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Catherine Godson, UCD Diabetes Research Centre, UCD Conway Institute, School of Medicine and Medical Sciences, University College Dublin, Dublin, Ireland. E-mail: email@example.com
The resolution of inflammation is an active process controlled by endogenous mediators with selective actions on neutrophils and monocytes. The initial phase of the acute inflammatory response is characterized by the production of pro-inflammatory mediators followed by a second phase in which lipid mediators with pro-resolution activities may be generated. The identification of these mediators has provided evidence for the dynamic regulation of the resolution of inflammation. Among these endogenous local mediators of resolution, lipoxins (LXs), lipid mediators typically formed during cell–cell interaction, were the first to be recognized. More recently, families of endogenous chemical mediators, termed resolvins and protectins, were discovered. LXs and aspirin-triggered LXs are considered to act as ‘braking signals’ in inflammation, limiting the trafficking of leukocytes to the inflammatory site. LXs are actively involved in the resolution of inflammation stimulating non-phlogistic phagocytosis of apoptotic cells by macrophages. Furthermore, LXs have emerged as potential anti-fibrotic mediators that may influence pro-fibrotic cytokines and matrix-associated gene expression in response to growth factors. Here, we provide a review and an update of the biosynthesis, metabolism and bioactions of LXs and LX analogues, and the recent studies on their therapeutic potential as promoters of resolution and fibro-suppressants.
Inflammation is a key process in effective host defence. It is a critical response to microbial invasion and tissue injury, and is characterized by site-specific accumulation and activation of leukocytes. The resolution of such inflammatory responses is necessary to re-establish homeostasis, limiting excessive tissue injury and minimizing the development of chronic inflammation, and depends on the biological actions of several anti-inflammatory and pro-resolving mediators, expressed by various cell types, as well as on apoptosis and clearance of inflammatory cells (Lawrence et al., 2002; Serhan and Savill, 2005; Serhan, 2007; Serhan et al., 2007). A failure of any step in this process may lead to chronic inflammation with possible further tissue destruction, fibrosis and eventually organ failure. The first evidence that the resolution of inflammation is an active rather than a passive process came with the discovery of pro-resolution biochemical signalling circuits (Serhan et al., 2000; 2007; Bannenberg et al., 2005). During the initial phase of inflammation, eicosanoids including prostaglandins and leukotrienes (LTs) play important role as local mediators in the development of an inflammatory condition, evoking potent chemotactic responses of leukocytes whose activation is coupled to the production of proinflammatory (Th1-derived cytokines) at sites of inflammation (Borgeat and Naccache, 1990). This is a biphasic process; the second stage is coupled to the biosynthesis of lipid mediators that actively limit inflammation and promote resolution. The new genus of pro-resolving mediators of molecules include lipoxins (LXs) and their aspirin-triggered carbon-15 epimers (ATL) (Levy et al., 2001; Serhan, 2005), as well as the recently discovered resolvins and protectins which are derived from ω-3 fatty acids (Serhan et al., 2000; 2008a,b). Resolvins and protectins were first identified in self-resolving murine exudates using the murine dorsal air pouch model of inflammation (Serhan et al., 2000). In parallel studies, it was demonstrated that prostaglandin E2 and D2 stimulate the translation of neutrophil 15-lipoxygenase (LO) involved in LX biosynthesis, providing evidence for class switching within the eicosanoid pathways during the evolution of an inflammatory exudate (Levy et al., 2001). Figure 1 shows the cellular and molecular mechanisms involved in the onset and resolution of inflammation.
In this review, we will give an overview and an update of the role of LXs as pro-resolution and anti-fibrotic agents with particular focus on the potential development of LX analogues as therapeutics.
Biosynthesis of LXs
The term LXs is an acronym for LO interaction products. These lipid mediators were first recognized to have dual anti-inflammatory and pro-resolution activities (Maderna and Godson, 2003; Kieran et al., 2004; McMahon and Godson, 2004; Serhan, 2005). 5S,6R,15S-trihydroxy-7,9,13-trans-11-cis-eicosatetraenoicacid (LXA4) and its positional isomer 5S,14R,15S-trihy-droxy-6,10,12-trans-8-cis-eicosatetraenoic acid (LXB4) are the principal species formed in mammals (Serhan et al., 1986a,b). LXs are typically formed by transcellular metabolism through distinct biosynthetic pathways depending on the cellular context (Kieran et al., 2004; McMahon and Godson, 2004; Chiang et al., 2005; Serhan, 2005). There are two main LO-mediated pathways of LX biosynthesis in human cells and tissues. The first of these involves the sequential lipoxygenation of arachidonic acid by 15-LO in epithelial cells and monocytes, and 5-LO in neutrophils (Serhan et al., 1984a,b). This pathway not only leads to LX biosynthesis, but also reduces LT formation, resulting in an inverse relationship between LT and LX byosynthesis in human leukocytes (Serhan, 1989). Indeed, it has recently been shown that in acute post-streptococcal glomerulonephritis up-regulation of 15-LO and subsequent LX biosynthesis supersede production of proinflammatory LTB4 (Wu et al., 2009). The second major route of LX formation involves platelet/leukocyte or platelet/leukocyte microaggregate interactions that promote LX formation by transcellular conversion of the 5-LO epoxide product, LTA4 to LXA4 and LXB4 by the LX-synthetase activity of the 12-LO in platelets (Serhan and Sheppard, 1990). Interestingly, platelets are not able to produce LXs on their own, but this pathway has been highlighted as a major route for LX formation within the vasculature where activated platelets become a major source of LXs after adhesion to neutrophils (Chiang et al., 2005; Serhan, 2005).
In addition to the transcellular routes, another recognized source of LX biosynthesis involves a form of cellular ‘priming’ with the esterification of 15-HETE in inositol-containing phospholipids within the membranes of human neutrophils (Brezinski and Serhan, 1990). Discovery of this pathway suggests that during disease or host defence, precursors of LX biosynthesis might be stored within the membranes of the inflammatory cells and released after stimulation (Brezinski and Serhan, 1990).
The signalling networks involved in LX formation show even greater complexity given the potential regulation of biosynthetic enzymes by specific cytokines (Serhan et al., 1996). For example, interleukin 4 (IL-4) and IL-13, putative negative regulators of inflammatory and immune responses, promote transcellular LX generation through enhanced expression of 15-LO in monocytes and epithelial cells (Nassar et al., 1994; Munger et al., 1999). Cytokines such as granulocyte–macrophage colony-stimulating factor (GM-CSF) and IL-3 up-regulate 5-LO transcripts (Ring et al., 1996), while pro-inflammatory cytokines such as IL-1β, IL-6 and tumour necrosis factor (TNF-α) have been shown to induce cyclooxygenase-2 (COX-2), thus potentially contributing to the formation of ATLs in vivo (Parente and Perretti, 2003).
Aspirin triggers the generation of epimeric forms of LXs (Claria and Serhan, 1995). Cells that express COX-2 (i.e. vascular endothelial cells, epithelial cells, macrophages, neutrophils) are able to produce ATLs by the actions of aspirin that triggers the endogenous formation of carbon-15 epimeric LXs, namely ATL (Claria and Serhan, 1995). In particular, in a cytokine primed milieu, aspirin acetylation of COX-2 switches the catalytic activity of the enzyme to an R-LO with the formation of 15R-HETE that is rapidly converted by 5-LO to 15-epimeric-LXA4 or 15-epimeric LXB4 (Claria and Serhan, 1995). Interestingly, ATL formation has been detected in vivo in various murine models of inflammation such as peritonitis (Chiang et al., 1998), dorsal air pouches (Perretti et al., 2002) and in aspirin-intolerant asthmatics (Sanak et al., 2000). Administration of low doses of aspirin to healthy subjects significantly increases plasma levels of ATL with a concomitant inhibition of thromboxane biosynthesis, suggesting that ATL may account for some of the beneficial effects of aspirin that are not strictly related to its anti-thrombotic actions (Chiang et al., 2004). A further synthetic route for the production of 15-epi LXA4 has been demonstrated in rat myocardium in response to statins and the PPAR-γ ligand pioglitazone (Birnbaum et al., 2006; 2007), providing a novel mechanism for immune regulation by statins.
Metabolic inactivation of LXs
LXs are rapidly generated in response to stimuli, act locally and undergo rapid metabolic inactivation. Using monocytes or isolated enzymes, it has been possible to demonstrate that the major route of LXs degradation is via dehydrogenation at C-15 and possibly by ω-oxidation at C-20 (Serhan et al., 1995; Clish et al., 2000). A similar inactivation pathway was also shown for LXB4 (Maddox et al., 1998). ATLs are converted in vitro to their 15-oxo-metabolite with a slower rate compared to native LXs, indicating that the hydrogenation step is highly specific (Serhan et al., 1995). Furthermore, ATLs, when generated in vivo, display longer biological half-life than native compounds and enhanced ability to evoke bioactions (Serhan et al., 1995; Maddox et al., 1997; Clish et al., 1999).
Synthetic LX analogues
The rapid inactivation and short half-life of LXs in vivo have prompted the development of novel analogues designed to resist metabolism, maintain their structural integrity and bioavailability and their potential beneficial bioactions. The initial design of metabolically stable LXA4 analogues focused on identifying poor substrates for PGDH, which maintained potency in in vitro assays. The discovery that 15-epi-LXA4 was equipotent in in vitro assays to LXA4, but was a poorer substrate for PGDH, provided support for exploiting these observations in novel analogue design. However, although 15-epi-LXA4 has enhanced metabolic stability over LXA4in vivo, its pharmacokinetics remain poor, which, in addition to low chemical stability, creates challenges for development of analogues with better therapeutic potential. Therefore, a series of LX and ATL analogues were designed with specific modifications of the native structures of LXA4 and LXB4, such as the addition of methyl groups on C-15 and C-5 of LXA4 and LXB4, respectively (Serhan et al., 1995), and phenoxyl or para-fluoro-phenoxyl groups at C-16 of both LXA4 and 15-epi ATL, protecting the molecules from the ω-oxidation and dehydrogenation in vivo (Serhan et al., 1995; Maddox et al., 1997; Clish et al., 1999). Consequently, these analogues were widely used in a number of studies exploring the biological functions of LX and ATL in experimental models of disease (Scalia et al., 1997; Takano et al., 1997; Filep et al., 1999; Hachicha et al., 1999; Jozsef et al., 2002; Ariel et al., 2003). A second generation of LX stable analogues, 3-oxa-LXA4 analogues, with enhanced chemical and metabolic stability, has shown potency and efficacy comparable to ATL in diverse animal models after topical, intravenous or oral delivery (Bannenberg et al., 2004a; Guilford et al., 2004). More recently, we have developed a stereoselective synthesis of chemically stable aromatic LXA4 and LXB4 analogues (O'Sullivan et al., 2007). This synthetic route establishes the required stereochemistry by way of Sharpless epoxidation, Pd-mediated Heck coupling and diastereoselective reduction reactions (Figure 2). LXs, ATL and their stable analogues share potent protective actions in controlling inflammation, and provide new opportunities to explore the actions and therapeutic potential for LXs and ATL as it will be outlined later in this review.
The binding of lipids and small peptides to the receptor occurs with different affinities and/or at discrete interaction sites, facilitating activation of distinct signalling pathways that depends on the cell type and system (Bae et al., 2003). N-glycosylation of ALXR is proposed to be important for ligand specificity and may play a role in switching receptor functions at local host defence sites, suggesting receptor versatility (Chiang et al., 2000).
Mouse and rat ALXR homologues have been cloned from a spleen cDNA library (Takano et al., 1997) and from peripheral blood leukocytes, respectively (Chiang et al., 2003). The overall homology between the human, murine and rat receptors is relatively high in particular in their second intracellular loop (100%) and between the sixth transmembrane domain (97%), suggesting important roles for these regions in ligand recognition and functional G protein coupling.
The partial antagonism of a subclass of peptide-LT receptors (CysLTs) is a potential mechanism through which LXs may contribute to the anti-inflammatory bioactions of LXs in several tissues and cell types other than leukocytes (Badr et al., 1989; McMahon et al., 2000; Gronert et al., 2001; Chiang et al., 2006). In mesangial cells, LXs (nanomolar) are potent inhibitors of proliferative responses to LTD4 by modulating LTD4-induced transactivation of the platelet-derived growth factor (PDGF) receptor and subsequent phosphotidylinositol 3-kinase activation and mitogenic responses (McMahon et al., 2000). The counter-regulatory responses identified for LX were insensitive to a CysLT1-specific receptor antagonist, but blocked by a non-selective antagonist (McMahon et al., 2002). These data are intriguing given the proposal that the interaction between CysLT1 and CysLT2 receptors regulates inflammatory responses such that activation of the CysLT2 receptor can exert a net inhibitory response on CysLT1 receptor responses (Jiang et al., 2007). By analogy, it might be proposed that LXA4 activation of the CysLT2 receptor regulates the pro-inflammatory response of the CysLT1; however, this has not been definitively demonstrated.
Further studies show that LXs inhibit proliferation induced by growth factors such as PDGF, epidermal growth factor (EGF) and connective tissue growth factor (CTGF) with a mechanism that involves cross-talk between AXLR and receptor tyrosine kinases (McMahon et al., 2000; 2002; Wu et al., 2006). This inactivation seems to be mediated through the coupling of the ALXR to the activation of the protein tyrosine phosphatase, SHP-2, and it is proposed that the association of the PDGF receptor β within lipid raft microdomains renders it susceptible to LXA4-mediated dephosphorylation by possible reactivation of oxidatively inactivated SHP-2 (Mitchell et al., 2007). The ALXR ligand annexin-1 also regulates protein phosphorylation of EGF and PDGF receptors (Mitchell et al., 2007).
It is noteworthy that LX-mediated dephosphorylation of intracellular proteins seems to be a recurrent feature of LXA4 signalling. In addition to dephosphorylation of receptor tyrosine kinases, LX-stimulated phagocytosis of apoptotic leukocytes as described below is dependent on dephosphorylation of myosin IIA (Reville et al., 2006). Recent evidence highlights the importance of LXA4 as regulators of eosinophil responses to GM-CSF through inhibition of protein tyrosine phosphorylation (Starosta et al., 2008). Additionally, LXA4 and ATL have been shown to regulate vascular endothelial growth factor (VEGF) receptor-2 phosphorylation in endothelial cells (Fierro et al., 2002; Cezar-de-Mello et al., 2006; 2008; Baker et al., 2009).
Another potential receptor for LXA4 is the aryl hydrocarbon receptor (AhR), a ligand-activated transcription factor. In a murine hepatoma cell line, LXA4 has been shown to bind and activate AhR (Schaldach et al., 1999). In dendritic cells, LXA4, signalling through AhR and ALXR modulate innate and acquired immune responses (Machado et al., 2006). It has recently been demonstrated that both LXA4 and ATL acting via the AhR inhibit innate immune responses of dendritic cells by up-regulating suppressor of cytokine signalling 2 (SOCS-2), which in turn promotes ubiquitinylation and degradation of TNF receptor-associated factor-6, a component of TNF-α, TLR signalling pathways (Machado et al., 2008). It should be noted that responses to the AhR require concentrations of LXA4 in the micromolar range, whereas cellular responses generated through ALXR (or CysLT) are typically maximal in the nanomolar range, and the Kd of the ALXR is subnanomolar (Fiore et al., 1994).
Anti-inflammatory, pro-resolution and anti-fibrotic effects of LXs
The actions of LXs and ATL are not limited to counter-regulating the evolution of inflammation, but also to promote resolution at different levels. LXs stimulate monocyte chemotaxis and adherence, without causing degranulation or release of reactive oxygen species (Maddox et al., 1997), suggesting that the actions of LXs are related to the recruitment of monocytes to sites of injury. These monocyte activities may be host protective in view of the important role of these cells in wound healing and resolution at inflammatory sites. Indeed, LXs and ATLs stimulate the in vitro clearance of apoptotic cells by human monocyte-derived macrophages in a non-phlogistic manner (Godson et al., 2000; Mitchell et al., 2002; Reville et al., 2006). LXs stimulate phagocytosis of exogenously administered excess apoptotic PMN in a murine model of thioglycollate-induced peritonitis in vivo, suggesting that LXs rapidly promote the clearance of apoptotic leukocytes within an inflammatory milieu (Mitchell et al., 2002). Consistent with a role for LX promoting the resolution of inflammation are the observations that LX-stimulated phagocytosis is associated with increased transforming growth factor-β1 (TGF-β1) release from macrophages, and a decrease of IL-8 and monocyte chemoattractant protein-1 (MCP-1) release (Godson et al., 2000). The effect of LXs on phagocytosis of apoptotic cells by macrophages is mediated by protein kinase C and PI-3-kinase (Godson et al., 2000; Mitchell et al., 2002). A modulatory role for cAMP is suggested by the observation that LX-induced phagocytosis is inhibited by a cell permeant cAMP analogue, and mimicked by a protein kinase A inhibitor (Godson et al., 2000). Furthermore, LXs prime macrophages for chemotaxis and phagocytosis, through myosin IIa assembly, re-organization of the cytoskeleton, promoting the cell polarization and formation of actin filaments and pseudopodia (Maderna et al., 2002; Reville et al., 2006). Assembly of non-muscle myosin is coupled to serine dephosphorylation, a process stimulated by LXA4 through a process that may involve phosphatase activation as described in mesangial cells (Mitchell et al., 2007).
Other ligands of ALXR, and in particular endogenous annexin-1 and its peptidomimetic Ac2-26, promote phagocytosis of apoptotic cells through a mechanism involving ALXR and changes in F-actin re-organization (Maderna et al., 2005). Interestingly, we have shown that cells undergoing apoptosis release annexin-1 that can then stimulate phagocytosis through ALXR (Scannell et al., 2007), demonstrating that the ALXR is activated by soluble ‘eat me’ signals released from apoptotic cells. Figure 5 illustrates the possible mechanisms of LXs in the phagocytosis of apoptotic cells and resolution of inflammation.
In addition to promoting resolution by non-phlogistic phagocytosis of apoptotic cells, LX can act to reprogramme cytokine-primed macrophages from a classic pro-inflammatory (M1) phenotype to an alternatively activated phenotype demonstrating enhanced phagocytic capacity for apoptotic cells (Mitchell et al., 2002). This feature may suggest novel therapeutic strategies in chronic inflammation characterized by massive macrophage infiltration.
As discussed earlier, LXs are potent inhibitors of mesangial cell proliferation in response to LTD4 and growth factors with a mechanism that involves cross-talk between AXL and receptor tyrosine kinases (McMahon et al., 2000; 2002; Mitchell et al., 2004). In addition, LXA4 can counteract PDGF-induced, fibrosis-related gene expression in mesangial cells, suggesting that LXA4 might act as a potential anti-fibrotic agent, preventing growth factor-induced mesangial matrix production and the progression of renal disease (Rodgers et al., 2005). PDGF-treated renal mesangial cells were shown to secrete factors that promote the onset of tubulointerstitial damage, as observed by epithelial-to-mesenchymal transformation in proximal tubular epithelial cells, an effect attenuated by pretreatment with LXA4 (Rodgers et al., 2005). Further to these data, Wu et al. demonstrated that TNF-α-induced proliferation and cytokine release, as well as CTGF-mediated release of fractalkine, MCP-1 and RANTES, were modulated by LXA4 in rat mesangial cells (Wu et al., 2005; 2006). In addition to evidence that LX can maintain the integrity of renal epithelia are data demonstrating that LXA4 stimulates the expression of ZO-1, claudin and occludin, and the maintenance of transepithelial resistance in cultured bronchial epithelial cells (Grumbach et al., 2009).
The synthetic LX analogue 15-epi-16-(para-fluoro)-phenoxy-LXA4 inhibits VEGF-induced endothelial cell proliferation and migration via inhibition of actin polymerization and assembly of focal adhesions (Fierro et al., 2002; Cezar-de-Mello et al., 2006). In addition, in endothelial cells, the 15-epi-16-(para-fluoro)-phenoxy-LXA4 induces the gene and protein expression of heme oxygenase-1 (HO-1), a key modulator of both innate and adaptative immunity (Nascimento-Silva et al., 2005). The pathophysiological importance of this finding is reflected by the fact that HO-1 synthesis triggered by ATL is required for the inhibition of TNF-α-induced adhesion molecule expression on endothelial cells which may impair leukocyte influx during the resolution phase of inflammation. Mice lacking 15-LO type I have an impaired HO-1 response. Topical application of LXA4 in these mice restores HO-1 expression and protects them from inflammatory challenge (Biteman et al., 2007).
The powerful anti-inflammatory, pro-resolution and more recently appreciated potential anti-fibrotic properties of LXs contribute to the overall anti-inflammatory mechanisms of LXs that can modulate the activation and migration of inflammatory cells.
LXs, ATLs and LX analogues in experimental model of diseases
There is reliable evidence that demonstrates that LXs or their stable analogue mimetics can reduce inflammation and symptoms in several experimental models of inflammatory disorders. As discussed earlier, the metabolism of LXs suggests that these molecules are highly susceptible to rapid inactivation; therefore, the availability of stable analogues has been a useful tool to extend the beneficial anti-inflammatory role of LXs to possible therapeutic applications.
The anti-inflammatory spectrum of activity of LXs is well documented in in vivo models of glomerulonephritis and acute renal failure (Badr et al., 1989; Papayianni et al., 1995; Ohse et al., 2004), as well as in in vitro models (McMahon et al., 2000; 2002; Mitchell et al., 2004; Rodgers et al., 2005). In a murine model of ischaemic renal injury (IRI) disease, administration of 15-epi-16-(para-fluoro)-phenoxy-LXA4, before onset of experimental ischaemia, resulted in a significant functional and morphological protection with a markedly reduced neutrophil infiltration to the IRI kidney, while maintaining glomerular function and morphology, and attenuating chemokine and cytokine responses including up-regulation of SOCS-2 (Leonard et al., 2002). Using a transcriptomic approach to investigate the mechanism underlying the protective action of LXA4, specific cohorts of genes whose expression was altered in renal IRI and modulated by 15-epi-16-(para-fluoro)-phenoxy-LXA4 were identified (Kieran et al., 2003). Some of these genes included chemoattractants, cytokines, chemokines and chemokine receptors, growth factors and their receptors, adhesion molecules and molecules implicated in maintaining epithelial barrier function such as claudins (Kieran et al., 2003). These data are especially noteworthy given the evidence that LXA4 regulates transepithelial resistance in bronchial epithelia by a mechanism that includes up-regulation of claudin expression. It has been proposed that defective LX biosynthesis in cystic fibrosis (Karp et al., 2004) and asthma (Levy, 2005) could contribute to compromised epithelial barrier function (Grumbach et al., 2009). In vivo models of peritonitis have frequently been used to highlight anti-PMN trafficking effects of LX analogues (O'Sullivan et al., 2007). Interestingly, a recent report demonstrated the effect of ajulemic acid (AjA), a synthetic cannabinoid, on enhanced LXA4 production, an effect attributed to the observed reduction in peritoneal infiltration in a mouse model where AjA treatment before zymosan-induced peritonitis was associated with LO-dependent LX generation (Zurier et al., 2009).
A second generation of LX/ATL analogues was designed to subvert metabolism by β-oxidation through insertion of a 3-oxa group and to have improved chemical stability (Guilford et al., 2004). The changes resulted in significantly enhanced stability and plasma half-life, maintaining similar biological activity with a better pharmacokinetic profile over the 15-epi analogue (Fiorucci et al., 2004; Guilford et al., 2004; Levy et al., 2007). The potent anti-inflammatory and protective actions of LXs in intestinal inflammation make them an attractive candidate as a potential therapy for various inflammatory conditions of the digestive system, including Crohn's disease and ulcerative colitis. Indeed, ATL is protective in intestinal inflammation in a mouse model of dextran sodium sulphate-induced colitis (Gewirtz et al., 2002), and the β-oxidation resistant 3-oxa-ATL (ZK-192) has been shown to potently attenuate trinitrobenzene sulphonic acid (TNBS)-induced colitis, a Crohn's disease model (Fiorucci et al., 2004). When orally administered, ZK-192 reduced TNBS colitis both in preventive and therapeutic regimens, attenuating weight loss, macroscopic and histological colon injury, mucosal neutrophil infiltration, colon wall thickening, as well as decreasing mucosal mRNA levels for several inflammatory mediators (Fiorucci et al., 2004).
In asthma, the ZK-994 LX/ATL analogue (5S,6R,7E,9E,13E,15S)-16-(4-fluoro-phenoxy)-3-oxa-5,6,15-trihydroxy-7,9,13-hexadecatrien-11-ynoic acid was effective in reducing airway inflammation and airway bronchoconstriction (Levy et al., 2007).
Recently, we have described the activity of new LX analogues that show the substitution of the reactive hexatriene system with an aromatic ring. Beside a capacity to stimulate in vitro phagocytosis of apoptotic cells by macrophages, these LX analogues show potent anti-inflammatory activity in vivo (O'Sullivan et al., 2007). We used an in vivo model of mouse peritonitis, and examined neutrophil trafficking to the peritoneal cavity in response to zymosan A challenge. When administered intravenously, (1R)-3a inhibited the acute inflammatory cell recruitment into mouse peritoneum.
The successful resolution of inflammation is an integral component of effective host defence. The various steps of resolution are regulated by endogenous mediators and by clearance of apoptotic cells by phagocytes. In this context, LXs are a class of lipid mediators that serve as local endogenous anti-inflammatory and pro-resolution signals. The potential therapeutic applications of LXs and their stable synthetic analogues are significant; it will be of interest to learn whether these or related agonists of resolution can be exploited in a therapeutic context to ensure the effective restoration of tissue homeostasis and prevention of fibrosis subsequent to an inflammatory response.
Work in the authors' laboratory is supported by the Science Foundation Ireland, EU FP6 Eicosanox Programme LSHM-CT-2004-005033 and The Government of Ireland Programme for Research in Third Level Institutions.
Note added in proof
During the final revision of this manuscript a new nomenclature for the FPR family of receptors was recommended by the International Union of Basic and Clinical Pharmacology LXXIII. On the basis of this classification, LXA4 is defined as an endogenous ligand for FPR2/ALX, instead of the previously used nomenclature of FPRL1/ALXR as used in this review (Ye et al., 2009).