- Open Access
Oleate ameliorates palmitate-induced reduction of NAMPT activity and NAD levels in primary human hepatocytes and hepatocarcinoma cells
Lipids in Health and Disease volume 16, Article number: 191 (2017)
Nicotinamide phosphoribosyltransferase (NAMPT) and nicotinamide adenine dinucleotide (NAD) levels are crucial for liver function. The saturated fatty acid palmitate and the unsaturated fatty acid oleate are the main free fatty acids in adipose tissue and human diet. We asked how these fatty acids affect cell survival, NAMPT and NAD levels in HepG2 cells and primary human hepatocytes.
HepG2 cells were stimulated with palmitate (0.5mM), oleate (1mM) or a combination of both (0.5mM/1mM) as well as nicotinamide mononucleotide (NMN) (0.5 mM) or the specific NAMPT inhibitor FK866 (10nM). Cell survival was measured by WST-1 assay and Annexin V/propidium iodide staining. NAD levels were determined by NAD/NADH Assay or HPLC. Protein and mRNA levels were analysed by Western blot analyses and qPCR, respectively. NAMPT enzyme activity was measured using radiolabelled 14C–nicotinamide. Lipids were stained by Oil red O staining.
Palmitate significantly reduced cell survival and induced apoptosis at physiological doses. NAMPT activity and NAD levels significantly declined after 48h of palmitate. In addition, NAMPT mRNA expression was enhanced which was associated with increased NAMPT release into the supernatant, while intracellular NAMPT protein levels remained stable. Oleate alone did not influence cell viability and NAMPT activity but ameliorated the negative impact of palmitate on cell survival, NAMPT activity and NAD levels, as well as the increased NAMPT mRNA expression and secretion. NMN was able to normalize intracellular NAD levels but did not ameliorate cell viability after co-stimulation with palmitate. FK866, a specific NAMPT inhibitor did not influence lipid accumulation after oleate-treatment.
Palmitate targets NAMPT activity with a consequent cellular depletion of NAD. Oleate protects from palmitate-induced apoptosis and variation of NAMPT and NAD levels. Palmitate-induced cell stress leads to an increase of NAMPT mRNA and accumulation in the supernatant. However, the proapoptotic action of palmitate seems not to be mediated by decreased NAD levels.
Nicotinamide phosphoribosyltransferase (NAMPT, also called visfatin or pre-B cell colony-enhancing factor (PBEF)) is a key enzyme of mammalian nicotinamide adenine dinucleotide (NAD) biosynthesis converting nicotinamide to nicotinamide mononucleotide (NMN) [1, 2]. By regulating intracellular NAD levels and the activity of NAD dependent enzymes, for example sirtuins, NAMPT is involved in the regulation of cellular metabolism . Moreover, NAMPT was shown to be differentially regulated in pathophysiological conditions like cancer , inflammatory disorders , heart diseases  and metabolic disorders, such as type 2 diabetes , obesity  and non-alcoholic fatty liver (NAFLD) [8,9,10,11]. Hepatic steatosis develops when triglycerides are accumulating in the liver due to insulin resistance, as a consequence of disturbed lipolysis in adipose tissue and de novo lipogenesis in the liver . An improvement of NAMPT protein and NAD levels by the bioflavonoid troxerutin or leucine was shown to protect mice with diet-induced obesity against steatosis, inflammation and glucose intolerance [13, 14] indicating an important role of NAMPT in the development of NAFLD. However, less is known about the regulation of hepatic NAMPT by the two main free fatty acids of human nutrition and adipose tissue, the monounsaturated fatty acid oleate (18:1) and the saturated fatty acid palmitate (16:0) [15, 16]. In this study, we investigated the impact of palmitate and oleate on NAMPT-mediated NAD biosynthesis in HepG2 cells and primary human hepatocytes. We could show that palmitate down regulated NAMPT activity and NAD levels while oleate ameliorated the negative effect of palmitate. However, hepatic NAD levels seemed to have no effect on hepatocyte survival or fat accumulation.
HepG2 cells were purchased from Leibniz Institute DSMZ (German Collection of Microorganisms and Cell Cultures) and cultured in MEM (Life Technologies) containing 10% fetal calf serum, 1% L-glutamine and 1% of streptomycin and penicillin (PAA Laboratories GmbH) at 37 °C in a humidified atmosphere of 5% CO2. Cells were passaged every 2 to 3 days. For experiments, cells were seeded in serum containing medium overnight. After washing with PBS, cells were serum starved for 24 h. Primary human hepatocytes were isolated as described before  and seeded in Williams’ Medium E containing 10% fetal calf serum, 1% L-glutamine and 1% of streptomycin and penicillin as well as 10–7 mol/L dexamethansone. Afterwards, cells were incubated with palmitate (0.5 mM), oleate (1.0 mM) or a combination of palmitate and oleate (0.5 mM/1 mM), dissolved as described previously, for 4 h, 24 h and 48 h, as well as nicotinamide mononucleotide (NMN; 0.5 mM) and FK866 (10 nM, Sigma-Aldrich). NMN was dissolved in serum free medium, FK866 in DMSO (dilution factor 1:1′000‘000) and palmitate and oleate in NaOH (dilution factor 1:200). All solvent controls had no impact on cell viability, NAMPT mRNA expression, protein levels and NAMPT activity as well as lipid accumulation (Additional file 1: Figure S1).
Cell viability assay
Cell viability was measured by using the Cell Proliferation Reagent WST-1 (Roche Diagnostics GmbH) according to manufacturer’s protocol. HepG2 cells were seeded in 96 well plates with 10,000 cells per well and cultured as described above. Subsequently, 10 μl of WST-1 reagent was added to each well and absorbance was determined at 450 nm using the Flurostar OPTIMA (BMG Labtech).
0.1 × 106 HepG2 cells per well were seeded in 12 well plates and cultured as indicated above. Additionally, cells were incubated with camptothecin (2 μM) (Sigma Aldrich) and etoposide (85 μM) (Merck Chemicals) as positive control for apoptosis for 24 h. Apoptosis was measured using the FITC Annexin V Apoptosis Detection Kit (BD Pharmingen™) as described before .
Protein extraction and western blot analyses
0.3 × 106 HepG2 cells per well were seeded in 6 well plates and incubated as described above. Cells were harvested in modified RIPA buffer containing 50 mM TrisHCl pH 7.4; 1% NP-40; 0.25% sodium deoxycholate; 1× Roche complete proteases inhibitor cocktail; 1 mM EDTA; 1 mM sodium orthovanadate, 1 mM sodium fluoride, 5 mM nicotinamide, 5 μM Trichostatin A and 1× Roche Complete protease inhibitor cocktail. Protein amount of cell lysates was determined using BCA protein assay (Pierce, Thermo Scientific). 10 μg or 30 μg protein was separated by SDS-PAGE and semi-dry transferred to nitrocellulose membranes as described before . For detection of NAMPT in the supernatant, 24 μl of samples were used and processed as described above.
NAD concentrations were measured using the EnzyChrom™ NAD+/NADH Assay Kit (E2ND-100, Biotrend) according to manufacturer’s protocol or by HPLC as described before .
Total RNA extraction and realtime qPCR
For total RNA extraction 0.3 × 106 HepG2 cells per well were seeded in 6 well plates. Total RNA was extracted by RNeasy Mini Kit (Qiagen) according to manufacturer’s protocol. 1000 ng of total RNA was transcribed into cDNA by M-MLV Reverse Transcriptase (Invitrogen). Afterwards, Taqman® analyses were performed using the qPCR Master Mix Plus Low ROX (Eurogentec) and the Applied Biosystems 7500 Real Time PCR System. NAMPT (forward: 5′-GCA-GAA-GCC-GAG-TTC-AAC-ATC-3′; reverse: 5′- TGC-TTG-TGT-TGG-GTG-GAT-ATT-G-3′; probe: 5′-TGG-CCA-CCG-ACT-CCT-ACA-AGG-TTA-CTC-AC-3′) was normalised to the mean of the housekeeping gene ß-actin (forward: 5′-CGA-GCG-CGG-CTA-CAG-CTT-3′; reverse: 5′-CCT-TAA-TGT-CAC-GCA-CGA-TTT-3′; probe: 5′-ACC-ACC-ACG-GCC-GAG-CGG-3′).
NAMPT enzyme activity
For determination of NAMPT activity 10 × 106 HepG2 cells were seeded in T175 culture flasks and cultured as described above. After lysis in 50 mM 0.1 M sodium phosphate buffer, pH 7.4, 30 μg of protein was added to the reaction buffer and incubated at 37 °C for 2 h. Afterwards the assay using radiolabelled 14C–nicotinamide was performed as described before .
Oil red O staining
HepG2 cells were grown in 24-well plates, fixed with phosphate buffered paraformaldehyde solution (Roth), washed with PBS and stained with Oil red O solution (stock solutions: 50 mg Oil red O powder in 100 ml isopropyl) for 15 min at 37 °C. After washing with PBS cells were photographed under the microscope. For quantification Oil red O was dissolved by adding isopropropanol (100%) to the samples. 100 μl of supernatant was added to a 96-well plate and measured at 510 nm using the Flurostar OPTIMA (BMG Labtech) .
Statistical analyses were performed with GraphPad Prism® software (5.03). Significance levels were calculated by one-way analysis of variance (ANOVA) followed by Bonferroni post hoc test (*p < 0.05; **p < 0.01; ***p < 0.001 compared to control; # p < 0.05; ## p < 0.01; ### p < 0.001 compared to palmitate, § p < 0.05; §§ p < 0.01; §§§ p < 0.001 in a time dependent manner). Data represent means ± SEM of three independent experiments.
Palmitate-induced cell death is rescued by oleate
To investigate the impact of palmitate and oleate on cell survival, HepG2 cells were incubated with palmitate (0.5 mM), oleate (1 mM) and a combination of both (0.5 mM/1 mM). After 4 h of incubation cell viability was unaltered. Palmitate decreased cell viability by 2.0-fold after 24 h (Additional file 2: Figure S2A). Viability further declined by 2.4-fold after 48 h (Fig. 1a). Oleate alone did not influence cell viability, but was able to ameliorate the negative impact of palmitate. Furthermore, oleate was able to normalize the number of apoptotic cells after palmitate-incubation (48 h) from 2.2-fold to control level (Fig. 1b).
Regulation of NAD salvage pathway by palmitate and oleate
NAD is known to play a central role in cellular metabolism as a redox partner or co-substrate for NAD-dependent enzymes. Therefore, intracellular total NAD concentration was measured in HepG2 cells and primary human hepatocytes. Palmitate decreased NAD concentration by 1.2-fold in HepG2 cells and by 3.2-fold in primary human hepatocytes (Fig. 2a) after 48 h. In line with these data, NAMPT activity in HepG2 cells was significantly decreased from 13.8 ± 0.02 cpm/ µg total protein x h to 6.2 ± 1.1 cpm/ µg total protein x h (2.4-fold) after 48 h of palmitate incubation (Fig. 2d). Incubation of HepG2 cells with palmitate led to higher NAMPT mRNA expression after 4 h and 24 h which was significantly increased by 5.2-fold after 48 h compared to control. In primary human hepatocytes, palmitate significantly increased NAMPT mRNA expression by 1.5-fold after 48 h (Fig. 2b). Interestingly, when we determined the NAMPT protein amount in lysates of HepG2 cells and primary human hepatocytes we found no significant changes in NAMPT protein level after stimulation with palmitate and oleate or its combination (Fig. 2c). Since hepatocytes are a source of extracellular NAMPT (eNAMPT)  and eNAMPT has been described as stress-response protein we analysed whether NAMPT was released by the cells and accumulated in the supernatant. After stimulation of HepG2 cells with palmitate NAMPT was secreted into the supernatant already after 4 h, a time point where we detected no cytotoxic effects. Extracellular NAMPT further increased in HepG2 cell supernatants time-dependently after 24 h and 48 h of palmitate treatment. Primary human hepatocytes released NAMPT into the supernatant after stimulation with palmitate after 48 h (Fig. 2e). Oleate alone had no impact on NAD concentration or NAMPT activity and release, but significantly restored palmitate-induced changes on NAMPT mRNA, −activity and NAD levels (Fig. 2a–d).
NMN does not counteract the palmitate-induced decrease in cell viability
To find out whether or not the decreased NAD levels were responsible for the reduction in cell viability after palmitate treatment, HepG2 cells were co-stimulated with the NAMPT enzyme product NMN. Although intracellular NAD levels were normalized (Fig. 3b), NMN was not able to rescue palmitate-induced cell viability reduction (Fig. 3a). As positive control, we tested whether NMN can improve cell viability of FK866-induced NAD depletion. NMN normalized the reduced cell viability and NAD levels (by 2.8-fold and 3.6-fold, respectively) caused by incubation with the specific NAMPT inhibitor FK866 (Fig. 3a, b).
A decreased NAMPT activity does not affect lipid accumulation
Lipid content of HepG2 cells after incubation with palmitate, oleate or the combination was assessed. After treatment with palmitate, no significant increase in intracellular lipids was detected, while oleate and a combination of oleate and palmitate treatment resulted in a 1.9-fold increase (Fig. 3c). Since NAMPT expression and NAD concentrations had been shown to be downregulated during the development of fatty liver disease  and NAMPT activity has been implicated in the regulation of lipid metabolism in the liver , we examined whether a decreased NAMPT activity and NAD levels would lead to higher lipid accumulation. Therefore, HepG2 cells were co-stimulated with FK866 (10 nM). However, FK866 treatment did not lead to alterations in intracellular lipid content in oleate-stimulated hepatocytes (Fig. 3c).
Disturbances in NAMPT and NAMPT-mediated NAD biosynthesis have been reported during the development of NAFLD [9, 23] and NAMPT is implicated in the regulation of lipid metabolism [22, 24]. However, the regulation of NAMPT expression and activity by free fatty acids in hepatocytes is incompletely understood. In our study we, therefore, examined the effect of the two main free fatty acids of human nutrition and adipose tissue, oleate (18:1) and palmitate (16:0) on hepatocyte viability and the regulation of hepatic NAMPT and NAD levels.
We could show that palmitate induces apoptosis in HepG2 cells which can be rescued by oleate. This is in line with several other studies. In INS-1E β-cells palmitate-induced apoptosis was rescued by oleate due to repression of endoplasmic reticulum stress (ER) via eukaryotic Initiation Factor 2α (eIF2α), X-box binding protein 1 (XBP1) and Chop . Stimulation of BiP by oleate or its overexpression restored palmitate-induced ER stress and apoptosis in HepG2 cells . Oleate is able to ameliorate palmitate-induced mitochondrial reactive oxygen species (ROS) generation, concomitant mitochondrial dysfunction and oxidative stress [27, 28].
Since it is known that inhibition of NAMPT-mediated NAD biosynthesis by the NAMPT-specific inhibitor FK866 reduces cell viability and induces apoptosis in hepatocytes , we asked whether or not NAMPT is affected by palmitate treatment. Incubation with palmitate led to decreased intracellular NAD levels in HepG2 cells as well as in primary human hepatocytes, which could be explained by a decreased NAMPT activity while intracellular NAMPT protein levels were maintained. How NAMPT activity is influenced by palmitate is still a matter of debate. Our data indicate that NAMPT activity is not associated with SIRT1 activity or ER stress (data not shown). Palmitate could lead to impaired β-oxidation, ROS production and calcium signalling . All of these processes depend on NAD and might play a role in decreased NAMPT activity and NAD levels induced by palmitate. It is known that NAMPT is only active as a dimer . It could be that palmitate increases the monomer to dimer ratio in the cell which decreases NAMPT activity and subsequently NAD levels. Interestingly, NAMPT mRNA levels increased and NAMPT accumulated in the supernatant already after 4 h. Our data are in line with earlier findings that resveratrol decreases NAMPT activity and induces NAMPT mRNA upregulation as well as NAMPT release in hepatocarcinoma cell lines . Furthermore, in human pancreatic islets glucose leads to an increase of NAMPT mRNA expression and accumulation of enzymatically active NAMPT in the supernatant . These findings point to a common mechanism used by different stress signals to induce NAMPT mRNA expression and concomitant release of NAMPT. In contrast to our study, palmitate decreases NAMPT release from 3 T3-L1 adipocytes , which implicates a cell-type dependent effect of palmitate. Serum NAMPT levels are altered in various diseases, for example in liver diseases [9, 34]. Since it is known that hepatocytes are a source of circulating NAMPT , it is of interest to fully understand the regulation of NAMPT release from different cells and organs into the circulation . In adipose tissue, NAMPT secretion is regulated by SIRT1 which deacetylates NAMPT at lysine 53 and thus increases NAMPT activity and secretion. Extracellular NAMPT (eNAMPT) counteracts palmitate-induced apoptosis by activating phosphoinositide 3-kinase (PI3-kinase)-dependent signaling pathways and down regulation of proapoptotic proteins, like B-cell lymphoma 2 (Bcl-2), cytochrome c and caspase 3 in pancreatic β-cells . Furthermore, eNAMPT protects against ER stress-induced apoptosis by activating the interleukin-6/Stat3 pathway via a non-enzymatic function .
Inhibition of intracellular NAMPT activity via FK866 leads to increased cell death which can be ameliorated by supplementation with the NAMPT enzyme product NMN . In our study, co-stimulation of hepatocytes with palmitate and NMN led to a normalization of NAD levels. However, cell viability was not ameliorated by NMN co-treatment. In contrast, oleate co-treatment completely reversed the palmitate-mediated cell viability decrease. This could be due to the fact that oleate triggers the conversion of palmitate to neutral triacylglycerides, which directly prevents palmitate from exerting adverse effects like promoting the accumulation of toxic diacylglycerides . Furthermore, it has already been shown that palmitate-induced apoptosis is driven by other cellular processes such as calcium-stimulated mitochondrial activation , autophagy , ER stress  or accumulation of ROS  which seemed to be independent of intracellular NAD levels. In animal studies it has been shown that alterations in NAMPT protein levels by pharmacological factors [13, 40] or by gene modification  improve hepatic triglycerides but in our study inhibition of NAMPT activity did not lead to a higher accumulation of triglycerides after oleate stimulation. This indicates that NAMPT is not involved in regulating triacylglyceride storage in our cell model. However, another study showed that NAMPT overexpression ameliorated hepatic triglyceride storage after oleate treatment .
We could show that palmitate decreased NAMPT activity and NAD levels in human hepatocytes and NAMPT acts as an early stress-response protein that is upregulated and secreted into the supernatant under lipotoxic stress. However, the pro-apoptotic effects of palmitate seem not to be mediated via intracellular NAD level. Oleate alone had no influence on the tested cellular responses but interestingly ameliorated the adverse impact of palmitate in combined treatment.
B cell lymphoma 2
eukaryotic Initiation Factor 2α
Nicotinamide adenine dinucleotide (NAD)
Non-alcoholic fatty liver (NAFLD)
Pre-B cell colony-enhancing factor (PBEF)
Reactive oxygen species
X-box binding protein 1
Rongvaux A, Galli M, Denanglaire S, Van Gool F, Drèze PL, Szpirer C, et al. Nicotinamide phosphoribosyl transferase/pre-B cell colony-enhancing factor/visfatin is required for lymphocyte development and cellular resistance to genotoxic stress. J Immunol. [Internet]. 2008 [cited 2015 May 22];181:4685–95. Available from: http://www.ncbi.nlm.nih.gov/pubmed/18802071.
Revollo JR, Grimm AA, Imai S. The NAD biosynthesis pathway mediated by nicotinamide phosphoribosyltransferase regulates Sir2 activity in mammalian cells. J Biol Chem. 2004;279:50754–63.
Sampath D, Zabka TS, Misner DL, O’Brien T, Dragovich PS. Inhibition of nicotinamide phosphoribosyltransferase (NAMPT) as a therapeutic strategy in cancer. Pharmacol Ther. [Internet]. 2015 [cited 2017 May 10];151:16–31. Available from: http://www.ncbi.nlm.nih.gov/pubmed/25709099.
Montecucco F, Cea M, Cagnetta A, Damonte P, Nahimana A, Ballestrero A, et al. Nicotinamide phosphoribosyltransferase as a target in inflammation- related disorders. Curr Top Med Chem. [Internet]. 2013 [cited 2015 May 22];13:2930–8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/24171767.
Romacho T, Azcutia V, Vázquez-Bella M, Matesanz N, Cercas E, Nevado J, et al. Extracellular PBEF/NAMPT/visfatin activates pro-inflammatory signalling in human vascular smooth muscle cells through nicotinamide phosphoribosyltransferase activity. Diabetologia [Internet]. 2009 [cited 2015 Jun 8];52:2455–63. Available from: http://www.ncbi.nlm.nih.gov/pubmed/19727662.
Imai S, Yoshino J. The importance of NAMPT/NAD/SIRT1 in the systemic regulation of metabolism and ageing. Diabetes Obes Metab. [Internet]. 2013 [cited 2015 May 29];15 Suppl 3:26–33 Available from: http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3819727&tool=pmcentrez&rendertype=abstract
Stastny J, Bienertova-Vasku J, Vasku A. Visfatin and its role in obesity development. Diabetes Metab Syndr Clin Res Rev. [Internet]. 2012 [cited 2015 May 29];6:120–4. Available from: http://www.ncbi.nlm.nih.gov/pubmed/23153983.
Kukla MM, Ciupińska-Kajor M, Kajor M, Wyleżoł M, Żwirska-Korczala K, Hartleb M, et al. Liver visfatin expression in morbidly obese patients with nonalcoholic fatty liver disease undergoing bariatric surgery. Pol J Pathol. [Internet]. 2010;61:147–53. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21225497.
Dahl TB, Haukeland JW, Yndestad A, Ranheim T, Gladhaug IP, Damås JK, et al. Intracellular nicotinamide phosphoribosyltransferase protects against hepatocyte apoptosis and is down-regulated in nonalcoholic fatty liver disease. J Clin. Endocrinol. Metab. [Internet]. 2010;95:3039–47. Available from: http://www.ncbi.nlm.nih.gov/pubmed/20392873.
Gaddipati R, Sasikala M, Padaki N, Mukherjee RM, Sekaran A, Jayaraj-Mansard M, et al. Visceral adipose tissue visfatin in nonalcoholic fatty liver disease. Ann Hepatol Off J Mex Assoc Hepatol. [Internet]. 2010;9:266–70. Available from: http://www.ncbi.nlm.nih.gov/pubmed/20720266.
Terra X, Auguet T, Quesada I, Aguilar C, Luna AM, Hernandez M, et al. Increased levels and adipose tissue expression of visfatin in morbidly obese women: the relationship with pro-inflammatory cytokines. Clin Endocrinol (Oxf). 2012;77:691–8.
Noureddin M, Rinella ME. Nonalcoholic Fatty Liver Disease, Diabetes, Obesity, and Hepatocellular Carcinoma. Clin Liver Dis. [Internet]. 2015 [cited 2015 May 4];19:361–79 Available from: http://www.sciencedirect.com/science/article/pii/S1089326115000136
Zhang Z-F, Fan S-H, Zheng Y-L, Lu J, Wu D-M, Shan Q, et al. Troxerutin improves hepatic lipid homeostasis by restoring NAD(+)-depletion-mediated dysfunction of lipin 1 signaling in high-fat diet-treated mice. Biochem Pharmacol. [Internet]. 2014;91:74–86. Available from: http://www.ncbi.nlm.nih.gov/pubmed/25026599.
Li H, Xu M, Lee J, He C, Xie Z. Leucine supplementation increases SIRT1 expression and prevents mitochondrial dysfunction and metabolic disorders in high-fat diet-induced obese mice. Am J Physiol Endocrinol Metab. 2012;303:E1234–44.
Zöllner N, Tatò F. Fatty acid composition of the diet: impact on serum lipids and atherosclerosis. Clin Investig. [Internet]. 1992 [cited 2015 May 29];70:968–1009. Available from: http://www.ncbi.nlm.nih.gov/pubmed/1472837.
Hodson L, Skeaff CM, Fielding BA. Fatty acid composition of adipose tissue and blood in humans and its use as a biomarker of dietary intake. Prog Lipid Res. [Internet]. 2008 [cited 2015 May 29];47:348–80. Available from: http://www.ncbi.nlm.nih.gov/pubmed/18435934.
Weiss TS, Pahernik S, Scheruebl I, Jauch K-W, Thasler WE. Cellular damage to human hepatocytes through repeated application of 5-aminolevulinic acid. J Hepatol. [Internet]. Elsevier; 2003 [cited 2015 Jun 22];38:476–82 Available from: http://www.journal-of-hepatology.eu/article/S0168827802004543/fulltext
Schuster S, Penke M, Gorski T, Gebhardt R, Weiss TS, Kiess W, et al. FK866-induced NAMPT inhibition activates AMPK and downregulates mTOR signaling in hepatocarcinoma cells. Biochem Biophys Res Commun. [Internet]. 2015 [cited 2017 Feb 13];458:334–40 Available from: http://linkinghub.elsevier.com/retrieve/pii/S0006291X15001503.
Garten A, Petzold S, Barnikol-Oettler A, Körner A, Thasler WE, Kratzsch J, et al. Nicotinamide phosphoribosyltransferase (NAMPT/PBEF/visfatin) is constitutively released from human hepatocytes. Biochem Biophys Res Commun. [Internet]. 2010 [cited 2017 Feb 13];391:376–81 Available from: http://linkinghub.elsevier.com/retrieve/pii/S0006291X09022414.
Ramírez-Zacarías JL, Castro-Muñozledo F, Kuri-Harcuch W. Quantitation of adipose conversion and triglycerides by staining intracytoplasmic lipids with Oil red O. Histochemistry [Internet]. 1992 [cited 2017 Aug 30];97:493–7. Available from: https://www.ncbi.nlm.nih.gov/pubmed/1385366.
Garten A, Petzold S, Barnikol-Oettler A, Körner A, Thasler WE, Kratzsch J, et al. Nicotinamide phosphoribosyltransferase (NAMPT/PBEF/visfatin) is constitutively released from human hepatocytes. Biochem Biophys Res Commun. [Internet]. 2010 [cited 2015 Jun 1];391:376–81 Available from: http://www.sciencedirect.com/science/article/pii/S0006291X09022414.
Tao R, Wei D, Gao H, Liu Y, DePinho RA, Dong XC. Hepatic FoxOs regulate lipid metabolism via modulation of expression of the nicotinamide phosphoribosyltransferase gene. J Biol Chem. [Internet]. 2011 [cited 2015 Mar 6];286:14681–90 Available from: http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3077665&tool=pmcentrez&rendertype=abstract.
Penke M, Larsen PS, Schuster S, Dall M, Jensen BAH, Gorski T, et al. Hepatic NAD salvage pathway is enhanced in mice on a high-fat diet. Mol Cell Endocrinol. [Internet]. 2015 [cited 2017 Feb 13];412:65–72 Available from: http://linkinghub.elsevier.com/retrieve/pii/S0303720715002993.
Bowlby SC, Thomas MJ, D’Agostino RB, Kridel SJ. Nicotinamide phosphoribosyl transferase (Nampt) is required for de novo lipogenesis in tumor cells. PLoS One [Internet]. 2012 [cited 2015 Jun 8];7:e40195 Available from: http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3387004&tool=pmcentrez&rendertype=abstract.
Sommerweiss D, Gorski T, Richter S, Garten A, Kiess W. Oleate rescues INS-1E β-cells from palmitate-induced apoptosis by preventing activation of the unfolded protein response. Biochem Biophys Res. Commun. [Internet]. 2013 [cited 2015 Jun 5];441:770–6. Available from: https://www.ncbi.nlm.nih.gov/pubmed/24189472.
Gu X, Li K, Laybutt DR, He M, Zhao H-L, Chan JCN, et al. Bip overexpression, but not CHOP inhibition, attenuates fatty-acid-induced endoplasmic reticulum stress and apoptosis in HepG2 liver cells. Life Sci [Internet]. 2010 [cited 2015 Jun 5]; 87:724–32. Available from: http://www.ncbi.nlm.nih.gov/pubmed/20970436.
Yuzefovych L, Wilson G, Rachek L. Different effects of oleate vs. palmitate on mitochondrial function, apoptosis, and insulin signaling in L6 skeletal muscle cells: role of oxidative stress. Am J Physiol. Endocrinol. Metab. [Internet]. 2010 [cited 2015 Jun 5];299:E1096–105 Available from: http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3006254&tool=pmcentrez&rendertype=abstract.
Egnatchik RA, Leamy AK, Jacobson DA, Shiota M, Young JD. ER calcium release promotes mitochondrial dysfunction and hepatic cell lipotoxicity in response to palmitate overload. Mol Metab. [Internet]. 2014 [cited 2015 Jun 21];3:544–53 Available from: http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=4099508&tool=pmcentrez&rendertype=abstract.
Egnatchik RA, Leamy AK, Noguchi Y, Shiota M, Young JD. Palmitate-induced activation of mitochondrial metabolism promotes oxidative stress and apoptosis in H4IIEC3 rat hepatocytes. Metabolism. [Internet]. 2014 [cited 2015 Jun 22];63:283–95 Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4099508/.
Wang T, Zhang X, Bheda P, Revollo JR, Imai S, Wolberger C. Structure of Nampt/PBEF/visfatin, a mammalian NAD+ biosynthetic enzyme. Nat Struct Mol Biol. 2006;13:661–2.
Schuster S, Penke M, Gorski T, Petzold-Quinque S, Damm G, Gebhardt R, et al. Resveratrol differentially regulates NAMPT and SIRT1 in Hepatocarcinoma cells and primary human hepatocytes. Avila MA, editor. PLoS One [Internet]. 2014 [cited 2017 Feb 13];9:e91045 Available from: http://dx.plos.org/10.1371/journal.pone.0091045.
Kover K, Tong PY, Watkins D, Clements M, Stehno-Bittel L, Novikova L, et al. Expression and regulation of nampt in human islets. PLoS One. 2013;8:e58767.
Karrasch T, Leszczak S, Bala M, Ober I, Martin J, Schmid A, et al. Short-term regulation of Visfatin release in vivo by oral lipid ingestion and in vitro by fatty acid stimulation. Exp Clin Endocrinol. Diabetes [Internet]. 2014 [cited 2015 Jun 8];122:126–34. Available from: http://www.ncbi.nlm.nih.gov/pubmed/24554513.
Auguet T, Terra X, Porras JA, Orellana-Gavaldà JM, Martinez S, Aguilar C, et al. Plasma visfatin levels and gene expression in morbidly obese women with associated fatty liver disease. Clin Biochem. 2013;46:202–8.
Dahl TB, Holm S, Aukrust P, Halvorsen B. Visfatin/NAMPT: a multifaceted molecule with diverse roles in physiology and pathophysiology. Annu Rev Nutr. [Internet]. 2012 [cited 2015 Jun 8];32:229–43. Available from: http://www.ncbi.nlm.nih.gov/pubmed/22462624.
Cheng Q, Dong W, Qian L, Wu J, Peng Y. Visfatin inhibits apoptosis of pancreatic β-cell line, MIN6, via the mitogen-activated protein kinase/phosphoinositide 3-kinase pathway. J Mol Endocrinol. [Internet]. 2011 [cited 2015 Jun 8];47:13–21. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21471274.
Li Y, Zhang Y, Dorweiler B, Cui D, Wang T, Woo CW, et al. Extracellular Nampt promotes macrophage survival via a nonenzymatic interleukin-6/STAT3 signaling mechanism. J Biol Chem. [Internet]. 2008 [cited 2015 Jun 8];283:34833–43 Available from: http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2596403&tool=pmcentrez&rendertype=abstract.
Cai N, Zhao X, Jing Y, Sun K, Jiao S, Chen X, et al. Autophagy protects against palmitate-induced apoptosis in hepatocytes. Cell Biosci. [Internet]. 2014 [cited 2015 May 28];4:28 Available from: http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=4045884&tool=pmcentrez&rendertype=abstract.
Kim D-S, Jeong S-K, Kim H-R, Kim D-S, Chae S-W, Chae H-J. Metformin regulates palmitate-induced apoptosis and ER stress response in HepG2 liver cells. Immunopharmacol. Immunotoxicol. [Internet]. 2010 [cited 2015 Jun 22];32:251–7. Available from: http://www.ncbi.nlm.nih.gov/pubmed/20038265.
Chang W-C, Jia H, Aw W, Saito K, Hasegawa S, Kato H. Beneficial effects of soluble dietary Jerusalem artichoke (Helianthus tuberosus) in the prevention of the onset of type 2 diabetes and non-alcoholic fatty liver disease in high-fructose diet-fed rats. Br J Nutr. [Internet]. 2014 [cited 2015 Apr 1];112:709–17. Available from: http://www.ncbi.nlm.nih.gov/pubmed/24968200.
Wang L-F, Wang X-N, Huang C-C, Hu L, Xiao Y-F, Guan X-H, et al. Inhibition of NAMPT aggravates high fat diet-induced hepatic steatosis in mice through regulating Sirt1/AMPKα/SREBP1 signaling pathway. Lipids Health Dis. [Internet]. 2017 [cited 2017 May 10];16:82. Available from: http://www.ncbi.nlm.nih.gov/pubmed/28449683.
Primary human hepatocytes were kindly provided by the “Virtual Liver Network”, a major national initiative on Systems Biology of the Liver. We want to thank Research Academy Leipzig and Integrated Research Training Group “Obesity Mechanisms “(CRC 1052) for support. The authors wish to acknowledge the skilled technical expertise of Anja Barnikol-Oettler. We want to thank Thomas Hermsdorf. We acknowledge support from the German Research Foundation (DFG) and Leipzig University within the program of Open Access Publishing.
Availability of data and materials
The datasets during and/or analysed during the current study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Solvent controls do not influence cell viability as well as intracellular NAMPT and NAD levels. HepG2 cells were stimulated with serum-free medium with and without DMSO (dilution factor: 1:1′000‘000) and serum free medium with 1% free fatty acid -BSA with and without NaOH (dilution 1:200). Neither DMSO nor NaOH altered cell viability measured by WST-1 assay (A), intracellular NAD levels measured by HPLC (B), NAMPT mRNA expression or protein abundance measured by qPCR or Western blot analysis (C,D), respectively, enzyme activity (E) and lipid accumulation stained with Oil-red O (F). Data were normalised to control (serum free medium) which was set 1. Data represent two or three independent experiments shown as means ± SEM. FFA: free fatty acid. (JPEG 691 kb)
Palmitate decreases cell viability after 24 h. After stimulation of HepG2 cells with palmitate and oleate for 4 h and 24 h at the indicated concentrations, cell viability was measured via WST-1 assay. Data were referred to control (serum free medium) and represent three independent experiments performed in triplicates shown as means ± SEM. ***p < 0.05 compared to control. (JPEG 51 kb)
About this article
Cite this article
Penke, M., Schuster, S., Gorski, T. et al. Oleate ameliorates palmitate-induced reduction of NAMPT activity and NAD levels in primary human hepatocytes and hepatocarcinoma cells. Lipids Health Dis 16, 191 (2017). https://doi.org/10.1186/s12944-017-0583-6