Myelin-phagocytosing macrophages modulate autoreactive T cell proliferation
© Bogie et al; licensee BioMed Central Ltd. 2011
Received: 15 March 2011
Accepted: 25 July 2011
Published: 25 July 2011
Multiple sclerosis (MS) is a chronic, inflammatory, demyelinating disease of the central nervous system (CNS) in which macrophages play a central role. Initially, macrophages where thought to be merely detrimental in MS, however, recent evidence suggests that their functional phenotype is altered following myelin phagocytosis. Macrophages that have phagocytosed myelin may be less inflammatory and may exert beneficial effects. The presence of myelin-containing macrophages in CNS-draining lymph nodes and perivascular spaces of MS patients suggests that these cells are ideally positioned to exert an immune regulatory role. Therefore we evaluated in this study the effect of myelin-phagocytosing macrophages on lymphocyte reactivity.
Thioglycolate-elicited rat peritoneal macrophages were loaded with myelin and cocultured with myelin-basic protein (MBP) or ovalbumin (OVA) reactive lymphocytes. Lymphocyte proliferation was determined by CFSE-labeling. The role of nitric oxide in regulating lymphocyte proliferation was assessed by addition of an inhibitor of inducible nitric oxide synthase to the coculture. In vivo immune regulation was investigated by treating MBP- and OVA-immunized animals subcutaneously with myelin. Cognate antigen specific lymphocyte proliferation and nitric oxide production were determined 9d post-immunization.
In this study we demonstrate that myelin-phagocytosing macrophages inhibit TCR-triggered lymphocyte proliferation in an antigen-independent manner. The observed immune suppression is mediated by an increase in NO production by myelin-phagocytosing macrophages upon contact with lymphocytes. Additionally, myelin delivery to primarily CD169+ macrophages in popliteal lymph nodes of OVA-immunized animals results in a reduced cognate antigen specific proliferation. In contrast to OVA-immunized animals, lymphocytes from MBP-immunized animals displayed an increased proliferation after stimulation with their cognate antigen, indicating that myelin-phagocytosing macrophages have dual effects depending on the specificity of surrounding lymphocytes.
Collectively our data show that myelin phagocytosis leads to an altered macrophage function that inhibits lymphocyte proliferation. Additionally, results from this study indicate that myelin-phagocytosing macrophages fulfill a dual role in vivo. On one hand they aggravate autoimmunity by activating myelin-reactive lymphocytes and on the other hand they suppress lymphocyte reactivity by producing NO.
Multiple Sclerosis (MS) is characterized as a chronic, inflammatory, neurodegenerative disease of the central nervous system (CNS). It is regarded to be an autoimmune disease as activated autoimmune lymphocytes are pivotal in orchestrating the immunopathological processes involved in myelin sheath damage [1–4].
Pathologically, MS is characterized by CNS infiltration of activated myelin-reactive lymphocytes and macrophages, resulting in an inflammatory microenvironment. Microglia and macrophages typically accumulate in the perivascular spaces and the brain parenchyma near terminal ovoids of transected axons . They are thought to be the primary effector cells in MS and its animal model, experimental allergic encephalomyelitis (EAE) [6–8]. Effector mechanisms of activated macrophages and microglia include the internalization of myelin, and the secretion of inflammatory and toxic mediators which negatively influence axonal and myelin integrity [9–22].
In contrast to their apparent detrimental role in MS, increasing evidence suggests an additional neuroprotective role for macrophages. Although two seemingly mutually exclusive processes, various studies have reported such a dual role of monocytes and macrophages in both injury and repair [23, 24]. In neurodegenerative models, remyelination is for instance often correlated with large numbers of macrophages and microglia in an inflammatory microenvironment [25–27]. Furthermore, as contact with CNS myelin debris inhibits oligodendrocyte progenitor maturation in vitro, and as macrophages have been described to actively phagocytose myelin debris, local clearance of myelin debris in the centre or vicinity of lesions is suggested to be a necessary prerequisite for axonal remyelination following demyelination . This hypothesis is supported by the fact that monocyte depletion and a consequent inability to clear the microenvironment of myelin debris, causes an impairment of oligodendrocyte progenitor differentiation in vivo [29, 30]. Finally, recent evidence indicates that monocyte-derived macrophages, peritoneal macrophages, microglia and dendritic cells (DCs) obtain anti-inflammatory characteristics following internalization of myelin [12–14, 31]. These studies clearly demonstrate that macrophages, besides their apparent role in neurodegeneration, may exert a neuroprotective influence on MS pathogenesis by clearance of myelin debris and by altering their phenotype following myelin internalization.
Perivascular macrophages, infiltrated macrophages and microglia are ideally positioned to influence infiltrating and infiltrated myelin-reactive lymphocytes. Indeed, CNS reactivation of autoreactive lymphocytes by local antigen presenting cells displaying myelin antigens is thought to initiate and maintain the inflammatory cascade observed in the brain of MS patients [3, 4, 32]. The presence of brain antigen-containing phagocytes in secondary lymph nodes in MS and EAE further emphasizes a possible crucial role of these cells in modulating the immune response during MS and EAE pathogenesis [33–35]. Phenotypical analysis of these macrophages further revealed that in contrast to neuronal antigen containing phagocytes, the majority of myelin-containing APCs express anti-inflammatory mediators. How brain antigens gain excess to CNS draining secondary lymph nodes, either chemotactically in the context of phagocytes or as soluble products, remains to be clarified [12, 36, 37].
In this study we investigated the capacity of myelin-phagocytosing macrophages (mye-macrophages) to influence lymphocyte proliferation. We show that mye-macrophages inhibit TCR-triggered lymphocyte proliferation in an antigen-independent manner. This process is mediated by an enhanced nitric oxide (NO) production. Furthermore, we demonstrate that myelin delivery to popliteal lymph nodes of OVA-immunized animals and uptake by primarily CD169+ macrophages reduces cognate antigen specific proliferation following restimulation ex vivo. The elevated production of NO detected in these lymph node cultures indicates that NO may also mediate the immune suppressive effects in vivo. In contrast, myelin delivery to popliteal lymph nodes did increase lymphocyte reactivity in MBP-immunized animals. Thus, mye-macrophages may play a suppressive role in CNS-draining lymph nodes during MS pathogenesis, depending on the nature of surrounding lymphocytes. Collectively our data provide evidence that myelin phagocytosis leads to an altered macrophage function that modulates lymphocyte responses.
Female Lewis rats, 6-8 weeks of age, were purchased from Harlan Netherlands B.V. (Horst, The Netherlands). Animals were housed in the animal facility of the Biomedical Research Institute of Hasselt University. Experiments were conducted in accordance with institutional guidelines and approved by the local Ethical Committee for Animal Experiments of Hasselt University.
Isolation of peritoneal rat macrophages
Three days prior to macrophage isolation, rats were injected intraperitoneally with 3 ml 3% thioglycolate (Sigma-Aldrich, Bornem, Belgium). Resident peritoneal macrophages were obtained by peritoneal lavage using 10 ml of ice-cold PBS (Lonza, Vervier, Belgium) supplemented with 5 mM ethylenediamine tetraacetic acid (EDTA; VWR, Leuven, Belgium). Peritoneal exudate cells (PECs) were cultured for 2 hours in RPMI 1640 medium. After 2 hours incubation at 37°C with 5% CO2, non-adherent cells were washed away. Remaining cells were >95% macrophages .
Myelin was purified from rat brain tissue by means of density-gradient centrifugation, as described previously . Myelin protein concentration was determined by using the BCA protein assay kit (Thermo Fisher Scientific, Erembodegem, Belgium). LPS content was determined using the Chromogenic Limulus Amebocyte Lysate assay kit (Genscript Incorperation, Aachen, Germany). Isolated myelin contained a neglectable amount of endotoxin (1.8 × 10-3 pg/μg myelin).
Isolated myelin was fluorescently labelled, according to the method of Van der Laan et al. . In short, 10 mg/ml myelin was incubated with 12.5 μg/ml 1,1"-diotadecyl-3,3,3',3',-tetramethylindocarbocyanide perchlorate (DiI; Sigma-Aldrich) for 30 min at 37°C. Next, a myelin phagocytosis assay was performed as previously described .
Immunization and in vivo myelin treatment
Lewis rats were injected subcutaneously with a 0.1 ml suspension containing 250 μg/ml guinea pig myelin basic protein (MBP) or ovalbumin (OVA), 2.5 mg/ml H37RA heat-killed mycobacterium tuberculosis (Difco, Detroit, USA) and 60 μl Complete Freunds adjuvant (Sigma-Alldrich) in both hind paws. Subsequently animals were injected subcutaneously with PBS, 2.6 × 106 latex beads (0.8 μm mean particle size, Sigma-Alldrich), 75 μg/animal of isolated myelin or OVA (d-4, 0, 4 and 8 pre- and post-immunization). MBP-immunized rats were weighted and scored daily according to the following neurological scale: 0 = no neurological abnormalities, 0.5 = partial loss of tail tonus, 1 = complete loss of tail tonus, 2 = hind limb paresis, 3 = hind limb paralysis, 4 = moribund, 5 = death.
Generation of antigen-specific lymphocytes
MBP and OVA-specific lymphocytes were obtained 9 days post-immunization by bilateral isolation of the inguinal and popliteal lymph nodes. Single-cell suspensions of harvested lymph nodes were obtained by grinding with a syringe plunger against a 70 μm cell strainer (Bellco Glass Inc., Vineland, USA). To enrich for antigen specific lymphocytes, lymph node cells were restimulated, as described previously . Briefly, lymph node cells were resuspended in stimulation medium: RPMI 1640 medium (Invitrogen, Merelbeke, Belgium) supplemented with 50 U/ml penicillin (Invitrogen), 50 U/ml streptomycin (Invitrogen), 20 μM 2-mercapto-ethanol (Sigma-Alldrich), 1% sodium pyruvate (Invitrogen), 1% MEM non-essential amino acids (Invitrogen), 2% deactivated autologous serum and 33 μg/ml MBP. After 2 days, cells were washed and resuspended in RPMI 1640 medium supplemented with 50 U/ml penicillin, 50 U/ml streptomycin, 20 μM 2-mercapto-ethanol, 10% fetal calf serum (FCS, Hyclone, Erembodegem, Belgium) and 6,5% supernatants of Concanavalin (ConA, Sigma-Alldrich) stimulated spleen cells. Following 2 days, cells were washed and resuspended in RPMI 1640 medium supplemented with 50 U/ml penicillin, 50 U/ml streptomycin, 20 μM 2-mercapto-ethanol and 10% fetal calf serum for 3 days.
CFSE-labeling of lymphocytes
A carboxyfluorescein diacetatesuccinimidyl ester (CFSE) stock (10 mM in DMSO, Invitrogen, Merelbeke, Belgium) was diluted in PBS (Biowhittaker™). Antigen-specific lymphocytes were resuspended in PBS supplemented with 0.05% BSA and 4 μM CFSE (20 × 106 cells/ml) for 7 min at 37°C with 5% CO2. Cells were washed and diluted in 0.5 ml culture medium for 30 min at 37°C with 5% CO2 to stabilize the CFSE-labeling. In parallel, to determine macrophage viability following a coculture with lymphocytes, macrophages were labeled with CFSE to distinguish them from unlabeled lymphocytes.
Coculture of macrophages with lymphocytes
Prior to coculture with CFSE labeled lymphocytes, isolated macrophages were seeded in flat-bottem 96-well plates (15 × 103 cells/well) in RPMI 1640 medium supplemented with 50 U/ml, 50 U/ml streptomycin and 10% FCS, and treated with 100 μg/ml of isolated myelin for three hours. Excess myelin was removed by washing twice with RPMI 1640 medium at 37°C. Subsequently, stimulation medium containing irradiated thymocytes (15 × 104, 3000 rad), CFSE-labeled MBP- or OVA-specific lymphocytes (15 × 104) and respectively 10 μg/ml MBP or 10 μg/ml OVA were added. Untreated macrophages were used as a control. To evaluate the involvement of respectively NO, arginase, indoleamine 2,3-dioxygenase (IDO) the phagocytosis process itself, direct cell-cell contact and IFNγ, 1.5 mM NG-Monomethyl-L-arginine (L-NMMA; VWR), 0.5 mM NG-Hydroxy-L-arginine (NOHA; VWR), 0.2 mM 1-Methyl-L-tryptophan (1-MT; Sigma Alldrich), latex beads (1:100), 100 μg/ml zymosan A (Sigma-Alldrich), transwell inserts (0.4 μm pore size, Sigma-Aldrich) or 10 μg/ml anti-rat IFNγ (Preprotech, London, UK) were tested in the coculture model.
Flow cytometry was used to assess proliferation and cell death of lymphocytes and macrophages after a 4 day coculture. Here, cells were stained with PE-conjugated mouse-anti-rat CD3 (Immunosource, Erembodegem, Belgium) or CD11b (AbD Serotec, Düsseldorf, Germany) and 7 aminoactinomycin D (7AAD, BD Biosciences).
Isolated lymph node cells (20 × 104) were cultured with MBP (10 μg/ml), OVA (10 μg/ml) or myelin-oligodendrocyte glycoprotein (MOG, 20 μg/ml). Additionally, 100 μg/ml of isolated myelin was added in some experiments. Following 48 hr, 1 μCi [3H]thymidine (Amersham, Buckinghamshire, UK) was added to the culture. Next, cells were harvested with an automatic cell harvester (Pharmacia, Uppsala, Sweden) and uptake of radioactivity was measured in a β-plate liquid scintillation counter (Wallac, Turku, Finland).
Coculture supernatants were collected and release of NO was determined using the griess reagent system (Promega, Leuven, Belgium), following the manufacturer's instructions. Absorbance was determined by using a microplate reader at 550 nm (Biorad Benchmark).
Histology and immunohistochemistry
Snap-frozen brain and spinal cord material was cut in respectively the coronal and sagittal plane with a Leica CM1900UV cryostat (Leica Microsystems, Wetzlar, Germany) to obtain 10 μm sections. The extent of demyelination and infiltration was determined by staining with Luxol Fast Blue (LFB; Gurr BDH, Poole, England). Briefly, aceton-fixed slides were incubated with LFB for 16 hr at 56°C, destained with 0.05% lithium carbonate, and counterstained with cresyl violet (VWR). Analysis was carried out using a Nikon eclipse 80i microscope and NIS Elements BR 3.10 software (Nikon, Tokyo, Japan).
DiI-labeled myelin migration to popliteal and inguinal lymph nodes was determined by immunohistochemistry. Popliteal and inguinal lymph nodes were snap-frozen directly following isolation and cut into 10 μm sections. Following fixation in respectively aceton for 10 min, sections and cells were blocked using 10% goat serum (Millipore, Brussels, Belgium) in PBS. Subsequently, sections and cells were stained with mouse-anti-rat CD169 (1/250 in PBS; Abd Serotec), a marker for macrophages in lymph nodes. As a secondary antibody Alexa fluor 488 F(ab')2 fragment of goat-anti mouse was used (1/500 in PBS; Invitrogen). Control staining was performed by omitting the primary antibody. Nuclear staining was performed using 4,6'-diamidino-2-phenylindole (DAPI; Invitrogen) for 10 min. Autofluorescence was minimalized by using 0.1% Sudan Black in 70% ethanol.
Data were statistically analyzed using GraphPad Prism for windows (version 4.03) and are reported as mean ± SEM. D'Agostino and Pearson omnibus normality test was used to test normal distribution. An analysis of variances (ANOVA) or two-tailed unpaired student T-test (with Welch's correction if necessary) was used for normally distributed data sets. The Kruskal-Wallis or Mann-Whitney analysis was used for data sets which did not pass normality. *P < 0,05, **P < 0,01 and ***P < 0,001.
Myelin-laden macrophages inhibit lymphocyte proliferation
To study whether mye-macrophages affect antigen-specific lymphocyte proliferation in a different manner compared to untreated macrophages, macrophages or mye-macrophages were cocultured for 4d with MBP- or OVA-reactive lymphocytes, irradiated thymocytes and purified MBP or OVA. Here it was demonstrated that mye-macrophages inhibit TCR-triggered lymphocyte proliferation more pronounced than untreated macrophages (Figure 1d and 1e). This process was independent of antigen-specificity, since both MBP and OVA-reactive lymphocytes showed the same reduction in proliferation. Proliferation differences were not due to an altered viability of lymphocytes or mye-macrophages (data not shown).
Inhibition of lymphocyte proliferation is independent of the phagocytosis process or myelin-antigen presentation
Like DCs, macrophages can act as messengers of innate and adaptive immunity by presenting antigen in context of MHC molecules. Mye-macrophages can therefore be assumed to process endogenous myelin and present it to myelin-reactive lymphocytes, possibly influencing reactivity of these lymphocytes. To determine whether the observed immune suppressive effects are dependent on antigen presentation, untreated macrophages and mye-macrophages were cocultured with MBP-reactive lymphocytes in the absence of MBP and irradiated thymocytes. Mye-macrophages did not affect lymphocyte proliferation (Figure 2b), suggesting that, at a macrophage/lymphocyte ratio of 1/10, mye-macrophages do not influence the proliferation of MBP-reactive lymphocytes. These results are in line with the observed equal inhibition of proliferation of both MBP and OVA-reactive lymphocyte by mye-macrophages.
Lipid components of myelin, like cholesterol and arachidonic acid-containing phosphatidylcholine, have been reported to directly inhibit proliferation of ConA stimulated lymphocytes [41, 42]. Accordingly, we assessed whether isolated myelin has a direct effect on lymphocyte proliferation. By culturing lymphocytes with increasing concentrations of isolated myelin, in the absence of macrophages, it was established that myelin itself, even at high concentrations, had no significant influence on lymphocyte reactivity (data not shown).
Together, these data indicate that direct effects of myelin on lymphocyte proliferation, myelin-antigen presentation and the phagocytosis process itself are not responsible for the observed effects on lymphocyte proliferation.
Macrophages inhibit lymphocyte proliferation by the production of nitric oxide
Macrophages have been reported to inhibit lymphocyte proliferation in vitro by mechanisms involving inducible nitric oxide synthase (iNOS), arginase I or IDO [43–55]. By administrating either an inhibitor of NOS (L-NMMA), arginase (NOR-NOHA) or IDO (1-MT) to the culture, the involvement of these enzymes was evaluated. Here we demonstrated that an increased activity of both IDO and arginase did not account for the increased inhibition of lymphocyte proliferation by mye-macrophages (Figure 2c). In contrast, administration of L-NMMA completely abrogated the inhibition of lymphocyte proliferation by both macrophages and mye-macrophages. Yet again, cocultures of both OVA and MBP-reactive lymphocytes were affected equally (data not shown). The importance of NO was further delineated by assessment of NO levels in the coculture supernatant of MBP-reactive lymphocytes. In contrast to cocultures of lymphocytes with latex beads or zymosan treated macrophages, a significantly increased concentration of NO was observed in the supernatants derived from cocultures with mye-macrophages, when compared to untreated macrophages (Figure 2d). This increased NO production by macrophages following myelin internalization was absent in monocultures (data not shown), indicating that the observed increased concentration of NO in the coculture with mye-macrophages was induced by lymphocytes. Lymphocyte-derived IFNγ has previously been described to induce NO production in macrophages . However, in our coculture model no increase in IFNγ in the supernatants of cocultures with mye-macrophages compared to untreated macrophages was found (data not shown). Correspondingly, IFNγ neutralization did neither abrogate the increased inhibition of proliferation by mye-macrophages or decrease the NO production in cocultures (data not shown). Nonetheless, when transwell inserts were used to restrict direct cell-cell contact, lymphocyte proliferation in cocultures of both untreated or myelin-treated approached control values (Figure 2e), indicating a role for direct cell-cell contact in the induction of NO.
Noteworthy, when lymph node cells, isolated 9 days post-immunization, were exposed directly to MBP and myelin, an even more pronounced myelin-mediated inhibition of lymphocyte proliferation was observed (Figure 2f). The latter indicates that local lymph node phagocytes show a similar immune suppressive response as peritoneal macrophages following myelin ingestion. Differences detected in proliferation were not due to an altered viability of lymphocytes (Figure 2f).
Myelin modulates lymph node proliferation in vivo
These results indicate that mye-macrophages have a dual influence on proliferation, depending on the nature of surrounding lymphocytes. On one hand they aggravate autoimmunity by activating myelin-reactive lymphocytes and on the other hand they have the capacity to suppress lymphocyte activation by the secretion of NO.
In this study we have established that macrophages that have phagocytosed myelin modulate the proliferation of autoreactive T cells. The observed inhibition of TCR-triggered lymphocyte proliferation by mye-macrophages was antigen-independent, as both OVA- and MBP-reactive lymphocytes show an identical reduction in proliferation following coculture with mye-macrophages in vitro. Additionally, when in vivo primed lymph node cultures were restimulated directly in vitro in the presence of myelin, an even more pronounced immune suppression was observed. These results indicate that both macrophages and lymph node phagocytes obtain immune suppressive properties following myelin internalization.
Macrophages may inhibit proliferation of lymphocytes in various manners, including IDO-mediated depletion of tryptophan, arginase-mediated lowering of L-arginine and lymphocyte CD3ζ expression, and NO-mediated reduction of tyrosine residue phosphorylation in the Jak3/STAT5 pathway and inhibition of caspase activity [43–52]. We demonstrate that the non-selective iNOS inhibitor L-NMMA completely reversed the observed inhibition of proliferation by both control and mye-macrophages while the other pathways were not involved. In line with this, an increased concentration of NO was demonstrated in the coculture supernatant of mye-macrophages, explaining the observed inhibition of lymphocyte proliferation by mye-macrophages.
Abrogation of direct cell-cell contact restored lymphocyte proliferation in our cocultures. This finding, together with the observed role of NO in the inhibition of lymphocyte proliferation, suggests that direct contact between both cell types is a necessary prerequisite for stimulating NO-mediated inhibition of lymphocyte proliferation by macrophages. On the other hand, NO might, due to extreme short half-life, not reach lymphocytes when direct contact is restricted. Future studies should therefore determine the mechanism behind the macrophage- and mye-macrophage-mediated inhibition of lymphocyte proliferation in our cocultures. Although lymphocyte-derived IFNγ is described to induce NO production by macrophages, we were unable to demonstrate a role for lymphocyte-produced IFNγ in the observed inhibition of lymphocyte proliferation .
As we demonstrated an increased, NO-mediated inhibition of lymphocyte proliferation by mye-macrophages in vitro, myelin-rich phagocytes in secondary lymph nodes might fulfill an identical suppressive role in vivo. CD169+ macrophages in lymph nodes are described to be primarily involved in uptake and relay of viral particles and immune complexes, and activation of follicular B lymphocytes [57–60]. We demonstrate that a subcutaneous injection of myelin in the footpad results in a notable migration of myelin towards CD169+ medullary and subcapsular sinus (SCS) macrophages in popliteal lymph nodes. Given the abundance of lipids in myelin, these results are in line with a recent report showing active phagocytosis of lipid-coated silica particles by SCS macrophages .
To explore the possible immune suppressive properties of mye-macrophages in vivo, OVA-immunized animals were treated subcutaneously in the footpad with myelin. Restimulated popliteal lymph nodes of myelin-treated animals display reduced OVA-induced proliferation compared to lymphocytes derived from untreated OVA-immunized animals. This effect is independent of interference of myelin proteins on OVA antigen presentation, as lymph node cultures of MBP-immunized animals treated subcutaneously with OVA did not reduce MBP reactivity. These results demonstrate that mye-macrophages suppress lymphocyte proliferation in vivo. In contrast, lymph node cultures derived from MBP-immunized animals that were treated with myelin showed an enhanced proliferative capacity. Although we demonstrated that mye-macrophages are unable to increase proliferation of MBP-reactive lymphocytes in vitro, the presence of other myelin-rich antigen-presenting cells, like migrated langerhans cells and local lymph node DCs, might explain the increased reactivity against MBP and MOG. Furthermore, B cells have been described to capture antigen-containing immune complexes from SCS macrophages processes and migrate to the T cell zone to influence antigen presentation [57, 60]. Finally, the discrepancy in literature regarding the skewing of macrophages following myelin internalization suggests that myelin can have divergent effects on macrophage polarization and its APC-like or immune suppressive properties, which may depend on the macrophage origin and local environmental stimuli. Likewise, the nature of surrounding lymphocytes, for example being myelin-protein, non-myelin or myelin-lipid specific, might determine whether the presence of mye-macrophages results in stimulation or suppression of lymphocyte activity. Future studies should therefore determine whether lymphocytes surrounding mye-macrophages in CNS draining lymph nodes recognize antigen presented by these cells and are hereby activated.
Interestingly, we demonstrated an increased capacity of lymph nodes cells from myelin treated, OVA-immunized animals to produce NO following LPS stimulation. These results indicate a direct role of macrophage-produced NO in the observed decrease in OVA reactivity in myelin-treated animals, as observed in vitro. The importance of NO in the control of inflammation in EAE is supported by studies showing an aggravation or inability to recover following treatment with an iNOS inhibitor in respectively the induction or the remission phase of EAE [62, 63]. Likewise, treatment with the NO-donor SIN-1 during the induction phase of EAE ameliorated EAE, which was correlated with a reduced immune cell infiltration and antigen-induced proliferation . Finally, EAE insusceptibility in rat strains like the Piebald Virol Glaxo and the Brown Norway strain was correlated with an increased production of immune suppressive NO following immunization [65, 66]. These results demonstrate that NO displays a disease-mitigating role in EAE by inhibiting lymphocyte proliferation. Based on these and our findings, we suggest that mye-macrophages in the perivascular space and CNS-draining lymph nodes can fulfill a suppressive role in MS by producing NO, hereby silencing autoreactive lymphocytes.
It is unclear which myelin components are responsible for the observed immune suppressive effects. To date, despite the abundance of lipids in myelin, most studies have mainly focused on the role of myelin proteins in neurodegenerative diseases. Interestingly, several lipids present in myelin have been reported to alter macrophage signaling and transcription. Intracellular, lipid sensors like LXR and PPAR, which are respectively activated by cholesterol derivates and non-esterified fatty acids, have recently been described as key regulators of lipid metabolism and inflammation, and may be activated following myelin internalization [67–69]. Similarly, individual lipids present in myelin can alter the macrophage or microglial response by binding to specific receptors and activating or blocking signalling cascades pivotal in inflammation [70–73].
Macrophages can adopt divergent phenotypes based on specific stimuli in their microenvironment [74–77]. Moreover, mye-macrophages have been described to display divergent phenotypes depending on the location in the lesion, suggesting that they are likely to exert diverse functions depending on their micro-location . By using thioglycolate-elicited PECs, as a representative model for infiltrating monocytes in EAE and MS, we established that myelin internalization results in an altered macrophage function, characterized by an increased production of NO . These mye-macrophages may have dual effects during MS pathogenesis. Whereas NO production by mye-macrophages can negatively influence neuronal integrity and block axonal conduction locally in the brain parenchyma, we show that NO also suppresses lymphocyte proliferation. Thus, depending on the surrounding cells, mye-macrophages can be involved in either limiting or promoting autoimmune-mediated demyelination.
We demonstrate that myelin phagocytosis leads to an altered macrophage function that inhibits lymphocyte proliferation. The observed immune suppression was mediated by an increased production of NO by mye-macrophages. Additionally, we establish that mye-macrophages fulfill an ambiguous role in vivo. On one hand mye-macrophages aggravate autoimmunity by activating myelin-reactive lymphocytes in secondary lymph nodes and on the other hand they suppress lymphocyte reactivity by producing NO.
We thank W. Leyssens for technical assistance. This work was supported by IWT Vlaanderen, FWO Vlaanderen, transnational University Limburg, Limburg Sterk Merk and Alma-in-Silico (EMR INT4.-1.3.-2008-03/003).
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