Ketogenic diet attenuates hepatopathy in mouse model of respiratory chain complex III deficiency caused by a Bcs1l mutation

Purhonen, Janne; Rajendran, Jayasimman; Mörgelin, Matthias; Uusi-Rauva, Kristiina; Katayama, Shintaro; Krjutskov, Kaarel; Einarsdottir, Elisabet; Velagapudi, Vidya; Kere, Juha; Jauhiainen, Matti; Fellman, Vineta; Kallijärvi, Jukka

doi:10.1038/s41598-017-01109-4

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Published: 19 April 2017

Ketogenic diet attenuates hepatopathy in mouse model of respiratory chain complex III deficiency caused by a Bcs1l mutation

Janne Purhonen^1,2,
Jayasimman Rajendran ORCID: orcid.org/0000-0003-3487-8260^1,2,
Matthias Mörgelin³,
Kristiina Uusi-Rauva¹,
Shintaro Katayama⁴,
Kaarel Krjutskov^1,4,5,7,
Elisabet Einarsdottir ORCID: orcid.org/0000-0003-3101-2285^1,4,7,
Vidya Velagapudi⁶,
Juha Kere ORCID: orcid.org/0000-0003-1974-0271^1,4,7,8,
Matti Jauhiainen⁹,
Vineta Fellman^1,10,11 &
…
Jukka Kallijärvi ORCID: orcid.org/0000-0003-3773-7025¹

Scientific Reports volume 7, Article number: 957 (2017) Cite this article

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Abstract

Mitochondrial disorders are among the most prevalent inborn errors of metabolism but largely lack treatments and have poor outcomes. High-fat, low-carbohydrate ketogenic diets (KDs) have shown beneficial effects in mouse models of mitochondrial myopathies, with induction of mitochondrial biogenesis as the suggested main mechanism. We fed KD to mice with respiratory chain complex III (CIII) deficiency and progressive hepatopathy due to mutated BCS1L, a CIII assembly factor. The mutant mice became persistently ketotic and tolerated the KD for up to 11 weeks. Liver disease progression was attenuated by KD as shown by delayed fibrosis, reduced cell death, inhibition of hepatic progenitor cell response and stellate cell activation, and normalization of liver enzyme activities. Despite no clear signs of increased mitochondrial biogenesis in the liver, CIII assembly and activity were improved and mitochondrial morphology in hepatocytes normalized. Induction of hepatic glutathione transferase genes and elevated total glutathione level were normalized by KD. Histological findings and transcriptome changes indicated modulation of liver macrophage populations by the mutation and the diet. These results reveal a striking beneficial hepatic response to KD in mice with mitochondrial hepatopathy and warrant further investigations of dietary modification in the management of these conditions in patients.

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Introduction

Mitochondrial disorders can manifest as hepatopathy, mainly in infants, with or without other organ manifestations¹. Only supportive treatments, such as adjustment of nutrition and vitamin supplementation to alleviate the metabolic imbalance, are available for these patients^{1, 2}.

Mutations in the BCS1L gene, encoding a CIII assembly factor, are the most common diagnosed cause of mitochondrial respiratory chain (RC) CIII (CIII) deficiency³. GRACILE syndrome⁴ (fetal growth restriction, aminoaciduria, cholestasis, liver iron overload, lactic acidosis, and early death during infancy) is caused by a homozygous missense mutation (c.232 A > G, p.S78G) in BCS1L ⁵. In liver mitochondria of the patients, Rieske iron-sulfur protein (RISP, UQCRFS1) incorporation into CIII is decreased resulting in reduced CIII activity⁶. We have generated a viable mouse model of CIII dysfunction by introducing the Bcs1l ^c.232A>G mutation into the mouse genome⁷. The homozygous mice display growth failure, low blood glucose, high blood lactate and progressive hepatopathy from the fourth week of age, recapitulating many of the main findings in the patients.

Carbohydrate-restricted high-fat ketogenic diets stimulate mitochondrial β-oxidation and ketone body production in the liver^{8, 9}. Ketone bodies can be utilized as an alternative energy source by the brain, heart and skeletal muscle. KDs are an established therapy in drug-resistant epilepsies and have been shown to increase the expression of genes related to tricarboxylic acid cycle and RC function, as well as the number of mitochondria in rat hippocampi^8,9,10. KDs have been proposed and tested as a therapy for mitochondrial disorders. Krebs et al. hypothesized that the course of postweaning-onset mitochondrial cardiomyopathy in Med30 mutant mice is affected by the considerable decrease in fat intake on shifting from maternal milk (42% fat) to the low-fat regular chow. Indeed, the researchers could extend the survival of the mutant mice by 40% by weaning them to high-fat ketogenic diet¹¹. Schiff et al. showed that high-fat diet-fed Harlequin mice with CI deficiency exhibit a slower progression of the neurodegenerative phenotype¹². In a mouse model of late-onset mitochondrial myopathy, KD decreased the amount of cytochrome c oxidase negative muscle fibers and prevented mitochondrial ultrastructural abnormalities in the muscle and normalized metabolic and lipidomic changes¹³. In a subsequent study by this group a modified Atkins diet caused muscle pain in the myopathy patients and selective lysis of abnormal muscle fibers, which was considered eventually beneficial for the muscle function¹⁴. Moreover, KD has been shown to increase mitochondrial mass in skeletal muscle¹³, heart¹⁵ and brown adipose tissue¹⁶.

With the hypothesis that KD may induce mitochondrial biogenesis to compensate reduced RC function, improve energy metabolism and ameliorate disease progression, we performed a dietary intervention to assess the effect of KD on liver disease in the Bcs1l mutant model of CIII dysfunction.

Results

KD induces persistent ketosis in Bcs1l mutant (Bcs1l ^G/G) mice

KD was fed to cohorts of mutant mice and wild-type (WT) littermates starting from weaning. To monitor ketosis in the feeding cohorts, blood β-hydroxybutyrate levels were measured at the time of sacrificing. WT mice on KD had significantly elevated β-hydroxybutyrate levels at P45, but after that the ketogenic effect decreased (Table 1). In contrast, the KD-fed Bcs1l ^G/G mice were ketotic during the entire intervention. Non-fasting blood glucose level of Bcs1l ^G/G mice was lower than in WT animals but similar on both diets. Plasma creatinine, urea and total protein were normal (Table 1). KD did not influence weight gain in either genotype (Supplementary Fig. 1). Bcs1l ^G/G mice tolerated KD from weaning for up to two and half months and thereafter showed behavioral decline suggesting adverse effect of the diet (data not shown).

Table 1 Biochemical parameters in whole blood and plasma, mean ± SD (n).

Full size table

KD delays liver fibrosis and inhibits stellate cell activation and hepatic progenitor cell response in Bcs1l ^G/G mice

In WT mice, KD had a minimal effect on liver histology (Fig. 1A) but caused a modest increase in liver triglyceride amount (Fig. 1C,F) and reduced liver glycogen content (Supplementary Fig. 2). Non-esterified fatty acid concentration was similar in all groups (Supplementary Fig. 3). Bcs1l ^G/G mice on control diet (CD) had early-stage hepatopathy characterized by expansion of portal triads with incipient fibrosis at P45 (Fig. 1A). Marked hepatocyte hypertrophy was observed centrivenously and to some degree throughout the lobules (Supplementary Fig. 4B,C). Apoptotic cells, single necrotic cells (Fig. 1E) and mitotic figures were frequent. Staining for the mitotic cell marker Ki-67 confirmed a proliferative response at P45, which tended to resolve by P95 (Supplementary Fig. 5). Collagen staining showed periportal fibrosis at P45 (Fig. 1B) and at P95 prominent pericellular fibrosis was also observed. Occasionally fibrotic septa connected two or more portal triads. Highly increased α-smooth muscle actin (α-SMA) immunostaining indicated stellate cell activation (Fig. 2A,B).

KD modulated progression of the hepatopathy in several ways (Figs 1 and 2): it reduced the number of apoptotic and necrotic cells, prevented expansion of portal areas and delayed progression of fibrosis (Fig. 1) and diminished liver glycogen content (Supplementary Fig. 2). The expansion of portal areas resembled hepatic progenitor cell response (ductular reactions and oval cell hyperplasia)¹⁷ (Fig. 1A and Supplementary Fig. 4D). Accordingly, immunostaining revealed aberrant expression of cytokeratin-7, a marker of bile ducts and hepatic progenitor cells (oval cells), mainly periportally but also across the parenchyma (Fig. 2A,C). The aberrant cytokeratin-7 expression was completely normalized by KD at P45 and attenuated at P95 (Fig. 2A,C). Also plasma alanine aminotransferase and alkaline phosphatase activities were reduced by KD (Table 1). Further details of the liver histology are shown in Supplementary Fig. 4.

KD normalizes the ultrastructure of hepatocyte mitochondria and improves CIII assembly and activity in Bcs1l ^G/G livers

Electron microscopy showed that in hepatocyte mitochondria of Bcs1l ^G/G mice the number of cristae was reduced and thickness increased as compared to WT mice (Fig. 3A–C). Both parameters were normalized in the KD-fed mice at all time points (P45-P171). The proportion of elongated mitochondria was increased by the mutation, KD and age of the mice (Fig. 3D). The elongated mitochondria in KD-fed Bcs1l ^G/G mice had also a larger cross-sectional area than the mitochondria in the mutant mice on CD (Fig. 3D).

Of the two main markers of mitochondrial mass, mtDNA copy number was unchanged between the groups (Fig. 4A), whereas citrate synthase (CS) activity was increased in Bcs1l ^G/G livers but not affected by KD (Fig. 4B). Western blot analysis of Bcs1l ^G/G liver lysates revealed, as expected⁷, reduced level of RISP and a similar amount of the earlier assembled CIII subunit CORE-1 as compared to WT lysates (Fig. 4C). The amount of neither CIII subunit was affected by KD in total liver lysates. VDAC1, a mitochondrial protein not part of the RC, was increased in liver lysates of the Bcs1l ^G/G mice on CD, as were also subunits of CI (NDUFA9) and CIV (COX1, cytochrome c oxidase I, MT-CO1). The level of these proteins was normalized by KD (Fig. 4C). CIII activity in isolated Bcs1l ^G/G liver mitochondria was reduced by approximately 70% on normal diet. KD increased CIII activity approximately 50% in both genotypes (Fig. 4D). Blue native gel electrophoresis (BNGE) and subsequent immunoblotting of intact complexes in isolated liver mitochondria showed that the amount of RISP in free CIII dimer and, in particular, in the fully assembled CI-CIII supercomplex was significantly increased in the mutant mice on KD as compared to CD (Fig. 4E). Free CI was abundant only in the mutant mice but normal levels of supercomplex-bound CI were observed. No gross differences were found in the amount of CII and CIV between the groups (Fig. 4E).

In skeletal muscle, CS activity was significantly increased by KD in both genotypes and RISP amount reduced in the mutant mice, but none of the RC complex subunits analyzed were changed (Supplementary Fig. 6). In brown adipose tissue, RISP level was reduced in the mutant mice but neither CS, RC subunits nor uncoupling protein 1 (UCP1) were changed (Supplementary Fig. 7).

Liver transcriptome changes reflect regenerative response, activated lysosomal function and upregulation of tricarboxylic acid cycle in early symptomatic (P40-45) Bcs1l ^G/G mice

Principal component analysis (Fig. 5A), profiles of differentially expressed genes (Fig. 5B) and pathway analyses (Supplementary Table 1) demonstrated that of the examined conditions the mutation had the greatest effect on the liver transcriptome (1200 differentially expressed genes). KD changed the expression of approximately 260 genes in WT mice and 460 genes in Bcs1l ^G/G mice. The largest block of up-regulated genes in Bcs1l ^G/G mice was related to translation and ribosomes (Fig. 5B,C and Supplementary Table 1), likely reflecting the regenerative response. Lysosome-related genes were also overrepresented among the up-regulated genes in Bcs1l ^G/G livers. The genes with the highest differential expression are listed in Supplementary Table 2.

The levels of transcripts encoding RC components were mostly unaltered between the groups (Supplementary Fig. 8). An exception was Uqrcb encoding a CIII subunit which was up-regulated 3.7-fold by KD in both genotypes (p < 0.0001). Of mitochondria-related genes, the majority of tricarboxylic acid cycle genes were induced by both the mutation and the diet (Fig. 4I). The hepatic expression of two circulating mitochondrial disease markers, Fgf21 ¹⁸ and Gdf15 ¹⁹ was up-regulated in Bcs1l ^G/G mice and Gdf15 expression was normalized by KD (Fig. 4H). Upstream regulatory analysis predicted that KD activated peroxisome proliferator-activated receptors (PPAR-α,-γ and -α), TFAM and PGC-1α and inhibited CREB, all transcriptional regulators of mitochondrial biogenesis (Fig. 5D). The observed mRNA level of Ppargc1a (PGC-1α) was increased in the Bcs1l ^G/G mice but not affected by the diet (Fig. 4G). Expression of a recently identified mitophagy and mitochondrial mass regulator Bnip3 ²⁰ was increased 1.4-fold (p = 0.02) and 1.8-fold (p < 0.001) by KD in WT mice and Bcs1l ^G/G mice, respectively. Bcs1l ^G/G mice on CD had decreased (-1.6-fold) expression of Bnip3 and related autophagy regulators, Atg3 (−1.8-fold) and Atg5 (−1.5-fold) compared to WT mice on CD (all p < 0.001).

Amino acid and lipid metabolism are altered at transcriptome and metabolite levels in Bcs1l ^G/G mice

The expression of multiple amino acid starvation response genes (i.e. Atf3, Atf4, Ddit3, Trib3, Asns and Txnip) was up-regulated in Bcs1l ^G/G mice (Supplementary Fig. 9). Amino acid metabolism-related genes were enriched in all comparisons (Fig. 5B,C and Supplementary Fig. 10A). Targeted plasma metabolomics revealed elevated concentrations of eight amino acids in the Bcs1l ^G/G mice (Supplementary Fig. 10B). In line with a probable increase in protein catabolism, gene expression pathway analyses predicted altered urea cycle activity in Bcs1l ^G/G livers (Fig. 5B,C), and, accordingly, the plasma level of arginine was decreased and ornithine and citrulline increased (Supplementary Fig. 10B).

Gene expression pathway analyses further suggested that hepatic lipid metabolism was profoundly altered by the mutation and the diet (Fig. 5B,C, Supplementary Fig. 11A and Supplementary Table 1). The expression of genes related to ketone body synthesis, bile acid biosynthesis and ω-3 and ω-6 fatty acid metabolism were up-regulated by KD (Fig. 5B,C). Several bile acid biosynthesis-related genes were down-regulated in Bcs1l ^G/G mice (Fig. 5B,C). Metabolomics analysis showed increased plasma concentrations of cholic acid and chenodeoxycholic (Supplementary Fig. 11B). Also, the concentrations of plasma carnitine and short-chain acylcarnitines were decreased by the mutation and KD further indicating altered lipid metabolism (Supplementary Fig. 11B).

KD modulates altered hepatic macrophage populations in Bcs1l ^G/G mice

In H&E-stained liver sections of Bcs1l ^G/G mice, cells with brownish cytoplasm and morphologically resembling macrophages were observed (Supplementary Fig. 12). These cells were PAS-diastase-positive and auto-fluorescent (Supplementary Fig. 12), suggesting that they were ceroid- or lipofuscin-laden macrophages. The number of these cells was decreased by KD. Immunostaining for macrophage/Kupffer cell markers showed similar number of hepatic macrophages with both F4/80 and IBA1 antibodies in WT mice (Fig. 2D,E). F4/80 is an established marker for tissue resident macrophages but some infiltrating monocyte-derived macrophages are negative or only weakly immunopositive for F4/80^{21, 22}. In the Bcs1l ^G/G livers F4/80 staining was reduced suggesting either loss of this marker or Kupffer cell depletion. However, the number of IBA1-expressing macrophages was increased in Bcs1l ^G/G livers and normalized by KD at P45 (Fig. 2A,E). In Bcs1l ^G/G livers the macrophages were larger and protruded out of sinusoids, or multiple macrophages surrounded a hepatocyte (Fig. 2A). Neutrophil count was marginally increased in the mutant livers (Supplementary Fig. 13).

Gene expression pathway analyses (Supplementary Table 1) indicated changes in four inflammation related pathways (Reactome database) in the Bcs1l/ ^G/G mice: formation of fibrin clot, infectious disease, MHC class II antigen presentation and phagosomal maturation (p < 0.0003 for all). Furthermore, one fifth of genes that were up-regulated more than 3-fold in Bcs1l/ ^G/G mice overlapped with genes that play a role in innate immune response (InnateDB²³). For example the macrophage marker gene Cd68 was up-regulated 8.5-fold (p < 0.0001) in the Bcs1l/ ^G/G mice and downregulated 2.4-fold (p = 0.0046) by KD. Comparison to various published macrophage gene expression profiles showed that most of the highly up-regulated genes in Bcs1l/ ^G/G livers were linked to activated macrophages (Fig. 6A). KD normalized the majority of these gene expression changes towards WT levels.

The expression of the central inflammation and fibrosis-related cytokines, tumor necrosis factor (Tnf) and transforming growth factor beta-1 (Tgfb1) was upregulated in Bcs1l/ ^G/G livers, which was in line with the activation predicted from transcriptomics data (Fig. 6D,E). Of these, Tnf expression was significantly normalized by KD (Fig. 6D,E).

KD normalizes perturbed hepatic glutathione metabolism in Bcs1l ^G/G mice

The expression of nine out of seventeen canonical glutathione S-transferase genes detected was up-regulated in Bcs1l ^G/G mice and normalized toward WT levels on KD (Fig. 7A). The most highly up-regulated glutathione transferase gene was Gsta1 (87-fold, p < 0.0001, Fig. 7B), which was down-regulated 4.4-fold by KD (p = 0.005). The expression of Glutathione synthetase (Gss) was increased 2-fold in Bcs1l ^G/G mutants (p < 0.001). In line with the gene expression data, total liver glutathione was increased in the Bcs1l/ ^G/G mice at P45 and normalized to WT levels on KD (Fig. 7C).

Discussion

Low-carbohydrate, high-fat diets are an established treatment in drug-resistant epilepsies. Studies in animal models have suggested that modulation of mitochondria-related functions, including reduced reactive oxygen species production, promotion of mitochondrial biogenesis and stimulation of glutathione biosynthesis contribute to their beneficial effects in the brain^8,9,10. Here, we demonstrate that KD ameliorated hepatopathy in CIII deficient Bcs1l mutant mice at the level of liver histology and liver enzymes, mitochondrial structure and function, and gene expression. Marked stellate cell activation and hepatic progenitor cell proliferation²⁴ indicate severe early liver injury in these mice despite relatively modest other histological changes. KD feeding reduced fibrosis, number of apoptotic/necrotic cells, and attenuated stellate cell and hepatic progenitor cell activation, suggesting that it either reduced the initial insult (CIII deficiency), affected fibrogenic processes in the liver or induced protective mechanisms (e.g. detoxification).

We found structural aberrations in mitochondria, the most striking of which was reduced number and increased thickness of cristae, in hepatocytes of Bcs1l ^G/G mice, and these alterations were prevented by KD. In a previous study, KD was shown to normalize overall mitochondrial structure in skeletal muscle in a mouse model of mitochondrial myopathy¹³. Mitochondrial cristae are structurally highly dynamic bioenergetic compartments and their shape is linked to RC function^{25, 26}. The reduced number and increased thickness of cristae in hepatocytes of Bcs1l ^G/G mice on CD might be related to disrupted RC complex organization²⁵. Starvation has been shown to cause elongation of mitochondria and both starvation and nonglycolytic substrates cause cristae remodeling, including increase in cristae number and reduced width in cultured cells. This process is thought to increase the efficiency of ATP production^27,28,29. It is tempting to speculate that the carbohydrate-restricted KD might have caused a similar starvation-like or substrate utilization-dependent mitochondrial adaptation in our mouse model, leading to normalization of cristae number and morphology.

To investigate if the normalized mitochondrial morphology reflected improved mitochondrial function, we measured CIII activity and assessed organization of respiratory chain complexes and supercomplexes in liver mitochondria. Indeed, CIII activity was increased by half in the mice on KD, which may have been sufficient to ameliorate the liver injury due to CIII dysfunction. Previously, a short term (<24 h) KD administration was also shown to increase combined CII and CIII activity in brain cortical mitochondria in a rat mode of traumatic brain injury³⁰. Typical markers of mitochondrial mass and biogenesis, such as Ppargc1a expression and citrate synthase activity were modestly increased in the mutant mice but not affected by the diet. MtDNA copy number was similar in all groups and none of the RC subunits analyzed were increased by KD. To the contrary, some RC subunits that were increased by the mutation were decreased to WT levels on KD. Transcriptome changes predicted activation of key regulators of mitochondrial biogenesis, PPAR-α,-γ and -α, PGC-1α and TFAM by KD, but apparently this transcriptional response did not result in increased mitochondrial mass. Ketone bodies have been shown to restore complex I stability and activity in a complex I deficient cell line³¹. Therefore, we assessed RC complex and supercomplex amount in liver mitochondria of the mice using BNGE. Despite that KD did not increase total amount of RISP in whole tissue lysate, more fully assembled CIII was found in isolated mitochondria from Bcs1l ^G/G mice on KD than on CD. This finding suggests improved CIII assembly or stability and offers an explanation for the increased CIII activity on KD. Dietary fat composition has been shown to affect phospholipid composition of mitochondrial membranes³² and affect respiratory chain supercomplex assembly and function^{33, 34}. Our KD contained a high proportion of polyunsaturated long-chain fatty acids, which may have had an effect on mitochondrial membrane composition and, subsequently, on CIII and supercomplex composition in our model.

Previously, a ketogenic diet, with a more extreme protein restriction than our formulation (see later discussion), decreased liver mitochondrial mass likely by up-regulating gene and protein expression of starvation induced mitophagy factor, BNIP3³⁵. We observed that KD increased hepatic Bnip3 expression in both genotypes. The Bcs1l ^G/G mice on CD had decreased Bnip3 transcript levels compared to WT mice along with reduced mRNA levels of the autophagy regulators Atg3 and Atg5 ³⁶. Taken together, our results indicate that the increased CIII activity and the beneficial effect of KD were not due to increased liver mitochondrial mass but likely to other adaptive mitochondrial responses such as improved mitochondrial quality control via autophagy and improved maintenance of cristae structure and RC function, including improved CIII assembly and activity.

Hepatic immune cells, including Kupffer cells and infiltrating monocyte-derived macrophages are key pro- and anti-fibrotic regulators³⁷. The Bcs1l ^G/G mice had substantially altered liver macrophage populations as shown by immunostainings and macrophage-related gene expression patterns, and these were clearly modulated by the diet. KD also reduced the number of ceroid-lipofuscin-laden macrophages in Bcs1l ^G/G livers, likely reflecting a reduced need for clearance of cellular debris due to reduced cell death. A reduced number of F4/80 positive macrophages, but increased total macrophage count, has been shown previously in the acute phase of liver injury^{21, 22}. These studies also identified the weakly F4/80-immunopositive subsets as infiltrating monocyte-derived macrophages. In contrast, the number of IBA1, CD68 and galectin-3 positive macrophages increases upon liver injury^{38, 39}. We observed depletion of F4/80-expressing macrophages in Bcs1l ^G/G livers but an increased number of IBA1-positive macrophages, the latter of which was reduced on KD. Expression of galectin-3 (Lgals3) and Cd68 was highly induced in Bcs1l ^G/G on CD and significantly less so on KD. Of interest, macrophage polarization and their inflammatory properties can be modified by mitochondrial function⁴⁰. The M1, or classically activated, subset of macrophages is mainly relying on anaerobic glycolysis whereas the M2, or alternative activated subset, is dependent on oxidative phosphorylation. The M2-like subsets are particularly important in tissue repair and resolution of inflammation⁴⁰. Interestingly, mice with global CI subunit Ndufs4 knock-out have systemic inflammation and osteopetrosis due to shift in macrophage polarization and osteoclast differentiation⁴¹.

In our model, components of the KD may have affected liver disease progression via mechanisms unrelated to energy metabolism. Docosahexanoid acid, a long-chain polyunsaturated n-3 fatty acid, can suppress mitochondrial membrane transition pore opening, a key event leading to apoptosis³². Indeed, we found significantly less dying hepatocytes in Bcs1l ^G/G mice on KD. Certain long-chain fatty acids and their derivatives are ligands for PPAR-α and -γ⁴². In our KD-fed mice, the expression of several PPAR-α- and PPAR-γ-regulated genes was altered in the liver transcriptome, suggesting that diet-dependent modulation of ligand binding to PPAR-α and -γ may have played a role. Other putative mediators are HCAR2, a receptor for the major ketone body β-hydroxybyturate, expressed in white adipose tissue and some immune cells including macrophages^{43, 44} and FFAR4 (free fatty acid receptor 4), the activation of which modulates macrophage polarization^{34, 35}. FFAR4 is activated by long-chain fatty acids and our KD formulation provided 2.8-fold more α-linolenic acid (C18:3 n-3) relative to energy content than the CD. The putative role of these receptors in mediating the effect of the KD should be further studied by administering ketone esters or the respective receptor agonists.

Induction of liver detoxification genes was minimal in Bcs1l ^G/G mice except for glutathione S-transferase (GST) genes. GSTs detoxify a variety of compounds, including oxidative stress-induced metabolites such as 4-hydroxynonenal⁴⁵. Some GSTs also possess peroxidase activity, and as such are antioxidant enzymes. In addition, the majority of GST genes contain antioxidant response element in their promoter region and are regulatory targets of NRF2, the major oxidative stress responsive transcription factor. The expression of several GST genes was highly induced in the liver of Bcs1l mice and this induction was partially reversed by KD feeding. Interestingly, the gene expression profile of GSTs in Bcs1l ^G/G mice showed similar induction of cytoplasmic GST genes as observed in the mouse liver when NRF2 pathway is over activated⁴⁶. As for oxidative stress, we found up-regulated expression of three genes encoding antioxidant enzymes (Gpx3, Gpx4 and Nqo1) in the liver of Bcs1l ^G/G mice as well as of glutathione synthetase. Intriguingly, catalase expression was downregulated 1.8 fold (data not shown). KD had no effect on the expression of these genes. In line with the gene expression data liver total glutathione content was increased in Bcs1l mice on CD but reduced to WT levels on KD. We interpret these results so that there was reduced need for detoxification and less cellular glutathione synthesized when the Bcs1l ^G/G mice were on KD.

A small retrospective study found KD treatment effective and relatively safe in respiratory chain defects related childhood epilepsy⁹. However, a KD intervention trial in mitochondrial myopathy patients had to be prematurely discontinued due to muscle pain and selective muscle fiber damage⁴⁷. We found that Bcs1l ^G/G mice showed eventual intolerance to the diet manifesting as more rapid behavioral decline after eleven weeks of feeding. Depleted glycogen stores might have led to an exacerbated energy crisis. However, blood glucose and lactate values at sacrificing time were not significantly different on the two diets. Common rodent KD formulations contain only 5E% protein and provide inadequate choline and methionine intake^{48, 49}. These KDs cause robust ketosis but also hinder growth of the mice and in some studies have caused adverse liver effects including steatosis^48,49,50. KD formulations with higher protein content are nutritionally more suitable but reduce the ketogenic effect in rodents⁵¹. In line with this we observed only transient ketosis in WT mice while the Bcs1l mice remained ketotic during the entire intervention. The KD-fed mice had similar weight gain as those mice on CD and no overt signs of protein malnutrition (weight loss or reduced plasma total protein), which is in line with findings from studies using KD with similar protein content (~9E%)^{48, 52}. Liver fat content was increased on KD in both genotypes but according to triglyceride measurements this increase did not fulfill the criteria of steatosis (50 mg/g, 57µMol/g triglycerides)⁵³. Our previous study showed a starvation-like condition and high levels amino acids in liver of Bcs1l mice at end-stage disease⁵⁴. In this study, metabolomics analysis showed similar elevation of plasma amino acids in Bcs1l ^G/G mice on both diets, which suggests that the probable catabolic state was not exacerbated by KD.

The present study shows that KD may have therapeutic potential in mitochondrial hepatopathies, currently incurable disorders. Further studies in animal models, and eventually in patients, should be designed to elaborate the effect of ketogenic diets on mitochondrial function and inflammatory processes in the context of respiratory chain deficiency.

Methods

Animal experiments

Congenic Bcs1l ^c.232A>G mice^{7, 55} were maintained by crossing heterozygotes to wild-type C57BL/6JCrl mice. The survival of the Bcs1l ^c.232A>G homozygous (Bcs1l ^G/G) mice in this background is on average 200 days. The animal ethics committee of the State Provincial Office of Southern Finland approved the animal experiments (permit numbers ESAVI-2010-07284/Ym-23 and ESAVI/6142/04.10.07/2014) and the experiments were carried out in accordance with the permits, Laboratory Animal Centre of the University of Helsinki practices and the Federation of Laboratory Animal Science Associations (FELASA) guidelines.

Litters were randomized to CD or KD. The CD (Teklad 2018, Harlan) was a cereal and soy-based rodent chow providing 18% of energy (E%) as fat, 58E% as carbohydrates and 24E% as protein. The KD (TD.96355, Harlan) was based on vegetable shortening, corn oil and casein, providing 90.5E% fat (1/3 as polyunsaturated fatty acids; 30.8 E% linoleic acid and 2.5E% α-linolenic acid), 0.4E% carbohydrates and 9.1 E% protein. Both diets provided approximately the same amount of choline (~8.5 mg/100 kJ) and methionine (~30 mg/100 kJ). The KD-chow was introduced into the cages from one week of age. From weaning on, the pups randomized to KD received ad libitum KD only. The CD and KD groups were sacrificed at postnatal age 40–45 days (which we refer as P45-group, n = 11–14/group) or P90-P114 (P95-group, n = 8–9/group). One cohort was followed until deterioration (P114-P173, n = 4/group). Both genders were used and for each homozygote a wild-type or heterozygote control was included. These control animals are referred to as wild-type (WT). The heterozygous mice are phenotypically wild-type⁷. Significant gender differences were not observed if not otherwise stated.

Sample collection

Blood glucose, lactate and ketone concentrations were measured from tail tip blood under brief isoflurane anesthesia. For other samples, the mice were sacrificed with carbon dioxide inhalation and cervical dislocation or, for blood collection via cardiac puncture, injected with a lethal dose of pentobarbital. The mice were not fasted prior to sample collection due to the hypoglycemia associated with the phenotype of the homozygotes. All samples were collected at the same time of the day during the light period of the mice. Blood was collected by cardiac puncture into Li-heparin tubes and plasma was separated and stored at −80 °C. Tissues were collected into 10% histology-grade formalin or snap frozen in liquid nitrogen and stored at −80 °C.

Histology and immunostaining

Liver sections were processed and stained with standard methods to assess general histology (hematoxylin-eosin), glycogen content (periodic acid-Shiff, PAS), neutral fat content (Oil Red O), fibrosis (Sirius Red) and ultrastructure (electron microscopy). Primary antibodies used in immunohistochemical staining are listed in Supplementary Table 3. Vectastain Elite peroxidase reagents (Vector Laboratories) were used for detection. Apoptotic and necrotic cells were counted from H&E-stained sections based on characteristic morphological features such as condensed hypereosinophilic cytoplasm, cell swelling and condensed, fragmented or dissolved nucleus according to published guidelines⁵⁶. All quantifications were performed in random-blind fashion. Technical details of the image analyses are described in Supplementary Materials and Methods.

Electron microscopy

Approximately 1 mm³ pieces of liver were fixed in 1.5% glutaraldehyde, 1.5% paraformaldehyde in 0.1 M Sörensen buffer pH 7.2, and processed for electron microscopy according to standard methods. Area, cristae number and thickness, and the shape of hepatocyte mitochondria were determined manually from images in Adobe Photoshop CS5. Cross sectional area was determined by manually selecting the longest and shortest axis of each mitochondria. Approximately 100 different hepatocytes were chosen at random locations and layers throughout at least 10 different specimen preparations. About five randomly chosen mitochondria per hepatocyte were measured, giving a total of approximately 500 mitochondria per independent sample.

Clinical chemistry and plasma metabolomics

Clinical chemistry parameters were measured from plasma samples using Siemens ADVIA1650 analyzer. Targeted plasma metabolomics (101 metabolites) was performed using an ACQUITY UPLC-MS/MS system as previously described⁵⁷.

Lipid analyses

Liver triglycerides were measured as enzymatic release of glycerol after methanol-chloroform extraction of lipids as previously described⁵⁸. The same lipid extracts were used to measure non-esterified fatty acids by an enzymatic colorimetric assay (Roche Diagnostics).

Protein analysis

Western blot analyses were used to quantify the amount of proteins in tissue lysates. The antibodies used are shown in Supplementary Table 3 and technical details in Supplementary Materials and Methods. For the quantifications, 28 independent samples were run in a random order. For representative blots, pooled lysates of 6–8 samples were used. The data were normalized to total protein transferred onto membrane as visualized and quantified by Stain-free imaging technology (Bio-Rad). Digitonin-solubilized respiratory chain complexes and supercomplexes were assessed with BNGE and immunoblotting as described earlier⁵⁵ except that Bio-Rad tank electroblotting apparatus and 1-hour transfer time was used. The BNGE analysis was performed twice on four mice per group with consistent results.

Enzyme activity assays

CIII activity in isolated mitochondria was measured with decylubiquinol as substrate and cytochrome c as final electron acceptor in a spectrophotometric assay⁷. Citrate synthase activity was measured with a commercial kit (Sigma-Aldrich Cat.no CS0720).

RNA sequencing (RNA-seq) and quantitative PCR (qPCR)

For library preparation, sequencing and data pre-processing we followed a published protocol⁵⁹ except that 10 ng total RNA from liver tissue rather than single cells were used. Differential gene expression analysis and read count normalization were performed with DESeq2 package for R⁶⁰. For gene set enrichment analyses and heat maps, the gene lists were filtered for absolute DESeq2 shrunken fold change of more than 1.4 and false discovery rate corrected p-value less than 0.1 if not otherwise stated. The enriched gene sets were retrieved from ConsensusPathDB⁶¹. Ingenuity Upstream Regulator Analysis (Qiagen) was used to predict activated or inhibited transcription regulators, cytokines and growth factors. Public microarray gene expression data sets were obtained from the Gene Expression Omnibus and analyzed using GEO2R (both by NCBI) (E-GEOD-32690)⁶² or from the ImmGen database⁶³ as a pre-analyzed data set (GSE1590)⁶³. The expression of 45 genes was verified by qPCR (Supplementary Fig. 12 and Supplementary Materials and Methods).

Mitochondrial DNA (mtDNA) copy number quantitation

mtDNA copy number in total liver genomic DNA was determined by measuring the relative amount of a mitochondrial (MT-Rnr1) and a nuclear gene (Actb) with qPCR.

Liver total glutathione was assessed with GSH-Glo™ Glutathione kit (Promega).

Statistics (excluding transcriptomics and metabolomics)

As a main strategy to test whether the groups differed, one-way ANOVA was performed. Significant ANOVA results were followed by three planned comparisons: 1) WT on CD vs WT on KD, 2) WT on CD vs Bcs1l ^G/G on CD and 3) Bcs1l ^G/G on CD vs Bcs1l ^G/G on KD. If the normality assumption of ANOVA was violated, Kruskal-Wallis test and Mann-Whitney U-tests were used instead. Two-way ANOVA was used where age of the mice needed to be included in the analysis. The Bonferroni correction was applied to the two-way ANOVA results.

Further information is provided in Supplementary Materials and Methods.

References

Fellman, V. & Kotarsky, H. Mitochondrial hepatopathies in the newborn period. Semin. Fetal. Neonat. M. 16, 222–228, doi:10.1016/j.siny.2011.05.002 (2011).
Article Google Scholar
Parikh, S. et al. A modern approach to the treatment of mitochondrial disease. Curr. Treat. Opt. Neurol. 11, 414–430, doi:10.1007/s11940-009-0046-0 (2009).
Article Google Scholar
Fernández-Vizarra, E. & Zeviani, M. Nuclear gene mutations as the cause of mitochondrial complex III deficiency. Front. Genet. 6, 134, doi:10.3389/fgene.2015.00134 (2015).
Article PubMed PubMed Central Google Scholar
Fellman, V., Rapola, J., Pihko, H., Varilo, T. & Raivio, K. O. Iron-overload disease in infants involving fetal growth retardation, lactic acidosis, liver haemosiderosis, and aminoaciduria. Lancet 351, 490–493, doi:10.1016/S0140-6736(97)09272-6 (1998).
Article CAS PubMed Google Scholar
Visapää, I. et al. GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L. Am. J. Hum. Genet. 71, 863–876, doi:10.1086/342773 (2002).
Article PubMed PubMed Central Google Scholar
Kotarsky, H. et al. Characterization of complex III deficiency and liver dysfunction in GRACILE syndrome caused by a BCS1L mutation. Mitochondrion 10, 497–509, doi:10.1016/j.mito.2010.05.009 (2010).
Article CAS PubMed Google Scholar
Leveen, P. et al. The GRACILE mutation introduced into Bcs1l causes postnatal complex III deficiency: a viable mouse model for mitochondrial hepatopathy. Hepatology 53, 437–447, doi:10.1002/hep.24031 (2011).
Article CAS PubMed Google Scholar
Branco, A. F. et al. Ketogenic diets: from cancer to mitochondrial diseases and beyond. Eur. J. Clin. Invest. 46, 285–298, doi:10.1111/eci.2016.46.issue-3 (2016).
Article PubMed Google Scholar
Kang, H. C., Lee, Y. M., Kim, H. D., Lee, J. S. & Slama, A. Safe and effective use of the ketogenic diet in children with epilepsy and mitochondrial respiratory chain complex defects. Epilepsia 48, 82–88, doi:10.1111/j.1528-1167.2006.00906.x (2007).
CAS PubMed Google Scholar
Bough, K. J. et al. Mitochondrial biogenesis in the anticonvulsant mechanism of the ketogenic diet. Ann. Neurol. 60, 223–235, doi:10.1002/ana.v60:2 (2006).
Article CAS PubMed Google Scholar
Krebs, P. et al. Lethal mitochondrial cardiomyopathy in a hypomorphic Med30 mouse mutant is ameliorated by ketogenic diet. Proc. Natl. Acad. Sci. USA 108, 19678–19682, doi:10.1073/pnas.1117835108 (2011).
Article ADS CAS PubMed PubMed Central Google Scholar
Schiff, M., Benit, P., Coulibaly, A. & Rustin, P. Fat supplementation slows down disease progression in complex I deficient Harlequin mice. J. Inherit. Metab. Dis. 34, S158–S158 (2011).
Google Scholar
Ahola-Erkkila, S. et al. Ketogenic diet slows down mitochondrial myopathy progression in mice. Hum. Mol. Genet. 19, 1974–1984, doi:10.1093/hmg/ddq076 (2010).
Article CAS PubMed Google Scholar
Ahola, S. et al. Modified Atkins diet induces subacute selective ragged-red-fiber lysis in mitochondrial myopathy patients. EMBO Mol Med 2, 1234–1247, doi:10.15252/emmm.201606592 (2016).
Article Google Scholar
Balietti, M. et al. A Ketogenic diet increases succinic dehydrogenase activity in aging cardiomyocytes. Ann N Y Acad Sci. 1171, 377–384, doi:10.1111/j.1749-6632.2009.04704.x (2009).
Article ADS CAS PubMed Google Scholar
Srivastava, S., Baxa, U., Niu, G., Chen, X. & Veech, R. L. A Ketogenic diet increases brown adipose tissue mitochondrial proteins and UCP1 levels in mice. IUBMB life 65, 58–66, doi:10.1002/iub.1102 (2013).
Article CAS PubMed Google Scholar
Williams, M. J., Clouston, A. D. & Forbes, S. J. Links between hepatic fibrosis, ductular reaction, and progenitor cell expansion. Gastroenterology 146, 349–356, doi:10.1053/j.gastro.2013.11.034 (2014).
Article PubMed Google Scholar
Suomalainen, A. et al. FGF-21 as a biomarker for muscle-manifesting mitochondrial respiratory chain deficiencies: a diagnostic study. Lancet Neurol 10, 806–818, doi:10.1016/S1474-4422(11)70155-7 (2011).
Article CAS PubMed Google Scholar
Yatsuga, S. et al. Growth differentiation factor 15 as a useful biomarker for mitochondrial disorders. Ann. Neurol. 78, 814–823, doi:10.1002/ana.v78.5 (2015).
Article CAS PubMed PubMed Central Google Scholar
Glick, D. et al. BNip3 regulates mitochondrial function and lipid metabolism in the liver. Mol. Cell. Biol. 32, 2570–2584, doi:10.1128/MCB.00167-12 (2012).
Article CAS PubMed PubMed Central Google Scholar
Ramachandran, P. et al. Differential Ly-6C expression identifies the recruited macrophage phenotype, which orchestrates the regression of murine liver fibrosis. Proc. Natl. Acad. Sci. USA 109, E3186–E3195, doi:10.1073/pnas.1119964109 (2012).
Article ADS CAS PubMed PubMed Central Google Scholar
Holt, M. P., Cheng, L. & Ju, C. Identification and characterization of infiltrating macrophages in acetaminophen-induced liver injury. J. Leuk. Biol. 84, 1410–1421, doi:10.1189/jlb.0308173 (2008).
Article CAS Google Scholar
Breuer, K. et al. InnateDB: systems biology of innate immunity and beyond - recent updates and continuing curation. Nucleic Acids Res. 41, D1228–D1233, doi:10.1093/nar/gks1147 (2013).
Article CAS PubMed Google Scholar
Eleazar, J. A. et al. Progenitor cell expansion: an important source of hepatocyte regeneration in chronic hepatitis. J. Hapatol. 41, 983–991, doi:10.1016/j.jhep.2004.08.017 (2004).
Article Google Scholar
Cogliati, S. et al. Mitochondrial cristae shape determines respiratory chain supercomplexes assembly and respiratory efficiency. Cell 155, 160–171, doi:10.1016/j.cell.2013.08.032 (2013).
Article CAS PubMed PubMed Central Google Scholar
Pernas, L. & Scorrano, L. Mito-morphosis: Mitochondrial fusion, fission, and cristae remodeling as key mediators of cellular function. Annu. Rev. Physiol. 78, 505–531, doi:10.1146/annurev-physiol-021115-105011 (2016).
Article CAS PubMed Google Scholar
Gomes, L. C., Di Benedetto, G. & Scorrano, L. During autophagy mitochondria elongate, are spared from degradation and sustain cell viability. Nat. Cell Biol. 13, 589–U207, doi:10.1038/ncb2220 (2011).
Article CAS PubMed PubMed Central Google Scholar
Patten, D. A. et al. OPA1-dependent cristae modulation is essential for cellular adaptation to metabolic demand. EMBO J. 33, 2676–2691, doi:10.15252/embj.201488349 (2014).
Article CAS PubMed PubMed Central Google Scholar
Rossignol, R. et al. Energy substrate modulates mitochondrial structure and oxidative capacity in cancer cells. Cancer Res. 64, 985–993, doi:10.1158/0008-5472.CAN-03-1101 (2004).
Article CAS PubMed Google Scholar
Greco, T., Glenn, T. C., Hovda, D. A. & Prins, M. L. Ketogenic diet decreases oxidative stress and improves mitochondrial respiratory complex activity. J. Cereb. Blood. Flow. Metab. 36, 1603–13, doi:10.1177/0271678X15610584 (2016).
Article CAS PubMed Google Scholar
Frey, S. et al. The addition of ketone bodies alleviates mitochondrial dysfunction by restoring complex I assembly in a MELAS cellular model. BBA Mol. Basis Dis. 1863, 284–291, doi:10.1016/j.bbadis.2016.10.028 (2017).
Article CAS Google Scholar
Khairallah, R. J. et al. Dietary supplementation with docosahexaenoic acid, but not eicosapentaenoic acid, dramatically alters cardiac mitochondrial phospholipid fatty acid composition and prevents permeability transition. BBA Bioenergetics 1797, 1555–1562, doi:10.1016/j.bbabio.2010.05.007 (2010).
Article CAS PubMed PubMed Central Google Scholar
Baker, C. D., Ball, W. B., Pryce, E. N. & Gohil, V. M. Specific requirements of nonbilayer phospholipids in mitochondrial respiratory chain function and formation. Mol. Biol. Cell 27, 2161–2171, doi:10.1091/mbc.E15-12-0865 (2016).
Article CAS PubMed PubMed Central Google Scholar
Bottinger, L. et al. Phosphatidylethanolamine and cardiolipin differentially affect the stability of mitochondrial mespiratory chain supercomplexes. J. Mol. Biol 423, 677–686, doi:10.1016/j.jmb.2012.09.001 (2012).
Article PubMed Google Scholar
Newell, C. et al. Tissue-specific impacts of a ketogenic diet on mitochondrial dynamics in the BTBRT + tf/j Mouse. Front. Physiol. 7, 654, doi:10.3389/fphys.2016.00654 (2016).
Article PubMed PubMed Central Google Scholar
Radoshevich, L. et al. ATG12 conjugation to ATG3 regulates mitochondrial homeostasis and cell death. Cell 142, 590–600, doi:10.1016/j.cell.2010.07.018 (2010).
Article CAS PubMed PubMed Central Google Scholar
Adhyatmika, A., Putri, K. S. S., Beljaars, L. & Melgert, B. N. The elusive antifibrotic macrophage. Front. Med. 2, 81, doi:10.3389/fmed.2015.00081 (2015).
Article Google Scholar
Wijesundera, K. K. et al. Expressions of Iba1 and galectin-3 (Gal-3) in thioacetamide (TAA)-induced acute rat liver lesions. Exp. Toxicol. Pathol. 65, 799–808, doi:10.1016/j.etp.2012.11.006 (2013).
Article CAS PubMed Google Scholar
Wijesundera, K. K. et al. M1-and M2-macrophage polarization in rat liver cirrhosis induced by thioacetamide (TAA), focusing on Iba1 and galectin-3. Exp. Mol. Pathol. 96, 382–392, doi:10.1016/j.yexmp.2014.04.003 (2014).
Article CAS PubMed Google Scholar
Mills, E. L. & O’Neill, L. A. Reprogramming mitochondrial metabolism in macrophages as an anti-inflammatory signal. Eur. J. Immunol. 46, 13–21, doi:10.1002/eji.201445427 (2016).
Article CAS PubMed Google Scholar
Jin, Z. X., Wei, W., Yang, M., Du, Y. & Wan, Y. H. Mitochondrial complex I activity suppresses inflammation and enhances bone resorption by shifting macrophage-osteoclast polarization. Cell Metab. 20, 483–498, doi:10.1016/j.cmet.2014.07.011 (2014).
Article CAS PubMed PubMed Central Google Scholar
Kliewer, S. A. et al. Fatty acids and eicosanoids regulate gene expression through direct interactions with peroxisome proliferator-activated receptors α and γ. Proc. Natl. Acad. Sci. USA 94, 4318–4323, doi:10.1073/pnas.94.9.4318 (1997).
Article ADS CAS PubMed PubMed Central Google Scholar
Taggart, A. K. et al. (D)-beta-Hydroxybutyrate inhibits adipocyte lipolysis via the nicotinic acid receptor PUMA-G. J. Biol. Chem. 280, 26649–26652, doi:10.1074/jbc.C500213200 (2005).
Article CAS PubMed Google Scholar
Rahman, M. et al. The β-hydroxybutyrate receptor HCA2 activates a neuroprotective subset of macrophages. Nat. Comm. 5, 3944, doi:10.1038/ncomms4944 (2014).
Article ADS CAS Google Scholar
Hayes, J. D., Flanagan, J. U. & Jowsey, I. R. Glutathione transferases. Ann. Rev. Pharmacol. Toxicol 45, 51–88, doi:10.1146/annurev.pharmtox.45.120403.095857 (2005).
Article CAS Google Scholar
Wu, K. C., Cui, J. Y. & Klaassen, C. D. Effect of graded Nrf2 activation on phase-I and -II drug metabolizing enzymes and transporters in mouse liver. PLoS One 7, e39006, doi:10.1371/journal.pone.0039006 (2012).
Article ADS CAS PubMed PubMed Central Google Scholar
Ahola, S. et al. Modified Atkins diet induces subacute selective ragged‐red‐fiber lysis in mitochondrial myopathy patients. EMBO Mol. Med. 8, 1234–1247, doi:10.15252/emmm.201606592 (2016).
Article CAS PubMed PubMed Central Google Scholar
Schugar, R. C., Huang, X., Moll, A. R., Brunt, E. M. & Crawford, P. A. Role of Choline Deficiency in the fatty liver phenotype of mice fed a low protein, very low carbohydrate ketogenic diet. PLoS One 8, e74806, doi:10.1371/journal.pone.0074806 (2013).
Article ADS CAS PubMed PubMed Central Google Scholar
Pissios, P. et al. Methionine and choline regulate the metabolic phenotype of a ketogenic diet. Mol. Metab. 2, 306–313, doi:10.1016/j.molmet.2013.07.003 (2013).
Article CAS PubMed PubMed Central Google Scholar
Garbow, J. R. et al. Hepatic steatosis, inflammation, and ER stress in mice maintained long term on a very low-carbohydrate ketogenic diet. Am. J. Physiol. Gastrointest. Liver Physiol. 300, G956–G967, doi:10.1152/ajpgi.00539.2010 (2011).
Article CAS PubMed PubMed Central Google Scholar
Bielohuby, M. et al. Induction of ketosis in rats fed low-carbohydrate, high-fat diets depends on the relative abundance of dietary fat and protein. Am. J. Physiol. Endocrinol. Metab. 300, E65–E76, doi:10.1152/ajpendo.00478.2010 (2011).
Article CAS PubMed Google Scholar
Nandivada, P. et al. Eucaloric ketogenic diet reduces hypoglycemia and inflammation in mice with endotoxemia. Lipids 51, 703–714, doi:10.1007/s11745-016-4156-7 (2016).
Article CAS PubMed Google Scholar
Kleiner, D. E. et al. Design and validation of a histological scoring system for nonalcoholic fatty liver disease. Hepatology 41, 1313–1321, doi:10.1002/hep.20701 (2005).
Article PubMed Google Scholar
Kotarsky, H. et al. Metabolite profiles reveal energy failure and impaired beta-oxidation in liver of mice with complex III deficiency due to a Bcs1l mutation. PLoS One 7, e41156, doi:10.1371/journal.pone.0041156 (2012).
Article ADS CAS PubMed PubMed Central Google Scholar
Davoudi, M., Kotarsky, H., Hansson, E. & Fellman, V. Complex I function and supercomplex formation are preserved in liver mitochondria despite progressive complex III deficiency. PLoS One 9, e86767, doi:10.1371/journal.pone.0086767 (2014).
Article ADS PubMed PubMed Central Google Scholar
Elmore, S. A. et al. Recommendations from the INHAND apoptosis/necrosis working group. Toxicol. Pathol. 44, 173–188, doi:10.1177/0192623315625859 (2016).
Article CAS PubMed PubMed Central Google Scholar
Nikkanen, J. et al. Mitochondrial DNA replication defects disturb cellular dNTP pools and remodel one-carbon metabolism. Cell Metab. 23, 635–648, doi:10.1016/j.cmet.2016.01.019 (2016).
Article CAS PubMed Google Scholar
Davoudi, M. et al. A mouse model of mitochondrial complex III dysfunction induced by myxothiazol. Biochem. Biophys. Res. Comm. 446, 1079–1084, doi:10.1016/j.bbrc.2014.03.058 (2014).
Article CAS PubMed Google Scholar
Krjutškov, K. et al. Single-cell transcriptome analysis of endometrial tissue. Hum. Reprod. 31, 844–853, doi:10.1093/humrep/dew008 (2016).
Article PubMed PubMed Central Google Scholar
Love, M. I., Huber, W. & Anders, S. Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biol. 15, 1–21 (2014).
Article Google Scholar
Kamburov, A. et al. ConsensusPathDB: toward a more complete picture of cell biology. Nucleic Acids Res. 39, D712–D717, doi:10.1093/nar/gkq1156 (2011).
Article CAS PubMed Google Scholar
Riquelme, P. et al. IFN-γ-induced iNOS expression in mouse regulatory macrophages prolongs allograft survival in fully immunocompetent recipients. Mol. Ther. 21, 409–422, doi:10.1038/mt.2012.168 (2013).
Article CAS PubMed Google Scholar
Gautier, E. L. et al. Gene expression profiles and transcriptional regulatory pathways underlying mouse tissue macrophage identity and diversity. Nat. Immunol. 13, 1118–1128, doi:10.1038/ni.2419 (2012).
Article CAS PubMed PubMed Central Google Scholar

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Acknowledgements

We thank Elisa Altay, Teija Toivonen, Eva Hansson, Ingegerd Fransson, Jatin Nandania and Jari Metso for technical assistance and Dr. Heike Kotarsky, Dr. Saara Tegelberg and MD Nikica Tomasic for helpful advice. We are thankful to Professor Hannu Sariola and MD PhD Hannu Jalanko for helpful advice on liver histology. Transcriptomics was assisted by Karolinska High throughput Center, with affiliation to SciLifeLab (https://www.scilifelab.se/facilities/khtc/). SNIC through Uppsala Multidisciplinary Center for Advanced Computational Science (UPPMAX) provided computation resources under Project b2014069. This study was supported by grants from Academy of Finland (grant 259296), Swedish Research Council (grant 521-2011-3877), Distinguished Professor Award at Karolinska Institutet (to Juha Kere), Strategic Research Program funding on Diabetes to Karolinska Institutet, Finnish Physicians’ Society, and Foundation for Pediatric Research in Finland and Folkhälsan Research Center.

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Folkhälsan Research Center, Helsinki, Finland
Janne Purhonen, Jayasimman Rajendran, Kristiina Uusi-Rauva, Kaarel Krjutskov, Elisabet Einarsdottir, Juha Kere, Vineta Fellman & Jukka Kallijärvi
Faculty of Medicine, University of Helsinki, Helsinki, Finland
Janne Purhonen & Jayasimman Rajendran
Division of Infection Medicine, Clinical Sciences, Lund University, Lund, Sweden
Matthias Mörgelin
Department of Biosciences and Nutrition, Karolinska Institutet, Huddinge, Sweden
Shintaro Katayama, Kaarel Krjutskov, Elisabet Einarsdottir & Juha Kere
Competence Centre on Health Technologies, Tartu, Estonia
Kaarel Krjutskov
Metabolomics Unit, Institute for Molecular Medicine, University of Helsinki, Helsinki, Finland
Vidya Velagapudi
Molecular Neurology Research Program, University of Helsinki, Helsinki, Finland
Kaarel Krjutskov, Elisabet Einarsdottir & Juha Kere
Department of Genetics and Molecular Medicine, King’s College London, England, UK
Juha Kere
National Institute for Health and Welfare, Helsinki, Finland
Matti Jauhiainen
Department of Clinical Sciences, Lund, Pediatrics, Lund University, Lund, Sweden
Vineta Fellman
Children’s Hospital, Helsinki University Hospital, University of Helsinki, Helsinki, Finland
Vineta Fellman

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Contributions

J.P., J.R., M.M., K.U.-R., S.K., V.V., E.E., J.Ke., M.J., V.F. and J.Ka. conceived and designed the experiments; J.P., J.R., M.M., K.U.-R., S.K., V.V., K.K. and J.Ka. performed the experiments; J.P. (sample collection, liver histopathology, qPCR, protein analyses, transcriptomics analyses and presentation), J.R. (animal data, sample collection, metabolomics), M.M. (electron microscopy), K.U.-R. (immunohistochemistry), S.K. (transcriptomics raw data preprocessing and analyses), V.V. (metabolomics), K.K. (RNAseq library preparation and quality assessment), E.E. (RNAseq sample handling and supervision), J.Ka. (immunohistochemistry, clinical chemistry); J.P., J.R., M.M., S.K., V.V., M.J., V.F. and J.Ka. analyzed the data; J.P., V.F. and J.Ka. wrote the draft and all authors revised it. All authors have contributed substantially to the work reported.

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Purhonen, J., Rajendran, J., Mörgelin, M. et al. Ketogenic diet attenuates hepatopathy in mouse model of respiratory chain complex III deficiency caused by a Bcs1l mutation. Sci Rep 7, 957 (2017). https://doi.org/10.1038/s41598-017-01109-4

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Received: 23 November 2016
Accepted: 23 March 2017
Published: 19 April 2017
DOI: https://doi.org/10.1038/s41598-017-01109-4

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