Additional correspondence: Dr. Jianli Wang, Institute of Immunology, Zhejiang University School of Medicine, Medical Research Building B803, 388 Yuhang Tang Road, Hangzhou, Zhejiang 310058, China e-mail: email@example.com
Bone marrow-derived macrophages (BMMs) treated with granulocyte-macrophage colony-stimulating factor (GM-CSF) or macrophage colony-stimulating factor (M-CSF), differentiate into GM-CSF-induced mouse bone marrow-derived macrophages (GM-BMMs) or M-CSF-induced mouse bone marrow-derived macrophages (M-BMMs), which have an M1 or M2 profile, respectively. GM-BMMs produce large amounts of proinflammatory cytokines and mediate resistance to pathogens, whereas M-BMMs produce antiinflammatory cytokines that contribute to tissue repair and remodeling. M-BMMs stimulated with lipopolysaccharide (LPS) are in an antiinflammatory state, with an IL-12lowIL-10high phenotype. However, the regulation of this process remains unclear. Klf10 belongs to the family of Krüppel-like transcription factors and was initially described as a TGF-β inducible early gene 1. IL-12p40 is upregulated in LPS-stimulated M-BMMs from Klf10-deficient mice, but downregulated during Klf10 overexpression. Klf11, another member of the Krüppel-like factor family, can also repress the production of IL-12p40. Furthermore, Klf10 binds to the CACCC element of the IL-12p40 promoter and inhibits its transcription. We have therefore identified Klf10 as a transcription factor that regulates the expression of IL-12p40 in M-BMMs.
Macrophages are critical in inflammation, tissue regeneration, and tolerance. Macrophages can be generated from bone marrow cells treated with granulocyte-macrophage colony-stimulating
factor (GM-CSF) and macrophage colony-stimulating factor (M-CSF) [1, 2] and then induced to become GM-CSF-induced mouse bone marrow-derived macrophage (GM-BMMs) or M-CSF-induced mouse bone marrow-derived macrophages (M-BMMs), which have a M1 (classic activated macrophages) or M2 (alternative activated macrophages) profile. Cytokines are also involved in macrophage polarization. M1 macrophages are induced by IFN-γ, with or without lipopolysaccharides (LPS), whereas M2 macrophages are generated through IL-4 or IL-13 stimulation [1, 3].
GM-BMMs and M-BMMs have different patterns of cytokine expression. GM-BMMs produce large amounts of nitric oxide (NO) and proinflammatory cytokines involved in resistance to pathogens, whereas M-BMMs produce fewer proinflammatory cytokines but more antiinflammatory cytokines responsible for tissue repair and tumor progression [1-3]. However, the transcription factors that regulate macrophage polarization remain largely undefined. IRF5 has been reported to promote the expression of M1-related genes , whereas IRF4 and Klf4 can control M2 macrophage polarization by regulating the expression of specific M2 markers [5, 6]. In addition, LPS-stimulated M-BMMs are in an antiinflammatory state with an IL-12lowIL-10high phenotype . Therefore, regulation of inflammatory cytokines such as IL-12 is important in maintaining the steady state of M-BMMs.
IL-12 (IL-12p70), a heterodimeric cytokine comprising the p40 and p35 subunits, is an important cytokine produced mainly by antigen-presenting cells and can regulate innate responses during infection . IL-12 can also induce interferon-γ production and trigger CD4+ T-cell differentiation into type 1 T helper (Th1) cells . Moreover, IL-12 is a phenotypic marker for GM-BMMs  and the ratio of IL-12 to IL-10 production is often used to define GM-BMMs and M-BMMs . Macrophages derived from IL-12p40-deficient mice have a bias toward M2 polarization . IL-12p40, a subunit shared by IL-12 and IL-23, is produced predominantly by activated monocytes, macrophages, and dendritic cells. Higher levels of the IL-12p40 subunit is produced than IL-12 and IL-23 heterodimers , the production of which is regulated by strict mechanisms. NF-κB family members are activated in the production of IL-12p40 . Several IFN-regulatory factors (IRFs) such as IRF5 and IRF8 are involved in IL-12p40 expression [13, 14]. Moreover, the CCAAT/enhancer-binding protein (C/EBP) family, including C/EBP α and C/EBP β, inhibits the production of IL-12p40 [15, 16].
The Krüppel-like factors (KLFs) are a family of transcriptional regulators with a highly conserved DNA-binding domain that consists of three C2H2-type zinc fingers capable of binding to a CACCC element or GC box consensus sequences [17, 18]. KLFs play different roles in biology through their divergent non-DNA-binding regions that function as trans-activation or trans-repression domains. A total of 17 members of mammalian KLFs have been identified thus far , some are found to play important roles in immune and hematopoietic cell biology by regulating gene transcription. For example, Klf1 (erythroid Krüppel-like factor) regulates β-globin expression during erythrocyte development [20, 21] and also affects IL-12p40 production in human macrophages . Klf4 has been reported as a key regulator in monocyte differentiation and macrophage activation [23-25]. Recent studies further demonstrated Klf4 as a novel regulator in M2 macrophage polarization .
Klf10 belongs to the KLF family and was initially identified in human osteoblasts as a TGF-β responsive gene . Thus, Klf10 is also called TGF-β inducible early gene 1 (TIEG1) . Osteoblasts from Klf10-deficient mice have been reported as defective in mineralization and in supporting osteoclast differentiation in vitro . Subsequent studies demonstrated that Klf10 is also essential in T-cell biology. Klf10 cooperates with Itch to regulate Foxp3 expression  and also regulates CD4+CD25− T cells and Treg cells by targeting TGF-β . TGF-β inhibits several LPS-induced inflammatory cytokines in macrophages  and contributes to resolve inflammation. Recent studies revealed that TGF-β also contributes to M2 macrophage polarization . However, as a TGF-β-induced gene, the function of Klf10 in innate immune cells such as macrophages has not been studied thus far.
Here, we demonstrate the role of Klf10 in regulating the production of inflammatory cytokines in M-BMMs. We found that Klf10 expression was downregulated upon TLR activation. The forced expression and loss function assay of Klf10 in M-BMMs revealed a repressive effect on IL-12p40. Moreover, we also observed a similar role for Klf11 as that of Klf10 in regulating IL-12p40 expression. Studies on this mechanism demonstrated that Klf10 inhibits the production of IL-12p40 by binding to the IL-12p40 promoter. Therefore, our observations support the importance of Klf10 as a key transcriptional repressor of inflammatory cytokines in M-CSF-induced macrophages.
Klf10 expression is downregulated upon TLR activation
Quantitative PCR (qPCR) analysis for the expression of the KLF family members in M-BMMs was conducted to determine whether the KLF family members can control the inflammatory factors in M-BMMs. The result shows that Klf3, Klf4, Klf6, Klf10, Klf11, and Klf13 have high mRNA level among all family members (Fig. 1A). We performed time course LPS treatment for M-BMMs to verify the response of these KLFs to innate immune stimuli. The qPCR results indicate that Klf3, Klf4, Klf6, and Klf13 exhibited a minor or no increase, whereas Klf10 and Klf11 significantly decreased (Fig. 1B). In addition, KLF expression and response to LPS were investigated in GM-BMMs, and the result was similar to that in M-BMMs (Supporting Information Fig. 1). The decline in Klf10 expression in M-BMMs was further verified by western blot analysis (Fig. 1C). This Klf10 downregulation can be induced by LPS even with a concentration as low as 10 ng/mL (Fig. 1D). LPS is a ligand for TLR4, which localizes on the cell surface. Klf10 expression also decreased when TLR3 and TLR9, located in intracellular vesicles , were activated by poly I:C and CpG (Supporting Information Fig. 2). TLR stimulation can result in NF-κB activation, and our observation reveals that Klf10 can respond sensitively to these TLRs. Klf10 is an NF-κB-targeted gene . Thus, we further demonstrate that Klf10 was downregulated in an NF-κB-dependent manner. We pretreated M-BMMs with BAY11–7082, an IκB-α inhibitor, to repress the NF-κB pathway and found that the decrease in Klf10 after LPS challenge can be abrogated (Fig. 1E). Meanwhile, the upregulation of inflammatory cytokines, such as IL-12p40 and IL-6, was abolished (Fig. 1E). These results indicate that klf10 may participate in TLRs and may control the production of inflammatory factors in M-BMMs.
Klf10 overexpression reduces production of IL12p40 in M-BMMs
Klf10 was overexpressed in M-BMMs to investigate whether it is involved in the regulation of inflammatory cytokines triggered by TLR4 signaling. The result shows that LPS-induced IL-12p40 was significantly inhibited at both the mRNA and protein levels, which also resulted in a decrease in IL-12p70. However, IL-12p35, the other subunit of IL-12p70, was unaffected (Fig. 2A). Other proinflammatory mediators, such as IL-6 and TNF-α, were slightly affected or unaffected by Klf10 (Fig. 2A and B). IL-10 is a key antiinflammatory factor that can suppress IL-12 and IL-6 expressions in M-BMMs. Thus, we found Klf10 had no effect on IL-10 (Fig. 2B), indicating that the suppression of IL-12p40 and IL-6 was not mediate by IL-10. These observations indicated that Klf10 overexpression inhibited the production of IL-12p40 induced by TLR4 signaling in M-BMMs.
Loss of Klf10 upregulates the production of IL-12p40 in M-BMMs
We further performed the loss of function assay with Klf10-deficient mice to verify the aforementioned observation. Surface markers of M-BMMs from WT and Klf10-deficient mice were first characterized by flow cytometry. The result reveal that the proportion of F4/80+CD11b+ mature M-BMMs did not differ between these two markers, indicating that Klf10 was not involved in the differentiation of M-BMMs (Supporting Information Fig. 3A). Moreover, we investigated the markers on M-BMMs such as costimulatory molecules CD80, CD86, TLR4 receptor, and MHC class II, and found that these markers were expressed normally (Supporting Information Fig. 3B). However, when we analyzed the inflammatory factors from these cells after LPS stimulation, IL-12p40 exhibited a significant upregulation at both the mRNA and protein levels in Klf10-deficient cells compared with that in WT cells (Fig. 3A). Meanwhile, the total IL-12p70 upregulated although the IL-12p35 subunit increased slightly, which was consistent with the result obtained from the klf10 over-expression assay (Fig. 3A). IL-12p40 is known to contribute to the production of NO  that is an important effect molecule of GM-BMMs, while here we found M-BMMs from klf10-deficient mouse released more NO as well (Fig. 3C), which may indicate a bias toward GM-BMM activation. The production of TNF-α and IL-10 did not exhibit a significant difference in M-BMMs from WT and Klf10-deficient mice, except for the slight increase of IL-6 (Fig. 3A and B). Type I interferon is reported to downregulate IL-12 expression [33, 34], while we found that expression of IFN-β was not evidently changed in our assay (Supporting Information Fig. 4). TGF-β is an inhibitor of IL-12 production , and its expression in Treg cells is downregulated in Klf10-deficient mice . However, we did not observe a decrease in TGF-β expression in M-BMMs of Klf10-deficient mice. The expression of several other specific markers linked with M-BMMs , such as CCL2, CCL5, CCL12, and CXCL10, were also investigated, and we found only a slight increase in CCL2 and CCL5 (Supporting Information Fig. 4). Moreover, we verified several markers in M-BMMs stimulated with IL-4, such as arginase-1 (Arg1), chitinase-like Ym1 (Chi3l3), found in inflammatory zone-1 (Fizz1, also called Retnla) and mannose receptor (Mrc1 encoding MR), and observed that they had similar expression levels in klf10-deficient and WT mice (data not shown). These results indicate that klf10 was not involved in the differentiation of M-BMMs but can repress the expression of IL-12p40 and IL-6 in these cells.
Loss of Klf10 does not affect the production of IL-12p40 in GM-BMMs
GM-BMMs can make more inflammatory factors than M-BMMs. Similar to other studies [7, 37, 38], we found that GM-BMMs produces more IL-12p40 and IL-6, but less IL-10 than M-BMMs (Fig. 4A). However, no differences were observed in the production of IL-12p40 and IL-6 in LPS-stimulated GM-BMMs between WT and Klf10-deficient mice compared with M-BMMs (Fig. 4A). Meanwhile, IFN-γ is reported as a priming agent for the enhancement of IL-12p40 production [14, 39]. The upregulation of IL-12p40 in Klf10-deficient mice compared with WT mice was also not found in GM-BMMs under the IFN-γ priming conditions (data not shown).
The expression of Klf10 in M-BMMs and GM-BMMs was first analyzed to investigate the reason for the aforementioned observations. However, no obvious difference was observed between them (Supporting Information Fig. 5). As shown above, GM-BMMs produce more inflammatory cytokines than M-BMMs. Deactivation of GM-BMMs was performed by using several inflammation inhibitors, such as dexamethasone, TGF-β, and IL-10, as previously described [40, 41], to investigate whether Klf10 functions in intense inflammation. The result shows that the expression of relevant cytokines decreased after deactivation. In addition, the expression of IL-12p40 and IL-6 was higher in GM-BMMs from Klf10-deficient mice than that from WT mice after deactivation (Fig. 4B). Moreover, the downregulation of Klf10 was abolished to some extent (Fig. 4C), which may enhance its inhibitive function on the cytokines. These data may indicate that Klf10 alone is insufficient to inhibit the inflammatory factors in GM-BMMs; other factors are possibly involved in the suppression of inflammation in deactivated GM-BMMs.
Klf11 plays similar roles as Klf10 in repressing IL-12p40 production
Klf11, another member of the KLF family, was also identified as a downregulated gene in LPS-stimulated M-BMMs. Klf11 is described as a TGF-β inducible early gene 2 and shares a highly conserved C-terminal DNA-binding domain with Klf10 . In addition, Klf10 and Klf11 have three repression domains in the N-terminal, which define them as a subfamily of repressor. We supposed that Klf11 may have a similar role in the regulation of inflammatory factors in M-BMMs. First, we found that overexpression of both Klf10 and Klf11 can inhibit the production of IL-12p40 and IL-6 in M-BMMs from WT mice and can rescue their overproduction in M-BMMs from Klf10-deficient mice (Fig. 5A). Therefore, we knocked down Klf11 through RNA-mediated interference. The efficiency of RNAi was confirmed by qPCR (Supporting Information Fig. 6A). The inhibition of Klf11 resulted in an increased production of IL-12p40 in WT cells, and this phenomenon was more notable in Klf10-deficient cells (Fig. 5B). Therefore, Klf10 and Klf11 may have a similar function in the regulation of IL-12p40. However, interference of Klf11 in the same conditions did not result in a significant change of IL-6 as that in the overexpression assay. Moreover, we used another SiRNA, as previously reported , to confirm the inhibitory function of Klf11 in the regulation of IL-12p40 (Supporting Information Fig. 6B and C). These data indicated that Klf11 can act similarly to Klf10 in the inhibition of IL-12p40 production.
Klf10 binds to the IL-12p40 promoter to inhibit its transcriptional activity
The KLF family members are characterized by a DNA-binding domain capable of binding to target genes to regulate their transcriptional activities and gene expressions. IL-12p40 promoter was sequenced to determine whether Klf10 can regulate the expression of IL-12p40 in a direct manner and a CACCC site was found therein (Fig. 6A). The binding site was highly conserved in mammals (Fig. 6B), similar to the CACCC-binding site of erythroid Krüppel-like factor in human macrophages. Subsequently, a series of luciferase reporter construct that can encode a WT IL-12p40 promoter (−283 to +99 bp), a mutant with 2-bp mutations in the CACCC site (at –233 bp), or a 5' deletion promoter construct (−223 bp) were constructed to investigate whether Klf10 can repress the transcription of IL-12p40. We found that Klf10 can significantly inhibit the transcriptional activity of the IL-12p40 promoter, but was unable to suppress the luciferase activity of these two mutants (Fig. 6C), suggesting that Klf10 may inhibit IL-12p40 by binding directly to the CACCC site of the promoter. ChIP assays were performed to determine whether Klf10 was recruited to the CACCC element of IL-12p40 promoter. Semi-qPCR and qPCR results verify that Klf10 can bind to the CACCC site of the IL-12p40 promoter (Fig. 6D and E). Therefore, we demonstrate that Klf10 inhibited the transcriptional activity of IL-12p40 by binding directly to the CACCC site of the IL12p40 promoter.
Macrophages are important mediators in immune responses to inflammation. The remarkable plasticity of macrophages has recently been the subject of intense investigation. M-CSF and GM-CSF are mediators involved in the regulation of macrophage heterogeneity. Macrophages induced by GM-CSF and stimulated with IFN-γ and LPS are characterized by a high expression of inflammatory cytokines and iNOS. By contrast, macrophages induced by M-CSF and then stimulated with IL-4 are responsible for the resolution of inflammation. Controlling the expression of inflammatory factors is critical in maintaining the antiinflammatory state in M-CSF-induced macrophages.
KLFs are important zinc finger transcription factors that can regulate the transcriptional activity of target genes, thereby affecting their expression. So far, Klf4 has been demonstrated to be critical during macrophage differentiation. Klf4 is expressed in a monocyte-restricted and stage-specific pattern during myelopoiesis . Recent studies identified Klf4 as a key regulator in M2 macrophage polarization . Klf4 is also related to macrophage activation. Klf4 overexpression can induce macrophage activation marker iNOS and inhibit TGF-β1 and Smad3 signaling .
Klf10, initially identified and named as TGF-β inducible early gene 1 in human osteoblasts , has been reported to have a critical role in T-cell biology [28, 29]. In this study, we demonstrated that Klf10 functions as a specific repressor to IL-12p40 in M-BMMs, whereas the expression of other cytokines, such as TNF-α and IL-10, were not obviously affected. IL-12p40 is a subunit shared by IL-12p70 and IL-23, and its regulation is important for both innate and adaptive immunity. IL-10 can suppress IL-12 by inhibiting the transcription of its encoding genes . TGF-β is also an inhibitor of IL-12 production through the reduction of the stability of IL-12 p40 mRNA . Type I interferons, such as IFN-α and IFN-β, can also inhibit the production of IL-12 . However, the aforementioned cytokines that regulate IL-12p40 were unaffected by Klf10 in our results. In addition, some transcription factors, such as IRF5, IRF8, C/EBP α, and C/EBP β, regulate the expression of IL-12p40. We found that the expression of these factors was not obviously affected in Klf10-deficient mice (data not shown). Therefore, Klf10 may directly regulate the expression of IL-12p40 in transcriptional levels. Most KLFs can bind to a CACCC element or a GC box sequence to regulate the transcription of target genes. We found a highly conserved CACCC element in the promoter of IL-12p40. Further studies through ChIP and luciferase reporter assays showed that Klf10 can bind to the CACCC site and inhibit the transcription of IL-12p40.
Klf10 is initially identified as a TGF-β responsive gene, and previous studies focused mainly on its roles in the TGF-β signaling pathway. Our study was the first to demonstrate the function of Klf10 in repressing IL-12p40 in M-BMMs upon TLR activation. TLRs can trigger intracellular signaling pathways, upregulate the expression of inflammatory factors and further contribute to the killing of microorganisms . Meanwhile, the TGF-β pathway is chiefly responsible for repressing the levels of inflammatory cytokines to maintain tolerance and to resolve inflammation . Although a deficiency in the expression of TGF-β in Treg cells from Klf10-deficient mice was reported, we did not observe a decrease in the expression of TGF-β in M-BMMs from Klf10-deficient mice (Supporting Information Fig. 4). This result indicates that Klf10 is unimportant in maintaining the expression of TGF-β in M-BMMs. TGF-β1 is a key factor involved in endotoxin tolerance, whereas smad3 and smad4 are also required in endotoxin tolerance [45, 46]. However, no obvious difference was observed between WT and Klf10-deficient cells in LPS-mediated endotoxin tolerance (Supporting Information Fig. 7). Therefore, Klf10 can inhibit the production of IL-12p40 in M-BMMs, which may not rely on the TGF-β pathway to some extent.
In conclusion, we demonstrate that Klf10 can repress the expression of IL-12p40 in M-CSF-induced macrophages and may help maintain the steady antiinflammatory state of such macrophages.
Materials and methods
Mice and reagents
C57BL/6 mice were purchased from Shanghai Slac Animal Inc. (Shanghai, China). Klf10-deficient mouse were originally from the laboratory of Dr. Thomas Spelsberg (Mayo Clinic, MN, USA). Mice were maintained in Experimental Animal Center of Zhejiang University. Experiments and animal care were performed in accordance with the guidelines of Zhejiang University. LPS (Escherichia coli 055:B5) and Poly I:C (P1038) were obtained from Sigma (St. Louis, MO, USA). Phosphorothioate-CpG ODN (5′-TCC ATG ACG TTC CTG ACG TT-3′) was synthesized by Sangon Biotech Co., Ltd. (Shanghai, China). Antibodies against Klf10 (sc-130408, sc-34544 X) were from Santa Cruz Biotechnology (Santa Cruz, CA, USA). HRP-conjugated anti-mouse IgG (7076) were from Cell Signaling Technology. Anti-mouse CD11b (M1/70), anti-mouse F4/80 (BM8), anti-mouse MHC Class II (M5/114.15.2), anti-mouse TLR4 (UT41), anti-mouse CD80 (16–10A1), and anti-mouse CD86 (GL1) antibodies were purchased from eBioscience (San Diego, CA, USA). The pGL-3 luciferase and pRL-TK-Renilla luciferase plasmids were from Promega (Fitchburg, WI, USA).
Recombinant vector encoding mouse Klf10 (mKlf10, GenBank Accession number NM_013692.2) and mouse Klf11 (mKlf11, GenBank Accession number NM_178357.3) were constructed by PCR-based amplification and subcloned into the pcDNA3 eukaryotic expression vector (Invitrogen, Carlsbad, CA, USA).
The primers were as followed:
Cell preparation and culture
Bone marrow cells were isolated from the tibia and femur and cultured in RPMI 1640 medium with 10% FBS (Hyclone, UT, USA), 2 mM glutamine, 100 units/mL penicillin-streptomycin, 10 ng/mL M-CSF (PeproTech, NJ, USA), or 20 ng/mL murine GM-CSF (R&D systems, MN, USA) at 37°C with 5% CO2 for 5 days to harvest M-BMMs or GM-BMMs, respectively. HEK293 cells were purchased from American Type Culture Collection (ATCC, Manassas, VA, USA) and cultured in DMEM supplemented with 2 mM glutamine, 100 units/mL penicillin and streptomycin, and 10% FBS at 37°C in the presence of 5% CO2.
Transient transfection into primary mouse bone marrow derived macrophage using Amaxa Mouse Macrophage Nucleofection kit (Cat. No. VPA-1009) was performed according to manufacturer's instruction. Transient transfection into HEK293 cells was performed by Lipofectamine 2000 (Invitrogen) according to the manufacturer's instruction.
To knock down Klf11 in M-BMMs from WT or klf10-deficient mouse, the ON-TARGET plus SMART pool mouse-TIEG3 (194655) or the negative control siRNA (Thermo Scientific Dharmacon, Lafayette, CO, USA) were transfected into M-BMMs using INTERFERinTM (Polyplus, Graffenstaden, France) according to the manufacturer's instruction. Another siRNA against Klf11 (5′- UGCAUGUGGACCUUUCGCUGUCAUG-3′) and control siRNA were synthesized by Shanghai GenePharma Co., Ltd. and were transfected using INTERFERinTM (Polyplus, Graffenstaden, France) according to the manufacturer's instruction.
RNA extraction and real-time qPCR
Total RNA was extracted using TRIzol reagent (Invitrogen, Cat. No.15596026). The cDNA was synthesized from total RNA using PrimeScript Reverse Transcriptase (Takara, Cat. No. DRR063A). Real-time PCR was accomplished with the ABI Prism 7500 analyzer (Applied Biosystems, Carlsbad, CA) using SYBR Premix Ex TaqTM (Takara, Cat. No. DRR041A). The corresponding primers were as follows:
Measurement of cytokines
Mouse IL-12p40, IL-12p70, TNF-α, IL-6, and IL-10 concentrations in cell culture supernatants were quantified by ELISA kits (eBioscience: IL-12/IL-23 total p40, Cat. No. 88–7100-22; IL-12p70, Cat. No. 88–7121-22; TNF-α, Cat. No. 88–7324-22; IL-6, Cat. No. 88–7064-22; IL-10, Cat. No. 88–7104-22) according to the manufacturer's instruction.
Detection of NO in culture supernatants
M-BMMs on day 5 from WT and Klf10-deficient mouse were stimulated with 1 μg/mL LPS for 12 and 24 h. Culture supernatants were analyzed for NO by the Griess reaction. Briefly, 50 μL supernatant was incubated with 50 μL Griess reagent for 5 min at room temperature, and NO2 level was determined by measuring the absorbance at 540 nm relative to the reference sample.
Whole cell lysates were prepared by complete Lysis-M kit (Roche; Cat. No. 04719956001) and the concentration was determined by the bicinchoninic acid protein assay (Thermo Scientific; Lot # MC 155209). The same amounts of protein were resolved on SDS-PAGE gels, transferred to polyvinylidene fluoride membrane. After blocking with 5% nonfat dry milk/PBS, the membranes were further incubated with the indicated primary antibodies overnight, reacted with a secondary antibody, and then protein bands were visualized by ECL.
Cells were harvested and incubated with relative antibodies for 30 min on ice, washed, and analyzed in a FACS calibur flow cytometer (Becton Dickinson).
Luciferase reporter assay
The promoter of IL-12p40 and its mutants were produced by PCR-based amplification and subcloned into the pGL3-Enhancer Vector to forming luciferase report plasmid.
Human embryonic kidney (HEK293) cells were cotransfected with 100 ng luciferase reporter plasmid, 10 ng thymidine kinase promoter-Renilla luciferase reporter plasmid, plus the pCDNA3-Klf10, or control vector. After 48 h, luciferase activities were determined by the Dual-Luciferase Reporter Assay System (Promega, Cat. No. E10910) according to the manufacturer's instructions.
The primers were as followed:
Chromatin-immunoprecipitation assays were done essentially as the manufacturer's protocol (Active motif, CHIP-ITTM Express). The immunoprecipitated DNA fragments were then analyzed by semi-qPCR and qPCR.
The primers used were as followed:
Data are presented as the mean ± SD. Statistical significance was determined by Student's t-test. A value of p < 0.05 was considered to be statistically significant.
We thank L. Lu for discussions; F. Xing for assistance with manuscript editing. This work was supported by grants from the National Basic Research Program of China (973 Program) (2012CB966603), the National Natural Science Foundation of China (J20111945), Zhejiang Provincial Natural Science Foundation of China (R20110298), Doctoral Fund of Ministry of Education of China (20110101120102), the Fundamental Research Funds for the Central Universities (2011QNA7001), and the National Technology Key Projects of China (008ZX1002-008).
Conflict of interest
The authors declare no financial or commercial conflict of interest.
GM-CSF-induced mouse bone marrow-derived macrophage
interferon regulatory factor
M-CSF-induced mouse bone marrow-derived macrophage