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Department of Microbiology and Immunology, Weill Medical College of Cornell University, New York, NY 10021
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Abstract |
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Introduction |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionDisclosuresReferences |
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Although the inflammatory response is critical in controlling the growth of pathogenic microorganisms, excessive cytokine production is harmful to the host and can even be fatal (3). Thus, the challenge faced by the immune system of an infected host is to respond with sufficient intensity and duration to control and eliminate the infection while minimizing nonspecific injury to host tissues. Monocytes are recognized as one of the key promoters of acute and chronic inflammatory responses. One intriguing feature of macrophage biology is the ability of activated macrophage populations to initially produce proinflammatory cytokines, such as TNF-
, IL-1
, IL-6, and IL-12 (4), and subsequently, the second phase of the macrophage response involves the production of IL-10, a potent immunosuppressive cytokine, which down-regulates the production of proinflammatory cytokines (5). The equilibrium of pro- and anti-inflammatory cytokine expression is of central importance for understanding how the immune system regulates responses to pathogenic infection (6).
IL-10 is one of the most potent and significant anti-inflammatory cytokines. It mediates the down-regulation of Th1 responses by inhibiting the production of most immune-activating cytokines (7, 8), thereby limiting and ultimately terminating inflammatory responses (9). This function is illustrated readily by the phenotype of IL-10-null mice, which acquires autoimmune manifestations of colitis due to an overabundance of IL-12 and IFN-
(9, 10) and exhibits increased resistance to microbial infection (11). The beneficial effect of IL-10 treatment for inflammatory conditions in both animal models and clinical diseases (recent review; Ref.9) suggests that the key functions of IL-10 are to maintain homeostasis of the immune system and to protect the host from excessive inflammation.
IL-10 gene regulation can occur both at the transcriptional and posttranscriptional levels (9, 12). However, current understanding of the mechanisms in IL-10 gene regulation remains rudimentary. A recent study from our laboratory (13) revealed that IL-10 and the protooncogene c-Maf induce their mutual expression in inflammatory macrophages, and c-Maf is a strong suppressor of IL-12 p40 gene transcription. c-Maf is the cellular counterpart of oncogenic v-Maf, which was identified originally in the genome of the acute transforming avian retrovirus AS42 and induces musculoaponeurotic fibrosarcoma (Maf)3 in vivo and transforms primary chicken embryo fibroblast in vitro (14). c-Maf belongs to the family of basic region leucine zipper domain transcription factors, and the cell lineage-specific targets of c-Maf have been identified; some examples include the following: IL-4 in Th2 cells (15), the crystalline genes in lens fiber cells (16, 17), insulin gene in islet cells (18), p53 (19), and L7 (20). In all these genes, c-Maf exerts its transcriptional role through binding to a Maf recognition element (MARE) (21). There are two forms of human c-Maf mRNA, c-Maf-long and c-Maf-short, as the result of differential splicing (22, 23). The first direct in vivo demonstration of a physiological role of c-Maf was provided by studies in c-Maf-null mice (16, 17, 24). Disruption of the c-Maf gene affected both intrauterine and postnatal survival (17). In addition, it has been shown that c-Maf is one of the master regulators for Th2 differentiation (15, 25), Therefore, c-Maf is both a developmentally and immunologically important gene. In the present study, we further investigated the molecular mechanisms by which c-Maf regulates IL-10 gene transcription in macrophages.
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Materials and Methods |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionDisclosuresReferences |
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c-Maf –/– mice were kindly provided by Dr. I. Cheng Ho of Harvard School of Public Health (Boston, MA) (17). Fetal liver-derived macrophages were prepared from gestation day 14.5 embryos by intercrossing c-Maf +/– mice as described previously (13).
Cells and reagents
RAW264.7 murine macrophage cell line (ATCC TIB-71), human monocytes isolation, and culturing were conducted as described previously (26). LPS (Escherichia coli serotype 0127:B8) was purchased from Sigma-Aldrich (catalog no. L-3129). The Abs were as follows: c-Maf (catalog no. A300-613A; Bethyl Laboratories), c-Maf (M153, sc-7866x; Santa Cruz Biotechnology), and c-fos (sc-52x; Santa Cruz Biotechnology). Recombinant human IL-4 and IFN- were purchased from Genzyme.
Reporter plasmids
The human IL-10 promoter-luciferase construct (pIL-10 (–1044/+30)-luc) was generously provided by Dr. L. Zaiegler-Heitbrock of University of Leicester (Leicester, U.K.) (27). For generation of the 5' successive deletion series, the upstream and downstream PCR primers were designed to include BamHI and XhoI restriction sites, respectively. The PCR products were ligated directly into pCR2.1 T/A vector and then subcloned into the same backbone of pIL-10 (–1044/+30)-luc plasmid by using BamHI/XhoI digestion. For the substitution mutants, an overlapping PCR procedure was used (28) by using a pair of overlapping internal primers that contain the mutant sequences. All constructs are relative to the transcriptional initiation site and confirmed by sequencing against the human IL-10 promoter (GenBank accession no. Z30175; Ref.29). The murine IL-4 promoter-driven luciferase construct, pIL-4 (–157/+68)-luc, was kindly provided by Dr. Richard Flavell of Yale University (New Haven, CT) (15). For the chimeric promoter constructs, the consensus MARE, 5'-TGCTGACTCAGCAACATTGTTGCTGACTCAGCAC-3'; –203/–170 wild type, 5'-TCATTTTTGCTTACGATGCAAAAATTGAAAACTA-3'; and –203/–170 mutant (M7), 5'-TCATTTTGTAGGCATCGTACAAAATTGAAAACTA-3' (core element underlined) were ligated to the upstream of the minimal herpes simplex virus thymidine kinase (TK) promoter (–109/+18)-luciferase vector, pTKluc (30), in both forward and reverse orientations. All plasmids were isolated using the Qiagen EndoFree Maxi kit (Qiagen).
Expression vectors for transcription factors
c-Maf expression vector (pCEFL/c-Maf) and its control vector (pCEFL) have been described before (23). There are two forms of c-Maf proteins as a result of alternative splicing: c-Maf-long and c-Maf-short (22, 23). The v-Maf dominant-negative mutant (DNM), Mxi-v-Maf, was kindly provided by Dr. K. Katoka (Tokyo Institute of Technology, Tokyo, Japan). Mxi-v-Maf is a fusion protein consisting of amino acids 1–70 of human Mxi1 that contains the Sin3 interaction domain fused to amino acids 19–369 of v-Maf, and this chimeric protein can bind to MARE sequence; however, Mxi1-Sin3 interaction domain masked the function of the Maf transactivation domain, thus acting as a DNM (31, 32). The Mxi-v-Maf is in the pGEM-4 vector (31).
Transient transfection and reporter assays
RAW264.7 cell transfections were performed by electroporation and followed by luciferase assay as described before (13). Results are expressed generally as mean ± SD from two to three independent experiments. All statistical analyses were performed with two-tailed Student’s t tests. Data were considered significant if p was <0.05.
Adenovirus-based expression vectors
Adenoviruses harboring human c-Maf-internal ribosomal entry site-enhanced green fluorescent protein (EGFP) or EGFP alone and their transduction of human monocyte-derived macrophages were as described before (13).
Chromatin immunoprecipitation (ChIP) assay
ChIP assay was performed by following the protocol in the ChIP Assay kit (Upstate Biotechnology). The presence of a selected DNA sequence of the human IL-10 gene was assessed by PCR. The primers used were sense (–206/–188), 5'-CAATCATTTTTGCTTACGA-3', and antisense (–147/–132), 5'-CCTTAGAGCTCCTCCT-3' (65-bp product). As a negative control, a separate region of the human IL-10 promoter was also included in the ChIP experiment. It is located between –3158 and –2947 upstream of the –206/–132 region. The pair of PCR primers used in this control were sense, 5'-AGTGAGAAGGCAGGCACCTA-3', and antisense, 5'-ATCCCCCACTGGAAAAATTC-3'. The PCR cycles were as follows: 95°C for 3 min, 60°C for 40 s, and 72°C for 30 s, 1 cycle; 95°C for 30 s, 60°C for 30 s, and 72°C for 30 s, 29 cycles; and 72°C for 7 min, 1 cycle.
RNase protection assay (RPA)
Total RNA was purified using Ultraspec RNA isolation system (Biotecx Laboratories). RPA was performed by using the Riboquant kit (BD Pharmingen), according to the manufacturer’s instructions. The mCK-2b and hCK2 template sets were used. The respective cytokine mRNAs were quantified by using the PhosphorImager and ImageQuant (ImageQuant 5.0; Molecular Dynamics) and normalized to the corresponding L32 and GAPDH controls.
Cytokine production by ELISA
BD Pharmingen OptEIA sets for mouse IL10, human IL-10, and human IL-12p40 were used.
Nuclear extract and recombinant human c-Maf
Nuclear extracts were isolated as described previously (33). The recombinant human c-Maf protein was synthesized by using pTNT Quick Coupled transcription/Translation System (Promega). In brief, both human c-Maf-long and -short form cDNA were cloned individually into pTNT vector under the T7 promoter and named pTNT/c-Maf and then proceeded to the pTNT reaction following the instruction.
EMSA
EMSA, competitive EMSA, and supershifts were performed as described previously (34). The following oligonucleotides were used as probes: MARE consensus, 5'-GGAATTGCTGACTCAGCATTACT-3'; –203/–170, 5'-TCATTTTTGCTTACGATGCAAAAATTGAAAACTA-3' (core element underlined); and NF-
B consensus, 5'-ATGTGAGGGGACTTTCCCAGGC- 3'.
Computational analysis of the IL-10 promoter region
Human IL-10 promoter region –1044/+30 was analyzed by the MatInspector V2.2 professional program (35) to predict transcription factor binding sites.
RT-PCR analysis of gene expression
Reverse transcription reactions were performed as previously described (13), and the following primers were used for PCR: human IL-10 (GenBank accession no. M57627) forward (position 104–129), 5'-AGTCTGAGAACAGCTGCACCCACTTC-3', and reverse (position 297–318), 5'-GGGCATCACCTCCTCCAGGTAA-3' (215-bp product, annealing temperature 60°C, 30 cycles). Because the cDNA sequences of c-Maf-short and c-Maf-long are identical until the position 1925 (22), the same upstream PCR primer for the two forms of c-Maf was used: sense (position 1571–1592), 5'-TGCACTTCGACGACCGCTTCTC-3'; antisense-short form (position 1957–1938), 5'-GGTGGCTAGCTGGAATCGCG-3' (GenBank accession no. AF055376, 386-bp product, annealing temperature 60°C, 
30 cycles); and antisense-long form (position 2040–2011), 5'-TGTACAGCTCTCACACAAATTTCATTTTGT-3' (GenBank accession no. AF055377, 469-bp product, annealing temperature 60°C, 30 cycles). Human GAPDH (GenBank accession no. M33197) was used as an internal control: sense (position 80–99), 5'-GAGTCAACGGATTTGGTCGT-3'; and antisense (position 298–317), 5'-TTGATTTTGGAGGGATCTCG-3' (238-bp product, annealing temperature 60°C, 28 cycles).
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Results |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionDisclosuresReferences |
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To characterize the role of c-Maf in the IL-10 gene expression in macrophages, we first examined the IL-10 mRNA expression in c-Maf –/– macrophages stimulated with LPS over a time course from 0 to 8 h. c-Maf mutant macrophages showed significantly impaired IL-10 mRNA expression relative to wild-type littermate macrophages after LPS stimulation throughout the time course (Fig. 1A), confirming our previous reporting (13). To address the question of whether c-Maf can activate the transcription of endogenous IL-10 gene in macrophages, a c-Maf overexpression approach was used. Human monocyte-derived macrophages were transduced with adenovirus-expressing human c-Maf or EGFP (as control).
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for 16 h, then treated with LPS for 4 h. The endogenous IL-10 mRNA expression was detected by RT-PCR (Fig. 1B) and RPA (Fig. 1C). Compared with the control adenovirus, c-Maf transduction of primary macrophages significantly enhanced LPS- or IFN-/LPS-stimulated IL-10 mRNA expression (compare lanes 2 and 3 to 4 and 5, respectively, in Fig. 1, B and C). c-Maf adenovirus transduction alone did not induce the endogenous IL-10 gene transcription (Fig. 1A, lane 1). Ectopic c-Maf expression can activate IL-10 gene transcription
Additionally, to demonstrate the transcriptional role of c-Maf in the regulation of IL-10 gene expression, the human IL-10 promoter (–1044/+30)-driven luciferase reporter was cotransfected with the human c-Maf expression plasmid into the mouse macrophage cell line RAW264.7, which has been used extensively to study macrophage cytokine gene expression (36, 37). The result shows that ectopically introduced c-Maf dose dependently up-regulated the IL-10 promoter activity (Fig. 2A). The short and long forms of c-Maf worked at similar efficiencies in activating the IL-10 promoter activity (Fig. 2B). Thus, the c-Maf-long form was used for all subsequent experiments. Next, we wanted to define the role of the endogenous c-Maf in IL-10 transcription. To address this issue, we used the well-characterized v-Maf-DNM (38). Protein blast analysis (
www.ncbi.nlm.nih.gov/BLAST/
) indicated that the bZIP-Maf identity between v-Maf (GenBank accession no. NP062191) and mouse c-Maf (GenBank accession no. I57555) or human c-Maf-short form (GenBank accession no. AAC27037 or human c-Maf-long form (GenBank accession no. AAC27038 is 98, 99, and 98%, respectively. These high degrees of homology suggest that v-Maf-DNM may be able to functionally block mammalian c-Maf. To verify whether the v-Maf-DNM, Mxi-v-Maf, could block the function of mammalian c-Maf, we first tested its activity on a mouse IL-4 promoter-driven luciferase reporter that has been shown to respond to c-Maf (15). The cotransfection of pIL-4 (–157/+68)-luc with c-Maf or c-Maf plus Mxi-v-Maf into RAW264.7 cells showed that Mxi-v-Maf strongly blocked the c-Maf-induced IL-4 transcription (data not shown), confirming its cross-species efficacy. We then cotransfected the pIL-10(–1044/+30)-luc with c-Maf or c-Maf plus Mxi-v-Maf. As shown in Fig. 2C, Mxi-v-Maf completely blocked ectopic c-Maf-induced IL-10 transcription. Moreover, when we cotransfected pIL-10(–1044/+30)-luc with Mxi-v-Maf into RAW264.7 cells, it also completely inhibited the constitutive as well as LPS-induced IL-10 promoter activity (Fig. 2D), suggesting that the endogenous c-Maf present in RAW264.7 cells (13) is not only required for LPS-induced IL-10 gene expression but also contributes to the basal level of IL-10 transcription.
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To identify the c-Maf response element(s) in the IL-10 promoter, a series of the 5' deletion mutants of IL-10 promoter-driven luciferase constructs were cotransfected with the c-Maf expression plasmid into RAW264.7 cells, and the luciferase activities were plotted relative to the activity of the full-length promoter (–1044/+30), which was set arbitrarily as 100%. Two constructs, –408 (no. 8) and –171 (no. 12) (Fig. 3), showed considerable decrease in their response to c-Maf, suggesting that the regions –511/–408 and –206/–171 may harbor c-Maf-responsive element(s). The complete loss of promoter activity in the –61 construct (no. 16) was likely due to the fact that the truncation was in the proximity of TATA-box, which is located at –59/–54 (see Fig. 5A for details).
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The above 5' deletion mutants have narrowed down the c-Maf-responsive elements to two possible regions on the IL-10 promoter. We then localized the exact c-Maf binding site on the IL-10 promoter by EMSA. Kataoka et al. have identified two types of DNA consensus sequences that are bound by v/c-Maf homodimers, a 13-bp TRE-type MARE and a 14-bp cyclic AMP-responsive element-type MARE. The former MARE contains an AP-1 (TGCTGACTCAGCA) binding site, whereas the latter harbors a cyclic AMP-responsive element (TGCTGACGTCAGCA) site (core element underlined). Computational analysis with the MatInspector V2.2 program (35) indicated that there is a putative Maf binding site located at –196/–184. To determine whether c-Maf could bind to the –206/–171 region, recombinant c-Maf protein (long form) was synthesized using the pTNT system, and it has been reported that the synthesized c-Maf protein from homodimers (15). A reciprocal competitive EMSA was used, i.e., by using 32P-labeled double-strand oligos in IL-10 promoter as probes and competed by the MARE consensus sequence, or the other way around, using the 32P-labeled MARE consensus sequence as the probe, then competed with the double-strand oligos derived from the IL-10 promoter. Three sets of double-strand oligos (–490/–470, –467/–435, and –430/–402) were used to cover the first c-Maf-responsive region (–511/–408) and one set of oligos to cover the second responsive region (–203/–170) based on the computational analysis. The three pairs of oligos (–490/–470, –467/–435, and –430/–402) that cover the first potential region (–511/–408) didn’t show any specific binding that could be competed off by cold MARE competitor, nor could they compete for binding to the MARE sequence (data not shown). However, for the second region, the –203/–170 probe formed a specific complex with recombinant c-Maf (Fig. 4A, lane 2, indicated by a black arrow), which could be efficiently competed off by an excess of cold –203/–170 sequence (Fig. 4A, lane 3, "self") or the consensus MARE sequence (Fig. 4A, lane 4, "non-self") but not by an irrelevant sequence (NF-B consensus; Fig. 4A, lane 5). Conversely, the MARE consensus sequence probe displayed very similar binding properties (Fig. 4B), indicating that the binding activities to the –203/–170 in human IL-10 promoter were comparable to the MARE consensus sequences. To further corroborate that this 13-bp (–196/–184) was a c-Maf-specific binding element, a series of 4- or 5-bp substitution mutants (M1–M6) or the entire 13-bp (–196/–184) substitution mutant (M7) were used as competitors against the wild-type –203/–170 probe for EMSA (Fig. 4C). As shown in Fig. 4D, M1 and M3–M6 oligos were able to compete off the majority of the c-Maf-binding activity against the wild-type probe, whereas M2 and the more extensive M7 oligos completely lost their ability to bind c-Maf. To verify the identity of the binding activity to the –203/–170 probe, a supershift assay was conducted using two sources of anti-c-Maf Abs. A c-Maf Ab (Bethyl Laboratories) strongly supershifted the complex (Fig. 4E, lane3), whereas the second c-Maf Ab (Santa Cruz Biotechnology) completely ablated this binding (Fig. 4E, lane 4), consistent with the reported behavior of these Abs (22). However, an anti-c-fos Ab did not have any effect on this complex (Fig. 4E, lane 5). Thus, these results confirm that c-Maf binds to the 13-bp MARE-like sequence located at –196/–184 of the IL-10 promoter with the most critical sequence motif of CTTAC. Similar results were obtained in the reciprocal competitive EMSA using RAW264.7 or human monocyte nuclear exact (data not shown). However, supershift with the nuclear extracts did not yield a clear confirmation (data not shown). We reasoned that this failure might be due to the low levels of endogenous c-Maf. Indeed, when we used nuclear extracts from RAW264.7 cells transiently transfected with the c-Maf expression vector to overexpress c-Maf, we did see a clear supershift (Fig. 4F, lane 3, indicated by the asterisk) or diminished the binding (Fig. 4F, lane 4). When we used nuclear extracts from HEK293 cells transduced with c-Maf-expressing adenovirus, which could render much higher gene expression in target cells, a very clear supershift or abrogation was observed by two anti-c-Maf Abs (Bethyl Laboratories and Santa Cruz Biotechnology; Fig. 4G, lanes 2 and 3, respectively) but not of anti-c-fos Ab (Fig. 4G, lane 4).
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To determine whether c-Maf could bind to the MARE-like sequence in the IL-10 promoter in vivo, ChIP assay was performed. This technique can establish whether a known transcription factor binds in the vicinity of a known regulatory element in living cells (39). As Fig. 5 demonstrates, in primary human monocyte-derived macrophages, c-Maf specifically bound to the IL-10 promoter in this region in vivo between –206 and –132 (Fig. 5B) but not to a separate region 3 kb upstream (Fig. 5C). Surprisingly, the binding was not inducible by LPS stimulation over a period of 30 h (Fig. 5D). The above data collectively suggest that c-Maf can bind to the –203/–170 sequence both in vitro and in vivo, and the core element for this binding resides in the 13-bp region at –196 to –184 in human IL-10 promoter.
The –196/–184 sequence acts as an enhancer
The above results provided evidence that –196/–184 in human IL-10 promoter is a MARE-like sequence. To test the function of this element in the induction of IL-10 promoter activity by c-Maf, a reporter construct with a 13-bp substitution (M7) was constructed on the backbone of –206/+30 of the IL-10 promoter. Compared with pIL-10 (–206)-luc, the response of pIL-10(–206)M7-luc to c-Maf was decreased by >50% and down to the level of the –171/+30 construct (Fig. 6A). Additionally, to characterize the function of this c-Maf response element, chimeric promoters were generated (Fig. 6B). Transient transfection of these constructs with c-Maf expression plasmid was performed in RAW264.7 cells. As shown in Fig. 6B, in the forward orientation, although the wild-type –206/–170 sequence, which contains the MARE-like element, was less potent in the response to c-Maf than that of the consensus MARE-containing TK promoter, the 13-bp M7 mutation resulted in a complete loss of its c-Maf response, decreasing to the basal level (Fig. 6B, upper panel). In the reverse orientation, although wild-type –206/–170 TK chimeric promoter showed an even greater response to c-Maf, the M7 mutant was still nonresponsive (Fig. 6B, lower panel). Taken together, these data additionally demonstrate that the 13-bp MARE-like sequence is a functional c-Maf response element; moreover, because it works in an orientation-independent manner, it may act as an enhancer element for IL-10 transcription.
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Additionally, we explored the physiological relevance of this transcription regulation, i.e., under what circumstance(s) is this c-Maf-mediated transcriptional regulation invoked? It is well known that inflammatory macrophages can be deactivated by IL-4 or IL-13 and play important roles in humoral immunity, homeostasis, and tissue injury repair (40, 41). On the basis of the established role of IL-4 in transcriptional regulation of c-Maf in Th cells (42, 43), we asked the two following questions: 1) Does IL-4 influence IL-10 production in human monocytes/macrophages? 2) Does IL-4 modulate c-Maf expression in human monocytes/macrophages?
To address the first question, human monocytes were treated with LPS or LPS + IL-4 and added at different time points relative to LPS. There was a differential impact of the IL-4 exposure on LPS-induced IL-10 and IL-12 p40 production. Addition of IL-4 together or 2 h after LPS stimulation enhanced IL-10 production (Fig. 7A) while strongly inhibiting IL-12 p40 production (Fig. 7B). IL-4 added at 16 h before LPS strongly enhanced IL-12 p40 and p70 (data not shown) synthesis, which is consistent with our previous report of the priming effect of IL-4 on IL-12 production (44). Furthermore, IL-4 added at +2 h dose dependently enhanced LPS-induced IL-10 production (Fig. 7C) while strongly suppressing IL-12 p40 production (Fig. 7D). These results are consistent with the reported effects of IL-4 on endotoxin-induced IL-10 production in murine macrophages (45). To address the second question, we examined the effect of IL-4 on the regulation of c-Maf mRNA expression. Human monocytes were treated with IL-4 in different doses for 2 h, and the total RNA was isolated for RT-PCR. Fig. 7E shows that IL-4 dose dependently stimulated c-Maf expression (both short and long forms) in resting monocytes, indicating that, as with Th cells (42, 43), IL-4 regulates c-Maf transcription also in macrophages. Control experiments in the nonadherent portion of the human PBMC with the same treatment indicated that the c-Maf mRNA expression observed was derived predominantly from monocytes and not from lymphocytes (data not shown). Additionally, we characterized the effect of LPS, IL-4, and LPS + IL-4 on the c-Maf mRNA expression. Human monocytes were treated with LPS, IL-4, or LPS + IL-4 for 8 h (at this time point, IL-10 mRNA reaches its peak (data not shown)). The total RNA was isolated for RT-PCR. Fig. 7F shows the following: 1) c-Maf was expressed constitutively in resting monocytes; 2) at 8 h, LPS did not stimulate an enhancement in c-Maf mRNA expression; and 3) IL-4 treatment enhanced and IL-4 + LPS further augmented c-Maf expression. ChIP assay in human monocytes also showed that IL-4 could by itself induce endogenous c-Maf binding to the IL-10 promoter at the MARE, even to a greater extent than LPS (compare lane 3 to lane 2 of Fig. 7G), and the LPS + IL-4 combination had an additive effect (Fig. 7G, lane 4). An important point to note is that although IL-4 alone stimulates high c-Maf expression, it is insufficient to induce IL-10 production by itself, and LPS treatment is required (Fig. 7A). This observation is consistent with the data shown in Fig. 1B, where we found that c-Maf adenovirus-mediated c-Maf overexpression alone did not induce IL-10 gene expression. Only by working together with LPS can the endogenous IL-10 gene be turned on. Furthermore, to investigate the role of c-Maf in IL-4-enhanced IL-10 expression, c-Maf-null macrophages were treated with LPS, IL-4, or LPS + IL-4. As shown in Fig. 7H, LPS-induced IL-10 production was enhanced strongly by IL-4 in cells heterozygous for c-Maf (p = 0.0086) but not in c-Maf–/– littermate-derived cells (p = 0.1453), demonstrating that c-Maf is at least partially required for IL-4-enhancement of LPS-induced IL-10 production.
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Discussion |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionDisclosuresReferences |
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A-crystallin promoter. The coactivation of c-Maf by CREB-binding protein/p300 requires histone acetyltransferase activity for crystalline gene expression (50), and their recruitment could modulate the chromatin structure, exposing the cis-elements for access by LPS-induced transcription factors and then turn on the IL-10 gene. Gene regulation is a complex process that involves the coordinated integration of distinct signal transduction pathways. Although c-Maf is essential for IL-10 transcription, c-Maf itself is not enough, and its ability to do so still requires LPS stimulation. This situation is analogous to many other factors that have been shown to be involved in the transcription of IL-10, e.g., CREB-1, activating transcription factor-1 (51, 52), C/EBP (53), SV40 promoter 1 (6, 54), SV40 promoter (55), and STAT3 (27). All these factors require an accompanying LPS stimulation, suggesting that multiple signal transduction pathways are involved in the activation of IL-10 expression (56). Furthermore, LPS-induced IL-10 gene transcription requires de novo protein synthesis because cycloheximide treatment before LPS stimulation can completely block IL-10 gene induction (6). Thus, we think that c-Maf works in concert with LPS-induced, yet-to-be-identified factors to activate the IL-10 gene. In support of this hypothesis, blocking AP-1 or CREB by AP-1-specific DNM (A-Fos) or CREB-DNM (57) strongly interfered with the capacity of c-Maf to activate IL-10 transcription (data not shown).
There is increasing evidence indicating that macrophages are a diverse and dynamic population of cells that can be activated through a number of distinct pathways and participate in a wide range of critical functions (41). In this study, we demonstrated that the IL-10-enhancing effect of IL-4 in LPS-activated human monocytes (Fig. 7, A and C) is similar to that shown in mouse macrophages (45). Then we investigated the modulation of c-Maf by IL-4 in human monocytes because it was reported that IL-4 could up-regulate c-Maf through Stat6 in Th cells (42). Our data demonstrates that IL-4 can regulate c-Maf expression and its binding to IL-10 promoter in human macrophages. Moreover, the characteristics of IL-4-enhanced IL-10 production (Fig. 7C) not only correlate well with its ability to stimulate c-Maf expression (Fig. 7E) in human monocytes but also show direct dependency on c-Maf (Fig. 7H). Considering that c-Maf is an essential transcription activator for IL-10 gene transcription, our data suggests that IL-4, which is derived mainly from activated Th2 cells, may exert its macrophage-regulating activity through stimulation of c-Maf. This idea is supported by the c-Maf overexpression experiment in human monocyte-derived macrophages, in which c-Maf overexpression enhanced LPS-induced IL-10 expression (Fig. 1, B and C), and by the study in c-Maf-null macrophages where rIL-4 failed to enhance LPS-induced IL-10 production (Fig. 7H).
Inflammation is a complex response, and it is an attempt to restore homeostasis (58). Macrophages are one of the main players in inflammatory immune responses. In this study, we demonstrated that c-Maf is an essential transcription factor for IL-10 production in inflammatory macrophages. This observation, together with our previous report that c-Maf is an inhibitor of IL-12 production, suggests that it may be an important factor in the homeostatic regulation. Our findings are one step further to understanding the intriguing and complex mechanisms of macrophage-gene regulation.
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Disclosures |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionDisclosuresReferences |
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Acknowledgments |
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Footnotes |
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1 This work was supported by National Institutes of Health Grant CA100223 (to X.M.). S.C. was supported in part by a Susan G. Komen Breast Cancer Foundation Postdoctoral Fellowship. 
2 Address correspondence and reprint requests to Dr. Xiaojing Ma, Department of Microbiology and Immunology, Weill Medical College of Cornell University, 1300 York Avenue, New York, NY 10021. E-mail address: xim2002{at}med.cornell.edu
3 Abbreviations used in this paper: Maf, musculoaponeurotic fibrosarcoma; MARE, Maf recognition element; TK, thymidine kinase; DNM, dominant-negative mutant; EGFP, enhanced green fluorescent protein; ChIP, chromatin immunoprecipitation; EMSA, electrophoretic mobility shift assay; RPA, RNase protection assay; TRE, 12-O-tetradecanoate-13-acetate-responsive element.
Received for publication October 28, 2004. Accepted for publication January 10, 2005.
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J. W. Leavenworth, X. Ma, Y.-y. Mo, and M. E. Pauza SUMO Conjugation Contributes to Immune Deviation in Nonobese Diabetic Mice by Suppressing c-Maf Transactivation of IL-4 J. Immunol., July 15, 2009; 183(2): 1110 - 1119. [Abstract] [Full Text] [PDF]
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J. Xu, Y. Yang, G. Qiu, G. Lal, Z. Wu, D. E. Levy, J. C. Ochando, J. S. Bromberg, and Y. Ding c-Maf Regulates IL-10 Expression during Th17 Polarization J. Immunol., May 15, 2009; 182(10): 6226 - 6236. [Abstract] [Full Text] [PDF]
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J. Dong, C. Ivascu, H.-D. Chang, P. Wu, R. Angeli, L. Maggi, F. Eckhardt, L. Tykocinski, C. Haefliger, B. Mowes, et al. IL-10 Is Excluded from the Functional Cytokine Memory of Human CD4+ Memory T Lymphocytes J. Immunol., August 15, 2007; 179(4): 2389 - 2396. [Abstract] [Full Text] [PDF]
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K. J. Staples, T. Smallie, L. M. Williams, A. Foey, B. Burke, B. M. J. Foxwell, and L. Ziegler-Heitbrock IL-10 Induces IL-10 in Primary Human Monocyte-Derived Macrophages via the Transcription Factor Stat3 J. Immunol., April 15, 2007; 178(8): 4779 - 4785. [Abstract] [Full Text] [PDF]
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Z. Yang, D. M. Mosser, and X. Zhang Activation of the MAPK, ERK, following Leishmania amazonensis Infection of Macrophages J. Immunol., January 15, 2007; 178(2): 1077 - 1085. [Abstract] [Full Text] [PDF]
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R. R. Flores, K. A. Diggs, L. M. Tait, and P. A. Morel IFN-{gamma} Negatively Regulates CpG-Induced IL-10 in Bone Marrow-Derived Dendritic Cells J. Immunol., January 1, 2007; 178(1): 211 - 218. [Abstract] [Full Text] [PDF]
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J. Shoemaker, M. Saraiva, and A. O'Garra GATA-3 Directly Remodels the IL-10 Locus Independently of IL-4 in CD4+ T Cells J. Immunol., March 15, 2006; 176(6): 3470 - 3479. [Abstract] [Full Text] [PDF]
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Z. H. Nemeth, C. S. Lutz, B. Csoka, E. A. Deitch, S. J. Leibovich, W. C. Gause, M. Tone, P. Pacher, E. S. Vizi, and G. Hasko Adenosine Augments IL-10 Production by Macrophages through an A2B Receptor-Mediated Posttranscriptional Mechanism J. Immunol., December 15, 2005; 175(12): 8260 - 8270. [Abstract] [Full Text] [PDF]
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M. Saraiva{paragraph}, J. R. Christensen, A. V. Tsytsykova, A. E. Goldfeld, S. C. Ley, D. Kioussis, and A. O'Garra Identification of a Macrophage-Specific Chromatin Signature in the IL-10 Locus J. Immunol., July 15, 2005; 175(2): 1041 - 1046. [Abstract] [Full Text] [PDF]
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, p < 0.01, compared with LPS treatment alone. E, Human monocytes were treated with different concentrations of IL-4 as indicated for 2 h, and total RNA was isolated for RT-PCR analysis of c-Maf expression (both short and long forms). GAPDH was analyzed as the internal control. F, Human monocytes were treated with IL-4 (1 ng/ml) or LPS (1 µg/ml) or both (IL-4 was added together with LPS) for 8 h, and total RNA was isolated for RT-PCR to examine the long- and short-form c-Maf mRNA expression. GAPDH was analyzed as the internal control. G, Human monocytes were treated with recombinant murine IL-4 (1 ng/ml) or LPS (1 µg/ml) or both (IL-4 was added at +2h) for 8 h, and ChIP assay was conducted as described in Fig. 5