LPS induces IL-10 production by human alveolar macrophages via MAPKinases- and Sp1-dependent mechanisms
© Chanteux et al. 2007
Received: 21 September 2006
Accepted: 04 October 2007
Published: 04 October 2007
IL-10 is a cytokine mainly produced by macrophages that plays key roles in tolerance to inhaled antigens and in lung homeostasis. Its regulation in alveolar macrophages (HAM), the resident lung phagocytes, remains however unknown.
The present study investigated the role of intracellular signalling and transcription factors controlling the production of IL-10 in LPS-activated HAM from normal nonsmoking volunteers.
LPS (1–1000 pg/ml) induced in vitro IL-10 production by HAM, both at mRNA and protein levels. LPS also activated the phosphorylation of ERK, p38 and JNK MAPkinases (immunoblots) and Sp-1 nuclear activity (EMSA). Selective inhibitors of MAPKinases (respectively PD98059, SB203580 and SP600125) and of Sp-1 signaling (mithramycin) decreased IL-10 expression in HAM. In addition, whilst not affecting IL-10 mRNA degradation, the three MAPKinase inhibitors completely abolished Sp-1 activation by LPS in HAM.
These results demonstrate for the first time that expression of IL-10 in lung macrophages stimulated by LPS depends on the concomitant activation of ERK, p38 and JNK MAPKinases, which control downstream signalling to Sp-1 transcription factor. This study further points to Sp-1 as a key signalling pathway for IL-10 expression in the lung.
Strategically located on the alveolar surface, alveolar macrophages represent highly specialized macrophages that function primarily in lung defence against inhaled particle matter, microorganisms and environmental toxins. Among microorganisms, gram-negative bacteria and more precisely, the lipopolysaccharide (LPS) component of the outer cell wall, is a very potent activator of macrophages. LPS binds to LPS-binding protein and is delivered to the cell surface receptor CD14, before being transferred to the transmembrane signaling receptor toll-like receptor 4 (TLR4) and its accessory protein MD2 . LPS stimulation activates several intracellular signaling pathways including the three mitogen-activated protein kinase (MAPK) pathways: extracellular signal-regulated kinases (ERK) 1 and 2, c-Jun N-terminal kinase (JNK) and p38. These signalling pathways in turn activate a variety of transcription factors which coordinate the induction of many genes encoding inflammatory mediators as well as anti-inflammatory cytokines.
The control of inflammatory responses is critical to the host to allow resolution and avoid tissue damage. IL-10 is a key anti-inflammatory factor and pleiotropic cytokine produced by a variety of cell types among which monocytes/macrophages are the main sources . IL-10 mediates the inhibition of pro-inflammatory cytokines such as TNF-α, IL-8, IL-6, IL-1β, IL-12 [3–7]. IL-10 has also been shown to inhibit antigen-presenting cell function, including the maturation of dendritic cells  and the expression of MHC class II and co-stimulatory molecules [9, 10]. IL-10 gene regulation can occur both at the transcriptional and posttranscriptional levels . Several studies have shown that the transcription factor Sp1 plays an important role in IL-10 transcription (an Sp1 responsive element in the IL-10 promoter is localized at -89 to -78) [12–14]. Moreover, detailed studies showed that p38 mitogen-activated protein regulates LPS-induced activation of Sp1 in THP-1, a human monocytic cell line . The STAT3 transcription factor may also bind to an element in the IL-10 promoter gene and the use of a dominant negative form of STAT3 was able to decrease IL-10 transcription . More recently, the protooncogene c-Maf has been shown to be an essential transcription factor for IL-10 gene expression in macrophages  while a role for C/EBP in cooperation with Sp1 has also been suggested . However, the intracellular signalling pathways governing IL-10 gene regulation in human alveolar macrophages are poorly understood. Thus, alveolar macrophages are the main source of IL-10 in the alveoli where they play an important role to control lung homeostasis. One study on human alveolar macrophages  showed that activation of PKC decreases IL-10 production whereas activation of protein phosphatases PP1 and PP2A enhance IL-10 secretion. In the present work, we evaluate the ability of human alveolar macrophages to produce IL-10 upon LPS stimulation and the role of MAPkinases (ERK, p38 and JNK) and Sp1 transcription factor as intracellular signals leading to IL-10 expression.
LPS from Salmonella typhimurium, PMSF, Nonidet, DTT, BSA, Tween 20, Thiazolyl Blue Tetrazolium Bromide and Actinomycin D were purchased from Sigma (Sigma Chemical Co., St Louis, MO). PD98059, SB203580 were purchased from BioMol (Plymouth Meeting, PA) and SP600125 from AG Scientific (San Diego, CA). Anti-CD14 was purchased from R&D Systems (Abingdon, UK). All other reagents were from VWR International (Darmstadt, Germany).
Isolation of Human Alveolar Macrophages (HAM)
HAM were obtained from bronchoalveolar lavages from normal non smoking volunteers as previously described . Briefly, the lavage fluid was passed through a layer of sterile gauze to remove gross mucus and then centrifuged at 500 g for 10 min at 4°C to separate cells from fluid. The cell pellet was washed twice in complete culture medium : RPMI 1640 medium (Cambrex Corporation, East Rutherford, NJ) supplemented with 10% decomplemented (30 min at 56°C) FCS, 2 mM L-glutamine, 100 U/ml penicillin and 100 μg/ml streptomycin. HAM were >95% pure with less than 1% of neutrophils and monocytes. HAM were allowed to adhere during 30 min and non-adherent cells were removed by two washes.
Nuclear extract and Electrophoretic Mobility Shif Assay (EMSA)
Nuclear extracts were prepared from HAM as described by Carter with minor modifications as reported previously . 1.106 HAM were washed in cold PBS and collected in 400 μl of ice-cold EMSA lysis buffer (10 mM HEPES pH 7.9, 10 mM KCl, 2 mM MgCl2, 2 mM EDTA, 1 mM DTT, 1 mM PMSF) supplemented with 10 μg/ml of each protease inhibitors (leupeptin, aprotinin, pepstatin, trypsin inhibitor) and then incubated on ice for 10 min. Nonidet (NP-40) 10% was added to lyse the cells which were vortexed and centrifuged 1 min at 4°C at 13000 rpm. Nuclei were resuspended in 25 μl of extraction buffer (50 mM Hepes pH 7.9, 10% glycerol, 50 mM KCl, 300 mM NaCl, 0,1 mM EDTA, 1 mM DTT, 0.5 mM phenylmethylsulfonylfluoride and protease inhibitors) for 30 min on ice. The nuclear suspension was then centrifuged 3 min at 13000 rpm and supernatant stored at -70°C until use. Proteins were assayed using the Blue coomassie method. Sp1 consensus oligonucleotides (5'-ATTCGATCGGGGCGGGGCGAGC-3') were purchased from Invitrogen Life Technologies (Carlsbad, CA) and were 3' biotinylated using Biotin 3' End DNA Labeling Kit (Pierce, Rockford, IL) following manufacturer's instructions. EMSA was performed using the LightShift Chemiluminescent EMSA kit (Pierce, Rockford, IL). Briefly, 2, 5 μg of nuclear extract was incubated at room temperature during 20 min with 20 fmol of biotinylated double-stranded oligonucleotide in presence of 50 ng of salmon sperm and reaction buffer. The protein-DNA complexes were separated on a 7% non-denaturating polyacrylamide gel and bands were visualized using Biorad Chemidocs XRS apparatus (Bio-Rad Laboratories, Hercules, CA).
RNA extraction and real-time PCR
Total RNA was extracted from 106 HAM using TRIzol reagent (Invitrogen) and 2 μg of total RNA was used to generate first strand cDNA synthesis using Superscript II (Invitrogen/Life Technologies, Carlsbad, CA). The reaction mix containing 1 μg of RNA, poly-dT, and 10 mM dNTP mix was diluted to 24 μl in sterile water, heated to 65°C for 5 min, and chilled on ice for 1 min. First strand synthesis was then performed in 50 μl total reaction volume by adding 50 mM Tris (pH 8.3), 75 mM KCl, 3 mM MgCl2, 20 mM DTT, 40 U of RNaseout, and 200 U of Superscript II reverse-transcriptase enzyme (Invitrogen) at 42°C for 1 h. The reaction was inactivated by heating at 72°C for 10 min. cDNA was stored at -20°C until amplification. The quantitative PCR was performed by real-time PCR on a Lightcycler System (Roche Applied Science, Basel, Switzerland) using predevelopped primers set for human IL-10 (Search LC, GmbH Heidelberg, Germany). PCR conditions were those described in manufacturer's instruction. The reaction mix contains 5 μl cDNA, 1 mM of primers, water and Master mix (Faststart DNA Master plus Sybr Green I-Roche Applied Science) in a final volume of 20 μl. β-actin primers were designed following sequence published in GenBank (access number : M10277) in two different exons. They were synthesized by Life technologies : sense : 5'-gtgacattaaggagaagctgtgcta-3' (position : 2294–2317), antisense : 5'-cttcatgatggagttgaaggtagtt-3' (position : 2588–2612). PCR conditions were : denaturation at 95°C, 10 s – hybridization, 60°C, 5 s – elongation, 72°C, 7 s. After amplification step, a melting curve is performed to ensure that only one product has been amplified. Moreover, separation of the products on 2% agarose gel confirmed the size of the amplicon.
IL-10 was assayed in the supernatant by ELISA using a pair of antibodies (BD Biosciences, San Diego, CA) following manufacturer's instructions. The sensitivity of the ELISA was 1.5 pg/ml.
5 × 105 HAM were collected in 200 μl Laemmli sample buffer and heated at 100°C, 5 min to denature proteins. 20 μl of protein lysate was loaded onto a 12% SDS-PAGE gel and run at 180 V for 1 h. Cell proteins were then transferred to nitrocellulose (Hybond-C, Amersham Biosciences, UK) membrane at 70 mA for 1 h 30 at room temperature. Membrane was blocked with 5% BSA in TTBS (Tris-Buffered saline with 0.1% Tween 20) for 1 h at room temperature, washed, and then incubated with the primary Ab 1/1000(anti-phospho ERK, anti-phospho p38 or anti-phospho JNK – Cell Signaling Technology, Beverly, MA) overnight at 4°C. The blots were washed 3 × 5 min with TTBS and incubated for 1 h with HRP-conjugated anti-rabbit IgG Ab 1/2000(Cell Signaling Technology, Beverly, MA). Immunoreactive bands were revealed using a chemiluminescent substrate (ECL, Amersham Biosciences, UK) and chemiluminescence was detected with chemidoc XRS apparatus. The intensity of each blot was measured with the densitometry program Quantity One (Bio-Rad Laboratories, Hercules, CA).
IL-10 mRNA degradation assay
1 × 106 HAM/well were stimulated with LPS (1 μg/ml) for 16 h, translation was stopped by using Actinomycin D (2.5 μg/ml) and then, PD98059, SB203580 or medium (25 μM) was added for various time periods. HAM were collected for RNA extraction and real time PCR for IL-10 mRNA was performed.
2.5 × 105 HAM/well were incubated with PD98059, SB203580, SP600125 (25 μM) or medium for 24 h. Supernatants were discarded and 100 μl of Thiazolyl Blue Tetrazolium Bromide (MTT, 1 mg/ml) was added to the cells for 1 h. DMSO was then used to stop the reaction and optical density was read at 550 nm.
Comparisons were performed using two-tailed paired t test or Mann-Wittney U test as appropriate. All analyses were performed using a statistics software package (GraphPad Prism, PA, USA). p values < 0.05 were considered as statistically significant.
LPS induces IL-10 secretion in human alveolar macrophages
To check if IL-10 production is CD14 dependent, we used an anti-CD14 blocking antibody. Preincubation of HAM with a neutralizing anti-CD14 (10 μg/ml) totally inhibits LPS-induced IL-10 (data not shown).
Activation of MAPkinases by LPS
MAPkinases are crucial for IL-10 production
MTT-based cytotoxicity assay of MAPk inhibitors in HAM. HAM were incubated for 24 h with PD98059, SB203580, SP600125 or medium at different concentrations, and cell viability was assessed by using the MTT reduction assay, as described in Methods. Results are mean ± SD of one representative experiment in triplicates (expressed as % of control); *p value < 0.05 (one sample t-test).
Concentration of inhibitors
96.2 ± 20.26
92.7 ± 14.2
92.6 ± 19.5
93.4 ± 14
85.3 ± 34.6
104.9 ± 33.5
79.9 ± 14.2
104.1 ± 15.7
110.1 ± 11
122.3 ± 6.9
82.8 ± 7.2
89.3 ± 9
104.6 ± 20.6
66.2 ± 10.1*
65.2 ± 9*
Role of Sp1 transcription factor in the production of IL-10
Effects of MAPkinases and Sp1 inhibitors on IL-10 mRNA
To assess a potential effect of PD and SB inhibitors on post-transcriptional mechanisms of regulation for IL-10 production, real time PCR for IL-10 mRNA was performed in HAM treated with Actinomycin D. Figure 8, panel B shows that both MAPK inhibitors did not affect significantly IL-10 mRNA degradation following LPS stimulation.
Lung homeostasis relies on the equilibrium between the induction of efficient innate defensive responses to inhaled infectious microorganisms and equally effective mechanisms to downregulate the inflammatory response to initiate resolution and tissue repair. As a predominant immune effector cell in the airspaces, the alveolar macrophage is critical to these defence processes. Thus they produce a vast array of cytokines and inflammatory mediators in particular after LPS stimulation, including TNF-α and IL-10 as prototypic pro-inflammatory and anti-inflammatory cytokines, respectively. While the signaling events that mediate TNF-α in HAM have been extensively studied [20–23, 19], those responsible for IL-10 production have not been well characterized.
The present study is the first one showing that ERK, p38, JNK and Sp1 are involved and essential in LPS-induced IL-10 expression in HAM. These factors act at the transcriptional level, as IL-10 mRNA stability was not affected by MAPK inhibitors. It is well known that LPS drives intracellular signaling pathways such as MAPKs and NF-κB [23, 24] to activate several pro-inflammatory genes including cyclooxygenase-2 , inducible nitric oxygen synthase , TNF-α and IL-1β . In the present study, we found that in HAM the MAPK signaling pathways were also involved in LPS-induced gene activation of IL-10, a major anti-inflammatory factor. A recent study in murine macrophage raw 264.7 cells also reported that MAPKs were necessary in IL-10 expression by LPS  whereas other studies showed that only MAPK p38 was essential for IL-10 expression induced by LPS and other ligands [29–33]. Our study not only showed that all MAPKs were necessary but that they also played an important role in the downstream activation of Sp1 trancription factor.
Sp1 is the founding member of a family of zinc finger transcription factors, which includes at least four Sp transcription factors [34, 35]. Among the Sp transcription factors, Sp1 has been extensively studied  and is known to be widely expressed and to play a role in the regulation of a vast array of genes. Thus, while not excluding a role for other nuclear factors our data confirm previous studies showing that IL-10 gene expression is controlled by the transcription factor Sp1 [13, 14, 37] since mithramycin, an inhibitor of Sp1, almost completely abrogated LPS-induced IL-10 production at the mRNA and protein level. EMSA assay confirmed this observation as it showed that mithramycin decreased the activation of the nuclear protein Sp1 after LPS stimulation. Transfection of HAM by antisense oligonucleotides to Sp1 could not be used as another approach to confirm the role of Sp1 in IL-10 induction by LPS, as after the time period required to silence Sp1 expression (minimum 16–20 hrs) following 4 hrs-transfection, HAMs were not anymore responsive to LPS for IL-10 production (data not shown). Interestingly, inhibition of MAPKs by their specific inhibitors, also abolished LPS-induced Sp1 activation. These results are in accordance with previous studies [14, 38–42] showing that Sp1 phosphorylation can be induced by ERK and p38 MAP kinases. In addition the present study also showed that JNK MAP kinase is also required for the activation of Sp1 induced by LPS. The three MAP kinases seem however to have different contributions to LPS-induced IL-10 in HAM, with a prominent role of p38 and ERK.
IL-10 production by alveolar macrophages has been debated since some authors described the inability of alveolar macrophages to produce IL-10 [43–45]. Other investigators related this to a reduced production of IL-10 to allergic inflammation . Our data clearly confirm IL-10 production by normal HAM [47–54], provide new information on the mechanisms involved in this production and complete the studies of Boehringer et al  who has studied the role of PP1 and PP2A in the regulation of LPS-induced IL-10 in HAM.
Our study demonstrates the contribution of MAP kinases to IL-10 expression in HAM upon endotoxin activation, indicating that ERK and p38 and to a lesser extent JNK are involved. In addition we show that ERK, p38 and JNK are able to trigger the phosphorylation of Sp1, the major transcription factor for the IL-10 gene. These findings are highly relevant to lung immunity, alveolar macrophages assuming front-line defense mechanisms and IL-10 representing a key factor for mucosal tolerance and resolution of inflammatory responses.
The authors thank J.-P. Vaerman for gift of IgA. H.C. was Chargé de Recherche of the Belgian Fonds National de la Recherche Scientifique. This work was supported by the Belgian Fonds National de la Recherche Scientifique Médicale (grant N°3.4598.05F), by an FSR grant (N° 1324.2004) and by a grant from GSK.
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