Nurr1 dependent regulation of pro-inflammatory mediators in immortalised synovial fibroblasts
© Davies et al; licensee BioMed Central Ltd. 2005
Received: 03 August 2005
Accepted: 25 November 2005
Published: 25 November 2005
Nurr1 is an orphan member of the nuclear receptor superfamily; these orphan receptors are a group for which a ligand has yet to be identified. Nurr1 has been shown to regulate the expression of a small number of genes as a monomeric, constitutively active receptor. These Nurr1 regulated genes are primarily associated with dopamine cell maturation and survival. However, previous reports have shown an increased expression of Nurr1 in the synovium of patients with rheumatoid arthritis (RA) suggesting a pro-inflammatory role for Nurr1 in RA. In this study we investigate the potential pro-inflammatory role of Nurr1 by monitoring Nurr1 dependent gene expression in an immortalised synoviocyte cell line, K4IM.
We overexpressed the wild type and a dominant negative form of the orphan nuclear receptor Nurr1, in a model synoviocyte cell line. Using the Affymetrix HG-U133 Genechips we demonstrate the effects on the transcriptome by the receptor. Further evidence of gene expression change was demonstrated using quantitative RT-PCR and ELISA analysis.
We show that Nurr1 regulates transcription of a small number of genes for pro-inflammatory modulators of which the most significant is interleukin-8 (IL-8). We also demonstrate increased synthesis and secretion of IL-8 further supporting a role for Nurr1 in inflammatory signalling pathways.
Using microarray analysis we show that elevated levels of Nurr1 leads to increased gene expression of pro-inflammatory genes: IL-8, Amphiregulin and Kit ligand in a model cell line. This data provides further evidence for an additional role for Nurr1 in inflammation and may play a role in the pathogenesis of rheumatoid arthritis.
Nuclear receptors can generally be described as ligand activated transcription factors that form a large superfamily of proteins. In humans 48 such receptors have been identified  and are involved with an extensive number of cellular processes throughout development and adult physiology . Nuclear receptors are activated through binding by a diverse range of natural and synthetically produced ligand molecules including hormones, fatty acids and antibiotics. In addition to the receptors known to bind ligand, a group of nuclear receptors exist for which a ligand has not been identified; these are termed the orphan nuclear receptors. Among this group of orphans is Nurr1 (NR4A2), a member of the NR4 group of orphan nuclear receptors together with Nur77 (NR4A1) and NOR-1 (NR4A3) . This family can bind as monomers to DNA response elements in the promoters of genes and activate transcription in the absence of ligand . Interestingly, this family of receptors are also capable of binding as a heterodimer with the 9-cis-retinoic acid receptor, RXR  or as a heterodimer with other Nur-family members . RXR as a heterodimer with Nurr1 remains active, suggesting that regulation can be modified by the use of specific rexinoids to enhance the response of these receptors to growth factors and therefore this could provide a novel therapeutic avenue for treatment of Nurr1 regulated disease.
The structure of Nurr1 has recently be solved highlighting differences between Nurr1 and the known liganded nuclear receptors . Based upon homology modelling, the region in Nurr1 that would normally contain the ligand-binding pocket has been shown to be substantially different from other nuclear receptors suggesting that there is insufficient space in the putative ligand binding pocket to accommodate a ligand. This may explain the observations that Nurr1 is able to activate transcription in a ligand independent manner and why no ligand has yet been reported for Nurr1.
In contrast to the majority of nuclear receptors, Nurr1 is encoded by an immediate early gene that is rapidly induced in cells in response to external stimuli such as cytokines. Nurr1 has been implicated in a number of human diseases including Parkinson's disease [8, 9], schizophrenia , alcohol dependence  and rheumatoid arthritis . In accordance with the nature of these diseases, the expression of Nurr1 is observed in the developing and adult CNS and within the inflamed synovium of the rheumatic joint [12–14].
A number of genes have been demonstrated to be regulated by Nurr1; many of these are involved with the development and maintenance of midbrain dopaminergic neurons. These include tyrosine hydroxylase , Ret tyrosine kinase  and the dopamine transporter (SLC6A3) . The Nur-family members have also been shown to play a pivotal role in regulating expression of CRH and pro-opiomelanocortin (POMC) within the hypothalamic-pituitary-adrenal (HPA) axis [6, 17–19]. These studies, carried out in mouse pituitary cells, also demonstrate that CRH is capable of causing increased expression of Nurr1, suggesting the presence of a positive feedback loop. More recently, studies in synovial tissue taken from the rheumatoid joint have shown Nurr1 to be highly expressed. In addition it has been demonstrated that inflammatory cytokines are capable of increasing Nurr1 expression through NF-κB and CREB dependent signalling and this elevation in Nurr1 leads to increased transcription of CRH [12, 20]. Whilst in the HPA axis, these close Nur-family members are capable of sharing overlapping roles, in primary synoviocytes, treatment with various cytokines shows predominantly Nurr1 upregulation . Therefore in rheumatic synovium it is proposed that Nurr1 is acting to exacerbate the inflammatory response by driving a Nurr1-CRH positive feedback loop, indicating its potential as a target for possible therapeutic intervention.
The purpose of this study was to further investigate the role of Nurr1 in regulating inflammatory processes in synovial cells, and by using transcript profiling to identify Nurr1 regulated genes in synoviocytes, which may be playing a role in the pathology of rheumatoid arthritis.
Plasmid expression constructs
A reporter gene construct was generated by ligating oligonucleotides representing 3 tandem repeated consensus Nurr1 binding sites (NurRE), into the SpeI/AflII site of the SW-gal construct as previously described , to generate the construct: pNurRE3gal. The sense strand oligonucleotides (5'-3') for the insert were as follows, 3XNurRE: ctagtgtgacctttattctcaaaggtcagtgacctttattctcaaaggtcagtgacctttattctcaaaggtcac. Construction of the control plasmid pCMV/hGH has been previously described . Dominant negative constructs were produced by fusing the DNA binding domain of Nurr1 (aa94–365) and the Drosophila engrailed domain (aa2–298) into the pcDNA3.1 expression vector to give pcDNA3.1-Nurr1-DN. The Nurr1 wild type gene was PCR amplified from whole brain RNA and cloned into the pcDNA3.1-V5-HIS vector and the DNA sequence verified.
K4IM cells (a generous gift from E. Murphy) were cultured in RPMI-1640 media supplemented with 10% (v/v) foetal calf serum (FCS), 2 mM glutamine and 50 μg/ml penicillin-streptomycin (Gibco BRL). HeLa cells were cultured in DMEM media supplemented with 10% (v/v) foetal calf serum (FCS), 2 mM glutamine and 50 μg/ml penicillin-streptomycin (Gibco BRL). For reporter gene assays, HeLa cells were cultured in phenol red-free DMEM supplemented with 0.5% (v/v) FCS, 2 mM glutamine and 50 μg/ml penicillin-streptomycin.
Reporter gene assays
24 hrs prior to transfection, 2.2 × 106 HeLa cells were seeded in a 9 cm2 dish, in full growth medium. Cells were transfected by calcium phosphate precipitation with a total of 20–25 μg DNA per 1 ml of precipitate as previously described . Generally, 10–15 μg of reporter construct was co-transfected with 2–5 μg of Nurr1 or empty vector DNA (pcDNA3.1) and including 0.5 μg CMV/hGH plasmid for data normalisation. 6 hrs post-transfection the cells were exposed to osmotic shock (15% glycerol in DMEM for 90 seconds) and the media replaced with phenol-red free DMEM supplemented with 0.5% FCS (assay medium). Cells were harvested 16–20 hrs later by incubating the cells with trypsin-EDTA (phenol red free) for 3 min at 37°C. Cells were counted, seeded into 96 well microtitre plates at 105 cells/well in 100 μl of assay medium and incubated for a further 16–20 hrs. β-galactosidase activity was measured using the spectrophotometric substrate, CPRG (Boehringer) as previously described . Briefly, 100 μl of a cocktail containing 7 μl 50 mM CPRG, 7 μl Z buffer pH7 (600 mM Na2HPO4; 400 mM NaH2PO4; 100 mM KCl; 10 mM MgSO4; 500 mM β-mercaptoethanol), 1 μl 20% SDS and 85 μl dH2O water was added directly to each well and the plates incubated at 37°C before an OD 570 nm measurement was taken. Incubation times varied depending on the individual assays but were typically 30 min–3 hrs. Secreted growth hormone from the cell supernatants was measured using a 2-antibody sandwich ELISA as previously described . β-galactosidase values were normalised using the hGH values.
Determination of IL-8 protein levels
IL-8 was quantified using ELISA (R&D systems – D8050). K4IM cells were resuspended in Amaxa solution "R" to a concentration of 0.4 × 106 cells per 100 μl. A total of 2 μg of DNA was transfected using the Amaxa Nucleofector following the manufacturer's protocol (A-23). Media was collected 48 hr post nucleofection and used undiluted in duplicate according to the manufacturer's instructions.
Sequences for Taqman RT-PCR. Sequences for primers and probes were designed using Primer Express (Applied Biosystems).
Size of product
Nucleofection was used to transfect the following three expression constructs into the K41M cell line: 1. pcDNA3.1 blank vector (control); 2. pcDNA3.1-Nurr1-WT (Nurr1 WT); 3. pcDNA3.1-Nurr1194–365EnR2–298 dominant negative (DN) co-transfected with pcDNA3.1-Nurr1-WT (Nurr1 DN/Nurr1 WT). Each transfection was carried out in triplicate, thus generating 9 samples from which RNA was extracted. Total RNA was extracted from each sample using RNeasy kit (Qiagen – 74104). RNA integrity and yield were analysed and quantified using the Agilent Bioanalyser 2100 with the RNA Nano6000 chip prior to synthesis of cRNA probes. Preparation of cRNA, hybridization and scanning of the HG-U133 GeneChip oligonucleotide arrays were performed according to the manufacturer's protocol (Affymetrix, Santa Clara, CA). GeneChip images were quantified and gene expression values were calculated by Affymetrix Microarray suite version 5.0 (Mas 5.0, Affymetrix). For statistical analysis a one-way analysis of variance (ANOVA) was used to compare Nurr1 WT to control samples. Prior to the test, probesets that were absent and/or had an expression signal less than 200 in all samples were removed. Probesets that had P-values less than 0.01 were considered statistically significant. A similar one-way ANOVA analysis across each probeset was used to compare Nurr1 DN to control samples. Candidate genes were retained if they showed greater than 1.5-fold upregulation, (p < 0.01) between the control and Nurr1 WT samples and yet no significant regulation (p < 0.01) between the control and Nurr1 DN samples. These remaining genes were then manually chosen for genes exhibiting an ideal profile (being changed with Nurr1 and returned towards basal activity with Nurr D/N).
Dominant negative Nurr1 blocks Nurr1 induced reporter gene expression
Analysis of Nurr1 mediated gene expression in K4IM cells
Differentially expressed genes following Nurr1 overexpression. K4IM cells were transfected in triplicate using the Amaxa Nucleofector system for each of the 3 conditions: 1. 5 μg pcDNA3.1 blank vector (control); 2. 2.5 μg pcDNA3.1-Nurr1-WT (Nurr1 WT) and 2.5 μg pCDNA3.1 blank vector; 3. 2.5 μg pcDNA3.1-Nurr1-DN dominant negative (DN) co-transfected with 2.5 μg pCDNA3.1-Nurr1-WT (Nurr1 DN/Nurr1 WT). Cells were cultured for 16 hours prior to RNA extraction. Genes were identified from the Affymetrix U133A chip showing significant change between blank vector transfected synoviocytes and Nurr1 transfected K4IM cells (>2 fold) and for genes not significantly changed between blank vector and Nurr1 D/N transfected cells (with a p-value of < 0.01). In each case genes were manually selected that showed subsequent return to basal levels with dominant negative cotransfection.
Official HUGO Symbol
Amphiregulin (schwannoma-derived growth factor)
Nurr1 dependent regulation of pro-inflammatory genes
Nurr1 dependent induction of IL-8 production in K4IM cells
This study was designed to explore the potential link between Nurr1, pro-inflammatory signalling and the pathogenesis of rheumatoid arthritis using a synovial fibroblast derived cell line, K4IM as a model system. Transcript profiling via Affymetrix microarrays was used to examine the consequences of elevated Nurr1 levels in K4IM cells. Overexpression of Nurr1 in K4IM cells resulted in constitutive activity of the receptor as shown by the reporter assay and this activity could be suppressed by cotransfection with a dominant negative Nurr1 construct (Figure 1). Given that Nurr1 is an immediate early gene  and that transactivation activity using the reporter system is observed within hours of transfection (data not shown), we harvested RNA 16 hours following transfection to maximise the chance of identifying Nurr1 primary targets as opposed to downstream secondary effects. To have confidence in the Nurr1 dependent transcription of elevated genes we compared expression profiles between cells transfected with Nurr1 alone or with a mix of Nurr1 and dominant negative Nurr1. Using our stringent cutoffs, only three genes: IL-8, Amphiregulin and Kit ligand were upregulated more than 2-fold and subsequently returned to basal levels by the presence of the Nurr1 dominant negative, confirming the Nurr1 dependence. A list of probesets of 1.5-fold increase between Nurr1-WT and blank vector control transfections is provided as a supplementary table to show genes that may be either increasing or decreasing in their expression following Nurr1 transfection (see Additional file 1). This small number of differentially expressed genes may be representative of both the short time period of expression and the specificity of Nurr1 signalling. Importantly all three have recognized roles in inflammation. We examined in further detail the Nurr1-dependent induction of these genes in K4IM cells and confirmed the microarray observations using Taqman quantitative RT-PCR. Of these three genes, the most highly induced gene was the inflammatory cytokine, IL-8 and for this reason we further demonstrated using an IL-8 ELISA that Nurr1 specifically induces release of IL-8 protein into the culture media from K4IM cells (Figure 3). IL-8 has an established role in neutrophil recruitment via the CXCR1/2 receptors 
Amphiregulin and Kit ligand also have demonstrated roles in inflammation [30, 31]. Transgenic mice expressing Amphiregulin under the control of keratin 14 promoter display early-onset synovial inflammation and severe skin pathology demonstrating a potential role for Amphiregulin in psoriasis and psoriatic arthritis . Kit ligand, also known as Stem Cell Factor (SCF), has been shown to play a role in activation of mast cells. Administration of SCF into the airways of normal mice results in a dose dependent increase in airway hyperreactivity via mast cell activation demonstrating the role of SCF in the development of allergic airway inflammation and hyperreactivity . In addition, activation of the Kit receptor by SCF leads to the phosphorylation of Akt which is necessary for IL-1-dependent NF-κB transactivation , Akt has been postulated to play a role in RA via its ability to regulate NF-κB and also promote resistance to apoptosis through a number of mechanisms [reviewed in ]. This role in cell cycle control remains consistent with other NR4 group members, in particular the Nur77 having an established role in TCR-mediated apoptosis of T hybridoma cells [34, 35].
Nurr1 has previously been shown to act as a point of convergence for multiple inflammatory signals via CREB-1 and NFκB signalling . Subsequent studies have shown Nurr1 and other NR4 family members to be involved in the inflammatory cascade of several stimuli, including TNFα-induced PAI-1 expression  and in LPS/TNFα stimulated macrophages . TNFα plays a critical role in the stimulation of leukocyte recruitment and cytokine production and antibodies which act by blocking TNFα signalling have been shown to have clinically beneficial effects in RA patients . Therefore we speculate that in addition to established NFκB signalling activating IL-8 expression , TNFα and other inflammation stimulators can act by regulating Nurr1 expression that in turn can regulate IL-8 expression either directly or indirectly. Ongoing work within our laboratory aims to address the exact mechanisms for Nurr1 activity on IL-8, Amphiregulin and Kit ligand gene expression.
In summary we have demonstrated using microarray analysis that elevated levels of Nurr1 leads to increased gene expression of IL-8, Amphiregulin and Kit ligand in the model cell line, K4IM. Moreover we have confirmed these Nurr1 dependent transcriptional changes using Taqman RT-PCR and demonstrated an increase in synthesis/secretion of IL-8 in cells transfected with Nurr1. We speculate that the elevated levels of Nurr1 observed in rheumatoid arthritis can potentially exacerbate the disease process in RA. Therefore, blocking the activation of Nurr1, or modifying the transactivation potential of Nurr1 through the use of rexinoids, methotrexate  or thiopurine analogues  represent a potential therapeutic option for rheumatoid arthritis and other inflammatory or allergic diseases.
The authors wish to thank Dr. H. Eibel (U. of Freiburg) for permission to use the K4IM cells, Dr. E. Murphy (U. of Dublin) for donation of the K4IM cells and for useful discussions, to members of the RIRA arthritis exploratory team and especially to Dr. J. Wardale for critical reading of this manuscript.
- Robinson-Rechavi M, Carpentier A, Duffraisse M, Laudet V: How many nuclear hormone receptors are there in the human genome?. Trends Genet. 2001, 17: 554-6. 10.1016/S0168-9525(01)02417-9.View ArticlePubMedGoogle Scholar
- Evans RM: The steroid and thyroid hormone receptor superfamily. Science. 1988, 240: 889-95.View ArticlePubMedGoogle Scholar
- A unified nomenclature system for the nuclear receptor superfamily. Cell. 1999, 97: 161-3. 10.1016/S0092-8674(00)80726-6.
- Sakurada K, Ohshima-Sakurada M, Palmer TD, Gage FH: Nurr1, an orphan nuclear receptor, is a transcriptional activator of endogenous tyrosine hydroxylase in neural progenitor cells derived from the adult brain. Development. 1999, 126: 4017-4026.PubMedGoogle Scholar
- Perlmann T, Jansson L: A novel pathway for vitamin A signaling mediated by RXR heterodimerization with NGFI-B and NURR1. Genes Dev. 1995, 9: 769-782.View ArticlePubMedGoogle Scholar
- Maira M, Martens C, Philips A, Drouin J: Heterodimerization between members of the Nur subfamily of orphan nuclear receptors as a novel mechanism for gene activation. Mol Cell Biol. 1999, 19: 7549-57.PubMed CentralView ArticlePubMedGoogle Scholar
- Wang Z, Benoit G, Liu J, Prasad S, Aarnisalo P, Liu X, Xu H, Walker NP, Perlmann T: Structure and function of Nurr1 identifies a class of ligand-independent nuclear receptors. Nature. 2003, 423: 555-560. 10.1038/nature01645.View ArticlePubMedGoogle Scholar
- Le WD, Xu P, Jankovic J, Jiang H, Appel SH, Smith RG, Vassilatis DK: Mutations in NR4A2 associated with familial Parkinson disease. Nat Genet. 2003, 33: 85-89. 10.1038/ng1066.View ArticlePubMedGoogle Scholar
- Xu PY, Liang R, Jankovic J, Hunter C, Zeng YX, Ashizawa T, Lai D, Le WD: Association of homozygous 7048G7049 variant in the intron six of Nurr1 gene with Parkinson's disease. Neurology. 2002, 58: 881-884.View ArticlePubMedGoogle Scholar
- Buervenich S, Carmine A, Arvidsson M, Xiang F, Zhang Z, Sydow O, Jonsson EG, Sedvall GC, Leonard S, Ross RG, Freedman R, Chowdari KV, Nimgaonkar VL, Perlmann T, Anvret M, Olson L: NURR1 mutations in cases of schizophrenia and manic-depressive disorder. Am J Med Genet. 2000, 96: 808-813. 10.1002/1096-8628(20001204)96:6<808::AID-AJMG23>3.0.CO;2-E.View ArticlePubMedGoogle Scholar
- Ishiguro H, Okubo Y, Ohtsuki T, Yamakawa-Kobayashi K, Arinami T: Mutation analysis of the retinoid X receptor beta, nuclear-related receptor 1, and peroxisome proliferator-activated receptor alpha genes in schizophrenia and alcohol dependence: possible haplotype association of nuclear-related receptor 1 gene to alcohol dependence. Am J Med Genet. 2002, 114: 15-23. 10.1002/ajmg.1620.View ArticlePubMedGoogle Scholar
- Murphy EP, McEvoy A, Conneely OM, Bresnihan B, Fitzgerald O: Involvement of the nuclear orphan receptor NURR1 in the regulation of corticotropin-releasing hormone expression and actions in human inflammatory arthritis. Arthritis Rheum. 2001, 44: 782-793. 10.1002/1529-0131(200104)44:4<782::AID-ANR134>3.0.CO;2-H.View ArticlePubMedGoogle Scholar
- Zetterstrom RH, Williams R, Perlmann T, Olson L: Cellular expression of the immediate early transcription factors Nurr1 and NGFI-B suggests a gene regulatory role in several brain regions including the nigrostriatal dopamine system. Brain Res Mol Brain Res. 1996, 41: 111-120. 10.1016/0169-328X(96)00074-5.View ArticlePubMedGoogle Scholar
- Law SW, Conneely OM, DeMayo FJ, O'Malley BW: Identification of a new brain-specific transcription factor, NURR1. Mol Endocrinol. 1992, 6: 2129-2135. 10.1210/me.6.12.2129.PubMedGoogle Scholar
- Wallen AA, Castro DS, Zetterstrom RH, Karlen M, Olson L, Ericson J, Perlmann T: Orphan nuclear receptor Nurr1 is essential for Ret expression in midbrain dopamine neurons and in the brain stem. Mol Cell Neurosci. 2001, 18: 649-663. 10.1006/mcne.2001.1057.View ArticleGoogle Scholar
- Sacchetti P, Dwornik H, Formstecher P, Rachez C, Lefebvre P: Requirements for heterodimerization between the orphan nuclear receptor Nurr1 and retinoid X receptors. J Biol Chem. 2002, 277: 35088-35096. 10.1074/jbc.M205816200.View ArticlePubMedGoogle Scholar
- Philips A, Lesage S, Gingras R, Maira MH, Gauthier Y, Hugo P, Drouin J: Novel dimeric Nur77 signaling mechanism in endocrine and lymphoid cells. Mol Cell Biol. 1997, 17: 5946-5951.PubMed CentralView ArticlePubMedGoogle Scholar
- Kovalovsky D, Refojo D, Liberman AC, Hochbaum D, Pereda MP, Coso OA, Stalla GK, Holsboer F, Arzt E: Activation and induction of NUR77/NURR1 in corticotrophs by CRH/cAMP: involvement of calcium, protein kinase A, and MAPK pathways. Mol Endocrinol. 2002, 16: 1638-1651. 10.1210/me.16.7.1638.View ArticlePubMedGoogle Scholar
- Murphy EP, Conneely OM: Neuroendocrine regulation of the hypothalamic pituitary adrenal axis by the nurr1/nur77 subfamily of nuclear receptors. Mol Endocrinol. 1997, 11: 39-47. 10.1210/me.11.1.39.View ArticlePubMedGoogle Scholar
- McEvoy AN, Murphy EA, Ponnio T, Conneely OM, Bresnihan B, Fitzgerald O, Murphy EP: Activation of nuclear orphan receptor NURR1 transcription by NF-kappa B and cyclic adenosine 5'-monophosphate response element-binding protein in rheumatoid arthritis synovial tissue. J Immunol. 2002, 168: 2979-2987.View ArticlePubMedGoogle Scholar
- Dixon G, Scanlon D, Cooper S, Broad P: A reporter gene assay for fungal sterol biosynthesis inhibitors. J Steroid Biochem Mol Biol. 1997, 62: 165-171. 10.1016/S0960-0760(97)00032-0.View ArticlePubMedGoogle Scholar
- Cerillo G, Rees A, Manchanda N, Reilly C, Brogan I, White A, Needham M: The oestrogen receptor regulates NFkappaB and AP-1 activity in a cell-specific manner. J Steroid Biochem Mol Biol. 1998, 67: 79-88. 10.1016/S0960-0760(98)00078-8.View ArticlePubMedGoogle Scholar
- Wigler M, Sweet R, Sim GK, Wold B, Pellicer A, Lacy E, Maniatis T, Silverstein S, Axel R: Transformation of mammalian cells with genes from procaryotes and eucaryotes. Cell. 1979, 16: 777-785. 10.1016/0092-8674(79)90093-X.View ArticlePubMedGoogle Scholar
- Paulsen RE, Weaver CA, Fahrner TJ, Milbrandt J: Domains regulating transcriptional activity of the inducible orphan receptor NGFI-B. J Biol Chem. 1992, 267: 16491-16496.PubMedGoogle Scholar
- Davis IJ, Hazel TG, Lau LF: Transcriptional activation by Nur77, a growth factor-inducible member of the steroid hormone receptor superfamily. Mol Endocrinol. 1991, 5: 854-859.View ArticlePubMedGoogle Scholar
- Lyon JJ, Watson RJ: Interference of Myb transactivation activity by a conditional dominant negative protein: functional interference in a cytotoxic T-cell line results in G1 arrest. Gene. 1996, 182: 123-128. 10.1016/S0378-1119(96)00531-8.View ArticlePubMedGoogle Scholar
- Castro DS, Hermanson E, Joseph B, Wallen A, Aarnisalo P, Heller A, Perlmann T: Induction of cell cycle arrest and morphological differentiation by Nurr1 and retinoids in dopamine MN9D cells. J Biol Chem. 2001, 276: 43277-43284. 10.1074/jbc.M107013200.View ArticlePubMedGoogle Scholar
- Haas C, Aicher WK, Dinkel A, Peter HH, Eibel H: Characterization of SV40T antigen immortalized human synovial fibroblasts: maintained expression patterns of EGR-1, HLA-DR and some surface receptors. Rheumatol Int. 1997, 16: 241-247. 10.1007/BF01375656.View ArticlePubMedGoogle Scholar
- Rampart M, Van Damme J, Zonnekeyn L, Herman AG: Granulocyte chemotactic protein/interleukin-8 induces plasma leakage and neutrophil accumulation in rabbit skin. Am J Pathol. 1989, 135: 21-25.PubMed CentralPubMedGoogle Scholar
- Cook PW, Brown JR, Cornell KA, Pittelkow MR: Suprabasal expression of human amphiregulin in the epidermis of transgenic mice induces a severe, early-onset, psoriasis-like skin pathology: expression of amphiregulin in the basal epidermis is also associated with synovitis. Exp Dermatol. 2004, 13: 347-356. 10.1111/j.0906-6705.2004.00183.x.View ArticlePubMedGoogle Scholar
- Campbell E, Hogaboam C, Lincoln P, Lukacs NW: Stem cell factor-induced airway hyperreactivity in allergic and normal mice. Am J Pathol. 1999, 154: 1259-1265.PubMed CentralView ArticlePubMedGoogle Scholar
- Cenni V, Sirri A, De Pol A, Maraldi NM, Marmiroli S: Interleukin-1-receptor-associated kinase 2 (IRAK2)-mediated interleukin-1-dependent nuclear factor kappaB transactivation in Saos2 cells requires the Akt/protein kinase B kinase. Biochem J. 2003, 376: 303-311. 10.1042/BJ20030028.PubMed CentralView ArticlePubMedGoogle Scholar
- Liu H, Pope RM: The role of apoptosis in rheumatoid arthritis. Curr Opin Pharmacol. 2003, 3: 317-322. 10.1016/S1471-4892(03)00037-7.View ArticlePubMedGoogle Scholar
- Liu ZG, Smith SW, McLaughlin KA, Schwartz LM, Osborne BA: Apoptotic signals delivered through the T-cell receptor of a T-cell hybrid require the immediate-early gene nur77. Nature. 1994, 367: 281-284. 10.1038/367281a0.View ArticlePubMedGoogle Scholar
- Woronicz JD, Calnan B, Ngo V, Winoto A: Requirement for the orphan steroid receptor Nur77 in apoptosis of T-cell hybridomas. Nature. 1994, 367: 277-281. 10.1038/367277a0.View ArticlePubMedGoogle Scholar
- Gruber F, Hufnagl P, Hofer-Warbinek R, Schmid JA, Breuss JM, Huber-Beckmann R, Lucerna M, Papac N, Harant H, Lindley I, de Martin R, Binder BR: Direct binding of Nur77/NAK-1 to the plasminogen activator inhibitor 1 (PAI-1) promoter regulates TNF alpha -induced PAI-1 expression. Blood. 2003, 101: 3042-3048. 10.1182/blood-2002-07-2331.View ArticlePubMedGoogle Scholar
- Pei L, Castrillo A, Chen M, Hoffmann A, Tontonoz P: Induction of NR4A orphan nuclear receptor expression in macrophages in response to inflammatory stimuli. J Biol Chem. 2005, 280: 29256-29262. 10.1074/jbc.M502606200.View ArticlePubMedGoogle Scholar
- Taylor PC, Peters AM, Paleolog E, Chapman PT, Elliott MJ, McCloskey R, Feldmann M, Maini RN: Reduction of chemokine levels and leukocyte traffic to joints by tumor necrosis factor alpha blockade in patients with rheumatoid arthritis. Arthritis Rheum. 2000, 43: 38-47. 10.1002/1529-0131(200001)43:1<38::AID-ANR6>3.0.CO;2-L.View ArticlePubMedGoogle Scholar
- Georganas C, Liu H, Perlman H, Hoffmann A, Thimmapaya B, Pope RM: Regulation of IL-6 and IL-8 expression in rheumatoid arthritis synovial fibroblasts: the dominant role for NF-kappa B but not C/EBP beta or c-Jun. J Immunol. 2000, 165: 7199-7206.View ArticlePubMedGoogle Scholar
- Ralph JA, McEvoy AN, Kane D, Bresnihan B, Fitzgerald O, Murphy EP: Modulation of orphan nuclear receptor NURR1 expression by methotrexate in human inflammatory joint disease involves adenosine A2A receptor-mediated responses. J Immunol. 2005, 175: 555-565.View ArticlePubMedGoogle Scholar
- Wansa KD, Muscat GE: TRAP220 is modulated by the antineoplastic agent 6-Mercaptopurine, and mediates the activation of the NR4A subgroup of nuclear receptors. J Mol Endocrinol. 2005, 34: 835-848. 10.1677/jme.1.01739.View ArticlePubMedGoogle Scholar
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