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(Arteriosclerosis, Thrombosis, and Vascular Biology. 2005;25:633.)
© 2005 American Heart Association, Inc.

Atherosclerosis and Lipoproteins

Oxidized Phospholipids Trigger Atherogenic Inflammation in Murine Arteries

Alexander Furnkranz; Andreas Schober; Valery N. Bochkov; Pavel Bashtrykov; Gerhard Kronke; Alexandra Kadl; Bernd R. Binder; Christian Weber; Norbert Leitinger

From the Department of Vascular Biology and Thrombosis Research (A.F., V.N.B., G.K., A.K., B.R.B., N.L.), University of Vienna, Austria; Wilheminen Hospital (A.F.), Vienna, Austria; the Department of Cardiovascular Molecular Biology (A.S., C.W.), University of Aachen, Germany; and the Cardiology Research Center (P.B.), Moscow, Russia.

Correspondence to Norbert Leitinger, Cardiovascular Research Center, University of Virginia, PO Box 801394, Charlottesville, VA 22908. E-mail nl2q{at}virginia.edu

	Abstract

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Objective— Lipoprotein-derived phospholipid oxidation products have been implicated as candidate triggers of the inflammatory process in atherosclerosis. However, in vivo evidence regarding the impact of oxidized phospholipids on the artery wall thus far has been elusive. Therefore, the aim of this study was to investigate if structurally defined oxidized phospholipids induce expression of atherogenic chemokines and monocyte adhesion in intact murine arteries.

Methods and Results— To model the accumulation of oxidized phospholipids in the arterial wall, oxidized 1-palmitoyl-2-arachidonoyl-sn-3-glycero-phosphorylcholine (OxPAPC) was topically applied to carotid arteries in mice using pluronic gel. Using quantitative reverse-transcriptase polymerase chain reaction (PCR) and immunohistochemistry, we show that OxPAPC induced a set of atherosclerosis-related genes, including monocyte chemotactic protein 1 (MCP-1) and keratinocyte-derived chemokine (KC), tissue factor (TF), interleukin 6 (IL-6), heme oxygenase 1 (HO-1), and early growth response 1 (EGR-1). OxPAPC-regulated chemokines were also expressed in atherosclerotic lesions of apolipoprotein E-deficient (ApoE^–/–) mice. In isolated perfused carotid arteries, OxPAPC triggered rolling and firm adhesion of monocytes in a P-selectin and KC-dependent manner.

Conclusion— Oxidized phospholipids contribute to vascular inflammation in murine arteries in vivo, initiating atherogenic chemokine expression that leads to monocyte adhesion; therefore, they can be regarded as triggers of the inflammatory process in atherosclerosis.

Oxidized phospholipids have been implied to play a role in atherogenesis; however, whether they trigger vascular inflammation in vivo is not known. Using a novel experimental approach, we demonstrate that oxidized phospholipids elicit atherogenic inflammation in murine arteries in vivo, implicating oxidized phospholipids as triggers of vascular inflammation.

Key Words: atherosclerosis • oxidized phospholipids • inflammation • chemokines • leukocyte adhesion

	Introduction

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Atherosclerosis is a chronic inflammatory disease involving accumulation of lipoproteins and mononuclear cells in the subendothelial space. Chemokines serve a vital role in supporting the inflammatory response of the arterial wall, leading to atherosclerotic plaque formation. In particular, genetic deletions of monocyte chemotactic protein 1 (MCP-1) or its receptor CCR2, as well as transplantation of bone marrow deficient in the IL-8 receptor homologue CXCR2,^1–3 have been shown to decrease monocyte accumulation and lesion formation in mice susceptible to atherosclerosis. Although our knowledge about the mechanisms underlying atherosclerosis and its complications has dramatically increased, the question about the initiating factors or triggers of atherogenesis remains unsolved. Accumulating evidence suggests retention of low-density lipoprotein (LDL) particles in the subendothelial space with subsequent oxidative modification as key steps in beginning atherosclerosis. Oxidized LDL has been shown to induce chemokines such as MCP-1 in vascular cells, but direct evidence from suitable animal models is scarce and it has been questioned if lipoproteins oxidized in vitro yield similar biological responses as lipoproteins oxidized in the arterial wall.⁴ Recently, considerable advances have been made in dissecting the molecular components of oxidized LDL responsible for its pro-atherogenic effect, allowing for the experimental use of defined compounds rather than complex lipoproteins. Initially, LDL oxidation gives rise to minimally oxidized LDL,⁵ the biological activity of which results primarily from oxidation of phospholipids, such as 1-palmitoyl-2-arachidonoyl-sn-3-glycero-phosphorylcholine (PAPC), yielding a series of oxidation products (OxPAPC), some of which have been structurally identified and shown to accumulate in atherosclerotic lesions.^6,7 The atherogenic potential of OxPAPC has been demonstrated in cell culture studies as shown by enhanced monocyte, but not neutrophil, binding to OxPAPC-stimulated endothelial cells, as well as induction of MCP-1 and IL-8.^8,9 However, static coculture systems only incompletely model the complex cellular interactions in the vessel wall and provide no information as to whether monocyte–endothelial interactions occur under flow. Moreover, in vivo, inactivation of oxidized phospholipids by protective enzymes such as paraoxonase or platelet-activating factor acetyl-hydrolase may occur, limiting the proinflammatory potential of these lipids. Therefore, the purpose of this study was to investigate if OxPAPC induces atherogenic chemokines or other inflammatory genes in the arterial wall in vivo and whether this would entail monocyte adhesion to the arterial endothelium.

	Methods

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Animals
C57BL/6J mice were purchased from the Institut fuer Versuchstierzucht und haltung (Himberg, Austria). ApoE^–/– mice on a C57BL/6J genetic background were acquired from the Proefdierencentrum (Leuven, Belgium). Mice were kept on a 12-hour dark/light cycle and received water and regular chow ad libitum.

Application of OxPAPC to Carotid Arteries
OxPAPC was obtained by air oxidation of dry PAPC (Sigma-Aldrich) as described previously.⁶ Immediately before surgical application, dry OxPAPC or PAPC was dissolved in cold 1% (wt/vol) F-127 pluronic gel (Sigma-Aldrich) in sterile water, followed by addition of 5 volumes of 50% (wt/vol) F-127. Sixty µL of F-127 with or without 50 µg OxPAPC, 50 µg PAPC, or 6 µg lipopolysaccharide (LPS) (Escherichia coli serotype 055:B5; Sigma-Aldrich) was applied to carotid vessels. At indicated time points, animals were euthanized, perfused for 5 minutes with PBS via the left ventricle, and the treated part of the common carotid artery was removed. For comparison of gene expression levels between ApoE^–/– and wild-type animals, mice were used at 12 months of age, at which time common carotid arteries of ApoE^–/– mice showed typical macrophage-rich lesions at the proximal and distal bifurcation.¹⁰ Relative quantification of gene expression was performed as described.¹¹ Details about surgical procedures, tissue harvesting, RNA isolation, quantitative reverse-transcriptase polymerase chain reaction (RT-PCR), used PCR primers (Table I), and immunohistochemistry are given in the online supplement (please see http://atvb.ahajournals.org).

Ex Vivo Perfusion Model
Cell rolling and arrest of calcein-labeled monocytic MM6 cells (1x10⁶/mL) on endothelium of common carotid arteries from 10- to 12-week-old C57Bl/6J mice were determined by epifluorescence videomicroscopy as described,¹² after preperfusion with OxPAPC or native PAPC (100 µg/mL, in sterile filtered MOPS-buffered physiological salt solution with 0.5% human serum albumin), for 4 hours at 37°C. Some carotid arteries were perfused with blocking antibody to KC (20 µg/mL, clone 124014; R&D Systems, Minneapolis, Minn) or P-selectin (30 µg/mL, RB40.34; Pharmingen, San Diego, Calif) for 20 minutes after OxPAPC treatment. Rolling flux was determined by counting the number of cells that rolled on the vessel wall for at least 1 second during an 8-minute period.

Statistical Analysis
Data are expressed as mean±SEM. Results were analyzed using unpaired Student t test (gene expression data) or 1-way ANOVA with Newman–Keuls post-test (ex vivo perfusion model). Differences were considered statistically significant at a value of P<0.05.

	Results

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Induction of Chemokine Expression by OxPAPC In Vivo
To investigate effects of oxidized phospholipids on the arterial wall in vivo, we applied F-127 pluronic gel with or without 50 µg OxPAPC to surgically exposed carotid arteries of C57BL/6 mice. This corresponds to a concentration of the bioactive phospholipids 1-palmitoyl-2-(5-oxovaleroyl)-sn-glycero-3-phosphorylcholine and 1-palmitoyl-2-glutaroyl-sn-glycero-3-phosphorylcholine of 30 µg/mL in the gel,⁹ which is lower than the concentrations measured in rabbit atherosclerotic lesions.¹³ F-127 dissolves within several hours and releases trapped lipids, allowing for topical exposure of arteries while minimizing systemic effects.¹⁴ We used this system to investigate differential expression between OxPAPC, native PAPC and mock-treated arteries of a set of atherosclerosis-related chemokines, including MCP-1 and KC (keratinocyte-derived chemokine, CXCL1), the murine chemokine closest related to human IL-8. Quantitative RT-PCR showed that treatment of carotid arteries for 6 hours with 50 µg OxPAPC in vivo increased vascular expression of MCP-1 (3.3±0.68-fold) and KC (4.8±0.22-fold), as compared with mock-treated arteries (Figure 1a). Immunohistochemistry of carotid arteries treated for 24 hours with OxPAPC confirmed these findings (Figure 1b), showing homogenous chemokine distribution throughout the vessel wall, a pattern also reported in atherosclerotic carotid arteries of ApoE^–/– mice.¹² In addition, treatment of carotid arteries with OxPAPC induced MIP-1 (3.3±0.57-fold) and MIP-1ß (3.6±0.59-fold), whereas RANTES, serum-derived factor-1, and eotaxin were not induced (Figure 1a). To confirm previous in vitro observations that nonoxidized PAPC is not biologically active,^6,13 we included a PAPC group in 1 experiment representing 3 animals. Application of 50 µg nonoxidized PAPC to carotid arteries did not influence gene expression levels as compared with mock-treated arteries (Figure 1c), demonstrating that oxidative modification of phospholipids was necessary to form pro-inflammatory agonists. Investigation of untreated contralateral carotid arteries, as well as other organs, revealed that systemic effects of OxPAPC were negligible (data not shown).

View larger version (46K): [in this window] [in a new window]   Figure 1. Chemokine induction by OxPAPC. a, OxPAPC induces MCP-1, KC, MIP-1, and MIP-1ß mRNA after 6 hours in murine carotid arteries, *P<0.05 (n=4). b, Vehicle- or OxPAPC-treated (24 hours) carotid arteries stained with antibody against MCP-1 (upper panel) or with antibody against KC (lower panel). Scale bar represents 20 µm. c, Native PAPC does not influence arterial gene expression after 6 hours. One experiment is shown representing pooled arteries from 3 animals. d, Chemokine mRNA expression in atherosclerotic carotids of ApoE–/– mice versus wild-type (WT) control animals. *P<0.05 (n=4).

Chemokine Expression in Murine Atherosclerosis
The chemokines tested in this study have been found in atherosclerotic lesions of varying species and different locations of the arterial tree. To investigate if OxPAPC-induced chemokines were also expressed in atherosclerotic arteries, we determined chemokine expression levels in carotid arteries of ApoE^–/– mice as compared with normal carotids from age-matched wild-type mice by quantitative RT-PCR. MCP-1, KC, MIP-1, and MIP-1ß showed enhanced expression in arteries of ApoE^–/– mice, whereas expressions of RANTES, serum-derived factor-1, and eotaxin were not increased (Figure 1d). Enhanced expression of CD68 indicated the presence of macrophages in lesions of ApoE^–/– mice (Figure 1d); however, we did not find increased CD68 in OxPAPC-treated arteries (Figure 1a), suggesting that chemokine production in OxPAPC-treated arteries was mainly by resident cells of the arterial wall.

OxPAPC Triggers Monocyte Rolling and Arrest in Native Murine Arteries
Chemokines support inflammation in atherogenesis by rapidly activating mononuclear leukocytes, leading to integrin-dependent cell arrest on inflamed endothelium, a prerequisite for transmigration.¹⁵ To investigate if oxidized phospholipids can trigger firm adhesion of circulating monocytes on arterial endothelium, we used isolated carotid arteries from C57BL/6 mice that had been perfused ex vivo for 4 hours with OxPAPC or native PAPC as control. Arteries were subsequently perfused with calcein-labeled monocytic Mono-Mac-6 (MM6) cells, and MM6 cell arrest was determined as described in Methods. We found that firm adhesion of MM6 cells was dramatically increased in OxPAPC-treated carotid arteries at the region of the bifurcation, whereas minimal adhesive interactions were observed in arteries treated with native PAPC (Figure 2a). Cell arrest was preceded by a short period of rolling in OxPAPC-treated arteries, which was negligible in control arteries treated with unoxidized PAPC (Figure 2b).

View larger version (14K): [in this window] [in a new window]   Figure 2. OxPAPC induces rolling and firm arrest of MM6 cells in isolated perfused carotid arteries. a, Preperfusion with OxPAPC, but not native PAPC, leads to firm arrest of MM6 cells in murine carotid arteries. Perfusion with a blocking antibody to KC (KC mAb) after treatment with OxPAPC reduces MM6 cell arrest to control (PAPC) levels. *P<0.01 versus PAPC, #P<0.05 versus OxPAPC (n=4 to 5). b, Preperfusion with OxPAPC leads to rolling of MM6 cells on endothelium of murine carotid arteries. Perfusion with a blocking antibody to KC (KCmAb, bar 3) after treatment with OxPAPC enhances rolling flux, whereas perfusion with a blocking antibody to P-selectin (Psel mAb, bar 4) reduces cell rolling to control (PAPC) levels. *P<0.01, **P<0.001 (n=3 to 6).

OxPAPC-Induced Monocyte Rolling and Arrest Are Mediated by P-Selectin and KC, Respectively
Among the chemokines found to be upregulated by OxPAPC in the artery wall, KC has been shown to play a dominant role in triggering monocyte arrest on early atherosclerotic endothelium in ex vivo perfused carotid arteries of ApoE^–/– mice.¹² We hypothesized that KC serves a similar function in OxPAPC-stimulated arteries. Preperfusion of a blocking KC antibody in OxPAPC-treated carotid arteries reduced MM6 cell arrest to levels seen in control arteries (Figure 2a), indicating that OxPAPC-induced monocyte arrest was critically dependent on KC.

Next, we were interested if OxPAPC-induced monocyte rolling would also involve mechanisms analogous to those in murine atherosclerosis. The selectin family of adhesion molecules mediates initial attachment and rolling of leukocytes on vascular endothelium,¹⁵ and functional blocking of P-selectin has been shown to abrogate monocyte rolling on atherosclerotic endothelium in isolated murine carotid arteries.¹⁶ Here, we found that preperfusion with a blocking P-selectin antibody abolished MM6 cell rolling in OxPAPC-treated arteries (Figure 2b), demonstrating a crucial role for P-selectin in OxPAPC-triggered monocyte rolling. However, preperfusion with a blocking KC antibody enhanced rolling flux (Figure 2b). In accord with this observation, continuous P-selectin–dependent monocyte rolling without arrest has been observed in atherosclerotic carotid arteries when blocking 4ß1 (VLA-4), the integrin on monocytes that mediates KC-triggered cell arrest.^12,17

OxPAPC Induces Expression of Other Atherosclerosis-Related Genes In Vivo
In addition to chemokines, OxPAPC induces several other atherosclerosis-related genes in cells of the artery wall in vitro. Recently, we showed induction of tissue factor (TF) by OxPAPC in human endothelial cells, accompanied by and dependent on the expression of early growth response-1 (EGR-1).¹⁸ Both genes have been implicated in human and experimental murine atherosclerosis.^19,20 To investigate if these effects would also be observed in the arterial wall in vivo, TF and EGR-1 mRNA levels were determined by quantitative RT-PCR in murine carotid arteries treated for 6 hours with OxPAPC or vehicle alone. OxPAPC treatment led to upregulation of both TF (2.6±0.62-fold) and EGR-1 (2.0±0.35-fold) transcripts in carotid arteries (Figure 3).

View larger version (13K): [in this window] [in a new window]   Figure 3. OxPAPC induces atherosclerosis-related genes in murine carotid arteries after 6 hours. P<0.05 (n=4) for all comparisons between vehicle and OxPAPC group.

IL-6 has been shown to be expressed in atherosclerotic lesions in mice.²¹ Furthermore, IL-6 has been reported to mediate effects of OxPAPC such as decreased hepatic paraoxonase expression in mice.²² Here, OxPAPC treatment induced IL-6 mRNA 3.5±0.6-fold compared with vehicle-treated arteries (Figure 3). In addition, OxPAPC has been shown to induce the protective gene heme oxygenase-1 (HO-1) in vascular cells in vitro.^23,24 Here, treatment of carotid arteries with OxPAPC induced HO-1 message 3.6±0.34-fold (Figure 3).

OxPAPC-Induced Inflammation Versus LPS-Induced Inflammation
Target gene expression induced by OxPAPC differs from that induced by other inflammatory mediators such as LPS or tumor necrosis factor-.^25–27 We have shown previously that expression of the adhesion molecules E-selectin, vascular cell adhesion molecule-1 (VCAM-1), or intercellular adhesion molecule-1 is not induced by OxPAPC in vitro.⁹ Consistently, quantitative RT-PCR, as well as immunohistochemistry, showed that treatment of carotid arteries with LPS effectively upregulated expression of E-selectin, VCAM-1, or intercellular adhesion molecule-1, whereas treatment with OxPAPC had no effect (Figure 4a and 4b). In contrast to LPS, OxPAPC did not upregulate P-selectin mRNA in murine arteries (Figure 4a), suggesting that monocyte rolling after OxPAPC treatment (Figure 2b) was mediated by surface translocation of P-selectin from Weibel–Palade bodies.²⁸

View larger version (23K): [in this window] [in a new window]   Figure 4. a, LPS, but not OxPAPC, induces vascular expression of E-selectin, intercellular adhesion molecule-1 (ICAM-1), and VCAM-1 mRNA after 6 hours. P<0.05 (n=3) for all comparisons between vehicle and LPS group. b, Vehicle, OxPAPC, or LPS-treated (24 hours) carotid arteries stained with antibody against VCAM-1. Scale bar represents 20 µm.

	Discussion

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A growing body of evidence suggests oxidized phospholipids as triggers of vascular inflammation in early atherosclerosis. Most importantly, component lipids of OxPAPC have been detected in atherosclerotic lesions in concentrations sufficient to stimulate vascular cells.^6,13 However, evidence for a direct contribution of oxidized phospholipids to vascular inflammation in vivo has not yet been obtained. Thus, to model the accumulation of oxidized phospholipids in the arterial wall during atherogenesis, we applied OxPAPC to the adventitia of carotid arteries of C57BL/6 mice using a slow-release preparation. The murine carotid artery consists of only 4 to 5 cell layers, facilitating penetration of the lipids through the vessel wall. The high sensitivity offered by real-time PCR allows quantifying gene expression from such minute samples. In this model, OxPAPC induced several chemokines in the carotid artery wall that are also expressed in human or experimental atherosclerosis.²⁹ Accordingly, investigation of atherosclerotic carotid arteries from ApoE^–/– mice revealed that OxPAPC-induced chemokines are expressed in atherosclerotic lesions in mice. Interestingly, the chemokines RANTES, eotaxin, and serum-derived factor-1 were not regulated by OxPAPC in murine arteries, nor were they differentially expressed in atherosclerotic versus normal arteries in ApoE^–/– mice. However, a nontranscriptional mechanism of RANTES deposition by activated platelets has been described.³⁰

Importantly, tissue composition differs between native arteries and established atherosclerotic lesions as indicated by high expression of the macrophage marker CD68 in arteries of ApoE^–/– mice. Thus, although not being representative of the complex cellular interactions in atherosclerotic lesions, our data indicate that OxPAPC accumulation triggers atherogenic chemokine expression and monocyte adhesion in the normal artery wall, underscoring the role of oxidized phospholipids in early lesion formation.⁵ Besides MCP-1 and KC, whose role in atherogenesis is firmly established, we found MIP-1 and ß to be expressed in OxPAPC-stimulated, as well as in atherosclerotic, arteries. MIP-1 and ß are members of the CC chemokine subfamily that attract monocytes and lymphocytes.²⁹ In addition, MIP-1ß induces TF activity in vascular smooth muscle cells.³¹

To investigate whether OxPAPC-induced chemokine expression resulted in arterial monocyte adhesion, a hallmark of early atherogenesis, we used ex vivo perfused carotid arteries, a model that has been used extensively to study monocyte–endothelial interactions in atherosclerosis.^12,16,17 In our study, OxPAPC stimulation led to monocyte rolling and firm adhesion in normal murine arteries. Firm adhesion of monocytes is mediated by arrest chemokines immobilized on the endothelial surface, leading to integrin activation or clustering on rolling leukocytes.¹⁵ It is not known which chemokines serve this function in OxPAPC-stimulated arteries; however, it has been shown that KC, but not MCP-1, triggers monocyte arrest on early atherosclerotic endothelium in isolated carotid arteries of ApoE^–/– mice.¹² Thus, we functionally blocked KC in OxPAPC-stimulated arteries, and the results demonstrated that OxPAPC-induced monocyte arrest was completely dependent on KC.

In addition, it has been shown that functional blocking of P-selectin abrogates monocyte rolling on atherosclerotic endothelium in mice in vivo,³² as well as in isolated carotid arteries.¹⁶ Here, we found that OxPAPC-induced monocyte rolling was also dependent on P-selectin in isolated carotid arteries. Although we did not find induction of P-selectin mRNA in OxPAPC-treated carotid arteries in vivo, oxidized LDL has been shown to induce surface translocation of preformed P-selectin from Weibel–Palade bodies.²⁸

Together, our data support a mechanism of OxPAPC-induced monocyte adhesion in which P-selectin mediates initial attachment and rolling on arterial endothelium, with subsequent activation and arrest triggered by immobilized KC. Although playing an important and nonredundant independent role in atherogenesis, MCP-1 is not involved in initial monocyte arrest on early atherosclerotic endothelium in murine carotid arteries.¹² Similarly, OxPAPC-induced MCP-1 could be rather involved in subsequent transmigration of adherent monocytes. Thus, our data are in accordance with observations on atherosclerotic vessels in mice and strongly suggestive of a role for oxidized phospholipids as triggers of monocyte recruitment to atherosclerotic lesions.

In ApoE^–/– mice, KC has been shown to act via VLA-4 on monocytes, which binds to VCAM-1 and fibronectin containing the CS-1 region.^12,17 We did not observe induction of VCAM-1 by OxPAPC; however, at sites of atherosclerosis predilection, such as the lesser curvature of the aortic arch, VCAM-1 is expressed in C57Bl/6J mice, possibly because of hemodynamic influences.³³ However, binding of monocytes to OxPAPC-stimulated endothelial cells is mediated by CS-1 fibronectin³⁴ and blocking CS-1 reduced atherosclerotic lesion formation in mice.³⁵

In addition to expression of chemokines, we found that OxPAPC induced expression of several other atherosclerosis-related genes. We demonstrate that oxidized phospholipids induce IL-6 transcripts in a native murine artery in vivo. Circulating levels of IL-6 predict future myocardial infarction in apparently healthy men.³⁶ Because IL-6 was shown to be expressed in atherosclerotic lesions in humans³⁷ and ApoE^–/– mice,²¹ atherosclerotic sites themselves likely contribute to elevated circulating IL-6 levels. Thus, our data suggest oxidized phospholipids contributing to IL-6 production in atherosclerosis. Moreover, we demonstrate induction of TF by OxPAPC. Enhanced TF expression has been demonstrated in atherosclerotic plaques,¹⁹ a process that may account for thrombotic events associated with early and advanced atherosclerosis. A transcription factor capable of binding to the TF promoter is EGR-1, which is critically involved in TF gene regulation.¹⁸ We have previously shown that OxPAPC increases EGR-1 as well as TF expression in cultured endothelial cells, and that TF induction by OxPAPC is dependent on EGR-1.¹⁸ Our data suggest that oxidized phospholipids contribute to EGR-1 expression in atherosclerosis, thereby enhancing expression of TF and possibly other EGR-1–inducible genes.²⁰ Finally, we found induction of HO-1 by OxPAPC in murine arteries. HO-1 is expressed in experimental as well as human atherosclerotic lesions,³⁸ where it is thought to counteract continuous oxidative stress by its antioxidant and anti-inflammatory properties. Thus, induction of HO-1 by oxidized phospholipids in the artery wall may constitute an adaptive response to limit the inflammatory reaction. It was demonstrated that formation of atherosclerotic lesions in ApoE^–/– mice was accompanied by decreased expression of various antioxidant enzymes, whereas HO-1 mRNA levels remained high during the course of atherogenesis,³⁹ indicating continuous stimulation likely to be caused by oxidized phospholipids.

Finally, we show that OxPAPC-induced expression of inflammatory genes in carotid arteries differs from that induced by LPS. Although LPS-induced or tumor necrosis factor-induced inflammation would result in adhesion and accumulation of neutrophils and monocytes, the gene expression pattern elicited by "lipid-induced inflammation" may determine monocyte specificity.

In conclusion, we have shown that oxidized phospholipids, known to accumulate in atherosclerotic lesions, induce expression of atherogenic chemokines and other inflammation-related genes in the arterial wall in vivo. Furthermore, we demonstrate a major role for KC in mediating oxidized phospholipid-induced monocyte adhesion to murine arteries. Thus, oxidized phospholipids can be considered as triggers of the inflammatory process in the vascular wall and therefore represent promising molecular targets to combat atherogenesis and its clinical consequences.

	Acknowledgments

 
This work supported by grants from the Austrian Science Fund (to F.W.F.); the Austrian National Bank; the Center for Molecular Medicine (CEMM); and the European Vascular Genomics Network (http://www.evgn.org), a Network of Excellence supported by the European Community’s sixth Framework Programme for Research Priority 1 "Life sciences, genomics and biotechnology for health" (Contact No. LSHM-CT-2003-503254).

	Footnotes

 
Current affiliation for G.K., A.K., and N.L.: Cardiovascular Research Center, University of Virginia, Charlottesville.

Received July 23, 2004; accepted November 23, 2004.

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