Insulin resistance is often associated with obesity and can precipitate type 2 diabetes. To date, most known approaches that improve insulin resistance must be preceded by the amelioration of obesity and hepatosteatosis. Here, we show that this provision is not mandatory; insulin resistance and hyperglycemia are improved by the modification of hepatic fatty acid composition, even in the presence of persistent obesity and hepatosteatosis. Mice deficient for Elovl6, the gene encoding the elongase that catalyzes the conversion of palmitate to stearate, were generated and shown to become obese and develop hepatosteatosis when fed a high-fat diet or mated to leptin-deficient ob/ob mice. However, they showed marked protection from hyperinsulinemia, hyperglycemia and hyperleptinemia. Amelioration of insulin resistance was associated with restoration of hepatic insulin receptor substrate-2 and suppression of hepatic protein kinase C ε activity resulting in restoration of Akt phosphorylation. Collectively, these data show that hepatic fatty acid composition is a new determinant for insulin sensitivity that acts independently of cellular energy balance and stress. Inhibition of this elongase could be a new therapeutic approach for ameliorating insulin resistance, diabetes and cardiovascular risks, even in the presence of a continuing state of obesity.


Insulin resistance is associated with obesity and is the major pathogenic indicator of early stages of type 2 diabetes. Epidemiological studies have shown that intake of excess saturated fatty acids is the principal lifestyle-related cause of insulin resistance and obesity-related diseases, including metabolic syndrome1. In general, it has been thought that dietary saturated fatty acids are detrimental, monounsaturated fatty acids are neutral and polyunsaturated fatty acids are beneficial, although intracellular events mediated by these fatty acids have not been fully characterized. During high-fat diet feeding, the influx of free fatty acids results in the accumulation of triglycerides, promoting a lipotoxic state, and this induces insulin resistance in skeletal muscle, adipose tissue and liver2. Intracellular accumulation of fatty acids activates both oxidative degradation and incorporation of these fatty acids into triglycerides as a protective adaptation against their cytotoxicity. When these mechanisms are overwhelmed, fatty acids may activate proinflammatory and stress-responsive signals such as the nuclear factor-κB and c-Jun N-terminal kinase pathways. These events, in turn, inhibit insulin signaling through abnormal phosphorylation or degradation of insulin signaling molecules, leading to metabolic deterioration3,4,5,6. Recent data also suggest that the Janus kinase (JAK)-signal transducer and activator of transcription (STAT)-3–suppressor of cytokine signaling (SOCS)-3 pathway that mediates leptin signals is involved in insulin resistance and leptin resistance7,8,9.

Lipogenesis is a key event in the energy storage system. The biosynthesis of fatty acids is sequentially catalyzed by the enzymes acetyl–coenzyme A (CoA) carboxylase, fatty acid synthase (FAS) and stearoyl-CoA desaturase (SCD)-1 (Supplementary Fig. 1a online). The entire pathway is controlled by the transcription factor sterol regulatory element–binding protein (SREBP)-1c (refs. 10–12). Saturated fatty acids, as well as high-carbohydrate diets, activate SREBP-1c and enhance lipogenesis10,13. Previously, we have shown that SREBP-1c inhibits insulin receptor substrate (IRS)-2 and contributes to insulin resistance in liver, implicating a link between lipogenesis and insulin resistance14. The elongation of long-chain fatty acids (ELOVL) family member 6 (Elovl6, also known as LCE and FACE) has been shown to be a target of SREBP-1 by microarray analysis of SREBP-1 transgenic mice, and it was predicted to be important for tissue fatty acid composition15,16. In this study, we have examined the effects of Elovl6 on obesity, hepatic steatosis and insulin resistance to better understand the roles of fatty acid composition in these obesity-related states.


Metabolic features of Elovl6-null mice

The Elovl6 gene product belongs to a highly conserved family of microsomal enzymes involved in the formation of long-chain fatty acids17. Functional analysis by expression experiments in cultured cells demonstrated that this enzyme has a role in the elongation of palmitate (16:0) to stearate (18:0), as well as in the elongation of palmitoleate (16:1n-7) to vaccinate (18:1n-7) (Supplementary Fig. 1a). To evaluate the importance of Elovl6 in vivo, Elovl6-null mice were created (Supplementary Fig. 2a–c online). Homozygous Elovl6 knockout (Elovl6−/−) mice had partial embryonic lethality, although surviving male and female mutants were fertile (Supplementary Fig. 2d). Gene disruption completely abolished hepatic Elovl6 expression, resulting in an effective loss of its activity in the liver; this indicates that the hepatic elongase activity for these reactions is essentially attributable to Elovl6 (Fig. 1a,b). The residual elongase activity of palmitoleate to vaccinate in Elovl6−/− liver may be attributed to Elovl5, which has been reported to have a weak activity for this reaction18. To determine whether the livers of Elovl6−/− mice contained fewer C18 fatty acids, hepatic fatty acid composition was determined (Fig. 1c,d). Consistent with the absence of elongation of C16 fatty acids to C18, hepatic concentrations of stearate and oleate (18:1n-9) were lowered, whereas those of palmitate and palmitoleate were heightened, as compared to wild-type mice. These trends were more prominent in the livers of mice fed a fat-free, high-sucrose diet (CHO) that enhances endogenous hepatic fatty acid synthesis10. This increase was significant enough to make palmitoleate, which is usually a minor fatty acid class, the second most abundant fatty acid present in livers of CHO-fed mice (Fig. 1d). The ratios of 18:0/16:0 and 16:1/18:1, the markers of the elongase activity, were consistently decreased and increased, respectively, in the livers of Elovl6−/− mice as compared to wild-type controls (Fig. 1e). The ratios of 18:1/18:0 and 16:1/16:0, indicative of desaturation through SCD-1 activity, were apparently higher, although the expression of SCD-1 was decreased (Fig. 1e). These data confirm the importance of Elovl6 in maintaining the hepatic contents of 18:0 and 18:1 through de novo synthesis of these fatty acids, despite the abundance of 18:0 and 18:1 in the diet. The fatty acid composition of plasma followed the same trend as that of the liver, but changes were minimal in skeletal muscle and adipose tissue (Supplementary Fig. 2).

Figure 1: Targeting of the Elovl6 gene.
Figure 1

(a) Northern blot analysis of Elovl6 expression in the livers of Elovl6+/+, Elovl6+/− and Elovl6−/− mice. Total RNA (15 μg) pooled equally from three mice was subjected to northern blotting, followed by hybridization with the Elovl6 cDNA. A cDNA probe for Rplp0 (which encodes acidic ribosomal phosphoprotein P0) was used to confirm equal loading. (b) Assessment of Elovl6 enzymatic activity in liver total membrane fractions (n = 5 per group) using four separate substrates, 16:0-CoA, 16:1-CoA, 18:0-CoA and 18:1-CoA. (c,d) Fatty acid composition of liver tissue in wild-type and Elovl6−/− mice fed either a normal chow (c) or a CHO diet (d) for 2 weeks (n = 3–5 per group). (e) The ratio of stearate (18:0) to palmitate (16:0), palmitoleate (16:1n-7) to oleate (18:1n-9), 18:1 to 18:0 and 16:1 to 16:0 in livers of wild-type and Elovl6−/− mice. Results are represented as means ± s.e.m. *P < 0.05, **P < 0.01 for Elovl6−/− mice as compared to wild-type controls.

Elovl6−/− mice appeared grossly normal, although they were slightly, but significantly, leaner than wild-type littermates, despite an identical daily food intake of standard laboratory chow (Fig. 2a–c). However, there was no difference in the size or the appearance of adipocytes from white and brown adipose tissues (Fig. 2d). Postprandial plasma concentrations of insulin and leptin were lower in Elovl6−/− mice than in wild-type mice, whereas no significant changes were observed in the amounts of plasma glucose or lipid (Fig. 2e and Supplementary Table 1 online). Hepatic total cholesterol and triglyceride levels were also not different between wild-type and Elovl6−/− mice on a chow diet (Supplementary Table 1). Because the Elovl6−/− mice had higher insulin sensitivity on a standard chow diet, we challenged these mice with a high-fat, high-sucrose diet (HF-HS) that is known to induce obesity, hepatosteatosis and insulin resistance19. This high-calorie diet markedly enhanced body weight gain in both wild-type and Elovl6−/− mice (which had identical daily food intakes) at a similar rate over the course of the study, although the slight, but significant, weight differences were sustained (Fig. 2a–c). Epididymal fat pad weight and total body fat percentage were markedly increased in both groups, with similar net increases (Supplementary Table 1 and Fig. 2b). In accordance with the observed increase in adiposity, white and brown adipocytes were enlarged similarly in both groups after they had been fed the HF-HS diet (Fig. 2d). There were no obvious histological changes in white or brown adipose tissue; this included no observed change in the extent of mononuclear cell infiltration, which has been shown to contribute to proinflammatory response and insulin resistance in obesity20,21. There was a trend toward more severe hepatosteatosis in Elovl6−/− mice than in wild-type mice on the HF-HS diet, as estimated from hepatic triglyceride and cholesterol abundance as well as by histological staining (Supplementary Table 1 and Fig. 2d). Overall, diet-induced obesity in Elovl6−/− mice was similar to that of normal controls.

Figure 2: Body weight, adiposity and glucose homeostasis in wild-type and Elovl6−/− mice fed a standard chow or HF-HS diet.
Figure 2

(a) Body weight changes of wild-type and Elovl6−/− mice fed a chow or HF-HS diet (n = 15–18 per group). Six-week-old male mice (n = 15–18) were fed a HF-HS diet for 12 weeks. (b) Average lean and fat mass and body weight and body fat gain by wild-type and Elovl6−/− mice fed a chow (n = 10 per group) or HF-HS diet (n = 8 per group). (c) Daily food intake in wild-type and Elovl6−/− mice provided ad libitum access to chow or HF-HS diet (n = 9–13 per group). (d) H&E-stained white adipose tissue (left), brown adipose tissue (middle) and liver (right) from wild-type and Elovl6−/− mice fed normal chow or HF-HS diet for 12 weeks. Scale bar, 50 μm. (e) Plasma glucose (left) and insulin (right) concentrations in wild-type (n = 18) and Elovl6−/− (n = 15) mice fed chow or HF-HS diet for 12 weeks. Results are represented as means ± s.e.m. *P < 0.05, **P < 0.01 for Elovl6−/− mice as compared to wild-type controls.

Elovl6 deletion protects against diet-induced insulin resistance

Wild-type mice on the HF-HS diet exhibited a robust elevation in plasma insulin accompanied by slight increases in plasma glucose in both fasted and fed states, indicating the emergence of insulin resistance (Fig. 2e). However, Elovl6−/− mice on the HF-HS diet showed a significant reduction in plasma insulin compared to wild-type mice, in both nutritional states. The ameliorative effects of Elovl6 deficiency on hyperinsulinemia was confirmed by a glucose tolerance test (GTT) (Fig. 3a). Wild-type mice on the HF-HS diet had markedly increased insulin abundance throughout the GTT. In contrast, HF-HS–fed Elovl6−/− mice exhibited a pattern of insulin response to glucose load nearly identical to that of mice on a chow diet. The protection from diet-induced insulin resistance in Elovl6−/− mice was more prominent during an insulin tolerance test (ITT) (Fig. 3b). Insulin sensitivity, as measured by the reduction in plasma glucose after insulin administration, was markedly reduced by the HF-HS diet in wild-type mice, whereas Elovl6−/− mice showed a nearly normal response to insulin. The area under the curve (AUC) of plasma insulin abundance during the GTT and the AUC of plasma glucose abundance during the ITT for the HF-HS–fed Elovl6−/− mice were significantly lower than those of the HF-HS–fed wild-type mice (Fig. 3c,d). A pattern of protection from insulin resistance similar to that observed in Elovl6 deficiency was also observed in old (age 6–8 months) mice on a normal chow diet and in body weight–matched mice on the HF-HS diet (Supplementary Fig. 3 online).

Figure 3: Protection from diet-induced insulin resistance in the absence of Elovl6.
Figure 3

(a) Plasma glucose (left) and insulin (right) concentrations during intraperitoneal GTTs in wild-type and Elovl6−/− mice fed standard chow or HF-HS diets for 12 weeks (n = 12 per group). (b) ITTs in wild-type and Elovl6−/− mice fed standard chow (0.5 U insulin per kg of body weight; left) or HF-HS diet (1.0 U insulin per kg of body weight; right) (n = 12 per group). (c,d) The AUCs during the GTTs (c) or ITTs (d). WT, wild-type. (e) Protection of islet hyperplasia in Elovl6−/− mice fed a HF-HS diet. H&E-stained sections of pancreases from wild-type and Elovl6−/− mice fed standard chow or HF-HS diet. Scale bar, 50 μm. (f) Immunoblot analysis of Ser473-phosphoylated Akt (pAkt) and total Akt in response to a bolus injection of insulin in liver and skeletal muscle. Experiments were performed on mice fed a regular chow or HF-HS diet for 12 weeks. (g) Densitometric quantification of all livers and muscle immunoblot analysis from f (n = 6 per group). (h) Phosphorylation of insulin receptor β (pIRβ), IRS-1 and IRS-2 induced by a bolus injection of insulin was assessed in livers of wild-type and Elovl6−/− mice on a regular chow and/or HF-HS diet. Blots are representative of three independent experiments. IP, immunoprecipitated; IB, immunoblotted; pY, phosphorylated tyrosine. Results are represented as means ± s.e.m. *P < 0.05, **P < 0.01 for Elovl6−/− mice as compared to wild-type controls.

Chronic hyperinsulinemia due to insulin resistance is associated with hyperplasia and hypertrophy of islets caused by the adaptive proliferation of β-cells to maintain blood glucose levels. Histology of pancreatic sections demonstrated that there was no observable difference in islet morphology between the wild-type and Elovl6−/− mice on a chow diet (Fig. 3e). Wild-type mice fed a HF-HS diet showed a marked increase in the number and size of islets, suggesting an adaptive enlargement of β-cell mass in response to insulin resistance. In contrast, islet hypertrophy was essentially absent in Elovl6−/− pancreas, presumably because Elovl6 deletion abrogated the development of diet-induced insulin resistance, despite the comparable obesity of the Elovl6−/− and wild-type mice.

Hepatic insulin signaling is preserved in Elovl6−/− mice

We studied insulin signaling in liver, muscle and white adipose tissue to estimate the contribution of these insulin-sensitive organs to the amelioration of diet-induced insulin resistance in Elovl6−/− mice (Fig. 3f,g and Supplementary Fig. 4a online). Insulin injection (5 units) induced phosphorylation of the major marker for insulin signaling, Akt (on Ser473), in each of these three tissues, with similar intensities in chow-fed wild-type and Elovl6−/− mice. In a reflection of their insulin resistance, wild-type mice on a HF-HS diet showed suppression of Akt phosphorylation in these organs, without alterations in total Akt protein concentration. Elovl6 deficiency restored the suppressed Akt phosphorylation only in the liver. Thus, amelioration of whole body insulin resistance in Elovl6−/− mice can be attributed to restoration of hepatic insulin sensitivity. These data are consistent with the observation that changes in fatty acid composition were prominent only in the livers of Elovl6−/− mice (Fig. 1c,d and Supplementary Fig. 2e–g). Restoration of Akt phosphorylation was accompanied by increased total and phosphorylated IRS-2 protein in Elovl6−/− livers, whereas phosphorylation of the insulin receptor and IRS-1 remained suppressed by the HF-HS diet in both genotypes (Fig. 3h), demonstrating that the restoration of insulin signaling in Elovl6−/− mice was mediated by the recovery of the hepatic IRS-2/Akt signaling pathway.

Recent studies have reported that stress or proinflammatory pathways such as the inhibitor of κB (IκB)-IκB kinase (IKK)-nuclear factor-κB, c-Jun N-terminal kinase and JAK–STAT-3–SOCS pathways impair insulin sensitivity, suggesting a link between inflammation and insulin resistance3,4,5,6,7,8,9. HF-HS feeding substantially regulated each of these pathways in the livers of wild-type mice contributing to insulin resistance (Supplementary Fig. 4b). Confoundingly, Elovl6 deficiency tended to slightly activate these signals. It has recently been reported that SOCS proteins act as negative regulators in insulin signaling7,8,9. Contrary to what would be predicted from the observed amelioration-of-insulin-resistance phenotype, SOCS-3 (encoded by Socs3) and cytokine-inducible SH2-containing protein (Cish) were highly upregulated in Elovl6−/− livers (Supplementary Fig. 4c). Collectively, these data show that amelioration of insulin resistance by Elovl6 deficiency is not mediated by suppression of these proinflammatory signals.

Gene expression in Elovl6−/− mice

To determine the molecular basis of these metabolic changes in the livers of Elovl6−/− mice, we examined the expression of genes involved in fatty-acid metabolism or glucose metabolism. Northern blot and real-time (RT) PCR analysis revealed that the HF-HS diet augmented hepatic expression of SREBP-1c (Srebf1) itself and of its target genes encoding lipogenic enzymes, including FAS (Fasn), Elovl6, SCD-1 (Scd1) and glycerol-3-phosphate acyltransferase (Gpam), in normal mice (Fig. 4a,b). The dietary induction of these genes was suppressed in Elovl6−/− mice. Consistently, expression of the nuclear active form of SREBP-1c protein was decreased (Fig. 4c). In contrast, expression of the forkhead box O1 and A2 proteins (Foxo1 and Foxa2), which have been reported to affect hepatic glucose and lipid metabolism22,23, was diminished by the HF-HS diet, but was not changed in Elovl6−/− mice (Fig. 4c). In a reflection of better insulin sensitivity, nuclear exclusion of Foxo1 induced by insulin treatment was more detectable in Elovl6−/− mice than in wild-type mice (Supplementary Fig. 4d). Inhibition of Scd1 expression caused by Elovl6 deficiency was prominent in mice on both normal and HF-HS diets. As we have previously reported, activation of SREBP-1c directly represses IRS-2, the main insulin signal mediator, and causes hepatic insulin resistance14. Therefore, suppression of SREBP-1c could contribute to the amelioration of hepatic insulin resistance in Elovl6−/− mice. Consistent with this notion, expression of Irs2, which was completely suppressed by the HF-HS diet in wild-type mice, was restored in the absence of Elovl6 (Fig. 4a–c). Meanwhile, genes related to fatty acid oxidation that are regulated by nuclear receptor peroxisome proliferator–activated receptor (PPAR)α (Ppara), such as those encoding carnitine palmitoyltransferase-1 (Cpt1a), medium-chain acyl-CoA dehydrogenase (Acadm), acyl-CoA oxidase (Acox1) and cytochrome P450 4a14 (Cyp4a14), were induced by HF-HS diet in wild-type mice as an adaptive response (Fig. 4a). However, expression of these oxidation genes, including Ppara, was considerably decreased in Elovl6−/− mice, despite the amelioration of insulin resistance in these mice. AMP-activated protein kinase (AMPK) has been shown to facilitate energy expenditure and contribute to insulin sensitivity after treatment with biguanides, anti-diabetic agents that activate AMPK24. The amount of the active form of AMPKα (phosphorylated on Ser485) was not changed in Elovl6−/− livers (Fig. 4c). Thus, these data implicate that Elovl6 deficiency suppressed both the synthesis and the degradation of fatty acids, resulting in a slightly increased hepatic triglyceride content. In support of this, fatty acid synthesis and oxidation were reduced in primary hepatocytes isolated from Elovl6−/− mice as compared to those from wild-type mice (Fig. 4d).

Figure 4: Effects of Elovl6 deficiency on mRNA and protein levels and fatty acid metabolism in the livers of wild-type and Elovl6−/− mice fed a regular chow or HF-HS diet.
Figure 4

(a,b) Northern blot (a) and RT-PCR (b) analysis of various mRNA levels in livers from wild-type and Elovl6−/− mice fed a standard chow or HF-HS diet for 12 weeks and sacrificed in a nonfasted state. (a) Total RNA was isolated from the livers of mice from each group (n = 3), pooled (15 μg) and subjected to northern blot analysis with the indicated cDNA probes. Fold changes of expression relative to chow-fed wild-type mice are shown. Ucp2, uncoupling protein-2; Ldlr, low-density lipoprotein receptor; Hmgcs1, hydroxymethylglutaryl-CoA synthase-1; Pklr, liver-type pyruvate kinase; Pck1, phosphoenolpyruvate carboxykinase-1, cytosolic. (b) Quantitative RT-PCR of RNA from livers of mice from each group (n = 9 per group). # indicates statistical significance between animals of the same genotype fed different diets, P < 0.01; * indicates statistical significance between wild-type and Elovl6−/− mice fed the same diet (P < 0.05). ND, not detectable. (c) Immunoblot analysis of SREBP-1, SREBP-2, Foxo1 and Foxa2 in nuclear extracts and IRS-2, Ser485-phosphorylated AMPKα (pAMPKα) and AMPKα in whole cell lysates from the livers of wild-type and Elovl6−/− mice fed a regular chow diet or HF-HS diet for 12 weeks. (d) The amount of fatty acid synthesis (left) and oxidation (right) in primary hepatocytes isolated from chow-fed wild-type and Elovl6−/− mice (n = 9 per group). d.p.m., decay per minute. (e) Diacylglycerol (left) and ceramide (right) content in the livers of wild-type and Elovl6−/− mice fed a regular chow diet or HF-HS diet for 12 weeks (n = 6 per group). (f) Immunoblot analysis determining membrane and cytosolic PKCε content in the livers of wild-type and Elovl6−/− mice fed a regular chow diet or HF-HS diet for 12 weeks (n = 6–8 per group). Blots are representative of three independent experiments. Results are represented as means ± s.e.m. *P < 0.05, **P < 0.01 for Elovl6−/− mice as compared to wild-type controls.

Diacylglycerol and ceramide have been thought to mediate insulin resistance in muscle and liver, accompanying accumulation of intracellular lipids25,26,27. We measured the contents of these lipid metabolites in the livers of wild-type and Elovl6−/− mice fed a chow or HF-HS diet (Fig. 4e). In wild-type mice, hepatic diacylglycerol content was elevated twofold by the HF-HS diet. Elovl6 deficiency did not affect the basal level on a normal chow, but inhibited the induction by HF-HS diet observed in Elovl6−/− mice. No marked genotypic and dietary differences were evident in hepatic ceramide content. Diacylglycerol accumulation has been reported to be linked to the increased protein kinase C (PKC) ε activity and impaired phosphorylation of IRS-2 tyrosine induced by insulin25,28. Hepatic PKCε activity, as measured by the ratio of the amount of PKCε in cellular membranes to that in the cytosolic fraction, was significantly increased in the livers of HF-HS–fed wild-type mice, but not in Elovl6−/− mice (Fig. 4f), implying that the protection from diet-induced insulin resistance observed in Elovl6−/− mice could be mediated at least partially through this diacylglycerol-PKCε pathway.

Contribution of hepatic Elovl6 to insulin resistance

To estimate the importance of hepatic Elovl6 on whole-body insulin sensitivity, and to distinguish the long-term and short-term effects of an absence of Elovl6, we used adenoviral RNA interference (RNAi) to specifically inhibit hepatic expression of Elovl6 (Fig. 5a–e). The Elovl6 RNAi adenovirus (Elovl6i) robustly suppressed hepatic Elovl6 expression and activity in C57BL6 mice on the HF-HS diet (Fig. 5a). Treatment with Elovl6i mimicked the hepatic changes observed in the liver of Elovl6−/− mice—it reduced expression of both Srebf1 and Ppara and induced Irs2 mRNA expression, and this was accompanied by a significant increase in hepatic triglycerides (Fig. 5a,b). Consequently, knockdown of hepatic Elovl6 significantly improved upon the increased plasma insulin level (P < 0.01) and impaired insulin sensitivity (as determined by ITT, P < 0.01) observed in mock-treated (LacZi), HF-HS–fed mice, even though there was no change in the plasma glucose level (Fig. 5c–e). Decreased plasma insulin was also observed by injecting Elovl6i into ob/ob (leptin-deficient, also known as Lep−/−) mice (data not shown). Conversely, injection of a small amount of Elovl6 adenovirus (Ad-Elovl6) into Elovl6−/− animals fed a HF-HS diet caused hepatic expression of this enzyme to return to the control level (Fig. 5f). The restoration of Elovl6 expression only in the liver canceled the protection from diet-induced hyperinsulinemia and insulin resistance in Elovl6−/− mice and was accompanied by increased Srebf1 and decreased Irs2 mRNA levels (Fig. 5f–h). In contrast, gene expression analysis in other energy organs, such as white fat, brown fat and skeletal muscle, in HF-HS–fed Elovl6−/− mice revealed no marked changes in the expression of genes involved in fatty acid oxidation, insulin sensitivity or lipogenesis, indicating that these organs do not contribute to the protection from insulin resistance noted in Elovl6−/− mice (Supplementary Fig. 5a–c). As an exception, Fasn expression was increased in these tissues. Insulin sensitivity was estimated in primary culture cells prepared from muscles of both groups (Supplementary Fig. 5d). There were no differences between wildtype and Elovl6−/− muscle cells in basal level, insulin-mediated induction or palmitate-mediated inhibition of glucose uptake (Supplementary Fig. 5d). Infection with Ad-Elovl6 did not restore the palmitatesuppressed uptake (Supplementary Fig. 5d). Thus, Elovl6 had no effects on the glucose uptake or insulin sensitivity of muscle cells. Taken together with the hepatic knockdown and restoration experiments, these data indicate that hepatic Elovl6 plays the major role in diet-induced insulin resistance.

Figure 5: Effects of hepatic Elovl6 expression on gene expression, fatty acid metabolism and insulin sensitivity.
Figure 5

(ae) Knockdown of hepatic Elovl6 by adenoviral expression of RNAi. Eight-week-old male C57BL6 mice were fed a HF-HS diet for 2 weeks, followed by tail vein injection with adenovirus encoding RNAi targeting Elovl6 (Elovl6i) or a LacZ (LacZi) control sequence. After 5–7 d of HF-HS feeding, mice were sacrificed in a nonfasted state. (a) Gene expression (left) and elongation activity (right) in the livers from LacZi and Elovl6i. The Elovl6i fold-change value is relative to the normalized value of LacZi control signal. (bd) Liver trigyceride (b) plasma glucose (c) and plasma insulin (d) levels in a fasted or fed state. (e) GTT (left) and ITT (0.75 U insulin per kg body weight; right) in mice infected with either LacZi or Elovl6i. (fh) Effect of adenovirus-mediated restoration of hepatic Elovl6 expression in Elovl6−/− mice. Six-week-old male Elovl6−/− mice were fed a HF-HS diet for 4 weeks and then treated with adenovirus encoding GFP (control) or Elovl6 for 5–7 d. (f) Northern blot analysis of gene expression in the livers of Elovl6−/− mice injected with adenovirus encoding GFP (Ad-GFP) or Elovl6 (Ad-Elovl6). (g) Plasma glucose (left) and insulin (right) concentrations of the Elovl6−/− mice injected with Ad-GFP or Ad-Elovl6 in the fed state. (h) ITT in mice infected with either Ad-GFP or Ad-Elovl6 (0.75 U per kg body weight). Results are represented as means ± s.e.m., n = 11–14 per group. *P < 0.05, **P < 0.01 for experimental mice as compared with their respective controls.

To determine whether overexpression of Elovl6 would affect hepatic gene expression and insulin signaling, mouse Hepa1c1c7 hepatoma cells were infected with Ad-Elovl6. Elovl6 overexpression markedly induced SREBP-1c at both the mRNA and nuclear protein levels (Fig. 6a). Furthermore, activation of this enzyme blocked insulin-stimulated phosphorylation of Akt (Fig. 6b). Thus, hepatic Elovl6 activity could induce SREBP-1c expression and oppose insulin signaling.

Figure 6: The effects of Elovl6 overexpression and palmitate/palmitoleate ratio on Hepa1c1c7 hepatoma cells and of Elovl6 deficiency on genetically obese mice.
Figure 6

(a,b) Overexpression of Elovl6 induces Srebf1 expression and insulin resistance in hepatoma cells. (a) Gene expression in Hepa1c1c7 cells infected with adenovirus expressing either Ad-GFP (n = 6) or Ad-Elovl6 (n = 6), as estimated by RT-PCR analysis (left). Immunoblot analysis of SREBP-1 in membrane (precursor) and nuclear extracts (mature) from Hepa1c1c7 cells infected with adenovirus expressing either Ad-GFP or Ad-Elovl6 (right). Ad-GFP is used as a negative control. (b) Elovl6 overexpression results in decreased Akt Ser473 phosphorylation in Hepa1c1c7 cells. Cells were stimulated with insulin for 10 min 16 h after adenovirus infection. (c,d) Effects of palmitate/palmitoleate ratio on Akt phosphorylation, c, and gene expression, d, in Hepa1c1c7 cells. Cells were supplemented with media alone (fatty acid–free) or media containing 200 μM palmitate (PA200), 200 μM palmitate + 200 μM palmitoleate (PA200 + POA200), 200 μM palmitate + 100 μM palmitoleate (PA200 + POA100), 200 μM palmitate + 50 μM palmitoleate (PA200 + POA50), or 200 μM palmitate + 10 μM palmitoleate (PA200 + POA10) for 16 h before insulin stimulation or RNA extraction. (eh) Loss of Elovl6 ameliorates insulin resistance in ob/ob mice. (e) Body weight changes (left) and body fat percentage (right) of wild-type (n = 11), ob/ob (n = 11) and ob/ob,Elovl6−/− mice (n = 10). (f,g) Plasma glucose (f) and insulin (g) concentrations in 6–8-week-old wild-type (n = 11), ob/ob (n = 11) and ob/ob,Elovl6−/− mice (n = 10). Mice were fasted for 24 h before experiments. (h) Plasma glucose levels during the GTT (left) and ITT (right) of 6–8-week-old ob/ob (n = 9) and ob/ob,Elovl6−/− (n = 9) mice. For ITT, insulin (2 U per kg body weight) was injected into each mouse after 6 h of fasting. Results are represented as means ± s.e.m. *P < 0.05, **P < 0.01 for experimental mice as compared with their respective controls.

To examine the physiological relevance of these data, we next asked whether insulin action and gene expression can be altered in liver cells as a function of the amount of cellular fatty acids regulated by Elovl6; we focused specifically on the effects of increasing the ratio of palmitoleate to palmitate. Hepa1c1c7 cells were cultured in medium supplemented with palmitate and with increasing concentrations of palmitoleate. Palmitate-alone treatment suppressed insulin-stimulated phosphorylation of Akt, and addition of palmitoleate restored it in a dose-dependent manner (Fig. 6c). Srebf1 and Ppara mRNA expression were increased by palmitate treatment and were returned to the baseline by palmitate and palmitoleate supplementation, (Fig. 6d). These experiments showed that the cellular contents, or the ratio of palmitoleate to palmitate, could be a determinant for the hepatic insulin sensitivity regulated by Elovl6. These findings suggest that the fatty acid composition observed in the Elovl6−/− liver is favorable for insulin action.

Leptin signaling in Elovl6 deficiency

Leptin is a key regulator of satiety and energy expenditure, thus determining energy metabolism and insulin sensitivity in the body29. Along with insulin resistance, diet-induced obesity by HF-HS was associated with leptin resistance, as evidenced by high plasma leptin levels and high leptin expression in adipose tissue in wild-type mice (Supplementary Table 1 and Supplementary Fig. 5a). Elovl6 deficiency improved leptin signaling, as judged by a marked decrease in plasma leptin in Elovl6−/− mice on both chow and HF-HS diets, irrespective of obesity. However, the food intake and resultant adiposity did not change in Elovl6−/− mice on the HF-HS diet (Fig. 2 and Supplementary Table 1). Livers from these mice did not show signs of the improved leptin signaling that was suppressed by HF-HS diet, as estimated by examining the amount of phosphorylation of STAT-3 and AMPK and fatty acid oxidation (Supplementary Fig. 4b and Fig. 4a). Furthermore, the effect of Elovl6 deficiency was evaluated in ob/ob mice, which showed severe obesity, insulin resistance and diabetes (Fig. 6e–h). ob/ob and Elovl6 double-mutant mice (ob/ob,Elovl6−/−) showed sustained, severe obesity and had similar increases in body weight, body fat (Fig. 6e) and liver triglyceride content (data not shown) when compared to wild-type mice. However, insulin resistance and hyperglycemia were markedly less severe in the ob/ob,Elovl6−/− mice than in the ob/ob mice, as estimated by GTTs and ITTs conducted in mice 6–8 weeks (Fig. 6f–h) and 16–18 weeks (data not shown) of age. Taken together, these data imply that the effect of Elovl6 on insulin sensitivity is independent of leptin. The mechanism by which Elovl6 deficiency decreases plasma leptin levels without changing adipocyte size is currently unknown, but must be related to enhanced insulin signaling.


Our current data establish the unique role of Elovl6 in hepatic lipogenesis. The major product of FAS, palmitate (16:0), is elongated by Elovl6 and desaturated by SCD-1 to yield oleic acid (18:1), the end product of mammalian fatty-acid synthesis. Recent studies in mouse models of ACC, FAS and SCD-1 deficiency, as well as our current data in Elovl6−/− mice, implicate various roles for endogenous fatty acid synthesis in energy metabolism (Supplementary Fig. 1). However, these deficiencies affect not only fatty acid synthesis, but also secondary activation of fatty acid oxidation. Liver-specific FAS knockout mice have phenotypes similar to those of PPARα-null mice, suggesting that some products of FAS are endogenous PPARα agonists that maintain fatty acid metabolism30. Scd1−/− mice are also protected from obesity and insulin resistance owing to activation of AMPK and fatty acid oxidation, implicating SCD-1 as a potential target for the treatment of diabetes31,32. Elovl6 and SCD-1 are structurally related and committed to consecutive reactions in lipogenesis; therefore, the improvement of insulin sensitivity in both knockout mice is not unexpected. It is possible that the decrease in Scd1 expression could partly contribute to the insulin-sensitizing effect of Elovl6 deficiency. However, in contrast to Scd1−/− mice, Elovl6−/− mice showed sustained obesity and low fatty acid oxidation in the liver, indicating that the mechanisms by which these two enzymes influence insulin sensitivity are not completely convergent. Thus, the conversion of palmitate to stearate is a key step in energy expenditure that discriminates between the physiological functions of Elovl6, a membrane-bound enzyme, and FAS, the multifunctional cytosolic enzyme that synthesizes fatty acids of up to 16 carbons in length.

The amelioration of insulin resistance in obese mice is usually accompanied by a loss of fat or body weight caused by decreased food intake33,34, enhanced lipid oxidation and/or decreased lipogenesis31,35,36. The Elovl6−/− mice are unique in that their insulin resistance was reduced without amelioration of obesity or hepatosteatosis. The restoration of hepatic insulin signaling in these mice could not be explained by changes in energy balance or proinflammatory signals. These data highlight the importance of tissue fatty acid composition in insulin sensitivity, especially the ratio of C18 to C16 fatty acids, which is controlled by Elovl6 activity. The precise molecular mechanism for this is currently unknown. Elovl6 inhibition results in the accumulation of palmitate, which is paradoxically the most potent dietary inducer of obesity and insulin resistance. Our studies show that the increase in the ratio of palmitoleate to palmitate prevents palmitate-induced Srebf1 expression and consequently rescues palmitate-induced insulin resistance. Furthermore, our preliminary data demonstrate that overexpression of Elovl6 leads to liver dysfunction, in addition to the induction of Srebf1 expression and insulin resistance in cells. These results suggest that the fatty acid composition of Elovl6−/− liver, namely the high ratio of 16:1/16:0 and the reduction in C18 fatty acids, may be protective against hepatic lipotoxicity and insulin resistance in HF-HS–fed mice (Supplementary Fig. 1b). Feeding normal mice a diet containing a single fatty acid demonstrated that palmitate alone or stearate alone can induce insulin resistance, but oleate alone cannot (Supplementary Fig. 5e). Elovl6−/− mice were insulin sensitive after palmitate ingestion, with elevations in liver triglyceride and cholesterol content. Thus, the conversion of palmitate to stearate is crucial for the emergence of insulin resistance. Notably, however, Elovl6−/− mice were again resistant to the insulin resistance–inducing effects of stearate. Thus, the protective effect of Elovl6 deficiency is not simply a result of stearate depletion, implicating that exogenous intake and endogenous production of fatty acids might have different effects on hepatic insulin sensitivity. Palmitoleate, the major final product of de novo fatty acid synthesis in Elovl6 deficiency, is efficiently incorporated into triglycerides and cholesterol esters, potentially contributing to the prevention of insulin resistance37. These observed effects may also be related to the reported benefits of macadamia nuts rich in palmitoleate in the prevention of diabetes and cardiovascular diseases38.

Ppara expression was reduced in Elovl6-deficient animals. Furthermore, Ad-Elovl6 and exogenous fatty acids administered in various 16:1/16:0 ratios regulate both Srebf1 and Ppara expression in a parallel fashion, although the co-regulation of these opposite regulators of fatty acid metabolism apparently contradicts nutritional adaptation. However, the suppression of Ppara expression in Elovl6-deficient mice does not explain the restoration of insulin sensitivity in these mice. It could instead be a result of the repression of SREBP-1c. Newly synthesized fatty acids could be ligands for PPARα and hepatocyte nuclear factor-4α (ref. 30). Elovl6 deficiency could deplete these ligands directly and/or indirectly through SREBP-1c suppression, leading to decreased activities of PPARα and hepatocyte nuclear factor-4α; it could further repress PPARα expression, as the PPARα promoter is a target of both factors (refs. 30,39,40 and T.Y. and H.S., unpublished data). Recently, we also found that knockdown of hepatic Srebf1 leads to suppression of Ppara in the liver (T.Y. and H.S., unpublished data). Secondary regulation of PPARα activity could be a part of SREBP-1c/Elovl6 regulation of lipogenesis.

It has been generally noted that different long chain fatty acids have distinct effects depending upon their extent of desaturation. However, our current study suggests that the length of fatty acids is also important for energy metabolism and insulin sensitivity.

To date, Elovl6−/− mice are the only known pure metabolic model in which obesity-induced insulin resistance is mitigated through modulation of hepatic metabolism without a concurrent amelioration of obesity. It has been reported that mice deficient for inducible nitric oxide synthase, adipocyte protein-2 (also known as fatty acid binding protein-4) and mal1 (also known as fatty acid binding protein-5) also maintain insulin sensitivity despite diet-induced obesity, but not through effects on the liver41,42,43. Our model helps in understanding the mechanism by which obesity and obesity-related disorders are sometimes dissociated and implicates a new strategy for the treatment of diabetes and cardiovascular diseases through intervention of Elovl6.


Generation of Elovl6−/− mice.

Elovl6+/− founder mice created at Lexicon Genetics through the use of a gene-trapping method44. We identified the integration site of the targeting cassette between exon 2 and 3 and developed a PCR-based assay that distinguishes between the three possible mouse genotypes (see Supplementary Methods online). We crossed Elovl6+/− founder mice (50% C57BL6 albino and 50% 129SvEvBrd strains) at least six times to transfer the null mutation onto the C57BL6 genetic background. We then intercrossed heterozygotes to obtain Elovl6+/+, Elovl6+/− and Elovl6−/− mice. We used only male mice for the present studies.

Animal experiments.

Mice were housed in a pathogen-free barrier facility with a 12-h light/dark cycle, with free access to water and a standard chow diet. In some experiments, we fed the mice a high-carbohydrate, fat-free diet10 or a high-fat, high-sucrose (HF-HS) diet19. We used age- and sex-matched littermates for each experiment, and we sacrificed mice in the early light phase in a nonfasted state. We isolated tissues immediately, weighed and kept in liquid nitrogen. We determined fat and lean mass by dual-energy X-ray absorptiometry using a PIXImus mouse densitometer (GE Medical Systems Lunar). All experiments were repeated at least three times. All animal husbandry and animal experiments were consistent with the University of Tsukuba's Regulation of Animal Experiment Committee.

Fatty acid elongation assay.

We assayed microsomal fatty acid elongation activity by measuring of [2-14C]malonyl-CoA incorporation into exogenous acyl-CoAs as described previously16.

Fatty acid composition of liver.

We measured the fatty acid composition by gas chromatography as described previously45.

Metabolic measurements.

We measured the concentrations of glucose, insulin, leptin, free fatty acids (FFAs), triglycerides, total cholesterol and alanine aminotransferase (ALT) in plasma and of triglycerides and total cholesterol in liver as previously described46. For intraperitoneal GTTs, mice were fasted overnight (for 16 h) and then injected intraperitoneally with D-glucose (20% solution; 2 g per kg body weight). For ITTs, mice in the randomly fed state were injected intraperitoneally with human regular insulin (Eli Lilly). We collected blood before injection and at different times after injection (as indicated in figures) and glucose and insulin values were determined. We determined diacylglycerol and ceramide contents in the liver lipid extracts by the diacylglycerol kinase assay as described previously47. We separated phosphorylated derivatives of diacylglycerol and thin-layer chromatography and visualized and quantified radioactive bands with an imaging analyzer.

In vivo insulin stimulation assay.

We fasted mice for 24 h and anesthetized them by injection of 30 mg/kg of pentobarbitone (Abbott Laboratories). We then opened the peritoneal cavity and injected either saline control or insulin (5 units) into the inferior vena cava. After 5 min, the liver, muscle and epididymal white adipose tissue were rapidly excised and immediately frozen in liquid nitrogen. We performed immunoprecipitation and immunoblot analysis of insulin signaling molecules using tissue homogenates.

Immunoblotting and immunoprecipitation.

We performed immunoblot analysis of tissue and cell lysates, membrane fractions and nuclear extracts as previously described10,14,48. We performed immunoprecipitation analysis of tissue lysates as previously described (ref. 14 and Supplementary Methods).

Total RNA preparation, northern blotting and RT-PCR analysis.

We performed total RNA preparation and blot hybridization with cDNA probes as previously described46. We performed quantitative RT-PCR analysis as described previously (ref. 49 and Supplementary Methods).

Determination of fatty acid synthesis and fatty acid oxidation in mouse primary hepatocytes in vitro.

Fatty acid synthesis and fatty acid oxidation in freshly isolated hepatocytes were measured as previously described50.

Preparation of recombinant adenovirus and adenovirus treatment.

We subcloned Elovl6-specific RNA interference (RNAi) constructs into the U6 entry vector (Invitrogen) using a primer specific for the Elovl6 coding sequence, 5′-GCGAGCCAAGTTTGAACTTCAGA-3′, and generated the recombinant adenoviral plasmid by homologous recombination with the pAd promoterless vector (Invitrogen). We subcloned mouse Elovl6-coding cDNA into the pENTR/D-TOPO vector (Invitrogen) and generated recombinant adenoviral plasmid by homologous recombination with pAd/CMV/V5-DEST vector (Invitrogen). We produced recombinant adenovirus in HEK293 cells and purified them as previously described14,48. We intravenously injected mice with adenoviruses expressing LacZ RNAi or Elovl6 RNAi at a dose of 1 × 109 PFU and adenoviruses expressing GFP or Elovl6 at a dose of 1 × 108 PFU. Cells were infected with adenoviruses expressing GFP or Elovl6 at a multiplicity of infection of 100 for 16 h.

Culture of Hepa1c1c7 cells.

Mouse hepatoma Hepa1c1c7 cells were cultured in MEMα supplemented with 10% FBS and 1% penicillin/streptomycin. For insulin-signaling analysis, we changed cells into serum-free medium 4 h before the experiment and then treated them with or without insulin (100 nM, 10 min). Cells were treated with fatty acids as described previously49.

Statistical analyses.

Data are expressed as means ± s.e.m. Differences between two groups were assessed using the unpaired two-tailed Student's t-test. Data sets involving more than two groups were assessed by ANOVA. Glucose and insulin tolerance tests were analyzed by repeated-measures ANOVA with Statview Software (BrainPower).

Note: Supplementary information is available on the Nature Medicine website.


  1. 1.

    , & Dietary fat, insulin sensitivity and the metabolic syndrome. Clin. Nutr. 23, 447–456 (2004).

  2. 2.

    Minireview: weapons of lean body mass destruction: the role of ectopic lipids in the metabolic syndrome. Endocrinology 144, 5159–5165 (2003).

  3. 3.

    et al. Local and systemic insulin resistance resulting from hepatic activation of IKKβ and NFβB. Nat. Med. 11, 183–190 (2005).

  4. 4.

    et al. IKK-beta links inflammation to obesity-induced insulin resistance. Nat. Med. 11, 191–198 (2005).

  5. 5.

    et al. Modulation of the JNK pathway in liver affects insulin resistance status. J. Biol. Chem. 279, 45803–45809 (2004).

  6. 6.

    et al. Endoplasmic reticulum stress links obesity, insulin action, and type 2 diabetes. Science 306, 457–461 (2004).

  7. 7.

    et al. Enhanced leptin sensitivity and attenuation of diet-induced obesity in mice with haploinsufficiency of Socs3. Nat. Med. 10, 734–738 (2004).

  8. 8.

    et al. Role of hepatic STAT3 in brain-insulin action on hepatic glucose production. Cell Metab. 3, 267–275 (2006).

  9. 9.

    et al. The dual function of hepatic SOCS3 in insulin resistance in vivo. Genes Cells 12, 143–154 (2007).

  10. 10.

    et al. Sterol regulatory element-binding protein-1 as a key transcription factor for nutritional induction of lipogenic enzyme genes. J. Biol. Chem. 274, 35832–35839 (1999).

  11. 11.

    Sterol regulatory element-binding proteins (SREBPs): transcriptional regulators of lipid synthetic genes. Prog. Lipid Res. 40, 439–452 (2001).

  12. 12.

    et al. Combined analysis of oligonucleotide microarray data from transgenic and knockout mice identifies direct SREBP target genes. Proc. Natl. Acad. Sci. USA 100, 12027–12032 (2003).

  13. 13.

    et al. Hyperlipidemic effects of dietary saturated fats mediated through PGC-1beta coactivation of SREBP. Cell 120, 261–273 (2005).

  14. 14.

    et al. SREBPs suppress IRS-2-mediated insulin signalling in the liver. Nat. Cell Biol. 6, 351–357 (2004).

  15. 15.

    , , , & Identification of a mammalian long chain fatty acyl elongase regulated by sterol regulatory element-binding proteins. J. Biol. Chem. 276, 45358–45366 (2001).

  16. 16.

    et al. Cloning and characterization of a mammalian fatty acyl-CoA elongase as a lipogenic enzyme regulated by SREBPs. J. Lipid Res. 43, 911–920 (2002).

  17. 17.

    , , & Elongation of long-chain fatty acids. Prog. Lipid Res. 43, 36–54 (2004).

  18. 18.

    et al. Regulation of hepatic fatty acid elongase and desaturase expression in diabetes and obesity. J. Lipid Res. 47, 2028–2041 (2006).

  19. 19.

    et al. Diet-induced insulin resistance in mice lacking adiponectin/ACRP30. Nat. Med. 8, 731–737 (2002).

  20. 20.

    et al. Obesity is associated with macrophage accumulation in adipose tissue. J. Clin. Invest. 112, 1796–1808 (2003).

  21. 21.

    et al. Chronic inflammation in fat plays a crucial role in the development of obesity-related insulin resistance. J. Clin. Invest. 112, 1821–1830 (2003).

  22. 22.

    , , & The forkhead transcription factor Foxo1 (Fkhr) confers insulin sensitivity onto glucose-6-phosphatase expression. J. Clin. Invest. 108, 1359–1367 (2001).

  23. 23.

    , , , & Foxa2 regulates lipid metabolism and ketogenesis in the liver during fasting and in diabetes. Nature 432, 1027–1032 (2004).

  24. 24.

    et al. Role of AMP-activated protein kinase in mechanism of metformin action. J. Clin. Invest. 108, 1167–1174 (2001).

  25. 25.

    et al. Mechanism of hepatic insulin resistance in non-alcoholic fatty liver disease. J. Biol. Chem. 279, 32345–32353 (2004).

  26. 26.

    et al. Mechanism by which fatty acids inhibit insulin activation of insulin receptor substrate-1 (IRS-1)-associated phosphatidylinositol 3-kinase activity in muscle. J. Biol. Chem. 277, 50230–50236 (2002).

  27. 27.

    et al. Inhibition of ceramide synthesis ameliorates glucocorticoid-, saturated-fat-, and obesity-induced insulin resistance. Cell Metab. 5, 167–179 (2007).

  28. 28.

    et al. Inhibition of protein kinase Cepsilon prevents hepatic insulin resistance in nonalcoholic fatty liver disease. J. Clin. Invest. 117, 739–745 (2007).

  29. 29.

    Obesity in the new millennium. Nature 404, 632–634 (2000).

  30. 30.

    et al. “New” hepatic fat activates PPARalpha to maintain glucose, lipid, and cholesterol homeostasis. Cell Metab. 1, 309–322 (2005).

  31. 31.

    et al. Loss of stearoyl-CoA desaturase-1 function protects mice against adiposity. Proc. Natl. Acad. Sci. USA 99, 11482–11486 (2002).

  32. 32.

    et al. Stearoyl-CoA desaturase 1 deficiency increases fatty acid oxidation by activating AMP-activated protein kinase in liver. Proc. Natl. Acad. Sci. USA 101, 6409–6414 (2004).

  33. 33.

    , , , & Mice lacking melanin-concentrating hormone are hypophagic and lean. Nature 396, 670–674 (1998).

  34. 34.

    et al. Reduced food intake and body weight in mice treated with fatty acid synthase inhibitors. Science 288, 2379–2381 (2000).

  35. 35.

    et al. Increased insulin sensitivity and obesity resistance in mice lacking the protein tyrosine phosphatase-1B gene. Science 283, 1544–1548 (1999).

  36. 36.

    , , & Continuous fatty acid oxidation and reduced fat storage in mice lacking acetyl-CoA carboxylase 2. Science 291, 2613–2616 (2001).

  37. 37.

    et al. Muscle-type specific intramyocellular and hepatic lipid metabolism during starvation in wistar rats. Diabetes 53, 528–534 (2004).

  38. 38.

    et al. Serum lipid effects of a monounsaturated (palmitoleic) fatty acid–rich diet based on macadamia nuts in healthy, young Japanese women. Clin. Exp. Pharmacol. Physiol. 31Suppl 2, S37–S38 (2004).

  39. 39.

    et al. Fatty acids and eicosanoids regulate gene expression through direct interactions with peroxisome proliferator-activated receptors alpha and gamma. Proc. Natl. Acad. Sci. USA 94, 4318–4323 (1997).

  40. 40.

    et al. Hepatocyte nuclear factor 4 is a transcription factor that constitutively binds fatty acids. Structure 10, 1225–1234 (2002).

  41. 41.

    & Targeted disruption of inducible nitric oxide synthase protects against obesity-linked insulin resistance in muscle. Nat. Med. 7, 1138–1143 (2001).

  42. 42.

    et al. Uncoupling of obesity from insulin resistance through a targeted mutation in aP2, the adipocyte fatty acid binding protein. Science 274, 1377–1379 (1996).

  43. 43.

    et al. Role of the fatty acid binding protein mal1 in obesity and insulin resistance. Diabetes 52, 300–307 (2003).

  44. 44.

    et al. Disruption and sequence identification of 2,000 genes in mouse embryonic stem cells. Nature 392, 608–611 (1998).

  45. 45.

    et al. Polyunsaturated fatty acids ameliorate hepatic steatosis in obese mice by SREBP-1 suppression. Hepatology 38, 1529–1539 (2003).

  46. 46.

    et al. Insulin-independent induction of sterol regulatory element-binding protein-1c expression in the livers of streptozotocin-treated mice. Diabetes 53, 560–569 (2004).

  47. 47.

    , & 1,2-Diacylglycerol and ceramide levels in insulin-resistant tissues of the rat in vivo. J. Biol. Chem. 265, 16880–16885 (1990).

  48. 48.

    et al. TFE3 transcriptionally activates hepatic IRS-2, participates in insulin signaling and ameliorates diabetes. Nat. Med. 12, 107–113 (2006).

  49. 49.

    et al. Granuphilin is activated by SREBP-1c and involved in impaired insulin secretion in diabetic mice. Cell Metab. 4, 143–154 (2006).

  50. 50.

    et al. Prevention of obesity in mice by antisense oligonucleotide inhibitors of stearoyl-CoA desaturase-1. J. Clin. Invest. 115, 1030–1038 (2005).

Download references


We thank T. Ide and H. Daitoku for technical help and/or useful comments. This work was supported by grants-in-aid from the Ministry of Science, Education, Culture and Technology of Japan; a grant for the Japan Foundation for Applied Enzymology; and a grant from The Naito Foundation.

Author information


  1. Department of Internal Medicine (Endocrinology and Metabolism) Graduate School of Comprehensive Human Sciences, 1-1-1 Tennodai, Tsukuba Ibaraki 305-8575, Japan.

    • Takashi Matsuzaka
    • , Hitoshi Shimano
    • , Toyonori Kato
    • , Ayaka Atsumi
    • , Takashi Yamamoto
    • , Noriyuki Inoue
    • , Mayumi Ishikawa
    • , Sumiyo Okada
    • , Naomi Ishigaki
    • , Hitoshi Iwasaki
    • , Yuko Iwasaki
    • , Tadayoshi Karasawa
    • , Shin Kumadaki
    • , Toshiyuki Matsui
    • , Yoshimi Nakagawa
    • , Akimitsu Takahashi
    • , Hiroaki Suzuki
    • , Sigeru Yatoh
    • , Hirohito Sone
    • , Hideo Toyoshima
    •  & Nobuhiro Yamada
  2. Center for Tsukuba Advanced Research Alliance University of Tsukuba, 1-1-1 Tennodai, Tsukuba Ibaraki 305-8575, Japan.

    • Takashi Matsuzaka
    • , Hitoshi Shimano
    • , Naoya Yahagi
    •  & Yoshimi Nakagawa
  3. Department of Metabolic Disease, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan.

    • Naoya Yahagi
    • , Motohiro Sekiya
    • , Ken Ohashi
    •  & Jun-ichi Osuga
  4. Department of Molecular Physiology and Biophysics, Vanderbilt University Medical Center, Nashville, Tennessee 37232, USA.

    • Alyssa H Hasty


  1. Search for Takashi Matsuzaka in:

  2. Search for Hitoshi Shimano in:

  3. Search for Naoya Yahagi in:

  4. Search for Toyonori Kato in:

  5. Search for Ayaka Atsumi in:

  6. Search for Takashi Yamamoto in:

  7. Search for Noriyuki Inoue in:

  8. Search for Mayumi Ishikawa in:

  9. Search for Sumiyo Okada in:

  10. Search for Naomi Ishigaki in:

  11. Search for Hitoshi Iwasaki in:

  12. Search for Yuko Iwasaki in:

  13. Search for Tadayoshi Karasawa in:

  14. Search for Shin Kumadaki in:

  15. Search for Toshiyuki Matsui in:

  16. Search for Motohiro Sekiya in:

  17. Search for Ken Ohashi in:

  18. Search for Alyssa H Hasty in:

  19. Search for Yoshimi Nakagawa in:

  20. Search for Akimitsu Takahashi in:

  21. Search for Hiroaki Suzuki in:

  22. Search for Sigeru Yatoh in:

  23. Search for Hirohito Sone in:

  24. Search for Hideo Toyoshima in:

  25. Search for Jun-ichi Osuga in:

  26. Search for Nobuhiro Yamada in:


T. Matsuzaka carried out most of the experiments, data analysis and prepared the figures with significant help from M.I., S.O., N. Ishigaki, H.I., Y.I. and T. Karasawa. H. Shimano developed the idea for and supervised the study, designed protocols, developed collaborations and wrote the manuscript. N. Yahagi contributed to many in vivo experiments and to training T. Matsuzaka in experimental techniques. T. Kato carried out measurements of fatty acid composition and assisted with hepatocyte isolations, fatty acid treatment to the cell and mice and adenoviral experiments. A.A. assisted with the in vivo adenoviral experiments. T.Y. assisted with PKCε analysis and cell-line experiments. N. Inoue assisted with ELISA measurements and developed the DXA protocols for analyzing fat. S.K. assisted with RT-PCR analysis. T. Matsui contributed to primary myotube culture and the 2-DG uptake assay. M.S. and K.O. participated in the experimental design and in training T. Matsuzaka in experimental techniques. A.H.H. reviewed the manuscript. Y.N. contributed to immunoblot analysis of insulin signaling, adenoviral work and discussion of the results. A.T. contributed to GTT, ITT, HF-HS diet–feeding to the mice and discussion of the results. H. Suzuki, S.Y., H. Sone, H.T. and J.O. contributed to experimental design, data analysis, interpretation and presentation. N. Yamada supervised the study, contributed crucial ideas to the project and reviewed the manuscript.

Corresponding author

Correspondence to Hitoshi Shimano.

Supplementary information

PDF files

  1. 1.

    Supplementary Text and Figures, Supplementary Table 1, Methods,

    Supplementary Methods, Supplementary Figs. 1–5, Supplementary Table 1

About this article

Publication history





Further reading