Polymorphonuclear neutrophils (PMNs) are a key component of the innate immune system. Their activation leads to the release of potent antimicrobial agents through degranulation. Simultaneously, PMNs release cell surface-derived microvesicles, so-called ectosomes (PMN-Ect). PMN-Ect are rightside-out vesicles with a diameter of 50–200 nm. They expose phosphatidylserine in the outer leaflet of their membrane and down-modulate monocyte/macrophage-activation in vitro. In this study, we analyzed the effects of PMN-Ect on maturation of human monocyte-derived dendritic cells (MoDCs). Intriguingly, exposing immature MoDCs to PMN-Ect modified their morphology, reduced their phagocytic activity, and increased the release of TGF-β1. When immature MoDCs were incubated with PMN-Ect and stimulated with the TLR4 ligand LPS, the maturation process was partially inhibited as evidenced by reduced expression of cell surface markers (CD40, CD80, CD83, CD86, and HLA-DP DQ DR), inhibition of cytokine-release (IL-8, IL-10, IL-12, and TNF-α), and a reduced capacity to induce T cell proliferation. Together these data provide evidence that PMN-Ect have the ability to modify MoDC maturation and function. PMN-Ect may thus represent an as yet unidentified host-factor influencing MoDC maturation at the site of injury, thereby possibly impacting on downstream MoDC-dependent immunity.
Many eukaryotic cells release small vesicles by ectocytosis (i.e., ectosomes (Ect)3), either spontaneously or in response to various stimuli (1, 2). Data on the function(s) of Ect have accumulated recently. Depending on their cellular origin, Ect have been associated with a broad spectrum of biological activities. Ect derived from endothelial cells have been described to bind monocytic cells and to induce procoagulant activity (3), whereas Ect derived from platelets and monocytes were shown to directly promote hemostasis and induce inflammation by activating endothelial cells (4, 5). As for monocyte-derived Ect, their proinflammatory potential has been linked to their potential to mediate the rapid secretion of IL-1β and to express tissue factor (6, 7, 8).
Activated human polymorphonuclear neutrophils (PMNs) release Ect at the time of degranulation. PMN-Ect have been well characterized (9, 10, 11). They are rightside-out vesicles with cytosolic content and a diameter of 50–200 nm and expose phosphatidylserine (PS) in the outer leaflet of their membrane. Contrasting other Ect, PMN-Ect have recently been shown to inhibit the inflammatory properties of human monocyte-derived macrophages in vitro. Induction of TGF-β1 secretion by macrophages and the exposure of PS on the surface of PMN-Ect were shown to contribute independently to this effect (11).
Dendritic cells (DCs) function as sentinels of the immune system, bridging innate and acquired immunity. In their tissue of residence, immature DCs (iDCs) internalize and proteolytically process self- and non-self Ags. When Ag uptake and processing occurs under inflammatory conditions, for example, conditions characterized by concomitant pattern recognition signals delivered to iDCs via pathogen-derived products, iDCs change their morphology, shut down phagocytosis, and increase expression of costimulatory molecules and secretion of cytokines. Simultaneously, DCs migrate into secondary lymphoid organs (i.e., spleen or lymph nodes). DCs activated and induced to mature under inflammatory conditions are then capable of priming and fully activating naive CD4+ and CD8+ T cells. By contrast, partially and/or “inappropriately” activated iDCs are thought to induce immunological tolerance to Ags presented on their surface (12, 13, 14, 15). The precise factors determining immunogenic vs tolerogenic DC-mediated priming remain to be defined.
PMN-Ect share important biological properties with apoptotic cells, including the expression of PS (9, 10, 11, 16). Apoptotic cells have been identified as major regulators of DC function both in vitro and in vivo (12, 13, 14, 15, 17, 18, 19, 20). PS, both on apoptotic cells as well as when incorporated into artificial liposomes, has been identified as a major factor influencing monocyte-derived dendritic cell (MoDC) maturation and function (21, 22, 23, 24). Furthermore, vesicles expressing PS released by tumor cells have recently been shown to down-regulate the activation of DCs, thus impairing the possible immune response against tumor Ags (25).
Although it is plausible that during the early phase of an immune response PMN-Ect interact with DCs, no data characterizing such interactions exist. In this study, we investigated the impact of PMN-Ect on MoDCs. Specifically, we examined the maturation of MoDCs in the presence/absence of PMN-Ect and the functional activity of MoDCs that were matured in the presence of PMN-Ect.
Materials and Methods
Collection of PMN-Ect
To isolate PMNs, a fresh buffy coat was diluted 1/1 (v/v) with PBS-EDTA (2 mM), mixed with 0.25 vol of 4% dextran T500 (GE Healthcare Bio-Sciences), and left for 30 min for erythrocyte sedimentation. Leukocyte-rich supernatant was aspirated and centrifuged for 10 min at 200 × g. The pellet was resuspended in 9 ml of ultrapure water to lyse erythrocytes. Isotonicity was restored by addition of 3 ml of KCl (0.6 M) and 40 ml of NaCl (0.15 M). Cells were then centrifuged for 10 min at 350 × g and resuspended in 20 ml of PBS-EDTA. This suspension was layered over 20 ml of Histopaque-1077 (Sigma-Aldrich) and centrifuged for 30 min at 350 × g. The PMN-rich pellet was recovered and washed twice in PBS-EDTA. All manipulations were performed at 4°C, thus minimizing PMN activation (10, 11).
For stimulation, pooled PMNs (1 × 107 cells/ml) from healthy blood donors were diluted 1/1 (v/v) in prewarmed (37°C) RPMI 1640 (Invitrogen Life Technologies) with 1 μM fMLP and incubated for 20 min at 37°C. PMNs were removed by centrifugation (4000 × g for 15 min at 4°C), and PMN-Ect contained in the supernatant were concentrated with Centriprep centrifugal filter devices (molecular mass 10,000 kDa cutoff; Millipore) and stored in aliquots at −80°C until use (10, 11).
Isolation, culture, and maturation of MoDCs
MoDCs were derived from monocytes isolated from fresh buffy coats. A buffy coat was diluted 1/1 (v/v) with HBSS (Invitrogen Life Technologies), layered over Histopaque-1077, and centrifuged for 30 min at 350 × g. PBMCs were washed and cultured in complete medium (RPMI 1640, 1% l-glutamine, 1% penicillin/streptomycin, and 10% FCS) for 1 h at 37°C in 6-well plates or in 75-ml flasks. After incubation, nonadherent cells were removed by washing twice with prewarmed RPMI 1640. The remaining adherent cells were then cultured in complete medium supplemented with 50 ng/ml GM-CSF and 50 ng/ml IL-4 (ImmunoTools). On days 2 and 5, the media including the supplements were replaced. On day 6, nonadherent immature MoDCs (iMoDCs) were harvested, counted, and plated in 6- or 24-well plates (1 × 105 cells/ml) in fresh medium containing GM-CSF and IL-4 (50 ng/ml each) (26, 27). On day 6, LPS (10 ng/ml final concentration; Sigma-Aldrich) and/or PMN-Ect was added. MoDCs and supernatants were collected 24 h later.
Flow cytometric analysis
Flow cytometric analyses of cell surface markers were performed using the following mouse mAbs conjugated with FITC: CD14, CD40, CD80, CD83, CD86, and HLA-DP DQ DR (Serotec) and with PE: CCR7 (BD Biosciences/BD Pharmingen). In each experiment, parallel stainings with isotype-matched controls IgG1-FITC, IgG2a-FITC (Serotec), and IgG2a-PE (BD Biosciences/BD Pharmingen) were performed. After each incubation, cells were spun down, resuspended in PBS/1% BSA, and labeled for 30–45 min at 4°C with appropriate Abs. After labeling, cells were washed twice in PBS/1% BSA and data were acquired with a FACSCalibur flow cytometer (BD Biosciences) and analyzed using Summit software (DakoCytomation). A minimum of 10,000 events were collected per dataset.
Detection of apoptosis
Detection of apoptotic and/or necrotic cells was performed using FITC-conjugated annexin V (AnV; BD Biosciences/BD Pharmingen) and Via-Probe (BD Biosciences/BD Pharmingen), a nucleic acid dye (7-aminoactinomycin D) used for the exclusion of nonviable cells. MoDCs were washed twice with cold PBS and resuspended in AnV-binding buffer (BD Biosciences/BD Pharmingen) at a concentration of 1 × 106 cells/ml. Aliquots of 100 μl were stained with 5 μl of AnV-FITC and 2 μl of Via-Probe and incubated for 15 min at room temperature in the dark. Samples were then diluted in 400 μl of binding buffer and analyzed by flow cytometry.
Endocytic activity of MoDCs was measured by assessing uptake of FITC-conjugated dextran (molecular mass, 40,000 kDa; Molecular Probes) (27). To that end, cells were incubated with 0.5 mg/ml FITC-conjugated dextran in complete medium for 15, 30, or 45 min at 37 and 4°C to measure specific uptake vs nonspecific binding, respectively. MoDCs were then washed three times and analyzed by flow cytometry.
Quantitation of cytokines by ELISA
Relevant supernatants were collected and spun for 10 min at 500 × g at 4°C to remove cellular debris. The concentrations of IL-8, IL-10, IL-12p70, TNF-α, and TGF-β1 were measured using OptEIA ELISA kits (BD Biosciences) according to the manufacturer’s instructions. All samples were measured in duplicates.
T cell proliferation assay
iMoDCs incubated for 24 h with 1) medium alone, 2) medium and PMN-Ect, 3) medium and LPS, and 4) medium and LPS and PMN-Ect were collected and washed twice to remove excess PMN-Ect and LPS. CD3+ T cells, obtained by positive magnetic selection with CD3+ microbeads (Miltenyi Biotec), were labeled with 0.25 mM CFSE at room temperature for 10 min in the dark. The reaction was stopped by adding cold complete medium. Cells were then washed twice with cold medium and seeded at a 1:1 ratio (if not stated otherwise) with MoDCs. After 5 days of culture, proliferation of CFSE-labeled T cells was assessed by flow cytometry.
PS blocking assay
On day 6, before coincubation with MoDCs, PMN-Ect were preincubated for 30 min at 4°C with recombinant AnV (50 μg/ml final concentration; BD Biosciences/BD Pharmingen) and then washed. MoDCs and supernatants were collected after 24 h.
Datasets were tested for normality. For normally distributed data, parametric analysis (two-tailed paired Student’s t test) and for non-normally distributed data nonparametric analysis (Wilcoxon-matched pairs test) were performed using GraphPad Prism software. Data are expressed as mean ± SEM. A p < 0.05 was considered statistically significant.
PMN-Ect modified the morphology of MoDCs
We first assessed the effects of PMN-Ect on MoDC morphology. Before LPS exposure, iMoDCs were round, whereas after 24 h of LPS maturation the name-giving dendritic morphology became evident (Fig. 1,A). The major finding was that the formation of dendrites was inhibited by PMN-Ect when MoDCs were matured with LPS. In line with the literature, there were no significant scatter modifications between iMoDCs and LPS-matured MoDCs (mMoDCs) (Fig. 1,B: Ø vs LPS) (21, 28). Intriguingly, the incubation of MoDCs with PMN-Ect, exposed or not to LPS, produced a shift of the scatter of the MoDCs (Fig. 1 B), indicating that the PMN-Ect had a direct effect on MoDC morphology. We could not detect a modification of PMN-Ect on MoDC viability, tested both via AnV and Via-Probe binding (data not shown).
PMN-Ect down-regulated the endocytic activity of MoDCs
We next examined whether PMN-Ect have an impact on the endocytic activity of MoDCs. MoDCs were incubated with FITC-conjugated dextran at 37°C to measure specific uptake and at 4°C to quantify nonspecific binding. As expected, mMoDCs lost partially their capacity to phagocytose dextran particles (Fig. 2). PMN-Ect significantly reduced the endocytic capacity of iMoDCs (Fig. 2,A) as well as mMoDCs (Fig. 2,B). Strikingly, PMN-Ect reduced iMoDC phagocytosis to the level of phagocytosis observed in mMoDCs. At 4°C no incorporation of FITC-conjugated dextran by MoDCs was observed (Fig. 2). These data indicate that PMN-Ect alter the endocytic capacity of MoDCs.
PMN-Ect down-regulated the phenotypic maturation of MoDCs
Having shown that PMN-Ect influence MoDC morphology and endocytic capacity, we next asked the question whether PMN-Ect impact on expression of surface markers of nonactivated vs mMoDCs as well. The data of six independent experiments were analyzed using the two-tailed paired Student t test. Of interest, iMoDCs exposed to PMN-Ect consistently expressed less CD40, CD86, and HLA-DP DQ DR than iMoDCs incubated without PMN-Ect (illustrated in Fig. 3), although these differences did not reach statistical significance.
As expected, coincubation of iMoDCs with LPS induced significant up-regulation of surface markers indicative of MoDC maturation (mMoDCs): CD40 (mean fluorescence intensity (MFI), 72.05 ± 10.02 vs 175.9 ± 36.74; p = 0.026), CD83 (6.308 ± 0.681 vs 17.48 ± 2.991; p = 0.007), CD86 (104.5 ± 18.11 vs 121 ± 20.01; p = 0.021), HLA-DP DQ DR (1049 ± 62.92 vs 1402 ± 74.28; p < 0.001). Up-regulation of CD80 was evident as well, but did not reach statistical significance (7.795 ± 1.019 vs 9.487 ± 1.282; p = 0.14; Fig. 3).
mMoDCs coincubated with PMN-Ect, in contrast, expressed significantly less CD40 (MFI, 175.9 ± 36.74 vs 127.1 ± 40.73; p = 0.027), CD80 (9.487 ± 1.282 vs 7.665 ± 0.9681; p = 0.019), CD83 (17.48 ± 2.991 vs 11.74 ± 1.932; p = 0.042), CD86 (121 ± 20.01 vs 78.93 ± 19.23; p = 0.002), and HLA-DP DQ DR (1402 ± 74.28 vs 1014 ± 124.8; p = 0.029) than mMoDCs alone (Fig. 3).
Together these data are evidence that PMN-Ect have the potential to modify MoDC maturation as judged by the expression pattern of various cell surface markers.
PMN-Ect inhibited the cytokine release of MoDCs
We next assessed whether the effect of PMN-Ect on MoDC phenotype was accompanied by changes in their release of cytokines (IL-8, IL-10, IL-12p70, and TNF-α). Levels of IL-8, IL-10, IL-12p70, and TNF-α remained unchanged when iMoDCs were incubated with PMN-Ect as compared with iMoDCs alone (Fig. 4). Compared with iMoDCs alone, secretion of each of these cytokines was up-regulated when iMoDCs were matured with LPS (IL-8: 274.8 ± 44.39 vs 24 346 ± 9410 pg/ml; p = 0.002; IL-10: 30.27 ± 12.98 vs 241.5 ± 51.72 pg/ml; p = 0.002; IL-12p70: 3.71 ± 0.52 vs 23.8 ± 3.14 pg/ml; p = 0.002; TNF-α: 107 ± 24.83 vs 3168 ± 912.9 pg/ml; p = 0.002).
Importantly, and in line with the effect of PMN-Ect on cell surface maturation markers, coincubation of mMoDCs with PMN-Ect strongly down-modulated the release of IL-10 (241.5 ± 51.72 vs 144.4 ± 56.56 pg/ml; p = 0.002), IL-12p70 (23.80 ± 3.140 vs 9.053 ± 1.629 pg/ml; p = 0.014), and TNF-α (3168 ± 912.9 vs 983.8 ± 361.9 pg/ml; p = 0.002) and slightly but significantly reduced the release of IL-8 (24 346 ± 9410 vs 17 237 ± 7071 pg/ml; p = 0.01).
Of note, variability in the absolute concentrations of cytokines was important and somewhat unpredictable. This variability might originate largely from the fact that for each experiment cells and PMN-Ect from different donors were used. For example, as shown in Fig. 4, cells from one donor reacted very strongly to LPS and, compared with other donors, released huge amounts of IL-8, IL-10, and TNF-α. Importantly, however, also in this donor a relative reduction was observed when iMoDCs were matured in the presence of PMN-Ect.
Because our results might have been modified by the fact that the PMN-Ect were from different donors than the MoDCs, we repeated the same studies using an autologous system. However, similar differences in the expression of surface markers and cytokine release were observed using PMN-Ect and MoDCs from the same donor (four independent experiments, data not shown).
MoDCs exposed to PMN-Ect released TGF-β1 and expressed less CCR7
Since TGF-β1 is known to be a central down-regulator of DCs, we measured its release when these cells were exposed to PMN-Ect. Strikingly, PMN-Ect increased the release of TGF-β1 from MoDCs in all experiments performed, whether the cells were immature (43.42 ± 19.64 vs 217 ± 46.61 pg/ml; p = 0.002) or LPS matured (90.63 ± 24.43 vs 260.3 ± 59 pg/ml; p = 0.002). Identical results were found whether the MoDCs and the PMN-Ect were from the same donor or not (Fig. 5 A).
MoDCs exposed to PMN-Ect stimulated T cell proliferation poorly
Given that PMN-Ect were found to impact on phenotypic maturation and the amount of inflammatory cytokines released by MoDCs, we next examined the immunostimulatory capacity of MoDCs exposed to PMN-Ect. When MoDCs were incubated with PMN-Ect without LPS, no significant effect on T cell proliferation was observed. By contrast, MoDCs coincubated with PMN-Ect at the time of LPS exposure induced significantly less T cell proliferation than their non-PMN-Ect-exposed counterparts (mean decrease in percent proliferating cells: 20.4%; p < 0.001; Fig. 6). The effect was seen using MoDCs suppressed by autologous and allogeneic PMN-Ect. The results observed in a MoDC:T cell ratio of 1 was also observed at a ratio of 1:10 (data not shown).
The activities of PMN-Ect were reversed by AnV binding
PS exposure on PMN-Ect has previously been shown using AnV binding (10). Since PS might be involved in the functional property of PMN-Ect to down-regulate the maturation of MoDCs, we coated first the PMN-Ect with recombinant AnV before adding them to the MoDCs. For mMoDCs, this coating reversed the inhibitory effects of PMN-Ect on expression of surface markers (for CD40, CD83, CD86, and HLA-DP DQ DR) (Fig. 7, cf LPS plus PMN-Ect and LPS plus PMN-Ect/AnV). We could not analyze the release of cytokines, because AnV per se induced an activation of MoDCs.
In the present study, we identified a new pathway by which activated human polymorphonuclear leukocytes, through the release of Ect, skew DC differentiation. It is likely that PMN-Ect released in vivo interact with tissue-resident iDCs at the site of injury or infection, i.e., when iDCs are exposed to maturation-inducing substances released from bacteria (14, 30). LPS and zymosan trigger, respectively, TLR4 and TLR2 receptors on iDCs (13, 31, 32) and induce maturation with release of specific cytokines (TNF-α, IL-12, etc.) and increased expression of costimulatory molecules such as CD80 and CD86, CD40, CD83, and HLA class II molecules (12, 15, 33). In this study, we showed that PMN-Ect inhibited the maturation of iMoDCs by LPS and induced new morphological and functional characteristics with a resulting reduced capacity to activate T cells. In addition, iMoDCs exposed to PMN-Ect released TGF-β1 and it might well be that to some or a larger extent TGF-β1 was responsible for the down-regulation of TLR4-mediated maturation of iDCs, as observed by others (15, 34), and of surface expression of CCR7 (29). During DC maturation, the up-regulated CCR7 is responsible for directing the migration of DCs to the lymph nodes. It has been shown that CCR7 controls the cytoarchitecture, the rate of endocytosis, the survival, the migratory speed, and the maturation of the DCs (35), so that a reduced expression of CCR7 might interfere with normal immune response. PMN-Ect have already been shown to induce the release of TGF-β1 from macrophages, a release, which was responsible in part for the inhibition of macrophage activation by LPS and zymosan (11). Hence, it appears that PMN-Ect have down-regulating properties at different levels in the inflammatory process, which lead to T cell activation. Interestingly, similar properties have been ascribed to cells undergoing apoptosis. Good evidence indicates that exposure of iDCs to apoptotic cells induces a tolerogenic – as opposed to an immunogenic-DC phenotype (12, 13, 15, 18, 20).
Together these observations highlight the complexity of the inflammatory process, which on one hand has to be amplified so as to trigger a specific immune response, but also has to limit excessive inflammation and prevent autoimmunity. For instance, apoptotic PMNs may have a protective role in allowing the termination of acute inflammation due to their overexpression of CCR5, which may adsorb CCL3 and CCL5 away from their targets, and thus act as “terminators” of chemokine signaling during the resolution of inflammation (36, 37). Ect are released at the early phase of PMN activation, when much phagocytic and inflammatory activity is still needed at the site of injury, whether this injury is related to cell necrosis and/or infection. But such local inflammation requires control as well and does not need systematically DCs to provoke T cell stimulation and an acquired immune response. Our results indicate that such early down-regulation is a property of PMN-Ect, which in the local context may participate in the control of autoimmune responses, similarly to what has been suggested for apoptotic cells (15, 19, 20, 22). However and by contrast to apoptotic cells, PMN-Ect have the particularity to be involved very early in inflammation, a time point, which might be crucial for determining later aspects of the cascade responsible for acquired immunity, in that sense not terminator of inflammation, but responsible for controlling the immune response.
Two aspects merit attention. First the effects of PMN-Ect on resting iMoDCs and then those on the maturation process of MoDCs induced by LPS. The morphological and phenotypic changes of iMoDCs cocultured with PMN-Ect were subtle. There was a minimal change in the forward and side scatters seen by FACS analysis and a nonsignificant but repeatedly observed very slight reduction of the expression of costimulatory molecules (CD40, CD86) and HLA class II molecules. However, iMoDCs that were exposed to PMN-Ect lost their phagocytic activity as indicated by a clearly reduced uptake of dextran particles. Thus, PMN-Ect may actively change the biological behavior of iDCs. Neither PS liposomes (a model of apoptotic cells) nor apoptotic primary cells (keratinocytes, monocytes, T and B cells) or cell lines were reported to induce similar functional changes in iDCs (21, 38). Recently, βig-h3, a protein expressed by iDCs and macrophages, has been shown to be involved in phagocytosis and suppressed during maturation of DCs. Whether PMN-Ect suppress the expression/production of βig-h3 remains an intriguing hypothesis (39). The comparisons between the expression of costimulatory and HLA class II molecules on iDCs induced by either apoptotic PMNs or PMN-Ect show divergent trends as well. Whereas both down-modulate CD40, CD80, and CD86 on iDCs, apoptotic PMNs increase CD83 and HLA class II, whereas PMN-Ect did the opposite (40). From the foregoing it seems evident that whereas there might be similarities in the responses induced by Ect and apoptotic cells, these responses are not identical.
Compared with their influence on iMoDCs, the impact of PMN-Ect on the LPS-induced maturation process of MoDCs was more obvious, significantly affecting phenotype, release of proinflammatory cytokines, and their immunogenicity vis-à-vis allogeneic T cells. Effects of PMN-Ect on LPS-induced maturation are analogous to those obtained with apoptotic cells and PS liposomes (19, 21, 24, 33, 38, 41, 42). Specifically, DCs exposed to PS liposomes before LPS maturation expressed significantly lower levels of CD40, CD80, CD83, CD86, HLA-ABC, and HLA-DR, secreted significantly less IL-10 and IL-12, and had impaired ability to activate allogeneic T cells (21). These data might indicate that PS per se plays a major role in interfering with the maturation process of DCs.
The mechanisms underlining the biological effects of PMN-Ect on DCs remain speculative. In many respects, they may be similar to those proposed for the down-regulation of DCs by apoptotic cells, including the high expression of PS, which in multiple experiments has been shown to allow specific binding of apoptotic cells to macrophages or DCs (16, 22, 43, 44, 45, 46). AnV is known to interfere with the binding of PS-expressing cells/particles to macrophages (11). In the experiments performed here, we could reverse the down-regulation of surface markers of MoDCs by PMN-Ect by incubating first the PMN-Ect with AnV, suggesting that the expression of PS on PMN-Ect was responsible for their property to modify MoDCs. However, PMN-Ect, which had bound AnV, induced by themselves the release of TNF-α by iDCs, indicating that AnV might have induced/blocked other interactions not directly related to PS as well.
Apoptotic cells and Ect released by the same type of cells express different sets of proteins. For instance, PMN-Ect express high levels of complement receptor 1 and CD66b (9, 10), whereas these molecules are down-regulated on apoptotic PMNs (47). Apoptotic cells express on their surface nuclear components (48), which will not be present on Ect released by live, activated cells. Thus, it is likely that diverse sets of proteins on dying cells vs Ect will allow different functional activities, although many of the basic properties might be very similar.
For instance, the specific release of TGF-β1 induced by the binding of PMN-Ect to iMoDCs is most likely one of the essential mediators reprogramming the DCs so that it has a lower reactivity to LPS. Indeed TGF-β is a major player in modulating the activity of iDCs and their maturation (15, 25, 49, 50). It is produced by iDCs exposed to apoptotic cells as well and under such conditions reprograms the DCs to become tolerogenic (15, 20). Whether iDCs exposed to PMN-Ect have similar properties, i.e., become tolerogenic, remains to be tested.
In conclusion, we suggest that, in addition to regulating macrophage activation (11), PMN-Ect may have the potential to influence the outcome of Ag-specific immunity by playing an active role in shaping DC-dependent immunity. In vivo models of inflammation/infection will now have to test the relevance of the here-proposed activities of PMN-Ect.
We thank Dr. Salima Sadallah and Brigitte Schneider for helpful suggestions and continuous support.
The authors have no financial conflict of interest.
The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.
This work was supported by Swiss National Science Foundation Grants 32000-116839 and PP00B-114850, the Roche Foundation for Anemia Research, and Fondazione per la Ricerca Sulla Trasfusione e Sui Trapianti.
Abbreviations used in this paper: Ect, ectosome; PMN, polymorphonuclear neutrophil; PS, phosphatidylserine; DC, dendritic cell; iDC, immature DC; MoDC, monocyte-derived DC; iMoDC, immature MoDC; mMoDC, matured MoDC; MFI, mean fluorescence intensity; AnV, annexin V; FSC, forward scatter; SSC, side scatter.