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【摘要】
Objective— Resident immune cells are a hallmark of atherosclerotic lesions. The sphingolipid analogue drug FTY720 mediates retrafficking of immune cells and inhibits their homing to inflammatory sites. We have evaluated the effect of FTY720 on atherogenesis and lipid metabolism.
Methods and Results— ApoE –/– mice on a normal laboratory diet received oral FTY720 for 12 weeks, which led to a 2.4-fold increase in serum cholesterol (largely VLDL fraction) and a 1.8-fold increase in hepatic HMGCoA reductase mRNA. FTY720 increased plasma sphingosine-1-phosphate and induced marked peripheral blood lymphopenia. A discoordinate modulation of B, T and monocyte cell numbers was found in peripheral lymphoid organs. Overall depletion of T cells was accompanied by a relative (2-fold) increase in regulatory T cell content paralleled by a similar increase in effector memory T cells (CD4+CD44hiCD62lo) as absolute numbers of both subpopulations remained essentially unchanged. Lymphocyte function was unaltered as indicated by anti-OxLDL antibodies and T cell proliferation. There were no changes in atherosclerotic lesions in early and established atherosclerosis.
Conclusions— FTY720 mediated peripheral lymphocyte depletion and retrafficking without altering function and overall balance of pro- and antiatherogenic lymphocyte populations. A net decrease in lymphocyte numbers occurred concomitantly with a more proatherogenic hypercholesterolemia resulting in unaltered atherogenesis.
Administration of the sphingolipid analogue FTY720 to ApoE –/– mice on normal laboratory diet altered lipid metabolism yielding pronounced hypercholesterolemia. Despite lymphocyte depletion and retrafficking the overall balance of pro- and antiatherogenic lymphocyte populations was not changed. Hypercholesterolemia appears to have counteracted the otherwise beneficial effect on atherogenesis.
【关键词】 atherosclerosis immune system immunosuppressive therapy leukocytes vascular biology
Introduction
Atherosclerosis is a chronic inflammatory disease elicited by lipid retention and modification in the arterial intima. Several inflammatory cell types such as macrophages and T-lymphocytes are believed to be intrinsically involved in the initiation and progression of arterial wall lesions. 1–3 Accumulating evidence suggests an important role for endogenous lysosphingolipids such as sphingosine-1-phosphate (S1P) in modulating immune cell trafficking, initiating angiogenesis, preserving vascular integrity, and enhancing eNOS-induced vasodilatation. All these effects are thought to be mediated via G protein–coupled receptors expressed on a variety of cell types. 4–6 The immunomodulator FTY720 acts as a sphingosine-1-phosphate mimetic and was shown effective in experimental models of transplantation and autoimmunity 7–9 with promising results in clinical trials for prevention of kidney graft rejection 10 and multiple sclerosis. 11 In vivo, FTY720 undergoes rapid phosphorylation to form the active compound FTY720-P, a sphingosine-1-phosphate (S1P) analogue. FTY720-P is an agonist of 4 of the 5 currently known G protein–coupled sphingolipid receptors (S1P 1, S1P 3, S1P 4, S1P 5 ). 12 FTY720 mediates redistribution of lymphocytes and other immune cells preventing their egress to inflamed tissues, while concomitantly preserving the functionality of lymphocytes. 13,14 Two recent reports have shown a protective effect on atherosclerosis for FTY720 in the LDLr –/– 15 and ApoE –/– 16 mouse model under conditions of a high-fat diet, attributing the effect to a decreased recruitment of inflammatory cells into the lesion. However, as perturbations occur on administration of a high-fat diet encompassing a pronounced monocytosis with a massive increase of macrophages 17 and T cells in lesions, 18,19 it appeared of great interest to analyze the protective potential of FTY720 in a more physiological mouse model of spontaneously developing atherosclerosis with less extreme lipid levels (ApoE –/– mice fed normal laboratory diet). This is the first study to show that hypercholesterolemia is induced by FTY720 treatment, which possibly counteracts its antiatherogenic effect on immune cell distribution.
Materials and Methods
For detailed Materials and Methods, please see the supplemental materials (available online at http://atvb.ahajournals.org).
Animals
Male ApoE –/– mice were obtained from Jackson Laboratories (Bar Harbor, Me). Ethical permission was obtained from the University of Heidelberg. Mice were fed a normal laboratory diet (ssniff Spezialdiäten GmbH). FTY720 (Novartis) was continuously administered for 12 weeks to the animals by drinking water calculated at a daily dose of 3 mg/kg/d. 7 8-week-old mice (n=7/group) and 26-week-old mice (n=10/group) were treated for 12 weeks with FTY720 to evaluate lesions in the aortic root 20 and innominate artery. 21
Tissue Processing
For RNA isolation the aortic arch, a predilection site for lesion development in ApoE –/– mice, 22 was dissected and snap-frozen. Lesion area and fractional area of the lesion were quantified and the results were expressed as the average of 8 sections per mouse. 20
Immunohistochemistry
Light microscopy was performed on 10-µm cryosections adjacent to the ORO-stained sections. Primary antibodies (CD4, CD8, CD19, CD68, vascular cell adhesion molecule -1, I-A b; all rat anti-mouse by BD Pharmingen) were titrated to optimum performance and applied to acetone-fixed cryosections followed by detection with the ABC alkaline phosphatase kit (Vector Laboratories). A thresholding technique using computerized ImagePro analysis on the aortic root sections was implemented.
Flow Cytometry
Flow cytometry was performed on a CyAn (Dako) after staining with the appropriate Ab; data were analyzed using Summit v4.3 software. Primary labeled antibodies used were CD19, CD3, CD4, CD8, F4/80, CD25, CD62L, CD44 from Pharmingen, FoxP3-PE was from eBioscience.
Functional Immune Assays
Splenocytes were harvested and cultured in duplicate in a 96-well plate at 5 x 10 5 cells per well after red blood cells lysis. Cells were incubated for 72 hours in the absence or presence of anti-CD3 antibody (1 µg/mL) followed by incorporation of 3 H-thymidine during the last 18 hours. ELISA methods were used to quantitate serum Ig isotypes to Ox-LDL. 23
Real-Time Polymerase Chain Reaction
RNA was isolated from the aortic arch using the RNeasy kit (Qiagen). Reverse transcription was performed using the Boehringer cDNA kit (Roche Diagnostics). The Roche real-time polymerase chain reaction (PCR) kit with SYBR Green (Roche Diagnostics) was used for quantitative PCR (LightCycler). Primer sequences were previously published. 24–28 Data were analyzed on the basis of the relative expression method with the formula 2 – C T, where C T = C T (sample)– C T (calibrator=average C T values of all samples), and C T is the C T of the housekeeping gene (β-actin) subtracted from the C T of the target gene.
Hematologic and Biochemical Parameters
Whole blood (EDTA) was analyzed by Cell Dyn 3500 hemocounter (Abbott). Serum total cholesterol and triglycerides were determined using a Monarch Automated Analyzer (ILS Laboratories Scandinavia AB). Fast protein liquid (FPLC) (Amersham Pharmacia) was performed for detection of cholesterol. 29 FTY720 serum levels were determined at Novartis by high-performance liquid chromatography (HPLC). S1P plasma levels were determined as described. 6 BD Cytometric Bead Array technique (Becton Dickinson and Company) was used to measure cytokine levels in serum.
Statistical Analysis
Values are expressed as mean±SEM unless otherwise indicated. Nonparametric Mann–Whitney U test was used to compare individual groups of animals. A level of P <0.05 was considered significant.
Results
Early Atherogenesis
Biochemical Markers and Drug Levels
FTY720 was administered continuously via the drinking water to 8-week-old ApoE –/– mice for a period of 12 weeks. A dose of 3 mg/kg/d yielded plasma drug levels of 3.08±1.99 ng/mL (mean±SD). FTY720 administration caused a 70% reduction in peripheral blood lymphocyte counts but did not influence other blood cells such as monocytes (supplemental Table I). Body weight did not differ between groups when fed a normal laboratory diet. However, there was a 2.4-fold increase in total serum cholesterol levels (supplemental Table I) with a marked elevation of the VLDL fraction ( Figure 1 A). Triglyceride levels were unaltered. To elucidate the mechanism leading to isolated hypercholesterolemia the effect of FTY720 on lipid metabolism was evaluated. Administration of FTY720 was associated with a significant increase in plasma levels of the natural analogue of FTY720-P—sphingosine-1-phosphate (S1P)—in the treated group (1318±39.0 ng/mL versus 1158±54.9 ng/mL, P =0.0476; Figure 1 B). As sphingosine had previously been shown to induce HMGCoA reductase 30 we analyzed mRNA from liver and intestinal tissue—2 key organs in lipid metabolism. Both hepatocytes and intestinal epithelial cells were recently shown to express S1P receptors. 31,32 Some genes involved in cholesterol/VLDL synthesis and uptake are sterol regulatory element-binding proteins (SREBPs), HMGCoA reductase, microsomal triglyceride transfer protein (MTP), scavenger receptor class B type I (SR-BI), and LDL receptor-related protein (LRP1). Figure 1C and 1 D illustrates that HMGCoA reductase transcript levels normalized to β-actin were upregulated (1.8-fold) in liver tissue of FTY720-treated animals (1.20±0.15 versus 0.68±0.05; P =0.033). These data indicate that FTY720 interfered with hepatic cholesterol metabolism.
Figure 1. Controls in black, FTY720 in white. A, Cholesterol lipoprotein profiles. B, Effect of FTY720 on S1P. RT-PCR data from liver (C) and intestine (D).
Cellular Composition in Immune Organs
Two distinct lymph node sites (axillary and inguinal), spleen, and peripheral blood were analyzed for cellular composition. FTY720 mediated a redistribution of B cells (CD19+) from peripheral blood into spleen and lymph nodes whereas T cells (CD4+ and CD8+) were depleted in all 3 lymphoid tissues ( Figure 2A and 2 B, spleen data not shown). The percentage of monocytes was unchanged in blood and spleen, but increased in lymph nodes. Analysis of regulatory T cells (CD4+FoxP3+) and memory effector T cells (CD4+CD44hiCD62Llo) showed no difference between groups when expressed as percentage of total parenchymal cells. However, when the distribution of Treg and memory effector T cells within the CD4+ T population was examined we found a significant (2-fold) relative increase among total CD4+ T cells for both, regulatory T cells, and memory effector T cells in the FTY720 treated animals ( Figure 2C through 2 F). This effect was attributable to the decline in total CD4+ T cell numbers on FTY720 administration whereas absolute cell numbers for Treg and memory effector cells remained essentially unchanged (supplemental Figure II). Data on Treg and memory effector T cells in blood are not shown as total CD4+ cell content was diminished to less than 1% of total cells in the FTY720 group obviating accurate interpretation and reasonable statistical analysis because of minimal cell numbers. As both subpopulations showed the same relative increase (2-fold), the overall balance of regulatory T cells and memory effector T cells was maintained in the FTY720 treated group. These data show a discoordinate modulation of lymphocyte populations with a preserved overall balance of pro-and antiatherogenic T cells.
Figure 2. Flow cytometry. Controls (black bars), FTY720 (open bars). A, Inguinal lymph node. B, Blood. C, Treg per CD4+. D, Treg among inguinal lymph node cells; frame: Treg per CD4+. E, Memory T cells per CD4+. F, CD4+CD44hi and CD4+CD62Llo cells among inguinal lymph node cells; frame: memory T cells per CD4+.
Serum Antibody and Cytokines Levels
Isotype analysis of serum antibodies against OxLDL, implicated in the pathogenesis of atherosclerosis, showed no significant differences between the 2 groups except for the subclass IgG1, which was lower in the treated group (0.28±0.03 versus 0.17±0.02, p = 0.004; Figure 3 A). Serum cytokine levels for interleukin (IL)-5, IL-10, and IFN- were similar in treated and control animals (data not shown). Anti-CD3 induced splenic T cell proliferation was not influenced by FTY720 administration as illustrated in Figure 3 B. Thus, functional properties of B and T cells remained essentially unaltered by FTY720 treatment.
Figure 3. Controls (black bars), FTY720 (open bars). A, Serum anti-OxLDL antibodies. OD values. B, Splenocyte proliferation assay.
Lesion Size, Cellular Composition, and Cytokine Pattern
Lesion size was measured to determine the effect of FTY720 on de novo atherogenesis. Morphometric analysis in the aortic root did not show any effect of FTY720 on lesion size (10.2 x 10 4 ±1.4 x 10 4 µm 2 in controls versus 12.5 x 10 4 ± 2.5 x 10 4 µm 2 in treated group; P =0,66) or fractional area of the lesion in (10.9±1.6% versus 14.3±2.2%; P =0,34) ( Figure 4A and 4 B and supplemental Figures III and IV). Immunohistochemical analysis of lesion composition yielded no significant differences in T, B cells or macrophage content (supplemental Table II). Expression of cytokine-induced genes (I-A b, VCAM-1) was not different. RT-PCR analysis of the aorta showed no significant differences in cytokine/mediator pattern (supplemental Figure V).
Figure 4. Controls (black circles), FTY720 (open circles). A, Lesion size in aortic root (ORO stain). B, Fractional area of the lesion.
Advanced Atherosclerosis
A second group of ApoE –/– mice on normal laboratory diet with established atherosclerotic lesions (26 weeks old) was treated orally with FTY720 at 3 mg/kg/d for 12 weeks. Similar results with respect to significant lymphopenia and changes in the lipid profile were found as in the early atherosclerosis experiment. All other parameters displayed no difference, comparable with the results in early atherosclerosis (supplemental Table III).
Lesion Size, Cellular Composition, and Cytokine Pattern
Quantitative analysis of the aortic root showed no significant differences between the 2 groups. Lesion size was similar comparing controls with treated animals (43.6 x 10 4 ± 4.0 x 10 4 µm 2 versus 38.5 x 10 4 ± 2.7 x 10 4 µm 2, P =0.15) and also the fractional area of the lesion (24.7±2.1% versus 23.6±1.2%, P =0.26). Immunohistochemical analysis of the advanced lesions detected no differences in T, B cell or macrophage content comparing treated animals with controls (data not shown). To evaluate whether FTY720 had any effect on plaque stability in advanced atherosclerosis we examined the innominate artery. 21 Lesion size, fractional area of the lesion, plaque thickness, thickness of the fibrous cap, amount of calcification, and intraplaque hemorrhage were not different between the 2 groups (data not shown). RT-PCR analysis of the aorta showed no significant differences in cytokine/mediator pattern (supplemental Figure VI).
Discussion
The concept of atherosclerosis as an inflammatory disease is supported by an increasing amount of data suggesting that immunomodulation may provide an effective tool to interfere with the development and progression of atherosclerosis. 1,2 In this study, the immunomodulatory sphingolipid analogue FTY720 mediated a pronounced peripheral lymphopenia, however without altering the immunologic balance toward a more protective profile leaving atherogenesis unchanged. This appears attributable to the novel finding of a 2.4-fold increase in cholesterol associated with proatherogenic fractions, primarily VLDL, on administration of the drug.
Three aspects appear noteworthy as to why administration of FTY720 has not been associated with hypercholesterolemia up to present. First, with respect to method only very few groups have performed a detailed plasma lipoprotein analysis as in our study. All currently analyzed clinical trials have not reported cholesterol levels and thus may have missed such an effect. 10,11 Second, the choice of animal model may influence the detected effects. In this respect, the ApoE –/– mouse presents a unique model—by means of its disturbed lipid clearance resulting in a massive elevation of plasma cholesterol levels primarily attributable to an increase in cholesterol-rich VLDL—and chylomicron remnant particles. ApoE –/– (and also LDLr –/– ) mice are sensitive to a high-fat diet, which leads to a marked increase in non-HDL cholesterol levels. 33 It is therefore likely that the effect of FTY720 on plasma cholesterol levels as observed in our study is masked on administration of a high-fat diet. This could explain why this effect was not observed in 2 recent studies on FTY720 in atherosclerosis in hyperlipidemic mouse models. 15,16 Third, the administered dose and route will greatly impact on drug levels and effect. The dose (3 mg/kg/body weight) administered in our study translated into drug levels of 3.1 ng/mL which is in the accepted therapeutic range of 1 to 5 ng/mL. 34
Despite drug-induced hypercholesterolemia, lesions were not larger in the treated ApoE –/– mice. This suggests a separate attenuating effect on atherosclerosis of FTY720 mediated by immunomodulation. Corroborating a previous study in C57BL/6J mice, we found a diminished peripheral lymphocyte cell pool, which the authors from that study 35 attributed predominantly to a decreased release of naïve lymphocytes from the thymus on long-term treatment with FTY720. Future work needs to delineate how long-term treatment differs from short-term treatment to explain this generalized peripheral lymphopenia. Two options are conceivable—either preserved inhibition of thymic lymphocyte egress 36 attributable to differential chemokine requirements in distinct lymphoid compartments 37 with long-term administration of FTY720, or peripheral depletion via ie, apoptosis. 38 Interestingly, we found maintained numbers of Treg and effector memory T cells in lymphoid tissues which argues against a "conventional" lymphodepletion and indicates a functional expansion of effector cells within an overall diminished peripheral lymphocyte pool. Thus, the ability to mount a systemic immune response was not disabled as evidenced by unaltered atherosclerosis-related OxLDL antibody profiles and splenic T cell proliferation. As to the source of Treg and effector memory cells, 2 options are conceivable. Either a thymic-derived natural Treg pool may be constantly self-regenerating in the periphery, or both CD4+ T cell subtypes are continuously regenerated in the periphery after antigen-induced activation. Our finding that effector memory T cell numbers were preserved indicates a peripheral source of at least the memory T cells as they are not derived from the thymus but rather are the result of peripheral antigen activation and subsequent continuous self-renewal. Recent data indicate that peripheral Treg may originate from memory T cells. 39 This may help explain our finding of preserved Treg counts and effector memory T cells as Treg would be regenerated from the peripheral memory T cell pool. In support of our findings, previous data show that FTY720 mediated sequestration of effector memory T cells into lymph nodes 8 and promoted accumulation of natural regulatory T cells, 40 the latter exerting protective effects on atherosclerosis. 41 However, lymphocyte retrafficking did not translate into a protective effect on atherosclerosis in our study which is in contrast to 2 very recent studies. 15,16 Three reasons may account for the discrepancy between these studies and the present one. First, in both studies animals were fed a high-fat diet which in itself causes a pronounced monocytosis and accumulation of macrophages and T cells in lesions. 17–19 In addition, hypercholesterolemia strongly promotes lymphocyte and macrophage activation. 42 Thus, the suppressive effect of FTY720 on inflammatory cell trafficking 5,12 as well as lymphocyte activation 15 may be facilitated under such conditions. Of note, inhibitory effects of FTY720 on splenic T cell proliferation were only observed in LDLr –/– mice exposed to high-fat diet but not when fed a normal laboratory diet (Nofer et al, unpublished results). We found a further increase in S1P plasma levels on FTY720 administration to high-fat fed mice when compared with control animals and FTY720-treated mice on normal diet (data not shown). This might translate into an enhanced effect of S1P on atherosclerosis-related effects (ie, eNOS-induced vasorelaxation 6 and reduced lymphocyte activation) in high-fat fed mice. Our data are supported by the recent finding that FTY720 inhibits sphingosine-1-phosphate lyase, the enzyme responsible for S1P degradation. 43 Normolipidemic C57BL/6J mice had significantly lower sphingolipid levels compared with hypercholesterolemic ApoE –/– mice. 44 Second, the treatment period in both studies was extended (16 and 20 weeks, respectively) enabling detection of even small protective effects on atherosclerosis. Third, the drug level was nearly 25-fold higher compared with our study (68 ng/mL versus 3 ng/mL) in 1 group which showed a decrease in lesion size in the aorta in LDLr –/– mice. Interestingly, in that study a second treatment group with a drug level more in line with levels obtained in our study, no protective effect on atherosclerosis could be detected in the aortic root. 15 In the other study drug levels were not measured. 16
Our study illustrates a link between sphingolipid and cholesterol metabolism and extends previous data. 30,43–45 We show that the sphingosine-1-phosphate (S1P) analogue FTY720 mediates an increase in S1P levels which is associated with increased hepatic HMG-CoA reductase gene expression leading to increased serum cholesterol levels. Further evidence for an interaction between sphingolipid and cholesterol metabolism comes from a recent study which showed that statins—HMG-CoA reductase inhibitors—induce endothelial S1P receptors and mediate vasorelaxation by enhanced eNOS production. 46 To establish the effect of sphingosine-1-phosphate agonists such as FTY720 on atherogenesis, it seems preferable to avoid extreme conditions such as the administration of high-fat diets to genetically hyperlipidemic animals. This will help extrapolate data derived from ongoing clinical trials. From the currently available data it appears safe to assume that FTY720 neither attenuates nor increases atherosclerosis in ApoE –/– mice.
Acknowledgments
We are grateful for the excellent technical assistance by Nadine Wambsganss, Inger Bodin and Ingrid Törnberg.
Sources of Funding
Grants supporting this work were from Novartis (Germany) and Deutsche Forschungsgemeinschaft (KL1398/2-1) to R.K. and T.J.D. (DE591/5-5/5-6), ADUMED Medical Research Foundation to J.R.N., Swedish Research Council, the Grönberg, the Novo Nordisk and the Swedish Heart-Lung Foundations, the Stockholm County Council (ALF) and the Karolinska Hospital to M.R. and G.K.H., respectively.
Disclosures
None.
【参考文献】
Binder CJ, Chang MK, Shaw PX, Miller YI, Hartvigsen K, Dewan A, Witztum JL. Innate and acquired immunity in atherogenesis. Nat Med. 2002; 8: 1218–1226.
Hansson GK, Libby P. The immune response in atherosclerosis: a double-edged sword. Nat Rev Immunol. 2006; 6: 508–519.
Khallou-Laschet J, Caligiuri G, Groyer E, Tupin E, Gaston AT, Poirier B, Kronenberg M, Cohen JL, Klatzmann D, Kaveri SV, Nicoletti A. The proatherogenic role of T cells requires cell division and is dependent on the stage of the disease. Arterioscler Thromb Vasc Biol. 2006; 26: 353–358.
Rosen H, Goetzl EJ. Sphingosine 1-phosphate and its receptors: an autocrine and paracrine network. Nat Rev Immunol. 2005; 5: 560–570.
Whetzel AM, Bolick DT, Srinivasan S, Macdonald TL, Morris MA, Ley K, Hedrick CC. Sphingosine-1 phosphate prevents monocyte/endothelial interactions in type 1 diabetic NOD mice through activation of the S1P receptor. Circ Res. 2006; 99: 731–739.
Nofer JR, van der Giet M, Tolle M, Wolinska I, von Wnuck Lipinski K, Baba HA, Tietge UJ, Godecke A, Ishii I, Kleuser B, Schafers M, Fobker M, Zidek W, Assmann G, Chun J, Levkau B. HDL induces NO-dependent vasorelaxation via the lysophospholipid receptor S1P3. J Clin Invest. 2004; 113: 569–581.
Hwang MW, Matsumori A, Furukawa Y, Ono K, Okada M, Iwasaki A, Hara M, Sasayama S. FTY720, a new immunosuppressant, promotes long-term graft survival and inhibits the progression of graft coronary artery disease in a murine model of cardiac transplantation. Circulation. 1999; 100: 1322–1329.
Habicht A, Clarkson MR, Yang J, Henderson J, Brinkmann V, Fernandes S, Jurewicz M, Yuan X, Sayegh MH. Novel insights into the mechanism of action of FTY720 in a transgenic model of allograft rejection: implications for therapy of chronic rejection. J Immunol. 2006; 176: 36–42.
Maki T, Gottschalk R, Ogawa N, Monaco AP. Prevention and cure of autoimmune diabetes in nonobese diabetic mice by continous administration of FTY720. Transplantation. 2005; 79: 1051–1055.
Tedesco-Silva H, Mourad G, Kahan BD, Boira JG, Weimar W, Mulgaonkar S, Nashan B, Madsen S, Charpentier B, Pellet P, Vanrenterghem Y. FTY720, a novel immunomodulator: efficacy and safety results from the first phase 2A study in de novo renal transplantation. Transplantation. 2005; 79: 1553–1560.
Kappos L, Antel J, Comi G, Montalban X, O?Connor P, Polman CH, Haas T, Korn AA, Karlson G, Radue EW. FTY720 D2201 Study Group. Oral fingolimod (FTY720) for relapsing multiple sclerosis. N Engl J Med. 2006; 355: 1124–1140.
Mandala S, Hajdu R, Bergstrom J, Quackenbush E, Xie J, Milligan J, Thornton R, Shei GJ, Card D, Keohane C, Rosenbach M, Hale J, Lynch CL, Rupprecht K, Parsons W, Rosen H. Alteration of lymphocyte trafficking by sphingosine-1-phosphate receptor agonists. Science. 2002; 296: 346–349.
Brinkmann V, Cyster JG, Hla T. FTY720: Sphingosine 1-phosphate receptor-1 in the control of lymphocyte egress and endothelial barrier function. Am J Transplant. 2004; 4: 1019–1025.
Singer II, Tian M, Wickham AL, Lin J, Matheravidathu SS, Forrest MJ, Mandala S, Quackenbush EJ. Sphigosine-1-phosphate agonists increase macrophage homing, lymphocyte contacts, and endothelial junctional complex formation in murine lymph nodes. J Immunol. 2005; 175: 7151–7161.
Nofer JR, Bot M, Brodde M, Taylor PJ, Salm P, Brinkmann V, van Berkel T, Assmann G, Biessen EA. FTY720, a synthetic sphingosine 1 phosphate analogue, inhibits development of atherosclerosis in low-density lipoprotein receptor-deficient mice. Circulation. 2007; 115: 501–508.
Keul P, Tolle M, Lucke S, von Wnuck Lipinski K, Heusch G, Schuchardt M, van der Giet M, Levkau B. The sphingosine-1-phosphate analogue FTY720 reduces atherosclerosis in apolipoprotein E-deficient mice. Arterioscler Thromb Vasc Biol. 2007; 27: 607–613.
Swirski FK, Libby P, Aikawa E, Alcaide P, Luscinskas FW, Weissleder R, Pittet MJ. Ly-6 chi monocytes dominate hypercholesterolemia-associated monocytosis and give rise to macrophages in atheromata. J Clin Invest. 2007; 117: 195–205.
Moos MP, John N, Grabner R, Nossmann S, Gunter B, Vollandt R, Funk CD, Kaiser B, Habenicht AJ. The lamina adventitia is the major site of immune cell accumulation in standard chow-fed apolipoprotein E-deficient mice. Arterioscler Thromb Vasc Biol. 2005; 25: 2386–2391.
Galkina E, Kadl A, Sanders J, Varughese D, Sarembock IJ, Ley K. Lymphocyte recruitment into the aortic wall before and during development of atherosclerosis is partially L-selectin dependent. J Exp Med. 2006; 203: 1273–1282.
Nicoletti A, Kaveri S, Caligiuri G, Bariety J, Hansson GK. Immunoglobulin treatment reduces atherosclerosis in apo E knockout mice. J Clin Invest. 1998; 102: 910–918.
Bea F, Blessing E, Bennett B, Levitz M, Wallace EP, Rosenfeld ME. Simvastatin promotes atherosclerotic plaque stability in apoE-deficient mice independently of lipid lowering. Arterioscler Thromb Vasc Biol. 2002; 22: 1832–1837.
Nakashima Y, Plump AS, Raines EW, Breslow JL, Ross R. ApoE-deficient mice develop lesions of all phases of atherosclerosis throughout the arterial tree. Arterioscler Thromb Vasc Biol. 1994; 14: 133–140.
Zhou X, Paulsson G, Stemme S, Hansson GK. Hypercholesterolemia is associated with a T helper (Th) 1/Th2 switch of the autoimmune response in atherosclerotic apoE-knockout mice. J Clin Invest. 1998; 101: 1717–1725.
Overbergh L, Giulietti A, Valckx D, Decallone B, Bouillon R, Mathieu C. The use of real-time reverse transcriptase PCR for the quantification of cytokine gene expression. J Biomol Tech. 2003; 14: 33–43.
Hamlet J, Demuth K, Paul JL, Delabar JM, Janel N. Hyperhomocysteinemia due to cystathionine beta synthase deficiency induces dysregulation of genes involved in hepatic lipid homeostasis in mice. J Hepatol. 2007; 46: 151–159.
Ameen C, Edvardsson U, Ljungberg A, Asp L, Akerblad P, Tuneld A, Olofsson SO, Linden D, Oscarsson J. Activation of peroxisome proliferator-activated receptor increases the expression and activity of microsomal triglyceride transfer protein in the liver. J Biol Chem. 2005; 280: 1224–1229.
Kamimura M, Viedt C, Dalpke A, Rosenfeld ME, Mackman N, Cohen DM, Blessing E, Preusch M, Weber CM, Kreuzer J, Katus HA, Bea F. Interleukin-10 suppresses tissue factor expression in lipopolysaccharide-stimulated macrophages via inhibition of Egr-1 and a serum response element/MEK-ERK1/2 pathway. Circ Res. 2005; 97: 305–313.
Merched AJ, Chan LC. Absence of p21 Waf1/Cip1/Sdi1 modulates macrophage differentiation and inflammatory response and protects against atherosclerosis. Circulation. 2004; 110: 3830–3841.
Parini P, Johansson L, Broijersen A, Angelin B, Rudling M. Lipoprotein profiles in plasma and interstitial fluid analyzed with an automated gel-filtration system. Eur J Clin Invest. 2006; 36: 98–104.
Gupta AK, Rudney H. Plasma membrane sphingomyelin and the regulation of HMG-CoA reductase activity and cholesterol biosynthesis in cell cultures. J Lipid Res. 1991; 32: 125–136.
Osawa Y, Uchinami H, Bielawski J, Schwabe RF, Hannun YA, Brenner DA. Roles for C 16 -ceramide and sphingosine 1-phosphate in regulating hepatocyte apoptosis in response to tumor necrosis factor-. J Biol Chem. 2005; 280: 27879–27887.
Kohno M, Momoi M, Oo ML, Paik JH, Lee YM, Venkataraman K, Ai Y, Ristimaki AP, Fyrst H, Sano H, Rosenberg D, Saba JD, Proia RL, Hla T. Intracellular role for sphingosine kinase 1 in intestinal adenoma cell proliferation. Mol Cell Biol. 2006; 26: 7211–7223.
Plump AS, Breslow JL. Apolipoprotein E and the apolipoprotein E-deficient mouse. Annu Rev Nutr. 1995; 15: 495–518.
Kahan BD, Karlix JL, Ferguson RM, Leichtman AB, Mulgaonkar S, Gonwa TA, Skerjanec A, Schmouder RL, Chodoff L. Pharmacodynamics, pharmacokinetics, and safety of multiple doses of FTY720 in stable renal transplant patients: a multicenter, randomized, placebo-controlled phase I study. Transplantation. 2003; 76: 1079–1084.
Morris MA, Gibb DR, Picard F, Brinkmann V, Straume M, Ley K. Transient T cell accumulation in lymph nodes and sustained lymphopenia in mice treated with FTY720. Eur J Immunol. 2005; 35: 3570–3580.
Matloubian M, Lo CG, Cinamon G, Lesneski MJ, Xu Y, Brinkmann V, Allende ML, Proia RL, Cyster JG. Lymphocyte egress from thymus and peripheral lymphoid organs is dependent on S1P receptor 1. Nature. 2004; 427: 355–360.
Yopp AC, Fu S, Honig SM, Randolph GJ, Ding Y, Krieger NR, Bromberg JS. FTY720-enhanced T cell homing is dependent on CCR2, CCR5, CCR7, and CXCR4: evidence for distinct chemokine compartments. J Immunol. 2004; 173: 855–865.
Hashimoto D, Asakura S, Matsuoka K, Sakoda Y, Koyama M, Aoyama K, Tanimoto M, Teshima T. FTY720 enhances the activation-induced apoptosis of donor T cells and modulates graft-versus-host disease. Eur J Immunol. 2007; 37: 271–281.
Akbar AN, Vukmanovic-Stejic M, Taams LS, Macallan DC. The dynamic co-evolution of memory and regulatory CD4+ T cells in the periphery. Nat Rev Immunol. 2007; 7: 231–237.
Ochando JC, Yopp AC, Yang Y, Garin A, Li Y, Boros P, Llodra J, Ding Y, Lira SA, Krieger NR, Bromberg JS. Lymph node occupancy is required for the peripheral development of alloantigen-specific foxp3+ regulatory T cells. J Immunol. 2005; 174: 6993–7005.
Ait-Oufella H, Salomon BL, Potteaux S, Robertson AK, Gourdy P, Zoll J, Merval R, Esposito B, Cohen JL, Fisson S, Flavell RA, Hansson GK, Klatzmann D, Tedgui A, Mallat Z. Natural regulatory T cells control the development of atherosclerosis in mice. Nat Med. 2006; 12: 178–180.
Wunder C, Churin Y, Winau F, Warnecke D, Vieth M, Lindner B, Zahringer U, Mollenkopf HJ, Heinz E, Meyer TF. Cholesterol glucosylation promotes immune evasion by Helicobacter pylori. Nat Med. 2006; 12: 1030–1038.
Bandhuvula P, Tam YY, Oskouian B, Saba JD. The immune modulator FTY720 inhibits sphingosine-1-phosphate lyase activity. J Biol Chem. 2005; 280: 33697–33700.
Park TS, Panek RL, Mueller SB, Hanselman JC, Rosebury WS, Robertson AW, Kindt EK, Homan R, Karathanasis SK, Rekhter MD. Inhibition of sphingomyelin synthesis reduces atherogenesis in apolipoprotein E-knockout mice. Circulation. 2004; 110: 3465–3471.
Hojjati MR, Li Z, Zhou H, Tang S, Huan C, Ooi E, Lu S, Jiang XC. Effect of myriocin on plasma sphingolipid metabolism and atherosclerosis in apoE-deficient mice. J Biol Chem. 2005; 280: 10284–10289.
Igarashi J, Miyoshi M, Hashimoto T, Kubota Y, Kosaka H. Statins induce S1P 1 receptors and enhance endothelial nitric oxide production in response to high-density lipoproteins. Br J Pharmacol. 2007; 150: 470–479.
作者单位：Department of Cardiology (R.K., F.B., E.B., M.P., H.A.K., T.J.D.), University Hospital Heidelberg, Germany; Department of Medicine (R.K., G.K.H.), Karolinska Institutet, Stockholm, Sweden; the Leibniz-Institute for Arteriosclerosis Research (J.R.N.), University of Münster, Germany; the Center f