treated wild-type BMM⌽, a significant reduction of Stat1 and Gbp4 expression was also detected (Fig.  6D). The reduction of Gbp4 expression roughly corresponded to the reduction observed with 2 ng/ml IL-10, a concentration similar to that present in supernatants of LPS-stimulated BMM⌽ (Fig. 3A). Thus, these results not only show that IL-10 signaling is functional in Nfkbiz Ϫ/Ϫ BMM⌽ but, moreover, indicate that the lack of IL-10 in Nfkbiz Ϫ/Ϫ BMM⌽ at least partially contributes to their enhanced M1 polarization.

Discussion
Growing evidence suggests that the induction of NF-B-regulated genes is not solely defined by the nuclear translocation of NF-B but that different NF-B target genes have individual expression profiles regarding kinetic, stimulus, or cell type, thereby ensuring a selectivity of an immune response. Several recent studies identified a subfamily of atypical IB proteins as important "specifiers" that select particular B-sites to be activated or repressed under certain conditions (14).
IB is mostly regarded as a pro-inflammatory regulator, as demonstrated e.g. by its requirement for Th17 differentiation and expression of particular pro-inflammatory cytokines. Nevertheless, Nfkbiz Ϫ/Ϫ mice show a pro-inflammatory phenotype and M1 hyperpolarization of macrophages (15,16,24,25), suggesting that so far unknown anti-inflammatory mediators might be controlled by IB. In this study, we found that induction of the potent anti-inflammatory cytokine IL-10 by LPS but also by TLR2 agonists (data not shown) was strictly dependent on IB and strongly reduced in Nfkbiz Ϫ/Ϫ mice. These results were supported by the finding that the doxycycline-inducible expression of ectopic IB in Raw264.7 macrophages tightly correlated with increasing Il10 mRNA levels. Moreover, reporter analysis revealed that the proximal B site of the Il10 promoter was responsible for IB-mediated Il10 expression. The recruitment of IB was associated with histone H3K4 trimethylation of the proximal promoter region as a marker of active gene transcription. Interestingly, in the absence of IB, H3K4 trimethylation did not occur, which, along with other lines of evidence, suggests that chromatin remodeling is essential for IB action. Thus, our results in knockout and overexpression models suggest that transcriptional regulation of Il10 directly depends on IB.
So far, the expression of IL-10 in macrophages is known to be primarily regulated by transcription factors such as SP1, C/EBP␤, IRF1, and STAT3 (28,(33)(34)(35), whereas a role of different NF-B proteins is relatively unknown. Because of the lack of a transcription activation domain, p50 NF-B homodimers, which retain their ability to bind to B sites, are thought to be transcriptional repressors. Interestingly, although not investigating atypical IB proteins, earlier studies already showed that p50 homodimers bind to the proximal Il10 promoter and activate Il10 transcription in primary macrophages (36).
Moreover, in contrast to IB, Bcl-3, a related atypical IB protein that also requires p50 for co-regulation, negatively regulates Il10 transcription in macrophages (27,37), although the exact role of Bcl-3 for Il10 expression is controversial (38). Bcl3 knockout mice show enhanced susceptibility to infection with Listeria monocytogenes, which is due to enhanced expression of IL-10, resulting in diminished levels of IL-12p70 and IFN␥. These results suggest that atypical IB proteins, such as Bcl-3 and IB, might regulate gene expression in an opposite manner, which is also underlined by the fact that IL-12p70 and IFN␥ are direct IB targets. Likewise, Bcl-3 and IB have an antagonistic effect on CCL2 expression in macrophages. Although Bcl-3 inhibits the expression of CCL2, IB promotes the expression of this chemokine (15,38). Another example of such opposite gene regulation by atypical IB proteins concerns IB and IB NS . For instance, although IB is required for IL-6, IL-12p40, and G-CSF expression (15,16), IB NS apparently inhibits transcription of these cytokines (39,40). Interestingly, our gene expression profiling suggest that atypical IB proteins might also influence each other at the transcriptional level and, moreover, compete with each other for p50-mediated DNA binding. Together, these findings suggest that atypical IB proteins form a complex network in controlling NF-B responses.
In addition to transcription factor binding, previous studies suggested that Il10 expression is regulated by changes in the chromatin structure at the IL10 locus. The histone deacetylase HDAC11 has been found to inhibit IL-10 expression (41), whereas phosphorylation of histone H3 at serine 10 is needed for transcriptional activation of the Il10 promoter (42). A recent study found that IB recruits the epigenetic modifier Tet2 to selective promoter regions independent of DNA meth-FIGURE 6. IL-10 partially attenuates the M1-hyperpolarized state of Nfkbiz-deficient bone marrow macrophages. A, BMM⌽ from wild-type and Nfkbiz Ϫ/Ϫ mice were cultured in the presence or absence of 1 g/ml LPS for 5 h. Cells were subsequently assayed for the indicated mRNA levels. Values were normalized to Gapdh and are mean Ϯ S.D. from four experiments. *, statistical significance comparing wild-type and knockout cells; N.D., not detectable. ctrl, control. B, wild type and Nfkbiz Ϫ/Ϫ BMM⌽ were stimulated with 1 g/ml LPS for the indicated times. The levels of Stat1, phospho-Stat1 (Tyr 701 ), and ␤-actin were analyzed by immunoblotting. An exemplary set of data is shown. C and D, Nfkbiz Ϫ/Ϫ BMM⌽ were cultured in the presence of 1 g/ml LPS or left untreated. After 4 h, the supernatants were replaced by medium supplemented with the indicated concentrations of IL-10 (C) or by supernatants from wild-type BMM⌽ (wt) challenged for 24 h with LPS (D). Samples for qRT-PCR were prepared after 4 h of incubation and analyzed for relative mRNA expression of Stat1 and Gbp4. Values are mean Ϯ S.D. from three experiments. ylation (43). IB further mediates chromatin remodeling by recruiting the SWI/SNF complex to target genes, thereby enhancing promoter accessibility (32). The same mechanism presumably underlies the regulation of Il10 expression because we found that Il10 promoter accessibility and H3K4 trimethylation were reduced in Nfkbiz Ϫ/Ϫ cells. Thus, it will be interesting to explore whether Bcl-3 and IB mediate their antagonistic effects at the Il10 promoter by recruiting distinct histone-modifying enzymes.
Although cells of the macrophage lineage are a major source of IL-10, several other cell types of the innate and adaptive immune system can express this cytokine (6,7). Further studies are needed to explore whether the strict control of IL-10 expression by IB is also relevant to other cell types. Our exemplary investigation of wild-type and Nfkbiz Ϫ/Ϫ MEFs indicates that the described mechanism is not restricted to macrophages. Interestingly, previous gene expression analysis revealed that IB-deficient macrophages show a bias toward M1 polarization, evidenced by the increased expression of certain M1 markers (15). It is worth mentioning that p50-deficient mice also show exacerbated M1-driven inflammation and reduced M2 polarization of their macrophages (44), although several phenotypic alterations are distinct between Nfkbiz Ϫ/Ϫ and p50-deficient mice.
In functional studies, we found that the increased mRNA expression of Stat1 and Gpb4 could be partially reverted not only by IL-10 supplementation but also by IL-10-proficient supernatants from wild-type macrophages even though no reduction in Cxcl9 expression was observed. It was not the intention of our study to investigate the role of IB-mediated IL-10 expression in macrophage polarization. Our results, however, indicate that decreased IL-10 expression contributes to at least some of the features of M1 polarization in Nfkbiz Ϫ/Ϫ mice. In line, IL-10-producing monocytes have been found to preferentially differentiate to M2 macrophages (45,46). Dysregulation of Il10 expression has been linked to several immune disorders. Transgenic mice overexpressing IL-10 in macrophages exhibit increased susceptibility to bacterial infections and septic shock (47). Excessive IL-10 secretion has also been linked to impaired tumor immune surveillance (48,49). In contrast, the absence of IL-10 results in spontaneous inflammatory bowel disease (8), emphasizing its protective role in inflammatory and autoimmune conditions. We did not detect spontaneous colitis in Nfkbiz Ϫ/Ϫ mice, which might be caused by the genetic background because intestinal lesions have been reported to be least severe in C57BL/6 mice (50). It is, however, worth mentioning that Nfkbiz Ϫ/Ϫ mice exhibit an increased susceptibility to dextran sodium sulfate-induced colitis. 4 In summary, we have uncovered an essential novel regulatory mechanism of Il10 gene regulation in macrophages. We demonstrate that IB through p50-mediated recruitment to the proximal Il10 promoter and subsequent histone H3 modification, enables transcription of the Il10 locus. Because IL-10 plays a beneficial role in several inflammatory diseases, Nfkbiz Ϫ/Ϫ mice are an interesting model system for evaluating IB as a potential therapeutic target in inflammatory diseases.