Endocannabinoids in Caenorhabditis elegans are essential for the mobilization of cholesterol from internal reserves

Proper cholesterol transport is crucial for the functionality of cells. In C. elegans, certain cholesterol derivatives called dafachronic acids (DAs) govern the entry into diapause. In their absence, worms form a developmentally arrested dauer larva. Thus, cholesterol transport to appropriate places for DA biosynthesis warrants the reproductive growth. Recently, we discovered a novel class of glycosphingolipids, PEGCs, required for cholesterol mobilization/transport from internal storage pools. Here, we identify other components involved in this process. We found that strains lacking polyunsaturated fatty acids (PUFAs) undergo increased dauer arrest when grown without cholesterol. This correlates with the depletion of the PUFA-derived endocannabinoids 2-arachidonoyl glycerol and anandamide. Feeding of these endocannabinoids inhibits dauer formation caused by PUFAs deficiency or impaired cholesterol trafficking (e.g. in Niemann-Pick C1 or DAF-7/TGF-β mutants). Moreover, in parallel to PEGCs, endocannabinoids abolish the arrest induced by cholesterol depletion. These findings reveal an unsuspected function of endocannabinoids in cholesterol trafficking regulation.


Results
Depletion of PUFAs leads to enhanced dauer formation. In a previous study, we have shown that C. elegans interrupts reproductive development and arrests as a dauer-like larva (L2*) with incomplete molting when grown for two generations without cholesterol 3 . More recently, we have found that this arrest can be abolished by supplementation of PEGCs, substances belonging to a novel class of lipids that mobilizes internal pools of cholesterol 10 . We were interested to further investigate this process and to identify other components that might be involved in it. We reasoned that strains aberrant in cholesterol mobilization would arrest already in the first generation without externally provided sterols. Indeed, a small screening performed on a mutant strain collection (Mende, F. and Kurzchalia, T.V., unpublished data) indicated that one of them, with inactive Δ 6desaturase [fat-3(ok1126)] showed growth defects already in the first, rather than in the second generation when grown without cholesterol. Unlike the wild type strain, that produced almost 100% gravid adults in the first generation without cholesterol, fat-3 displayed a high incidence of arrested larvae ( Fig. 1a) with typical dauer morphology (Supplementary Figure 1). This mutant strain bears a large deletion in the coding region of gene fat-3, and is null for FAT-3 desaturase. Animals accumulate linoleic and α-linolenic acids and are unable to produce the major C20 PUFAs found in C. elegans: arachidonic (20:4 (n-6), AA) and eicosapentanoic acid (20:5(n-3), EPA) 16,17 .
Next, we set out to confirm the interaction between the PUFA biosynthesis pathways and the dauer formation regulating pathways. In particular, we tested the interaction with the DAF-7/TGF-β pathway that regulates dauer development by affecting sterol trafficking and metabolism 10,18,19 . In our previous study we have shown that temperature-sensitive daf-7 mutants with "dauer formation constitutive" (Daf-c) phenotype are hypersensitive to cholesterol depletion and form dauer larvae in the absence of external cholesterol already at the semi-permissive growth temperature despite internally stored sterols 10 . We reasoned that if the biosynthesis of PUFAs is connected with this regulatory pathway, depletion of PUFAs should enhance the phenotype of daf-7. To this end, we generated a double mutant strain for fat-3(ok1126) and daf-7(e1372) and scored dauer formation. When grown at the semi-permissive growth temperature (20° C), daf-7(e1372);fat-3(ok1126) double mutants formed significantly more dauers (~85%) than the parental daf-7 strain (<10%) (Fig. 1b,c). Moreover, enhanced dauer formation in double mutants was fully abolished when the medium was supplemented with DA (Fig. 1b). These results suggest that a decrease in the synthesis of C20 PUFAs could be leading to deficiency of DAs. We speculated that depletion of PUFAs might exacerbate cholesterol deficiency due to a decrease in its delivery rate from storage sites to the locations of DA production. Therefore, we tested whether very high cholesterol availability in the growth medium was sufficient to compensate for the loss of FAT-3 in daf-7;fat-3 animals. As shown in Fig. 1d, providing a high-cholesterol diet did promote dauer recovery of daf-7;fat-3 mutants.
Arachidonic acid-containing endocannabinoids abolish dauer formation of daf-7;fat-3 and daf-7;fat-4 mutants. Then, we asked which PUFA-derived molecules could be responsible for the dauer arrest of daf-7;fat-3 double mutants. PUFAs are metabolized into many potent bioactive compounds such as eicosanoids and endocannabinoids 20 . The latter, shown in Fig. 2a previous studies have shown that N-acylethanolamines (NAEs) antagonize dauer formation in C. elegans 12 . Using high-performance liquid chromatography coupled to mass spectrometry (HPLC MS/MS), we found that, in agreement with a previous report 21 Table 1). We also determined that these arachidonic acid-containing endocannabinoids are synthesized by daf-7 (Fig. 2b). In contrast, both fat-3 and daf-7;fat-3 strains do not synthesize PUFA-derived endocannabinoids to detectable levels (Fig. 2b). Next, we tested the capability of the detected endocannabinoid molecules to suppress dauer formation of daf-7;fat-3. We found that supplementation of the media with 2-AG and AEA significantly reduced the Daf-c phenotype of daf-7;fat-3 worms (Fig. 2c). In contrast, EPEA failed to rescue the Daf-c phenotype of daf-7;fat-3 (Fig. 2a,c).Treatment with AA, which is both a precursor as well as the hydrolytic breakdown product of both 2-AG and AEA 15 , was unable to promote reproductive growth of daf-7;fat-3 (Fig. 2c). However, in a previous study, we have established the use of fatty acid methyl esters (FAMEs) instead of the corresponding free fatty acids due to the much higher rescue activities of the former 22 . FAMEs are more active presumably because membranes (a) Unlike wild-type worms, fat-3(ok1126) mutants are incapable of synthesizing PUFAs and undergo a dauerlike arrest in the first generation when grown in cholesterol-free media. One-way analysis of variance p < 0.001. All pairwise multiple comparison procedures (Holm-Sidak method), (*) indicates statistically significant difference with fat-3/solvent, p < 0.001. Bars represent mean values and error bars represent standard errors. The number of independent experiments is n = 3 for all conditions. (b) While daf-7 worms form ~10% dauers at 20 ºC, fat-3 worms do not form dauers. In stark contrast, double mutant daf-7;fat-3 forms ~85% dauers at 20 ºC, and addition of DA suppresses dauer formation almost completely. One-way analysis of variance p < 0.001. All pairwise multiple comparison procedures (Holm-Sidak method): (*) indicates statistically significant difference with daf-7, p < 0.001. Bars represent mean values and error bars represent standard errors. The number of independent experiments is n = 5 for daf-7, and n = 13 for fat-3 and daf-7; fat-3. are more permeable for them. Indeed, addition of AA-methyl ester (methyl-AA) to daf-7;fat-3 worms significantly reduced the Daf-c phenotype (Fig. 2c). This raised the question whether methyl-AA is a precursor of 2-AG and/or AEA 23 or AA has an effect by itself. In order to find out whether methyl-AA serves as a precursor of 2-AG and AEA, lipid extracts of fat-3 and daf-7;fat-3 mutants fed with methyl-AA were analyzed by LC-MS/MS. This analysis revealed that indeed these mutants were capable to synthesize both 2-AG and AEA (Supplementary Table 1) upon methyl-AA supplementation. Importantly, we found that noladin 24 (Fig. 2a), a non-hydrolysable analog of 2-AG, was also able to rescue the Daf-c phenotype of daf-7;fat-3 to an extent comparable to the effect of 2-AG, demonstrating that the endocannabinoids are not merely precursors for other AA-derived compounds (Fig. 2c).
Although AA-derived endocannabinoids rescue the dauer phenotype of daf-7;fat-3, it could be argued that this double mutant is unable to synthesize dihommo-γ-linolenic acid [20:3(n-6)] (DGLA) and eicosatetraenoic acid [20:4(n-3)], [ETA (n-3)] and that endocannabinoids derived from these C20 PUFAs could serve the same function as 2-AG or AEA. To answer this question we generated daf-7;fat-4 double mutant strain that synthesizes DGLA and ETA (n-3), but is unable to synthesize AA 25 due to its deficiency in Δ5 fatty acid desaturase enzyme FAT-4. daf-7;fat-4 double mutant displays a very strong Daf-c phenotype similar to the one observed in daf-7;fat-3 (Supplementary Figure 2a). Furthermore, supplementation of the growth medium with an excess of cholesterol, DA, 2-AG and noladin ether substantially lowers dauer formation in daf-7;fat-4 ( Supplementary Figures 2a and  2b). These results demonstrate the specificity of AA-derived endocannabinoids to rescue the enhanced dauer formation of daf-7 animals deprived of C20 PUFAs. Taken together, we conclude that endocannabinods containing AA residues are the active compounds promoting reproductive development.
Endocannabinoids do not substitute for DA. As shown above, both endocannabinoids and DAs are able to rescue the dauer constitutive phenotype displayed by daf-7;fat-3 (Figs 1b and 2c). This raised the possibility that the endocannabinoid compounds were merely substituting for DAs as DAF-12 ligands. To address this question, we tested whether 2-AG and AEA were able to compensate for the deficiency of DAF-9 cytochrome P450 enzyme, necessary for the production of DA from cholesterol 6,26 . As seen in Supplementary Figure 3, unlike DA, 2-AG and AEA failed to inhibit dauer formation in daf-9(dh6) mutants. This indicates that these endocannabinoids cannot substitute for DA. Thus, it seems likely that these endocannabinoids inhibit dauer formation by enhancing the synthesis of DAs.

Endocannabinoids rescue the arrest induced by cholesterol depletion through its mobilization.
Our previous studies have demonstrated that PEGCs also enhance the synthesis of DAs by mobilization of internal pools of maternally deployed cholesterol 10 . Because of this activity, PEGCs are also able to abolish the developmental arrest caused by cholesterol starvation in the second generation of worms grown on sterol-depleted medium 10 . We asked whether endocannabinoids could similarly inhibit the arrest of cholesterol-depleted worms. Indeed, addition of 2-AG to sterol-lacking medium resulted in formation of many late stage (L4) larvae and adults in the N2 wild-type strain in the second generation, whereas the untreated worms arrested mainly as L2* larvae as published before (Fig. 3a) 3 .
We next set out to investigate whether AEA and 2-AG have the ability to mobilize internal reserves of sterols in C. elegans. First, we made use of daf-7 mutants which are hypersensitive to cholesterol starvation. They form dauers already in the first generation even at permissive temperature (15˚C) when the external cholesterol source is missing. Although these worms receive high amounts of maternal cholesterol, they are unable to use this sterol for DA synthesis presumably due to an impairment in mobilizing sterols efficiently 10 . We found that upon cholesterol deprivation, 2-AG rescues the dauer arrest of daf-7 animals grown without cholesterol (Fig. 3b). Next, we investigated the interaction of endocannabinoids with the NPC1 sterol-trafficking system 27 . As mentioned earlier, cholesterol transport in C. elegans is partly mediated by the NPC1 homologs NCR-1 and NCR-2 28 . Because of this, double mutant ncr-2(nr2023);ncr-1(nr2022) displays constitutive dauer formation 5 . This dauer formation can be rescued by supplementation with DAs 5,7 . As seen in Fig. 3c, 2-AG could also largely suppress ncr-2;ncr-1 dauer formation. Moreover, the Daf-c phenotype of ncr-2;ncr-1, as well as of daf-7, was diminished by RNAi against faah-1, a gene encoding a conserved fatty acid amide hydrolase (FAAH) enzyme, responsible for the breakdown of N-acylethanolamines such as AEA and EPEA in worms 12 ( Fig. 3d and Supplementary Figure 4).
The ability of the AA-derived endocannabinoids to rescue the development of cholesterol-depleted worms pointed out to the possibility that the endogenous production of these compounds might be enhanced in response to cholesterol withdrawal. This could be a mechanism to optimize cholesterol mobilization when the diet is not rich in sterols. In agreement with this hypothesis, we found that removing cholesterol from the growth medium resulted in a reproducible two-fold increase in 2-AG levels in N2 animals already in the first generation (Supplementary Table 2). Taken together, our data suggest that in C. elegans endocannabinoids exert their effects on post-embryonic development by enhancing the efficiency of cholesterol trafficking and the utilization of internal pools.
Endocannabinoids and PEGCs are acting through parallel pathways. Next, we examined how 2-AG and AEA are connected to recently discovered PEGCs: Can endocannabinoids rescue PEGCs deficiency? And vice versa, can PEGCs rescue endocannabinoid deficiency?
To induce PEGCs deficiency, we inhibited the synthesis of their precursors, the glucosylceramides (GlcCer). For this, two approaches have been used. Firstly, we decided to decrease C15iso and C17iso monomethyl branched-chain fatty acids (mmBCFA), needed for the synthesis of the long-chain base in C. elegans 29 (Supplementary Figures 5 and 6). For this, we applied RNAi of LET-767, the major 3-ketoacyl-CoA reductase, necessary for the elongation of long-chain and branched-chain fatty acids. RNAi of LET-767 in wild type worms leads to multiple developmental phenotypes in the first generation and early larval arrest in the second generation (L1-L2) 22 . Indeed, RNAi against LET-767 in daf-7 mutants grown at 20 °C significantly increases the Daf-c phenotype of the strain (Fig. 4a). GC-MS analysis of the relative fatty acid profiles of control and let-767 RNAi animals confirmed that RNAi treatment leads to a strong decrease in the levels of C15iso and C17iso mmBCFAs, but not of PUFAs (Supplementary Table 3). Accordingly, as seen in Fig. 4b, supplementation with C17iso mmBCFA methyl esters rescued the let-767 RNAi-induced dauer arrest of daf-7 worms. Astoundingly, both 2-AG and AEA also rescued the dauer formation observed in daf-7 animals subjected to let-767 RNAi (Fig. 4b). To exclude the possibility that endocannabinoids act by elevating levels of mmBCFAs, i.e. by inducing (a) not yet identified alternative 3-ketoacyl-CoA reductase(s), we performed GC-MS analysis of mmBCFA in daf-7 let-767 RNAi worms in the presence of 2-AG (Supplementary Table 4). This experiment clearly shows that endocannabinoid treatment does not increase mmBCFA. In consistency with impaired cholesterol trafficking in daf-7 let-767 (RNAi), dauer formation was partly inhibited by high cholesterol levels in the medium (Fig. 4c).
The second approach to deplete PEGCs was to treat daf-7 with PDMP, an inhibitor of the final glucosylation step in the synthesis of GlcCer (Supplementary Figure 6). We found that DA, high cholesterol and endocannabinoids rescue daf-7 dauers generated in the presence of PDMP (Fig. 4d) 10 . However, as expected, PDMP treatment could not be rescued by addition of mmBCFA C17iso methyl ester because PDMP inhibits a later step of the synthesis of PEGCs. Thus, PEGCs deficiency could be rescued by supplementation with endocannabinoids.
In another set of experiments, we investigated whether PEGCs could abolish dauer formation in the endocannabinoids deficient strain daf-7;fat-3. As seen in Fig. 4e, synthetic mmPEGC-C22, the major PEGC species found in worms 10 , can partially rescue the dauer formation induced by the absence of endocannabinoids. Taking altogether, we propose that two unrelated lipid species, endocannabinoids and PEGCs, regulate worm cholesterol transport/mobilization through parallel pathways.

Discussion
The major finding of our study is that the endocannabinoids 2-AG and AEA regulate the transport/mobilization of cholesterol in C. elegans, which results in enhanced DA production. Several lines of evidence support this notion: endocannabinoids (i) abolish the developmental arrest caused by cholesterol depletion in wild-type and daf-7 worms, (ii) stimulate the reproductive development of daf-7 worms with diminished glucosylceramide/ PEGC synthesis and (iii) rescue ncr-2;ncr-1 mutants with aberrant cholesterol transport.  Based on our data, we propose a tentative scheme of the interaction between endocannabinoids and PEGC in the control of cholesterol transport (Fig. 4f). Multiple reactions produce the precursors diacylglycerol (DAG), N-acyl-phosphatidylethanolamine (NAPE), and GlcCer required for the synthesis of 2-AG, AEA and PEGCs, respectively. The conversions of these precursors to the active compounds are carried out by not yet identified enzymes in C. elegans. 2-AG and AEA are probably produced by enzymes homologous to the mammalian DAG lipase (DAGL) and NAPE-specific phospholipase D (NAPE-PLD) 30 , although alternative biosynthetic pathways also exist 12,20,31 . The enzymatic system required for PEGCs production is completely unknown. Intriguingly, PEGCs cannot be synthesized in the absence of functional NCR-1 and NCR-2 proteins 10 . This suggests that in worms PEGCs mediate cholesterol transport downstream of NPC1. Endocannabinoids and PEGCs act in parallel to stimulate the mobilization/transport of cholesterol. This leads to delivery of the latter to DAF-9, production of DA and inhibition of the dauer-promoting activity of DAF-12. It should be noted that, in addition to their effect as regulators of cholesterol mobilization, endocannabinoids might also stimulate the synthesis of DA via regulation of alternative signaling pathways such as the monoaminergic neurotransmission, GPCR and MAP kinase -mediated cascades, etc. 32,33 . PEGCs, on the other hand, could also display pleiotropic effects due to their specific glycospingolipid structure: they might physically interact with cholesterol or affect its distribution by regulating different properties of the cellular membranes: their topology, fluidity or permeability 34 .
One important implication of the fact that the endocannabinoids and GlcCer/PEGCs act in parallel is that endocannabinoids might be involved in the regulation of a plethora of other known glucosylceramide-dependent processes in worms. These include the activation of the nutrient-sensing TOR signaling, the establishment of epithelial polarity in intestinal cells, foraging behavior and sensory neuron maturation 29,[35][36][37] . Future studies will reveal the relationships between glycosphingolipids, cholesterol and endocannabinoids in the control of these processes.
Many of the physiological effects produced by endocannabinoids are not completely understood. Some of them may reflect their influence on cholesterol trafficking. In higher organisms, many aspects of the intracellular cholesterol transport are regulated by the transcription factors LXR and SREBP 1 . Intriguingly, LXR is one of the vertebrate homologs of DAF-12, which binds oxysterols 38 . This points to the interesting possibility that LXR and DAF-12 might have similar endocannabinoid-dependent activities in regard to the control of cholesterol homeostasis. On the other hand, endocannabinoids and endocannabinoid agonists are known to increase the hepatic expression of SREBP in mice 39 . Whether 2-AG and AEA could also operate via SREBP in worms is worth investigating.
Finally, deregulation of cholesterol and lipid homeostasis has major consequences on development and disease. Cholesterol metabolism in particular is closely interrelated with cardiovascular disease in humans. It is well known that dietary supplementation with omega-6 polyunsaturated fatty acids (PUFAs) reduces the risk of cardiovascular disease. In part, this is attributable to the observation that increased plasma levels of omega-6 PUFAs favorably affect plasma LDL-cholesterol and HDL-cholesterol levels 40,41 . While it is widely accepted that lipid metabolism is linked to cholesterol homeostasis 38,42 , exactly how PUFAs control cholesterol balance and metabolism remains largely unexplored. Hence, our findings point up the exciting scenario that the role of PUFA-derived endocannabinoids could be conserved in humans. Thus, unraveling the mechanisms by which endocannabinoids affect sterol-regulated processes in C. elegans could have important implications for the better understanding of human pathological conditions associated with impaired cholesterol homeostasis, such as atherosclerosis, non-alcoholic fatty liver disease and Niemann-Pick type C disease.

Materials and Methods
Materials. 2 The worm strain N2 Bristol and the single mutants daf-7(1372), fat-3(ok1126), fat-4 (ok958), ncr-1;ncr-2 (JT10800) were obtained from Caenorhabditis Genetics Center (CGC). daf-9(dh6);dhEx24 was provided by Prof. A. Antebi. Growth and maintenance of worm strains. Worms were routinely propagated on nematode growth medium (NGM) agar plates seeded with E. coli OP50 46 . Saturated cultures of E. coli OP50 or NA22 grown in lysogeny broth (LB) medium were concentrated 10 times and spread on NGM-agar plates. Worms were placed on the plates either as mixed stage populations or as embryos obtained by hypochlorite treatment. The temperature-sensitive Daf-c mutants were grown at 15 °C to grow in the reproductive mode and at 25 °C to arrest as dauer larvae.
errors. The number of independent experiments is n = 2 for all conditions. [DA] = 1 µM. [mmPEGC-C22] = 0.5 mM. (f) Endocannabinoids and PEGCs act in parallel to promote transport/mobilization of cholesterol from internal pools. Endocannabinoids are synthesized from their precursors DAG and NAPE most probably by DAGL and NAPE-PLD enzymatic activities. The enzyme(s) that produce(s) PEGC from d17iso-GlcCer is(are) unknown but the synthesis is dependent on NCR-1/2. Both endocannabinoids and PEGCs have the ability to mobilize cholesterol. The latter is then delivered to the sites of DAF-9 mediated DA synthesis. After systemic distribution of DA within the organism, it binds and inhibits the dauer-promoting activities of DAF-12. DAG -diacylglycerol; NAPE -N-acyl-phosphatidylethanolamine; DAGL -DAG lipase; NAPE-PLD -NAPE-specific phospholipase D.
SCIENTIFIC REPORTS | (2018) 8:6398 | DOI:10.1038/s41598-018-24925-8 RNAi by feeding. RNAi against let-767 was performed with E. coli HT115 double-stranded RNA (dsR-NA)-producing strain from the Ahringer library. RNAi was performed in the first generation. Bleached embryos were left to hatch overnight in M9 at 20 °C and the resulting L1s were seeded to RNAi plates and grown at 20 °C or 15 °C according to the experiment. Similarly, faah-1 RNAi was performed in the first generation. Unlike the experiments with let-767, the worms subjected to faah-1 RNAi were seeded on the dsRNA-producing E. coli as embryos. Finally, the dauer phenotype was scored after 72 h or 144 h, depending on the assay. For biochemical analysis worms were harvested from RNAi plates after 72 h.

Dauer formation assays.
In general, 80-100 L1s or embryos were transferred to NGM plates seeded with E. coli (HT115) containing RNAi against let-767, faah-1 or empty vector as a negative control. The supplementation with endocannabinoids (final concentration 50 µM), arachidonic acid (final concentration 50 µM), methyl esters from different fatty acids (final concentration 50 µM), mm-PEGC-C22 (final concentration 10 µM) and DL-threo-PDMP (final concentration 20 µM) was added to the bacteria immediately prior to seeding. The final concentrations of these compounds were calculated according to the volume of the NGM agar used for the preparation of the plates. It should be noted that the active concentrations of mm-PEGC-C22 published before 10 have been calculated according to the volume of the bacterial loan seeded on the agar/agarose surface. If calculated using the latter method, the concentration of mm-PEGC-C22 used here would be 500 µM. Finally, after 72 h the percentage of dauers was scored. Δ 4 -DA and Δ 7 -DA 43,44 were used alternatively in dauer rescue experiments with working concentrations that were chosen (1 µM and 90nM, respectively).
To determine dauer formation of daf-9(dh6) strain, embryos were placed on NGM plates with E. coli complemented with Δ 7 -DA or endocannabinoids. dhEx24 is an extrachromosomal array carrying active DAF-9 and nuclear GFP. After 3 days daf-9 null worms were identified on the basis of the absence of GFP signal and dauer formation was scored 47 .
Cholesterol deprivation assay. The protocol from Matyash et al. 3 was carried out. Briefly, to produce sterol-depleted media, agar was replaced by agarose (Sigma-Aldrich) that was washed three times with chloroform to deplete the trace sterols in it. E. coli NA22 was grown in low-glucose, sterol-free DMEM culture medium (Sigma-Aldrich). Bacteria were rinsed with M9 before use and concentrated 20 times. Then the plates were seeded with 100 µl of bacteria and the supplements were added (or solvent carrier as negative control). 80-100 L1s were plated, incubated at 15° C for 6 days, and finally scored for percentage of dauers formed.

Lipid extraction and endocannabinoid analysis by HPLC-MS/MS. The protocol is an adaptation
from Folch (1957) 48 . Lipid extracts were generated from approximately 100 mg of frozen worm pellets belonging to N2, daf-7, fat-3 and daf-7;fat-3 grown at 20 °C. The pellets were thawed on ice in 1.3 ml methanol and subjected to 4 min sonication on ice. After sonication, 1000 ppb of the internal standard 2-AG-d5 were added followed by 2.6 ml chloroform and 1.3 ml 0.5 M KCl/0.08 M H 3 PO 4 to a final ratio of 1:2:1. Samples were vortexed and then sonicated in an ultrasonic water bath for 15 min. After vortexing twice for 1 min, samples were centrifuged for 10 min at 2.000 g to induce phase separation. The lower phase was collected into a clean glass tube, dried under nitrogen and re-suspended in 100 µl of acetonitrile.

Generation of daf-7;fat-3 and daf-7;fat-4 double mutant strains. Homozygous fat-3(ok1126) male
worms were crossed to daf-7(e1372) hermaphrodites. The hermaphrodites from the progeny laid eggs that at 25 °C developed into dauers or adults. The dauers were relocated to 15 °C to re-enter reproduction and their progeny was screened using PCR for homozygous daf-7(e1372);fat-3(ok1126) individuals. Using an equivalent strategy, homozygous fat-4(ok958) male worms were crossed to daf-7(e1372) hermaphrodites. The hermaphrodites from the progeny laid eggs that at 25 °C developed into dauers or adults. The dauers were relocated to 15 °C to re-enter reproduction and their progeny was screened using PCR for homozygous daf-7(e1372);fat-4(ok958) individuals.

GC-MS determination of fatty acid methyl-ester content. Lipid extraction was performed using
Bligh and Dyer 49 method. Briefly, the N2 and fat-3 were grown at 20 °C on E. coli OP50 for 72 h and then harvested from plates with 5-10 ml of M9 buffer. For the interference assay with let-767 RNAi, daf-7 worms were grown on E. coli OP50 with TH115 empty vector as a control, and with RNAi against let-767 at 20 °C for 72 h. Subsequently, worms were harvested as described above. Thereafter, worms were washed three times with M9 buffer to eliminate excess bacteria. The worm pellet was transferred to a glass tube and 3 ml of a chloroform:methanol 1:2 mixture was added. Dibutylhydroxytoluene (BHT) was added as an antioxidant at a final concentration SCIENTIFIC REPORTS | (2018) 8:6398 | DOI:10.1038/s41598-018-24925-8 of 5 µg/ml. The samples were incubated for 12 h at −20 °C. After incubation the samples were centrifuged and the supernatants were transferred to a new tube. 1 ml of KCl (1M) and 1 ml of chloroform were added to the samples, the samples were mixed by vortexing and then centrifugated for 2 min at 2000 g. Finally, the organic phases were transferred to new tubes and dried under N 2 flow. Chemical General Information. 1 H and 13 C NMR spectra were acquired on a Bruker Avance II 300 MHz (75.13 MHz) using CDCl 3 as solvent. Electrospray Ionization High-Resolution Mass Spectra (ESI-HRMS) were recorded on a Bruker MicrOTOF II with lock spray source. IR spectra were obtained using an FTIR Shimadzu spectrometer. Chemical reagents were purchased from commercial suppliers and used without further purification, unless otherwise noted. Solvents were analytical grade or were purified by standard procedures prior to use. Yields were calculated for material judged homogeneous by thin layer chromatography (TLC) and nuclear magnetic resonance ( 1 H-NMR). All reactions were monitored by thin layer chromatography performed on silica gel 60 F254 pre-coated aluminum sheets, visualized by a 254 nm UV lamp, and stained with an ethanolic solution of 4-anisaldehyde. Column flash chromatography was performed using silica gel 60 (230-400 mesh).

2-AG-d 5 preparation.
For obtaining 2-AG-d 5 as a deuterated internal standard for quantification assays, we followed a three-step protocol: differential protection, esterification and deprotection. Differential protection step: In order to only protect primary alcohols, a solution of glycerol-d 8 (38 mg, 0.18 mmol) in anhydrous dichloromethane (5 ml) under inert atmosphere was prepared and cooled at −78 ºC. Then, collidine (54 mg, 0.36 mmol) and tert-butyl dimethyl silyl chloride (TBDMSCl, 70 mg, 0.54 mmol) was added. The mixture reacted for 3 h at −78 ºC, then warmed to room temperature and stirred for additional 12 h. Brine was added and the solution was extracted with dichloromethane. The combined organic extracts were dried over sodium sulfate and evaporated. Products were purified by column chromatography on silica gel with increasing hexane/ethyl acetate gradients. 1-O,3-O-Bis(TBDMS) glycerol-d 6 was obtained as a colorless liquid in 44% yield (55 mg). For the esterification step, a solution of 1-O,3-O-Bis(TBDMS) glycerol-d 6 (10 mg, 0.03 mmol) in anhydrous dichloromethane (2 ml) under inert atmosphere was prepared and cooled at 0 ºC. Next, arachidonic acid (36 mg, 0.12 mmol), 4-dimethylaminopyridine (15 mg, 0.12 mmol) and N,N'-dicyclohexylcarbodiimide (15 mg, 0.12 mmol) were added in that order. The mixture reacted for 3 h at 0 ºC, and was then warmed to room temperature and stirred for additional 12 h. Water was added and the solution was extracted with dichloromethane. Combined organic extracts were dried over sodium sulfate and evaporated. Products were purified by column chromatography on silica gel with increasing hexane/ethyl acetate gradients. 1-O,3-O-bis(TBD MS)−2-AG-d 5 was obtained as a yellowish liquid in 80% yield (15 mg). For the deprotection step, a solution of 1O,3O-Bis(TBDMS)−2-AG-d 5 (15 mg, 0.025 mmol) in tetrahydrofuran (2 ml) was prepared. Then, a 1M solution of tetrabutylammonium fluoride (150 ml, 0.15 mmol) was added cautiously dropwise. Once the reaction was complete (1 h), water was added and the solution was extracted with dichloromethane. Combined organic extracts were dried over sodium sulfate and evaporated. A quantitative amount of product 2-AG-d 5 (10 mg, quantitative) was obtained as a yellowish liquid.
Methyl-ester preparation. For the derivatization of fatty acids prior to GC-MS analysis, 0.5 ml of anhydrous sodium methoxide 0.5 M were added to the lipid samples and then incubated 30 min at room temperature. Then 1 ml of HCl (2 N) was added for neutralization of the reaction. The fatty acid methyl esters were extracted with hexane and finally resuspended in 500 ml of hexane.
For obtaining the AA and C17iso methyl-esters used for supplementation assays we followed a protocol based on Walker et al. 50 . Briefly, a solution of diazomethane in diethyl ether was added cautiously dropwise to a stirred solution of the appropriate fatty acid (50 mg, 0.16 mmol) in dichloromethane (5 ml) until the yellow color persisted. The excess of the reagent was vented under a nitrogen purge. The solvent was evaporated and the product dried under vacuum to provide the methyl ester as a colorless oil (54 mg, quantitative) that was used without further purification.
Gas chromatography coupled to mass spectrometry (GC-MS). The methyl ester analysis was performed in a Shimadzu GC-2010 Plus equipment. The column used was a Supelco WAX-10 (Sigma Aldrich) 100% polyethyleneglycol. The helium flux was 1 ml/min and the heating program was 180 °C (0 min to 32 min) and then a gradient increasing 3 °C/min from 180 °C to 240 °C. The split was 1/30 and the ionization voltage was 70 eV with an ionic range from 50 to 600 Da. The ion specters were registered as relative abundance in function of mass/charge (m/z). Peak assignation was done using the mixture of standards of fatty acid methyl esters AGs Supelco (Sigma Aldrich).