Cytokine-stimulated T cells induce macrophage IL-10 production dependent on phosphatidylinositol 3-kinase and p70S6K: implications for rheumatoid arthritis
© BioMed Central Ltd 2001
Received: 18 July 2001
Accepted: 6 September 2001
Published: 10 October 2001
IL-10 is an anti-inflammatory cytokine produced in the joint in rheumatoid arthritis by macrophages and infiltrating blood lymphocytes. Regulation of its expression is poorly understood, but previous findings have suggested that physical interactions with T cells may play a role. This report investigates signalling mechanisms involved in the production of macrophage IL-10 upon interaction with fixed, cytokine-stimulated T cells (Tck). Elutriated monocytes were differentiated to macrophages by macrophage-colony-stimulating factor (M-CSF) and co-cultured with fixed T cells chronically stimulated in a cytokine cocktail of IL-2/IL-6/tumour necrosis factor (TNF)-α in the presence or absence of wortmannin and LY294002, inhibitors of phosphatidylinositol 3-kinase (PI3K), or of rapamycin, an inhibitor of p70 S6-kinase (p70S6K). Spontaneous IL-10 production by rheumatoid arthritis synovial-membrane mononuclear cells (RA-SMCs) and co-cultures of rheumatoid arthritis T cells (RA-Ts) and macrophages was also assessed. RA-T and Tck induction of macrophage IL-10 production was suppressed by cell separation and inhibition of PI3K and p70S6K. PI3K involvement was also shown by phosphorylation of the downstream effector protein kinase B. Spontaneous IL-10 production by RA-SMCs was also inhibited by LY294002 and depletion of the nonadherent (T-cell-enriched) fraction of the cell population. IL-10 production in RA-SMCs and M-CSF-primed macrophages, activated by interaction with Tck, is PI3K- and p70S6K-dependent.
KeywordsIL-10 macrophage PI3K rheumatoid arthritis T cells
IL-10 is an anti-inflammatory cytokine spontaneously produced by monocytes/tissue macrophages in the rheumatoid joint , regulating IL-1 receptor antagonist (IL-1Ra)/IL-1β and tumour necrosis factor (TNF)-α in rheumatoid synovium [1,2]. Histological studies of synovium in rheumatoid arthritis (RA) have established that macrophages are in close contact with T cells in the inflamed interstitium , suggesting that contact signals between macrophages and T cells may be of importance in vivo in modulating cytokine production. Direct, contact-mediated interaction between monocytes and activated lymphocytes in vitro induced synthesis of IL-1β, TNF-α, IL-10 and metalloproteinases [4,5,6,7,8]. The mechanisms of T-cell activation determine the monocyte cytokine profile. T cells can be activated antigen-independently using a combination of inflammatory cytokines (IL-2, IL-6 and TNF-α) or IL-15 alone , suggesting a role for bystander activation of T cells in RA. These cytokine-stimulated cells (Tck) did not induce monocyte production of IL-10 , whereas T cells activated through the T cell receptor (TCR)/CD3 system did.
Macrophages differentiated in vitro from monocytes mimic tissue macrophages present in the synovial joint. Thus, differentiation might influence the profile and amount of cytokines. Macrophages primed with macrophage-colony-stimulating factor (M-CSF) produce IL-10 in response to CD40 ligation . We therefore investigated whether differentiation of monocytes to macrophages, cells more representative of the rheumatoid synovium, would alter the ability of T cells stimulated antigen-independently to induce IL-10.
The signalling mechanisms by which T-cell interactions induce macrophage IL-10 are unclear. We have shown that the lipid kinase phosphatidylinositol 3-kinase (PI3K) and its downstream substrate p70 S6-kinase (p70S6K) mediate IL-10-induced responses . However, little is known about IL-10 production, although PI3K mediates CD45-ligation-induced monocyte TNF-α production . The aim of this study was to investigate signalling pathways downstream of cell-to-cell contact between T cells and macrophages involved in IL-10 production in the context of PI3K and p70S6K.
Materials and methods
Isolation of RA synovial-membrane mononuclear cells and enrichment of CD3+ cells
Mononuclear cells from synovial membranes in rheumatoid arthritis (RA-SMCs) were prepared by collagenase and DNase digestion of membranes as described elsewhere . T cells were enriched using Dynabeads coated with anti-CD3 antibodies in accordance with the manufacturer's specifications (Dynal, Bromborough, Wirral, UK). The resulting RA synovial-membrane T cells (RA-Ts) were fixed in glutaraldehyde before co-culture (see below). Nonadherent cells were depleted from RA-SMCs by adherence (see Supplementary materials and methods).
Purification of T lymphocytes and monocytes
Human peripheral blood mononuclear cells (PBMCs) were obtained from density centrifugation of buffy coats from human venous blood through Ficoll/Hypaque density centrifugation medium (Nycomed Pharma AS, Oslo, Norway). PBMCs were centrifugally elutriated in a Beckman JE6 elutriator (Beckman RIIC Ltd, High Wycombe, Bucking-hamshire, UK). Lymphocyte and monocyte purity was assessed by flow cytometry: T cells were routinely >90% pure and monocytes >85% pure.
Stimulation and fixation of T lymphocytes
T cells were stimulated for 8 days in 25 ng/ml TNF-α, 25 ng/ml IL-2 and 100 ng/ml IL-6, using an established technique . Lymphocytes were fixed in glutaraldehyde in accordance with the method previously described .
Differentiation of monocytes to macrophages
Monocytes were differentiated with M-CSF for 7 days in accordance with the protocol used previously . Adherent cells were washed and removed from the plastic with cell-dissociation medium (Sigma, Poole, UK). The resulting adherent cells were washed and resuspended in RPMI-1640/10% FCS medium (BioWhittaker Europe Ltd, Verviers, Belgium) ready for use.
Cognate co-culture assay
M-CSF-primed macrophages were plated at 1 × 105 cells/well and allowed to settle in 96-well flat-bottomed plates for 1 hour before addition of autologous T cells. Macrophages were pretreated for 1 hour with the PI3K inhibitors wortmannin and LY294002 or the p70S6K inhibitor rapamycin. Fixed Tck or RA-Ts were added to achieve a predetermined T:macrophage ratio of 5:1 for maximal cytokine production and incubated for 24 hours, after which supernatants were harvested and stored at -20°C until ELISA. Alternatively, co-cultures were set up in 12-well plastic tissue-culture plates at a T:macrophage ratio of 5:1 with the macrophage density set at 5 × 106 per well, for western blot analysis of phosphorylated protein kinase B (phospho-PKB) and phosphorylated p70S6K (phospho-p70S6K). The culture was stimulated for 30 min, after which cells were lysed (see Supplementary materials and methods).
Cytokine determination by ELISA
IL-10 sandwich ELISAs were carried out in accordance with the manufacturer's specifications (PharMingen International, Oxford, UK). Assay was performed with a standard curve of recombinant human (rhu)IL-10 from 13–10,000 pg/ml  and showed no cross-reactivity with any cytokine tested.
Western blot analysis of phospho-PKB and phospho-p70S6K
After co-culture, cells were lysed on ice for 15 min in lysis buffer (see Supplementary materials and methods) and separated by SDS-PAGE and were western blotted in accordance with the method described elsewhere . Phosphorylated proteins were detected using antibodies raised against phospho-PKB (ser473) and phospho-p70S6K (thr389) and were compared with total protein kinase B (PKB) and p70S6K.
Tck induce macrophage-derived IL-10
Tck induction of macrophage IL-10 is PI3K- and p70S6K-dependent
Because activation of p70S6K is both PI3K-dependent [14,15] and PI3K-independent [16,17], we investigated whether p70S6K is involved in Tck induction of IL-10, using rapamycin, the inhibitor of mammalian target of rapamycin (mTOR), an upstream activator of p70S6K. Rapamycin dose-dependently suppressed macrophage IL-10 (control cells produced 192 ± 13 pg/ml, versus 38 ± 7 pg/ml for cells in 1 nM rapamycin) (Fig. 2d). Western blot analysis showed that p70S6K and its nuclear isoform p85S6K are activated upon macrophage interaction with Tck: p70S6K was phosphorylated at Thr389 (Fig. 2e, lane 2). Activation of p70S6K was PI3K-independent, however, as it was not suppressed by wort-mannin (lane 3) or LY294002 (lane 4).
RA-Ts induce IL-10 production by peripheral blood monocytes
RA-T induction of macrophage IL-10 production is PI3K- and p70S6K-dependent
Spontaneous IL-10 production by RA-SMCs is suppressed by depletion of nonadherent cells
Wortmannin and LY294002 differentially regulate spontaneous production of IL-10 by RA-SMCs
M-CSF-primed macrophages, unlike monocytes, produce IL-10 when stimulated by Tck. The ability of M-CSF-primed macrophages to produce IL-10 in response to Tck as well as other stimuli such as CD40 ligation  indicates that M-CSF priming per se is essential for IL-10 production, biasing membrane-receptor expression or signalling networks. M-CSF is required to preprogramme monocyte differentiation, as addition to monocyte co-culture failed to induce IL-10. M-CSF is readily detected in the RA joint (reviewed ), and this may explain why IL-10 is found in RA-SMC cultures .
Tck may represent the T-cell phenotype in the rheumatoid synovium [6,9], and interaction with M-CSF-primed macrophages may mimic the mechanism of IL-10 production in the rheumatoid joint. In support of this hypothesis, spontaneous IL-10 production by RA-SMCs was reduced upon depletion of the nonadherent (T-cell enriched) fraction of the cell population. In addition, RA-Ts and Tck both induced macrophage IL-10. However, RA-Ts also induced monocyte IL-10 whereas Tck did not, suggesting that although these two types of T cell express similar phenotypes, there maybe undefined membrane proteins present on RA-Ts or that there may be higher expression of such proteins in RA-Ts than in Tck.
PI3K positively regulates Tck-induced macrophage IL-10 production. Spontaneous IL-10 production by RA-SMCs was also PI3K-dependent, as LY294002 inhibited cytokine production. Wortmannin, however, did not affect IL-10 production, in contrast with Tck, which induced IL-10 in macrophages. This difference in sensitivity to wortmannin between macrophages and RA-SMCs may represent a potency effect or differential utilisation of PI3K isoforms. The distal PI3K signalling molecules, PKB and p70S6K [19,20,21,22] were also activated. The suppression of macrophage IL-10 by rapamycin suggests that PI3K-dependent IL-10 production is p70S6K-dependent. Upstream regulators of p70S6K include mTOR , PI3K , MAPK (mitogen-activated protein kinase)  and PKB . It is unclear whether p70S6K is downstream of PI3K or represents an alternative, independent pathway. Several studies have found p70S6K to be PI3K-dependent [14,15] as well as PI3K-independent, downstream of PKC and p42/44 MAPK [16,17]. We have found that macrophage IL-10 requires PI3K and p70S6K activation; however, p70S6K activation appears to be PI3K-independent, as neither of the PI3K inhibitors suppressed p70S6K phosphorylation.
These data show that the interaction between Tck and macrophages induces the anti-inflammatory cytokine IL-10. The production of this cytokine resulting from such interactions is regulated by PI3K and p70S6K. Studies of the signalling pathways involved in the regulation of proinflammatory and anti-inflammatory mediators may define therapeutic targets for chronic inflammatory diseases such as RA.
M-CSF-primed monocytes produce IL-10 upon interaction with Tck. We observed that the signalling pathway involved in macrophage IL-10 production and in RA synovial tissue cells is PI3K- and p70S6K-dependent.
(For more methodologies and results, see Supplementary material)
Supplementary materials and methods
IL-2, IL-6 and TNF-α were kind gifts from Dr U Gubler (Hoffmann-La Roche, Nutley, NJ), Dr P Ramage (Sandoz, Pharma Ltd, Basel, Switzerland) and Dr W Stec (Centre of Macromolecular Studies, Lodz, Poland), respectively. IL-10 and TNF-α ELISA reagents were purchased from PharMingen International (Oxford, UK). The inhibitors LY294002, wortmannin and rapamycin were purchased from Sigma (Poole, Dorset, UK) and antibodies against PKB, and p70S6K from New England BioLabs (UK) Ltd (Hitchin, Hertforshire, UK). All reagents were tested for the presence of lipopolysaccharide/endotoxin contamination and were found to be below the lower level of detection of the limulus amaebocyte assay (BioWhittaker, Berkshire, UK).
Isolation of RA synovial-membrane mononuclear cells and enrichment of CD3+ cells
RA synovial-membrane mononuclear cells (RA-SMCs) were obtained from samples of synovial-membrane tissue provided by the Rheumatology Clinic, Charing Cross Hospital, London, UK. All patients gave their signed consent, and ethical approval was obtained from the Riverside Research Ethics Committee (London). Patients met the American College of Rheumatology (ACR) 1987 revised criteria for RA.
In brief, tissue was cut into small pieces and digested in medium containing 0.15 mg/ml DNAse type I (Sigma, UK) and 5 mg/ml collagenase (Roche, UK) for 2 hours at 37°C. Cell debris was excluded by passing cells through a nylon mesh. Cells were then washed and collected in RPMI/10% FCS at a density of 1 × 106 cells/ml and used immediately for spontaneous cytokine production by RA-SMCs, or CD3+ T cells/nonadherent cells were depleted from adherent cells. T cells were enriched using direct, positive selection using Dynabeads (Dynal) coated with anti-CD3 antibodies. Mononuclear cells (1 × 107) were treated with 100 μl anti-CD3-coated Dynabeads for 20 min at 4°C under conditions of constant rotation. Cells attached to beads were separated from unbound cells by using a magnetic particle concentrator (Dynal) and cultured for 6 hours at 37°C. Detached cells were removed from the beads by washing them twice in medium, in the presence of the magnet. CD3+ T cells obtained were of high purity (>95%) and viability (>90%). RA CD3+ T cells were predominantly CD4+ CD45RO+. In addition, the T-cell activation markers human leukocyte antigen (HLA)-DR and CD69 were also present, suggesting that RA CD3+ T cells were of an activated, memory phenotype closely resembling that of Tck . The resulting RA-Ts were suspended in RPMI 1640 medium ready for fixation before co-culture assays (see below). Nonadherent cells were depleted from RA-SMCs: briefly, RA-SMCs were adjusted to a density of 2 × 106 cells/ml in RPMI 1640/5% FCS and left to adhere to plastic 6-well plates for 2 hours at 37°C, after which nonadherent cells were removed and adherent cells washed twice in RPMI 1640 medium. Adherent cells were removed and cultured overnight, and again nonadherent cells were washed off with RPMI 1640 medium. The resulting adherent RA-SMCs were harvested and resuspended to a density of 2 × 106cells/ml ready for comparison of their IL-10 production with spontaneous production by whole-population RA-SMCs.
RA-Ts isolated from synovial tissue by positive selection using magnetic beads coated with anti-CD3 antibodies may become activated by the beads. Therefore, we investigated the ability of such beads to further stimulate these cells. We found that CD3+ separated RA-Ts behaved like nonadherent (T-cell enriched, >70% CD3+) RA-SMCs with respect to the ability to induce monocyte or macrophage production of IL-10 and TNF-α. Also, stimulation of RA-Ts for 48 hours in culture by immobilised anti-CD3 did not significantly alter upregulation of the activation markers CD69 and HLA-DR or proliferation when compared with RA-Ts alone. In addition, our group has noted that with respect to macrophage cytokine production and activation marker analysis, RA-T cells positively selected using beads coated with anti-CD2 antibodies behaved like nonadherent (T-cell-enriched) RA-SMCs and RA-Ts separated using anti-CD3 antibodies. RA-T cells are generally of an activated phenotype (predominantly CD45RO+ HLA-DR+CD69+), and, unlike their unstimulated peripheral blood counterparts, are not significantly stimulated upon separation by anti-CD3 coated magnetic beads.
Purification of T lymphocytes and monocytes
Human PBMCs were obtained from density centrifugation of human venous blood buffy coats, purchased from the North London Blood Transfusion Service (Colindale, UK) through Ficoll/Hypaque (specific density 1.077 g/ml; Nycomed Pharma). PBMCs were centrifugally elutriated in a Beckman JE6 elutriator. Lymphocyte and monocyte purity were assessed by flow cytometry of fluorochrome-conjugated anti-CD3, anti-CD19, anti-CD14 and anti-CD45 antibodies (Becton Dickinson, Oxford, UK). Both types of cell were routinely >90% pure (T cells, >90% CD3+, <4% CD19+, <3% CD14+; and monocytes, >90% CD14+, <0.5% CD19+, <8% CD3+).
Stimulation and fixation of T lymphocytes
Purified T cells were routinely resuspended in RPMI 1640/10% human AB+ serum at a density of 1 × 106/ml and stimulated for 8 days at 37°C/5%CO2, in a modified version of the technique developed by Unutmaz and colleagues . To generate Tck, we cultured the lymphocytes for 8 days in the presence of saturating levels of the cytokines TNF-α (25 ng/ml), IL-2 (25 ng/ml) and IL-6 (100 ng/ml). Lymphocytes were then harvested and washed twice in PBS before fixation for 1 min on ice in PBS/0.05% glutaraldehyde. This fixation solution was neutralised to pH7.0 by addition of an equal volume of 0.2 M glycine/RPMI. Fixed cells were washed twice in RPMI medium and finally resuspended in RPMI/5% FCS and stored at 4°C until the experiment. Cells were routinely used up to 3 days after fixation without any reduction in magnitude of the cytokine response induced in the cognate assay.
Cognate co-culture assay
M-CSF-primed macrophages were washed in serum-free RPMI 1640 medium and plated at a density of 1 × 105 cells/well in RPMI 1640/10% FCS and were allowed to settle in 96-well flat-bottomed plate wells for at least 1 hour before addition of autologous T cells (cytokine profiles/amplitudes were irrespective of whether T cells were autologous or allogeneic MHC-mismatched, data not shown). When necessary, macrophages were pretreated for 1 hour with the PI3K inhibitors wortmannin or LY294002, or with the p70S6K inhibitor rapamycin. For maximal cytokine production, fixed allogeneic T cells or CD3+ RA-T cells were added to achieve a predetermined T-cell:macrophage ratio of 5:1. Each well was topped up to 200 μl with RPMI 1640/10% FCS. Each test condition was carried out in triplicate in each assay. The resulting co-culture assay was incubated at for 37°C/5%CO2 24 hours. All inhibitor concentrations used in this study were noncytotoxic to macrophages or RA-SMCs as determined by trypan blue exclusion and MTT assays. Supernatants were harvested and stored at -20°C until ELISA. In the case of phospho-PKB and phospho-p70S6K, the cognate co-culture was set up in 12-well plastic tissue-culture plates at a T-cell:macrophage ratio of 5:1, with the macrophage density set at 5 × 106per well. Culture was stimulated for 30 min at 37°C, and the cells were then lysed (see western blot analysis).
Western blot analysis of phospho-PKB and p70S6K
T cells and macrophages were co-cultured at a ratio of 5:1, where macrophages were seeded at a density of 5 × 106 cells/ml in 24-well plates in RPMI 1640/10% FCS. When inhibitors were used, the macrophages were pretreated for 1 hour before stimulation by the addition of fixed T cells and stimulated for 30 min before harvesting of cell lysates. The stimulation time was previously defined as optimal for activation of both PKB and p70S6K. After stimulation, cells were lysed on ice for 15 min in lysis buffer (1% NP-40, 200 mM NaCl, 0.1 mM EDTA, 1 mM dithiothreitol, 1 mM Na3VO4, 1 mM NaF, 1 mM phenylmethylsulfonyl fluoride, 10 μg/ml leupeptin, 10 μg/ml pepstatin and 10 μg/ml aprotinin). Lysed samples were separated on 10% SDS-polyacrylamide gel and western blotted onto a nitrocellulose membrane. Phosphorylated proteins were detected using antibodies raised against phospho-PKB and phospho-p70S6K, followed by anti-rabbit horseradish peroxidase conjugate and detection by enhanced chemiluminescence (ECL; Amersham Pharmacia Biotech UK Ltd, Little Chalfont, Buckinghamshire, UK). Protein bands were visualised by autoradiography using Hyperfilm (Amersham Pharmacia Biotech UK Ltd).
Data were compared using GraphPad Prism version 3.0 (GraphPad Software, Inc, San Diego, CA, USA). Statistical significances were determined by Student's t-test.
Tck induce macrophage-derived IL-10 and TNF-α
Previously, we found that Tck induced the production of TNF-α but not IL-10 in monocytes from peripheral blood, and we wished to find out whether M-CSF-differentiated macrophages would produce IL-10 and the proinflammatory cytokine TNF-α in response to the same stimulus. M-CSF-primed macrophages produced 192 ± 13 pg/ml IL-10 (see Fig. 1) upon interaction with Tck. In addition, M-CSF-primed macrophages produced 158 ± 23 pg/ml TNF-α. In this procedure, fixed Tck did not secrete any cytokines but induced cytokine production by physical contact with the macrophages, as separation of the two cell types by a semipermeable membrane abrogated the production both of IL-10 and of TNF-α. Figure 1 shows a representative experiment of IL-10 production; other experiments varied in the amount of cytokine produced (176 ± 7 to 1567 ± 134) but resulted in similar cytokine profiles. Differences in the amount of cytokine produced are thought to be a consequence of donor variation between blood packs.
The effects of Tck on cytokine production were specific to interaction of Tck or RA-Ts with monocytes/macrophages, as the addition of an exogenous cytokine cocktail (IL-2/ IL-6/TNF-α) did not induce macrophage IL-10 production as did fixed, unstimulated T cells in the presence of these cytokines (data not shown). In addition, membrane turnover would make it unlikely that surface binding of IL-2/ IL-6/TNF-α would regulate IL-10 production; if it did, monocytes would be likely to produce IL-10 in this co-culture.
Tck induction of macrophage IL-10 and TNF-α is PI3K-dependent
Tck induction of macrophage IL-10 and TNF-α is p70S6K-dependent
Tck induction of macrophage IL-10 and TNF-α is p70S6K-dependent. Previously, it had been reported that the activation of p70S6K is both PI3K-dependent [14,15] and PI3K-independent [16,17]. It was therefore of interest to find out whether p70S6K activation was involved in Tck induction of IL-10, using rapamycin, the inhibitor of mTOR, an upstream activator of p70S6K. Rapamycin suppressed IL-10 by M-CSF-primed macrophages in a dose-dependent manner. In Fig. 2d, IL-10 production was inhibited from control levels of 192 ± 13 pg/ml to 38 ± 7 pg/ml by 1 nM rapamycin with an IC50 value of 6 pM (P = 0.006). In addition, TNF-α was also inhibited by rapamycin, from control (510 ± 33 pg/ml) to 56 ± 6 pg/ml at 1 nM (P = 0.0013) (IC50 = 16 pM) (Supplementary Fig. 1c). Western blot analysis showed that p70S6K and its nuclear isoform, p85S6K, are activated upon macrophage interaction with fixed Tck. p70S6K was phosphorylated at Thr389 upon this interaction (see Fig. 2c, lane 2). The activation of p70S6K was not dependent on PI3K activity, however, as it was not suppressed by the PI3K inhibitors wortmannin (lane 3) or LY294002 (lane 4) but was inhibited by rapamycin (data not shown).
RA-Ts induce macrophage IL-10 and TNF-α production
Spontaneous IL-10 and TNF-α production by RA-SMCs is suppressed by removal of nonadherent cells
Wortmannin and LY294002 differentially regulate spontaneous IL-10 and TNF-α production by RA-SMCs
RA-T cell induction of macrophage IL-10 and TNF-α production is PI3K-dependent
Supplementary discussion and conclusion
PI3K appears to play a role in Tck and RA-T induction of macrophage cytokine production, but caution is needed when interpreting data using specific inhibitors. It is well established that LY294002 and wortmannin are PI3K inhibitors, with LY294002 being the more specific. However, at high concentrations, wortmannin can inhibit several other enzymes, including phospholipase A2, phosphatidylinositol 4-kinase, phospholipase D and myosin light-chain kinase. To ascribe PI3K specificity to the observations being described, these inhibitors were routinely tested for the ability to inhibit PI3K by abrogation of PKB phosphorylation. In addition, the specificity of PI3K was validated by the TNF-α augmentation (see Supplementary Figure 1) where both wortmannin and LY294002 resulted in similar responses. Because wortmannin irreversibly inhibits PI3K, its lack of effect on RA-SMC IL-10 production over 24 hours may reflect the turnover rate for PI3K in these cells, which probably differs from that observed with M-CSF-primed macrophages.
The supplementary data presented here suggest that the signalling pathways involved in Tck-induced macrophage IL-10 and TNF-α share a common component, p70S6K. PI3K however, differentially regulates IL-10 and TNF-α production – IL-10 positively, and TNF-α negatively. Negative regulation of TNF-α would appear to be independent of IL-10, as neutralisation of endogenous IL-10 does not affect wortmannin's augmentation of macrophage TNF-α upon interaction with Tck (data not shown). These observations of PI3K involvement appear to be reproducible by RA-SMCs and RA-T/macrophage co-culture, potentially validating the Tck/macrophage model for the study of cytokine production with respect to cellular interactions in the rheumatoid joint. These data suggest that the PI3K pathway is a potential therapeutic target, activation of which may induce IL-10 while concomitantly suppressing TNF-α production, redressing the balance between pro-inflammatory and anti-inflammatory cytokines produced in the rheumatoid joint.
50% effective dose
enzyme-linked immunosorbent assay
fetal calf serum
human leukocyte antigen
50% inhibitory concentration
peripheral blood mononuclear cell
phosphate-buffered saline [solution]
protein kinase B
mononuclear cells from synovial membranes in rheumatoid arthritis
T cells from synovial membranes in rheumatoid arthritis
Roswell Park Memorial Institute [medium]
cytokine-stimulated T cells
tumour necrosis factor.
We thank Dr Ferdinand Lali for help in setting up phospho-western blots and Dr Abhilash Jain, Mr Gurdeep Kahlon and Mrs Sarah Field for obtaining and preparing RA-SMCs. This work was funded by a Wellcome Trust project grant.
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