Elk-3 Is a Transcriptional Repressor of Nitric-oxide Synthase 2
2003; Elsevier BV; Volume: 278; Issue: 41 Linguagem: Inglês
10.1074/jbc.m308179200
ISSN1083-351X
AutoresYen‐Hsu Chen, Matthew D. Layne, Su Wol Chung, Kuniaki Ejima, Rebecca M. Baron, Shaw‐Fang Yet, Mark A. Perrella,
Tópico(s)Cancer, Hypoxia, and Metabolism
ResumoThe inducible isoform of nitric-oxide synthase (NOS2), a key enzyme catalyzing the dramatic increase in nitric oxide by lipopolysaccharide (LPS), plays an important role in the pathophysiology of endotoxemia and sepsis. Recent evidence suggests that Ets transcription factors may contribute to NOS2 induction by inflammatory stimuli. In this study, we investigated the role of Ets transcription factors in the regulation of NOS2 by LPS and transforming growth factor (TGF)-β1. Transient transfection assays in macrophages showed that Ets-2 produced an increase in NOS2 promoter activity, whereas the induction by Ets-1 was modest and NERF2 had no effect. Elk-3 (Net/Erp/Sap-2a) markedly repressed NOS2 promoter activity in a dose-dependent fashion, and overexpression of Elk-3 blunted the induction of endogenous NOS2 message. Mutation of the Net inhibitory domain of Elk-3, but not the C-terminal-binding protein interaction domain, partially alleviated this repressive effect. We also found that deletion of the Ets domain of Elk-3 completely abolished its repressive effect on the NOS2 promoter. LPS administration to macrophages led to a dose-dependent decrease in endogenous Elk-3 mRNA levels, and this decrease in Elk-3 preceded the induction of NOS2 mRNA. In a mouse model of endotoxemia, the expression of Elk-3 in kidney, lung, and heart was significantly down-regulated after systemic administration of LPS, and this down-regulation also preceded NOS2 induction. Moreover, TGF-β1 significantly increased endogenous Elk-3 mRNA levels that had been down-regulated by LPS in macrophages. This increase in Elk-3 correlated with a TGF-β1-induced down-regulation of NOS2. Taken together, our data suggest that Elk-3 is a strong repressor of NOS2 promoter activity and mRNA levels and that endogenous expression of Elk-3 inversely correlates with NOS2. Thus, Elk-3 may serve as an important mediator of NOS2 gene expression. The inducible isoform of nitric-oxide synthase (NOS2), a key enzyme catalyzing the dramatic increase in nitric oxide by lipopolysaccharide (LPS), plays an important role in the pathophysiology of endotoxemia and sepsis. Recent evidence suggests that Ets transcription factors may contribute to NOS2 induction by inflammatory stimuli. In this study, we investigated the role of Ets transcription factors in the regulation of NOS2 by LPS and transforming growth factor (TGF)-β1. Transient transfection assays in macrophages showed that Ets-2 produced an increase in NOS2 promoter activity, whereas the induction by Ets-1 was modest and NERF2 had no effect. Elk-3 (Net/Erp/Sap-2a) markedly repressed NOS2 promoter activity in a dose-dependent fashion, and overexpression of Elk-3 blunted the induction of endogenous NOS2 message. Mutation of the Net inhibitory domain of Elk-3, but not the C-terminal-binding protein interaction domain, partially alleviated this repressive effect. We also found that deletion of the Ets domain of Elk-3 completely abolished its repressive effect on the NOS2 promoter. LPS administration to macrophages led to a dose-dependent decrease in endogenous Elk-3 mRNA levels, and this decrease in Elk-3 preceded the induction of NOS2 mRNA. In a mouse model of endotoxemia, the expression of Elk-3 in kidney, lung, and heart was significantly down-regulated after systemic administration of LPS, and this down-regulation also preceded NOS2 induction. Moreover, TGF-β1 significantly increased endogenous Elk-3 mRNA levels that had been down-regulated by LPS in macrophages. This increase in Elk-3 correlated with a TGF-β1-induced down-regulation of NOS2. Taken together, our data suggest that Elk-3 is a strong repressor of NOS2 promoter activity and mRNA levels and that endogenous expression of Elk-3 inversely correlates with NOS2. Thus, Elk-3 may serve as an important mediator of NOS2 gene expression. Sepsis is a systemic inflammatory response to severe infection that frequently progresses to refractory hypotension, multiple organ system failure, and death (1Bone R.C. Ann. Intern. Med. 1991; 115: 457-469Crossref PubMed Scopus (1238) Google Scholar). In a subset of patients, the release of bacterial cell wall-derived lipopolysaccharide (LPS 1The abbreviations used are: LPS, lipopolysaccharide; NO, nitric oxide; NOS, NO synthase(s); iNOS, inducible NOS; TGF-β1, transforming growth factor-β1; NID, Net inhibitory domain; CID, C-terminal-binding protein interaction domain; TCF, ternary complex factors; IFN, interferon. or endotoxin) initiates a cascade of inflammatory events (2Parrillo J.E. N. Engl. J. Med. 1993; 328: 1471-1477Crossref PubMed Scopus (1507) Google Scholar). This response to infection is mediated, in part, by macrophage activation and the release of proinflammatory cytokines (3Bone R.C. Grodzin C.J. Balk R.A. Chest. 1997; 112: 235-243Abstract Full Text Full Text PDF PubMed Scopus (765) Google Scholar). Among the mediators induced by these signal cascades, nitric oxide (NO) acts as a key regulator of hypotension and end organ damage (4Rees D.D. Monkhouse J.E. Cambridge D. Moncada S. Br. J. Pharmacol. 1998; 124: 540-546Crossref PubMed Scopus (79) Google Scholar, 5Titheradge M.A. Biochim. Biophys. Acta. 1999; 1411: 437-455Crossref PubMed Scopus (395) Google Scholar). The production of nitric oxide from l-arginine is catalyzed by NO synthases (NOS) (6Stuehr D.J. Biochim. Biophys. Acta. 1999; 1411: 217-230Crossref PubMed Scopus (816) Google Scholar). Of the three isoforms of NOS identified in mammalian cells, the expression of NOS2 is inducible by many proinflammatory stimuli, such as interleukin-1β, tumor necrosis factor-α, interferon-γ, and bacterial LPS, depending on the target cell. Thus, the study of NOS2 gene regulation is of particular importance in our understanding and management of sepsis and other inflammatory disorders. Ets proteins are a family of transcription factors that share a unique and highly conserved, winged helix-turn-helix DNA-binding domain (7Wasylyk B. Hahn S.L. Giovane A. Eur. J. Biochem. 1993; 211: 7-18Crossref PubMed Scopus (811) Google Scholar, 8Dittmer J. Nordheim A. Biochim. Biophys. Acta. 1998; 1377: F1-F11PubMed Google Scholar). Ets proteins are involved in the transcriptional regulation of genes important for determining tissue specificity, cellular differentiation, and cellular proliferation by binding to GGA(A/T) sites in the promoters/enhancers of these genes (7Wasylyk B. Hahn S.L. Giovane A. Eur. J. Biochem. 1993; 211: 7-18Crossref PubMed Scopus (811) Google Scholar, 8Dittmer J. Nordheim A. Biochim. Biophys. Acta. 1998; 1377: F1-F11PubMed Google Scholar, 9Wasylyk B. Hagman J. Gutierrez-Hartmann A. Trends Biochem. Sci. 1998; 23: 213-216Abstract Full Text Full Text PDF PubMed Scopus (447) Google Scholar). Several reports have demonstrated a vital role for Ets family proteins in the regulation of mammalian immunity (8Dittmer J. Nordheim A. Biochim. Biophys. Acta. 1998; 1377: F1-F11PubMed Google Scholar, 10Anderson K.L. Perkin H. Surh C.D. Venturini S. Maki R.A. Torbett B.E. J. Immunol. 2000; 164: 1855-1861Crossref PubMed Scopus (148) Google Scholar, 11Zhang L. Eddy A. Teng Y.T. Fritzler M. Kluppel M. Melet F. Bernstein A. Mol. Cell. Biol. 1995; 15: 6961-6970Crossref PubMed Scopus (138) Google Scholar). Additional reports have also revealed that Ets family proteins regulate gene expression in non-immune cell types. For example, Dube et al. (12Dube A. Yasmin A. Sato T.N. Libermann T.A. Oettgen P. Circ. Res. 1999; 84: 1177-1185Crossref PubMed Scopus (93) Google Scholar) showed that the Ets transcription factor NERF2 is an important mediator of the vascular-specific expression of TIE2 in endothelial cells. In addition, ESE-1 represents a novel mediator of vascular inflammation (13Rudders S. Gaspar J. Madore R. Voland C. Grall F. Patel A. Pellacani A. Perrella M.A. Libermann T.A. Oettgen P. J. Biol. Chem. 2001; 276: 3302-3309Abstract Full Text Full Text PDF PubMed Scopus (85) Google Scholar). Interestingly, a target gene of ESE-1 in vascular cells and macrophages is NOS2 (13Rudders S. Gaspar J. Madore R. Voland C. Grall F. Patel A. Pellacani A. Perrella M.A. Libermann T.A. Oettgen P. J. Biol. Chem. 2001; 276: 3302-3309Abstract Full Text Full Text PDF PubMed Scopus (85) Google Scholar). Due to the potential importance of Ets factors in immune cells and vascular inflammation, we wanted to determine whether other members of the Ets superfamily could regulate NOS2 gene expression. Beyond the induction of NOS2 by proinflammatory stimuli, previous work from our laboratory has focused on the role of transforming growth factor (TGF)-β1 in the down-regulation of NOS2 after its induction by proinflammatory cytokines and LPS (14Perrella M.A. Yoshizumi M. Fen Z. Tsai J.-C. Hsieh C.-M. Kourembanas S. Lee M.-E. J. Biol. Chem. 1994; 269: 14595-14600Abstract Full Text PDF PubMed Google Scholar, 15Perrella M.A. Patterson C. Tan L. Yet S.-F. Hsieh C.-M. Yoshizumi M. Lee M.-E. J. Biol. Chem. 1996; 271: 13776-13780Abstract Full Text Full Text PDF PubMed Scopus (74) Google Scholar, 16Perrella M.A. Hsieh C.-M. Lee W.-S. Shieh S. Tsai J.-C. Patterson C. Lowenstein C.J. Long N.-C. Haber E. Shore S. Lee M.-E. Proc. Natl. Acad. Sci. U. S. A. 1996; 93: 2054-2059Crossref PubMed Scopus (75) Google Scholar, 17Pellacani A. Wiesel P. Razavi S. Vasilj V. Feinberg M.W. Chin M.T. Reeves R. Perrella M.A. J. Biol. Chem. 2001; 276: 1653-1659Abstract Full Text Full Text PDF PubMed Scopus (32) Google Scholar). TGF-β1 inhibited NOS2 at the level of gene transcription (14Perrella M.A. Yoshizumi M. Fen Z. Tsai J.-C. Hsieh C.-M. Kourembanas S. Lee M.-E. J. Biol. Chem. 1994; 269: 14595-14600Abstract Full Text PDF PubMed Google Scholar), and this effect occurred in part by downregulating the expression of high mobility group (HMG)-I/Y protein (17Pellacani A. Wiesel P. Razavi S. Vasilj V. Feinberg M.W. Chin M.T. Reeves R. Perrella M.A. J. Biol. Chem. 2001; 276: 1653-1659Abstract Full Text Full Text PDF PubMed Scopus (32) Google Scholar), an architectural transcription factor. However, we hypothesized that other mechanisms may exist for the inhibition of the NOS2 gene by TGF-β1. Among the Ets family members, a candidate gene known to have transcriptional repressive activity is Elk-3 (Net/Erp/Sap-2a) (18Giovane A. Pintzas A. Maira S.M. Sobieszczuk P. Wasylyk B. Genes Dev. 1994; 8: 1502-1513Crossref PubMed Scopus (202) Google Scholar, 19Lopez M. Oettgen P. Akbarali Y. Dendorfer U. Libermann T.A. Mol. Cell. Biol. 1994; 14: 3292-3309Crossref PubMed Scopus (109) Google Scholar, 20Price M.A. Rogers A.E. Treisman R. EMBO J. 1995; 14: 2589-2601Crossref PubMed Scopus (247) Google Scholar, 21Nozaki M. Onishi Y. Kanno N. Ono Y. Fujimura Y. DNA Cell Biol. 1996; 15: 855-862Crossref PubMed Scopus (20) Google Scholar, 22Maira S.M. Wurtz J.M. Wasylyk B. EMBO J. 1996; 15: 5849-5865Crossref PubMed Scopus (78) Google Scholar). Elk-3 is a member of the ternary complex factors (TCF) subfamily of Ets proteins, along with Elk-1 and Sap-1. TCFs have been shown to participate in the response of the cell to Ras and growth signals. Important structural domains of TCFs include domains A (Ets domain that mediates DNA binding), B (interaction with serum-response factor), C (activation domain), and D (mitogen-activated protein (MAP) kinase docking domain) (22Maira S.M. Wurtz J.M. Wasylyk B. EMBO J. 1996; 15: 5849-5865Crossref PubMed Scopus (78) Google Scholar, 23Yang S.-H. Bumpass D.C. Perkins N.D. Sharrocks A.D. Mol. Cell. Biol. 2002; 22: 5036-5046Crossref PubMed Scopus (52) Google Scholar). When compared with Elk-1 and Sap-1, Elk-3 is unique in that it exhibits strong transcription repressor activity under basal conditions. Prior studies have shown that this inhibitory effect occurs through the Net inhibitory domain (NID) (22Maira S.M. Wurtz J.M. Wasylyk B. EMBO J. 1996; 15: 5849-5865Crossref PubMed Scopus (78) Google Scholar) and the C-terminal-binding protein interaction domain (CID) (24Criqui-Filipe P. Ducret C. Maira S.M. Wasylyk B. EMBO J. 1999; 18: 3392-3403Crossref PubMed Scopus (137) Google Scholar). The present study was designed to investigate the role of Ets transcription factors in the regulation of NOS2 by LPS and TGF-β1 in vitro and in vivo. Cell Culture and Reagents—Murine macrophages (RAW 264.7) were cultured as described previously (25Ejima K. Layne M.D. Carvajal I.M. Nanri H. Ith B. Yet S.-F. Perrella M.A. Antioxid. Redox. Signal. 2002; 4: 569-575Crossref PubMed Scopus (29) Google Scholar), and NIH/3T3 cells were cultured according to recommendations from American Type Culture Collection. LPS from Escherichia coli (serotype O26:B6) was purchased from Sigma, and human recombinant TGF-β1 and interleukin-1β (IL-1β) and murine recombinant interferon (IFN)-γ were purchased from PeproTech Inc. (Rocky Hill, NJ). Plasmid Constructs and DNA Probes—The mouse NOS2 luciferase reporter plasmids, iNOS(–1485/+31), iNOS(–815/+31), iNOS(–518/+31), and iNOS(–234/+31) in the pGL2-Basic vector (Promega) were described previously (14Perrella M.A. Yoshizumi M. Fen Z. Tsai J.-C. Hsieh C.-M. Kourembanas S. Lee M.-E. J. Biol. Chem. 1994; 269: 14595-14600Abstract Full Text PDF PubMed Google Scholar, 15Perrella M.A. Patterson C. Tan L. Yet S.-F. Hsieh C.-M. Yoshizumi M. Lee M.-E. J. Biol. Chem. 1996; 271: 13776-13780Abstract Full Text Full Text PDF PubMed Scopus (74) Google Scholar). Ets-1, Ets-2, NERF2, and Elk-3 (Erp)-cloned into pCI expression vector (Promega), and iNOS(–234/+31)ETSm with a mutation in the Ets binding site located at bp –190 to –180, were generous gifts from Dr. Peter Oettgen, Boston, MA. Elk-3ΔA (Elk-3 without the A domain, see Fig. 5B, upper panel) was generated by subcloning the PCR product, using primers: 5′-CATGCCATGGCCAGCCGCAACGAGTACC-3′ and 5′-ATAGTTTAGCGGCCGCTGTGGGGAACTGGAAAAGTGT-3′, into pCMV/myc/nuc expression vector (Invitrogen) at the NcoI and NotI sites. Site-directed Mutagenesis—Site-directed mutagenesis of Elk-3 was performed by a PCR method using Pfu Turbo polymerase (Stratagene) followed by DpnI digestion to remove unmutated plasmids. We altered the NID and the CID of Elk-3 to produce N1, N2, C1, C2, and C3 mutants (schematic structures as described in Fig. 5A, upper panel) as described previously (22Maira S.M. Wurtz J.M. Wasylyk B. EMBO J. 1996; 15: 5849-5865Crossref PubMed Scopus (78) Google Scholar, 24Criqui-Filipe P. Ducret C. Maira S.M. Wasylyk B. EMBO J. 1999; 18: 3392-3403Crossref PubMed Scopus (137) Google Scholar). All constructs were confirmed by sequencing. Transient Transfections of RAW 264.7 Cells and Reporter Activity Assays—iNOS(–1485/+31), iNOS(–234/+31), and iNOS(–234/+31)ETSm reporter constructs were used for transient transfection assays. For assays in RAW 264.7 cells, 4 × 105 cells/well were plated in duplicate on 6-well plates and incubated overnight. Using FuGENE 6 transfection reagent (Roche Applied Science), cells were transfected with 0.5 μg of a NOS2 reporter plasmid plus the indicated amounts of expression constructs, Ets-1, Ets-2, NERF2, Elk-3 (wild or mutated type). The total amount of plasmid DNA was kept constant among groups by normalizing with empty pCI vector. Twenty-four h later, LPS (10 ng/ml) was given to the indicated wells. The cells, incubated with or without LPS for 24 h, were harvested for assessment of luciferase activity using Promega's luciferase assay system. As described previously (13Rudders S. Gaspar J. Madore R. Voland C. Grall F. Patel A. Pellacani A. Perrella M.A. Libermann T.A. Oettgen P. J. Biol. Chem. 2001; 276: 3302-3309Abstract Full Text Full Text PDF PubMed Scopus (85) Google Scholar), we omitted co-transfection of a second plasmid for determination of transfection efficiency because many commonly used viral promoters contain binding sites for Ets factors, thus leading to potential artifacts when used in conjunction with Ets expression plasmids. At least 2–3 independent experiments, carried out in duplicate, were performed for each experimental condition. Transient Transfections of NIH/3T3 cells—pCI or Elk-3 (6 μg of each) were transfected into NIH/3T3 cells (100-mm dishes) using FuGENE 6 transfection reagent, according to the manufacturer's instructions. After overnight incubation, LPS (2 μg/ml), IL-1β (10 ng/ml), and IFN-γ (100 units/ml) were added to NIH/3T3 cells. Fibroblasts, similar to smooth muscle cells (15Perrella M.A. Patterson C. Tan L. Yet S.-F. Hsieh C.-M. Yoshizumi M. Lee M.-E. J. Biol. Chem. 1996; 271: 13776-13780Abstract Full Text Full Text PDF PubMed Scopus (74) Google Scholar), are not as sensitive to LPS stimulation alone as are macrophages and therefore require the addition of proinflammatory cytokines for NOS2 induction. After 24 h of treatment, RNA was harvested for Northern blot analysis. Mouse Model of Endotoxemia—Wild-type male C57BL/6 mice were injected intraperitoneally with LPS (10 mg/kg) or vehicle (saline). Heart, kidney, and lung tissues were harvested from the mice 4 and 12 h after LPS/vehicle was administrated. All endotoxemia experiments in mice were performed in accordance with National Institutes of Health guidelines and approved by the Harvard Medical Area Standing Committee on animals. RNA Isolation and Northern Blot Analysis—RNeasy Mini RNA isolation kit (Qiagen) was used to extract total RNA from cultured cells and mouse tissues. Northern blot analysis was performed as described previously (26Chen Y.-H. Layne M.D. Watanabe M. Yet S.-F. Perrella M.A. J. Biol. Chem. 2001; 276: 47658-47663Abstract Full Text Full Text PDF PubMed Scopus (30) Google Scholar). The signal intensity was measured on a Phosphor-Imager using ImageQuant software (Amersham Biosciences). Statistics—Where indicated, comparisons between groups were made by factorial analysis of variance followed by Fisher's least significant difference test. Elk-3 Represses NOS2 Promoter Activity—To explore the role of Ets factors in transcriptional regulation of the NOS2 promoter in macrophages, we transfected RAW 264.7 cells with expression constructs for several Ets proteins (including Ets-1, Ets-2, NERF2, and Elk-3) and assessed promoter activity of the iNOS(–1485/+31) reporter construct. Using transient transfection assays in the absence of LPS, we found that Ets-2 stimulated NOS2 promoter activity (∼3-fold induction, p < 0.05), whereas the Ets-1 induction was modest (<2-fold, not significant) and NERF2 had no effect (Fig. 1). After 24 h of treatment with LPS, NOS2 promoter activity with control empty plasmid (pCI) was induced ∼7-fold, and the addition of Ets-2 with LPS produced a 16-fold induction (p < 0.05). In the presence of LPS, Ets-1 induced NOS2 promoter activity 12-fold, although this was not significantly different from NOS2 promoter activity transfected with control plasmid (7-fold). NERF2 had no additional effect on NOS2 promoter activity, even in the presence of LPS. Elk-3, in contrast, showed a strong repressive effect (80–85% at a concentration of 200 ng/well, p < 0.05) on the promoter activity of iNOS(–1485/+31), in the presence or absence of LPS. Elk-3 Represses NOS2 Promoter Activity in a Dose-dependent Manner—We next wanted to determine whether the effect of Elk-3 on LPS-mediated NOS2 induction was contingent on Elk-3 plasmid concentration. As shown in Fig. 2, the repressive effect of Elk-3 on the NOS2 promoter in the presence of LPS was dose-dependent. At a concentration of 200 ng/well, Elk-3 repressed LPS-induced NOS2 promoter activity to a level not statistically different from baseline, and a >95% reduction occurred at an Elk-3 concentration of 800 ng/well. These data suggest that Elk-3 is a strong repressor of NOS2 promoter activity in macrophages and that Elk-3 at higher concentrations can completely abrogate the induction of NOS2 by LPS. Overexpression of Elk-3 Represses Endogenous NOS2 mRNA Levels—To determine whether overexpression of Elk-3 could regulate endogenous NOS2 expression, we performed transient transfection analyses of NIH/3T3 cells in the presence or absence of proinflammatory stimuli (LPS, IL-1β, and IFN-γ). NIH/3T3 cells were used because of their higher transfection efficiency when compared with RAW 264.7 cells. After transfection with the control empty plasmid (pCI) or Elk-3, we treated NIH/3T3 cells with LPS (2 μg/ml), IL-1β (10 ng/ml), and IFN-γ (100 units/ml) and then harvested total RNA after 24 h. Northern blot analysis revealed that when compared with control pCI plasmid, overexpression of Elk-3 repressed endogenous NOS2 mRNA that had been induced by LPS, IL-1β, and IFN-γ (Fig. 3). Ets Binding Site in the Downstream NOS2 Promoter (–190 to –180) Contributes to Ets-1 and Ets-2, but Not Elk-3, Alteration in NOS2 Promoter Activity—A critical Ets binding site in the downstream NOS2 promoter (bp –190 to –180) is important for the regulation of NOS2 promoter activity by the Ets transcription factor ESE-1 (13Rudders S. Gaspar J. Madore R. Voland C. Grall F. Patel A. Pellacani A. Perrella M.A. Libermann T.A. Oettgen P. J. Biol. Chem. 2001; 276: 3302-3309Abstract Full Text Full Text PDF PubMed Scopus (85) Google Scholar). To evaluate the function of this Ets binding site on Ets-1, Ets-2, and Elk-3 regulation of the NOS2 promoter, we performed deletion analysis and site-directed mutagenesis of the NOS2 promoter. Using several different NOS2 deletion constructs, iNOS(–1485/+31), iNOS(–815/+31), iNOS(–518/+31), and iNOS(–234/+31), we found that all of the constructs responded similarly to Ets-2 and Ets-1 induction, or Elk-3 repression, in RAW 264.7 cells (data not shown). However, mutation of the downstream Ets site (bp –190 to –180) in the iNOS(–234/+31) construct led to a significant blunting of LPS-induced NOS2 promoter activity by Ets-2 and Ets-1 (p < 0.05), when compared with wild-type promoter activity (Fig. 4). In contrast, mutation of this Ets site had no effect on the ability of Elk-3 to repress NOS2 promoter activity that was induced by LPS. NID and Ets Domains Are Important for Elk-3 Repression of NOS2 Promoter—Previous studies (22Maira S.M. Wurtz J.M. Wasylyk B. EMBO J. 1996; 15: 5849-5865Crossref PubMed Scopus (78) Google Scholar, 24Criqui-Filipe P. Ducret C. Maira S.M. Wasylyk B. EMBO J. 1999; 18: 3392-3403Crossref PubMed Scopus (137) Google Scholar) have shown that two important and unique inhibitory domains, NID and CID, contribute to the repressive effects of Elk-3 (Fig. 5A, upper panel). To study the role of these Elk-3 inhibitory domains on NOS2 promoter activity, we mutated the same sites of NID and CID as described previously (22Maira S.M. Wurtz J.M. Wasylyk B. EMBO J. 1996; 15: 5849-5865Crossref PubMed Scopus (78) Google Scholar, 24Criqui-Filipe P. Ducret C. Maira S.M. Wasylyk B. EMBO J. 1999; 18: 3392-3403Crossref PubMed Scopus (137) Google Scholar) to generate N1, N2, C1, C2, and C3 mutants (Fig. 5A, upper panel). As shown in Fig. 5A, in the lower panel, whereas various mutations of CID (C1, C2, and C3) had no effect on NOS2 promoter repression by Elk-3, the N2 mutant of NID had a reduced inhibitory effect as compared with wild-type Elk-3 (p < 0.05). Even more impressively, deletion of the Ets (A) domain of Elk-3 (Fig. 5B, upper panel) abolished its inhibitory effect on NOS2 promoter activity (Fig. 5B, lower panel). Elk-3 Is Down-regulated by LPS in Cultured Macrophages and Mouse Tissues—To investigate the endogenous regulation of Elk-3 expression in the presence of LPS, we harvested total RNA from RAW 264.7 cells that were treated with increasing doses of LPS (from 0 to 100 ng/ml) for 6 h. By Northern blot analysis, we found that mRNA levels of Elk-3 decreased in a dose-dependent fashion as the LPS dose increased (Fig. 6A). Data from mRNA levels of three independent experiments showed that LPS significantly decreased Elk-3 mRNA levels after 6 h at a dose of 1 ng/ml (p < 0.05), and the expression of NOS2 mRNA began to increase at this same dose (Fig. 6B, p < 0.05). Maximal suppression of Elk-3 mRNA (94% decrease) occurred at an LPS dose of 100 ng/ml, whereas NOS2 mRNA was dramatically induced. Furthermore, we investigated the relationship between Elk-3 and NOS2 expression in mice during endotoxemia. Northern blot analysis showed that the expression of Elk-3 was strongly repressed in mouse kidney, lung, and heart tissues 4 h after the administration of LPS, whereas NOS2 was induced (Fig. 7). By 12 h after LPS administration, the mRNA levels of Elk-3 increased and the mRNA levels of NOS2 decreased, reverting back toward their respective baseline levels. Taken together, these data demonstrate that endogenous expression of Elk-3 inversely correlates with NOS2 expression after treatment with LPS.Fig. 7Expression of Elk-3 inversely correlates with NOS2 mRNA in tissues from mice with endotoxemia. Male C57BL/6 mice were injected intraperitoneally with LPS (10 mg/kg) or vehicle (saline). The mice were killed at 4 or 12 h after vehicle or LPS administration, and total RNA was extracted from kidney, lung, and heart tissues. Northern blot analysis was performed as described under “Experimental Procedures,” using 32P-labeled Elk-3, NOS2, and 18 S rRNA probes. This experiment was performed two independent times.View Large Image Figure ViewerDownload Hi-res image Download (PPT) TGF-β1 Reverses the Suppression of Elk-3 by LPS and Decreases NOS2 Expression—We have reported previously that TGF-β1 significantly down-regulates NOS2 promoter activity and mRNA levels that had been induced by proinflammatory cytokines or LPS in vascular smooth muscle cells and macrophages, respectively (14Perrella M.A. Yoshizumi M. Fen Z. Tsai J.-C. Hsieh C.-M. Kourembanas S. Lee M.-E. J. Biol. Chem. 1994; 269: 14595-14600Abstract Full Text PDF PubMed Google Scholar, 15Perrella M.A. Patterson C. Tan L. Yet S.-F. Hsieh C.-M. Yoshizumi M. Lee M.-E. J. Biol. Chem. 1996; 271: 13776-13780Abstract Full Text Full Text PDF PubMed Scopus (74) Google Scholar, 17Pellacani A. Wiesel P. Razavi S. Vasilj V. Feinberg M.W. Chin M.T. Reeves R. Perrella M.A. J. Biol. Chem. 2001; 276: 1653-1659Abstract Full Text Full Text PDF PubMed Scopus (32) Google Scholar). Since endogenous Elk-3 expression inversely correlates with NOS2 message, and overexpression of Elk-3 represses the induction of NOS2 by an inflammatory stimulus, we wanted to determine whether TGF-β1 (10 ng/ml) would increase Elk-3 mRNA that had been down-regulated by LPS (10 ng/ml). Total RNA was harvested from RAW 264.7 cells at various time points after LPS administration, as shown in Fig. 8. Northern blot analysis revealed that after LPS administration, Elk-3 mRNA levels decreased rapidly (as early as 1 h, data not shown), with a maximal suppression by 6 h (Fig. 8). Moreover, this decrease in Elk-3 mRNA by LPS preceded the induction of NOS2. TGF-β1 significantly increased Elk-3 mRNA levels that had been down-regulated by LPS, and this increase in Elk-3 correlated with a TGF-β1-induced down-regulation of NOS2. Since overexpression of Elk-3 can down-regulate LPS-induced NOS2 (Figs. 1, 2, 3), these data suggest that TGF-β1 may down-regulate NOS2, in part, by up-regulating Elk-3. The inflammatory response is a key component of host defense, but excessive activation of the immune system and subsequent release of vasoactive mediators, as occurs in endotoxemia and sepsis, may be fatal (3Bone R.C. Grodzin C.J. Balk R.A. Chest. 1997; 112: 235-243Abstract Full Text Full Text PDF PubMed Scopus (765) Google Scholar). Overproduction of NO, through LPS and proinflammatory cytokine activation of NOS2, acts as a key regulator of hypotension and end organ damage (4Rees D.D. Monkhouse J.E. Cambridge D. Moncada S. Br. J. Pharmacol. 1998; 124: 540-546Crossref PubMed Scopus (79) Google Scholar, 5Titheradge M.A. Biochim. Biophys. Acta. 1999; 1411: 437-455Crossref PubMed Scopus (395) Google Scholar). Due to the detrimental consequences of an exaggerated response to infection, the immune system must be tightly controlled to prevent a massive systemic reaction leading to multiple organ failure and death. The effects of proinflammatory cytokines can be counterbalanced by the production of anti-inflammatory mediators (3Bone R.C. Grodzin C.J. Balk R.A. Chest. 1997; 112: 235-243Abstract Full Text Full Text PDF PubMed Scopus (765) Google Scholar). Thus, understanding the endogenous mediators responsible for the transcriptional regulation of NOS2 (either up-regulation or down-regulation) may provide important insight into the pathophysiology of systemic inflammatory processes such as endotoxemia and sepsis. In collaboration with Rudders et al (13Rudders S. Gaspar J. Madore R. Voland C. Grall F. Patel A. Pellacani A. Perrella M.A. Libermann T.A. Oettgen P. J. Biol. Chem. 2001; 276: 3302-3309Abstract Full Text Full Text PDF PubMed Scopus (85) Google Scholar), we reported previously that ESE-1, a member of the immune modulatory family of Ets proteins, regulates NOS2 expression and is a mediator of vascular inflammation. In the present study, we extend these findings by investigating the role of additional Ets transcription factors in the regulation of NOS2 by LPS and TGF-β1. Transient transfection assays in macrophages showed that Ets-2, similar to ESE-1 (13Rudders S. Gaspar J. Madore R. Voland C. Grall F. Patel A. Pellacani A. Perrella M.A. Libermann T.A. Oettgen P. J. Biol. Chem. 2001; 276: 3302-3309Abstract Full Text Full Text PDF PubMed Scopus (85) Google Scholar), increased NOS2 promoter activity. Induction of NOS2 by Ets-1 was modest, and NERF2 had no effect (Fig. 1). In contrast, Elk-3 markedly repressed NOS2 promoter activity (Figs. 1 and 2), and overexpression of Elk-3 blunted the induction of endogenous NOS2 by proinflammatory mediators (Fig. 3). Among the Ets family of proteins, Elk-3 is a member of the TCF subfamily, and it is known to have transcriptional repressive activity (18Giovane A. Pintzas A. Maira S.M. Sobieszczuk P. Wasylyk B. Genes Dev. 1994; 8: 1502-1513Crossref PubMed Scopus (202) Google Scholar, 19Lopez M. Oettgen P. Akbarali Y. Dendorfer U. Libermann T.A. Mol. Cell. Biol. 1994; 14: 3292-3309Crossref PubMed Scopus (109) Google Scholar, 20Price M.A. Rogers A.E. Treisman R. EMBO J. 1995; 14: 2589-2601Crossref PubMed Scopus (247) Google Scholar, 21Nozaki M. Onishi Y. Kanno N. Ono Y. Fujimura Y. DNA Cell Biol. 1996; 15: 855-862Crossref PubMed Scopus (20) Google Scholar, 22Maira S.M. Wurtz J.M. Wasylyk B. EMBO J. 1996; 15: 5849-5865Crossref PubMed Scopus (78) Google Scholar). Two important inhibitory domains have been identified in the Elk-3 protein, NID (22Maira S.M. Wurtz J.M. Wasylyk B. EMBO J. 1996; 15: 5849-5865Crossref PubMed Scopus (78) Google Scholar) and CID (24Criqui-Filipe P. Ducret C. Maira S.M. Wasylyk B. EMBO J. 1999; 18: 3392-3403Crossref PubMed Scopus (137) Google Scholar). The NID, with a helix-loop-helix protein-protein interaction motif, produces its repressive effect by altering both DNA binding and gene transactivation (9Wasylyk B. Hagman J. Gutierrez-Hartmann A. Trends Biochem. Sci. 1998; 23: 213-216Abstract Full Text Full Text PDF PubMed Scopus (447) Google Scholar). On the other hand, CID interacts with a co-repressor, C-terminal-binding protein, to produce its repressive effect (24Criqui-Filipe P. Ducret C. Maira S.M. Wasylyk B. EMBO J. 1999; 18: 3392-3403Crossref PubMed Scopus (137) Google Scholar). In regard to NOS2 gene transactivation by an inflammatory stimulus, mutation of NID, but not CID, partially alleviated the repressive effect of Elk-3 (Fig. 5A). We also found that deletion of the Ets (A) domain of Elk-3 completely abolished its repressive effect on the NOS2 promoter (Fig. 5B). These data suggest that although NID contributes, the Ets domain is necessary for Elk-3 repression of NOS2 gene transactivation. TGF-β1 is a pleiotrophic growth factor involved in a broad spectrum of cellular activities, including the modulation of immune function (27Massague J. Annu. Rev. Cell Biol. 1990; 6: 597-641Crossref PubMed Scopus (3010) Google Scholar). Mice deficient in TGF-β1 exhibit widespread, uncontrolled inflammation and tissue necrosis, leading to death (28Shull M.M. Ormsby I. Kier A.B. Pawlowski S. Diebold R.J. Yin M. Allen R. Sidman C. Proetzel G. Calvin D. Annunziata N. Doetschman T. Nature. 1992; 359: 693-699Crossref PubMed Scopus (2653) Google Scholar, 29Kulkarni A.B. Huh C.G. Becker D. Geiser A. Lyght M. Flanders K.C. Roberts A.B. Sporn M.B. Ward J.M. Karlsson S. Proc. Natl. Acad. Sci. U. S. A. 1993; 90: 770-774Crossref PubMed Scopus (1663) Google Scholar). These data suggest that TGF-β1 is an important anti-inflammatory mediator. Furthermore, TGF-β1 is known to decrease macrophage responsiveness to LPS (30Randow F. Syrbe U. Meisel C. Krausch D. Zuckermann H. Platzer C. Volk H.D. J. Exp. Med. 1995; 181: 1887-1892Crossref PubMed Scopus (392) Google Scholar) and to prevent NOS2 expression in response to proinflammatory cytokines (14Perrella M.A. Yoshizumi M. Fen Z. Tsai J.-C. Hsieh C.-M. Kourembanas S. Lee M.-E. J. Biol. Chem. 1994; 269: 14595-14600Abstract Full Text PDF PubMed Google Scholar, 31Nathan C. Xie Q.-w. Cell. 1994; 78: 915-918Abstract Full Text PDF PubMed Scopus (2758) Google Scholar, 32Tsunawaki S. Sporn M. Ding A. Nathan C. Nature. 1988; 334: 260-262Crossref PubMed Scopus (755) Google Scholar, 33Forstermann U. Schmidt H.H. Kohlhaas K.L. Murad F. Eur. J. Pharmacol. 1992; 225: 161-165Crossref PubMed Scopus (74) Google Scholar). We have shown previously that TGF-β1 inhibited NOS2 induction at the level of gene transcription (14Perrella M.A. Yoshizumi M. Fen Z. Tsai J.-C. Hsieh C.-M. Kourembanas S. Lee M.-E. J. Biol. Chem. 1994; 269: 14595-14600Abstract Full Text PDF PubMed Google Scholar), and this effect occurred in part by down-regulating the expression of the architectural transcription factor high mobility group (HMG)-I/Y protein (17Pellacani A. Wiesel P. Razavi S. Vasilj V. Feinberg M.W. Chin M.T. Reeves R. Perrella M.A. J. Biol. Chem. 2001; 276: 1653-1659Abstract Full Text Full Text PDF PubMed Scopus (32) Google Scholar). In addition, we demonstrated that the administration of TGF-β1 to rats inhibited NOS2 expression in vivo and that TGF-β1 arrested LPS-induced hypotension and decreased mortality (16Perrella M.A. Hsieh C.-M. Lee W.-S. Shieh S. Tsai J.-C. Patterson C. Lowenstein C.J. Long N.-C. Haber E. Shore S. Lee M.-E. Proc. Natl. Acad. Sci. U. S. A. 1996; 93: 2054-2059Crossref PubMed Scopus (75) Google Scholar). Since our current data revealed that during an LPS response, endogenous expression of Elk-3 inversely correlated with NOS2 expression (Figs. 6 and 7), we wanted to determine whether the anti-inflammatory mediator TGF-β1 would alter the expression of Elk-3 during an inflammatory stimulus such as LPS. In the present study, TGF-β1 significantly increased Elk-3 mRNA levels that had been down-regulated by LPS in macrophages. This increase in Elk-3 correlated with a TGF-β1-induced down-regulation of NOS2 (Fig. 8). Our data suggest that TGF-β1 induction of Elk-3 is another mechanism by which TGF-β1 may down-regulate NOS2 gene transcription after its induction by proinflammatory stimuli. The present study provides further insight into the regulation of the NOS2 gene by Ets factors. Ets-2 is able to increase NOS2 promoter activity; however, more impressively, Elk-3 is a potent repressor of NOS2 gene transactivation. Overexpression of Elk-3 can even suppress endogenous NOS2 that is induced by LPS and proinflammatory cytokines. The ability of Elk-3 to repress NOS2 depends on an inhibitory domain (NID, not CID) and the Ets domain of Elk-3. Moreover, endogenous Elk-3 mRNA is rapidly down-regulated by LPS, and this down-regulation precedes the induction of NOS2. Conversely, endogenous Elk-3 mRNA is induced by TGF-β1, and this induction is associated with a down-regulation of NOS2. Our data demonstrate that Elk-3 is a repressor of the NOS2 gene and that endogenous expression of Elk-3 inversely correlates with NOS2 expression. Thus, we propose that Elk-3 contributes to the tight control of NOS2 gene regulation in the setting of pro- and anti-inflammatory stimuli and that Elk-3 may serve as an important mediator of the NOS2 gene. We thank Dr. Peter Oettgen for generous gifts of NOS2 promoter construct iNOS(–234/+31)ETSm, Ets-1, Ets-2, NERF2, and Elk-3 (Erp) plasmids.
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