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Jornal Brasileiro de Pneumologia

Print version ISSN 1806-3713On-line version ISSN 1806-3756

J. bras. pneumol. vol.42 no.3 São Paulo May/June 2016

http://dx.doi.org/10.1590/S1806-37562015000000133 

BRIEF COMMUNICATION

Analysis of the stability of housekeeping gene expression in the left cardiac ventricle of rats submitted to chronic intermittent hypoxia

Guilherme Silva Julian1 

Renato Watanabe de Oliveira1 

Sergio Tufik1 

Jair Ribeiro Chagas1  2 

1Departamento de Psicobiologia, Universidade Federal de São Paulo, Escola Paulista de Medicina - UNIFESP-EPM - São Paulo (SP) Brasil.

2Departamento de Biociências, Universidade Federal de São Paulo - UNIFESP-Baixada Santista - Santos (SP) Brasil.

ABSTRACT

Obstructive sleep apnea (OSA) has been associated with oxidative stress and various cardiovascular consequences, such as increased cardiovascular disease risk. Quantitative real-time PCR is frequently employed to assess changes in gene expression in experimental models. In this study, we analyzed the effects of chronic intermittent hypoxia (an experimental model of OSA) on housekeeping gene expression in the left cardiac ventricle of rats. Analyses via four different approaches-use of the geNorm, BestKeeper, and NormFinder algorithms; and 2−ΔCt (threshold cycle) data analysis-produced similar results: all genes were found to be suitable for use, glyceraldehyde-3-phosphate dehydrogenase and 18S being classified as the most and the least stable, respectively. The use of more than one housekeeping gene is strongly advised.

Keywords: Cell hypoxia; Reference standards; Sleep apnea, obstructive; Cardiovascular diseases; Models, animal; Polymerase chain reaction

Obstructive sleep apnea (OSA), which is a sleep-related breathing disorder with a high worldwide prevalence,1,2 causes various metabolic, oxidative, and sympathetic disturbances, increasing the risk of cardiovascular disease. 3 The most widely used animal model of OSA, particularly when the focus is on its cardiovascular consequences, is the chronic intermittent hypoxia (CIH) model.3 The CIH model mimics many of the putative pathological effects of OSA, such as increased blood pressure and sympathetic activity.4

Real-time PCR is the most commonly used tool to study gene expression of specific targets. In order to obtain reliable results in quantitative real-time PCR, it is necessary to use appropriate reference genes, or housekeeping genes (HKGs),5 as internal controls for gene expression normalization, which is essential to the evaluation of relative gene expression. However, using certain unstable genes as HKGs can strongly compromise data reliability.6,7 Therefore, each experimental condition should have an HKG selection step in order to obtain good quality data. The three most widely used algorithms for HKG selection are those provided by the computer programs geNorm,8 BestKeeper,9 and NormFinder.10

To our knowledge, there have been no studies assessing the stability of HKG expression in the left ventricle, or any other cardiac structure, using in vivo models of hypoxia, most such studies having been performed in vitro. Therefore, the objective of the present study was to report the selection of HKGs in the left cardiac ventricle of rats submitted to CIH, using the geNorm, BestKeeper, and NormFinder algorithms to analyze the expression stability of five commonly used HKGs. Our results provide important information for HKG selection in future studies employing a CIH model.

Twenty-two adult male Wistar Hannover rats were submitted to CIH (8 h/day) as described previously.11 All experimental procedures were performed in accordance with current ethical and practical guidelines for the use of laboratory animals.12 This study was approved by the Animal Research Ethics Committee of the Federal University of São Paulo (Protocol no. 2025/11).

Animals were assigned to one of three experimental groups: control (n = 6); CIH (six weeks of CIH, n = 7); and CIH+N (six weeks of CIH, followed by two weeks of recovery in normoxia, n = 8). The CIH protocol is described in detail elsewhere,11 as is the rationale behind the use of a two-week recovery period in the CIH+N group.13

After six weeks (the end of the CIH protocol) or eight weeks (the end of the CIH+N protocol), animals were euthanized by rapid decapitation. Subsequently, the heart was rapidly removed and washed with saline, after which the left ventricle was dissected. All tissues were rapidly dissected on dry ice and stored at −80°C until extraction.

Total RNA was extracted using TRIzol reagent (Thermo Fisher Scientific Inc., Waltham, MA, USA) and treated with DNase. Quantitative real-time PCR was performed with SYBR Green, as described previously.11 For our HKG evaluation, we chose five of the most commonly used genes, from different gene pathways: eukaryotic 18S ribosomal RNA (rRNA); beta-actin (ACTB ); beta-2-microglobulin (β2M ); glyceraldehyde-3-phosphate dehydrogenase (GAPDH ); and hypoxanthine guanine phosphoribosyl transferase (HPRT ). The primer sequences for all of those HKGs are described elsewhere.11

Gene expression stability was evaluated using the programs geNorm (Gene Quantification: http://download.gene-quantification.info/), NormFinder (Department of Molecular Medicine, Aarhus University Hospital, Aarhus, Denmark: http://moma.dk/normfinder-software), and BestKeeper (Gene Quantification: http://download.gene-quantification.info/). The geNorm program calculates the average expression stability (M-value) for each gene, lower M-values indicating greater stability. 8 The NormFinder program provides a stability value number for each gene, lower stability values indicating less stability. 10 The BestKeeper program calculates a Pearson's correlation coefficient for each gene, values of p closer to 1.0 indicating greater stability. 9 We also analyzed all of the 2−ΔCt (threshold cycle) data by one-way ANOVA.14 To test for normality and homogeneity, we employed the Kolmogorov-Smirnov test and Levene's test, respectively. The level of statistical significance was set at p < 0.05.

Our evaluation of RNA quality and integrity demonstrated intact 18S and 28S rRNA. Optimization of primer conditions and cDNA concentrations was performed and described previously.11 The 2−ΔCt values, analyzed independently, did not achieve significance (p > 0.05 for all), although 18S expression trended toward significance (p = 0.076 vs. p > 0.4 for the remaining genes; data not shown). These data indicate that, although all five HKG candidates are suitable for use, the expression of 18S demonstrates a tendency to show greater variability between groups.

In our BestKeeper analysis to identify the best HKGs in CIH models, all five candidate genes presented values that were acceptable (p < 0.01). According to the BestKeeper ranking, GAPDH was the best candidate, followed by ACTB . In addition, 18S presented the lowest Pearson's correlation coefficient, indicating that it was the least stable of the five HKG candidates. All BestKeeper Pearson's correlation coefficients are described in Table 1 and depicted in Figure 1A.

Figure 1 BestKeeper, geNorm, and NormFinder stability analyses of housekeeping genes in the left ventricle of rats submitted to chronic intermittent hypoxia. R: Pearson's correlation coefficient; M-value: average expression stability; ACTB: beta-actin; HPRT: hypoxanthine guanine phosphoribosyl transferase; β2M: beta-2-microglobulin; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; and 18S: eukaryotic 18S ribosomal RNA. 

Table 1 Rankings of left ventricle candidate housekeeping genes, by the stability of their expression, from the BestKeeper, geNorm, and NormFinder evaluations. 

Rank BestKeeper geNorm NormFinder
Gene Ra Gene M-valueb Gene Stability valueb
1 GAPDH 0.774 GAPDH 0.3877 GAPDH 0.0759
2 ACTB 0.745 β2M 0.4377 ACTB 0.1085
3 β2M 0.727 ACTB 0.4641 β2M 0.1094
4 HPRT 0.713 HPRT 0.4945 HPRT 0.1095
5 18S 0.588 18S 0.5182 18S 0.1176

R: Pearson's correlation coefficient; M-value: average expression stability; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; ACTB: beta-actin; β2M: beta-2-microglobulin; HPRT: hypoxanthine guanine phosphoribosyl transferase; and 18S: eukaryotic 18S ribosomal RNA. aValues closer to 1.0 (the higher values in this scenario) indicate greater stability. bLower values indicate greater stability.

In our geNorm analysis, all five candidate genes presented M-values lower than 1.5, which is considered to be the cut-off value for suitability,8 in all analyses. According to the geNorm ranking, GAPDH was the best candidate gene, followed by β2M . In addition, 18S presented the highest M-value and was ranked as the least stable gene. All geNorm M-values are described in Table 1 and depicted in Figure 1B. The BestKeeper and geNorm algorithms produced very similar results, the only difference being in terms of the second best HKG candidate.

In our NormFinder analysis, all five candidate genes presented stability values below 0.15, the cut-off value for suitability.10 Similar although not identical to the BestKeeper results, the NormFinder algorithm identified GAPDH as the best candidate gene, followed by β2M . In addition, 18S presented the highest stability value and was therefore ranked as the least stable gene. All NormFinder stability values are described in Table 1 and depicted in Figure 1C.

The NormFinder HKG ranking was identical to that of BestKeeper, GAPDH and ACTB being ranked as the most stable genes, whereas 18S was ranked as the least stable. However, the geNorm ranking showed a slight difference-ACTB in third position and β2M in second position. The data from all three algorithms corroborate those reported in a previous study involving cardiosphere-derived cells (endogenous cardiac stem cells, candidates for restoring lost tissue) and evaluating the influence of aging on gene stability. The authors found that ACTB , GAPDH , and β2M were the most stable HKGs in both adult or neonatal cardiosphere-derived cells under conditions of normoxia or hypoxia. 15 Although our study involved the left ventricle portion of the heart, which is composed of several cell types, the tissue origin is the same as that of the cardiosphere-derived cells analyzed by those authors. Conversely, in a study employing an animal model of left ventricular diastolic dysfunction, GAPDH was found to be the second most stable gene, underscoring its stability in vivo.16 In addition, ACTB presents good stability in models using different hypoxia stimuli, such as various cell types submitted to hypoxia in vitro7,15 and various brain structures submitted to hypoxia in vivo.11

Although analyses of β2M have shown it to be unstable in some brain structures and cell lines,7,11 our analysis of tissue from the left ventricle ranked β2M among the most stable candidate genes. Our data underscore those of several other studies, which classified β2M as one of the most stable candidate genes, in cardiosphere-derived cells under hypoxic conditions15 and in human chondrocytes cultured at oxygen concentrations of 5% and 1%.17

In the present study, HPRT was found to be among the least stable candidate genes. However, it can be considered suitable for use because it presented acceptable stability in the geNorm and BestKeeper analyses. Our data are in conflict with those of some previous studies, in which HPRT has been reported to be one of the most stable genes, in cultures of cells submitted to acute hypoxia7 and in an in vivo model of ischemia in the right ventricle.18 Nevertheless, our data corroborate those of another previous study involving cardiosphere-derived cells, in which HPRT was found to be among the least stable genes under conditions of hypoxia.19 The discrepancies among these studies might be due to differences in the origin of the tissue evaluated (cardiac tissue vs. prostate, kidney, and breast tissues) and in the experimental condition (hypoxia vs. ischemia).

Our data corroborate those of several other studies that classified 18S as an unsuitable HKG. In studies employing in vitro models of hypoxia, 18S has been found to be inappropriate as an HKG in the LNCaP (prostate cancer) cell line20,21 and in locust muscle cells,6 as it has in studies employing in vivo models of CIH in various brain structures.11 Our data corroborate those of previous studies demonstrating 18S sensitivity to different hypoxia stimuli. To our knowledge, this is the first study to evaluate 18S expression in cardiac tissue under hypoxic conditions.

Our study has some limitations. The CIH model mimics only one of the four major factors of OSA. In addition, analyses of the stability of HKG expression can demonstrate inter-model and even inter-structure variability.7,11 Therefore, the results of HKG expression studies are not generalizable to all structures or to all models of hypoxia. Nevertheless, the results of present study demonstrate that all of the HKGs tested are suitable for use, although it is inadvisable to use 18S. In addition, the geNorm, BestKeeper, and NormFinder algorithms produced very robust results, with little variation among the three. However, to obtain reliable data, the use of more than one HKG is strongly advised.

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Study carried out in the Departamento de Psicobiologia, Universidade Federal de São Paulo, Escola Paulista de Medicina - UNIFESP-EPM - São Paulo (SP) Brasil; and in the Departamento de Biociências, Universidade Federal de São Paulo -UNIFESP-Baixada Santista - Santos (SP) Brasil.

Financial support: This study received financial support from the Associação Fundo de Incentivo à Pesquisa (AFIP, Association for the Incentive Funding of Research), the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq, National Council for Scientific and Technological Development; Fellowship Grant nos. 301974/2011-0 and 310040/2011-6 to ST and JRC, respectively), the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES, Office for the Advancement of Higher Education), and the Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP, São Paulo Research Foundation; Grant nos. 2011/15060-4 and 2011/16011-6 to GSJ and RWO, respectively).

Received: June 04, 2015; Accepted: October 11, 2015

Correspondence to: Jair Ribeiro Chagas. Rua Napoleão de Barros, 925, 3º andar, CEP 04024-002, São Paulo, SP, Brasil. Tel./fax: 55 11 2149-0144. E-mail: jchagas1@gmail.com

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