Gene expression results in lipopolysaccharide-stimulated monocytes depend significantly on the choice of reference genes
© Piehler et al; licensee BioMed Central Ltd. 2010
Received: 16 September 2009
Accepted: 4 May 2010
Published: 4 May 2010
Gene expression in lipopolysaccharide (LPS)-stimulated monocytes is mainly studied by quantitative real-time reverse transcription PCR (RT-qPCR) using GAPDH (glyceraldehyde 3-phosphate dehydrogenase) or ACTB (beta-actin) as reference gene for normalization. Expression of traditional reference genes has been shown to vary substantially under certain conditions leading to invalid results. To investigate whether traditional reference genes are stably expressed in LPS-stimulated monocytes or if RT-qPCR results are dependent on the choice of reference genes, we have assessed and evaluated gene expression stability of twelve candidate reference genes in this model system.
Twelve candidate reference genes were quantified by RT-qPCR in LPS-stimulated, human monocytes and evaluated using the programs geNorm, Normfinder and BestKeeper. geNorm ranked PPIB (cyclophilin B), B2M (beta-2-microglobulin) and PPIA (cyclophilin A) as the best combination for gene expression normalization in LPS-stimulated monocytes. Normfinder suggested TBP (TATA-box binding protein) and B2M as the best combination. Compared to these combinations, normalization using GAPDH alone resulted in significantly higher changes of TNF-α (tumor necrosis factor-alpha) and IL10 (interleukin 10) expression. Moreover, a significant difference in TNF-α expression between monocytes stimulated with equimolar concentrations of LPS from N. meningitides and E. coli, respectively, was identified when using the suggested combinations of reference genes for normalization, but stayed unrecognized when employing a single reference gene, ACTB or GAPDH.
Gene expression levels in LPS-stimulated monocytes based on RT-qPCR results differ significantly when normalized to a single gene or a combination of stably expressed reference genes. Proper evaluation of reference gene stabiliy is therefore mandatory before reporting RT-qPCR results in LPS-stimulated monocytes.
Cells from the mononuclear phagocyte system play central roles in the pathophysiological processes of inflammation  and infection  Lipopolysaccharide (LPS), a cell membrane component of gram-negative bacteria, is a potent stimulator of immune responses of the mononuclear phagocyte system . Stimulation of monocytes with LPS is a frequently employed model system to study inflammatory responses [4–8] and coagulation [9, 10]. One approach to investigate cellular processes is by gene expression studies. Due to its high sensitivity, specificity, dynamic range and straightforwardness, quantitative reverse-transcription polymerase chain reaction (RT-qPCR) has become one of the most frequently used techniques to measure gene expression. For comparison of expression levels between certain conditions of a cell or organ gene expression quantities need to be normalized to a standard. Several approaches have been proposed to achieve adequate normalization, but expression levels of internal reference genes, habitually called housekeeping genes, are mainly used . Studies from the past years have undoubtedly shown that stability assessment of internal reference genes for each experimental condition is a prerequisite for valid normalization of gene expression and reliable gene expression results [12–15]. This notion has therefore also been included in the recently published MIQE guidelines describing "M inimum I nformation for publication of Q uantitative real-time PCR E xperiments" .
In contrast to the fact that gene expression analysis in LPS-stimulated cells from the mononuclear phagocyte system is frequently employed - documented by about 1500 PubMed entries on "LPS, monocyte and gene expression" (as accessed by September 1st, 2009) - a systematic evaluation of reference gene stability has, to our knowledge, not been published yet. Moreover, a thorough review of the literature of the last years indicated that most of the published RT-qPCR results in LPS-stimulated monocytes were normalized to either GAPDH or ACTB alone, although normalization to a single reference gene is only rarely justified .
In the present study, mRNA expression levels of twelve candidate reference genes were assessed by RT-qPCR in human monocytes stimulated with LPS from different bacteria. The software applications geNorm [15, 17], Normfinder [12, 18] and Bestkeeper [14, 19] were subsequently used to calculate the most stably expressed reference genes and to determine the optimal number of reference genes required for reliable normalization of gene expression data. These results were then applied to normalize expression levels of genes known to be involved in immune response and to evaluate different normalization strategies. We show that gene expression levels in LPS-stimulated monocytes are significantly dependent on the choice of reference genes which emphasizes the importance of reference gene evaluation in the frequently employed model system of LPS-stimulated monocytes
Stability of reference gene expression
Candidate reference and target genes.
Candidate Reference Genes
Beta chain of MHC I
C-terminal binding protein 1
Involved in cellular proliferation.
Glycolysis and gluconeogenesis
Golgi autoantigen, golgin subfamiliy A, 1
Phosphoglycerate kinase 1
(Peptidylprolyl isomerase A)
(Peptidylprolyl isomerase B)
Associated with the secretory pathway
Succinate dehydrogenase complex, subunit A
Transmembrane BAX inhibitor motif containing 4
Involved in apoptosis
TATA box binding protein
Tumor necrosis factor
Descriptive statistics of candidate reference and target genes as calculated by BestKeeper.
Candidate Reference Genes
SD [± Cq]
CV [% Cq]
GM [C q ]
AM [C q ]
Min [C q ]
Max [C q ]
SD [± C q ]
CV [%C q ]
i) geNorm analysis
In addition to a ranking regarding the expression stability of each gene, geNorm also calculates a normalization factor for each sample based on the most stable reference genes and reports the optimal number of required reference genes. Figure 2B illustrates the determination of the optimal number of reference genes based on the pairwise variation of sequential normalization factors with increasing number of reference genes included for normalization factor calculation. According to the geNorm developers' original publication data, the authors propose 0.15 as the cut-off, below which the optimal number of reference genes is achieved and the inclusion of an additional reference gene not required. In our study, V2/3 (0.13) is already below this cut-off implying that the employment of the two best-performing reference genes (PPIB and B2M) is likely to result in reliable gene expression normalization of target genes (Figure 2B). However, as the authors of the original publication explicitly recommend the minimal use of the three most stable internal control genes for normalization of RT-qPCR results , we decided to calculate the normalization factor based on the three best-scoring reference genes (PPIB, B2M and PPIA) for further analysis.
ii) Normfinder analysis
We noted that, due to different mathematical approaches of the two programs, Normfinder ranked ACTB as the most stable, single reference, whereas the same gene performed poorly in the geNorm analysis.
iii) Bestkeeper analysis
Bestkeeper correlation analysis
BestKeeper index vs.
Coefficient of correlation [r]
Unfortunately, neither the software nor the original publication presents a ranking of reference gene stability (besides SD calculations) or suggests an optimal number of reference genes for reliable normalization of expression levels based on the BestKeeper index. Taking this into account and the fact that BestKeeper is founded on similar principles as geNorm, which also identified the candidate genes PPIA, B2M and PPIB as the most stable genes, it was opted not to use BestKeeper results for further analysis.
Evaluation of different normalization strategies
After identification of the most stably expressed reference genes in primary human monocytes stimulated with LPS, we were interested in validating our data and whether different normalization strategies significantly change gene expression results. For this, we quantified the mRNA expression of two target genes (TNF-α and IL10) known to be significantly regulated upon LPS stimulation of monocytes and, based on our data, used different approaches to normalize the expression levels of these target genes. The following normalization approaches were applied: (i) A normalization factor calculated by geNorm based on the three most stably expressed genes (PPIB, B2M and PPIA; denoted gN comb), (ii) the geometric mean of the best combination of two genes as recommended by Normfinder (B2M and TBP; denoted NF comb), (iii) the single best gene as suggested by Normfinder (ACTB), and (iv) another gene frequently used for gene expression normalization, GAPDH. Subsequently, we investigated whether these strategies resulted in significantly different expression results.
Expression level changes of TNF-α and IL10 in LPS-stimulated monocytes based on different normalization strategies.
Nm LPS stim/non-stim
Ec LPS stim/non-stim
Nm LPS stim/non-stim
Ec LPS stim/non-stim
Our study is, to our knowledge, the first report investigating expression stability of a panel of candidate reference genes in the frequently employed inflammation model of LPS-stimulated monocytes. We used three different programs (geNorm, Normfinder and Bestkeeper) to evaluate the expression stability of twelve candidate reference genes and, based on these results, investigated different normalization strategies applied to the mRNA levels of two target genes, TNF-α and IL10, in monocytes stimulated with LPS from E. coli and N. meningitides, respectively.
In LPS-stimulated monocytes, ACTB and GAPDH are mainly used as reference genes. In our study, we chose commonly used reference genes from the literature (ACTB, GAPDH, B2M, PGK1, PPIA, PPIB, SDHA, TBP and UBC) [12, 14, 15, 21]. In addition, we included three novel reference genes, CTBP1, GOLGA1 and TMBIM4, which were identified by Lee et al. using statistical analysis of large human microarray datasets from various experimental conditions and therefore called universal housekeeping genes . Published microarray-based gene expression results of resting and activated mononuclear cells would probably result in several promising candidate reference genes. Comparison of our chosen reference genes with a previous, microarray gene expression study from our group using stimulation conditions identical to this study showed that several candidate reference genes investigated here (B2M, PGK1, PPIB, TMBIM4 and UCB) were among the least regulated (fold-change <0,2) genes (data not shown) . This indicates that the reference gene panel evaluated in this study included several promising candidates.
One of the main findings from our study is that several genes, like GAPDH, ACTB or UBC, which probably due to traditional reasons are still frequently used for normalization of RT-qPCR data, exhibit substantial variation in LPS-stimulated and non-stimulated monocytes. These findings clearly suggest that these genes disqualify as single internal control genes in LPS-stimulated monocytes. This observation is supported by several other studies which have shown significant variability of traditional "housekeeping" genes in different experimental conditions rendering them unsuitable as internal standards [11, 13, 23–29]. For example, Glare et al. demonstrated strong downregulation (10 times) of both GAPDH and ACTB in inflamed biopsy tissue of asthmatic patients compared to healthy controls or treated patients .
The evaluation of candidate reference gene stability depends on the method used. Surprisingly, Normfinder evaluated ACTB as the most stable single gene, whereas geNorm and BestKeeper found ACTB to be one of the least stable genes. This discrepancy is probably due to the different algorithms used in the programs. geNorm calculates the average pairwise variation for a candidate reference gene with all other tested genes and BestKeeper focuses on the coefficient of variation of a gene across all samples, whereas Normfinder employs a model-based approach which, in addition to the overall expression level variation, also takes intra- and intergroup variation into account. Even if such a discrepancy in ACTB stability has been reported before , the expression level changes observed in the present study resulted in highly similar findings, both for the target genes TNF-α and IL-10 (Figure 3), and for the candidate reference genes (Figure 4), when using the best combination of reference genes as suggested by geNorm or Normfinder.
Instability of normalization genes is likely to introduce a bias in reported gene expression results. In our study, we showed that normalization to GAPDH indicated significantly higher expression levels of target genes than normalization to a combination of stably expressed genes, resulting in an overestimation of the fold change in gene expression. Moreover, we observed a significant difference in TNF-α mRNA levels in monocytes stimulated with LPS from N. meningitides or E. coli when using a normalization strategy based on several stably expressed reference genes. In contrast, no significant difference between TNF-α mRNA levels in monocytes stimulated with E. coli and N. meningitides LPS, respectively, was observed when normalized to either ACTB or GAPDH alone. These false-negative results illustrate that slight changes in gene expression differences and affection of metabolic pathways may be overlooked when normalizing mRNA levels to single genes and not to a combination of stably expressed genes. Our findings that gene expression results vary depending on the chosen normalization strategy are not without precedence. For example, Dheda et al. nicely showed that a significant upregulation of IL4 in patients with tuberculosis compared to healthy controls can be masked when RT-qPCR results are normalized to an inappropriate reference gene, in this case GAPDH . Moreover, treatment of tuberculosis patients led to a (nonsignificant) decrease in IL4 expression when a validated reference gene was used. In contrast, normalization of IL4 to GAPDH resulted in a 5-fold up regulation indicating persistence of the disease as opposed to the clinical, biochemical and radiological improvement of the patient . Together with our results, these documentations of erroneous results introduced by the choice of inappropriate reference genes strongly advocate for the demand to make systematic validation of reference genes obligatory for reported gene expression analyses [16, 31].
The absence of universal reference genes with constant expression levels in any experimental condition demands the documentation of the validity of the employed reference genes for each experimental setup. This is also true for our study, as different experimental conditions, such as type and concentration of activator, incubation time or cell type, may require a different set of valid reference genes for proper gene expression normalization. Even if the reference genes evaluated as stably expressed in the present study may be considered as candidate reference genes in subsequent studies with similar conditions of monocyte stimulation, the quest for valid reference genes must be repeated and the reference gene stability must be documented for each activation process.
In the present study, we showed that gene expression levels in LPS-stimulated monocytes based on RT-qPCR results differ significantly when normalized to a single gene or a combination of stably expressed reference genes. The importance of our findings is highlighted by the fact that a review of the literature on gene expression in LPS-stimulated monocytes of the last years exhibited that the large majority of the published RT-qPCR results were normalized to a single gene, mainly GAPDH or ACTB, and that a systematic comparison of different normalization strategies was lacking. Our results indicate that normalization of RT-qPCR data to GAPDH or ACTB alone leads to imprecise gene expression results in LPS-stimulated monocytes and that the employment of several, stably expressed reference genes is mandatory. Due to the absence of universal reference genes, however, the state-of-the-art evaluation of reference gene stability has to be documented for each experimental setup and tailored to every activation process.
Isolation of monocytes
PBMC from six consenting, healthy donors (Blood Bank, Oslo University Hospital, Ulleval, Norway) were isolated from EDTA whole blood (450 ml) by density gradient centrifugation as previously described . Monocytes were purified from PBMC by counter-current elutriation centrifugation using a Beckman J-6M/E centrifuge to a purity of >90% as assessed by flowcytometry using CD14 as marker (data not shown) and cryopreserved in RPMI 1640 (Gibco) containing 25% (v/v) fetal calf serum (FCS) and 10% (v/v) DMSO at -150°C until further use.
Monocytes were thawed, resuspended and cultivated in RPMI 1640 with 5% (v/v) FCS containing 2% (v/v) of a penicillin/streptomycin solution and seeded at a density of 0.75 million cells per well in 24 wells microtiter plates (Costar). The cells were cultured at 37°C in a 5% CO2 atmosphere in the absence or presence of 1 μg LPS from E. coli (strain O55:B5, Cambrex BioScience) or N. meningitides (strain 44/76, B15:P1.16), respectively, in a total volume of 1 ml for 3 hours. Meningococcal endotoxin was a kindly gift of Klaus Bryn at the National Institute of Public Health, Norway . After centrifugation of the microtiter plates at 500 g and 20°C for 7 minutes, the supernatants were discarded and the cells lysed in 750 μl of lysis/binding buffer (MagNa Pure LC RNA Isloation Kit-High Performance, Roche) and stored at -80°C until parallel total RNA isolation.
RNA isolation and cDNA synthesis
Total RNA from cell lysates was isolated using the MagNa Pure LC RNA Isloation Kit-High Performance on a MagNA Pure LC Instrument (Roche) and the RNA HP blood external lysis protocol according to the manufacturer' instructions. The concentration and purity of isolated total RNA were measured using a NanoDrop ND-1000 spectrophotometer (Thermo Scientific). RNA amounts isolated from 0.75 million monocytes were between 425 ng and 995 ng. Absorbance ratios at 260/280 nm above 1.8 and a mean 260/230 nm absorbance ratio of 1.8 indicated that all RNA samples were pure and free of protein and without contamination by organic solvents. RNA integrity was assessed by micro-fluidic capillary electrophoresis using an Agilent 2100 Bioanalyzer and the RNA 6000 Pico Chip Kit (Agilent Technologies). All RNA samples exhibited RNA integrity numbers (RIN) above 9 indicating no RNA degradation and optimal RNA quality for downstream RT-qPCR applications .
First-strand cDNA was synthesized from 100 ng total RNA using the Omniscript RT Kit (Qiagen) and Oligo (dT) primers. The reverse transcription step was performed in duplicate at a GeneAmp PCR System 9600 (Perkin Elmer) at 37°C for 60 min and 95°C for 5 min. Finally, duplicate cDNA samples were pooled and diluted 1:2 in RNase/DNase free water prior to use in RT-qPCR. cDNAs were stored at -20°C.
Quantitative real-time PCR (qPCR)
Traditional reference genes and genes recently proposed to be stably expressed under certain conditions were chosen from the literature [12, 14, 15, 22, 35]. cDNA specific, pre-designed primers and probes for altogether twelve candidate reference genes and two target genes were purchased from Applied Biosystems. Table 1 shows symbols and names including the assay IDs of the genes investigated in this study.
qPCR reactions were performed on a ABI 7900 HT Fast Real-Time PCR System (Applied Biosystems) in a 96-well microtiter plate format and a final volume of 20 μl using 2 μl cDNA (diluted 1:2), 10 μl 2 × TaqMan Fast Universal PCR MasterMix (Applied Biosystems), 1 μl gene specific 20 × Gene Expression Assay Mix (Applied Biosystems) and 7 μl RNase/DNase free water. The cycling conditions were as follows: 20 s polymerase activation at 95°C followed by 40 cycles of 95°C for 1s and 60°C for 20 s. All samples were amplified in duplicate and two non-template controls per primer pair were included in each run. Expression levels were obtained as individual Cq values for each gene using the SDS RQ manager v 1.2 (Applied Biosystems) with standard settings and following instructions of the vendor. PCR efficiency for each primer-probe set was calculated using 10-fold dilutions (1:1 to 1:100 000) of pooled cDNA. Individual Cq values were plotted against the logarithm of the dilution factor, and both Pearson's correlation coefficient (r) and PCR efficiency (E) for each assay were determined from the respective plot. r2 were obtained from the lines of best fit from the Microsoft Office Excel software and PCR efficiencies were calculated according to the formula E = 10^(-1/slope) (Table 1). Efficiency plots for each gene are shown in Additional File 3.
Analysis of gene expression data
To evaluate the gene expression stability of candidate reference genes, the software applications geNorm version 3.5 [15, 17] NormFinder version 0.953 [12, 18] and BestKeeper version 1 [14, 19] were used according to the developers' manuals. Where necessary, raw Cq values were transformed into linear scale expression quantities using the delta-Cq method and E as base. Differential gene expression results were calculated using the Pfaffl method  when normalizing to a single gene (ACTB and GAPDH) or to the geometric mean of the best combination of two genes (B2M and TBP) as suggested by Normfinder. In the case of the Normfinder normalization strategy, the geometric mean of the B2M and TBP Cq values in each sample were used as the reference gene Cq in the Pfaffl equation, with Ereference gene = 2. For normalization using the three best performing genes as suggested by geNorm (PPIB, B2M and PPIA), the according normalization factor was calculated and applied. All differential gene expression results are expressed as the geometric mean. Statistical significance was assessed by Wilcoxon matched pairs signed ranks test using SPSS version 16.0. Paired Student's t test was also performed and resulted in highly similar findings (data not shown). Results with p < 0.05 were considered statistically significant.
Meningococcal endotoxin was a kindly gift of Klaus Bryn at the National Institute of Public Health, Norway. This work was partially financed by a grant from Helse Øst RHF (200500428-243), Norway.
- Auffray C, Sieweke MH, Geissmann F: Blood monocytes: development, heterogeneity, and relationship with dendritic cells. Annu Rev Immunol. 2009, 27: 669-692. 10.1146/annurev.immunol.021908.132557.View ArticlePubMedGoogle Scholar
- Serbina NV, Jia T, Hohl TM, Pamer EG: Monocyte-mediated defense against microbial pathogens. Annu Rev Immunol. 2008, 26: 421-452. 10.1146/annurev.immunol.26.021607.090326.PubMed CentralView ArticlePubMedGoogle Scholar
- Brandtzaeg P, Bjerre A, Ovstebo R, Brusletto B, Joo GB, Kierulf P: Neisseria meningitidis lipopolysaccharides in human pathology. J Endotoxin Res. 2001, 7: 401-420.PubMedGoogle Scholar
- Toltl LJ, Beaudin S, Liaw PC: Activated protein C up-regulates IL-10 and inhibits tissue factor in blood monocytes. J Immunol. 2008, 181: 2165-2173.View ArticlePubMedGoogle Scholar
- Ovstebo R, Olstad OK, Brusletto B, Moller AS, Aase A, Haug KB, Brandtzaeg P, Kierulf P: Identification of genes particularly sensitive to lipopolysaccharide (LPS) in human monocytes induced by wild-type versus LPS-deficient Neisseria meningitidis strains. Infect Immun. 2008, 76: 2685-2695. 10.1128/IAI.01625-07.PubMed CentralView ArticlePubMedGoogle Scholar
- Martin M, Rehani K, Jope RS, Michalek SM: Toll-like receptor-mediated cytokine production is differentially regulated by glycogen synthase kinase 3. Nat Immunol. 2005, 6: 777-784. 10.1038/ni1221.PubMed CentralView ArticlePubMedGoogle Scholar
- Hashimoto S, Morohoshi K, Suzuki T, Matsushima K: Lipopolysaccharide-inducible gene expression profile in human monocytes. Scand J Infect Dis. 2003, 35: 619-627. 10.1080/00365540310015926.View ArticlePubMedGoogle Scholar
- Moller AS, Ovstebo R, Westvik AB, Joo GB, Haug KB, Kierulf P: Effects of bacterial cell wall components (PAMPs) on the expression of monocyte chemoattractant protein-1 (MCP-1), macrophage inflammatory protein-1alpha (MIP-1alpha) and the chemokine receptor CCR2 by purified human blood monocytes. J Endotoxin Res. 2003, 9: 349-360.PubMedGoogle Scholar
- Ahamed J, Niessen F, Kurokawa T, Lee YK, Bhattacharjee G, Morrissey JH, Ruf W: Regulation of macrophage procoagulant responses by the tissue factor cytoplasmic domain in endotoxemia. Blood. 2007, 109: 5251-5259. 10.1182/blood-2006-10-051334.PubMed CentralView ArticlePubMedGoogle Scholar
- Luyendyk JP, Schabbauer GA, Tencati M, Holscher T, Pawlinski R, Mackman N: Genetic analysis of the role of the PI3K-Akt pathway in lipopolysaccharide-induced cytokine and tissue factor gene expression in monocytes/macrophages. J Immunol. 2008, 180: 4218-4226.PubMed CentralView ArticlePubMedGoogle Scholar
- Huggett J, Dheda K, Bustin S, Zumla A: Real-time RT-PCR normalisation; strategies and considerations. Genes Immun. 2005, 6: 279-284. 10.1038/sj.gene.6364190.View ArticlePubMedGoogle Scholar
- Andersen CL, Jensen JL, Orntoft TF: Normalization of real-time quantitative reverse transcription-PCR data: a model-based variance estimation approach to identify genes suited for normalization, applied to bladder and colon cancer data sets. Cancer Res. 2004, 64: 5245-5250. 10.1158/0008-5472.CAN-04-0496.View ArticlePubMedGoogle Scholar
- Dheda K, Huggett JF, Chang JS, Kim LU, Bustin SA, Johnson MA, Rook GA, Zumla A: The implications of using an inappropriate reference gene for real-time reverse transcription PCR data normalization. Anal Biochem. 2005, 344: 141-143. 10.1016/j.ab.2005.05.022.View ArticlePubMedGoogle Scholar
- Pfaffl MW, Tichopad A, Prgomet C, Neuvians TP: Determination of stable housekeeping genes, differentially regulated target genes and sample integrity: BestKeeper--Excel-based tool using pair-wise correlations. Biotechnol Lett. 2004, 26: 509-515. 10.1023/B:BILE.0000019559.84305.47.View ArticlePubMedGoogle Scholar
- Vandesompele J, De PK, Pattyn F, Poppe B, Van RN, De PA, Speleman F: Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol. 2002, 3: RESEARCH0034-10.1186/gb-2002-3-7-research0034.PubMed CentralView ArticlePubMedGoogle Scholar
- Bustin SA, Benes V, Garson JA, Hellemans J, Huggett J, Kubista M, Mueller R, Nolan T, Pfaffl MW, Shipley GL, et al, et al.,: The MIQE guidelines: minimum information for publication of quantitative real-time PCR experiments. Clin Chem. 2009, 55: 611-622. 10.1373/clinchem.2008.112797.View ArticlePubMedGoogle Scholar
- geNorm. [http://medgen.ugent.be/~jvdesomp/genorm/]
- Normfinder. [http://www.mdl.dk/publicationsnormfinder.htm]
- BestKeeper. [http://gene-quantification.com/bestkeeper.html]
- Hellemans J, Mortier G, De PA, Speleman F, Vandesompele J: qBase relative quantification framework and software for management and automated analysis of real-time quantitative PCR data. Genome Biol. 2007, 8: R19-10.1186/gb-2007-8-2-r19.PubMed CentralView ArticlePubMedGoogle Scholar
- Suzuki T, Higgins PJ, Crawford DR: Control selection for RNA quantitation. Biotechniques. 2000, 29: 332-337.PubMedGoogle Scholar
- Lee S, Jo M, Lee J, Koh SS, Kim S: Identification of novel universal housekeeping genes by statistical analysis of microarray data. J Biochem Mol Biol. 2007, 40: 226-231.View ArticlePubMedGoogle Scholar
- Dheda K, Huggett JF, Bustin SA, Johnson MA, Rook G, Zumla A: Validation of housekeeping genes for normalizing RNA expression in real-time PCR. Biotechniques. 2004, 37: 112-119.PubMedGoogle Scholar
- Schmittgen TD, Zakrajsek BA: Effect of experimental treatment on housekeeping gene expression: validation by real-time, quantitative RT-PCR. J Biochem Biophys Methods. 2000, 46: 69-81. 10.1016/S0165-022X(00)00129-9.View ArticlePubMedGoogle Scholar
- Arukwe A: Toxicological housekeeping genes: do they really keep the house?. Environ Sci Technol. 2006, 40: 7944-7949. 10.1021/es0615223.View ArticlePubMedGoogle Scholar
- Bustin SA, Nolan T: Pitfalls of quantitative real-time reverse-transcription polymerase chain reaction. J Biomol Tech. 2004, 15: 155-166.PubMed CentralPubMedGoogle Scholar
- Selvey S, Thompson EW, Matthaei K, Lea RA, Irving MG, Griffiths LR: Beta-actin--an unsuitable internal control for RT-PCR. Mol Cell Probes. 2001, 15: 307-311. 10.1006/mcpr.2001.0376.View ArticlePubMedGoogle Scholar
- Tricarico C, Pinzani P, Bianchi S, Paglierani M, Distante V, Pazzagli M, Bustin SA, Orlando C: Quantitative real-time reverse transcription polymerase chain reaction: normalization to rRNA or single housekeeping genes is inappropriate for human tissue biopsies. Anal Biochem. 2002, 309: 293-300. 10.1016/S0003-2697(02)00311-1.View ArticlePubMedGoogle Scholar
- Glare EM, Divjak M, Bailey MJ, Walters EH: beta-Actin and GAPDH housekeeping gene expression in asthmatic airways is variable and not suitable for normalising mRNA levels. Thorax. 2002, 57: 765-770. 10.1136/thorax.57.9.765.PubMed CentralView ArticlePubMedGoogle Scholar
- Hibbeler S, Scharsack JP, Becker S: Housekeeping genes for quantitative expression studies in the three-spined stickleback Gasterosteus aculeatus. BMC Mol Biol. 2008, 9: 18-10.1186/1471-2199-9-18.PubMed CentralView ArticlePubMedGoogle Scholar
- Guenin S, Mauriat M, Pelloux J, Van WO, Bellini C, Gutierrez L: Normalization of qRT-PCR data: the necessity of adopting a systematic, experimental conditions-specific, validation of references. J Exp Bot. 2009, 60: 487-493. 10.1093/jxb/ern305.View ArticlePubMedGoogle Scholar
- Lund PK, Joo GB, Westvik AB, Ovstebo R, Kierulf P: Isolation of monocytes from whole blood by density gradient centrifugation and counter-current elutriation followed by cryopreservation: six years' experience. Scand J Clin Lab Invest. 2000, 60: 357-365. 10.1080/003655100750019260.View ArticlePubMedGoogle Scholar
- Brandtzaeg P, Bryn K, Kierulf P, Ovstebo R, Namork E, Aase B, Jantzen E: Meningococcal endotoxin in lethal septic shock plasma studied by gas chromatography, mass-spectrometry, ultracentrifugation, and electron microscopy. J Clin Invest. 1992, 89: 816-823. 10.1172/JCI115660.PubMed CentralView ArticlePubMedGoogle Scholar
- Fleige S, Pfaffl MW: RNA integrity and the effect on the real-time qRT-PCR performance. Mol Aspects Med. 2006, 27: 126-139. 10.1016/j.mam.2005.12.003.View ArticlePubMedGoogle Scholar
- Coulson DT, Brockbank S, Quinn JG, Murphy S, Ravid R, Irvine GB, Johnston JA: Identification of valid reference genes for the normalization of RT qPCR gene expression data in human brain tissue. BMC Mol Biol. 2008, 9: 46-10.1186/1471-2199-9-46.PubMed CentralView ArticlePubMedGoogle Scholar
- Pfaffl MW: A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res. 2001, 29: e45-10.1093/nar/29.9.e45.PubMed CentralView ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.