Selection of reference genes in different myocardial regions of an in vivo ischemia/reperfusion rat model for normalization of antioxidant gene expression
© Vesentini et al; licensee BioMed Central Ltd. 2012
Received: 23 September 2011
Accepted: 29 February 2012
Published: 29 February 2012
Changes in cardiac gene expression due to myocardial injury are usually assessed in whole heart tissue. However, as the heart is a heterogeneous system, spatial and temporal heterogeneity is expected in gene expression.
In an ischemia/reperfusion (I/R) rat model we evaluated gene expression of mitochondrial and cytoplasmatic superoxide dismutase (MnSod, Cu-ZnSod) and thioredoxin reductase (trxr1) upon short (4 h) and long (72 h) reperfusion times in the right ventricle (RV), and in the ischemic/reperfused (IRR) and the remote region (RR) of the left ventricle. Gene expression was assessed by Real-time reverse-transcription quantitative PCR (RT-qPCR). In order to select most stable reference genes suitable for normalization purposes, in each myocardial region we tested nine putative reference genes by geNorm analysis. The genes investigated were: Actin beta (actb), Glyceraldehyde-3-P-dehydrogenase (gapdh), Ribosomal protein L13A (rpl13a), Tyrosine 3-monooxygenase (ywhaz), Beta-glucuronidase (gusb), Hypoxanthine guanine Phosphoribosyltransferase 1 (hprt), TATA binding box protein (tbp), Hydroxymethylbilane synthase (hmbs), Polyadenylate-binding protein 1 (papbn1). According to our findings, most stable reference genes in the RV and RR were hmbs/hprt and hmbs/tbp/hprt respectively. In the IRR, six reference genes were recommended for normalization purposes; however, in view of experimental feasibility limitations, target gene expression could be normalized against the three most stable reference genes (ywhaz/pabp/hmbs) without loss of sensitivity. In all cases MnSod and Cu-ZnSod expression decreased upon long reperfusion, the former in all myocardial regions and the latter in IRR alone. trxr1 expression did not vary.
This study provides a validation of reference genes in the RV and in the anterior and posterior wall of the LV of cardiac ischemia/reperfusion model and shows that gene expression should be assessed separately in each region.
Cardiac muscle is a heterogeneous system and many parameters such as blood flow and perfusion [1–3], patterns of ion channel activation [4–6] differ in distinct heart regions. As gene expression is concerned, spatial heterogeneity between cardiac chambers as well as between left and right ventricle have long been recognized [7, 8]. However, mounting evidences suggest that also conduction velocity, repolarization heterogeneities, and arrhythmia susceptibility in different left ventricle (LV) regions can be attributable to regional differences in their protein expression pattern and function [9, 10]. The spatial, functional and temporal heterogeneity that is distinctive becomes especially relevant in the injured heart [11–13].
In vivo occlusion of the left anterior descending (LAD) coronary artery followed by reperfusion is extensively used as an animal model of ischemic heart disease. Upon coronary obstruction, restoration of blood flow to the ischemic myocardium modulates the size of myocardial infarct and the chance of cell survival. However, this process, termed reperfusion, per se can also induce injury. The exact mechanism of reperfusion injury has not yet been clarified, although it probably involves cellular overload of calcium, mitochondrial impairment and oxidative stress-induced damage . The role of endogenous antioxidants in reperfusion injury has been studied extensively, although results are not always consistent (for a review see [15, 16]). In fact, activity or gene expression of antioxidant enzymes has been reported to either increase or decrease upon ischemia/reperfusion (I/R) [17–23]. This may be due to different experimental conditions and/or to variation of cardiac endogenous antioxidant expression at different times of reperfusion .
Although experimental in vivo ischemia most commonly involves mono-vasal occlusion, very few investigations have been addressed to comparative analysis on tissues from different LV regions [9, 11–13], as most reports on small animal models analyzed the total or partial left ventricular tissue [24–26] or even both ventricles combined .
The working hypothesis of the present study is that gene expression analysis performed separately in LAD territory and in the remaining cardiac regions is required as a prior condition for an accurate study of the effects of ischemia and reperfusion.
Real-time reverse-transcription quantitative PCR (RT-qPCR) is the method of choice for analyzing gene expression . However, selection of appropriate internal reference genes or housekeeping genes is necessary for reliable results in RT-qPCR. Reference gene expression should remain constant in the tissues of interest  and in the established experimental conditions. The lack of these requirements may lead to erroneous or inaccurate results [30–33].
Previously, single reference genes have been widely used to normalize expression of the target genes. However, numerous reports have stated that classic reference genes may vary extensively in different experimental conditions and tissues and are therefore unsuitable for normalization purposes in the absence of an accurate validation [32, 34, 35]. For example, one of the most traditionally used genes for normalization has been gapdh although several publications show that its expression is variable and not suitable for normalizing mRNA levels [36–38].
Normalization against multiple internal reference genes has now become a prerequisite for correct expression analysis  and software programs devoted to evaluation of expression stability and selection of the most suitable reference genes under different experimental conditions have been developed [40, 41]. This requirement is paramount in a complex tissue such as the myocardium that is composed by multiple cell types and especially during ischemia-reperfusion where also not specific RNA degradation can take place.
In an in vivo rat model of myocardial I/R we focused on gene expression of three antioxidant enzymes ubiquitously expressed--mitochondrial and cytosolic superoxide dismutase (MnSod and Cu-ZnSod respectively) and cytosolic thioredoxin reductase (trxr1)--whose role in the protection of ischemia/reperfusion injury has been investigated extensively [16, 42, 43]. Short (4 h) and long (72 h) reperfusion times were considered in order to evaluate the role of these antioxidant enzymes during two different phases of cardiac wound healing: the necrosis/apoptosis and the proliferation phase respectively [44, 45].
The first endpoint of our study was to evaluate a set of candidate reference genes for their use in normalizing RT-qPCR data in three distinct regions of the heart, namely the right ventricle, the central LAD ischemic/reperfused area of the left ventricle, and its undamaged posterior wall.
The second endpoint of the study was to verify alterations in MnSod, Cu-ZnSod and trxr1 gene expression level upon ischemia/reperfusion-induced oxidative stress in the different heart areas at the two different times of reperfusion.
Results and discussion
Selection of reference genes
It is noteworthy that, as previously reported by Brattelid et al.,  in a rat model of post-infarction heart failure, the highest stability was observed in genes encoding proteins involved in DNA synthesis/transcription, independently of the myocardial area analyzed, thus confirming that they are a suitable alternative to the widely used metabolic gene gapdh as reference genes
Target gene expression analysis
Regarding MnSod, there was an evident drop in expression level in all three cardiac regions upon long reperfusion time only (Figure 3A). In the RV and in the RR MnSod expression decreased of 54 and 40% with respect to sham (p < 0.01 and p < 0.05 respectively). In the IRR, expression level decreased of 83% with respect to sham (p < 0.001).
A decrease in MnSod activity upon ischemia and reperfusion has been previously described [46, 47]. However, our experimental setting disclosed that although a decrease of expression occurs in all cardiac regions, it is greater in the IRR and occurs only in the long reperfusion time, corresponding to the proliferative phase of wound healing during which fibroblasts and endothelial cells proliferate and matrix proteins are produced . On the contrary, Cu-ZnSod expression did not vary with respect to sham in the RV and RR at all times. However, in the IRR, after long reperfusion there was a drop of 83% (p < 0.01 vs sham) (Figure 3B).
Finally trxr1 expression levels did not vary significantly upon I/R during either short nor long reperfusion with respect to sham in all cardiac regions (Figure 3C).
We tested whether results obtained by normalization in the IRR against the six reference genes retained significance also when normalizing with a progressively reduced number of genes. Analysis was performed only on mitochondrial and cytoplasmic SOD, the genes that exhibited a significant variation of expression.
These data suggest that in the rat model of in vivo cardiac I/R, expression analysis may be accurately performed by selecting the appropriate reference genes for each region and even reducing the number of reference genes suggested by geNorm analysis. This becomes reasonable considering the hands-on implications (laboratory costs and time) and in consideration of the limiting quantity of the sample that occurs when a spatial analysis is carried out on small-sized experimental models (rats and mice).
In summary, gene expression of both reference and target genes reflects cardiac heterogeneity in the ischemic and reperfused heart.
geNorm analysis has shown that reference gene stability varies among the three myocardial regions analyzed: hmbs, hprt and hmbs, tbp, hprt are suitable reference genes in the right ventricle and in the Remote region respectively. Although in the ischemic reperfused region instability is higher, three reference genes could be sufficient for adequate normalization (ywhaz, pabp, hmbs).
We show that Cu-ZnSod and MnSod, but not trxr1 expression, varies in the different heart regions during the proliferative phase of post-ischemic wound healing.
Previous investigations report differences in gene expression of antioxidant enzymes in post-infarcted myocardium of rats [13, 23, 47, 48]. However, excluding a few cases [13, 48], gene expression is most commonly studied in the whole heart in spite of specific spatial differences in gene expression of both reference and target genes. Whenever a region-specific variability in gene expression occurs, as is the case of Cu-ZnSod reported in our study, analysis of the heart as a whole could lead to misleading results by either an over- or under-estimation bias.
A more general survey of spatial and temporal expression of antioxidant-coding genes could offer useful knowledge of the relation between the different phases of cardiac repair as well as constitute possible therapeutic targets.
Although our study was limited to the assessment of antioxidant gene changes related to ischemia-reperfusion, it has a more general value addressing the challenging problems of choice and validation of reference genes which apply to other target genes as well, involved in cardiac pathological processes.
All experiments were performed according to the guidelines of D.Lgs 116 (1992) and conformed to the "Guiding Principles for Research Involving Animals and Human Beings, " approved by the American Physiological Society.
Twenty male Wistar rats (8-10 weeks, 250-300 g) were anesthetized by intraperitoneal injection of Zoletil 100® + xylazine (50 mg/Kg and 3 mg/Kg respectively). The heart was exposed through a left lateral thoracotomy and LAD coronary was occluded for 30 min in 15 animals. Then the knot around the vessel was opened and unrestrained reperfusion allowed. At the end of reperfusion, animals were killed. Under deep anesthesia, hearts were arrested in diastole by lethal KCl injection. The hearts were then excised and washed for 10 min with cold Krebs-Henseleit bicarbonate buffer in Langendorff configuration.
Reperfused animals were divided into two groups: "short reperfusion time", which were reperfused for 4 h after the reopening of the LAD (n = 9) and "long reperfusion time", which were reperfused for 72 h after the reopening of the LAD (n = 6).
A control group of sham-operated animals underwent all surgical procedures except for the occlusion of the LAD and were killed in correspondence with the short (n = 3) and the long (n = 2) reperfusion times.
Hearts were cut below the plane of LAD occlusion and tissue samples were obtained from a) the right ventricle wall (RV), b) the core of the LAD territory, i.e., the ischemic reperfused region (IRR) in the left ventricular wall, c) the left ventricular free wall remote to LAD region (RR). In sham-operated animals tissues were harvested from analogously termed corresponding regions; IRR of sham-operated animals corresponded to the area beside the LAD in the left ventricle. Samples were snap frozen in liquid nitrogen and stored at -80°C until RNA purification was undertaken.
RNA extraction, quantification and retrotranscription
Frozen samples were transferred to Tri Reagent (Sigma) and homogenized using TissueLyser (Qiagen) according to manufacturer's instructions.
Concentration of RNA was determined by measuring optical density at 260 nm. Integrity of total RNA was assessed by electrophoresis on 1.2% agarose gels. cDNA was obtained from 1 μg of total RNA using the iScript (Bio-Rad Laboratories, Hercules, CA, USA) retrotranscription kit.
Reference gene selection and real-time PCR
Primer sequences of target genes and candidate reference genes for normalization
Forward primer (5'-3')
Reverse primer (5'-3')
Amplic on length
tyrosine 3-monooxygenase/tryptophan 5- monooxygenase activation protein zeta polypetide
Ribosomal protein L13A
Hypoxantine guanine phosphoribosyl transferase
TATA box binding protein
poly(A) binding protein, nuclear 1
Manganese Superoxide dismutase
Copper-Zinc Superoxide dismutase
Thioredoxin reductase 1
Real-time PCR was performed using iQ SYBRGreen Supermix (Bio-Rad Laboratories). Reactions contained 1X SYBR Green SuperMix (BioRad), 300 nM of each primer and 100 ng of template in a 25 μl final volume reaction. After an initial denaturation step at 95°C for 3 min, amplification was performed with 40 cycles of denaturation at 95°C for 15 s and annealing at 60°C for 30 s. Amplification was followed by melting curve analysis: a single homogeneous peak confirmed specific amplification for each primer pair.
Relative expression levels of reference genes were determined with the comparative threshold cycle (Cq) method. Relative expression levels of target genes were normalized to the geometric mean of most stable genes as indicated by geNorm software. All samples were run in duplicate and the mean value of each duplicate was used for all further calculations.
Serial cDNA dilution curves were produced to calculate the amplification efficiency for all genes. A graph of threshold cycle vs log10 picograms of diluted sample series was produced. The slope of the curve was used to determine the amplification efficiency according to Pfaffl : Efficiency = 10(-1/slope). Amplification efficiency values are reported in Table 1.
Gene expression stability and selection of the most suitable reference genes were evaluated with geNorm analysis. To determine the number of optimal genes required for normalization the software calculated pairwise variation (Vn/n+1) between Normalization Factor NFn and NFn+1.
Data are expressed as mean ± SE. Comparisons were made by two-way repeated measures ANOVA. When a significant effect of a factor was indicated, the post-hoc Bonferroni test was used to isolate the statistical differences. Analyses were performed using SPSS 13 (SPSS Inc. Chicago, Il, USA), and a p-value of less than 0.05 was considered statistically significant.
We gratefully acknowledge Mrs Alison Frank for language revision of the manuscript.
This work was supported by the Consiglio Nazionale delle Ricerche, Italy (grant CNR-DG.RSTL.035.007-035) and Scuola Superiore Sant'Anna, Italy (grant PNAZ.M6009AL).
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