Genes & Genetic Systems
Online ISSN : 1880-5779
Print ISSN : 1341-7568
ISSN-L : 1341-7568
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Preliminary assessment of differential expression of candidate genes associated with atherosclerosis
Joan BlinZalinah AhmadLekhraj Rampal S/O Gyanchand RampalNorhafizah MohtarrudinAbdul Karim Haji TajudinRohayu Shahar Adnan
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2013 年 88 巻 3 号 p. 199-209

詳細
ABSTRACT

Identifying susceptible genes associated with the pathogenesis of atherosclerosis (ATH) may contribute toward better management of this condition. This preliminary study was aimed at assessing the expression levels of 11 candidate genes, namely tumor protein (TP53), transforming growth factor, beta receptor II (TGFBR2), cysthathionenine-beta-synthase (CBS), insulin receptor substrate 1 (IRS1), lipoprotein lipase (LPL), methylenetetrahydrofolate reductase (MTHFR), thrombomodulin (THBD), lecithin-cholesterol acyltransferase (LCAT), matrix metallopeptidase 9 (MMP9), low density lipoprotein receptor (LDLR), and arachidonate 5-lipoxygenase-activating protein (ALOX5AP) genes associated with ATH. Twelve human coronary artery tissues (HCATs) were obtained from deceased subjects who underwent post-mortem procedures. Six atherosclerotic coronary artery tissue (ACAT) samples representing the cases and non-atherosclerotic coronary artery tissue (NCAT) samples as controls were gathered based on predetermined inclusion and exclusion criteria. Gene expression levels were assessed using the GenomeLab Genetic Analysis System (GeXP). The results showed that LDLR, TP53, and MMP9 expression levels were significantly increased in ACAT compared to NCAT samples (p < 0.05). Thus, LDLR, TP53, and MMP9 genes may play important roles in the development of ATH in a Malaysian study population.

INTRODUCTION

Cardiovascular disease (CVD) has been the leading cause of death in Malaysia for the last 45 years (Rampal et al., 2008). Atherosclerosis (ATH) is one of the underlying causes of CVD. Atherosclerosis (ATH) was formerly regarded as a lipid storage disease. It is known to be involved in ongoing inflammatory responses and processes (Libby et al., 2002). The development of ATH consists of three main phases, and inflammation plays a central role in all phases of atherosclerotic development (Spagnoli et al., 2007). In addition to inflammation, the deposition of cholesterol in the arterial wall also plays an important role in the pathogenesis of ATH. Different genes play important roles in the initiation and modulation of atherosclerotic disease through different mechanisms, either through up regulation or down regulation of these genes (Humphries and Ordovas, 2001). In our study, we aimed to determined the differential expressions of 11 candidate genes namely tumor protein (TP53), transforming growth factor, beta receptor II (TGFBR2), cysthathionenine-beta-synthase (CBS), insulin receptor substrate 1 (IRS1), lipoprotein lipase (LPL), methylenetetrahydrofolate reductase (MTHFR), thrombomodulin (THBD), lecithincholesterol acyltransferase (LCAT), matrix metallopeptidase 9 (MMP9), low density lipoprotein receptor (LDLR), and arachidonate 5-lipoxygenase-activating protein (ALOX5AP) genes associated with ATH development. Genes such as LCAT, LDLR, ALOX5AP, and LPL are able to influence plasma cholesterol level. LCAT gene is a major determinant of plasma high-density lipoprotein (HDL) concentration. Previous study showed that heterozygosity of the LCAT gene leads to LCAT enzyme deficiency, which is associated with both atherogenic lipid profile and vascular abnormalities (Ayyobi et al., 2004). A high level of plasma LDL on the other hand is a contributing factor for coronary artery disease (Tveten et al., 2012). Increased expression level of ALOX5AP in adipose tissue has also been linked with the risk of CVD (Kaaman et al., 2006). Meanwhile, proatherogenic role of LPL has been described previously in different studies (Werba et al., 2001; Mead et al., 1999).

Thrombomodulin, a product of THBD gene, is a glycoprotein receptor expressed on the endothelial cell surface and is involved in an anticoagulation pathway. Binding of thrombomodulin with thrombin activates protein C, which in turn inhibits procoagulant pathway (Salomaa et al., 2001). Thus, reduced THBD expression could impair its function in coagulation cascade. TP53 is a tumor suppression protein 53 known to participate in diverse cellular stress, the cell cycle, and apoptosis (Levine et al., 2006). Apoptosis is a programmed cell death and known to cause a number of common and threatening vascular diseases, including atherosclerosis (Mallat and Tedgui, 2000). Meanwhile, TGF-beta superfamily plays a key role in the maintenance of normal blood vessel wall structure, and defects in genes encoding these superfamily members have been linked to a range of cardiovascular syndrome (Grainger, 2007).

Other genes such as MTHFR, CBS, MMP9, and IRS1 were also reported to be involved in the development of ATH. MTHFR and CBS enzymes are predominantly involved in folate and homocysteine metabolism. A defect in the gene encoding the MTHFR enzyme impairs the ability to produce folate. The reduction in folate activity leads to increased homocysteine levels in the blood, which is associated with an increased risk of developing ATH (Varga et al., 2005). Mild impairment of CBS function is also correlated with increased homocysteine concentration. The involvement of matrix metalloproteinases (MMPs) in the early stage of plaque development has been suggested by Loftus et al. (2002). The IRS1 gene however, has commonly been correlated with a higher risk of developing diabetes type 2 (Kovacs et al., 2003). However, previous study reported that the IRS1 gene also plays a role in CVD development (Baroni et al., 1999).

Atherosclerotic cardiovascular disease remains a growing public health burden in developed countries (Miller et al., 2007). Malaysia also has a hard time coping with the CVD burden every year. Much effort has been invested in screening, treating and preventing the disease. The high morbidity and mortality associated with ATH indicate the need for a better understanding of the underlying molecular events leading to disease etiology and progression.

With technological advancements, the world has been waiting for better ways of coping with this disease. One strategy for the ideal management of the disease is suggested to be the personalized medicine approach. However, this facet of medicine, which is moving closer to more precise, predictable and powerful medicine, can only be achieved through a thorough understanding of the disease genetics. The promise of personalized medicine, which allows us to provide better diagnoses, safer drug prescribing, and more effective treatment, depends on a detailed understanding of the genes and gene variants that contribute to disease susceptibility, progression (Seo et al., 2004) and treatment response. Thus, identifying the candidate genes associated with the development of the disease is a fundamental step.

The GenomeLab Genetic Analysis System (GeXP) is a novel technological platform for quantitative multiplexed gene expression analysis. GeXP is able to provide a better approach for the identification of multiple genes in a single reaction, which is important in studying a complex disease, such as atherosclerotic cardiovascular disease (Drew et al., 2011).

MATERIALS AND METHODS

Samples

A total of 12 human coronary artery tissues (HCATs) were obtained from deceased subjects who had undergone a post-mortem procedure performed by an assigned medical officer in the Forensic Department of Hospital Serdang and Hospital Kuala Lumpur, Malaysia. The study was conducted after approval by the Ethics Committee of National Medical Research (NMRR-08-1592-2721), Ministry of Health, Malaysia, and the Ethics Committee of Faculty of Medicine and Health Sciences, Universiti Putra Malaysia (UPM). Six samples of atherosclerotic coronary artery tissue (ACAT) and six samples of non-atherosclerotic coronary artery tissue (NCAT), representing cases and controls, respectively, were gathered for the study. Our ACAT samples were defined as HCATs obtained from deceased subjects who died from ischemic heart disease (IHD) with the clear presence of an atheroma (mild, moderate or severe atheroma with 10% to 95% stenosis) within the tissue lining of left anterior descending (LAD) of left coronary artery tissue. Samples of NCAT were HCATs taken from deceased subjects who died from motorcycle vehicle accident (MVA) showing no atheroma at the lining of the same stated tissue region and were declared healthy by the pathologists involved in the post-mortem procedure. Other inclusion criteria for ACAT and NCAT samples included male Malaysian nationals only. All of the tissue samples were only taken from deceased subjects who had undergone the post-mortem within 24 hours between death and the execution of the autopsy. Subjects with conflicting diseases, such as diabetes and chronic inflammatory disease, were excluded from our study. The tissue characteristics were grossly examined and confirmed by a certified pathologist in the Forensic Department of both hospitals before being released to be used in this study. Microscopic examinations of ACAT samples were also performed to confirm the presence of atheroma, measuring the degree of stenosis, clinical complications, and the presence of superimposed thrombosis events. During the procedure, a 3.0 cm tissue sample was excised 1.2 cm away from the ostium of the LAD of left coronary artery. The tissue was cleaned by trimming excess fat tissues covering the artery using a sterile dissecting kit. Approximately 1.5 cm of each tissue was transferred into a 2 ml tube containing 1.5 ml of RNAlater solution, and the remaining 1.5 cm of tissue was preserved in formalin solution for microscopic examination with hematoxylin and eosin (H & E) staining. All of the samples were immediately stored at 4℃ and transported to a laboratory in UPM as soon as possible. Table 1 shows demographic data of both ACAT and NCAT samples.

Table 1. Characteristic of tissue samples
CharacteristicsACAT (n=6)NCAT (n=6)
Mean age (years)52.33±3.18034.67±4.372
Age range (years)47–5826–40
Sex
 Male66
 Female
Cause of death
 IHD6
 Non-IHD6

(–) sign indicate no applicable data.

Result was represented as Mean ± SD.

Ischemic heart disease (IHD).

Atherosclerotic coronary artery tissue (ACAT).

Non-atherosclerotic coronary artery tissue (NCAT).

Paraffin-embedded tissue and microscopic slide preparations

All formalin-fixed ACAT samples were cut longitudinally and processed using an automatic tissue processor (LEICA TP1020) for tissue dehydration. Next, the tissues were embedded by placing them in a mold filled with melted paraffin wax, and they were allowed to solidify. The paraffin-embedded tissues were then trimmed and sectioned into 3 μm sections for microscopic slide preparation. All prepared microscopic slides underwent H & E staining with an autostainer (Tissue-Tek® PrismaTM). Next, the dried slides were mounted with DPX and examined under a microscope.

Total RNA isolation

Total ribonucleic acid (RNA) was isolated from each 40 mg of tissue sample using a PerfectPure RNA Tissue Kit (5-Prime, USA). The isolation steps were carried out according to the manufacturer’s instructions. Briefly, tissue sample was immersed in lysis solution containing TCEP [tris (2-carboxyethyl) phosphine]. It was then thoroughly homogenized using Polytron® PT 1600E benchtop homogenizer (Kinematica, Lucerne, Switzerland). Approximately 10 μl of Proteinase K Solution (20 mg/ml) (Fermentas, Lithuania) was added into the lysate followed by vortexing and incubation on ice. Preclear column was used to remove large particulates. The RNA binding was then performed using Purification Column. The column was washed with Wash 1 solution before subjected to DNase treatment. After incubation, the column was washed with DNase Wash Solution. The washing step was repeated twice. Next, the Purification Column was transferred into a new collection tube and the sample was subjected to Wash 2 solution. This washing step was also repeated twice. The column was then transferred into a new collection tube. Elution Solution was added to the Purification Column to elute the RNA. The sample was then centrifuged to collect the eluted RNA sample into collection tube. The concentration and purity of yielded RNA were determined by the ratio of absorbance at 260 nm and 280 nm using a NanoDrop ND-1000 spectrophotometer (Nano-Drop Technologies, Wilmington, DE, USA).

Gene expression analysis

The Beckman Coulter (Fullerton, CA, USA) GenomeLab Gene Expression Profiler (GeXP) genetic analysis system was used to study the gene expression pattern of 11 candidate genes that were proposed to mediate ATH development in humans. These 11 candidate genes were selected based on previous reports on their associations with the risk of ATH development in human (Table 2). The GenomeLab GeXP Start Kit (GenomeLab), ThermoStart Taq DNA polymerase (Thermo Scientific), and capillary array for DNA separation (GenomeLab) were purchased from Beckman Coulter (Fullerton, CA, USA). The oligo (dT) multiplex primers were supplied by 1st BASE.

Table 2. Summary table of candidate genes used for differential gene expressions analysis using GeXP
Gene nameGene locusGene product/descriptionMechanism/FunctionReferences
EzrinaX51521EzrinHousekeeping gene
TP53NM_000546Tumor protein 53InflammationBeiras-Fernandez et al., 2011
TGFBR2NM_003242Transforming growth factor, beta receptor IIInflammationten Dijke and Arthur, 2007
CBSL14577Cystathionenine-beta-synthaseEnzyme activityVarga et al., 2005
IRS1NM_005544Insulin receptor substrate 1Enzyme activityBaroni et al., 1999
LPLNM_000237Lipoprotein lipaseCholesterol transportWerba et al., 2001
MTHFRBC053509Methylenetetrahydrofolate reductaseEnzyme activityVarga et al., 2005
THBDNM_000361ThrombomodulinCoagulation factorsChan et al., 2006
LCATNM_000229Lecithin-cholesterol acyltransferaseCholesterol transportAyyobi et al., 2004
ATP5OaX83218ATP synthase, H+ transporting, mitochondrial F1 complex, O subunitHousekeeping gene
MMP9NM_004994Matrix metallopeptidase 9Enzyme activityWang et al., 2011
LDLRNM_000527Low density lipoprotein receptorCholesterol transportTveten et al., 2012
KnarbKanamycin resistance geneInternal control
RPLP0aNM_001002Ribosomal protein, large, P0Housekeeping gene
ALOX5APNM_001629Arachidonate 5-lipoxygenase-activating proteinCholesterol transportKaaman et al., 2006
a  Gene used for normalization.

b  Internal control KANR gene.

Multiplex primer design

Multiplex primer sets were designed using GenomeLab eXpress Profiler software by importing the accession number of the candidate genes into the eXpress Designer module of the software. The fragment sizes of primer pairs were designed in the range of 150 to 342 nucleotides to yield PCR products that had a 7 nucleotides difference from each other. Each primer was designed together with a universal primer sequence from 5’ to 3’ with the software. In addition to the candidate genes, three housekeeping genes (ezrin, ATP synthase, and ribosomal protein) were included for normalization. These genes were chosen because their product sizes were ideally distributed along the whole length of the panel. Primers were also designed to amplify a kanamycin resistance gene RNA transcript (supplied with the GeXP assay kit, Beckman Coulter, Fullerton, CA, USA) that was used to spike each reverse transcription reaction and served as an internal reaction integrity control (Vansant et al., 2006; Chen et al., 2007; Ismail et al., 2010). Finally, all of the primers were pooled for GeXP multiplex analysis. The genes and primer sequences are listed in Table 2 and Table 3.

Table 3. Summary of reverse and forward primers sequences used in GeXP analysis
Gene nameProduct sizeLeft sequence (5’ to 3’)Right sequence (5’ to 3’)Reverse primer (nM)
Ezrina 150 dGCCTAGAGGCTGACCGTATG eTGTGTATTCTGCAAGCTCCG 4000
TP53 187 dGTCAGAAGCACCCAGGACTT eCTCCCAAACATCCCTCACAG 4000
TGFBR2 201 dCGGCTCCCTAAACACTACCA eTATCCCCACAGCTTACAGGG 4000
CBS 208 dGTTTGCGTGTTTGGGTTTTT eGAGGGGAAATGATTGCTTCA 4000
IRS1 215 dGGGTGCTGGCCTATTAGTGA eTGCATTCATTGCCATTTGTT 4000
LPL 222 dGCTGCAACAATCTGGGCTAT eCACGGTGCCATACAGAGAAA 4000
MTHFR 243 dGAGGAAACAGCAGCCTCAAC eGACAGCTCCCTCAGCAGTTC 4000
THBD 250 dCGTGGGCTAGGGATGACTAA eAAGTGGGGCTTGCTTCATAA 4000
LCAT 257 dTGGAAGGACCGCTTTATTGA eAGCTGGGTGTGGAAATGAAC 8000
ATP5Oa 281 dATTGAAGGTCGCTATGCCA eTCGACCATTTTCAGCAAGC 8000
MMP9 293 dAATCCTACTCCGCCTGCAC eTCGCTGTCAAAGTTCGAGGT 4000
LDLR 314 dCACCACGGTGGAGATAGTGA eCTGTCTCGAGGGGTAGCTGT 4000
Knarb 325 dATCATCAGCATTGCATTCGATTCCTGTTTG eATTCCGACTCGTCCAACATC 1000
RPLP0a 330 dCTGATGGGCAAGAACACCAT eTGCCCCTGGAGATTTTAGTG 4000
ALOX5AP 342 dGGTCTACACTGCCAACCAGAA eTGGTGGTGGAGATCGTCTTT 4000
a  Housekeeping gene.

b  Internal control.

c  Housekeeping gene used for normalization.

d  Universal left sequence= 5’-AGGTGACACTATAGAATA…-3’.

e  Universal right sequence= 5’-GTACGACTCACTATAGGGA…-3’.

Note: Universal left and right sequence tags are linked to the left and right primer sequence of each gene, respectively.

Reverse transcription

Semi-quantitative reverse transcription polymerase chain reaction (RT-PCR) was performed using the GenomeLab GeXP Start Kit (GenomeLab) from Beckman Coulter (Fullerton, CA, USA). A total of 250 ng total RNA per well was used in the RT-PCR. A pool of all reverse primers was prepared at final concentrations of 4.0 μM to 8.0 μM in a final volume of 500 μl. Three different controls were performed for RT-PCR, including a reverse transcriptase minus (RT Minus) control (without reverse transcriptase), a no template control (without RNA) and kanamycin resistance gene RNA amplification as an internal reaction integrity control during cDNA synthesis. A total reaction volume of 20 μl for each sample was prepared and mixed gently followed by brief centrifugation. The RT-PCR mixture was incubated in a thermal cycler with the following program: 1 min at 48℃, 60 min at 42℃, and 5 min at 95℃, with a final hold at 4℃.

Polymerase chain reaction

Polymerase chain reaction (PCR) was then performed on each sample by adding 9.3 μl of cDNA from each previous RT-PCR to a pool of all forward primers at 0.2 μM in a final reaction volume of 20 μl containing 4 μl of 5X PCR buffer, 4 μl 25 mM MgCl2 (Thermo-Start) and 0.7 μl Thermo-Start DNA Polymerase (7 U). PCR was performed in a thermal cycler under the following conditions: 10 min at 95℃, followed by 35 cycles of 30 s at 94℃, 20 s at 55℃, and 1 min at 68℃, with a final hold at 4℃.

Fragment analysis

Sample loading solution (SLS) was prepared by adding 37.5 μl of SLS buffer (Beckman Coulter, Fullerton, CA, USA) and 0.5 μl of CEQ DNA size standard-400 (Beckman Coulter, Fullerton, CA, USA) to each reaction. Next, 2.0 μl of each PCR product was added into each well of a Beckman 96-well CEQ electrophoresis plate containing the SLS mixture. GeXP separates PCR products based on size through capillary gel electrophoresis. The dye signal strength was then measured in arbitrary units of optical fluorescence, which was defined as the fluorescent signal minus background (Ismail et al., 2010). The GeXP software matches each fragment peak with the appropriate gene. It then reports the peak height and area-under-the-curve (AUC) for all peaks in the electropherogram (Rai et al., 2009). Gene expression data were gathered and normalized to the internal control gene (KanR) with AUC set at 1 and evaluated with GenomeLab GeXP Quant Tool software (Beckman Coulter, Fullerton, CA, USA). For this data set, we chose ATP5O as our housekeeping normalization gene due to its ideal expression level. The data were then imported into the analysis module of eXpress Profiler software for gene normalization using our chosen ATP5O housekeeping gene and for subsequent analysis. Finally, all multiplexes were combined into one Excel data file for further statistical analysis.

Statistical analysis

Statistical analysis was carried out using Statistical Package for Social Sciences (SPSS) version 17.0. Student’s t-test was performed to compare the mean expression levels of each candidate gene between ACAT and NCAT samples. Significant differences were obtained at p values less than 0.05 (p<0.05).

RESULTS

Pathological cardiac findings by gross examinations

Gross examination findings showed the presence of severe atheroma in ACAT samples. These tissues were less elastic in structure compared to NCAT samples. In the most severe cases, the tissues were hardened, with abundant plaque accumulating along the arterial wall. NCAT samples, however, showed a clean lumen, with no atheroma observed along the wall of the coronary artery. In addition, the tissues were more elastic in structure than ACAT samples. Fig. 1 shows the gross examination images of ACAT and NCAT samples.

Fig. 1.

Gross examinations of left coronary artery tissues obtained from deceased subjects. A & B: NCAT samples with no evidence of atheroma formation. C & D: ACAT samples with the presence of severe atheroma (> 50% of stenosis), composed of fibrous plaque.

Pathological cardiac findings by microscopic examinations

The ACAT samples consisted of both stable and unstable atheromas, with 40% to 85% stenosis. Stable atheromas were composed of a thick fibrous cap (> 65 μm thickness), with no inflammatory cells within the plaques. In contrast, unstable atheromas (as shown in Fig. 1, C and D) were characterized by fibrous caps that were less than 65 μm thick, and the plaques were mainly composed of inflammatory cells, foaming macrophages, and necrotic cells. Fig. 2 shows stable and unstable atheromas with different degrees of stenosis and the presence of inflammatory cells, foaming macrophages, cholesterol clefts, calcification, and an old thrombus with evidence of organization and recanalization in the atheroma tissues.

Fig. 2.

A. The open, needle-like spaces in the atheromatous plaque are cholesterol clefts (cc). B. This section of coronary artery demonstrates remote thrombosis (t) with recanalization and organization. C. There is a large area of calcification (ca) on the upper left, which appear bluish on this H & E stain. D. This section of unstable atheroma shows numerous foam cells (fc), cholesterol clefts (cc) and the presence of a few dark blue inflammatory cells scattered within the atheroma. E. Stable atheroma with 40% stenosis. F. Unstable atheroma with 85% stenosis. Note: inflammatory cells (ic), lumen (lu), atheroma plaque (P), intima layer (I), media layer (M), adventitia layer (A), arrow indicating the thickness of atheroma; original magnification × 40 (C, E, &F); original magnification × 100 (A & D); original magnification × 200 (B).

Differential expression of candidate genes analysis in ACAT and NCAT samples

Prior to the quantitative analysis, optimization procedures were carried out for RT-PCR and GeXP analysis protocols. Each gene-specific primer pair was first tested in a single-plex reaction before analysis of the multiplex primer mix of the 11 selected gene-specific primers was carried out. This initial experiment was performed to confirm that no false fragments were produced and that only a single peak of the expected size was generated from each of the single-plex reaction analyses. During the multiplex assay, it was initially found that some of the candidate genes yielded low signal peaks in the gene panel. Thus, gene-specific reverse primer concentrations were optimized to improve detection in the multiplex reactions. The primer concentrations that gave optimal signal detection are listed in Table 3. Although we included three housekeeping genes in the multiplex reaction mixture, only two genes (e.g ATP5O and RPLPO) were chosen for normalization based on their expression levels suitability (Fig. 3). ATP5O normalized data revealed significantly altered expression of three candidate genes (LDLR, TP53, and MMP9) (Fig. 4A). LDLR, TP53, and MMP9 expressions were significantly up-regulated in ACAT samples. ATP5O normalized data also indicated up-regulation of TGFBR2, CBS, MTHFR, THBD, LCAT, and ALOX5AP gene expression in ACAT samples. However this data was not significant. Down-regulation of IRS1 and LPL expressions indicated in this analysis was also not significant. Meanwhile, RPLPO normalized data revealed fewer significantly altered expressions in the candidate genes when compared to ATP5O normalized data (Fig. 4B). The RPLPO normalized data demonstrated that MMP9 and TP53 expressions were significantly up-regulated in ACAT samples. Other genes showed broadly similar expression to those in ATP5O normalized data, with no significant result obtained. Table 4 displays the summary information of expression pattern from data being normalized by both housekeeping genes. This table compares ATP5O and RPLPO normalized data where expression pattern of candidate genes was marked together with its differential expression in fold change.

Fig. 3.

Representative electropherograms showing quantitative multiplex GeXP of candidate genes related to atherosclerosis using custom design GeXP multiplex assay. A: Candidate genes expression in atherosclerotic coronary artery tissue (ACAT) samples. B: Candidate genes expression in non-atherosclerotic coronary artery tissue (NCAT) samples. Housekeeping genes (a: Ezrin; j: ATP5O; n: RPLP0). Candidate genes (b: TP53; c: TGFBR2; d: CBS; e: IRS1; f: LPL; g: MTHFR; h: THBD; i: LCAT; k: MMP9; l: LDLR; o: ALOX5AP). Internal control gene (m: Knar). The size of detected amplicons in ACAT (A) and NCAT samples (B) are shown. The amplicons sizes were varying in two to three nucleotides from the actual product size.

Fig. 4.

Differential expression of 11 candidate genes assessed using GeXP analysis. Gene expression is normalized to two housekeeping genes ATP5O (A) and RPLPO (B) respectively. Each value was represented as Mean ± SD. * indicates significance at p<0.05.

Table 4. Gene expression pattern using ATP5O and RPLPO normalized data
Candidate genesATP5O normalized dataRPLPO normalized data
Gene expressionFold changeGene expressionFold change
TP53↑*1.963↑*1.245
TGFBR21.4391.421
CBS1.2021.672
IRS1–0.825–0.352
LPL–0.652–0.422
MTHFR1.7731.103
THBD1.7011.728
LCAT2.6471.134
MMP9↑*1.773↑*1.538
LDLR↑*3.9134.018
ALOX5AP1.2381.415

Note: Data normalized to ATP5O and RPLPO genes. (* indicates significance at p<0.05; ↑ indicates up-regulated gene; ↓ indicates down-regulated gene; and negative (–) sign indicates decrease in fold change.

DISCUSSION

The aim of this study was to assess the differential expression of 11 candidate genes associated with the risk of developing ATH in a Malaysian study population. These genes are important in physiological cellular and metabolic functions, such as the cholesterol transport pathway, the coagulation cascade, the inflammatory process and enzyme activities, thus, were classified into four different mechanisms or pathways based on their functions in the human body. Peripheral blood is the easiest source of RNA for differential expression of candidate genes experiments in both human and animal models. However, gene expression studies have been carried out recently using tissue samples instead for a better understanding of the gene expression pattern of a disease at a specific location. In our study, coronary artery tissue was used to study the differential expression of candidate genes in disease (ACAT) and non-disease (NCAT) samples. In this study, pathological cardiac findings for each tissue were confirmed by performing gross and microscopic examinations. These steps were crucial to ensure that all of the ACAT samples used in our study showed evidence of atheroma within the stated tissue region. Human coronary artery tissues were selected based on predetermined criteria as mentioned in the methods section. Subjects with conflicting diseases, such as diabetes and chronic inflammatory disease, were excluded from our study because complications of diabetes usually lead to CVD; thus, the possibility that the subject had already developed an initial stage of CVD. ATH itself is also closely linked to a disease of the inflammatory response. Patients with a chronic inflammatory disease might have a similar pattern of differential gene expression as those suffering from atherosclerotic disease. By taking these into account, we tried to avoid any potential interference in our study.

An ideal gene for normalization is one that shows consistency in expression levels and whose signal intensity is approximately half of the intensity of the candidate genes. For this matter, ATP50 and RPLPO were chosen for data normalization and subsequent statistical analysis in this study. In our study, four candidate genes related to cholesterol transport were assessed for their expression levels in ACAT and NCAT samples. Our findings showed that cholesterol transport-related genes, such as LCAT, LDLR, and ALOX5AP, were expressed from one-to four-fold higher in ACAT compared to NCAT samples. The LPL gene, in contrast, showed a slight down-regulation in atherosclerotic tissue of less than one-fold (Table 4). However, these differences were not statistically significant. Although the role of the LCAT gene in ATH is controversial, a previous study showed that heterozygocity of the LCAT gene leads to LCAT enzyme deficiency, which is associated with both atherogenic lipid profile and vascular abnormalities (Ayyobi et al., 2004). According to our findings, the LCAT expression pattern was slightly increased in ACAT samples compared to NCAT samples. However, there was no significant difference in this pattern. This result seemed to contradict the previous theory on LCAT expression levels being related to ATH (Hoeg et al., 1996). Kaaman et al. (2006) reported that the mRNA expression level of ALOX5AP in subcutaneous adipose tissue was increased in obese subjects and normalized following weight reduction. They suggested that the increased gene expression of ALOX5AP in adipose tissue was associated with an insulin-resistance phenotype, which was a risk factor for CVD. In our findings, there was only a slight increase in the ALOX5AP expression level in ACAT samples compared to NCAT samples. However, the significant increase in the LDLR gene expression profile suggested its positive association with ATH development. This finding corroborates the ideas of Salazar et al. (2000) who demonstrated that the LDLR gene polymorphism is associated with coronary artery disease (CAD) in Brazilian Caucasian women. The LDLR gene plays an important role in mediating the cellular uptake of plasma low-density lipoprotein (LDL). In general, high LDL levels and low HDL levels are associated with a high risk of CVD. Thus, the over-expression of the LDLR gene in this study may be an indicator that this gene could be associated with an increased risk of developing ATH in Malaysia.

Factors such as thrombin and fibrin have been known to contribute to ATH initiation and progression via the activation of tissue factor in the coagulation cascade (Marutsuka et al., 2005). Thrombin and fibrin act as procoagulant agents during blood clotting. One of the most frequent events in patients with acute myocardial infarction is blood clot formation resulting from plaque disruption in coronary arteries. Plaque disruption normally leads to the formation of a thrombus, which is carried by the blood stream and could cause vessels to become plugged. This condition reduces the blood supply to the heart, which leads to unstable angina, acute coronary syndrome, and in the worst scenario, sudden death. Thus, an endogenous anticoagulant factor, such as protein C, is important in maintaining the homeostatic balance in the coagulation cascade to prevent thromboembolic disease (Ohlin et al., 2004). Thrombomodulin, a product of the THBD gene, is known to play an opposite role to thrombin and fibrin. During the coagulation cascade, thrombomodulin binds to thrombin to activate protein C. Activated protein C inhibits the procoagulant pathway by degrading activated factors V and VIII (Salomaa et al., 2001). The thrombomodulin-thrombin complex changes the activity of thrombin from pro-coagulation to anti-coagulation (Zhao et al., 2005). The inhibition of further thrombin formation in the coagulation cascade by the thrombomodulin-thrombin complex thereby limits blood coagulation. In addition, this complex inhibits fibrinolysis by cleaving thrombin-activatable fibrinolysis inhibitor (TAFI) into its active form. Because thrombomodulin is an important link between coagulation and fibrinolysis, the down-regulation of its gene expression level could impair its function in anti-coagulation. In our study, we assessed the expression level of the THBD gene in both ACAT and NCAT samples to determine its association with ATH development. We found a slight increase in THBD gene expression in ACAT compared to NCAT samples, although this increase was not significant. The up-regulated pattern of the THBD gene level in our study seemed to clash with the theory of THBD function. However, the conflicting data might be due to the small sample size.

Two of the candidate genes in this study are inflammation-related genes. In our findings, both TP53 and TGFBR2 showed higher expression levels in ACAT compared to NCAT samples. Although the difference in TGFBR2 gene expression in ACAT and NCAT samples was not significant, the expression of the TP53 gene was significantly increased in ACAT compared to NCAT samples. Its expression level is low in normal cells but high in transformed cell lines. We found in our study that the TP53 level was up regulated in ACAT, suggesting that the TP53 gene contributes to the progression of ATH development. These findings further support the idea of Beiras-Fernandez et al. (2011), who suggested that polymorphisms in the TP53 gene increased the risk of CAD progression. A previous study also suggested that cellular death by apoptosis occurs within atherosclerotic lesions (Lesauskaite et al., 2003). Thus, because the TP53 gene can promote apoptosis, it is not surprising that the loss of TP53 functions leads to an increased progression of ATH.

In a complex disease such as ATH, enzyme activities greatly influence the complex cascade of ATH development. MTHFR, CBS, MMP9, and IRS1 genes were assessed for their association with ATH development due to their involvement in the important pathways within atherosclerotic lesion development. We found an increase in MTHFR and CBS expression in ACAT compared to NCAT samples. However, due to limited sample size, we were unable to demonstrate significant differences in their expression between the two groups. The expression of the MMP9 gene was significantly increased in ACAT compared to NCAT samples. In normal adult tissue, the expression of matrix metalloproteinases (MMPs) is usually low. Although a slight down-regulation of IRS1 gene expression was noted, there was no significant difference in the gene expression level reported in this study (less than one-fold decrease). Matrix metalloproteinases (MMPs) are a family of 24 proteins with different substrate specificities. They include extracellular matrix (ECM) and cell surface proteins (Newby, 2007). In normal adults, the expression of MMPs is low. However, during physiological and pathological remodeling processes, their expression is up-regulated. The increased of MMPs expressions has also been reported within atherosclerotic plaques (Sukhova et al., 1999). Thus, our present findings seem to be consistent with other research, which found a similar pattern of MMP9 expression in atherosclerotic tissues. As mentioned earlier, the slight decrease in IRS1 gene expression level in ATH tissue was not significant. Nevertheless, the pattern of IRS1 gene expression was in agreement with previous studies performed by other researchers. This insignificance could most likely be due to our small sample size.

In conclusion, our preliminary findings showed that the LDLR, TP53, and MMP9 genes were possible predictors for susceptibility factors in developing ATH. Although the other candidate genes had been suggested to have an association with CAD in previous studies, they did not show a significant association in this present study. The main reason for this result is most likely due to the relatively small number of ACAT and NCAT samples, which limited our findings. Further studies with a larger sample size are recommended to conclude the influence of these genes on ATH progression with certainty. This will help in revealing a more significant association of candidate genes associated with ATH development in a Malaysian study population.

ACKNOWLEDGMENT

We thank all the staff and forensic pathologists at the Forensic Department of Hospital Serdang, Serdang, Selangor, and Hospital Kuala Lumpur, Kuala Lumpur, Malaysia, respectively, for help in supplying the samples involved in this study. Special appreciation is also extended to Miss Chow Woan Yun from Beckman Coulter for her excellent technical assistance. This study was supported by the IRPA 06-02-04-0482 research grant.

REFERENCES
 
© 2013 by The Genetics Society of Japan
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