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Anne Brunet, Alway M336, 300 Pasteur Drive, Stanford University, Stanford CA 94305, USA. Tel.: +1 650 725 8042; fax: +1 650 725 1534; e-mail: email@example.com
Dietary restriction (DR) has the remarkable ability to extend lifespan and healthspan. A variety of DR regimens have been described in species ranging from yeast to mammals. However, whether different DR regimens extend lifespan via universal, distinct, or overlapping pathways is still an open question. Here we examine the genetic pathways that mediate longevity by different DR regimens in Caenorhabditis elegans. We have previously shown that the low-energy sensing AMP-activated protein kinase AMPK/aak-2 and the Forkhead transcription factor FoxO/daf-16 are necessary for longevity induced by a DR regimen that we developed (sDR). Here we find that AMPK and FoxO are necessary for longevity induced by another DR regimen, but are dispensable for the lifespan extension induced by two different DR methods. Intriguingly, AMPK is also necessary for the lifespan extension elicited by resveratrol, a natural polyphenol that mimics some aspects of DR. Conversely, we test if genes previously reported to mediate longevity by a variety of DR methods are necessary for sDR-induced longevity. Although clk-1, a gene involved in ubiquinone biosynthesis, is also required for sDR-induced lifespan extension, we find that four other genes (sir-2.1, FoxA/pha-4, skn-1, and hsf-1) are all dispensable for longevity induced by sDR. Consistent with the observation that different DR methods extend lifespan by mostly independent genetic mechanisms, we find that the effects on lifespan of two different DR regimens are additive. Understanding the genetic network by which different DR regimens extend lifespan has important implications for harnessing the full benefits of DR on lifespan and healthspan.
Restricting nutrients without malnutrition extends lifespan and reduces age-dependent decline and diseases in virtually all species (Masoro, 2005). Although a single term [dietary restriction (DR)] is often used to refer to this intervention, there exist a number of methods of restricting nutrients that all result in lifespan extension in species ranging from yeast to mice (Goodrick etal., 1990; Mair etal., 2005; Masoro, 2005; Dilova etal., 2007; Mair & Dillin, 2008; Piper & Bartke, 2008; Skorupa etal., 2008). Whether the different methods of restricting nutrients converge on a common pathway to extend lifespan or whether independent mechanisms are elicited depending on how DR is achieved is still unclear.
The nematode Caenorhabditis elegans provides a good model to study the genetics of lifespan in response to different DR regimens. There exist eight distinct methods of manipulating the diet that all extend lifespan to varying degrees in C. elegans, allowing comparison across DR regimens (Table 1). The standard worm diet consists of attenuated E. coli bacteria (OP50) placed on agarose plates. The DR methods in worms are: (i) a genetic mutation (eat-2) that reduces the pharyngeal pumping rate of the worms, thereby decreasing food intake (Avery, 1993; Lakowski & Hekimi, 1998); (ii and iii) two different methods of diluting the bacteria in liquid cultures (bacterial DR: bDR and liquid DR: lDR) (Klass, 1977; Houthoofd etal., 2003; Bishop & Guarente, 2007; Panowski etal., 2007); (iv and v) two chemically defined liquid medias that induce DR-like phenotype in C. elegans (axenic medium and chemically defined liquid medium: CDLM) (Houthoofd etal., 2002a; Szewczyk etal., 2006); (vi) the dilution of peptone in the agarose plates, which reduces the growth of bacteria (DP: dilution of peptone) (Hosono etal., 1989); (vii) the total absence of bacteria on plates (dietary deprivation: DD) (Kaeberlein etal., 2006; Lee etal., 2006); and (viii) a method that we recently described where bacteria are serially diluted on plates (solid DR: sDR) (Greer etal., 2007).
Table 1. Eight methods of dietary restriction in C. elegans
Independent laboratories calculate lifespan starting at different ages (birth vs. young adult).
While UV-killed bacteria were used in some experiments with sDR and resveratrol, most experiments were performed with live bacteria.
sDR is normally initiated at a post-reproductive age (day 4 of adulthood), but when initiated at day 1 of adulthood, sDR decreases fertility (data not shown).
We have recently discovered that the low energy-sensing kinase AMPK/aak-2 is necessary for longevity induced by sDR in worms (Greer etal., 2007). AMPK can act upstream of the Forkhead transcription factor FoxO/daf-16 to extend lifespan, perhaps via direct phosphorylation (Greer etal., 2007). Like AMPK, FoxO is necessary for longevity induced by sDR (Greer etal., 2007). In contrast, neither AMPK nor FoxO are necessary for the longevity induced by eat-2 (Lakowski & Hekimi, 1998; Curtis etal., 2006). In addition, FoxO is not necessary for longevity induced by other DR methods (bDR, lDR, axenic medium, and DD) (Houthoofd etal., 2003; Kaeberlein etal., 2006; Lee etal., 2006; Bishop & Guarente, 2007; Panowski etal., 2007). Similarly, in Drosophila, FoxO is not absolutely necessary for DR-induced longevity (Giannakou etal., 2008; Min etal., 2008), although FoxO alters the optimal food concentration required for longevity (Clancy etal., 2002; Giannakou etal., 2008; Min etal., 2008). In mammals, the role of AMPK and FoxO in DR-induced longevity has not been examined yet. While a series of genes have been identified as playing important roles in longevity induced by different DR methods, the comparison of the importance of these genes in diverse DR regimens has not been performed. Identifying the different genetic pathways by which the various methods of restricting nutrients promote longevity is important for harnessing the full benefits of DR on lifespan.
Here we test whether distinct DR methods are mediated by specific or common genetic pathways. We find that while AMPK and FoxO are necessary for longevity induced by sDR and by peptone dilution in plates, these genes are not absolutely required for eat-2 and bDR to extend lifespan. Intriguingly, AMPK, but not FoxO, is necessary for the DR mimetic resveratrol to extend lifespan in worms. We then test whether sDR is mediated by genes that were previously found to mediate longevity by other DR methods or DR mimetics. We find that sir-2.1, pha-4, skn-1, and hsf-1 are all dispensable for sDR-induced lifespan extension, but that clk-1 is necessary for this regimen to extend lifespan. Finally, we show that sDR further enhances the lifespan of eat-2 mutant worms, indicating that these two DR methods act additively to promote longevity. Our results are compatible with a model in which sDR induces lifespan extension by a mechanism that is different from, but overlapping with, that of other DR methods. Understanding how different methods of DR induce lifespan extension is pivotal for the identification of all the components of the gene network that orchestrates maximal longevity extension in response to nutrient deprivation.
AMPK/aak-2 and FoxO/daf-16 are necessary for sDR-induced lifespan extension across a gradient of bacteria on plates
Assessing lifespan at only two concentrations of food (ad libitum vs. DR) does not distinguish genes that are truly involved in mediating DR from genes that affect the optimal response to food concentrations required to elicit the DR effect (e.g. chico in flies) (Clancy etal., 2002). Therefore, to test if AMPK/aak-2 and FoxO/daf-16 mediated lifespan extension in response to DR or affected the optimal response to food concentration, we performed lifespan experiments using a gradient of bacterial concentrations. The lifespan extension of WT worms as a function of bacteria concentration follows a parabola-shaped curve (Fig. 1), with moderate reduction of food intake leading to beneficial effects on lifespan (DR) and severe reduction of food intake having detrimental effects leading to death (starvation) (Piper & Partridge, 2007; Mair & Dillin, 2008). In contrast, the lifespan of worms carrying a null mutation in the aak-2 or in the daf-16 gene (aak-2(ok524) and daf-16(mu86)) was never extended, regardless of the concentration of bacteria (Fig. 1A,B; Tables S1A and S1B in Supporting Information). These results indicate that AMPK/aak-2 and FoxO/daf-16 are necessary for lifespan extension in response to sDR and that mutations in these genes do not lead to a shift of the overall organismal dependence on food.
The dependency of sDR on AMPK and FoxO was also observed with independent backcrossed worm strains (aak-2(rr48) for AMPK and daf-16(m26) or daf-16(mgDf50) for FoxO) (Fig. 5, data not shown), with bacterial strains from independent laboratories (data not shown), and in the presence or absence of FUdR, an inhibitor of worm reproduction (Figure S1; Table S1C). Together with our previous findings (Greer etal., 2007), these results indicate that AMPK and FoxO are necessary to mediate longevity induced by sDR, a regimen that restricts food intake in worms.
AMPK and FoxO are necessary for the lifespan extension due to peptone dilution
We next asked how general the role of AMPK and FoxO was in longevity induced by different methods of restricting nutrients. Dilution of peptone in bacterial plates extends worm lifespan because it is considered to reduce bacterial growth on the plates (Hosono etal., 1989). We find that the dilution of peptone in bacterial plates extends lifespan in an AMPK/aak-2 and FoxO/daf-16 dependent manner (P < 0.0001 by two-way anova) (Fig. 2A; Table S2). This result indicates that AMPK and FoxO are also necessary for lifespan extension induced by another method of restricting nutrients.
AMPK and FoxO are not completely necessary for bDR and eat-2 induced longevity
FoxO/daf-16 was shown not to be entirely necessary for longevity induced by the dilution of bacteria in liquid cultures (bDR) (Houthoofd etal., 2003; Panowski etal., 2007). However, the importance of AMPK in bDR-induced lifespan extension has never been examined. We tested whether AMPK and FoxO were required for lifespan extension in response to a gradient of bacteria concentrations in liquid culture. Combining the results of three independent experiments (Fig. 2B), we found that bDR significantly extended the lifespan of WT (N2), aak-2(ok524), and daf-16(mu86) mutant worms (P < 0.0001), indicating that AMPK and FoxO are dispensable for the entire lifespan extension induced by bDR. In two of these experiments, bDR extended WT (N2) lifespan to a larger extent than aak-2 and daf-16 mutant worm lifespan (P < 0.0001 by two-way anova) (Figure S2A and S2B; Table S3). In one experiment however, bDR extended the lifespan of WT (N2) worms to a similar extent as that of aak-2 and daf-16 mutant worms (P = 0.1528 and 0.6643 respectively by two-way anova) (Figure S2C; Table S3). Note that in one of the assays (Figure S2A), starvation was not reached, which may alter the interpretation of the experiment. However, when this assay was omitted for statistical analysis, we still found that bDR extended WT (N2) lifespan to a larger extent than aak-2 and daf-16 mutant worm lifespan (P < 0.001 by two-way anova). Although the parameters for these variations are unknown, these results suggest that AMPK and FoxO are dispensable for bDR to extend lifespan, but that they play a modulatory role in the extension of lifespan by this regimen.
Finally, as previously reported, we confirmed that AMPK/aak-2 and FoxO/daf-16 were completely dispensable for the lifespan extension of eat-2(ad1116) mutant worms, a genetic way to mimic DR (Lakowski & Hekimi, 1998; Curtis etal., 2006) (Fig. 2C,D; Table S4). Together, these results indicate that AMPK and FoxO are required for longevity induced by some (sDR and DP) but not all (bDR and eat-2) DR methods.
Resveratrol extends lifespan in an AMPK-dependent, but FoxO-independent, manner
Resveratrol extends lifespan in many species and has been suggested to act as a DR mimetic (Sinclair, 2005). Resveratrol has recently been found to activate AMPK in cultured cells and in mice (Baur etal., 2006; Zang etal., 2006; Dasgupta & Milbrandt, 2007; Hwang etal., 2007). We thus asked whether AMPK was necessary for increased longevity induced by resveratrol in C. elegans. Resveratrol induced a modest, but statistically significant, increase in WT (N2) worm lifespan. In contrast, resveratrol did not increase the lifespan of aak-2(ok524) mutant worms, suggesting that AMPK is necessary for the beneficial effects of resveratrol on lifespan (Fig. 3A; Table S5), as was proposed by (Bass etal., 2007). Similar to what was previously reported (Viswanathan etal., 2005), we found that resveratrol still extended the lifespan of daf-16(mu86) mutant worms (Fig. 3B; Table S5), indicating that resveratrol extends lifespan by eliciting an AMPK-dependent, FoxO-independent pathway. Therefore, activation of AMPK is not always coupled to that of FoxO, even though AMPK's ability to extend lifespan is dependent on the presence of FoxO (Greer etal., 2007). This result suggests that AMPK also regulates other substrates to extend lifespan, which is consistent with published findings (Apfeld etal., 2004; Narbonne & Roy, 2006). Therefore, these results suggest that different ways of manipulating nutrients and chemical compounds extend lifespan via independent and non-linear genetic pathways.
sir-2.1, pha-4, skn-1, and hsf-1 are not necessary for sDR-induced lifespan extension
Having shown that FoxO and AMPK were important for some, but not all, DR methods, we next tested if conversely, genes that have been implicated in lifespan extension by resveratrol or by other DR regimens were necessary for sDR to extend lifespan.
We first asked if sir-2.1, which encodes a Sirtuin family protein deacetylase, was required for lifespan extension in response to sDR. sir-2.1 has been found to mediate lifespan extension by resveratrol in some studies (Wood etal., 2004; Viswanathan etal., 2005), but not others (Bass etal., 2007). We used a mutant strain carrying a deletion in the sir-2.1 gene, which is predicted to be a null mutant (sir-2.1(ok434)) (Wang & Tissenbaum, 2006). We found that sDR increased the lifespan of both WT and sir-2.1 mutant worms to the same extent (Fig. 4A; Table S6). There was no statistically significant difference between the effects of sDR on the longevity of WT worms vs. sir-2.1 mutant worms (P = 0.1240 by two-way anova). These results indicate that sir-2.1 is not necessary for lifespan extension by sDR.
We then tested the importance of the Forkhead transcription factor FoxA/pha-4, a gene involved in eat-2 and bDR-induced longevity (Panowski etal., 2007), in lifespan extension induced by sDR. We used a temperature sensitive allele of FoxA/pha-4, smg-1(cc546ts); pha-4(zu225), and its control counterpart smg-1(cc546ts) (Gaudet & Mango, 2002). When shifted to the restrictive temperature smg-1(cc546ts); pha-4(zu225) display very little PHA-4 protein and the phenotype of smg-1(cc546ts); pha-4(zu225) is similar to that of the pha-4(q490) null mutant (Kaltenbach etal., 2005; Kiefer etal., 2007). We found that sDR extended lifespan of both the control strain (smg-1(cc546ts)) and the inducible pha-4 mutant strain (smg-1(cc546ts); pha-4(zu225)) (Fig. 4B; Table S7A) (P = 0.3724 by two-way anova). These results indicate that FoxA/pha-4 is not necessary for sDR induced lifespan extension. Consistent with this observation, we found that sDR still increased the lifespan of worms in which FoxA/pha-4 was knocked-down by RNAi, but did not extend the lifespan of worms in which FoxO/daf-16 was knocked-down (Figure S3; Table S7B). These findings suggest that FoxO, but not FoxA, is required for sDR-induced longevity.
We also examined if skn-1, a gene encoding a transcription factor necessary for lDR to extend lifespan (Bishop & Guarente, 2007), was required for longevity in response to sDR. We used a loss of function mutant strain of skn-1, skn-1(zu135), which displays a premature stop codon in all three isoforms of SKN-1 (a, b, and c) (Bishop & Guarente, 2007; Tullet etal., 2008). We showed that sDR extended lifespan of WT worms and skn-1(zu135) mutant worms to a similar extent (P = 0.5567 by two-way anova). Although it is formally possible that some SKN-1 activity remains in the skn-1(zu135) mutant strain, these findings nevertheless suggest that skn-1 is not necessary for sDR-induced longevity (Fig. 4C; Table S8).
Finally, we asked if hsf-1, which encodes a heat-shock responsive transcription factor involved in longevity in response to DD (Steinkraus etal., 2008), was necessary for sDR-induced lifespan extension. We used a mutant strain of hsf-1 (hsf-1(sy441)) that contains a premature stop codon that eliminates the transactivation domain of HSF-1 and is likely to be a null mutant (Hajdu-Cronin etal., 2004). We found that sDR still extended the lifespan in hsf-1(sy441) mutant worms similarly to WT worms (P = 0.2843 by two-way anova), indicating that hsf-1 is not necessary for sDR-induced longevity (Fig. 4C; Table S9).
Together, these data indicate that four genes (sir-2.1, pha-4, skn-1, and hsf-1) that have been previously implicated in longevity in response to a variety of DR methods and DR mimetics do not mediate lifespan extension by sDR. These findings further corroborate the observation that different DR regimens evoke independent pathways.
clk-1 is necessary for sDR-induced lifespan extension
The clk-1 gene encodes a demethoxyubiquinone hydroxylase that is necessary for the biosynthesis of ubiquinone, a component of the electron transport chain (Ewbank etal., 1997; Miyadera etal., 2001). clk-1 mutant worms live longer than their WT counterparts (Lakowski & Hekimi, 1996) and their long lifespan is not further extended by the eat-2 mutation (Lakowski & Hekimi, 1998), suggesting that clk-1 is necessary for eat-2 induced lifespan extension. Although the clk-1 allele, clk-1(e2519), is unlikely to be a null mutant (Lakowski & Hekimi, 1996), we tested if clk-1 was important for sDR-induced lifespan extension. We found that clk-1(e2519) mutant worms, similarly to aak-2(ok524) and aak-2(rr48) mutant worms, no longer responded to sDR (Fig. 5; Table S9). These results suggest that clk-1 is necessary for sDR-induced longevity and are compatible with the observation that clk-1 longevity like sDR-induced lifespan is dependent on daf-16. Although the interpretation of these results is difficult because of the lack of a null allele for clk-1 (Gems etal., 2002), clk-1 may mediate two independent methods of DR, eat-2 and sDR. Thus, in addition to the genes that are specific to DR methods, there may also exist overlapping mechanisms underlying DR-induced longevity.
The effects of sDR and eat-2 on lifespan are additive
The observation that sDR is mediated by AMPK, FoxO, and clk-1 whereas eat-2 is mediated by FoxA and clk-1, raised two possibilities: (i) clk-1 is a common mechanism between both methods of DR but each method also triggers specific pathways in parallel; and (ii) each DR regimen is sensed by different pathways (e.g. by FoxO vs. FoxA), which both converge on clk-1. To distinguish between these two possibilities and to test whether sDR and eat-2 had additive effects on longevity, we tested the combined effect of sDR and eat-2 on lifespan. We found that sDR further extended the long lifespan of eat-2 mutant worms (Fig. 6, Table S4). Thus, both DR regimens are additive and can extend lifespan by up to 57% when combined. Although the eat-2 mutation is not a null mutation, which renders the interpretation of these experiments more difficult, these findings also suggest that eat-2 and sDR evoke mostly independent, though overlapping, pathways to extend lifespan.
In this study, we performed a side-by-side comparison of the role of different genes in lifespan extension elicited by a variety of DR regimens. Our results uncover the importance of the low energy-sensing protein kinase, AMPK, in longevity due to some forms of DR and to resveratrol, a compound that extends lifespan and mimics some aspects of DR in many species. In addition, our findings provide further evidence that, contrary to the assumption that DR is independent of the insulin–FoxO pathway in invertebrates, the FoxO transcription factor daf-16 actually plays a role in DR-induced longevity, depending on how DR is elicited (Fig. 7A). Importantly, our results show that DR is not a uniform condition that triggers a universal and linear genetic pathway. Rather, diverse DR regimens evoke mostly independent genetic pathways, depending on how DR is achieved (Fig. 7B). Identifying the specific genes that mediate DR-induced longevity in C. elegans is likely to have important implications for other species, including yeast, flies, and mammals, because of the conservation of the genes studied and because of the existence of different DR regimens in these other species as well. Understanding the genetic network by which different DR methods extend lifespan should also help harness the effects of this environmental intervention on lifespan and healthspan and will be particularly important to achieve the full benefits of DR.
Parameters that may affect the mechanisms of DR-induced longevity
Different DR regimens may evoke distinct genetic pathways because some nutrients may be more limiting than others depending on the DR method. For example, sDR might reduce carbohydrates more prominently than amino-acids, which would render it dependent on AMPK and FoxO, while other methods (eat-2, bDR) may reduce amino-acids more readily, which would evoke TOR, a well-known amino-acid responsive pathway (Avruch etal., 2006), and the FoxA/pha-4 transcription factor, which has recently been found to be downstream of TOR (Sheaffer etal., 2008). DR could also trigger different genetic mechanisms depending on the time at which DR is initiated or the tissues/cells by which it is sensed.
Alternatively, different DR regimens may evoke independent pathways because the way in which DR is initiated may trigger other non-DR signaling pathways that in turn have beneficial effects on lifespan. For example, diluting bacteria in sDR might also lead to the reduction in bacterial pathogenicity, which could in turn affect the insulin-FoxO pathway. However, if pathogenicity were the sole cause for premature death, concentrating bacteria above the ad libitum concentration would be detrimental, which we have found not to be the case. We have also shown that sDR is not simply due to a reduction in bacterial pathogenicity because sDR reduces worm fertility (data not shown) and because sDR performed with UV-killed bacteria also extends lifespan (Greer etal., 2007). The way sDR is achieved (by adding diluted amounts of E. coli every 2 days) may induce cycles of feeding and fasting that may cause this method to be AMPK and FoxO dependent whereas other DR methods (eat-2) maintain a more constant bacteria concentration throughout lifespan. sDR may also induce a mild oxidative stress response that could trigger the activation of the AMPK and FoxO pathways, as these pathways are known to transduce stress stimuli (Henderson & Johnson, 2001; Apfeld etal., 2004; Schulz etal., 2007; Lee etal., 2008). Although such stress may be part of DR itself (see the ‘hormesis theory’ of DR (Sinclair, 2005)), it is possible that the other DR methods do not require oxidative stress to extend lifespan.
Conversely, other methods of inducing DR could trigger non-DR signaling pathways. For example, the eat-2 mutation, which affects the acetylcholine receptor, may have other effects in addition to reducing pharyngeal pumping. Liquid methods of DR may also evoke other parameters (e.g. altered oxygen consumption (Honda etal., 1993) or forced exercise (Retzlaff etal., 1966) since worms actively swim in liquid) that may interact with reduction in nutrients to result in lifespan extension in a manner that is dependent on specific genes. Identifying the parameters that are embedded in or interact with DR methods will be important to gain complete insight into the mechanisms by which DR extends lifespan.
Mechanisms of DR in other species
An important question is whether the genetic mechanisms identified to regulate longevity in response to DR in C. elegans are conserved between species. The existence of different DR regimens that extend lifespan in yeast, flies, and mice raises the possibility that some of the mechanisms sensing the restriction of specific nutrients are conserved throughout evolution.
For example, in flies, a number of different methods of restricting diet extend lifespan (for a comprehensive review see (Piper & Partridge, 2007)). Two methods of DR in flies, dilution of yeast (Min etal., 2008) and dilution of both sugar and yeast (Giannakou etal., 2008) have been found to be independent of the Drosophila FoxO transcription factor, dFOXO, although dFOXO modifies the response to DR (Giannakou etal., 2008). While the role of AMPK in DR has not been tested yet, the histone deacetylases Rpd3 and Sir2, and the tumor suppressors Dmp53 and Tsc2, a member of the TOR pathway, have all been shown to be necessary for lifespan extension in different methods of DR in flies (Rogina etal., 2002; Kapahi etal., 2004; Rogina & Helfand, 2004; Bauer etal., 2005). The main method in which DR is initiated in flies, which reduces amino-acids, may primarily evoke the TOR and FoxA pathway rather than the AMPK or FoxO pathway (Kapahi etal., 2004).
In mice, reduction of the total amount of food which mice receive every day (Weindruch etal., 1986) or alternating days of feeding and fasting (EOD) both extend lifespan (Goodrick etal., 1990). The specific genetic components involved in DR in mice have not been as extensively analyzed yet, although the deletion of Sirt1, the mouse Sir2 ortholog, abrogates the beneficial effect of DR on behavioral activity (Chen etal., 2005) and mice expressing additionally copies of the Sirt1 gene have metabolic parameters similar to those induced by DR (Bordone etal., 2007). A reduction of the protein concentration (Goodrick, 1978) or of the amount of methionine in the diet also extend mouse lifespan (Orentreich etal., 1993), raising the possibility that the TOR pathway might be critical in longevity induced by these methods. While the importance of AMPK or FoxO in longevity induced by DR in mammals is still unknown, emerging evidence suggests that these pathways play some role in DR. First, EOD and a 40% restriction of food activate AMPK in the liver of rats (Pallottini etal., 2004). Short term DR (60% reduction of food for 5 days) also activated AMPK in the hippocampus of mice (Dagon etal., 2005). Second, the lifespan of mice that are deficient for the growth hormone receptor is not extended by a 30% reduction of food (Bonkowski etal., 2006). The deficiency in growth hormone receptor is thought to act via a reduction in IGF-1 and insulin levels, which would lead to FoxO activation. These observations raise the possibility that FoxO may mediate longevity in response to DR in mice.
Role of AMPK in longevity induced by ‘DR mimetics’
A gene network mediating longevity in response to DR
The pathways that regulate aging in response to DR are unlikely to be linear. Our findings indicate that resveratrol requires AMPK, but not FoxO, to extend lifespan, yet FoxO is necessary to mediate AMPK's effects on lifespan (Greer etal., 2007). Similarly, lifespan extension due to resveratrol is thought to be sir-2.1 dependent (although not in all studies (Bass etal., 2007)) and daf-16 independent (Wood etal., 2004; Viswanathan etal., 2005), yet the lifespan extension in response to sir-2.1 overexpression is daf-16 dependent (Tissenbaum & Guarente, 2001). These observations suggest that genetic pathways branching downstream of Sir-2 and AMPK probably exist and that negative and positive feedback mechanisms may also be involved. For example, AMPK substrates other than FoxO may contribute to AMPK lifespan extension, as proposed (Apfeld etal., 2004; Narbonne & Roy, 2006). The identification of additional AMPK substrates will be important for understanding the mechanisms of AMPK action on longevity. Our study may provide an explanation for the controversies regarding the implication of daf-16 downstream of pro-longevity genes (Lakowski & Hekimi, 1996; Murakami & Johnson, 1996; Braeckman etal., 1999; Henderson etal., 2006; Wang & Tissenbaum, 2006; Hansen etal., 2007). Lifespan assay protocols might inadvertently induce sDR, which would render lifespan daf-16 dependent. Thus, maintaining worms on ad libitum concentrations of food throughout lifespan experiments is likely crucial to prevent confounding variables, which could influence whether longevity is dependent on daf-16.
Finally, it is interesting to note that the genes involved in mediating different DR methods encode proteins from similar families (the Forkhead transcription factors FoxO and FoxA or the nutrient sensing kinases AMPK and TOR). In addition, the pathways mediating DR-induced longevity have already been shown to cross-talk extensively, at least in mammalian systems (e.g. AMPK and mTOR, Sir2 and AMPK) (Greer & Brunet, 2008). These observations underscore that DR-induced longevity is likely to be mediated by a network of genes rather than by linear pathways. Manipulating more than one ‘node’ in this network may allow additive or even synergistic lifespan and healthspan benefits.
Materials and methods
Worm strains and RNA interference
N2 and daf-16(mu86) strains were a kind gift from Dr Man-Wah Tan. The aak-2(ok524), aak-2(rr48), sir-2.1(ok434), skn-1(zu135), hsf-1(sy441), clk-1(e2519), daf-16(mgDf50), daf-16(m26), and daf-16(mu86), strains were provided by the Caenorhabditis Genetics Center. The eat-2(ad1116), daf-16(mu86); eat-2(ad1116), N2, and a three times backcrossed aak-2(ok524) strains were generously provided by Cynthia Kenyon. The smg-1(cc546ts) and smg-1(cc546ts); pha-4(zu225) strains were generously provided by Susan Mango. The aak-2(ok524) strain was crossed to eat-2(ad1116) to generate the double mutant strain aak-2(ok524); eat-2(ad1116). Unless otherwise noted, aak-2(ok524) and daf-16(mu86) strains were used. HT115 (DE3) bacteria transformed with vectors expressing dsRNA of the genes of interest were obtained from the Ahringer library (a gift from Dr M.-W. Tan) and were grown at 37 °C and seeded onto standard nematode growth medium (NGM) plates containing Ampicillin (100 µg mL−1) and IPTG (0.4 mm). Adult worms were placed on standard NGM plates and removed after 4–6 h to obtain synchronized populations of worms. L1 or L4 worms obtained from these synchronized populations were placed on NGM plates containing Ampicillin (100 µg mL−1) and IPTG (0.4 mm) seeded with the respective bacteria. Each vector was sequenced to verify the presence of the appropriate gene of interest.
Worm lifespan assays were performed at 20 °C unless noted differently. Worm populations were synchronized by placing young adult worms on NGM plates seeded with the E. coli strain OP50–1 (unless otherwise noted) for 4–6 h and then removed. OP50–1 is a strain derived from OP50 that contains a streptomycine resistance gene (Kawli & Tan, 2008). The hatching day was counted as day 1 for all lifespan measurements. Worms were changed every other day to new plates to eliminate confounding progeny, and were marked as dead or alive. Worms were scored as dead if they did not respond to repeated prods with a platinum pick. Worms were censored if they crawled off the plate or died from vulval bursting. For each lifespan assay, 90 worms per condition were used in three plates (30 worms per plate). The data were plotted in StatView 5.0.1 using the Kaplan–Meier Survival curves and statistical significance was determined by Log-rank (Mantel-Cox) tests. Lifespan assays were repeated at least once unless otherwise mentioned. Representative Kaplan-Meier survival curves are shown in the figures. For lifespan assays performed on a gradient of bacterial concentrations mean and standard error values were taken from Kaplan–Meier Survival curves plotted in StatView 5.0.1 and plotted in Excel. Representative curves are presented unless noted otherwise. For smg-1 and smg-1; pha-4 lifespan assays, worms were grown at permissive temperature 24 °C until the first day of adulthood when they were switched to 15 °C which allows for the degradation of pha-4(zu225) (Gaudet & Mango, 2002).
OP50–1 bacteria were serially diluted from 5 × 1012 to 5 × 104 bacteria mL−1. Bacteria were resuspended in S Medium to inhibit bacterial growth. Adult worms were placed on these various concentrations of bacteria starting at day 7 of life (day 4 of adulthood). Worms placed on a gradient of bacterial concentrations ranging from 5 × 104 to 5 × 107 bacteria mL−1 died 2 days after being placed on these extreme DR diets. For specific assays, sDR was considered 5 × 108 bacteria mL−1 and ad libitum was 5 × 1011 bacteria mL−1 (Greer etal., 2007).
Peptone dilution assays
Assays were performed as in (Hosono etal., 1989). Synchronized populations of worms were obtained by placing adult worms on plates with decreasing concentrations of peptone (from 2.5 to .0025 g L−1 with 150 µL of 5 × 1012 bacteria mL−1 seeded on each plate) and removing the worms after 4–6 h. Worms were switched every other day to fresh plates and were scored as alive as described above.
Liquid DR assays
Assays were performed as in (Panowski etal., 2007). Briefly worms were grown until day 1 of adulthood on NGM plates seeded with 150 µL of 5 × 1011 bacteria mL−1. They were then transferred for 1 day to NGM plates with FUdR (100 mg L−1) seeded with 150 µL of 5 × 1011 bacteria mL−1. Approximately 20 worms were then placed in each well of a 12-well plate with 1 mL of S-basal supplemented with cholesterol (5 mg L−1), Ampicillin (50 µg L−1), Kanamycin (10 µg L−1), Tetracycline (1 µg L−1) and FUdR (100 mg L−1) containing OP50–1 bacteria at various concentrations (from 3.33 × 109 to 5 × 1011 bacteria mL−1). Approximately 90 total worms were used for each condition (4 wells containing approximately 22 worms per well). Plates were gently shaken at 20 °C and worms were scored as alive as described before. Live worms were switched to fresh liquid medium containing the appropriate dilution of bacteria every third day.
Statistical analysis of lifespan was performed on Kaplan–Meier survival curves in StatView 5.0.1. For statistical comparison of independent replicates, Fischer's combined probability tests were performed. To compare the interaction between genotype and food concentration, two-way anova tests were performed in Prism 4.0 c using the mean and standard error values obtained from the Kaplan–Meier survival curves. To compare the interaction between genotype and food concentration in an independent manner, regression analyses were also performed on raw lifespan data using a Cox proportional hazard analysis in r 2.7.1. The values from the Fisher's combined probability tests, two-way anova, and Cox proportional hazard analysis are included in the supplemental tables.
We thank Andy Dillin, Cynthia Kenyon, Susan Mango, and Man-Wah Tan for generously sharing protocols, reagents, and for helpful discussion. We thank Keith Blackwell for helpful suggestions. We thank Alex McMillan, Art Owen, and Dario Valenzano for help with statistical analysis. We thank Max Banko and Hirokazu Fukui for experimental help. We thank members of the Brunet laboratory as well as Paul Greer, Stuart Kim, Judy Lieberman, and Adolfo Sanchez-Blanco for critically reading the manuscript. We are grateful to Theresa Stiernagle and the Caenorhabditis Genetics Center funded by the National Center for Research Resources of the NIH for providing worm strains. This research was supported by an NIH grant (NIA AG026648–01), an American Institute for Cancer Research grant, and by a gift from the Glenn Foundation to A.B. E.L.G. was supported by a PHS grant (CA 09302) from the NCI and by an NSF graduate fellowship.
Since this manuscript was accepted, another method of DR in C. elegans, termed IF for intermittent fasting, has been reported. This DR method is dependent on RHEB-1 and FoxO/daf-16, but independent of AMPK/aak-2 (Honjoh S, Yamamoto T, Uno M, Nishida E (2009) Signalling through RHEB-1 mediates intermittent fasting-induced longevity in C. elegans. Nature 457, 726–730.)