Eosinophil recruitment and activation: the role of lipid mediators

Eosinophils are effector cells that migrate toward several mediators released at inflammatory sites to perform their multiple functions. The mechanisms driving eosinophil selective accumulation in sites of allergic inflammation are well-established and involve several steps controlled by adhesion molecules, priming agents, chemotactic, and surviving factors. Even though the majority of studies focused on role of protein mediators like IL-5 and eotaxins, lipid mediators also participate in eosinophil recruitment and activation. Among the lipid mediators with distinguish eosinophil recruitment and activation capabilities are platelet activating factor and the eicosanoids, including leukotriene B4, cysteinyl leukotrienes, and prostaglandin D2. In this review, we focused on the role of these four lipid mediators in eosinophil recruitment and activation, since they are recognized as key mediators of eosinophilic inflammatory responses.

Eosinophils are nowadays considered as multifunctional cells that have long been associated with allergy and parasitic infections. They are immunomodulatory cells that participate both in innate and adaptive immune response via expression of various receptors and secretion of a variety of mediators. To perform their functional activities, first eosinophils must migrate to sites of inflammatory reaction. Over the last years, a number of mediators and receptors involved in the regulation of eosinophil recruitment have been identified. Besides adhesion molecules and cytokines, eosinophil mobilization is mostly coordinated by a broad range of bioactive mediators known as chemokines. These molecules are an increasing family of small proteins with common structural motifs that via activation of their specific receptors play an important role not only in selective recruitment of eosinophils but also in subsequent eosinophil activation in sites of eosinophilic inflammation. Even though the main efforts in this research area are directed toward peptidic mediators, like chemokines, a growing body of data has unveiled key roles of lipid mediators in regulating eosinophil migration and activation. Among bioactive lipids, eicosanoids are a large family of distinctive mediators derived from arachidonic acid (AA) metabolization regularly found at high levels in inflammatory sites. Displaying from pro-to anti-inflammatory, pro-resolution, and even immunomodulatory functions, these molecules are key mediators in the pathogenesis of diverse inflammatory diseases, such as asthma, infection, and cancer. This review will first explore the role of some of the most well-studied lipid mediators on eosinophil migration. Then, it will summarize the impact of a varied of these mediators on eosinophil activation, focusing on eosinophil secretory function of leukotriene C 4 (LTC 4 ) synthesis/release. also migrate toward different factors distinct from chemokines such as C5a (Klebanoff et al., 1977), interleukin-5 (IL-5; Wang et al., 1989), granulocyte-macrophage colony-stimulating factor (GM-CSF; Secor et al., 1990), and lipid mediators. Indeed, AA metabolites as leukotrienes and prostaglandins (PGs), as well as, platelet activating factor (PAF) are considered major players in the pathogenesis of asthma and other forms of allergic inflammation, in part because they control eosinophil influx and activation.
Within a variety of cell types, phospholipase A 2 -driven AA mobilization followed by the oxidative metabolism of free AA mediated by either two cyclooxygenases (COX, PG H synthase) or a family of lipoxygenase (LO) enzymes culminate with the generation of bioactive lipid mediators with roles in eosinophilic inflammation. Specifically concerning those with ability to elicit eosinophil recruitment, newly synthesized lipid mediators may comprise:

LEUKOTRIENE B 4
Leukotriene B 4 (LTB 4 ) is a lipid mediator with potent chemoattractant properties that is rapidly generated from activated innate immune cells such as neutrophils, macrophages, and mast cells. Elevated levels of LTB 4 have been reported in various allergic diseases and these levels have been related to disease activity and eosinophilia (O'Driscoll et al., 1984;Wardlaw et al., 1989;Shindo et al., 1993). LTB 4 can bind to two highly conserved G protein-coupled receptors (GPCRs), LTB 4 receptor 1 (BLT1) and the considered low-affinity BLT2 (Toda et al., 2002;Yokomizo, 2011). LTB 4 serves as a potent chemoattractant through ligation of BLT1 on target cells. Expression and function of LTB 4 receptors on eosinophils remained for long time controversial, in part because LTB 4 -driven activity seemed to have some selectivity toward neutrophils. However, while strong demonstration of BLT1 expression in human eosinophils is still pending, functional assays using LTB 4 as agonist and specific BLT1 antagonists have provided evidences of expression of active BLT1 on human eosinophils. For instance, it has been shown a BLT1-driven LTB 4 ability to trigger calcium influx in human eosinophils (Murray et al., 2003a). On the other hand, murine (m)BLTR was cloned while searching for novel chemoattractant receptors in murine eosinophils and demonstrated that it encodes a functional receptor for LTB 4 which are able to trigger chemotaxis of mouse eosinophils (Figure 1, left panel; Spada et al., 1997;Huang et al., 1998). Reinforcing both in vitro data and in vivo assays with BLT1 antagonists, in vivo studies using BLT1-deficient mice have confirmed that ligation of BLT1 by LTB 4 is a key event for recruitment of eosinophils (Tager et al., 2000) However, it is noteworthy that while mouse eosinophils may generate only negligible amounts of LTB 4 , human eosinophils are not LTB 4 producers, representing major cellular sources of cysteinyl LTs (Weller et al., 1983). Based on the prominent eosinophil feature of recurrently depend on autocrine/paracrine stimulation to regulate their own functions, it seemd to be potentially more important the role of cysteinyl LTs in inducing eosinophilic responses, including autocrine/paracrine roles in induction of eosinophil chemotaxis and activation.

CYSTEINYL LEUKOTRIENES
Leukotriene C 4 and its extracellular derivatives LTD 4 and LTE 4 have many well recognized actions as mediators of allergic response, causing bronchoconstriction, mucous hypersecretion, increased microvascular permeability, and bronchial hyperresponsiveness. Additional but not as well-established effect is the ability of cysteinyl LTs to control eosinophil activities, including those related to tissue infiltration. Involvement of cysteinyl LTs in eosinophil influx is an in vivo phenomenon which was firstly demonstrated in guinea-pigs (Chan et al., 1990), but also observed in human (Laitinen et al., 1993) and reinforced by the anti-allergic effects of CysLT1 antagonists which, in addition to inhibiting allergic symptoms, also inhibit eosinophil recruitment during airway allergic inflammation (Peters-Golden, 2008). Even though cysteinyl LTs display negligible eosinophilotactic activity in vitro (Figure 1, left panel; Fregonese et al., 2002), cysteinyl LTs contribute to several mechanisms involved in mouting tissue FIGURE 1 | Schematic mechanisms of LTB 4 -, LTC 4 -, PAF-, or PGD 2 -induced eosinophil chemotaxis and LTC 4 synthesis. Left eosinophil scheme displays the ability of the four lipid mediators to trigger eosinophil chemotaxis by activating receptor-mediated distinct intracellular signaling. In contrast, the right eosinophil scheme shows that only PGD 2 and PAF are capable of activating LTC 4 synthesizing machinery, yet again by eliciting distinct signaling, but both by a lipid body-dependent mechanism. The right scheme also illustrates that both leukotrienes LTB 4 and LTC 4 , even thought activate their specific receptors in eosinophils (see left panel), failed to trigger lipid body biogenesis or LTC 4 synthesis. eosinophilia, since: (i) cysteinyl receptor CysLT1 appears to play a role in eosinophilopoeisis, inasmuch as CysLT1 antagonism in vivo limits IL-5-responsive eosinophil differentiation and maturation (Saito et al., 2004); (ii) cysteinyl LTs are able to significantly upregulate adhesion molecules, such as Mac-1 expression (Fregonese et al., 2002;Saito et al., 2004); (iii) direct administration of LTC 4 induce a rapid and significant reduction in leukocyte rolling velocity, further increasing cell adherence odds (Kanwar et al., 1995); (iv) cysteinyl LTs induce RANTES production from isolated lung cells, which in turn might cause RANTES-driven migration of eosinophils into airways (Kawano et al., 2003).

PLATELET ACTIVATING FACTOR
One major chemoattractant for eosinophils is the etherlinked phospholipid, PAF. PAF (1-O-alkyl-2-acetyl-sn-glycero-3phosphocholine) is another potent lipid mediator synthesized by a range of cell types, including monocytes/macrophages, mast cells, platelets, neutrophils, endothelial cells as well as eosinophils. PAF is capable of eliciting both chemokinesis and chemotaxis in vitro and triggering eosinophil influx and accumulation in vivo (Wardlaw et al., 1986;Kimani et al., 1988;Martins et al., 1989;Kato et al., 2004). Acting via a single class of identified receptor -named PAFR -a seven-trans-membrane G proteincoupled receptor, PAF evokes not only migration-related activities but also a variety of eosinophilic functional responses (Grigg, 2012). Of note, while it became more and more clear that human and mouse eosinophils shared profound dissimilarities , both express functional active PAFR which mediates eosinophilotactic activity of PAF in human and mouse cells by a pertussis toxin (PTX)-sensitive manner. Several studies have tryed to characterize the signaling pathways involved in PAFinduced eosinophil chemotaxis, and although still controversial, it is now recognized that eosinophilotactic responses triggered by PAF depend on activation of mitogen-activated protein (MAP) kinases, while upstream signaling events are regulated by activation of phosphoinositide 3-kinase (PI3K; Figure 1, left panel; Dent et al., 2000;Miike et al., 2000). Indeed, these findings are in agreement with the demonstration that PI3K inhibitors suppress PAF-mediated tissue eosinophilia in diseases such as asthma (Mishra et al., 2005).

PROSTAGLANDIN D 2
Prostaglandin D 2 has emerged as a key mediator of allergic diseases such as asthma (Matsuoka et al., 2000), in part due to its now wellcharacterized ability to promote potent eosinophil chemotaxis and activation (Powell, 2003). PGD 2 -driven cellular functions are all mediated by high-affinity interaction with two receptors, namely D prostanoid receptor 1 (DP 1 ) and chemoattractant receptorhomologous molecule expressed on T helper type 2 cell (Th2) cells (CRTh2, also known as DP 2 ). Whilst DP 1 is coupled to Gαs protein and signals through elevation of intracellular levels of cyclic adenosine monophosphate (cAMP), DP 2 is coupled to Gαi and its activation leads to elevation of intracellular calcium, reduction in cAMP (Sawyer et al., 2002) and downstream activation of PI3K (Xue et al., 2007). Eosinophils co-express both the classic DP 1 receptors coupledto adenylyl cyclase, as well as, PTX-sensitive DP 2 (Monneret et al., 2001).
Prostaglandin D 2 -mediated eosinophilotactic effect is due to direct activation of the DP 2 receptor expressed on eosinophil surface (Monneret et al., 2003). Several pharmacological studies show the involvement of DP 2 in the establishment of eosinophilia in models of allergic inflammation. For instance, intratracheal injection of PGD 2 or selective DP 2 agonist induced eosinophilia in rats, whereas the use of selective DP 1 agonist failed to trigger eosinophil accumulation (Emery et al., 1989). Likewise, intratracheal administration of DP 2 agonist or PGD 2 induced specific airway eosinophilia in mice previously exposed to the allergen or IL-5 (Shiraishi et al., 2005). DP 2 antagonist abrogated the PGD 2induced mobilization of eosinophils from the bone marrow of the guinea-pig confirming a crucial role of DP 2 in this response (Royer et al., 2008). A specific DP 2 agonist not only increased eosinophil recruitment at inflammatory sites but also the pathology in two in vivo models of allergic inflammation: atopic dermatitis and allergic asthma (Spik et al., 2005). Concurring, selective DP 2 , but not DP 1 antagonists were capable to inhibit eosinophil accumulation in a model of PGD 2 -induced eosinophilic pleurisy . In vitro, PGD 2 is able to promote additional migration-related activities, such as increased expression of cell adhesion molecules CD11b and L-selectin, calcium mobilization, actin polymerization, chemokinesis and a rapid change in eosinophil morphology (Gervais et al., 2001;Monneret et al., 2001). Of note and as illustrated in Figure 1 (left panel), these and other in vitro studies have collectively unveiled that PGD 2 -driven eosinophil chemotaxis may be determined by a balance between opposing downstream signaling pathways: cAMPdependent inhibitory DP 1 versus prevailing stimulatoryDP 2 intracellular effects (Monneret et al., 2003;Ulven and Kostenis, 2006;Sandig et al., 2007). However, further studies appears to be still needed to fully explain PGD 2 mechanisms of actions, since recently it has been shown that DP 1 and DP 2 may form heteromers representing a distinct functional signaling unit on eosinophil membrane with non-changed ligand-binding features (Sedej et al., 2012). In fact, these are not the first findings showing the ability of DP 1 receptors to amplify the biological response to DP 2 activation in eosinophils (Mesquita-Santos et al., 2011) a process that, although may not play roles in eosinophil migration, it appears to be critical to PGD 2 -induced eosinophil activation (see below).

DO LIPID MEDIATORS ACTIVATE EOSINOPHIL EFFECTOR FUNCTIONS?
At the sites of eosinophilic accumulation, through their ability to secrete a range of cytokines, basic proteins, reactive oxygen species as well as lipid mediators, eosinophils contribute to the physiopathology of a growing list of conditions including classical eosinophil-related diseases such as bronchial asthma, novel and quite surprising pathologies such as cancer, multiple sclerosis, Duchene muscular dystrophy as well as physiological process such as mammary development . While the regulation of eosinophil migration to the inflammatory focus is a critical stage in eosinophilic pathologies, understanding the mechanisms by which eosinophil activation is stimulated and its consequences appear to be even more important in defining potential targets for therapeutic interventions, since the specific stimulatory molecules, its receptors and signaling pathways involved in www.frontiersin.org eosinophil activation and subsequent mediator secretion may each be susceptible to inhibition. Indeed among different parameters of eosinophil activation, eosinophil secretory activity may represent the most attractive target to development of therapeutical maneuvers. Upon activation, eosinophil may engage both in secretion of pre-formed granule-stored contents, including eosinophil specific toxic proteins, enzymes, cytokines, chemokines, and other bioactive mediators, as well as de novo synthesized/released molecules including oxygen free radicals but prominently lipidic AA-derived mediators. The unique eosinophil pattern of oxidative metabolism of AA generates a specific array of eicosanoids. Eosinophils can synthesize lipoxin A 4 (LXA 4 ) and the aptly named after eosinophils, eoxin C 4 (EXC 4 ), besides the prostanoids thromboxane B 2 (TXB 2 ), PGE 2 and the recently identified PGD 2 . However, when properly stimulated, eosinophils prominently synthesize cysteinyl LTs. Of note, eosinophils are a major cellular source of cysteinyl LTs and have been identified as the principal LTC 4 synthase expressing cells in bronchial mucosal biopsies of asthmatic subjects (Bandeira-Melo and Weller, 2003). Hence, much interest in understanding the regulation of eicosanoid formation in eosinophils has focused on the mechanisms that regulate eosinophil cysteinyl LTs formation and release. Briefly, free AA can be metabolized within eosinophils by 5-LO, which is the limiting enzyme of leukotriene synthesis. 5-LO catalyzes a two-step reaction. First, 5-LO targets free AA in concert with the 5-LOactivating protein (FLAP) to insert one oxygen molecule into the 5 position of AA to form 5S-hydroperoxyeicosatetraenoic acid (HPETE), then transforms 5-HPETE into an unstable allylic epoxide, named LTA 4 . The subsequent metabolism of LTA 4 also differs between leukocytes. In neutrophils, for instance, LTA 4 hydrolase enzymatically hydrolyses 5-LO-metabolite LTA 4 to LTB 4 . In contrast within human eosinophils, which do not express LTA 4 hydrolase and therefore are incapable of LTB 4 synthesis, a specific glutathione S-transferase, named LTC 4 synthase (LTC 4 S), catalyzes the adduction of reduced glutathione (a tripeptide composed by glutamic acid, glycine, and cysteine) to LTA 4 to form LTC 4 . After energy-dependent export, LTC 4 is converted to LTD 4 and LTE 4 through sequential enzymatic removal of the glutamic acid by γ-glutamyl transpeptidases and then the glycine by dipeptidases. Therefore, because these LTs share a cysteine, LTC 4 and its extracellular derivatives LTD 4 and LTE 4 are collectively called cysteinyl LTs.
Similar to how we presented the roles of lipid mediators in inducing eosinophil migration, here we will also summarize some activating roles of LTB 4 , cysteinyl LTs, PAF and PGD 2 , but we will give special emphasis to a prototype parameter of eosinophil activation: eosinophil ability to activate LTC 4 synthesizing machinery.

LEUKOTRIENE B 4
Even though LTB 4 receptors have been indirectly and directly found to be expressed on human and murine eosinophils, respectively, there are not many successful studies reporting LTB 4 -driven eosinophil activation. Mainly using as cell model guinea-pig eosinophils, it has been shown that LTB 4 was capable of stimulating eosinophil recruitment, release of AA, homotypic eosinophil aggregation, as well as, rapid and transient activation of the NADPH oxidase (Faccioli et al., 1991;Lindsay and Giembycz, 1997;Teixeira et al., 1999). Of note, the intracellular mechanisms that mediate LTB 4 -induced NADPH oxidase activation involve mediation by lyn kinase, PKC, and PLA 2 , but occurs essentially independently of changes in the intracellular calcium, phospholipase D, PI3K, and ERK1/2 (Perkins et al., 1995;Lindsay et al., 1998a,b;Lynch et al., 1999) Specifically regarding induction of LTC 4 synthesizing function, stimulation of human eosinophils with LTB 4 failed to mount a LTC 4 synthesizing response (Figure 1,  right panel). In addition, eosinophil stimulation with LTB 4 was also unable to trigger synthesis of other eicosanoids such as PGE 2 or even the biogenesis of lipid bodies -organelles, which compartmentilize AA metabolism within eosinophils and other cell types, and that are promptly assembled under stimulation that leads to eicosanoid synthesis (Bozza et al., 1997b).

PLATELET ACTIVATING FACTOR
Human eosinophils are prominent among cell populations that respond to PAF stimulation displaying, besides chemotaxis, numerous PAF-driven functions, including migration-related activities such as adhesion and expression of cell surface molecules, as well as, secretory functions, including superoxide production and release of cationic granule proteins and stored cytokines (Wardlaw et al., 1986;Kroegel et al., 1989;Zoratti et al., 1991;Takizawa et al., 2002;Dyer et al., 2010). Equally important is the notion that although only one PAFR has been identified, PAF-driven signaling has emerged as a complex phenomenon, displaying differences between eosinophil chemotactic versus secretory functions and therefore suggesting the existence of yet non-characterized receptors (Kato et al., 2004).
It is noteworthy that PAF was the first stimulus to have its lipid body-dependent mechanism of eliciting LTC 4 synthesis characterized. PAF, acting via its G-protein-linked receptor induces lipid body formation via a downstream signaling involving PKC and phospholipase C (PLC) activation (Figure 1, right panel; Bozza et al., 1996Bozza et al., , 1997aBozza et al., , 1998. Even more relevant to PAF ability of inducing LTC 4 synthesis, it was the demonstration that the major enzymes involved in the enzymatic conversion of AA into LTC 4 , 5-LO, and LTC 4 synthase, were found compartmentalized within PAF-induced newly assembled eosinophil lipid bodies (Bozza et al., 1997a(Bozza et al., , 1998 and that these enzymes were functional and producing LTC 4 within theses organelles (Bandeira-Melo et al., 2001).
Inasmuch as eosinophils express functional receptors for cysteinyl LTs, it has been investigated their potential role as stimuli of eosinophil activation. Indeed, a series of reports showed cysteinyl LTs ability to affect various eosinophil responses. For instance, cysteinyl LTs promote CysLT 1 -dependent calcium influx on HL-60 (Thivierge et al., 2000;Murray et al., 2003b). We have also shown that LTC 4 , LTD 4 , and LTE 4 induced a dose-and timedependent, vesicular transport-mediated release of pre-formed IL-4 from eosinophils derived in vitro from human cord blood progenitors (Bandeira-Melo et al., 2002a). Although some controversy exist (Murray et al., 2003b), cysteinyl LTs also appear to be able to induce in vitro survival of human eosinophils by activation of CysLT 1 receptors (Lee et al., 2000;Becler et al., 2002). It is noteworthy that in addition to their recognized activities as paracrine mediators, eicosanoids like cysteinyl LTs are now also recognized to display autocrine effects. Indeed, eosinophil-derived cysteinyl LTs exert autocrine effects to enhance eosinophil survival triggered by GM-CSF, as well as, mast cell-and lymphocytederived molecules (Lee et al., 2000). Moreover, the capacity of eotaxin to stimulate the vesicular transport-mediated release of pre-formed IL-4 from human eosinophil granules is dependent of an endogenous LTC 4 , formed at eosinophil lipid bodies, that acting as an intracrine signaling molecule regulates this CCR3elicited IL-4 release (Bandeira-Melo et al., 2002c). Thus, LTC 4 may act intracellularly as intracrine signal transducing mediators. Indeed, cysteinyl LTs-responsive receptors have been identified on the membranes of intracellular eosinophil granule organelles and appear to function mediating cysteinyl LTs-stimulated secretion from within eosinophil granules, including those granules found extracellularly (Neves et al., 2010). On the other hand ans as illustrated in Figure 1 (right panel), specifically regarding the ability of activating LTC 4 synthesis, none endogenous or exogenous cysteinyl LTs displayed the ability to trigger lipid body biogenesis or to elicit their own synthesis (Bandeira-Melo et al., 2002c).

PROSTAGLANDIN D 2
Besides migration-related cell functions, it is now wellcharacterized that PGD 2 is a potent inducer of eosinophil activation, being capable of promoting eosinophil secretory activity. For instance, PGD 2 is capable of triggering eosinophil degranulation, which appears to be induced by the selective DP 2 agonist but not by selective DP 1 agonist, suggesting for DP 2 a role in modulating, not only eosinophil migration, but also activation (Gervais et al., 2001). We have also shown that, in addition to its eosinophilotactic activity, PGD 2 controls allergy-relevant eosinophil activation parameter: the increased LTC 4 -synthesizing capacity of these cells (Mesquita-Santos et al., 2006). Indeed, other eosinophilotactic mediators, including eotaxin, RANTES, and PAF are capable of triggering LTC 4 synthesis within eosinophils through activation of their cognate Gαi-coupled chemotactic receptors (e.g., CCR3; Bozza et al., 1996;Bandeira-Melo et al., 2001). However, PGD 2 -induced LTC 4 synthesis, surprisingly and distinctly from other parameters of eosinophil activation evoked by PGD 2 , was not mediated by the stimulatory activation of DP 2 receptors while being counter-balanced by a parallel inhibitory cAMP-dependent DP 1 receptor activation. On contrary, it does depend on a novel kind of interaction between the PGD 2 receptor types expressed on eosinophils (Figure 1, right panel). Eosinophil LTC 4 synthesis triggered by PGD 2 is controlled by complementary stimulatory events between DP 1 receptor-activated lipid bodies and concurrent DP 2 receptor signaling . While PGD 2 emerges as a potent inflammatory mediator of allergic disorders and as an interesting therapeutic target, because of the mandatory dual activation of DP 1 and DP 2 receptors for increasing eosinophil LTC 4 synthesis, either DP 1 or DP 2 receptor antagonists might be highly effective candidates as anti-allergic tools to control cysteinyl LTs production regulated by the activation of eosinophils at sites of allergic reactions. On the top of that, we had recently also found out that upon proper stimulation, both human and mouse eosinophils can produce significant amounts of biologically relevant PGD 2 (Luna-Gomes et al., 2011) . PGD 2 intracellular synthesis within eosinophils led to PGD 2 receptor-mediated paracrine/autocrine functions, contributing to eosinophil activation. Indeed, eosinophil-derived PGD 2 appears to be capable of regulating both eosinophil motility, as well as, lipid body-driven LTC 4 synthesis within eosinophils stimulated with eotaxin, for instance.

FINAL REMARKS
It is clear that several relevant aspects of lipid mediator impact on eosinophil biology need to be further characterized, however knowledge on this subject had evolved dramatically in the last decades. Among the most significant advances on eosinophil/lipid mediator axis are: (i) the recognition that eosinophils express the multitude of lipid mediator receptors on their surface, even those receptor pairs with apparently opposing functional outcomes under activation; (ii) the appreciation that not only eosinophil migration is elicited by lipid mediators, but maybe even more therapeutically relevant, activation of eosinophil secretory functions; and (iii) the acknowledgment of a wide-ranging induced signaling and consequently functional potentiality for lipid mediator-stimulated eosinophils that have still unpredicted impact to surrounding eosinophilic immuno-pathologies.
Still of special interest for eosinophil biology with roles in maximizing eosinophil functional potentialities is the rising observations unraveling intricate interactions between lipid mediators (such as LTC 4 and PGD 2 ) and eosinophil-relevant chemokines and other proteic stimuli. Possibly the most illustrative example of such cross-talking is eosinophil stimulation by eotaxin, a key mediator in the development of allergic eosinophilia that is known by its potent eosinophilotactic activity and has emerged as a potent mediator of eosinophil activation. Among a number of data on eotaxin/AA metabolites interdependency, some hallmarks are the sequencial events: (i) eotaxin particular ability to acutely enhance PGD 2 synthesis by eosinophils by stimulating CCR3 receptors (Mesquita-Santos et al., 2006;Luna-Gomes et al., 2011); (ii) the subsequent autocrine/paracrine induction of lipid body biogenesis and lipid body-located LTC 4 synthesis by eosinophil-derived PGD 2 (Luna-Gomes et al., 2011); followed by (iii) LTC 4 -driven intracrine induction of piecemeal degranulation of granule-stored IL-4 by eotaxin-stimulated eosinophils (Bandeira-Melo et al., 2002c). Nevertheless, eotaxin is not the only example of such lipid/protein cooperation. It is still noteworthy that cell types other than eosinophils also undergo such lipid mediator/protein mediator cross-talking in regulating cell activation. Either infection-elicited or oxLDL-driven MCP1, for instance, www.frontiersin.org besides its known CCR2-driven chemotactic function, appear as a key activator of lipid body biogenic and leukotriene synthesizing machineries within macrophagic cells (Pacheco et al., 2007;Silva et al., 2009). Once more specifically regarding eosinophils, synergistic effects on eliciting eosinophil chemotaxis have been also described between PGD 2 and at least the cytokines IFN-γ and TNF-α (El-Shazly et al., 2011), as well as, between DP 2 activation and vasoactive intestinal peptide VIP (El-Shazly et al., 2013). Moreover, RANTES, IL-16 and MIF are also proteic mediators capable of activating eicosanoid synthesizing machinery within eosinophils culminating with the generation of LTC 4 and PGD 2 , that in turn intracrinally or autocrinally mediate eosinophil secretory functions (Bandeira-Melo et al., 2002b,c;Vieira-de-Abreu et al., 2011).