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Essential roles of PKA, iNOS, CD95/CD95L, and terminal caspases in suppression of eosinopoiesis by PGE2 and other cAMP-elevating agents.

1. Introduction

Eosinophils, which are prominent in allergic inflammation [1], develop from bone-marrow colony-forming progenitors through lineage-committed, non-colony-forming cells (precursors) to terminally differentiated, mature granulocytes, under the influence of interleukin-5 (IL-5) [2, 3]. IL-5 is also an important mobilization, survival, and activation factor for terminally differentiated eosinophils. Nevertheless, prostaglandin E2 (PGE2), a ubiquitous inflammatory mediator, is able to override IL-5-induced survival signals [4, 5], ultimately inducing apoptosis in developing eosinophils. This regulatory effect is dependent on the inducible NO synthase isoform (iNOS), for PGE2 is ineffective in bone-marrow lacking a functional iNOS, due to either gene inactivation or pharmacological blockade. iNOS-deficient bone-marrow is nevertheless susceptible to inhibition by NO, as shown by the ability of NO-releasing chemicals to suppress eosinopoiesis, indicating that NO acts downstream from PGE2. PGE2 induces cellular markers of apoptosis (annexin V binding, TUNEL labeling, and nucleosome release). It also requires CD95 ligand (CD95L, CD158) at a second critical step, downstream from iNOS [4], to suppress eosinopoiesis. This dual requirement for iNOS and CD95L, in an ordered sequence, as well as the biochemical evidence of apoptosis, led us to propose that eosinopoiesis is regulated by PGE2 through an iNOS-CD95L-dependent proapoptotic pathway. In human asthma and experimental models of asthma, where eosinophil infiltrates are a prominent feature of the chronic pulmonary inflammation, eosinopoiesis is rapidly and selectively upregulated following airway allergen exposure [6, 7]. We have recently shown that the stimulatory effects of airway allergen exposure on bone-marrow eosinopoiesis are prevented by diethylcarbamazine, which acts in vivo through a mechanism dependent on both iNOS and CD95L [8]. In vitro, diethylcarbamazine directly suppresses eosinopoiesis in bone-marrow culture, an effect also prevented by iNOS blockade and inactivation [8].

Importantly, the ability of PGE2 to induce apoptosis during eosinophil development is blocked by previous exposure to dexamethasone. This shows that interference with the signaling sequence started by PGE2 is part of the modulatory effects of a widely used anti-inflammatory drug. When apoptosis is blocked by dexamethasone, a maturation-promoting activity in PGE2 is unveiled, as shown by changes in a4 integrin expression, cell aggregation, and cytological maturation of eosinophils in BM culture [9]. This suggests that different signaling and effector events are mobilized by the same ligand/receptor interactions, depending on the presence or absence of immunomodulators, like glucocorticoids. This added complexity further highlights the need for characterization of these events in each experimental condition.

On the other hand, PGE2-induced suppression of eosinopoiesis is effectively blocked by cysteinyl-leukotrienes (CysLT), which are important mediators of inflammation in asthmatic lungs [5]. In IL-5-stimulated bone-marrow culture, CysLT greatly enhance eosinopoiesis [5]. CysLT further mediate the enhancing effects of eotaxin and interleukin-13, both significant players in allergic pulmonary inflammation [10]. These observations not only demonstrate that the iNOS-CD95L pathway is relevant to the pathophysiology of experimental asthma but also further highlight the need to define the precise steps which may be blocked by CysLT and cytokines which act through CysLT.

Given the pathway's ability to transduce both negative and positive influences from various diffusible mediators and immunomodulators, we examined its relationship to other regulatory molecules. PGE2 signals through EP2 receptors, which activate adenylyl cyclase and, consequently, cAMP-dependent protein kinase (PKA) [11]. PGE2 and cAMP-elevating agents suppress colony formation by a variety of myeloid lineages, including eosinophils [12]. Adrenergic hormones/neurotransmitters, which share these signaling mechanisms with PGE2, are known physiological regulators of bone-marrow function [13]. We have therefore compared the effects of a widely used [beta]-adrenergic ligand (isoproterenol) and of other cAMP-inducing/mimetic agents on eosinopoiesis with those of PGE2 and addressed the roles played by adenylyl cyclase, PKA, iNOS, NO, CD95L/CD95, and terminal caspases, in the actions of these modulators and mediators.

2. Methods

2.1. Animals. Mice of the BALB/c (both wild-type and CD95L-deficientgld mutants) [14] and C57BL/6 backgrounds (both wild-type and iNOS-deficient knockout mice) [15], bred at CECAL-FIOCRUZ, Rio de Janeiro, Brazil, and CD95deficient Ipr mutants of the C57BL/6 background [16], bred at Faculdade de Medicina da USP, Ribeirao Preto, Brazil, were used at 6-8 weeks of age, following institutionally approved (CEUA#L010/04 and CEUA#L-002/09) protocols. Where indicated, eosinophil-null mutant mice, which lack a high-affinity binding site for the GATA-1 transcription factor [17], required for eosinophil lineage commitment, and wild-type BALB/c controls were used to confirm that eosinophils were responsible for NO production.

2.2. Reagents. FCS was from Hyclone (Logan, UT); culture media RPMI 1640 from RHyClone, Thermoscientific, (Waltham, MA); PGE2 (ref.14010) from Cayman Chemical Company (Ann Arbor, MI); recombinant murine (rm) IL-5 from Pharmingen (San Diego, CA), rmFlt3-Ligand (CAT# 250-31L) from Peprotech (Rocky Hill, NJ) and rmSCF (CAT# 455-MC) from R&D Systems (Minneapolis, MN); Hanks' Balanced Salt Solution, without Phenol Red (HBSS/PhR-) (ref.H6648), L-nitroarginine (ref.N5501), sodium nitroprusside (SNP) (ref.S0501), isoproterenol hydrochloride (ref.I6504), cholera toxin (ref.C8052), anti-iNOS antibody (ref.N9657), H-89 dihydrochloride hydrate (H89) (ref.B1427) selective PKA inhibitor ([K.sub.i] = 48 nM), Bisindolylmaleimide II (Bis) (ref.B3056) dual PKA/PKC inhibitor (Ki = 3.0 [micro]M and 6.0 [micro]M, resp.), adenylyl cyclase inhibitor SQ 22,536 (ref.S153), 6-Isopropoxy-9-oxoxanthene-2-carboxylic acid (AH6809) (ref.A1221), selective murine EP2 antagonist [18], and 2-acetylhydrazide 10(11H)-carboxylic acid, 8-chloro-dibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid (SC19220) (ref.S3065), preferential EP1 receptor antagonist from Sigma Chemical Co. (St Louis, MO); dibutyryl cyclic AMP (ref.D0260), forskolin (ref.F6886), ZVAD-fmk (ref.V116), dexamethasone 21-phosphate disodium salt (ref.D1159), and aminoguanidine hydrochloride, a selective iNOS inhibitor (ref.396494) from Sigma-Aldrich (St. Louis, MO); biotinylated anti-mouse IgG antibody (ref. SC-2040) from Santa Cruz Biotechnology (Santa Cruz, CA, USA.); rolipram from Sanofi (Montpellier, France); 4-amino-5-methylamino-2,7-difluorescein diacetate (DAFFM) (ref.D23844) from Invitrogen (Sao Paulo, Brazil) [19]; liquid diaminobenzidine (DAB+) (ref. K3467) solution from Dako Cytomation (Dako Denmark A/S, Glostrup, Denmark).

2.3. Bone-Marrow Culture. Liquid bone-marrow culture conditions were routinely used because they allow addition of agonists and inhibitors at different times, which cannot be done in clonal culture systems, where proper mixing and diffusion of substances added after plating is restricted by the semisolid media. The previously reported effects of PGE2 and cAMP-elevating agents [12] in semisolid culture are nevertheless consistent with their suppressive effects in liquid culture as detailed here (see Results Section 3.1). Eosinophilopoiesis in liquid culture was strictly dependent on IL-5 [7], and culture conditions were adequate for demonstrating both enhancing and suppressive effects [12]. BM cells were collected from both femurs of naive mice, washed, counted in a haemocytometer, seeded at 106 in 1 mL of RPMI 1640 medium, 10% FCS, and rmIL-5 (1ng/mL; optimal dose, as previously defined [7]) in 24-well clusters, and incubated at 37[degrees]C, 5% C[O.sub.2]/95% air for 7 days. Where indicated, cultures received PGE2, isoproterenol, or one of the cAMP-elevating agents (dibutyryl-cAMP, rolipram, cholera toxin, or forskolin) known to duplicate the effects of PGE2 in semisolid culture [12]. Unless otherwise indicated, each agonist was added only once, immediately after IL-5, at the beginning of the culture period. In selected experiments, PGE2 was added at various times after initiation of the culture [9]. Where indicated, cultures also received EP inhibitors (AH6809 or SC19220), iNOS inhibitor (aminoguanidine) [8], adenylyl cyclase inhibitor (SQ22536), or protein kinase A and C inhibitors (H89 or Bis) or caspase inhibitor (zVAD-fmk) [20]. In this case, inhibitors were added before both IL-5 and the agonists they were expected to antagonize. Bone-marrow cells, both before (day 0) and after (day 7) culture, were resuspended, collected, counted, cytocentrifuged, and stained for eosinophil peroxidase (EPO), a murine eosinophil lineage-specific marker present from the earliest precursors to terminally differentiated eosinophils [21]. EPO+ cells were counted at 400x under oil. Eosinophil numbers were calculated from total and differential counts. EPO+ cell counts are in excellent agreement with counts of Giemsastained eosinophils and with detection of CCR3+ cells by immunofluorescence [9]. For BALB/c bone-marrow cultures established for 7 days with IL-5 alone, our largest series in this study, yield was 15.81(+1.18) x [10.sup.4] eosinophils/mL (mean [+ or -] SEM, n = 29), from an initial inoculum of 106 bone-marrow cells/mL. Where indicated, bone-marrow cultures were initially expanded in RPMI 1640 medium, 20% FCS, with flt3 ligand (100 ng/mL), and stem cell factor (100 ng/mL) for 4 days, before changing the stimulus for an additional 4 days to IL-5 alone or combined with PGE2 or isoproterenol, as described by Dyer et al. [22].

2.4. Studies on iNOS Expression and NO Production. For immunocytochemical detection of iNOS, bone-marrow liquid cultures were established with IL-5, alone or in association with [PGE.sub.2], dexamethasone (dex.), or both for 48 h, before resuspension, collection, fixation (1% paraformaldehyde), and staining of the cells. Nonspecific binding was prevented by preincubation for 1 h in PBS containing 10% FCS. The slides were washed (3x, PBS with 1% FCS) and incubated for 1 h with primary anti-iNOS antibody, diluted 1: 100. Unbound antibody was removed by washing as above, before incubation for 1 h with secondary rat anti-mouse IgG antibody, conjugated to alkaline phosphatase, diluted 1: 500. Unbound antibody was removed, and the reaction was developed with the Fast Red chromogen as recommended by the manufacturer. Images shown in Results Section 3.2, Figure 2 were taken with an Olympus PM-C35DX camera from an Olympus BX-50 microscope, with an Olympus UPLANAPO (Order #OB92, Spectra Services, Ontario, NY) 40x oil objective with iris (NA 1.00-0.50; WD 0.12 mm). For direct quantitation of NO generation [19], [10.sup.6] bone-marrow cells from iNOS-deficient C57BL/6 and the respective wild-type control mice were preincubated with DAF-FM (10 [micro]M) in a 100 [micro]L volume ofHBSS/PhR-, supplementedwith 100 [micro]M L-Nitroarginine, for 30 minutes at 37[degrees]C, before washing in HBSS/PhR-, supplemented with 100 [micro]M L-arginine, for 10 minutes, at 500 x g, and further incubation for 8h in 2mL of this medium in the presence of IL-5 (1 ng/mL), alone or in association with dibutyryl cAMP ([10.sup.-6] M), aminoguanidine ([10.sup.-4] M), or combinations of these agents. Separate control experiments evaluated eosinophil-deficient bone-marrow [17] in these conditions. Cells were collected, washed in PBS, and submitted to flow cytometry in a FACSCalibur (Becton-Dickinson) with analysis by the SUMMIT software (v4.3, Dako), with gating in the granulocyte region, defined on the basis of forward and side scatter profiles.

2.5. Statistical Analysis. Data (mean [+ or -] SEM) were analyzed by factorial analysis of variance with the Tukey HSD correction, using Systat for Windows version 4 software from Systat Inc. (Evanston, IL). Significance was set at <0.05. In all panels where data are presented as % eosinophilopoiesis suppression, defined as (EPO+ cell counts in experimental cultures/EPO+ cell counts in control cultures with IL-5 alone) x 100, this mode of display was chosen for the sake of clarity, since what is shown is the ability of a negative agent (receptor antagonist or cyclase/kinase inhibitor) to reverse the effect of a different negative agent (suppressive ligand, such as PGE2 or dbcAMP), thereby evoking a positive response.

3. Results

3.1. Effects of PGE2. PGE2 dose-dependently suppressed eosinophil production in BALB/c bone-marrow cultures (Figure 1(a)), as shown by the significantly decreased numbers of eosinophils recovered from 7-day cultures, established in the presence of IL-5 associated with PGE2 at [10.sup.-6][-10.sup.-8] M (but not at [10.sup.-9][-10.sup.-10] M), relative to the IL-5 controls. In the presence of IL-5 alone (Figure 1(b), closed squares), eosinophil numbers were significantly increased, relative to the BM inoculum (day 0), from day 4 onwards. In the presence of IL-5 and PGE2 ([10.sup.-7] M, open squares), eosinophil recovery was also significantly increased, relative to the bone-marrow inoculums, from day 4 onwards. Nevertheless, significant differences were still observed between PGE2-treated and the respective control cultures for the entire period from day 3 to day 7, showing long-lasting suppression by PGE2. The effects of PGE2 ([10.sup.-7] M) depended on the timing of its introduction in the culture, as significantly decreased eosinophil recovery, relative to IL-5 controls, was observed following addition at days 0-1, but not at later times (Figure 1(c)). In the absence of IL-5, PGE2 had no significant effect during a short (2h) preincubation period, followed by media replacement and further culture in IL-5 alone for 7 days (not shown). Longer preincubation periods were not examined, as viability decreased in the absence of IL-5, even if no PGE2 is present (not shown). The long-lasting suppressive effect of PGE2 on eosinophilopoiesis depended on terminal caspases, because it was abolished by the caspase inhibitor, zVAD-fmk (4-40 [micro]M). zVAD-fmk had no effect by itself, even at the highest concentration tested (Figure 1(d)).

Together, these observations indicate that, while PGE2 must act during the initial 24 h of culture, its suppressive effect, which involves apoptotic mechanisms, only becomes detectable 48 h later.

3.2. Relationship of iNOS Expression to the Effects ofPGE2 and Dexamethasone. Because PGE2 requires iNOS to suppress eosinophilopoiesis [4] and because dexamethasone prevents iNOS expression [23], we next evaluated whether iNOS expression was detectable in eosinophils and enhanced by PGE2 as well as suppressed by dexamethasone, paralleling the effects of these drugs on eosinophilopoiesis.

As shown in Figure 2 (upper panel), iNOS was easily detected by immunocytochemistry in eosinophils (upper right) present at 2 days of culture in IL-5 associated with PGE2 ([10.sup.-7] M). The strong cytoplasmic (see insert) staining of most, but not all, eosinophils present in a representative cluster strikingly contrasts with the faint staining in controls exposed to IL-5 alone (upper left). Importantly, staining was undetectable (lower left) in cultures exposed to IL-5 plus dexamethasone ([10.sup.-7] M) and very weak in cultures exposed to both dexamethasone and PGE2 (lower right), confirming that dexamethasone prevents the upregulation of iNOS in the presence of PGE2. These patterns of iNOS expression were consistent with the detection ofiNOS protein by immunoblotting in the corresponding culture conditions in separate control experiments (not shown). Both the timing of iNOS expression and its sensitivity to dexamethasone are consistent with a mechanistic relationship between upregulation of iNOS expression by PGE2 and suppression of eosinophilopoiesis.

3.3. Role of Prostanoid Receptors and Caspases. We next examined the postreceptor events that might provide a link between receptor activation by PGE2 and the induction of apoptosis at later times. We focused on cAMP-related mechanisms, because PGE2 binds to EP receptors, including two subtypes (EP2 and EP4) which primarily activate adenylyl cyclase through Gs [24]. We first evaluated whether isoproterenol, a ligand that binds to a receptor ([beta]-adrenergic) unrelated to EP, would duplicate the effects of PGE2, since it mobilizes the same intracellular signaling mechanisms starting at a different surface receptor. Isoproterenol (10-6-10-7 M, but not [10.sup.-8][-10.sup.-9] M) significantly suppressed eosinophilopoiesis in BALB/c bone-marrow cultures (Figure 3(a)). As previously shown for PGE2 (Figure 1(d)), the effect of isoproterenol was abolished by caspase inhibitor zVAD-fmk (Figure 3(b)), showing that terminal caspases are one effector mechanism required for the effectiveness of these two unrelated ligands. The involvement of EP receptors in the actions of PGE2 and their irrelevance to the actions of isoproterenol were confirmed by the use of the selective murine EP2 antagonist [18], AH6809, and of the EP1-selective antagonist, SC19220, which were both effective against PGE2 but ineffective against isoproterenol (Figure 3(c)). Because it has been recently reported that preexposure for 4 days to flt3L plus SCF primes bone-marrow for increased eosinopoiesis in the presence of IL-5 [22], we further examined the effect of priming on the suppressive activity of both ligands, comparing cultures of primed and unprimed bone-marrow cells cultured for comparable periods (Figure 3(d)). Priming by flt3L/SCF greatly increased eosinopoiesis, as judged from eosinophil recovery at 4 days of culture in IL-5 (compare with Figure 1(b)). However, no loss of effectiveness was found for either PGE2 (77.6 [+ or -] 4.2%) or isoproterenol (83.0 [+ or -] 6.6%), which were at least as effective after priming as in nonprimed cultures (Figures 1(d) and 3(b), resp.).

3.4. Role of Adenylyl Cyclase. The involvement of adenylyl cyclase in transducing the signals delivered at distinct surface receptors by PGE2 and isoproterenol was confirmed by the effectiveness of SQ22536 against both agonists (Figure 4(a)). Finally, the sensitivity of the effects of both PGE2 and isoproterenol to the PKA selective inhibitor, H89 (Figure 4(b)), and the dual PKA/PKC inhibitor, Bis (Figure 4(c)), supports the hypothesis that these unrelated ligands share a requirement for PKA as a critical intracellular signaling mechanism.

3.5. Effects of Receptor-Independent Agonists. To further establish the relationship of these intracellular signaling mechanisms to iNOS, we subsequently examined whether receptor-independent agonists, that either induce or mimetize increased intracellular cAMP levels, would duplicate the effects of PGE2 and isoproterenol and whether their effects would be sensitive to iNOS blockade or inactivation.

We initially confirmed a requirement for iNOS in the actions of isoproterenol, since these were prevented by selective iNOS inhibitor aminoguanidine, which had no significant effect in the absence ofisoproterenol (Figure 5(a)). Next, we examined the effects of a wide panel of receptor-independent substances, which act to induce or to mimic elevation of intracellular cAMP levels by unrelated biochemical mechanisms. These included (a) forskolin, which directly activates adenylyl cyclase; (b) rolipram, which inhibits phosphordiesterase, leading to accumulation of its substrate, cAMP; (c) dibutyryl cAMP, which mimics the effects of cAMP and permeates cell membranes; (d) cholera toxin, which activates adenylyl cyclase by its effects on G proteins. All shared the ability to suppress eosinophilopoiesis in IL-5-stimulated bone-marrow cultures, in the absence but not in the presence of aminoguanidine (Figure 5(b)).

For all of the agents listed above, we further confirmed the essential role for iNOS in these regulatory effects, by comparing the lack of response in iNOS-deficient bone-marrow to the responses of wild-type cells (Figures 5(c) and 5(d)). Together, these observations demonstrate the mechanistic link between cAMP signaling, iNOS function, and eosinophilopoiesis suppression.

3.6. Direct Evidence for NO Production in Response to cAMP Rise. To directly confirm that NO was generated by iNOS in bone-marrow cells exposed in the presence of IL-5 to a PKA-activating stimulus, we examined by flow cytometry NO production over an 8-hour period, using an NO-sensitive probe (DAF-FM). Bone-marrow from BALB/c mice was stimulated by IL-5 (1ng/mL), alone or in association with dibutyryl-cAMP (10-6 M) (Figures 6(a)-6(c)). Dibutyryl-cAMP increased the number of eosinophils emitting an NO-specific fluorescent signal (Figure 6(b)) relative to IL5 controls (Figure 6(a)), and this increase was abolished by aminoguanidine (Figure 6(c)), confirming that the NO-specific signal was generated through iNOS.

Next, bone-marrow from iNOS-deficient mice (Figure 6(e)) and from wild-type C57BL/6 controls (Figure 6(d)) was examined in these conditions. As expected, in iNOS-deficient bone-marrow (Figure 6(e)), dibutyryl-cAMP plus IL-5 induced no increase in NO-specific signal relative to the IL-5 controls; by contrast, the same agonistic combination increased NO-specific fluorescence relative to the IL-5 controls in wild-type bone-marrow (Figure 6(d)). This effect was blocked by aminoguanidine (Figure 6(d)). Blockade by aminoguanidine of the NO signal in wild-type bone-marrow response to dibutyryl-cAMP was statistically significant (Figure 6(f)).

In separate control experiments with bone-marrow from mice lacking eosinophils, due to deletion of the GATA-1 high-affinity binding site required for eosinophil lineage commitment [17], no significant difference in NO-specific signals was observed between samples exposed to IL-5 plus dibutyryl-cAMP and IL-5 controls, in numbers of positive cells (P = 0.499) or in median fluorescence intensity (P = 0.408).

3.7. Role ofCD95. Finally, we addressed the issue of whether all of these different ligands converge on the same pathway to apoptosis, namely, that involving CD95L and its receptor, CD95 (Fas). CD95L-deficient bone-marrow was refractory to the suppressive effects of PGE2, cholera toxin, and isoproterenol, unlike that of wild-type BALB/c controls (Figure 7(a)). CD95-deficient bone-marrow was equally resistant to suppression by PGE2, isoproterenol, dibutyryl cAMP, and rolipram, in sharp contrast to the great sensitivity of wild-type C57BL/6 controls (Figure 7(c)). We further examined whether sodium nitroprusside (SNP), an NO donor, would be able to act on bone-marrow lacking CD95L (Figure 7(b)) and CD95 (Figure 7(d)). In agreement with previous observations made with a different NO-releasing chemical, SNAP [4], gld bone-marrow cells were totally resistant to SNP; by contrast, SNP retained its effectiveness in Ipr bone-marrow cells.

4. Discussion

This is, to our knowledge, the first study to establish a sequence of events strictly required for suppression of eosinopoiesis by any soluble ligand. By clearly identifying the critical steps and the experimental tools that allow their dissection, we were able to define a proapoptotic pathway which (a) begins on surface receptors; (b) requires adenylate cyclase followed by PKA signaling; (c) induces iNOS followed by iNOS-mediated NO production; and (d) ultimately triggers apoptosis through an interaction between two well-defined surface molecules, CD95L and CD95.

As discussed below, this pathway can now be unambiguously distinguished from another sequence of events, which is initiated by the same ligand/receptor interaction but modified by glucocorticoid priming of the target cells, in a way that culminates in terminal differentiation, not in apoptotic cell death.

Therefore, the present study demonstrates how a combination of pharmacological and genetic approaches allows one to define signals involved in cellular differentiation, as opposed to cell death, in a single hemopoietic lineage.

Furthermore, by demonstrating that [beta]-adrenergic stimuli can duplicate the effects of PGE2, this study broadens the spectrum of soluble ligands that can downregulate bone-marrow responses to allergen challenge and raises the issue of whether sympathetic fibers, abundant in bone-marrow [25], can play an attenuating or modifying role in the hematological response to allergen challenge.

The complete initial separation of pathways by ligation of distinct surface receptors by PGE2 and isoproterenol was documented by the use of the appropriate antagonists. Subsequent convergence of these pathways was demonstrated by the identical effect of blocking adenylyl cyclase on the responses to both agonists, as well as the reproduction of their effects with a wide panel of receptor-independent agonists. Sharing of both iNOS and the downstream effector molecules by these converging pathways was directly demonstrated by the inability of all the agonists tested to suppress eosinopoiesis in mice lacking iNOS, CD95L, or CD95.

Our experiments confirmed a mechanistic link between induction and activity of NO synthase, NO generation, and CD95-dependent apoptosis. Our observations are consistent with a role for NO in inducing and activating CD95L and/or CD95, as suggested by the ability of NO donors to suppress eosinophilopoiesis in bone-marrow of wild-type but not CD95L-deficient mice [4].

By the second day of exposure to IL-5, the cultured eosinophils become refractory to PGE2, even though eosinophil numbers increase essentially between days 3 and 6. This suggests that the apoptosis observed at later times is the outcome of a process initiated during the initial 24 h. Since a significant impact on eosinophil numbers is first demonstrable at 72 h, the required steps should take place up to that point. Again, such an estimate is consistent with our demonstration of strong iNOS induction at the midpoint in this interval (48 h).

We have previously demonstrated that bone-marrow cultures exposed to IL-5 in association with dexamethasone accumulate large numbers of cytologically immature eosinophils, forming aggregates, as a result of the increased expression of [alpha]4 integrins. In these conditions, iNOS expression is undetectable (Figure 2), and apoptosis is prevented [4]. The addition of PGE2 to these cultures downregulates a4 expression, decreases cellular aggregation, and allows terminal cytological differentiation, but no apoptosis occurs. These observations are entirely consistent with the evidence from this study that PGE2, in the presence of dexamethasone, did not induce iNOS expression.

One can propose, therefore, that PGE2 induces two different sequences of events in the same target population: (a) in the absence of dexamethasone, it acts in the initial 24 h to start a programme involving PKA activation and inducing iNOS and NO, ultimately leading to apoptosis; (b) in the presence of dexamethasone, it fails to induce iNOS and NO, and apoptosis is avoided, but downmodulation of a4 integrins and terminal differentiation are induced. While this reinforces the notion that iNOS and NO are essential elements in the proapoptotic programme, it also allows us to predict that the maturation induced by PGE2 in dexamethasone-exposed cells is independent of iNOS. This issue will be addressed in a separate report.

A related issue which requires further investigation is whether cysteinyl-leukotrienes also affect iNOS expression, an effect which would account for their ability to enhance eosinophil survival in bone-marrow culture [5] as well as the context of asthma [26].

Eosinophils, which express IL-5 receptors, were also shown to express iNOS by immunocytochemistry and contribute to NO production by iNOS by flow cytometry. This is consistent with evidence from other groups [27]. The hypothesis that all critical steps take place in the bone-marrow eosinophils themselves is consistent with the high effectiveness of PGE2 and isoproterenol inflt3L/SCF-primed cultures, which produce functional eosinophils at high purity [22]. Although this pattern of IL-5 receptor expression and enzyme induction tends to restrict the critical events to a single lineage, NO is highly diffusible through cell membranes. Indeed, cells which do not produce NO themselves remain susceptible to the effects of NO produced by neighboring cells. In this study, iNOS expression was heterogeneous among eosinophils in the same clusters. While cells strongly expressing iNOS and producing large amounts of NO are relatively resistant to this product, since they sustain its production for extended periods, iNOS-negative cells in their neighborhood might be susceptible to NO-induced apoptosis. This would be consistent with our observation of nuclear changes suggestive of apoptosis in the neighborhood of iNOS-positive eosinophils (Figure 2). Future studies might address this issue by examining whether eosinophils expressing iNOS at high levels by day 2 are identical with, or distinct from, the cells that ultimately undergo CD95-dependent apoptosis at later times.

Interestingly, in the presence of millimolar concentrations of an NO-releasing chemical, SNP, an apparent disconnection between the impact of the mutations Ipr and gld was observed in our study: while gld made bone-marrow resistant to the direct effect of an NO donor (Figure 7(b)), Ipr had no impact on susceptibility to the same agent (Figure 7(d)). The refractoriness of gld bone-marrow strengthens the conclusion that NO is not directly cytotoxic but essentially a signaling molecule. Importantly, this signal may be more effective in the presence of IL-5, as in our study, than in its absence [28]. Disruption of this NO signal, unexpectedly, was observed with gld but not with Ipr, even though Ipr bone-marrow was as resistant to all of the previously characterized pro-apoptotic stimuli as gld bone-marrow. A possible explanation is that cells from C57BL/6-lpr/lpr mice, which carry an early transposable element inserted into intron 2 of the fas gene, retain expression of CD95 at low levels and present residual responses to CD95L+ effector cells [29-31]. Differences in the genetic background of the gld and lpr strains may also contribute to these apparent discrepancies [29].

While we provided direct evidence that dexamethasone blocks this pathway at one defined step, namely, the induction of iNOS, additional studies are needed, however, to define whether the downstream effector molecules, CD95 and CD95L, are also targets of dexamethasone. This possibility would be consistent with the involvement of CD95 in both apoptosis and terminal differentiation, as reported for other hemopoietic lineages: in murine erythrocytes, terminal caspases as well as CD95 played a role in inducing terminal differentiation, while sustained Raf-1 activation prevented terminal differentiation [32]; in murine bone-marrow transplantation protocols, expression and ligation of CD95 correlated with better survival and differentiation potential of donor hemopoietic cells, rather than with susceptibility to apoptosis induced by CD95L [33, 34].


PGE2:  Prostaglandin E2
CD95L: Ligand for death receptor CD95
IL-5:  Interleukin-5
CysLT: Cysteinyl-leukotrienes
PKA:   cAMP-dependent protein kinase
EPO:   Eosinophil peroxidase
ZVAD:  Caspase inhibitor zVAD-fmk.

Authors' Contribution

B. de Luca and P. Xavier-Elsas made equally essential contributions to the execution and design of the experiments, respectively, and should therefore be considered joint first authors, listed in alphabetical order; Pedro Xavier-Elsas wrote the paper; Maria Ignez Gaspar-Elsas and Fernando Queiroz Cunha supervised the study, critically reviewed the paper and provided essential reagents; Maria Augusta Arruda and Thiago Mattar Cunha designed the inhibitor studies; Ricardo A. Luz evaluated NO production; Carla Jones evaluated iNOS expression; Tulio Queto and Monica Barradas studied flt3L/SCF effects.


This work was supported by fellowships (Research Productivity Fellowships to Pedro Xavier-Elsas, Maria Ignez Gaspar-Elsas, and Fernando Queiroz Cunha; Ph.D. fellowship to Ricardo A. Luz) and Grants (470377/2011-9 to Pedro Xavier-Elsas) from CNPq; Capes Fellowships to Bianca de Luca and Tulio Queto; and Grants from FAPERJ (E-26/111.555/2010 and E-26/103.138/2011) to Pedro Xavier-Elsas.


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Bianca de Luca, (1) Pedro Xavier-Elsas, (2) Monica Barradas, (2) Ricardo A. Luz, (2) Tulio Queto, (1) Carla Jones, (2) Maria Augusta Arruda, (3) Thiago Mattar Cunha, (4) Fernando Queiroz Cunha, (4) and Maria Ignez Gaspar-Elsas (1)

(1) Department of Pediatrics, Instituto Nacional de Saude da Mulher, da Crianca e do Adolescente Fernandes Figueira, FIOCRUZ, Avenue Rui Barbosa 716, 22250-020 Rio de Janeiro, RJ, Brazil

(2) Department of Immunology, Instituto de Microbiologia Professor Paulo de Goes, Universidade Federal do Rio de Janeiro, CCS, Bloco I, Room I-2-066, 22205-020, Rio de Janeiro, Brazil

(3) Farmanguinhos, FIOCRUZ, Avenue Comandante Guaranys No. 447, Jacarepagua, 22775-903 Rio de Janeiro, RJ, Brazil

(4) Department of Pharmacology, Faculdade de Medicina da USP, Avenue Bandeirantes 3900, Monte Alegre, 14049-900 Ribeirao Preto, SP, Brazil

Correspondence should be addressed to Pedro Xavier-Elsas;

Received 12 August 2013; Accepted 12 September 2013

Academic Editors: B. Cardaba, A. A. Manfredi, J. W. Steinke, and L. Virag
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Title Annotation:Research Article
Author:de Luca, Bianca; Xavier-Elsas, Pedro; Barradas, Monica; Luz, Ricardo A.; Queto, Tulio; Jones, Carla;
Publication:The Scientific World Journal
Article Type:Report
Date:Jan 1, 2013
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