- Research Paper
- Open Access
Identification of Mest/Peg1 gene expression as a predictive biomarker of adipose tissue expansion sensitive to dietary anti-obesity interventions
Genes & Nutrition volume 10, Article number: 27 (2015)
Food components with anti-obesity properties are commonly evaluated using mouse models of diet-induced obesity. The ability of these components to reduce or prevent white adipose tissue (WAT) accumulation is usually tested in feeding trials of several weeks duration in order to detect significant effects on fat mass expansion. Here, we aimed to identify early, predictive biomarkers for WAT expansion. We performed a 5-day high-fat diet (HFD) feeding trial with C57BL/6J mice using different established anti-obesity interventions: epigallocatechin gallate, replacing dietary lipids by n-3 PUFA, and increasing dietary protein. WAT gene expression was analyzed of genes known to be similarly affected by short- and long-term HFD. Gene expression of Leptin and Mest (mesoderm-specific transcript) was increased by HFD and normalized by all anti-obesity interventions. In a second experiment, translatability to whole blood-based expression data was assessed. Mice were challenged for 21 days with a HFD without or with simultaneous treatment with anti-obesity bioactives, hydroxytyrosol or resveratrol, and compared for parameters including Leptin and Mest expression in whole blood at day 5. While Leptin mRNA could not be detected in mouse whole blood, there was an induction of Mest mRNA by HFD which was suppressed by hydroxytyrosol. Moreover, Mest expression in whole blood at day 5 positively correlated with adiposity and negatively with lean body mass and the subcutaneous/visceral fat ratio at day 21. We conclude that gene expression of Leptin and Mest in WAT and of Mest in whole blood represent early, predictive markers of adipose tissue expansion of potential usefulness in nutritional studies and trials.
Obesity prevalence is increasing worldwide not only in industrialized but also in developing and transition countries, and nearly three million deaths each year are obesity related (Scully 2014). One approach in combatting obesity is the use of dietary interventions consisting of altered dietary nutrient composition or supplementation of bioactive ingredients in order to prevent and/or treat obesity. For an effective development of this approach, early biomarkers of adipose tissue expansion that are both predictive of fat accumulation in the long-term and sensitive to dietary anti-obesity interventions are of great interest, as their availability can, in the first place, expedite the screening and evaluation of candidate ingredients/conditions in animal trials. Of particular interest are biomarkers of this type derived from easily accessible, non-invasive samples, since they could serve to monitor early responsiveness to the dietary intervention without the need to euthanize the animals and, most important, in human intervention trials. Among accessible samples, blood cells are increasingly being investigated as a source of transcript-based biomarkers in nutritional and obesity studies. It has been shown that gene expression in blood cells can mirror gene expression changes in key tissues in energy homeostasis and respond to both internal and external stimuli (Reynes et al. 2015; Oliver et al. 2013; de Mello et al. 2012).
In a previous study, we used a systematic gene profiling (transcriptomic) approach to evaluate the predictability of short-term, high-fat diet (HFD)-induced changes in adipose tissue gene expression for long-term changes. We identified a set of genes in white adipose tissue (WAT) of mice which are regulated by HFD and whose short-term expression changes (after only 5 days of dietary challenge) are highly predictable for long-term changes (after 12 weeks) (Voigt et al. 2013). We considered this a promising step to establish well-defined, early biomarkers that could shorten animal trials considerably to allow a more rapid and efficient screening of health-promoting food compounds. The current investigation was undertaken with the primary aim to validate this idea. To this end, we conducted short-term (5 day) HFD challenge and intervention trials in mice applying, on top of the HFD, three different dietary interventions which have previously been shown to reduce the development of obesity and associated disorders albeit acting through different physiological mechanisms, i.e., supplementation of epigallocatechin gallate (EGCG) from green tea (Friedrich et al. 2012), replacing part of the dietary lipids by n-3 PUFA (Kus et al. 2011), and a high dietary protein content (Freudenberg et al. 2012). Using quantitative real-time PCR gene expression in epididymal WAT, we identified gene expression of Leptin and Mest [mesoderm-specific transcript (Mest), also known as paternally expressed gene 1 (Peg1)] as early markers of adipose tissue expansion whose HFD-induced expression changes in fat tissue were normalized by the different anti-obesity interventions. Interestingly, in an independent experiment using a different HFD and additional anti-obesity bioactives, we demonstrate similar changes for Mest gene expression in whole blood of mice, thus going one step further in the characterization of Mest gene expression as a biomarker of adipose tissue expansion sensitive to dietary intervention.
Materials and methods
Animals, diets and interventions
The experiments were performed in accordance with the national and European ethical guidelines for the use and care of laboratory animals. Experiment 1 was approved by the ethics committee of the Ministry for Environment, Health and Consumer Protection (State Brandenburg, Germany, Permission No. 23-2347-8-2009) and Experiment 2, by the Bioethical Committee of the University of the Balearic Islands (No. 8453, 18-06-2010).
Male C57BL/6JRcc mice were obtained from Harlan and Harlan Laboratories GmbH, housed individually at 22 °C with a 12-h light/dark cycle with ad libitum access to food (standard chow, ssniff Spezialdiäten GmbH, Soest, Germany) and water. At the age of 11–12 weeks, they were divided into 5 different groups matched for body weight (n = 9–10) and assigned to one of 5 different semisynthetic diets (Table 1) and fed for 5 days ad libitum. Overall diet composition was based on BIOCLAIMS low-fat diet (LFD) and HFD (Voigt et al. 2013; Hoevenaars et al. 2012). Group 1 was a LFD control group, and group 2 a HFD control group. Both diets have the same components. They are matched in protein energy content and only differ in their carbohydrate/fat content. Groups 3–5 were HFD-based intervention groups. Group 3 (HFD + EGCG) was fed HFD supplemented with 0.5 % of EGCG (TEAVIGO, kindly provided by DSM Nutritional Products Ltd., Basel, Switzerland). TEAVIGO is an extract of green tea (Camellia sinensis), which contains over 94 % of EGCG and <0.1 % caffeine. Group 4 (HFD + EPAX) received the HFD supplemented with n-3 long-chain polyunsaturated fatty acid concentrate (46 % DHA, 14 % EPA, wt/wt, as triacylglycerols; product EPAX 1050 TG; kindly provided by EPAX a.s., Lysaker, Norway) which replaced 15 % wt/wt of dietary lipids. In group 5 (HFD/HP), protein content was increased (to 43 energy%) at the expense of carbohydrates.
Body weight and food intake were recorded daily. After 5 days, mice were killed by cardiac puncture between 8.00 and 12.00 a.m. after isoflurane anesthesia, 2 h after food withdrawal. Li-heparinized plasma was obtained, and epididymal WAT (eWAT) was snap-frozen in liquid nitrogen and stored at −80 °C until analysis. Body composition was determined before the diet switch and at day of dissection using quantitative magnetic resonance (QMR; Bruker’s Minispec MQ10, Houston, TX, USA) as described (Klaus et al. 2005; Katterle et al. 2008).
Four groups of 7-week-old C57BL/6J male mice were used (from CRL España, Barcelona, Spain): a control group fed a defined LFD (D12450J from Research Diets Inc., New Brunswick, NJ, USA) with 10 % energy as fat (LF group), a group fed a defined HFD with 45 % energy as fat (D12451 from Research Diets Inc.) and treated with vehicle (sodium chloride 0.9 %) (HF group) and groups fed the same HFD and treated with resveratrol (30 mg/kg bw/day) or hydroxytyrosol (20 mg/kg bw/day), respectively (HF + RSV and HF + HT groups) (n = 10 animals/group). 3-Hydroxytyrosol [≥98 % (HPLC)] and resveratrol [≥99 % (GC)] were obtained from Sigma (Madrid, Spain). Initial body weight was equal for all animals (20.1 ± 0.17 g, n = 40). The animals were housed 2–3 per cage at 22 °C, with a 12-h light/dark cycle (lights on at 08:00) and free access to food and water. The duration of the experiment was 21 days. Treatments were conducted daily and by oral administration, between 9.00 and 12.00 a.m. Body weight and food intake were regularly monitored. Body composition was analyzed using EchoMRI-700™ analyzer (LCC, Houston, TX, USA) after 4 and 20 days of dietary challenge and intervention. Whole blood (~150 μL) was taken from facial vein on day 5 and 21 of experiment, at the start of the light cycle, and stored in RNAlater ® (Ambion®, Life Technologies, Alcobendas, Spain) at −80 °C. On day 21, the animals were euthanized under fed conditions within the first 2 h of the light cycle. WAT depots (epididymal, retroperitoneal and inguinal) were dissected in their entirety and weighed. Inguinal WAT biopsies were fixed with paraformaldehyde for histological examination. Blood collected from the neck was used to measure glucose levels and for the preparation of serum, which was stored at −80 °C until analysis.
Random blood glucose was measured before dissection using an automatic device [Accu-Chek Aviva system (Roche Diagnostics)]. Plasma or serum non-esterified fatty acids (NEFA), plasma cholesterol and plasma triglycerides (TG) were measured using colorimetric and enzymatic standard methods (NEFA C kit, Wako Chemicals GmbH, Neuss, Germany; Serum TG Determination Kit, Sigma-Aldrich, Inc., Steinheim, Germany; Cholesterol liquicolor, Human GmbH, Wiesbaden, Germany, respectively) according to the manufacturer’s instructions. Serum insulin levels were measured using commercial ELISA kits [ALPCO Diagnostics, USA (Experiment 1), Mercodia, Uppsala, Sweden (Experiment 2)].
RNA extraction and gene expression analysis
RNA isolation from adipose tissue samples was performed as described before (Keipert et al. 2014). Blood samples stored in RNAlater ® were used for total blood RNA extraction using Mouse RiboPure™-Blood RNA Isolation Kit (Ambion®, Life Technologies) and following the manufacturer’s instructions. Quantitative real-time PCR was performed essentially as described before (Keipert et al. 2014; Petrov et al. 2015) and followed the MIQE guidelines (Bustin et al. 2009).
Adipose tissue histology
Specimens of inguinal WAT lobules were fixed by immersion in 4 % paraformaldehyde in 0.1 M phosphate buffer (pH 7.4) overnight at 4 °C, dehydrated in a graded series of ethanol, cleared in xylene, and embedded in paraffin blocks. Five-micrometer-thick sections were stained with hematoxylin/eosin to assess tissue morphology using a Zeiss Axioskop 2 microscope equipped with an AxioCam ICc3 digital camera (Carl Zeiss, Barcelona, Spain) as described before (Petrov et al. 2015).
Data are presented as mean ± SEM. Statistical significance of differences between groups was assessed by one-way ANOVA and least-significant difference (LSD) post hoc comparisons using SPSS 1.9 for windows (SPSS, Chicago, IL, USA) or GraphPad Prism 5 (GraphPad Software, Inc., La Jolla, CA, USA). Threshold of significance was set at P < 0.05. Values not sharing a common letter are statistically different. Simple correlations with all animals were assessed by Pearson’s correlation coefficients using SPSS 1.9 for windows (SPSS, Chicago, IL, USA). Threshold of significance was set at P < 0.05.
Leptin and Mest gene expression in adipose tissue as early markers of adipose tissue expansion sensitive to dietary intervention
Obesity-prone mice were challenged with 5 days of feeding either a HFD or one of three versions of the same HFD incorporating anti-obesity ingredients or composition changes, and compared with mice on a LFD. As expected, HFD feeding resulted in an increased overall energy intake. This was attenuated by EGCG supplementation but not by the other treatments (Table 2). Initial and final body weights were not different between the groups. Final fat mass was slightly increased in the HFD and the HFD + PUFA groups compared to the LFD group (Table 2). When the increase (i.e., the difference between day 0 and day 5) was calculated, there was a small but significant increase in both body weight and body fat content in the HFD group compared to LFD (Fig. 1a, b). This was completely inhibited by the high-protein (HFD/HP) intervention, with HFD + EGCG showing small but non-significant effects and HFD + PUFA showing no effects. Other phenotypic characteristics such as eWAT weight, liver weight and TG content as well as blood glucose, insulin and NEFA content were not affected as expected, due to the brevity of the dietary intervention. Interestingly, HFD feeding resulted in a decrease in plasma TG levels which was also seen in the EGCG and PUFA intervention but not in the HP intervention group (Table 2).
Using quantitative RT-PCR, gene expression was analyzed in eWAT, focusing on the genes which were previously identified to show similar regulation after 5 days and 12 weeks of HFD feeding (Voigt et al. 2013). The aim was to identify genes that can serve as robust biomarkers for adipose tissue expansion to be used in short-term intervention trials. Selection criteria were the following: (1) gene expression is affected by 5-day feeding of a HFD and (2) gene expression is normalized to LFD control values by a dietary anti-obesity intervention. As shown in Table 3, genes of lipid metabolism were mostly downregulated by HFD irrespective of the dietary intervention. Genes of carbohydrate metabolism were affected by HFD and dietary interventions without any consistent pattern. Genes of oxidative phosphorylation were not significantly affected. Genes coding for secreted proteins tended to be upregulated by HFD with minor effects of the interventions. Interestingly, Rbp4 gene expression was downregulated in HFD + EGCG and HFD/HP compared to the HFD group but not by PUFA supplementation.
Finally, of all genes analyzed in eWAT, only 2 fulfilled our criteria as predictive biomarkers for adipose tissue expansion, i.e., Mest/Peg1 and the Leptin gene. Leptin gene expression in eWAT was significantly increased after 5 days of HFD (Fig. 1c), even though eWAT weight was not yet significantly increased. All 3 anti-obesity interventions decreased Leptin gene expression similar to levels comparable to LFD control levels. A similar pattern could be seen for Mest gene expression. Although the increase by HFD was not quite significant in the post hoc test, ANOVA showed a highly significant effect (P = 0.0007) and all three anti-obesity interventions reduced Mest expression to values even slightly below the LFD control values (Fig. 1d). The only other gene showing a similar expression pattern was Serpine 1 (Table 3) coding for plasminogen activator inhibitor-1, however, without reaching statistical significance.
Mest gene expression in whole blood as an early marker of adipose tissue expansion sensitive to dietary intervention
Obesity-prone mice were challenged for 21 days with a HFD without or with simultaneous daily oral treatment with putative anti-obesity bioactives (hydroxytyrosol or resveratrol), and compared with mice on a LFD for parameters including Leptin and Mest expression in whole blood after 5 days of HFD feeding. There were no significant differences between groups in cumulative energy intake over the 21-day experimental period (not shown). Although final body weight was not affected by 21 days of HFD (not shown), body weight gain was greater in the HFD-fed groups compared with the LF group. This was evident already after only 3 days on the HFD (Fig. 2a), as expected from previous results [(Voigt et al. 2013) and current Experiment 1]. Hydroxytyrosol-treated mice showed a trend to reduced body weight gain on the HFD that reached statistical significance between days 15 and 18. After 4 days, animals on the HFD treated with vehicle already had increased percent body fat content compared with the LF group, whereas the difference did not reach statistical significance for the animals on the HFD treated with either of the two bioactives (Fig. 2b). Body fat content at day 20 (Fig. 2c), adiposity index (defined as the sum of the mass of all WAT depots dissected expressed as percentage of body weight) at day 21 (not shown) and subcutaneous (inguinal) WAT depot mass at day 21 (Fig. 2d) were similarly increased in the three HFD-fed groups relative to the LF group. However, the accrual of visceral fat (epididymal and retroperitoneal depots) was decreased in the hydroxytyrosol- and, to a lesser extent, the resveratrol-treated mice (Fig. 2e, f), which therefore displayed a higher subcutaneous/visceral fat ratio at the end of the experiment compared with the vehicle-treated HF group (Fig. 2g). Moreover, although subcutaneous (inguinal) WAT depot mass was similarly increased by HFD irrespective of bioactive treatment, hydroxytyrosol- and resveratrol-treated mice displayed smaller inguinal WAT adipocytes at the end of the experiment, as evidenced by morphological examination (Fig. 3). Collectively, these results indicate that the bioactives tested, especially hydroxytyrosol, beneficially impacted on body adiposity, counteracting the effects of the obesogenic diet. Additionally, the increase in blood glucose levels following 21 days of HFD was ameliorated by bioactive treatment, especially hydroxytyrosol (Fig. 2h), while serum insulin and NEFA levels showed no significant differences between groups (Fig. 2i, j).
Gene expression analysis of Mest in whole blood revealed a considerable (~80 %) acute increase after 5 days on the HFD that was markedly attenuated after a more prolonged challenge of 21 days (Fig. 4a, b). The acute increase of Mest expression in whole blood upon HFD feeding was suppressed by simultaneous treatment with hydroxytyrosol, but not with resveratrol (Fig. 4a). Additionally, mRNA levels of Mest in whole blood after 21 days on HFD tended to be lower in the two groups of mice fed the HFD and treated with bioactive compared with the HFD group that received the vehicle (Fig. 4b). Remarkably, when all animals in Experiment 2 were included, Mest expression in total blood at day 5 positively correlated with adiposity and negatively with lean body mass and the subcutaneous/visceral fat ratio at the end of the experiment (Fig. 4c–e). In fact, Mest expression in total blood at day 5 positively correlated with the mass of all WAT depots at the end of the experiment and the positive correlation was maintained for Mest expression in total blood at day 21 and eWAT mass (not shown). Leptin mRNA was barely detectable in whole blood by Q-PCR, because in most samples analyzed Ct (cycle threshold) values were above 35 and thus close to or below detection threshold.
Predictive biomarkers of WAT accretion are of interest since they can serve to shorten animal trials assaying novel ingredients or other dietary interventions for anti-obesity activity and, particularly if linked to easily accessible non-invasive samples, to proof effects and identify responders in human intervention trials of this type. They may, therefore, find applicability in the substantiation of health claims made on food regarding obesity, adiposity and related health problems. In the current work, we sought to derive such biomarkers starting from previous gene expression profiling data of WAT after short- and long-term HFD feeding in mice (Voigt et al. 2013). First, dietary anti-obesity intervention strategies on top of a HFD were used to identify short-term gene expression changes in mouse WAT that were both predictive of long-term changes and sensitive to dietary interventions. Second, genes identified were assessed in whole blood in an independent experiment using additional anti-obesity bioactives. Our results suggest that Mest expression in WAT and whole blood could be used as a predictive biomarker for fat mass expansion.
Altogether, five different anti-obesity interventions have been used here which have been previously shown to reduce the development of obesity and associated disorders albeit acting through different physiological mechanisms. Dietary supplementation of EGCG, the green tea bioactive polyphenol, prevented the development of HFD-induced obesity in a dose-dependent manner in mice after 4 weeks (Klaus et al. 2005). This was shown to be due to decreased intestinal fat absorption and transport (i.e., higher energy excretion) and increased oxidation of dietary lipids linked to a reduced incorporation of dietary lipids into various tissues (Friedrich et al. 2012). Another intervention was the replacement of 15 % of dietary lipids with EPAX-1050, a triglyceride mixture containing 60 % of n-3 LC-PUFAs from marine origin. The experimental setup was the same which has been shown to reduce feed efficiency, fat depots and liver TG content, and to increase insulin sensitivity after 8 weeks of HFD feeding in mice (Kus et al. 2011) linked to an increased metabolic flexibility of skeletal muscle, with n-3 LC-PUFA supporting complete oxidation of fatty acids in mitochondria (Horakova et al. 2012). A third intervention was an increase in the protein content of the HFD to over 40 %. This has been shown to result in decreased body weight, body fat and hepatic TG accumulation, as well as increased insulin sensitivity compared to a HFD with adequate protein content after 20 weeks of feeding (Freudenberg et al. 2012). It was suggested that the positive effects of high-protein diets on metabolic syndrome associated traits are acutely due to satiety effects possibly linked to amino nitrogen intake and the subsequent suppression of liver lipogenesis (Freudenberg et al. 2013). Finally, hydroxytyrosol and resveratrol are two phenolic phytochemicals abundant in extra-virgin olive oil and grapes and red wine, respectively. For these two compounds, beneficial effects on metabolic health have been demonstrated, including an anti-obesity action in animals (Cao et al. 2014; Aguirre et al. 2014) which has been related to interactions with adipogenesis and adipocyte lipid and energy metabolism (Hao et al. 2010; Drira and Sakamoto 2014; Mercader et al. 2011; Gomez-Zorita et al. 2013) among other mechanisms. The dietary interventions chosen thus represent a broad range of treatments shown to attenuate or prevent the development of HFD-induced obesity and associated features of the metabolic syndrome in different studies.
Studies indicate that WAT rapidly responds to changes in the nutritional status with changes in gene expression (Voigt et al. 2013). Therefore, we first sought to identify genes whose modulations in WAT by 5 days of HFD feeding were similarly counteracted by three different anti-obesity intervention treatments (EGCG from green tea, n-3 PUFA and high dietary protein content). Using gene expression profiling, we have previously shown that about 80 % of all genes differentially expressed in eWAT after 5 days of HFD feeding were downregulated. These downregulated genes were mainly related to metabolic pathways such as lipogenesis, carbohydrate metabolism and mitochondrial function (Voigt et al. 2013). Our current analysis showed that none of these genes fulfilled our criteria for robust biomarkers. Although their downregulation by HFD could mainly be confirmed, their expression levels were not normalized by the anti-obesity interventions suggesting that genes crucial for lipid and glucose metabolism are not suitable as robust early biomarkers for adipose tissue health and expansion. Much less genes were upregulated by HFD such as genes coding for secreted proteins including leptin, serpine 1, haptoglobin and rbp4. Of these genes, only Leptin and Mest/Peg1 gene expression was consistently normalized by the different anti-obesity interventions. Thus, we show that gene expression of both Leptin and Mest was not only increased by short-term HFD feeding, but more importantly that their expression levels were completely normalized to LFD control levels in the HFD groups with simultaneous anti-obesity treatments.
Since its first discovery more than 20 years ago (Zhang et al. 1994), leptin has been well established as an adipose tissue-derived adipokine reflecting adipose tissue mass (Friedman 2014). It is long known that Leptin gene expression is correlated with adipocyte lipid content (Maffei et al. 1995), but surprisingly, the exact molecular mechanisms regulating its gene expression and secretion are still unknown today. Our data suggest that Leptin gene expression might be acutely down- or upregulated by catabolic or anabolic state of adipocytes, respectively.
Mest has also been known for about 20 years when it was discovered as a mesodermal imprinted, paternally expressed gene (Kaneko-Ishino et al. 1995) important for embryonic development (Lefebvre et al. 1998). Later it was shown to be highly expressed in adipose tissue, and its expression was linked to adipocyte differentiation (Kadota et al. 2012; Takahashi et al. 2005). Although the exact biochemical function of the Mest product is still unknown, it is suggested to play a role in adipocyte differentiation by inhibition of the Wnt signaling pathway (Jung et al. 2011). Several lines of evidence point to Mest as an acute marker of adipose tissue and fat cell expansion: Mest gene expression was highly increased in WAT of obese mice in diet-induced obesity as well as in genetic obesity (Takahashi et al. 2005; Okada et al. 2009; Moraes et al. 2003; Jura et al. 2015) which was linked to a positive energy balance during the most rapid phase of fat mass expansion (Nikonova et al. 2008; Kozak et al. 2010). Across several mouse strains, Mest expression in WAT was found to be associated with body weight (Anunciado-Koza et al. 2015). It has previously been shown that Mest expression in WAT was significantly increased already after 2 days of HFD feeding (Nikonova et al. 2008). In rats, dietary treatments during the suckling period that differentially affected inguinal adipocyte size at weaning also affected Mest gene expression of the same depot similarly (Musinovic et al. 2014). Differences in Mest gene expression observed in mouse WAT biopsies at an early age correlated with adiposity after 8 weeks of HFD feeding in mice (Koza et al. 2006). Furthermore, overexpression of Mest in 3T3-L1 adipocytes and transgenic mice led to an increased expression of adipocyte gene markers and considerably enlarged adipocytes (Takahashi et al. 2005). Together, this suggests that Mest is not only a biomarker for fat mass expansion but also causally linked to adipose expansion. In humans, evidence has been provided that epigenetic malprogramming of MEST may contribute to obesity predisposition throughout life, and of decreased blood MEST methylation in adults with morbid obesity compared with normal-weight controls (El Hajj et al. 2013).
In the first approach, we identified Leptin and Mest gene expression in WAT as early, predictive biomarkers of WAT accretion. In the second approach, we aimed to assess the translatability of these findings to whole blood-based expression data. The level of expression of Leptin gene in mouse blood is defined “low” by the web-based software anatomy tool of Genevestigator V3 (https://genevestigator.com/gv/index.jsp) (Hruz et al. 2008), and expression of the Leptin gene was found to be undetectable in rat peripheral blood mononuclear cells (Reynés B, Oliver P and Palou A, personal communication). In line with these observations, only Mest gene expression could be consistently detected in whole blood of our mice. Our results are first to reveal an induction of Mest gene expression in whole blood following the intake of an obesogenic diet. Remarkably, this was especially strong in the short term (day 5) although still evident after a more prolonged HFD challenge (21 days). Importantly, this response was suppressed or attenuated by simultaneous treatment with anti-obesity bioactives, hydroxytyrosol and, to a lesser extent, resveratrol. Importantly, treatment with these bioactives, particularly hydroxytyrosol, ameliorated other HFD-induced changes in our model system, such as increased blood glucose levels, visceral WAT gain and subcutaneous adipocyte size, thus favouring a healthier phenotype and adipose organ and validating their use as anti-obesity agents in our design. Most remarkably, Mest expression in total blood at day 5 correlated with measures of body composition at day 20–21, in a sense that greater Mest expression was associated with increased adiposity, decreased percent lean body mass and relatively more visceral fat (decreased subcutaneous/visceral fat ratio). To our knowledge, these results are first to show the potential of Mest gene expression in whole blood as an early, predictive marker of WAT expansion.
Leptin and Mest gene expression in eWAT and Mest gene expression in whole blood were upregulated by short-term (5 days) HFD feeding and normalized by different dietary interventions previously shown to have anti-obesity effects in the long-term. Leptin and Mest gene expression in fat depots as well as Mest gene expression in whole blood can thus be considered as predictive markers of adipose tissue accretion which could be useful for the rapid screening and evaluation of bioactive compounds/interventions with potential anti-obesity action.
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The research leading to these results has received funding from the European Union’s Seventh Framework Program FP7 2007-2013 under Grant Agreement No. 244995 (BIOCLAIMS Project). The authors thank Mario Rodríguez-Baeza for his help in experiment 2 during his Master studies. Excellent technical assistance provided by Antje Sylvester, Carolin Borchert and Enzo Ceresi is acknowledged.
Conflict of interest
Anja Voigt and Joan Ribot have contributed equally to this work.
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Voigt, A., Ribot, J., Sabater, A.G. et al. Identification of Mest/Peg1 gene expression as a predictive biomarker of adipose tissue expansion sensitive to dietary anti-obesity interventions. Genes Nutr 10, 27 (2015) doi:10.1007/s12263-015-0477-z
- Whole blood
- Mesoderm-specific transcript (Mest/Peg1)
- Epigallocatechin gallate (EGCG)
- n-3 PUFA
- High-protein diet