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Abdominal aortic aneurysm (AAA), characterized by a localized dilation of the abdominal aorta, is a life-threatening vascular pathology. Because of the current lack of effective treatment for AAA rupture, prevention is of prime importance for AAA management. Calorie restriction (CR) is a nonpharmacological intervention that delays the aging process and provides various health benefits. However, whether CR prevents AAA formation remains untested. In this study, we subjected Apoe−/− mice to 12 wk of CR and then examined the incidence of angiotensin II (AngII)–induced AAA formation. We found that CR markedly reduced the incidence of AAA formation and attenuated aortic elastin degradation in Apoe−/− mice. The expression and activity of Sirtuin 1 (SIRT1), a key metabolism/energy sensor, were up-regulated in vascular smooth muscle cells (VSMCs) upon CR. Importantly, the specific ablation of SIRT1 in smooth muscle cells abolished the preventive effect of CR on AAA formation in Apoe−/− mice. Mechanistically, VSMC-SIRT1–dependent deacetylation of histone H3 lysine 9 on the matrix metallopeptidase 2 (Mmp2) promoter was required for CR-mediated suppression of AngII-induced MMP2 expression. Together, our findings suggest that CR may be an effective intervention that protects against AAA formation.
Abdominal aortic aneurysm (AAA) is a permanent, localized dilation of the abdominal aorta (Johnston et al., 1991). Mortality after AAA rupture can be as high as 80% (Logan and Bourantas, 2000; Verhoeven et al., 2008). Because of the lack of medical therapy, AAA treatment mainly consists of surgery when the dilation occurs quickly or reaches a diameter larger than 5.5 cm (Bown et al., 2013; Lederle, 2013). Thus, prevention is particularly important for AAA management. In addition to uncontrollable risk factors such as advancing age, male gender, and family history, controllable risk factors such as smoking and abdominal obesity greatly contribute to the onset of AAA (Nordon et al., 2011). Epidemiological studies have revealed that an increased waist-to-hip ratio is independently associated with AAA (Golledge et al., 2007; Stackelberg et al., 2013). Likewise, studies in mice have suggested that obese mice are more susceptible to AAA than lean mice (Police et al., 2009), and weight loss suppresses the expansion of established AAAs (Police et al., 2010). Although the development of AAA is related to metabolic disorders, it remains unknown whether improving systemic metabolism prevents the formation of AAA.
Calorie restriction (CR), which consists of decreasing caloric intake without causing malnutrition, is the only nonpharmacological intervention to slow the aging process in a wide variety of organisms ranging from yeast to primates (Piper and Bartke, 2008; Colman et al., 2009, 2014; Fontana et al., 2010). Studies on unconventional CR imply that CR may also reduce mortality in humans (Strom and Jensen, 1951; Willcox et al., 2007). Furthermore, cross-sectional studies and randomized controlled trials have demonstrated that CR effectively improves systemic metabolic parameters and prevents obesity and insulin resistance (Weiss et al., 2006; Fontana et al., 2007; Weiss and Holloszy, 2007). As a healthy food regimen, CR reduces risk factors of atherosclerosis and related cardiovascular diseases (CVDs) in humans (Fontana et al., 2004, 2007; Lefevre et al., 2009). Despite the metabolic and cardiovascular benefits of CR, whether CR represents an effective strategy for AAA prevention remains untested.
In the present study, we investigated the influence of CR on AAA formation in mice. We observed that CR significantly altered the systemic metabolic state of Apoe−/− mice and inhibited angiotensin II (AngII)–induced AAA formation in Apoe−/− mice. Notably, we observed a significant up-regulation of Sirtuin 1 (SIRT1) in vascular smooth muscle cells (VSMCs) under CR, and importantly, specific knockout of VSMC-derived SIRT1 (VSMC-SIRT1) abolished the prevention of AAA by CR. These results revealed that SIRT1 in VSMCs plays a critical role in mediating the preventive effect of CR on AAA formation.
To investigate the influence of CR on AAA formation, Apoe−/− mice were calorie restricted or fed ad libitum (AL) for 12 wk, a strategy that has been widely used to investigate the effects of CR in mice (Hallows et al., 2011; Cerletti et al., 2012). After this 12-wk dietary intervention, mice in the experimental group received 4 wk of AngII infusion to induce AAA formation, whereas the control group received saline infusion (Fig. 1 A). During the experiment, AL mice displayed stable weight gain, whereas the weights of CR mice sharply decreased in the first 4 wk and then slightly increased in the remaining 12 wk (Fig. 1 B). However, no significant difference in body weight (BW) was observed between the AngII-infused mice and the control mice under the same dietary conditions. The liver weight–to-BW ratio was comparable in the four mouse groups (Fig. 1 C). Nonetheless, the epididymal white adipose tissue (eWAT)–to-BW ratio was markedly decreased after 16 wk of CR, notwithstanding that AngII infusion did not affect the eWAT-to-BW ratio (Fig. 1 D). These results indicate that CR constrains BW gain and fat storage in Apoe−/− mice.
We next examined the energy expenditure (EE) and respiratory quotient (RQ) of all groups of mice using indirect calorimetry. The results revealed that CR significantly reduced EE and decreased RQ in Apoe−/− mice, whereas AngII treatment did not notably affect the EE and RQ of Apoe−/− mice (Fig. 1, E and F), suggesting that CR mice tend to use more lipids rather than carbohydrates as an energy source compared with AL mice. We further examined systemic glucose and lipid metabolism in CR Apoe−/− mice. The fasting glucose levels were not significantly different between the four groups (Fig. 1 G). We analyzed the glucose regulatory function of these mice using an intraperitoneal glucose tolerance test (IPGTT). After glucose injection (2 g/kg BW), AL mice had higher increases in blood glucose levels than CR mice within 60 min, regardless of AngII treatment (Fig. 1 G), indicating that CR improves glucose tolerance in Apoe−/− mice. CR also notably decreased serum triglyceride levels in Apoe−/− mice, whereas AngII infusion did not affect the lipid profile of Apoe−/− mice (Table 1). Altogether, the results described in this section demonstrate that CR alters systemic metabolism in Apoe−/− mice, thus indicating the success of the mouse model construction for further analysis of the effect of CR on AAA formation.
Apoe−/− mice with AngII infusion is a widely used animal model for AAA formation (Daugherty et al., 2000; Daugherty and Cassis, 2004). In the present study, AngII infusion increased systolic blood pressure (SBP) in both CR and AL mice, whereas CR had no notable effect on AngII-induced elevation of SBP (Table 1). There were no gross differences in morphology between the aortas of AL control (AL-Con; saline infusion) and CR-Con Apoe−/− mice (Fig. 2 A). 59% (29/49) of AL Apoe−/− mice developed AAA after AngII infusion, which is consistent with a previous study (Trivedi et al., 2013). In contrast, only 33% (11/33) of CR-AngII Apoe−/− mice developed AAA (Fig. 2 C). Over the 4 wk of AngII infusion, 29% (14/49) of AL-AngII Apoe−/− mice died from aortic aneurysm rupture, whereas only 6% (2/33) of CR-AngII Apoe−/− mice died (Fig. 2 D).
AngII infusion markedly increased the aortic weight–to-BW ratio and maximal abdominal aortic diameter in Apoe−/− mice (Fig. 2, B and E). These effects were significantly alleviated by CR (Fig. 2, B and E). Elastin van Gieson (EVG) staining of the suprarenal aortas also demonstrated that the elastic lamina in the aortas of AL-Con and CR-Con Apoe−/− mice was intact and regularly arranged (Fig. 2, F and G). The aortic elastin was seriously degraded and disrupted in AL-AngII Apoe−/− mice, whereas the aortic elastin was more preserved in CR-AngII Apoe−/− mice compared with AL-AngII Apoe−/− mice (Fig. 2, F and G). Elastin is generated by medial VSMCs, and AAA is characterized by a loss of VSMCs (López-Candales et al., 1997). We therefore examined the density of VSMCs in the aortic media. Immunohistochemistry (IHC) of α smooth muscle actin (αSMA), a marker of VSMCs, in suprarenal aortas revealed that although there were no significant differences in VSMC density in the aortic media between the AL-Con and CR-Con Apoe−/− mice, the VSMC density in the aortic media was markedly lower in AL-AngII Apoe−/− mice compared with AL-Con Apoe−/− mice, and CR-AngII Apoe−/− mice had a higher VSMC density in the aortic media compared with AL-AngII Apoe−/− mice (Fig. 2, H and I). These observations suggested that CR alleviates the decrease in VSMC density caused by AngII infusion. In addition to elastin degradation and VSMC loss, AngII-induced cytokine expression and oxidative stress in the aortas of Apoe−/− mice were also reduced by CR (not depicted). Apart from AAAs induced by AngII infusion, consistent with a previous study (Daugherty et al., 2010), we observed that the maximal diameters of ascending aortas of Apoe−/− mice were markedly increased upon AngII infusion. Nevertheless, in the present study, the maximal diameters of ascending aortas of AL-AngII–treated Apoe−/− mice were comparable to those of CR-AngII–treated Apoe−/− mice (not depicted). Collectively, the results in this section suggest that a calorie-restricted diet effectively reduces the formation of AngII-induced AAAs and ameliorates the severity of AAAs in Apoe−/− mice.
Previous studies have revealed that the gene expression profiles in metabolic tissues, such as liver and skeletal muscle, are reprogrammed by CR in mice. The most significantly changed genes are involved in energy metabolism, which include oxidative phosphorylation, glucose metabolism, and lipid metabolism (Lee et al., 1999; Renaud et al., 2014). In the present study, we examined the metabolic state of the liver after 12-wk CR in the Apoe−/− mouse. We examined mRNA expression of Ndufs8, Sdhb, Uqcrc1, Cox5b, and Atp5a1, which encode the subunits of mitochondrial respiratory chain complexes I to V, respectively. The results demonstrated that the mRNA expression of these genes in the liver was significantly increased in response to CR (Fig. 3 A). Moreover, the mRNA expression levels of Hk4 (a gene related to glycolysis) and Pnpla2 (a gene related to lipolysis) in the liver were significantly increased in response to CR (Fig. 3 B). These results suggest that CR up-regulates the expression of oxidative respiratory chain complex genes and promotes glycolysis and lipolysis in the liver.
We next examined these metabolism-related indices in the aortas of Apoe−/− mice to investigate the downstream effectors in the aortas that mediate the effect of CR on AAA formation. In contrast to the liver, the mRNA expression levels of oxidative phosphorylation complexes in aortas were comparable between AL-Con and CR-Con Apoe−/− mice (Fig. 3 C). Furthermore, there were no significant differences in real-time PCR results for the aortic expression levels of genes related to glycolysis (e.g., Hk1 and Pkm), fatty acid β-oxidation (e.g., Cpt1a and Acadl), lipolysis (e.g., Lipe and Pnpla2), and fatty acid synthesis (e.g., Fasn) between the AL-Con and CR-Con Apoe−/− mice (Fig. 3 D). All of these results indicated that CR does not significantly change the expression levels of oxidative phosphorylation complexes and the expression of genes related to glucose and lipid metabolism in aortas.
Metabolic/energy sensors, including SIRT1, SIRT3, AMP-activated protein kinase α (AMPKα), and mechanistic target of rapamycin (mTOR), have been reported to be involved in the response to CR in different contexts (Blagosklonny, 2010; Cantó and Auwerx, 2011; Guarente, 2013). To probe the mechanism of how CR protects against AAA formation, we examined the expression levels of these proteins in the aortas of 12-wk–CR Apoe−/− mice. Western blots demonstrated that SIRT1 protein expression was significantly up-regulated, whereas SIRT3 expression levels remained unchanged in the aortas of CR-Con Apoe−/− mice compared with AL-Con Apoe−/− mice (Fig. 4 A). Western blots also demonstrated that the total amounts of AMPKα and mTOR and their active forms (phosphorylated AMPKα and phosphorylated mTOR) did not change significantly in the aorta in response to CR (Fig. 4 A). In addition to SIRT1 protein levels, SIRT1 deacetylase activity also markedly increased in the aorta upon CR (Fig. 4 B). To determine the cell type in the aorta in which SIRT1 was up-regulated upon CR, we evaluated SIRT1 expression in VSMCs using immunofluorescence (IF). We observed that SIRT1 was mainly located in VSMCs (marked with αSMA), and SIRT1 expression in medial VSMCs increased after 12 wk of CR (Fig. 4 C). Although macrophages are also reportedly involved in AAA development (Longo et al., 2002; Wang et al., 2010), in the present study, there were few macrophages infiltrating the aortic walls after 12 wk of CR, as indicated by IHC for macrophages (Mac-3; not depicted). These results indicate that VSMC-SIRT1 plays a potentially important role in mediating the beneficial effects of CR in the aorta.
To further confirm the response of SIRT1 in VSMCs to CR, we conducted in vitro experiments using VSMCs isolated from the suprarenal region of abdominal aortas of Apoe−/− mice that were incubated with the serum of AL-Con or CR-Con Apoe−/− mice. Western blots demonstrated that SIRT1 expression was markedly increased in VSMCs incubated with the serum from CR-Con Apoe−/− mice for 48 h compared with those cells incubated with serum from AL-Con Apoe−/− mice. However, the expression levels of SIRT3, AMPKα, and mTOR, as well as AMPKα and mTOR, activities were not significantly changed in VSMCs after incubation with CR-Con Apoe−/− mouse serum (Fig. 4 D). Consistent with the in vivo findings, the mRNA levels of respiratory chain subunits and key enzymes involved in glucose and lipid metabolism were all comparable between the AL serum–incubated and CR serum–incubated VSMCs (Fig. 4, E and F). These results suggest that despite the unchanged metabolism in VSMCs, VSMC-SIRT1 is responsively up-regulated upon CR.
To investigate the role of VSMC-SIRT1 in mediating the protective effect of CR on AAA formation, we generated Apoe−/− mice that expressed a truncated and inactive form of SIRT1 specifically in smooth muscle cells (SVKO;Apoe−/− mice) using the SM22α–Cre mouse model, as previously described (Fig. 5, A and B; Gorenne et al., 2013). We observed that the WT SIRT1 protein was almost completely depleted, and a shorter truncated SIRT1 protein was expressed in the aorta of SVKO;Apoe−/− mice (Fig. 5, C and D). We performed the 12-wk CR followed by 4 wk of AngII infusion in these mice. We observed that CR decreased both BW (Fig. 5 E) and the eWAT weight–to-BW ratio (Fig. 5 F) but did not affect the liver weight–to-BW ratio (Fig. 5 G) in SVKO;Apoe−/− mice. EE and RQ decreased in response to CR in SVKO;Apoe−/− mice (Fig. 5, H and I). Blood triglyceride levels were also reduced by CR (Table 2). The blood glucose levels within 60 min after glucose challenge were significantly lower in the CR SVKO;Apoe−/− mice compared with AL SVKO;Apoe−/− mice (Fig. 5 J). These results suggest that smooth muscle–specific SIRT1 ablation does not affect the effects of CR on systemic metabolism, implicating that systemic metabolic changes lie upstream of the up-regulation of aortic SIRT1 expression in response to CR.
After AngII infusion, 70% (14/20) of AL Sirt1flox/flox;Apoe−/− mice and 32% (6/19) of CR Sirt1flox/flox;Apoe−/− mice developed AAAs (Fig. 6, A–C). However, the incidence of AAA was 64% (16/25) for AL-AngII SVKO;Apoe−/− mice and 71% (15/21) for CR-AngII SVKO;Apoe−/− mice, which were not remarkably different (Fig. 6, A–C). Furthermore, CR reduced AngII-induced mortalities in Sirt1flox/flox;Apoe−/− mice, whereas the mortalities caused by aortic rupture in AL-AngII and CR-AngII SVKO;Apoe−/− mice were also not significantly different (Fig. 6 D). AngII infusion caused a notable increase in the total aortic weight–to-BW ratio and the aortic maximal diameter in both AL and CR groups of SVKO;Apoe−/− mice (Fig. 6, B and E). No significant differences were observed in these indices between the AL-AngII and CR-AngII SVKO;Apoe−/− mice (Fig. 6, B and E). In addition, there was no significant difference between the maximal diameters of ascending aortas of the AL and CR groups of SVKO;Apoe−/− mice upon AngII infusion (not depicted). EVG staining results showed that CR preserved elastin degradation in Sirt1flox/flox;Apoe−/− mice after AngII administration. However, there were no differences in the degree of elastin degradation in SVKO;Apoe−/− mice in either the AL-AngII or CR-AngII groups (Fig. 6, F and G). All of these results suggest that the preventive effect of CR on AngII-induced AAA formation was reduced by VSMC-SIRT1 ablation.
Extracellular matrix degradation plays a critical role in AAA formation, and MMP2 and MMP9 are particularly important in this process (Longo et al., 2002). We examined the effect of CR on the expression and activities of MMP2 and MMP9 in the aortas of Apoe−/− mice. There were no significant differences in the protein and mRNA levels of MMP2 and MMP9 between the AL-Con and CR-Con Apoe−/− mouse aortas (Fig. 7, A and C). However, compared with AL-Con Apoe−/− mice, there was a dramatic up-regulation of MMP2 and MMP9 protein and mRNA levels in the aortas of AL-AngII Apoe−/− mice; this up-regulation was significantly suppressed in the aortas of CR-AngII Apoe−/− mice compared with AL-AngII Apoe−/− mice (Fig. 7, A and C). Consistently, gelatin zymography demonstrated lower MMP2 activity in the aortas of CR-AngII Apoe−/− mice compared with AL-AngII Apoe−/− mice (Fig. 7 B). Particularly, MMP2 showed remarkably higher expression levels and activity compared with MMP9 (Fig. 7, B and C), suggesting that MMP2 is the predominant MMP in aortas. We therefore examined Mmp2 mRNA levels in the aortas of SVKO;Apoe−/− mice by quantitative real-time PCR. The results demonstrated that the AngII-induced up-regulation of Mmp2 expression was not attenuated by CR in SVKO;Apoe−/− mice (Fig. 7 D), indicating that CR inhibits AngII-induced MMP2 expression in a VSMC-SIRT1–dependent manner.
We next investigated the mechanism by which SIRT1 regulates MMP2 expression during CR. SIRT1 is a histone H3 lysine 9 (H3K9) and H4K16 deacetylase (Vaquero et al., 2004), and studies have demonstrated that the subtle enhancement of histone acetylation in the promoter can increase target gene transcription (Taylor et al., 2013; Ryall et al., 2015). Therefore, we analyzed the histone acetylation state in the aortas of Apoe−/− and SVKO;Apoe−/− mice in response to CR. Western blots demonstrated that the overall H3K9 and H4K16 acetylation (H3K9ac and H4K16ac) levels in Apoe−/− mouse aortas were not significantly changed upon CR either with or without AngII infusion (Fig. 8 A). Moreover, CR and AngII infusion did not change the overall H3K9 and H4K16 acetylation levels in aortas when SIRT1 was ablated (Fig. 8 A). Thus, we performed chromatin immunoprecipitation (ChIP) followed by quantitative PCR using mouse aortas with antibodies against H3K9ac and H4K16ac to examine whether CR affected the in vivo H3K9ac and H4K16ac levels on the Mmp2 promoter. Specific primers complementary to the regions at −919 to −784 bp, −669 to −485 bp, −404 to −261 bp, and −260 to −105 bp in the Mmp2 promoter were designed. The results demonstrated that both H3K9ac and H4K16ac levels were significantly higher than normal IgG on the four regions of the Mmp2 promoter, but no significant differences in the H3K9ac and H4K16ac levels were observed among the four Mmp2 promoter regions in the aortas of Apoe−/− mice (Fig. 8, B and C). ChIP assay results further showed that CR did not markedly influence H4K16ac or H3K9ac levels on the Mmp2 promoter without AngII infusion in the aortas of Apoe−/− mice (Fig. 8, D and E). However, H3K9ac levels on the Mmp2 promoter were remarkably increased upon AngII stimulation. After the treatment of AngII, CR significantly reduced H3K9ac levels in the regions of −919 to −784 bp, −669 to −485 bp, and −260 to −105 bp on the Mmp2 promoter in the aortas of Apoe−/− mice (Fig. 8 D), whereas H4K16ac levels in the Mmp2 promoter were not significantly affected by CR even in AngII-treated Apoe−/− mice (Fig. 8 E). Hence, these results indicate that CR specifically prevents the increase of AngII-induced H3K9ac on the Mmp2 promoter.
To investigate whether SIRT1 mediates the suppressive effect of CR on AngII-induced H3K9ac increase, the aortas of AngII-treated SVKO;Apoe−/− mice were used for H3K9ac ChIP assay. The results showed that CR did not significantly change H3K9ac levels on the Mmp2 promoter in AngII-treated SVKO;Apoe−/− mice (Fig. 8 D). Hence, VSMC-SIRT1 is required for the prevention of AngII-induced H3K9ac increase on the Mmp2 promoter. We next examined the expression and activity of SIRT1 upon AngII infusion. The results showed that, although AngII infusion did not significantly affect SIRT1 expression, AngII treatment decreased SIRT1 deacetylase activity and nicotinamide adenine dinucleotide (NAD+) availability in the aortas of Apoe−/− mice (Fig. 8, F–H). Additionally, ChIP against SIRT1 showed that AngII-treatment reduced the recruitment of SIRT1 onto the Mmp2 promoter, particularly in the −669 to −485 bp region (Fig. 8, I and J). These results suggest that AngII infusion decreases SIRT1 deacetylase activity to increase H3K9ac levels on the Mmp2 promoter, which may contribute to increased MMP2 expression in the aorta upon AngII infusion. All the results described in this section suggest that the CR-mediated increase in the aortic expression of SIRT1 may provide a prerequisite for lower histone H3K9ac levels on the Mmp2 promoter, thereby preventing the increase in MMP2 expression after AngII infusion.
In the present study, we used a mouse model to determine that CR protects against AAA formation. We observed that 12 wk of CR remarkably reduced AngII-induced AAA formation in Apoe−/− mice. Furthermore, we observed a significant increase of VSMC-SIRT1 in aortas in response to CR. The smooth muscle–specific ablation of SIRT1 reduced the effectiveness of CR in preventing AAA. Our findings suggest a critical role for VSMC-SIRT1 in mediating the protective effects of CR on AAA formation.
As a calorie intake intervention, CR influences systemic metabolism. Consistent with previous studies (Guo et al., 2002; McCurdy and Cartee, 2005; Boily et al., 2008), in our mouse model, we observed that CR affected systemic metabolic indices by decreasing BW, EE, and RQ and improving glucose regulatory function. In addition to systemic metabolic changes, CR also reprograms local metabolism in different tissues, including the liver (Renaud et al., 2014), skeletal muscle (McCurdy and Cartee, 2005), and the heart (Sung et al., 2011). However, it remains unknown whether CR has an effect on glucose and lipid metabolism in the aorta. Although we observed an increase in the expression of key glycolysis and lipolysis enzymes and oxidative phosphorylation complex subunits in Apoe−/− mouse livers after CR, no significant alteration of these molecules was observed in aortas. Our findings suggest that despite the remarkable metabolic reprogramming in the liver, a 12-wk CR diet does not cause detectable changes in aortic glucose and lipid metabolism in Apoe−/− mice.
Although no significant metabolic changes were observed in the aortas upon CR, SIRT1 expression and activity was up-regulated in the aortas of Apoe−/− mice. In contrast, the expression of other metabolic/energy sensors, including SIRT3, AMPKα, and mTOR, was not significantly changed in the aortas. Furthermore, SIRT1 expression was significantly increased in VSMCs incubated with serum from CR mice. Studies from other groups have also demonstrated that serum from CR animals increases SIRT1 expression in human coronary artery endothelial cells and HEK293T cells (Cohen et al., 2004; Csiszar et al., 2009). These results indicate that SIRT1 is sensitive to circulating factors that are altered upon CR. A previous study has demonstrated that many metabolites, and lipids in particular, were altered in C57BL/6J mouse serum upon CR (Collino et al., 2013). Palmitic acid also reportedly decreases SIRT1 expression in human monocytes (THP-1) in vitro (de Kreutzenberg et al., 2010). Here, we observed that CR significantly decreased triglyceride levels in Apoe−/− mouse serum. Thus, the alteration of serum lipids by CR may contribute to SIRT1 up-regulation in the VSMCs of the aortic media. In addition, a recent study showed that [N1]methylnicotinamide stabilizes SIRT1 to regulate hepatic metabolism (Hong et al., 2015). Hence, the changes of circulatory metabolites, such as [N1]methylnicotinamide, may also contribute to the increase of vascular SIRT1 upon CR. More importantly, we demonstrated that SIRT1 ablation in VSMCs reduced the preventive effect of CR on AAA formation but did not diminish the effect of CR on systemic metabolism. Although it remains to be elucidated exactly what metabolites mediate the up-regulation of VSMC-SIRT1 in response to CR, our findings suggest that VSMC-SIRT1 up-regulation is critical for the prevention of AngII-induced AAA formation during CR.
Epigenetic mechanisms underlie many aspects of the effects of CR on CVD prevention and health maintenance (Li et al., 2011b). As a metabolic sensor and a histone deacetylase, SIRT1 regulates CVDs by epigenetically regulating transcriptional factors and histones (Liu et al., 2014). Endothelial SIRT1 has been previously demonstrated to improve endothelial function and prevent atherosclerotic diseases by deacetylating H3K9 and H4K16 in target gene promoters (Zhou et al., 2011; Wan et al., 2014). However, it remains unclear whether SIRT1 in VSMCs participates in the epigenetic regulation of AAA formation. In the present study, we observed that VSMC-SIRT1 was a main sensor of CR in the aorta and that VSMC-SIRT1 was required for the CR-mediated prevention of AngII-induced AAA. MMP2 activation aggravated extracellular matrix degradation and promoted VSMC apoptosis, which is an important mechanism underlying AAA formation (Nataatmadja et al., 2003). We observed in the present study that CR suppressed the increase of Mmp2 transcription and prevented the decrease of VSMC density in the aortas of Apoe−/− mice with AngII-induced AAAs. Moreover, the epigenetic regulation of MMP2 expression by SIRT1-dependent H3K9ac in the Mmp2 promoter contributed to the CR-mediated inhibition of MMP2 expression after AngII infusion. VSMC-SIRT1 reportedly plays an important role in attenuating vascular remodeling by deacetylating transcription factors, thus regulating the expression of downstream molecules (Li et al., 2011a; Gao et al., 2014). MMP2 expression can be regulated by transcription factors such as NF-κB (Lin et al., 2010) and activator protein 1 (Bergman et al., 2003), which are also substrates of SIRT1 for deacetylation (Yeung et al., 2004; Zhang et al., 2010). Further studies will elucidate whether the modulation of transcription factors and histones by SIRT1 work in concert to regulate MMP2 expression in response to CR. In addition to the suppression of MMP2 expression and medial degradation, we also observed that CR decreased cytokine expression and 8-OHdG staining in the aortas of Apoe−/− mice after AngII infusion (unpublished data). These functions of CR may further contribute to protection against AAA progression.
In conclusion, the present study provides the first evidence that reducing calorie intake reduces AAA formation in mice. Moreover, VSMC-SIRT1 plays a critical role in mediating the protective effect of CR on AAA formation. Our findings support the benefit of a calorie-restricted lifestyle for AAA prevention and suggest that SIRT1 is a promising molecular target for the treatment of AAA.
Apoe−/− mice on C57BL/6J background were obtained from Peking University. We established SVKO mice using a Cre/LoxP strategy. Sirt1flox/flox mice that expressed SIRT1exon4 flanked by LoxP sites on the 129 background were purchased from The Jackson Laboratory (stock no. 008041). SM22α-Cre+/+ mice on the 129 background with a Cre-recombinase gene inserted into the endogenous transgelin (SM22α) locus were purchased from The Jackson Laboratory (stock no. 006878). These mice were backcrossed with mice on the C57BL/6J background for at least 10 generations to yield Sirt1flox/flox mice and SM22α-Cre+/− mice on the C57BL/6J background. They were further crossed with Apoe−/− mice to generate Sirt1flox/flox;Apoe−/− and SM22α-Cre+/−;Apoe−/− mice. Male SM22α-Cre+/−;Sirt1flox/flox;Apoe−/− mice were crossed with female Sirt1flox/flox;Apoe−/− mice, both on the C57BL/6J background, to generate SVKO;Apoe−/− mice (SM22α-Cre+/−;Sirt1flox/flox;Apoe−/−). All of the mice were genotyped by PCR using tail clip samples. The primers used for genotyping are listed in Table S1. All of the animal protocols were approved by the Animal Care and Use Committee at the Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, and Peking Union Medical College.
8-wk-old male Apoe−/− or SVKO;Apoe−/− mice were housed individually and randomly allocated into four groups. AL-Con mice and AL-AngII mice were fed AL with AL food for 16 wk. CR-Con mice and CR-AngII mice were fed a 10%-restricted diet for the first week and a 25%-restricted diet for the remaining experimental period of the CR diet. The AL and CR food were made according to the composition of AIN-93M, as previously described (Pugh et al., 1999). During the last 4 wk, AL-AngII and CR-AngII mice received subcutaneous AngII infusions in a dose of 1.44 mg/kg/d delivered via osmotic pumps (model 2004; Alzet). AL-Con and CR-Con mice received saline as a control. The detailed procedure was performed as previously described (Satoh et al., 2009). In the last week of the experiment, the mice underwent indirect calorimetry, IPGTT, and SBP measurement. After sacrifice, maximal diameters of suprarenal abdominal aortas and maximal diameters of ascending aortas were measured using Image Pro Plus software (Media Cybernetics) by a researcher blind to group assignment. AAA incidence was calculated based on a definition of aneurysm as an external width of the suprarenal aorta that was increased by ≥50% compared with aortas from saline-infused mice as previously described (Satoh et al., 2009).
Whole-body metabolic states of the mice were tested by indirect calorimetry in a comprehensive lab animal monitor system (Columbus Instruments) for 2 d after 1 d of habituation according to the manufacturer’s instructions. Light and feeding conditions were kept the same as in the home cages. EE and RQ were calculated using the equations: EE (kcal/h) = (3.818 × VO2) + (1.232 × VCO2) and RQ = VO2/VCO2. VO2 stands for the volume of oxygen consumed per hour, and VCO2 stands for the volume of carbon dioxide produced per hour. Because of the huge difference in BW between the AL and CR mice, we compared their metabolic rates by normalizing to the metabolic size, as reflected by the BW0.75 of each mouse (Zhou et al., 2012).
Before IPGTT, the mice were fasted overnight. Fasting blood glucose levels were measured with blood that was collected via tail tip cutting using a portable glucose meter (Yuyue). Mice were injected intraperitoneally with 2 g/kg BW d-glucose dissolved in saline, and blood glucose levels were measured at 15, 30, 60, and 120 min after glucose injection.
SBP was measured in the last week of AngII infusion. SBP was measured using tail-cuff plethysmography (BP-2000 System; Visitech Systems) as previously described (Li et al., 2011a).
Mice were fasted overnight and anesthetized before blood collection. Blood was collected from the abdominal vena cava before euthanasia, allowed to clot for 20–30 min, and centrifuged at 3,000 g for 20 min. Serum was collected from the centrifuged samples and stored at −70°C until use. The serum was thawed, and triglyceride and cholesterol levels were measured at the Peking Union Medical College Hospital clinical laboratory.
After the mice were executed, aortas from the ascending aorta to the furcation of the common iliac artery were isolated. After macroscopic analysis, suprarenal abdominal aortas were subjected to histology analysis. The aortas and adventitia were fixed with 4% paraformaldehyde-PBS for 24 h and embedded in paraffin, and serial sections were made using suprarenal abdominal aortas and four sections (5 µm each) at 500-µm intervals as previously described (Satoh et al., 2009). Paraffin sections were stained with EVG or used for IF staining and IHC staining. The grade of elastin degradation was quantified by a researcher who was blinded to the group assignment according to the criteria previously described (Satoh et al., 2009). The grades were as follows: score 1, no degradation; score 2, mild elastin degradation; score 3, severe elastin degradation; and score 4, aortic rupture. The primary antibodies used in IF and IHC staining were αSMA (A2547, Sigma-Aldrich; ab5694, Abcam) and SIRT1 (07-131; EMD Millipore). The secondary antibodies used in IF staining were Alexa Fluor 488–conjugated goat anti–mouse IgG and Alexa Fluor 594–conjugated goat anti–rabbit IgG. Nuclei were stained with Hoechst Stain solution (B2261; Sigma-Aldrich). All of the pictures were taken with the same settings.
Total RNA was extracted using TRIzol reagent (Invitrogen) and first-strand cDNA was synthesized from 3 µg RNA using a reverse transcription system (New England Biolabs, Inc.) according to the manufacturer’s instructions. Quantitative real-time PCR was performed using Green Premix Ex Taq reagent (Takara Bio Inc.) on a Mastercycler machine (Eppendorf) with cDNA as a template. Primers were designed to span exon boundaries to avoid genomic DNA amplification. Target mRNA expression was calculated relative to Actb. Primer sequences are provided in Table S2.
Western blotting was performed as previously described (Zhou et al., 2011). The primary antibodies used were SIRT1 (07-131; EMD Millipore), SIRT3 (5490; Cell Signaling Technology), AMPKα (9957; Cell Signaling Technology), phosphorylated AMPKα (9957; Cell Signaling Technology), mTOR (2983; Cell Signaling Technology), phosphorylated mTOR (2971; Cell Signaling Technology), GAPDH (5174; Cell Signaling Technology), MMP2 (sc13595; Santa Cruz Biotechnology, Inc.), MMP9 (ab38898; Abcam), H3K9ac (ab10812; Abcam), H3 (ab1791; Abcam), H4K16ac (07-329; EMD Millipore), and H4 (05-858; EMD Millipore). Western blots were quantified densitometrically using Image Pro-Plus software (Media Cybernetics), the intensity values were calculated relative to GAPDH, H3, or H4, and the values were normalized to AL-Con values.
Freshly isolated mouse aortas were homogenized with immunoprecipitation buffer (P0013; Beyotime Biotechnology). SIRT1 was immunoprecipitated with SIRT1 antibodies (07-131; EMD Millipore) from whole aortic homogenates (200 µg protein). Aortic SIRT1 activity was assessed using a SIRT1 deacetylase activity assay kit (CS1040; Sigma-Aldrich) according to the manufacturer’s instructions.
Freshly isolated mouse aortas were used for measuring aortic NAD+/NADH levels following the manufacturer’s instructions (ab65348; Abcam).
VSMCs for culture were isolated from suprarenal abdominal aortas of 2–3-mo-old 20–25-g WT male mice and maintained in DMEM containing 10% FBS at 37°C in a humidified atmosphere of 5% CO2 and 95% air, as previously described (Ishida et al., 1999). Four to five passages of VSMCs at 70–80% confluence were incubated in DMEM containing 10% serum from AL-Con or CR-Con Apoe−/− mice for 48 h. Mouse serum was thawed and heat inactivated at 56°C for 30 min before use in cell culture experiments.
MMP activity was measured as previously reported (Hawkes et al., 2010). Aortic homogenates (5 µg protein) were electrophoresed in SDS-PAGE gels containing gelatin. The gels were washed in 2.5% Triton X-100 for 30 min and incubated for 12–40 h in zymography development buffer (0.05 M Tris-HCl, pH 8.8, 5 mM CaCl2, and 0.02% NaN3) at 37°C. The gels were subsequently stained with Coomassie brilliant blue.
Freshly isolated mouse aortas were carefully stripped out of the adventitial layer and chopped into small pieces. Aortic tissue was digested with 0.05% trypsin-EDTA (BRL 25300; Gibco) for 5 min at 37°C, followed by the addition of 9 ml of 10% FBS-DMEM to stop digestion. ChIP assays were performed using aortic tissues as previously described (Wang et al., 2008). The antibodies used in ChIP included anti-H3 (ab1791; Abcam), H3K9ac (ab10812; Abcam), H4 (05-858; EMD Millipore), H4K16ac (07-329; EMD Millipore), SIRT1 (07-131; EMD Millipore), and normal rabbit IgG (sc-2027; Santa Cruz Biotechnology, Inc.). DNA was detected by quantitative real-time PCR. Specific primers were designed to amplify the Mmp2 promoter. The primer sequences are provided in Table S3.
Quantitative results are expressed as the means ± SEM. The normality and the homogeneity of variance of the data were tested. To compare among three or more groups, a one-way ANOVA plus a posthoc analysis (Bonferroni test) was used for normally distributed variables, and a Kruskal-Wallis test plus a posthoc analysis (Dunn’s multiple comparison test) was used for variables not passing a normality or equal variance test. Two-way repeated-measures ANOVA was used for BW data and IPGTT data that were repeatedly measured. Fisher’s exact test was applied to the comparisons of aneurysm incidence. The log-rank (Mantel-Cox) test was used for survival analysis. All statistical analyses were performed using Prism 6.0 (GraphPad Software). A p-value <0.05 was considered to be statistically significant.
Table S1 shows primers used for genotyping. Table S2 shows primers used for measuring relative mRNA expression. Table S3 shows primers used in tissue ChIP assays.
This work is supported by grants from the National Natural Science Foundation of China (91339201, 81422002, 31571193, and 31271227) and the National Basic Research Program of China (2011CB503902).
The authors declare no competing financial interests.