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Altered Gene Expression Pattern in Peripheral Blood Mononuclear Cells in Patients with Acute Myocardial Infarction

Altered Gene Expression Pattern in Peripheral Blood Mononuclear Cells in Patients with Acute Myocardial Infarction

  • Marek Kiliszek, 
  • Beata Burzynska, 
  • Marcin Michalak, 
  • Monika Gora, 
  • Aleksandra Winkler, 
  • Agata Maciejak, 
  • Agata Leszczynska, 
  • Ewa Gajda, 
  • Janusz Kochanowski, 
  • Grzegorz Opolski



Despite a substantial progress in diagnosis and therapy, acute myocardial infarction (MI) is a major cause of mortality in the general population. A novel insight into the pathophysiology of myocardial infarction obtained by studying gene expression should help to discover novel biomarkers of MI and to suggest novel strategies of therapy. The aim of our study was to establish gene expression patterns in leukocytes from acute myocardial infarction patients.

Methods and Results

Twenty-eight patients with ST-segment elevation myocardial infarction (STEMI) were included. The blood was collected on the 1st day of myocardial infarction, after 4–6 days, and after 6 months. Control group comprised 14 patients with stable coronary artery disease, without history of myocardial infarction. Gene expression analysis was performed with Affymetrix Human Gene 1.0 ST microarrays and GCS3000 TG system. Lists of genes showing altered expression levels (fold change >1.5, p<0.05) were submitted to Ingenuity Pathway Analysis. Gene lists from each group were examined for canonical pathways and molecular and cellular functions. Comparing acute phase of MI with the same patients after 6 months (stable phase) and with control group we found 24 genes with changed expression. In canonical analysis three pathways were highlighted: signaling of PPAR (peroxisome proliferator-activated receptor), IL-10 and IL-6 (interleukin 10 and 6).


In the acute phase of STEMI, dozens of genes from several pathways linked with lipid/glucose metabolism, platelet function and atherosclerotic plaque stability show altered expression. Up-regulation of SOCS3 and FAM20 genes in the first days of myocardial infarction is observed in the vast majority of patients.


Acute myocardial infarction (MI) remains the leading cause of death despite the substantial progress in diagnosis and therapy in recent decades. In the acute phase of MI increased leukocyte count, a non-specific marker of inflammation, is the risk factor for future cardiovascular events and predicts mortality in those with STEMI [ST-segment elevation MI], NSTEMI (non-STEMI) or unstable angina [1], [2]. It has also been shown that an elevated leukocyte count predicts 1-year mortality independently of the risk factors for coronary artery disease across the entire spectrum of acute coronary syndromes (ACS) [3]. The mechanisms linking activation of inflammation and ACS are complex – inflammation seems to be linked to the initiation and progression of atherosclerosis [4]. Obtaining novel insights into the pathophysiology of myocardial infarction by analyzing gene expression patterns in leucocytes should aid the discovery of novel biomarkers of MI and elaboration of novel therapeutic strategies. The aim of our pilot study was the first attempt at establishing leukocyte gene expression signatures of the acute phase of MI.

Materials and Methods


Patients presenting with STEMI were included in the Ist Chair and Departament of Cardiology of Medical University of Warsaw in 2010. We sought to include consecutive patients that agreed to participate in the study (due to technical aspects of blood collection, only patients admitted between Sunday and Thursday were taken into consideration). All the patients underwent coronary angiography and angioplasty of infarct related artery. Pharmacological treatment was according to current guidelines [5]. Blood was collected on the 1st day of myocardial infarction (admission), after 4–6 days (discharge), and after 6 months. Participation in the study had no influence on the pharmacological treatment and procedures underwent by the patients. Control group comprised patients with proven coronary artery disease: with coronary angiography (at least one stenosis exceeding 50% or previous coronary angioplasty of previous coronary artery bypass graft), or with non-invasive tests (positive exercise test) and no history of myocardial infarction. The study was approved by the Bioethics Committee of the Medical University of Warsaw and all patients gave written informed consent.

RNA Isolation

Sodium-heparinized blood was collected from 28 patients at the three time points. Peripheral blood mononuclear cells (PBMC) were purified using BD Vacutainer® CPT™ Cell Preparation Tube according to the manufacturer’s instructions (Becton, Dickinson and Co. Franklin Lakes, NJ,USA).

Total RNA was isolated from PBMC with the MagNA Pure Compact System (Roche Diagnostics GmbH, Germany) according to the manufacturer’s recommendations. RNA samples were quantified by UV absorption (Nanodrop, LabTech International, UK) and their quality was checked with the RNA 600 Nano Assay Kit using Bioanalyzer© in accordance with the manufacturer’s procedures (Agilent, Santa Clara, CA, USA). Samples with an RNA integrity number of eight or above were considered suitable for use in microarrays. RNA samples were stored at −80°C until further analysis.

Table 2. Differentially expressed genes common to both analyses: admission versus 6 months after MI and admission versus control.

Figure 1. Top canonical pathways associated with acute phase of STEMI.

Ingenuity Pathway Analysis of gene sets differentially expressed on the first day of myocardial infarction versus 6 months after MI or versus control group was performed. Functional categories are represented on the x-axis. The significance is expressed as the negative exponent on the p-value calculated for each function on the y-axis of the diagram, increasing with bar height.

Table 4. Differentially expressed genes common to both analyses: admission versus control and discharge versus control.

cDNA Microarrays

RNA (100 ng) was reverse transcribed, amplified, and labeled with biotin using the whole transcript sense target labeling kit and hybridized for 16 h at 45°C to Human Gene 1.0 ST arrays (Affymetrix, Santa Clara,CA, USA), according to the manufacturer’s instructions. Following hybridization, the probe arrays were washed and stained on a fluidics station and immediately scanned on an Affymetrix GCS 3000 GeneArray Scanner.

Figure 2. Expression data from microarray experiments for chosen genes.

The y-axis represents the log2 normalized intensity of the gene and the x-axis represents analyzed groups. The line inside the box and whiskers represents the median of the samples in a group. Points present relative expression levels in individual patients at admission (blue), at discharge (green), 6 month after MI (violet) and from control group (red). Numbers indicate the coded identity of a particular patient. SOCS3– suppressor of cytokine signaling 3; ST14– MT-SP1/matriptase; AQP 9– aquaporin 9; MYBL1– v-myb myeloblastosis viral oncogene homolog (avian)-like 1; STAB1– stabilin 1; ASGR2– asialoglycoprotein receptor 2.

Data Analysis of Microarrays

Quality controls were performed using Microarray Suite 5.0 software provided by Affymetrix ( according to the manufacturer’s recommendations. Affymetrix raw gene array data were processed using the Partek Genomics Suite software (Partek Inc., St. Louis, MO, USA).

Comparisons were performed between MI group at day one of day 4–6 on the one hand and MI group at 6 months or control on the other. Lists of genes showing significant differences in expression levels between groups were submitted to Ingenuity Pathway Analysis (Ingenuity® Systems, for canonical pathways and subjected to network analyses.

Determination of mRNA Levels by qRTPCR

Total RNA was converted into cDNA using the QuantiTect Reverse Transcription Kit (QIAGEN, Germany) according to the manufacturer’s recommendations.

qPCR amplification was performed using a using LightCycler 1.5 and LightCycler 480 Instruments, and LightCycler FastStart DNA Master SYBR Green I and LightCycler 480 SYBR Green I Master (Roche Diagnostics GmbH, Germany) according to the manufacturer’s instructions. The Pfaffl model [6] and the relative expression software tool (REST-MCS©-version 2) [7] were used to estimate changes in the relative mRNA levels of a 24 genes in order to validate the results obtained in the microarray study. We determined the relative expression levels of the selected genes at the 1st day of myocardial infarction (on admission), 6 months after MI and in the control group, using samples from six randomly chosen patients from both groups. Data normalization was carried out against transcripts of the HPRT and TUBB genes. The sequences of all primers and qPCR amplification parameters are available in supplementary data (Table S1).

Statistical analysis.

Continuous variables are presented as mean ±SD (standard deviation). Categorical variables are presented as frequencies. Statistical significance of the results was estimated by variance analysis (ANOVA). Differences were considered statistically significant at a nominal significance of p<0.05 and a fold change >1.5 in expression between the admission, discharge and control groups.


Twenty-eight patients with ST-segment elevation myocardial infarction (STEMI) were included. All the patients completed the follow-up visit 6 months after admission. The control group comprised 14 patients. Basic characteristics of the groups are shown in table 1.


On the first day of MI 91 genes showed a significantly different level of expression compared with 6 months after MI. Of those, 57 were annotated, including three pairs of duplicate genes. Of the 54 unique annotated genes with altered expression 51 were up- and three down-regulated at day 1 versus 6 months (Table S2). In turn, a comparison of gene expression on the first day of MI with the control group identified 491 genes a significantly differentially expressed (212 annotated, including 14 pairs of duplicate genes, 85 were up- and 127 down-regulated, Table S3). Twenty-four genes were shared between the two comparisons (MI vs. after 6 months and MI vs. control, Table 2).

In a canonical analysis of the genes with altered expression several pathways were found, the most significant being: signaling of PPAR (peroxisomal proliferator-activated receptor), IL-6 (interleukin 6) signaling, and IL-10 (interleukin 10) signaling. These pathways were common for both comparisons (Figure 1).

Additionally, a comparison between day one and after 6 months revealed significant changes in glucocorticoid receptor signaling and activation of LXR/RXR (liver × receptor/retinoid × receptor). In contrast, analysis of the day one MI group versus the control highlited genes associated with Complement System, Coagulation System, Natural Killer Cell Signaling, and Extrinsic Prothrombin Activation Pathway.

In the molecular and cellular function categories Cellular Growth and Proliferation, Cell-To-Cell Signaling and Interaction, and Cell Movement were markedly changed in both analyses.

To validate the microarray results, mRNA levels of twenty-four genes shared between the two comparisons were quantified by qRT-PCR (Table 3). Results of validation confirmed the microarray data and for most of the genes the fold-changes calculated by qRT-PCR exceeded the microarray ones.


On the 4th–6th day after MI expression of 34 genes was changed relative to 6 months after MI: 18 with annotation including two pairs and one gene represented by seven probes, which makes 10 unique genes, all upregulated (Table S4). In a canonical analysis five most significant pathways were: Primary Immunodeficiency Signaling, B Cell Development; Communication between Innate and Adaptive Immune Cells; Systemic Lupus Erythematosus Signaling; Role of Macrophages, Fibroblasts and Endothelial Cells in Rheumatoid Arthritis.

Analysis of 4th–6th day after MI versus the control group indicated 302 differentially expressed genes with 98 of them annotated, including three pairs of duplicates; 26 up- and 72 down-regulated (Table S5). Association with Hematopoiesis from Pluripotent Stem Cells, Primary Immunodeficiency Signaling, Natural Killer Cell Signaling, Complement System, and EIF2 Signaling canonical pathways was found.

Genes Shared between Admission and Discharge

Taking into account genes common to the two analyses of gene expression on admission and on discharge versus after 6 months, only two transcripts showed significantly altered expression: FAM20A and SOCS3. In contrast, when the same admission and discharge groups were compared with the control 75 genes were shared between the two comparisons, including 39 down-regulated small non-coding RNA transcripts (Table 4).

Additionally, we undertook a patient-by-patient analysis of the most differently expressed genes between all groups. The direction of change was the same in all patients although the relative levels of expression differed markedly between patients (Figure 2).


We have shown here that in leukocytes of STEMI patients tens of genes show altered expression during or soon after MI relative to the stable coronary artery disease. Interestingly, at the day of the infarct they include mainly genes and pathways directly or indirectly linked with lipid/glucose metabolism, platelet function and atherosclerotic plaque stability. On discharge, many genes related to specific immune response (encoding immunoglobulins) show altered expression. Comparing the admission and the discharge profiles with the control group, a strikingly high number of small non-coding RNA transcripts (most frequent small nucleolar RNA, snoRNA) show altered expression. Those snoRNAs are known to act as guide molecules for site-specific methylation and pseudouridylation of other RNAs. snoRNA-guided modifications of mRNA seem possible and could affect splicing, translation or mRNA stability. However, the clinical significance of snoRNA is not known [8].

Gene Expression

Below we discuss selected literature references indicating a possible relevance of individual genes showing altered expression in this study (see Table 2) to the functioning of the cardiovascular system.

We have shown up-regulation of SOCS3 and FAM20 genes in the first 4–6 days of myocardial infarction. SOCS3 is one of the eight proteins of the SOCS group that block the JAK (Janus kinase) tyrosine kinase activity and the activation of STAT factors [9]. Expression of SOCS3 has been shown to be significantly reduced in balloon-injured porcine coronary arteries [10]. Recently it was reported that the progression of LV remodeling after AMI was prevented in SOCS3-deficient mice. SOCS3 deletion enhanced multiple cardioprotective signaling pathways including STAT3, AKT, and extracellular signal-regulated kinase (ERK)-1/2, while inhibiting myocardial apoptosis and fibrosis [11].

The FAM20 family comprises secreted proteins with potential roles in regulating differentiation and functioning of hematopoietic and other tissues. The FAM20A mRNA is only expressed during early stages of hematopoietic development [12]. The role of FAM198B is unknown.

ST14 (MT-SP1/matriptase) of plays roles in growth factor activation, receptor activation and inactivation, protease activation, and ectodomain shedding [13]. In atherosclerotic lesions, enhanced mRNA and protein expression of ST14 was found relative to nondiseased vessels [14]. Asialoglycoprotein receptor (ASGPR) is a hepatic lectin responsible for selective binding and internalization of galactose/N-acetylgalactosamine-terminating glycoproteins by hepatic parenchymal cells [15]. ASGR plays a role in regulating platelet life span and activation [16], which suggest a potential link of ASGR with coronary disease and acute coronary syndromes. The aquaporin (AQP) family members are fundamental in transmembrane water movements [17]. The specific function of AQP9 is to maximize glycerol influx and urea efflux during gluconeogenesis, as this channel is more permeable to glycerol and urea than to water [18]. Using an AQP9-knockout mice model it has been shown that AQP9 is important for hepatic glycerol metabolism and may play a role in glycerol and glucose metabolism in diabetes mellitus [19].

Early growth response-1 (EGR1) plays a role in the pathogenesis of atherosclerotic lesions, intimal thickening after acute vascular injury, ischemic pathology, angiogenesis, allograft rejection, and cardiac hypertrophy. Aditionally, EGR-1 regulates expression of molecules critically linked with atherogenesis and lesion progression [20], [21], [22]. Peroxisome proliferator-activated receptor G (PPARG), a member of the PPAR subfamily of nuclear hormone receptors, has a key role in adipogenesis, insulin sensitivity, and glucose and lipid metabolism, and also plays a major role in vascular biology, modulating atherosclerosis progression and vascular endothelial function [23], [24]. Killer cell lectin-like receptor subfamily C, member 2 (KLRC2) and member 4 (KLRC4) are expressed primarily in natural killer (NK) cells and are a family of transmembrane proteins characterized by a type II membrane orientation and the presence of a C-type lectin domain. NK cells are an important component of the innate immune system through target cell killing and cytokine production. A direct evidence for NK cell involvement in atherogenesis is scant, although some researchers have localized NK cells to the human atherosclerotic plaque [25], [26]. RNASE2– RNase A family, 2 (liver, eosinophil-derived neurotoxin) is a distinct cationic protein of the eosinophil’s large specific granule known primarily for its ability to induce ataxia, paralysis, and central nervous system cellular degeneration [27]. FCGR1A – Fc fragment of IgG, high affinity 1A, receptor (CD64) is unique within the FCGR family which mediates important immune defense functions by inducing cell surface changes on human leukocytes [28], [29]. Activating FCGRs can induce phagocytosis, antigen presentation, the production of reactive oxygen species (ROS) and cytokines [28].

Canonical Analysis

Activation of PPAR changes gene transcription to modulate several clinically important metabolic functions: it improves the lipid profile and corrects hyperglycaemia and insulin resistance [30]. Interestingly, PPAR and retinoid × receptor (RXR) cooperate in metabolic regulation. Numerous PPAR agonists are used in clinical setting (fibrates) or are currently under investigation for therapeutic application (thiazolidinediones).

IL-6 seems to have proatherogenic effects. Its serum concentration is elevated in acute myocardial infarction [31] and predicts events in the follow-up [32]. IL-6 has been shown to enhance fatty lesion development in mice [33]. IL-6 signaling is regulated by a family of endogenous JAK kinase inhibitor proteins, suppressors of cytokine signaling (SOCS) [34]. SOCS3 has a differential effect on IL-6 and IL-10 receptor signaling: the IL-6 receptor signaling is down-regulated by SOCS3, whereas that by IL-10 receptor is not [35]. In mice, leukocyte-derived IL-10 prevents the development of advanced atherosclerosis and plays a critical role in the modulation of the cellular and collagen plaque composition [36]. On the other hand, an elevated baseline plasma level of IL-10 has been reported as a strong and independent predictor of long-term adverse cardiovascular outcome in patients with acute coronary syndrome [37].

LXR/RXR plays important roles in cholesterol metabolism and regulates a number of immune and inflammatory pathways that have the potential to modulate development of atherosclerotic lesion [38].

Study Limitations

Since no data on gene expression in STEMI has been published so far (means, standard deviations, etc.), we conducted a pilot study with a rather small number of patients. The results should be confirmed on a larger and independent cohort. Our group was homogenous (STEMI patients only, with angioplasty of infarct-related artery) and well-characterized clinically. We compared expression with two controls: the same group after six months (this approach has several strengths: age, sex and risk factors are the same, and the STEMI phase can be compared with the subsequent stable phase of the coronary artery disease) and an independent control group with coronary artery disease, but without myocardial infarction. Our aim was to find genes showing changed expression specifically during MI, but not those associated with stable coronary artery disease (that is why we did not take healthy controls). Thanks to such choice also the treatment of both groups was comparable, with the exception of a clopidogrel and – obviously – heparin. Our control group was older than the experimental group, but when we compared age 1st or 4th quartile of the study group with the controls, the major results were the same (data not shown). Obviously the left ventricle ejection fraction was different – but this cannot be avoided. Other clinical factors were not significantly different.


ST-segment elevation myocardial infarction alters expression of several groups of genes. On admission, several genes and pathways that could be directly or indirectly linked with lipid/glucose metabolism, platelet function and atherosclerotic plaque stability were affected (signaling of PPAR, IL-10, IL-6). Analysis at discharge highlighted specific immune response (upregulation of immunoglobulins). Highly significant and substantial upregulation of SOCS3 and FAM20 genes expression in the first 4–6 days of myocardial infarction in all patients is the most robust observation of our work.

Supporting Information

Table S1.

Primers sequences and reaction conditions used for Real-time PCR.


Table S2.

Annotated genes with expression at admission significantly different from 6 months after MI.


Table S3.

Annotated genes with expression at admission significantly different from control.


Table S4.

Annotated genes with expression at discharge significantly different from 6 months after MI.


Table S5.

Annotated genes with expression at discharge significantly different from control.


Author Contributions

Conceived and designed the experiments: MK BB MG GO. Performed the experiments: MK MM AW EG JK. Analyzed the data: MK BB MG GO. Contributed reagents/materials/analysis tools: BB MG AM AL. Wrote the paper: MK BB. Critucal review of the manuscript: JK GO.


  1. 1. Barron HV, Harr SD, Radford MJ, Wang Y, Krumholz HM (2001) The association between white blood cell count and acute myocardial infarction mortality in patients ≥65 years of age: findings from the cooperative cardiovascular project. J Am Coll Cardiol 38: 1654–1661.
  2. 2. Mueller C, Neumann FJ, Perruchoud AP, Buettner HJ (2003) White blood cell count and long term mortality after non-ST elevation acute coronary syndrome treated with very early revascularisation. Heart 89: 389–392.
  3. 3. Ndrepepa G, Braun S, Iijima R, Keta D, Byrne RA, et al. (2009) Total leucocyte count, but not C-reactive protein, predicts 1-year mortality in patients with acute coronary syndromes treated with percutaneous coronary intervention. Clin Sci (Lond) 116: 651–658.
  4. 4. Libby P, Ridker PM, Hansson GK (2011) Progress and challenges in translating the biology of atherosclerosis. Nature 19 473: 317–325.
  5. 5. Van de Werf F, Bax J, Betriu A, Blomstrom-Lundqvist C, Crea F, et al. (2008) Management of acute myocardial infarction in patients presenting with persistent ST-segment elevation. The Task Force on the management of ST-segment elevation acute myocardial infarction of the European Society of Cardiology. European Heart Journal 29: 2909–2945.
  6. 6. Pfaffl MW (2001) A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Research 29: e45.
  7. 7. Pfaffl MW, Horgan GW, Dempfle L (2002) Relative expression software tool (REST) for group-wise comparison and statistical analysis of relative expression results in real-time PCR. Nucleic Acids Research 30: e36.
  8. 8. Holley CL, Topkara VK (2011) An Introduction to Small Non-coding RNAs: miRNA and snoRNA. Cardiovasc Drugs Ther 25: 151–159.
  9. 9. Tamiya T, Kashiwagi I, Takahashi R, Yasukawa H, Yoshimura A (2011) Suppressors of Cytokine Signaling (SOCS) Proteins and JAK/STAT Pathways: Regulation of T-Cell Inflammation by SOCS1 and SOCS3. Arterioscler Thromb Vasc Biol 31: 980–985.
  10. 10. Gupta GK, Dhar K, Del Core MG, Hunter WJ 3rd, Hatzoudis GI, et al (2011) Suppressor of cytokine signaling-3 and intimal hyperplasia in porcine coronary arteries following coronary intervention. Exp Mol Pathol 91: 346–52.
  11. 11. Oba T, Yasukawa H, Hoshijima M, Sasaki K, Futamata N, et al. (2012) Cardiac-Specific Deletion of SOCS-3 Prevents Development of Left Ventricular Remodeling After Acute Myocardial Infarction. J Am Coll Cardiol 59: 838–852.
  12. 12. Nalbant D, Youn H, Nalbant SI, Sharma S, Cobos E, et al. (2005) FAM20: an evolutionarily conserved family of secreted proteins expressed in hematopoietic cells. BMC Genomics 27: 6–11.
  13. 13. Darragh MR, Bhatt AS, Craik CS (2008) MT-SP1 proteolysis and regulation of cell-microenvironment interactions. Front Biosci 13: 528–539.
  14. 14. Seitz I, Hess S, Schulz H, Eckl R, Busch G, et al. (2007) Membrane-type serine protease-1/matriptase induces interleukin-6 and -8 in endothelial cells by activation of protease-activated receptor-2: potential implications in atherosclerosis. Arterioscler Thromb Vasc Biol 27: 769–775.
  15. 15. Weigel PH (1994) Galactosyl and N-acetylgalactosaminyl homeostasis: a function for mammalian asialoglycoprotein receptors. Bioessays 16: 519–524.
  16. 16. Sørensen AL, Rumjantseva V, Nayeb-Hashemi S, Clausen H, Hartwig JH, et al. (2009) Role of sialic acid for platelet life span: exposure of beta-galactose results in the rapid clearance of platelets from the circulation by asialoglycoprotein receptor–expressing liver macrophages and hepatocytes. Blood 114: 1645–1654.
  17. 17. Magni F, Sarto C, Ticozzi D, Soldi M, Bosso N, et al. (2006) Proteomic knowledge of human aquaporins. Proteomics 6: 5637–5649.
  18. 18. Carbrey JM, Gorelick-Feldman DA, Kozono D, Praetorius J, Nielsen S, et al. (2003) Aquaglyceroporin AQP9: solute permeation and metabolic control of expression in liver. Proc Natl Acad Sci USA 100: 2945–2950.
  19. 19. Rojek AM, Skowronski MT, Füchtbauer EM, Füchtbauer AC, Fenton RA, et al. (2007) Defective glycerol metabolism in aquaporin 9 (AQP9) knockout mice. Proc Natl Acad Sci U S A 104: 3609–3614.
  20. 20. Khachigian LM (2006) Early Growth Response-1 in Cardiovascular Pathobiology. Circ Res 98: 186–191.
  21. 21. Khachigian LM, Lindner V, Williams AJ, Collins T (1996) Egr-1-induced endothelial gene expression: a common theme in vascular injury. Science 271: 1427–1431.
  22. 22. Harja E, Bucciarelli LG, Lu Y, Stern DM, Zou YS, et al. (2004) Early growth response-1 promotes atherogenesis: mice deficient in early growth response-1 and apolipoprotein E display decreased atherosclerosis and vascular inflammation. Circ Res 94: 333–339.
  23. 23. Asnani S, Theuma P, Fonseca VA (2003) PPARgamma agonists and vascular risk factors: potential effects on cardiovascular disease. Metab Syndr Relat Disord 1: 23–32.
  24. 24. Zhang L, Chawla A (2004) Role of PPARG in macrophage biology and atherosclerosis. Trends Endocrinol Metab 15: 500–505.
  25. 25. Vanderlaan PA, Reardon CA (2005) Thematic review series: the immune system and atherogenesis. The unusual suspects: an overview of the minor leukocyte populations in atherosclerosis. J Lipid Res 46: 829–838.
  26. 26. Millonig G, Malcom G, Wick G (2002) Early inflammatory-immunological lesions in juvenile atherosclerosis from the Pathobiological Determinants of Atherosclerosis in Youth (PDAY) Study. Atherosclerosis 160: 441–448.
  27. 27. Rosenberg HF, Tenen DG, Ackerman SJ (1989) Molecular cloning of the human eosinophil-derived neurotoxin: a member of the ribonuclease gene family. Proc Natl Acad Sci U S A 86: 4460–4464.
  28. 28. van der Poel CE, Spaapen RM, van de Winkel JG, Leusen JH (2011) Functional Characteristics of the High Affinity IgG Receptor, FcgammaRI. The Journal of Immunology 186: 2699–2704.
  29. 29. Ohta Y, Stossel TP, Hartwig JH (1991) Ligand-sensitive binding of actin-binding protein to immunoglobulin G Fc Receptor I (FcGRI). Cell Press 67: 275–282.
  30. 30. Jandeleit-Dahm KAM, Calkin A, Tikellis C, Thomas M (2009) Direct antiatherosclerotic effects of PPAR agonists. Curr Opin Lipidol 20: 24–29.
  31. 31. Kaminski KA, Kozuch M, Bonda T, Wojtkowska I, Kozieradzka A, et al. (2009) Coronary sinus concentrations of interleukin 6 and its soluble receptors are affected by reperfusion and may portend complications in patients with myocardial infarction. Atherosclerosis 206: 581–587.
  32. 32. Tan J, Hua Q, Li J, Fan Z (2009) Prognostic value of interleukin-6 during a 3-year follow-up in patients with acute ST-segment elevation myocardial infarction. Heart Vessels 24: 329–334.
  33. 33. Huber SA, Sakkinen P, Conze D, Hardin N, Tracy R (1999) Interleukin-6 exacerbates early atherosclerosis in mice. Arterioscler Thromb Vasc Biol 19: 2364–2367.
  34. 34. Yoshimura A, Naka T, Kubo M (2007) SOCS proteins, cytokine signalling and immune regulation. Nat Rev Immunol 7: 454–465.
  35. 35. Ait-Oufella H, Taleb S, Mallat Z, Tedgui A (2011) Recent advances on the role of cytokines in atherosclerosis. Arterioscler Thromb Vasc Biol 31: 969–979.
  36. 36. Potteaux S, Esposito B, van Oostrom O, Brun V, Ardouin P, et al. (2004) Leukocyte-derived interleukin 10 is required for protection against atherosclerosis in low-density lipoprotein receptor knockout mice. Arterioscler Thromb Vasc Biol 24: 1474–1478.
  37. 37. Cavusoglu E, Marmur JD, Hojjati MR, Chopra V, Butala M, et al. (2011) Plasma interleukin-10 levels and adverse outcomes in acute coronary syndrome. Am J Med 124: 724–730.
  38. 38. Calkin AC, Tontonoz P (2010) Liver × Receptor Signaling Pathways and Atherosclerosis. Arterioscler Thromb Vasc Biol 30: 1513–1518.