Logo of jlrAbout JLRASBMBJLRContactSubscriptionsSubmissionsThis Article
J Lipid Res. 2010 Jan; 51(1): 103–111.
PMCID: PMC2789770

Allele-specific regulation of MTTP expression influences the risk of ischemic heart disease[S]


Promoter polymorphisms in microsomal triglyceride transfer protein (MTTP) have been associated with decreased plasma lipids but an increased risk for ischemic heart disease (IHD), indicating that MTTP influences the susceptibility for IHD independent of plasma lipids. The objective of this study was to characterize the functional promoter polymorphism in MTTP predisposing to IHD and its underlying mechanism. Use of pyrosequencing technology revealed that presence of the minor alleles of the promoter polymorphisms -493G>T and -164T>C result in lower transcription of MTTP in vivo in the heart, liver, and macrophages. In vitro experiments indicated that the minor -164C allele mediates the lower gene expression and that C/EBP binds to the polymorphic region in an allele-specific manner. Furthermore, homozygous carriers of the -164C were found to have increased risk for IHD as shown in a case-control study including a total of 544 IHD patients and 544 healthy control subjects. We concluded that carriers of the minor -164C allele have lower expression of MTTP in the heart, mediated at least partly by the transcription factor CCAAT/enhancer binding protein, and that reduced concentration of MTTP in the myocardium may contribute to IHD upon ischemic damage.

Keywords: promoter activity, lipotoxicity, lipid accumulation, myocardium

The microsomal triglyceride transfer protein (MTTP) is essential for formation of apolipoprotein B (apoB)-containing lipoproteins. The liver and the intestine have the highest tissue expression of MTTP and secrete triacylglycerol (TAG)-rich VLDLs and chylomicrons, respectively (1). MTTP is also expressed in other cells such as cardiomyocytes (2) and macrophages (3). The heart secretes apoB100-containing lipoproteins and it has been proposed that cardiac lipoprotein secretion protects the heart against accumulation of lipids that are toxic to the myocardium (4). This theory is supported by the finding that MTTP expression is inversely correlated with the concentration of TAGs in the myocardium. Thus, ischemia-induced TAG accumulation in the myocardium might be mitigated by increased MTTP expression in the myocardium (5).

The -493G>T single nucleotide polymorphism (SNP) in MTTP (rs1800591) has been associated with metabolic traits and ischemic heart disease (IHD) (6). Homozygosity for the minor -493T allele appeared to confer an increased risk for IHD in two studies, the West of Scotland Coronary Prevention Study (WOSCOPS) and the Uppsala Longitudinal Study of Adult Men (ULSAM), together comprising 680 patients with IHD (6).

The -493G>T polymorphism is in linkage disequilibrium (LD) with two other SNPs in MTTP, the -164T>C (rs1800804) and Ile128Thr (rs3816873) (7, 8). It is not known which of these three SNPs are functional in vivo, and few studies have addressed tissues other than the liver and intestine. The MTTP promoter is well characterized, and it has been shown that the first 200bp in the proximal promoter determines the basal expression and regulation of MTTP (9).

We hypothesized that MTTP promoter polymorphisms alter the expression of the gene in the heart, thereby affecting lipid accumulation in the myocardium and thus, susceptibility to ischemia. Against this background, we investigated the in vivo allele-specific mRNA expression of MTTP in human heart, liver, and macrophages. We also characterized the underlying mechanism to the allele-specific gene expression and investigated the association between the MTTP polymorphisms and IHD in a Swedish case-control study.


Biopsies from the human heart

Nine left ventricular biopsies were obtained from subjects who were heterozygous for the -493G>T, -164T>C, and Ile128Thr SNPs. The biopsies were from a biobank of left ventricular biopsies taken from patients undergoing heart valve surgery. The nine biopsies obtained were all from patients with tricuspid valves. The nine patients were of Caucasian origin and none of them had type 2 diabetes (T2D). Basic characteristics are shown in Supplementary Table I. Subjects had given their written informed consent to participate. The study was approved by the ethics committee at the Karolinska Institutet, Stockholm, Sweden.

Liver biopsies from individuals with hepatic steatosis

Liver samples were obtained from 25 Caucasian subjects with various degrees of liver steatosis. Total RNA was isolated and cDNA generated according to standard protocols. Twelve of these individuals were found to be heterozygous for the MTTP polymorphisms and were subsequently examined. None of the 12 individuals suffered from T2D. Basic characteristics are shown in Supplementary Table I. Subjects had given their written informed consent to participate. The study was approved by the ethics committee of the Helsinki University Hospital (10).

Primary monocytes from healthy individuals

A total of 16 healthy individuals with known genotypes for the -493G>T, -164T>C and Ile128Thr polymorphisms were recruited among Caucasian participants from a previous population screening (6). Of these individuals, six were heterozygous for the MTTP polymorphisms, six were homozygous for the major alleles and four were homozygous for the minor alleles. Basic characteristics are shown in Supplementary Table I. The study was approved by the ethics committee at the Karolinska Institutet, Stockholm, Sweden. Approximately 100 ml blood was drawn from each individual and primary blood monocytes were isolated using Ficoll-Paque according to the manufacturer's instructions (GE Healthcare Bio-Sciences). The isolated primary cells were differentiated into macrophages by PMA treatment as described (11). To allow complete differentiation, the cells were cultured for another 60 h at 37°C. The macrophages were cultured under basal conditions. Total RNA was isolated and reverse transcribed using Superscript II (Invitrogen). Subjects gave their informed consent to participate.

Allele-specific gene expression assay

The Ile128Thr polymorphism in MTTP was used as a marker for the allele-specific expression of the -493G>T and -164T>C polymorphisms. Pyrosequencing technology (Biotage) was used to compare the relative allelic expression in subjects heterozygous for these three SNPs. A fragment of approximately 100 base pairs surrounding the Ile128Thr polymorphism was amplified by PCR from cDNA or genomic DNA. Forward primers were biotinylated. Single-stranded PCR fragments were separated and sequenced with the use of PyroGold reagents and the PSQ 96MA Pyrosequencing machine and software version 2.0.2. To normalize signals from different fluorescent dyes, a standard curve for the cDNA assay was used as shown in Supplementary Fig. I. Genomic DNA with expected perfect 1:1 allele ratio was included as a control. The method has been described elsewhere (12). Primer sequences are given in Table 1.

Primers and oligonucleotides used in current study

Transient transfections and luciferase assay

Minimal promoter constructs containing the -164T>C SNP (-179 to -148) were based on four sets of complementary oligonucleotides. The oligonucleotides were annealed and cloned into the pGL3-promoter vector (SDS Promega) using BglII and BamH1 restriction sites as described (13). Longer promoter fragments were amplified from genomic DNA from two subjects homozygous for the major or minor alleles of the -493G>T and -164T>C SNPs, respectively. The amplified MTTP promoter region spans from -593 to +27, relative to the transcriptional start site. For cloning purposes, the primers were flanked by Nhe1 and BglII restriction sites. The amplified PCR products were cloned into pGL3-basic vector (SDS Promega). The longer promoter fragments includes proximal promoter and the transcription start site and do not require a reporter that contains promoter sequence to generate transcriptional activity, as measured by the luciferase assay. All constructs were verified by DNA sequencing according to the manufacturer's protocol (ABI). Primer and oligonucleotide sequences are given in Table 1.

The cell lines used in this study (HepG2, Huh7, and HeLa) were maintained in Dulbecco's modified Eagle's medium, supplemented with 10% FBS and 0.6% penicillin-streptomycin, in 6-well plates. The Dual Luciferase Reporter Assay System from SDS Promega was used for the transfection assays. The cells received fresh medium 3 h before transfection. The cells were then cotransfected with 3 μg/well CaCl2 precipitated pGL3-promoter or pGL3-basic vector and 1 μg/well control vector pRL-TK. The luciferase and Renilla luciferase activities were measured 48 h after transfection according to the manufacturer's protocols. Assays were performed under basal conditions or in the presence of 100 nM insulin. Insulin was added 48 h prior to harvesting the cells. All assays were performed in triplicate.

In order to investigate if CCAAT/enhancer binding proteins (C/EBPs) had any direct effect in the allele-specific expression of MTTP, HeLa cells, which do not express MTTP and only express C/EBP at low levels, were cotransfected with plasmids comprising the MTTP promoter (-593 to +27) and PCMV5 expression vectors containing C/EBPα, C/EBPβ, or C/EBPδ. The C/EBP expression vectors were a kind gift from Dr. Magnus Nord, Karolinska Institutet. Transient transfections and luciferase assay were performed as described above.


For electrophoretic mobility shift assays (EMSAs), complementary oligonucleotides containing the -164 polymorphic site, C/EBP consensus, and a sterol response element (SRE), which binds sterol response element binding protein 1 (SREBP-1), were annealed. Nuclear extracts were prepared from HepG2 or Huh7 liver cell lines as described (14), and competitive EMSAs were performed with labeled oligonucleotide corresponding to 50,000 cpm and 100-fold excess for competition with cold oligonucleotide. To investigate the potential binding of SREBP-1, HepG2 cells were transfected with an SREBP-1 expression vector before harvesting. Successful cloning was verified by sequencing (ABI). For the supershift assay, 1 μg/lane of human anti-SREBP-1 antibody was added to the mixture and incubated for 10 min at room temperature before loading onto the gel. The antibodies were a kind gift from Dr. Jay Horton, Southwestern Medical Center, Dallas, TX. The EMSA experiment was performed as described (15). Primer sequences are shown in Table 1.

Case-control study (INTERGENE)

The case-control study is part of the INTERGENE study and includes 544 validated IHD patients and 544 age- and sex-matched control subjects living in the Västra Götaland region of Sweden. INTERGENE is a cohort designed to study the interplay between genetic susceptibility, environmental factors, lifestyle, gender, and established risk factors in cardiovascular disease. The patients were survivors of acute coronary syndrome (ACS) and were identified from the same source population as the sampled cohort. There was no lower age limit for the first event and the upper age limit was 75. ACS comprises both acute myocardial infarction [International Classification of Diseases (ICD) 10: I21.0-I21.9] and unstable angina pectoris (ICD 10: I20.0). Previously-known coronary cases with new attacks as well as first time patients were included. The patients and controls were 61.1 ± 8.4 and 61.2 ± 8.4 years old, respectively, and 28% were women. The participants had given their informed written consent to participate. The study was approved by the local ethics committee. Full description of the study is available at www.sahlgrenska.gu.se/intergene (16).


Genomic DNA from subjects included in the case-control cohort and in the allele-specific gene expression assay was isolated from venous blood according to standard protocols. The subjects were genotyped for the -493G>T (rs1800591G>T) and the -164T>C (rs1800804T>C) polymorphisms by TaqMan Technology (ABI). The call rates were above 96% for both the -493G>T and -164T>C assays. The -493G>T and -164T>C position are relative MTTP transcription start site according to RefSeq NM_000253.1.

Statistical analyses

Statistical analyses were conducted using the SAS 9.1.3 software (SAS Institute, Inc., Cary, NC). Hardy-Weinberg equilibrium and differences in genotype distributions were assessed using χ2 tests. Pairwise linkage disequilibrium was estimated using a maximum-likelihood Expectation Maximization algorithm implemented in the Haploview 4.0 software (17). Continuous variables that did not adhere to a normal distribution were normalized by logarithmic transformation prior to statistical analyses. Differences between groups were estimated by unpaired t-test and one-way ANOVA using Fisher's protected least significant difference test for post hoc analysis. Odds ratios (ORs) with corresponding 95% confidence intervals (CI) were calculated using logistic regression analysis and adjusted for age and gender. Linear regression was applied on the standard curve used in the allele-specific gene expression assay. The Wilcoxon sign rank test was employed to detect any differences in allelic ratio as measured by pyrosequencing technology. P values < 0.05 were considered significant.


Allele-specific gene expression of MTTP in the human heart, liver, and macrophages

To investigate whether the -493G>T and -164T>C SNPs influence transcriptional activity in vivo, the allele-specific gene expression of MTTP was analyzed by pyrosequencing technology in human tissue biopsies from the heart, liver, and macrophages.

The pyrosequencing technology was employed because the method can detect small differences in relative gene expression from each chromosome with high accuracy. Analyses need to be performed in material from individuals heterozygous for the polymorphism(s) of interest. Any imbalance in expression levels between two alleles is, thus, measured within the same individual, hence, minimizing the cis- and trans-acting effects. The allele-specific gene expression of MTTP was measured in individuals heterozygous for the -493G>T, -164T>C, and Ile128Thr polymorphisms that are in perfect LD. The results show that the expression of the minor alleles of the MTTP polymorphisms was significantly lower compared with the major alleles in the heart (P = 0.004), liver (P = 0.001), and macrophages (P = 0.031) (Fig. 1). Genomic DNA from the same individuals was used as control and the allele ratio for the DNA was 50% as expected (Fig. 1). Thus, the minor -493T/-164C alleles are expressed at lower levels than the major -493G/-164T alleles in vivo.

Fig. 1.
In vivo allele-specific gene expression of MTTP in heart, liver, and macrophages. The pyrosequencing assay measured the relative amount (%) of the major 128Ile and the minor 128Thr alleles in heterozygous individuals, thus revealing the allele-specific ...

Allele-specific MTTP promoter activity

In contrast to the above in vivo result, our previous in vitro results showed that the minor -493T allele has increased promoter activity compared with the -493G allele when using minimal promoter constructs (13). Inasmuch as the -493G>T and -164T>C polymorphisms are on the same haplotype, we set out to determine whether the -164T>C SNP influences transcriptional activity per se or in combination with the -493G>T SNP. For this purpose, transient transfection assays were performed in a hepatoma cell line (HepG2) that endogenously expresses MTTP. Transfections using minimal promoter constructs spanning only the -164 site showed that the minor -164C allele conferred a 30% decrease in transcriptional activity compared with the major -164T allele (P = 0.004) (Fig. 2).Constructs containing both the minor -493T and the -164C alleles (-593 to +27) also resulted in a 30% decrease in transcriptional activity compared with constructs containing both major -493G/-164T alleles (P = 0.02) (Fig. 2). Insulin is known to downregulate the MTTP promoter activity (18) and the insulin-response element is present in the proximal promoter of MTTP (bp -123 to -112) (9); therefore, the cells were treated with 100 nM insulin as a positive control. Addition of insulin further decreased the MTTP promoter activity by 30% (P = 0.004) compared with untreated cells, showing that the reporter gene constructs responded to insulin treatment as expected (Fig. 2). The difference in promoter activity between the major -493G/-164T alleles and the minor -493T/-164C alleles was attenuated when cells were treated with insulin (Fig. 2). The in vitro results are in agreement with the in vivo results and indicate that the minor -164C allele mediates the decreased transcriptional activity.

Fig. 2.
Transcriptional activity of MTTP promoter constructs. Relative luciferase activity from constructs spanning the -164T>C polymorphic site from position -179 to -148 in the MTTP promoter and from constructs spanning both the -164T>C and ...

Allele-specific binding of C/EBP to the -164T>C polymorphic site

The -164 polymorphic site comprises both a putative C/EBP response element and a putative SRE (Fig. 3A). The major -164T allele is homologous to the C/EBP response element. MatInspector predicted a C/EBP binding site across the -164 polymorphic region when the promoter sequence containing the major T-allele was used (Core Similarity = 1.000). When the T allele was changed to the C allele, MatInspector could not predict the C/EBP binding site. MatInspector did not predict any SRE across the -164 polymorphic site with either the T or C allele, respectively. However, earlier studies showed that a putative SRE similar to the one found in the LDL-receptor (LDLR) gene is present across the -164 region (9, 19). The minor -164C allele shows higher homology with the putative SRE (Fig. 3A). EMSAs were performed to investigate potential binding of these nuclear factors.

Fig. 3.
Allele-specific binding of nuclear factor to the -164 polymorphic site. A: DNA sequence from position -173 to -156 in the MTTP promoter. The -164T>C site is shadowed in gray. Sequence containing the major T-allele shows homology to the C/EBP binding ...

The major -164T allele oligonucleotide bound more strongly to nuclear factors compared with the minor -164C allele oligonucleotide. A 100-fold excess of an unlabeled -164T oligonucleotide competed against this binding whereas a nonspecific DNA sequence had no effect on the binding (Fig. 3B).

Competitive EMSA with labeled C/EBP consensus oligonucleotide and -164T and -164C oligonucleotides showed that an excess of unlabeled C/EBP oligonucleotide competes the binding of nuclear factors to the -164T oligonucleotide. In contrast, we could not detect any binding of C/EBP to the -164C allele (Fig. 3C).

The SRE across the -164 polymorphic site, similar to the one found in the LDLR promoter, is known to bind SREBP-1 (19). The binding of SREBP-1 to the polymorphic site at position -164 was investigated using nuclear extracts from HepG2 cells overexpressing SREBP-1. The LDLR-SRE consensus oligonucleotide was used as a positive control. Supplementation with SREBP-1 antibody generated a clear supershift of the LDLR-SRE complex but no supershift was detected for the nuclear complexes containing the -164T or the -164C oligonucleotides (Fig. 4A, B). These results indicate that C/EBP bound more strongly to the major -164T allele than the minor -164C allele and that SREBP-1 did not bind to the -164 polymorphic site in an allele-specific manner.

Fig. 4.
Binding of SREBP-1 to LDLR-SRE but not to the -164 site. A: EMSA with nuclear extract from the liver cell line HepG2, overexpressing SREBP-1 and the radioactive probe comprising the LDLR-SRE consensus sequence (lanes 1–3), the major -164T allele ...

C/EBPs mediate allele-specific gene expression of the MTTP gene

In order to investigate if C/EBPs affect the promoter activity of MTTP per se in an allele-specific manner, transient transfection assays were performed in HeLa cells. HeLa cells do not have endogenous expression of MTTP, which minimizes the background signals and allows detection of any direct influences of C/EBPs on the transcription of the two promoter variants (i.e., -493G/-164T and -493T/-164C), respectively. For this purpose, HeLa cells were cotransfected with pGL3-basic containing the promoter constructs (-593 to +27) and expression vectors containing C/EBPα, C/EBPβ, or C/EBPδ, respectively. In accordance with the results based on EMSA experiments, the presence of C/EBPα and C/EBPδ increased the transcriptional activity for the major -493G/-164T alleles compared with the minor -493T/-164C alleles (Fig. 5). We conclude that C/EBPα and C/EBPδ are critical for the effect on transcriptional activity mediated by the -164T>C polymorphism.

Fig. 5.
C/EBP isoforms influence MTTP promoter activity in an allele-specific manner. Relative luciferase activity measured in HeLa cells cotransfected with luciferase pGL3-basic vector containing the MTTP promoter spanning from position -593 to +27, and PMCV5 ...

Association of the MTTP -164T>C promoter polymorphism with IHD

The relationship between the -164T>C SNP and IHD was investigated in a Swedish case-control cohort (INTERGENE) consisting of 544 patients and 544 sex- and age-matched control subjects. The subjects were genotyped for the -493G>T and -164T>C SNPs, which were found to be in perfect LD (D' = 1.0, r2 = 1.0).

The minor allele frequency of the -164T>C polymorphism in the MTTP promoter was 0.25 in patients and 0.22 in controls and the genotype distributions adhered to the Hardy-Weinberg equilibrium in both groups. Homozygous carriers of the minor -164C allele (or the -493T allele) were found to have a higher risk for IHD after adjustment for age and gender: 1.76 (1.03–2.99) [OR (95% CI)], P = 0.038. The OR for heterozygous individuals was 1.13 (0.88–1.45), P = 0.36.


In this study, we demonstrated an allele-specific expression of MTTP predisposing to IHD. In summary, the minor alleles of the -493G>T and -164T>C SNPs conferred lower expression of MTTP in the human heart, liver, and macrophages. In vitro experiments revealed that the minor -164C allele is critical in mediating the lower transcriptional activity. C/EBP did not bind to the minor -164C allele but had strong affinity for the major -164T allele. Finally, homozogosity for the -164C allele was associated with increased risk of IHD. On the basis of these results, we propose that the -164T>C SNP alters the MTTP expression and, thus, influences the susceptibility to IHD.

It is postulated that MTTP is important in the heart for secretion of intracellular lipids, which may be toxic to the myocardium at high concentration (5, 20). The finding that the minor -164C allele conferred decreased MTTP mRNA expression compared with the major -164T allele is consistent with our previous study showing that individuals carrying the -493T allele, and hence also the minor -164C allele, have lower MTTP mRNA concentrations in the atrium of the heart compared with carriers of the common allele (6). Of note, homozygote individuals also had electrocardiogram abnormalities independent of preexisting heart disease (6). Furthermore, it has been shown that decreased transcription of MTTP mRNA is inversely correlated with intracellular TAG concentrations in human hearts (5). Cardiac lesions and excessive deposition of lipochrome pigment have been reported in abetalipoproteinema, a rare recessive monogenic disease caused by mutation in MTTP (21, 22). Furthermore, tissue-specific knockout mice that lack MTTP expression in the heart show cardiac lipid accumulation (4). Taken together, these results suggest that a functional MTTP protein is important for cardiac lipid metabolism and that the minor alleles of the three MTTP polymorphisms examined here, specifically the -164C variant, contribute to TAG accumulation in the myocardium.

Cardiac lipid accumulation has been proposed to contribute to the high mortality following infarction in subjects with T2D (23). Ischemia in the heart induces both MTTP and APOB expression in the myocardium and increases cardiac lipoprotein production and MTTP expression is negatively related to TAG storage in myocardial cells (5). Animal studies have shown that overexpression of apob impedes cardiac TAG accumulation (24) and protects against lipotoxic cardiomyopathy (25). Furthermore, it has recently been shown that overexpression of MTTP decreases fat accumulation and increases secretion of apoB100-containing particles (26), together suggesting that MTTP has a protective role against lipotoxicity.

MTTP is also expressed in antigen-presenting cells such as macrophages (3). In the atherosclerotic lesion, macrophages internalize oxidized LDL through the scavenger receptor, a process eventually converting them into foam cells. Little is known about the function of MTTP in macrophages but it is conceivable that MTTP is involved in foam cell formation and plaque development. In this study, the minor MTTP -164C allele was associated with lower expression of MTTP in macrophages but whether this contributes to foam cell formation and progression of atherosclerosis or plaque instability needs to be elucidated.

MTTP is highly expressed in the liver and is crucial for the formation of VLDL (1). The expression of the minor MTTP -164C allele in liver deviated slightly from that of the major -164T allele (Fig. 1), and no association between the -164T>C SNP and plasma lipid or lipoprotein concentrations was found in the case-control cohort (data not shown). It seems reasonable to assume that the high constitutive expression of MTTP in the liver attenuates the downstream effects of the allele-specific gene expression mediated by the -164T>C SNP on plasma lipid and lipoprotein concentrations. Of note, the samples used in our study were obtained from both healthy individuals and patients. The monocytes were isolated from healthy individuals whereas the liver biopsies were obtained from individuals with various degrees of liver fat content and the heart biopsies from patients undergoing aortic heart valve surgery. Despite this diverse background of individuals, the results were similar in all three tissues/groups.

In this study, we showed, both in vivo and in vitro, that the minor allele of the -164T>C SNP resulted in lower transcription of the gene. This is in contrast with our earlier in vitro results from HepG2 cells, showing that the minor allele of the -493G>T polymorphism was associated with higher promoter activity compared with the major allele, using minimal promoter constructs comprising only the -493G>T SNP (13). However, an additional effect of the -493G>T polymorphism cannot be excluded from these experiments, which would require constructs of the same length with only one polymorphic site included in each promoter construct. Nonetheless, genetic linkage studies have shown that these two polymorphisms are always inherited together. Rubin et al. (27) recently reported that the minor alleles of the -493G>T and -164T>C SNPs result in higher promoter activity compared with the major alleles when Caco-2 cells originating from human intestine were transfected with MTTP promoter constructs spanning from -966 to -1 not including the transcriptional start site. However, they could not detect any significant differences in allele-specific promoter activity when Huh7 liver cells were used (27). Of note, these two promoter studies did not include in vivo analyses and it has recently been shown that in vitro analyses often fail to predict in vivo effects of regulatory polymorphisms (28), indicating the need for assessing the effect of polymorphisms in native tissues.

We previously reported that the Ile128Thr polymorphism influences the interaction between MTTP and apoB. The threonine allele had decreased thermal stability and weakened binding to apoB compared with the isoleucine allele (29). Taken together, our results suggest that homozygosity for the minor -164C and 128Thr alleles has both reduced MTTP expression and a less functional protein.

Here, we showed that the -164T>C SNP predisposed to IHD in a study of 544 patients and 544 control subjects. We also showed that the -164T>C and the -493G>T SNPs were in perfect allelic association. This is in agreement with previous results from the WOSCOPS and ULSAM studies where the -493TT genotype was associated with higher risk of IHD (6). Of note, analyses based on combined data from the INTERGENE, WOSCOPS, and ULSAM studies yielded a common Mantel-Haenszel OR of 1.64 (1.20–2.25) with a Cochran-Mantel-Haenszel Statistic of 9.49 (P = 0.002), the odds ratios being homogeneous across all studies (P = 0.14, Breslow-Day test).

In contrast to the above result, there was no significant association between the -493G>T or -164T>C SNPs and cardiovascular end points in the Framingham Offspring Study (consisting of 212 IHD patients and 2,510 control subjects) (30) and the ECTIM study (consisting of 622 male patients with myocardial infarction and 728 age-matched controls from Ireland and France) (31). Possible explanations for the lack of association in these studies might be different study designs and ethnicities. Validation in prospective studies is needed as well as more in-depth knowledge about the function and regulation of MTTP in the heart and macrophages. In addition, the influence of other polymorphisms that are in allelic association with the studied SNPs cannot be excluded. However, the -493G>T, -164T>C, and Ile128Thr are in perfect LD and lie in a haploblock clearly distinguished from the 3′ region of the gene, including the 3′-UTR in MTTP (Supplementary Fig. II). Any influences of potential functional polymorphisms located 3′ in MTTP are, thus, unlikely. The -164T>C polymorphism lies in the proximal promoter of MTTP that has been shown to regulate the basal transcription of the gene (9). Therefore, it is likely that the -164T>C polymorphism has a profound effect on the observed allele-specific gene expression. However, other polymorphic sites may also affect the expression and regulation of MTTP.

In summary, we have shown that the minor MTTP -164C variant resulted in lower expression of MTTP in the heart, liver, and macrophages, most likely due to a reduced binding of C/EBPs. The -164C allele was associated with increased risk for IHD and we postulate that lower concentration of MTTP results in increased lipid accumulation in the myocardium and, thus, increased susceptibility to IHD. We hypothesize that MTTP inhibitors could have severe long-term side effects related to myocardial function and it is important not only to study MTTP in the liver, but also in the heart and other tissues, to fully understand its potential side effects when used as a drug target.


The authors thank the patients and the healthy individuals for their participation; Professor Mai-Lis Hellenius, Karolinska Institutet, for clinical expertise regarding recruit by genotype; Dr Jacob Odeberg, Karolinska Institutet, for his input and know-how about pyrosequencing methodology, and Dr Fredrik Karpe, Oxford, for his scientific advice concerning this project



acute coronary syndrome
apolipoprotein B
CCAAT/enhancer binding protein
confidence interval
electrophoretic mobility shift assay
International Classification of Diseases
ischemic heart disease
linkage disequilibrium
low density lipoprotein receptor
microsomal triglyceride transfer protein
odds ratio
single nucleotide polymorphism
sterol response element
sterol response binding protein 1

This work was supported by the Swedish Medical Research Council [12659], the Heart and Lung Foundation, the Swedish Diabetes Foundation, the Swedish Foundation for Strategic Research, Karolinska Institutet Funds, and a donation by Fredrik Lundberg.

[S]The online version of this article (available at http://www.jlr.org) contains supplementary data in the form of one table and two figures..


1. Shoulders C. C., Shelness G. S. 2005. Current biology of MTP: implications for selective inhibition. Curr. Top. Med. Chem. 5: 283–300 [PubMed]
2. Nielsen L. B., Veniant M., Boren J., Raabe M., Wong J. S., Tam C., Flynn L., Vanni-Reyes T., Gunn M. D., Goldberg I. J., et al. 1998. Genes for apolipoprotein B and microsomal triglyceride transfer protein are expressed in the heart: evidence that the heart has the capacity to synthesize and secrete lipoproteins. Circulation. 98: 13–16 [PubMed]
3. Dougan S. K., Salas A., Rava P., Agyemang A., Kaser A., Morrison J., Khurana A., Kronenberg M., Johnson C., Exley M., et al. 2005. Microsomal triglyceride transfer protein lipidation and control of CD1d on antigen-presenting cells. J. Exp. Med. 202: 529–539 [PMC free article] [PubMed]
4. Bjorkegren J., Veniant M., Kim S. K., Withycombe S. K., Wood P. A., Hellerstein M. K., Neese R. A., Young S. G. 2001. Lipoprotein secretion and triglyceride stores in the heart. J. Biol. Chem. 276: 38511–38517 [PubMed]
5. Nielsen L. B., Perko M., Arendrup H., Andersen C. B. 2002. Microsomal triglyceride transfer protein gene expression and triglyceride accumulation in hypoxic human hearts. Arterioscler. Thromb. Vasc. Biol. 22: 1489–1494 [PubMed]
6. Ledmyr H., McMahon A. D., Ehrenborg E., Nielsen L. B., Neville M., Lithell H., MacFarlane P. W., Packard C. J., Karpe F. 2004. The microsomal triglyceride transfer protein gene-493T variant lowers cholesterol but increases the risk of coronary heart disease. Circulation. 109: 2279–2284 [PubMed]
7. Ledmyr H., Karpe F., Lundahl B., McKinnon M., Skoglund-Andersson C., Ehrenborg E. 2002. Variants of the microsomal triglyceride transfer protein gene are associated with plasma cholesterol levels and body mass index. J. Lipid Res. 43: 51–58 [PubMed]
8. Neville M. J., Clarke R., Evans J. G., Rubinsztein D. C., Karpe F. 2007. Absence of relationship between MTTP haplotypes and longevity. J. Gerontol. A. Biol. Sci. Med. Sci. 62: 202–205 [PubMed]
9. Hagan D., Kienzle B., Jamil H., Hariharan N. 1994. Transcriptional regulation of human and hamster microsomal triglyceride transfer protein genes. Cell type-specific expression and response to metabolic regulators. J. Biol. Chem. 269: 28737–28744 [PubMed]
10. Westerbacka J., Kolak M., Kiviluoto T., Arkkila P., Siren J., Hamsten A., Fisher R. M., Yki-Jarvinen H. 2007. Genes involved in fatty acid partitioning and binding, lipolysis, monocyte/macrophage recruitment, and inflammation are overexpressed in the human fatty liver of insulin-resistant subjects. Diabetes. 56: 2759–2765 [PubMed]
11. Whatling C., Bjork H., Gredmark S., Hamsten A., Eriksson P. 2004. Effect of macrophage differentiation and exposure to mildly oxidized LDL on the proteolytic repertoire of THP-1 monocytes. J. Lipid Res. 45: 1768–1776 [PubMed]
12. Wang H., Elbein S. C. 2007. Detection of allelic imbalance in gene expression using pyrosequencing. Methods Mol. Biol. 373: 157–176 [PubMed]
13. Karpe F., Lundahl B., Ehrenborg E., Eriksson P., Hamsten A. 1998. A common functional polymorphism in the promoter region of the microsomal triglyceride transfer protein gene influences plasma LDL levels. Arterioscler. Thromb. Vasc. Biol. 18: 756–761 [PubMed]
14. Alksnis M., Barkhem T., Stromstedt P., Ahola H., Kutoh E., Gustafsson J., Poellinger L., Nilsson S. 1991. High level expression of functional full length and truncated glucocorticoid receptor in Chinese hamster ovary cells. Demonstration of ligand-induced down-regulation of expressed receptor mRNA and protein. J. Biol. Chem. 266: 10078–10085 [PubMed]
15. Lundell K., Thulin P., Hamsten A., Ehrenborg E. 2007. Alternative splicing of human peroxisome proliferator-activated receptor delta (PPARdelta): effects on translation efficiency and trans-activation ability. BMC Mol. Biol. 8: 70. [PMC free article] [PubMed]
16. Berg C. M., Lappas G., Strandhagen E., Wolk A., Toren K., Rosengren A., Aires N., Thelle D. S., Lissner L. 2008. Food patterns and cardiovascular disease risk factors: the Swedish INTERGENE research program. Am. J. Clin. Nutr. 88: 289–297 [PubMed]
17. Barrett J. C., Fry B., Maller J., Daly M. J. 2005. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics. 21: 263–265 [PubMed]
18. Lin M. C., Gordon D., Wetterau J. R. 1995. Microsomal triglyceride transfer protein (MTP) regulation in HepG2 cells: insulin negatively regulates MTP gene expression. J. Lipid Res. 36: 1073–1081 [PubMed]
19. Sekar N., Veldhuis J. D. 2004. Involvement of Sp1 and SREBP-1a in transcriptional activation of the LDL receptor gene by insulin and LH in cultured porcine granulosa-luteal cells. Am. J. Physiol. Endocrinol. Metab. 287: E128–E135 [PubMed]
20. Boren J., Veniant M. M., Young S. G. 1998. Apo B100-containing lipoproteins are secreted by the heart. J. Clin. Invest. 101: 1197–1202 [PMC free article] [PubMed]
21. Dische M. R., Porro R. S. 1970. The cardiac lesions in Bassen-Kornzweig syndrome: report of a case, with autopsy findings. Am. J. Med. 49: 568–571 [PubMed]
22. Kott E., Delpre G., Kadish U., Dziatelovsky M., Sandbank U. 1977. Abetalipoproteinemia (Bassen-Kornzweig syndrome). Acta Neuropathol. 37: 255–258 [PubMed]
23. Sharma S., Adrogue J. V., Golfman L., Uray I., Lemm J., Youker K., Noon G. P., Frazier O. H., Taegtmeyer H. 2004. Intramyocardial lipid accumulation in the failing human heart resembles the lipotoxic rat heart. FASEB J. 18: 1692–1700 [PubMed]
24. Nielsen L. B., Bartels E. D., Bollano E. 2002. Overexpression of apolipoprotein B in the heart impedes cardiac triglyceride accumulation and development of cardiac dysfunction in diabetic mice. J. Biol. Chem. 277: 27014–27020 [PubMed]
25. Yokoyama M., Yagyu H., Hu Y., Seo T., Hirata K., Homma S., Goldberg I. J. 2004. Apolipoprotein B production reduces lipotoxic cardiomyopathy: studies in heart-specific lipoprotein lipase transgenic mouse. J. Biol. Chem. 279: 4204–4211 [PubMed]
26. Chen Z., Newberry E. P., Norris J. Y., Xie Y., Luo J., Kennedy S. M., Davidson N. O. 2008. ApoB100 is required for increased VLDL-triglyceride secretion by microsomal triglyceride transfer protein in ob/ob mice. J. Lipid Res. 49: 2013–2022 [PMC free article] [PubMed]
27. Rubin D., Schneider-Muntau A., Klapper M., Nitz I., Helwig U., Folsch U. R., Schrezenmeir J., Doring F. 2008. Functional analysis of promoter variants in the microsomal triglyceride transfer protein (MTTP) gene. Hum. Mutat. 29: 123–129 [PubMed]
28. Cirulli E. T., Goldstein D. B. 2007. In vitro assays fail to predict in vivo effects of regulatory polymorphisms. Hum. Mol. Genet. 16: 1931–1939 [PubMed]
29. Ledmyr H., Ottosson L., Sunnerhagen M., Ehrenborg E. 2006. The Ile128Thr polymorphism influences stability and ligand binding properties of the microsomal triglyceride transfer protein. J. Lipid Res. 47: 1378–1385 [PubMed]
30. Couture P., Otvos J. D., Cupples L. A., Wilson P. W., Schaefer E. J., Ordovas J. M. 2000. Absence of association between genetic variation in the promoter of the microsomal triglyceride transfer protein gene and plasma lipoproteins in the Framingham Offspring Study. Atherosclerosis. 148: 337–343 [PubMed]
31. Herrmann S. M., Poirier O., Nicaud V., Evans A., Ruidavets J. B., Luc G., Arveiler D., Bao-Sheng C., Cambien F. 1998. Identification of two polymorphisms in the promoter of the microsomal triglyceride transfer protein (MTP) gene: lack of association with lipoprotein profiles. J. Lipid Res. 39: 2432–2435 [PubMed]

Articles from Journal of Lipid Research are provided here courtesy of American Society for Biochemistry and Molecular Biology

Save items

Related citations in PubMed

See reviews...See all...

Cited by other articles in PMC

See all...


  • Gene
    Gene records that cite the current articles. Citations in Gene are added manually by NCBI or imported from outside public resources.
  • GEO Profiles
    GEO Profiles
    Gene Expression Omnibus (GEO) Profiles of molecular abundance data. The current articles are references on the Gene record associated with the GEO profile.
  • HomoloGene
    HomoloGene clusters of homologous genes and sequences that cite the current articles. These are references on the Gene and sequence records in the HomoloGene entry.
  • MedGen
    Related information in MedGen
  • PubMed
    PubMed citations for these articles
  • Substance
    PubChem chemical substance records that cite the current articles. These references are taken from those provided on submitted PubChem chemical substance records.

Recent Activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...