Nicotinamide phosphoribosyltransferase (NAMPT) is a pleiotropic protein implicated in the pathogenesis of acute respiratory distress syndrome, aging, cancer, coronary heart diseases, diabetes, nonalcoholic fatty liver disease, obesity, rheumatoid arthritis, and sepsis. However, the underlying molecular mechanisms of NAMPT in these physiological and pathological processes are not fully understood. Here, we provide experimental evidence that a Nampt gene homozygous knockout (Nampt−/−) resulted in lethality at an early stage of mouse embryonic development and death within 5–10 days in adult mice accompanied by a 25.24±2.22% body weight loss, after the tamoxifen induction of NamptF/F × Cre mice. These results substantiate that Nampt is an essential gene for life. In Nampt−/− mice versus Nampt+/+ mice, biochemical assays indicated that liver and intestinal tissue NAD levels were decreased significantly; histological examination showed that mouse intestinal villi were atrophic and disrupted, and visceral fat was depleted; mass spectrometry detected unusual higher serum polyunsaturated fatty acid containing triglycerides. RNA-seq analyses of both mouse and human pediatric liver transcriptomes have convergently revealed that NAMPT is involved in key basic cellular functions such as transcription, translation, cell signaling, and fundamental metabolism. Notably, the expression of all eight enzymes in the tricarboxylic acid cycle were decreased significantly in the Nampt−/− mice. These findings prompt us to posit that adult Nampt−/− mouse lethality is a result of a short supply of ATP from compromised intestinal absorption of nutrients from digested food, which leads to the exhaustion of body fat stores.
Nicotinamide phosphoribosyltransferase (NAMPT) was initially named pre-B-cell colony-enhancing factor (PBEF)1 as it synergized the pre-B-cell colony-formation activity of stem cell factor and interleukin 7. NAMPT catalyzes the condensation of nicotinamide with 5-phosphoribosyl-1-pyrophosphate to yield nicotinamide mononucleotide, an intermediate in the biosynthesis of NAD.2 In 2005, Fukuhara et al.3 reported Nampt as a Visfatin, which was enriched in visceral fat with insulin-mimetic function. The list of NAMPT’s physiological roles is continuously growing. The dysregulation of NAMPT gene has been implicated in several human diseases.4 However, the underlying molecular mechanisms are not fully understood.
Loss-of-function experiments reveal the functions of a gene. The most dramatic phenotype is lethality, defining a gene as essential.5 Recently, three groups reported that there are about 2000 core genes essential for life in several types of human cells.6, 7, 8 They also found that the essentiality of some genes is context-dependent and affects viability in a cell-type-specific manner.9 It is more logical to establish any essential gene in an animal model, by exploring the terminal phenotypes and the various molecular mechanisms underlying lethality. The mouse has long been regarded as an ideal model system for this purpose. Conservation between humans and mice is underscored by strong one-to-one orthologous relationships between genes of the two species.10 We have previously reported that the Nampt gene DNA coding sequence between mouse and human is 96% identical.11 Hence, the homozygous Nampt gene knockout in mice would offer an attractive model to decipher fully the Nampt gene’s pleiotropic roles, by probing molecular mechanisms underlying lethality in adult mice.
Here, we provide experimental evidence that the Nampt gene homozygous knockout (Nampt−/−) resulted in mouse embryonic lethality at an early stage. We also established Nampt gene conditional knockout mice and found that induced Nampt−/− adult mice died within 5–10 days, accompanied by a 25.24±2.22% body weight loss. These results substantiate that Nampt is an essential gene in vivo. RNA-seq analyses of both mouse and human pediatric liver transcriptomes revealed that Nampt is involved in key basic cellular functions such as transcription, translation, cell signaling, and fundamental metabolism. Particularly, expression of all eight enzymes in the tricarboxylic acid cycle(TAC) in Nampt−/− adult mice were decreased significantly, which suggests that depletion of cellular ATP energy sources may be the main culprit of adult Nampt−/− mouse death.
Homozygous Nampt gene knockout mice are embryonically lethal
To study the biological functions of the Nampt gene, we established the Nampt gene-trapped mouse model (Figure 1a). To confirm the mutant ES cell line, RT-PCR results showed that the cell line only expresses about 50% Nampt mRNA of the Nampt+/+ wild-type control, and western blotting demonstrated that cellular Nampt protein in the Nampt+/− ES cell line is decreased significantly (Figure 1b). The validated ES cell lines were injected into blastocysts of pseudopregnant female C57BL/6N mice at the Johns Hopkins University transgenic mouse core facility to generate the Nampt+/− knockdown mouse model. To facilitate mouse genotyping needs, we sequenced the whole region of Nampt gene intron-7, including the inserted gene-trap cassette (Supplementary Figure 1), and designed three PCR primers (two forward and one reverse) to detect Nampt wild-type (Nampt+/+), Nampt heterozygous (Nampt+/−), and Nampt knockout (Nampt−/−) mice as indicated in Figure 1c. Representative genotyping images of Nampt+/+, Nampt+/−, and Nampt−/− mice are presented in Figure 1f. To generate Nampt−/− knockout mice, Nampt+/− male and female mice were bred. At embryonic day 11.5, Nampt+/+ and Nampt+/− embryos both have normal development with 40–45 pairs of somites, and normal embryo size. Nampt−/− embryos are much smaller in size, and display unclear abnormal embryo structure (Figure 1d). To establish the Nampt−/− embryonic lethality, we performed a β-gal staining of mouse embryos at 8.5 d.p.c. stage, as the inserted gene-trap vector β-Geo can express β-gal. A representative normal size Nampt+/− embryo has a diffused brown color staining as in the Nampt+/+ embryo, while an undeveloped Nampt−/− embryo shows strong dark blue staining (Figure 1e). These results corroborate that the Nampt−/− mice are lethal at an early embryonic stage.
Nampt is an essential gene for adult mouse survival
As Nampt−/− mice are embryonically lethal, we cannot use Nampt−/− mice for a complete ‘loss of function’ study and hence we generated a Nampt conditional knockout mouse line (NampF/F). The Nampt gene spans over 36.9 kb and contains 11 exons and 10 introns, thus preventing the convenient floxing of its entire gene. We decided to introduce loxP sites into introns flanking exon 2. A Neo selection cassette flanked by FRT sites was inserted adjacent of the loxP site within intron-1 as well (Figure 2a). The Namptflox(Neo) targeting vector was introduced into mouse embryonic stem cells (mES), which were then injected into C57BL/6 host blastocysts to generate chimeric mice (Supplementary Figure 2). Namptflox(Neo)/+ heterozygous mice were crossed with the ACTB::FLPe deleter mouse line to remove the PGK-Neo cassette, which has been reported to interfere with gene expression (Figure 2a). Namptflox/+ mice were backcrossed with C57BL/6J wild-type mice for 10 generations before being considered as a pure C57BL/6 background, and subsequently intercrossed to obtain homozygous Namptflox/flox mice. All the genotypes were confirmed by PCR analysis (Figure 2b) and tissue expression levels of Nampt protein were verified by western blotting (Figure 2c). Namptflox/flox mice were born at a normal Mendelian ratio and were viable without displaying any obvious defect. To conditionally induce cre-loxP recombination, Namptflox/flox mice were mated to UbcCreERT2 mice. After 4-day intraperitoneal administration of tamoxifen (TMX), Namptflox/flox mice (n=10) displayed rapid weight loss. These mice became dehydrated, less active on day 3 after injection and reached >20% weight loss within 5–10 days before dying (Figure 2e). Dissection of dying Nampt−/− mice showed fat tissue depletion and intestinal abnormality in TMX-treated UbcCreERT2: Namptflox/flox mice (Figure 2d). The Nampt protein expression levels were dramatically reduced in TMX-treated UbcCreERT2: Namptflox/flox mice after day 5(Figure 2c). Histological examination revealed that Nampt depletion induced severe intestinal villus atrophy and the disruption of normal architecture (Figure 2f) compared with the wild-type control mice.
Abnormal serum lipid profile in Nampt−/− mice
To characterize the rapid catabolism of visceral fat in Nampt−/− mice, we analyzed the serum lipid content in these mice (Supplementary Table 1) by UHPLC-qTOF MS method. Principal component analysis revealed that each experimental group clustered as a unique entity (Figure 3a). One hundred forty-one lipids were significantly and differentially expressed among the four experimental groups (Supplementary Table 1 and Supplementary Figure 3). A heatmap of the top 10 differentially presented lipids is displayed in Figure 3b. High molecular weight Triacylglyceride (TG) with long polyunsaturated carbon side chains (~4 or more double bonds) were more prevalent in the 10 and 20% weight loss group compared with the control groups (Figure 3c,Supplementary Table 1 and Supplementary Figure 3). Conversely, TGs with a lower number of side chain carbons and fewer double bonds were less abundant in the control mice than in the mice with weight loss, especially the 20% weight loss group. In contrast to TG levels, phosphatidylcholine lipid (PC) levels were less abundant in the Nampt knockout mice with 10 and 20% weight loss relative to the tamoxifen and vehicle control mice (Figure 3d, Supplementary Table 1 and Supplementary Figure 3).
Liver transcriptome profile in Nampt−/− mice
To comprehensively investigate the effect of the Nampt gene knockout on the mouse liver transcriptome profile, we used RNA-seq to determine and compare hepatic gene expression changes between Nampt−/− and wild-type Nampt+/+ mice. A total 4638 genes with significantly differential expression (P-value <0.05) in Nampt−/− mice were identified, of which 2434 genes were upregulated and 2204 genes were downregulated (Supplementary Table 2). A total 2443 genes (52.6%) had >2-fold change (Figure 4a). Most of the genes (97.5%) were protein-coding genes, 34 genes were lincRNAs, 19 were antisense RNAs, and 232 genes coded for transcription factors. GO biological process and KEGG pathway enrichment for the 4638 genes were calculated (Supplementary Table 3 and Supplementary Table 4). The results showed that 476 biological processes and 57 significant KEGG pathways were enriched (P-value <0.05). GO biological process showed that 1050 genes were involved in 106 metabolic processes and 272 genes were involved in 43 biosynthetic processes. In 91 metabolic processes and 40 biosynthetic processes, there were more downregulated genes than upregulated genes (Supplementary Table 5). The examined KEGG pathways include metabolism of xenobiotics by cytochrome P450, drug metabolism, fatty acid metabolism, glutathione metabolism, nitrogen metabolism, and the citrate cycle, glycolysis/gluconeogenesis, and nicotinate and nicotinamide metabolism (Supplementary Table 4), which are pertinent to liver and Nampt functions. These results suggest that most metabolic and biosynthetic processes have been slowed down in Nampt−/− mice.
As adult Nampt−/− mice showed the similar intestinal villus atrophy and damage (Figure 2f) as adult replication protein A subunit3 (Rpa3, another proven essential gene) knockout mice, we compared expression levels of the liver Rpa3 gene and three other genes(Trp53, Atr and Mapk7), whose conditional homozygous knockouts caused the death,5, 12, 13 between Nampt−/− versus Nampt+/+ mice, to determine whether the Nampt−/− caused lethality is due to downregulation of these genes. Only the Rpa3 gene expression was significantly downregulated in Nampt−/− mice versus Nampt+/+ mice (2.40±0.75 versus 5.19±0.87, Supplementary Figure 4).
As intestinal swelling (Figure 2d), villus atrophy, and damage (Figure 2f) occurred in Nampt−/− mice, we surveyed significantly differentially expressed genes in 13-ion-associated transport processes of Nampt−/− mouse liver tissues, which may provide information about the gastrointestinal absorption or transport of ions and nutrients from the food supply. As presented in Figure 4b, 8 out of 13-ion-associated transport processes were downregulated. Furthermore, 47.3% of genes in the whole electron transport chain (53 genes in total) were downregulated, indicating that the normal function of the electron transport chain has been compromised (Supplementary Table 6). In mitochondrial ATP biosynthesis coupled electron transport, more genes were inhibited. The same trend was true of three other ATP involved processes (Figure 4c). Of note is that the expression of 16 enzymes in TCA were downregulated, except Pcx, which catalyzes the carboxylation of pyruvate to oxaloacetate involved in gluconeogenesis (Figure 4d).
We further focused on the analysis of those genes involved in carbohydrate and lipid metabolism (Supplementary Table 7). Most genes in glycolysis were downregulated, but most genes in gluconeogenesis were upregulated (Figure 4e). Expressions of 29 of 32 enzymes involved in fatty acid metabolism were downregulated (Figure 4f). These findings suggest that the Nampt gene knockout may result in a decrease of glucose and fatty acid metabolism and an augmentation of glucose synthesis by gluconeogenesis in mouse livers. We also noticed that the expression of the lipase-encoding genes (Lipc, Lipg), 2, 4-dienoyl CoA reductase genes (Decr1, Decr2), and the enoyl-CoA isomerase (Eci1) were all downregulated in Nampt−/− mice compared with the Nampt+/+ control mice. This may explain the increased accumulation of serum high polyunsaturated fatty acid containing TGs in Nampt−/− mice compared with the Nampt+/+ control mice (Figure 3c). To investigate whether the reduced circulating phosphatidylcholine (PC) levels in Nampt−/− mice (Figure 3d) might be explained by changes in transport, we examined the expression profiles for genes encoding PC transporters in our RNA-seq data (Supplementary Table 8). The expressions of several PC transporters, including Abca3, Abcb4, Pcyt1a, and Stard7, were decreased significantly in Nampt−/− mice compared with the Nampt+/+ mice.
Effect of Nampt gene knockout on NAD metabolism and NAD-involved gene expression
Nampt is a key enzyme in the cellular NAD synthesis of a mammalian salvage pathway from nicotinamide. However, the global effect and full repertoire of gene pools affected by the Nampt gene knockout are not fully characterized. The adult Nampt−/− mice have afforded us the opportunity to realize this goal. Figure 5a displays that in Nampt−/− mice, expression of nicotinamide nucleotide adenylyltransferase 1(Nmnat1), which catalyzes the formation of NAD+ from nicotinamide mononucleotide (NMN), was decreased significantly. Ectonucleotide pyrophosphatase/phosphodiesterase 3(Enpp3), which catalyzes the hydrolysis of pyrophosphate bonds in NAD+ to regenerate NMN, Nudix (nucleoside diphosphate linked moiety X)-type motif 12 (Nudt12), which cleaves NAD+ to AMP and NMN, and Nicotinamide riboside kinase 1 (Nmrk1), which catalyzes the nicotinamide-β-riboside to form NMN were all downregulated. Expression of three enzyme genes, Nt5c2: 5′-nucleotidase, cytosolic II (Nt5c2), 5′-nucleotidase, cytosolic IIIB (Nt5c3b), and Purine-nucleoside phosphorylase (Pnp), were all upregulated. Activation of these genes contributes to the generation of nicotinamide from NMN. All these interactions led to the decreased synthesis of NMN and hence NAD. Indeed, we found that NAD levels in liver tissue and jejunum tissue were decreased significantly in Nampt−/− mice versus Nampt+/+ mice and paralleled to their body weight loss. In liver tissues, NAD levels are significantly lower in 20 and 15% body weight loss groups than the control group (9.10±1.27 and 11.27± 2.27 versus 13.94±1.35 pmole/mg tissue protein; Figure 5b). In jejunum tissue, NAD levels are significantly lower in 20 and 15% body weight loss groups than the control group (2.66±0.59 and 2.93±0.38 versus 5.06±1.40 pmole/mg tissue protein). In both tissues, NAD levels are decreased in 5% body weight loss group too.
NAD is a critical cofactor for sirtuin protein deacetylase. We examined the Nampt gene knockout on the expression of seven sirtuin genes. RNA-seq revealed that expression of Sirt3, 4, and 5 in mitochondria were decreased significantly while expression of Sirt1 in nuclei was increased significantly in Nampt−/− mice versus Nampt+/+ mice (Figure 5d). Sirtuin protein controls mitochondrial function through the deacetylation of targets that include the FOXO protein family. We then examined the effect of sirtuin downregulation on the expression status of the liver-expressed FOXO protein family. Liver Foxo4 gene expression was inhibited significantly in the Nampt−/− mice (Figure 5d). Sirtuin–Foxo signaling may control the expression of a number of genes. Figure 5e shows that acetylated proteins are one of the two top affected protein families, accounting for 20% of 4638 significantly differently expressed genes in Nampt−/− versus Nampt+/+ mice.
Co-expressed genes of human NAMPT gene in human prenatal and pediatric livers
To relate what we learned about potential functions of the Nampt gene in mouse liver to NAMPT’s role in human liver, we examined the expression patterns of the NAMPT gene and its co-expressed genes in human prenatal and pediatric liver from an existing RNA-seq data set. The goal of this ‘guilt-by-association’ coexpression relationship analysis was to provide insights into potential functional roles of NAMPT and associated genes. After birth, expression of the NAMPT gene was upregulated significantly (171.98±18.47 FPKM postnatally, n=52 versus 5.69±1.34 FPKM prenatally, n=10, P<0.01; Figure 6a). Expression of NAMPT genes positively correlated with the children’s development and growth until puberty (Figure 6b). A total 1064 genes displayed the same expression pattern as the NAMPT gene (Supplementary Table 9). GO biological process enrichment of these co-expressed genes found that they are involved in several important processes: transcription, translation, regulation of cell death, metabolism, and noncoding RNA processing (Figure 6c). The top five involved molecular and cellular functions of these co-expressed genes include gene expression, cell death and survival, protein synthesis, cellular functions and maintenance, and molecular transport (Figure 6d). These results suggest that NAMPT may have similar roles in these processes and functional categories.
Our study represents the first scientific report, with concrete experimental evidence in a C57BL/6J mouse model, that Nampt is an essential gene in vivo. This claim is supported by the findings that the Nampt gene homozygous knockout (Nampt−/−) mice were embryonically lethal and Nampt−/− adult mice died within 5–10 days with 25.24±2.22% body weight loss. Although several groups – including ours – previously noted that Nampt gene homozygous knockout mice were embryonic lethal, none of them reported physical evidence.3, 14, 15, 16, 17 Here, we have presented the morphological and genotyping evidence of mouse embryos at both 8.5 and 11.5 d.p.c. (Figures 1d and e), clearly demonstrating that Nampt−/− mouse embryos had significantly smaller sizes and abnormal gross structures, and died before organogenesis. This ‘gold standard’ of evidence authenticates that the Nampt gene is an essential gene in living organisms.
In adult Nampt−/− mice, we found seven phenotypes: death at 5–10 days after the induction >20% body weight loss (Figure 2); decreased cell NAD levels of both liver and intestinal tissues (Figures 5b and c); intestinal swelling (Figure 2d); atrophic intestinal villi (Figure 2f); visceral fat depletion (Figure 2d); higher serum TG and lower serum PC levels (Figure 3). To unravel the molecular underpinnings of these processes, we utilized RNA-seq18 to profile mouse liver transcriptomes to gain transcriptional insights into the essential role of Nampt in living organisms. Several important themes have emerged. First, 4638 differentially expressed genes in Nampt−/− mouse livers (Figure 4a and Supplementary Table 2) affect 476 biological processes and 57 significant KEGG pathways, corroborating Nampt’s pleiotropic functions. Second, our study found that liver tissue and jejunum tissue NAD levels were decreased significantly in Nampt−/− mice versus Nampt+/+ mice (Figures 5b and c), confirming Nampt’s key role in cell NAD synthesis.2, 16, 19 RNA-seq revealed that in Nampt−/− mice, key enzymes in two other salvage pathways and the de novo synthesis pathway of NAD synthesis were significantly decreased. It would be of interest to determine whether NAMPT directly or indirectly inhibits expression of these genes. Third, RNA-seq analysis of mouse liver transcriptomes in Nampt−/− mice versus Nampt+/+ mice have provided a number of novel insights into the essential role of the Nampt gene. In Nampt−/− mice, genes encoding acetylated proteins and genes in gluconeogenesis were upregulated while genes in glycolysis, lipase and tricarboxylic acid cycle were downregulated (Figure 4d). TCA shutdown would decrease ATP synthesis. Without enough ATP, those ATP-dependent transporters – such as those in intestine involved in nutrient absorption or transport – would cease to function. RNA-seq analysis indicated that expression of most ion transporter genes were inhibited significantly in Nampt−/− mice (Figure 4b). In addition, ATP is needed to maintain normal tissue structural integrity. In Nampt−/− mice, the short supply of ATP may be responsible for disrupted intestinal architecture and villus atrophy (Figure 2f). This may also be due to the high rate of cell turnover in this tissue, which makes it more susceptible to energy deficiency. This could explain why, in clinical trials of cancer treatment, oral administration of FK866 or CHS828,20, 21 which inhibits NAMPT enzymatic activity, caused unwanted side effects dominated by gastrointestinal symptoms. It suggests that alternative routes of drug administration may avoid or minimize gastrointestinal side effects, and achieve better therapeutic efficacy. Of interest is that we found that Rpa3 gene expression was decreased by more than 50% in Nampt−/− mice (Supplementary Figure 4). The phenotype of disrupted intestinal architecture and villus atrophy in Nampt−/− mice looks similar to those in Rpa3−/− mice.5 It remains to be elucidated whether this effect is due to the direct regulation of the Nampt gene knockout on Rpa3 gene expression.
NAD is a critical cofactor for sirtuin protein deacetylase. In Nampt−/− mice, expression of mitochondrial Sirt3, Sirt4, and Sirt 5, especially Sirt3, were all diminished significantly while nuclear Sirt1 was augmented (Figure 5f), suggesting that Sirt3, instead of Sirt1, may have a key role in life among seven sirtuin proteins. This is in line with previous evidence by Yang et al.22 Sirtuins can regulate transcription by deacetylating transcription factors such as FOXO family. Among several common FOXO genes, expression of FOXO4 was inhibited significantly. The dysregulated Sirt3–Foxo4 axis may set up a chain of reaction to engender the dysregulation of a number of genes in Nampt−/− mice, becoming a death axis in Nampt−/− mice. Based on the transcriptional insights, we sum up a tentative schema in Figure 5f to explain Nampt−/−-induced death process. Briefly, the homozygous Nampt gene knockout causes a decrease in cell NAD synthesis, which leads to the dysregulation of NAD-dependent genes such as those encoding acetylated proteins including Sirt3–Foxo4 axis and especially the suppression of eight enzymes in TCA cycle. The resultant decreased ATP output may adversely affect other genes including Rpa3, ion and nutrient transporters, as well as disrupt normal intestinal tissue architecture, which hinders normal nutrient absorption and transport into the visceral organs and forces the mobilization and exhaustion of fat storage and all energy sources, culminating in mouse death.
It should be pointed out that Nampt’s functional roles may not solely depend on its enzymatic activity on NAD synthesis.23, 24, 25 In Nampt−/− mice, liver and intestinal NAD levels were only 20–30% lower than those in surviving adult Nampt+/+ mice. Thus, it is warranted to explore whether the disruption of non-enzymatic functions of Nampt also has a critical role in the dying phenotype of adult Nampt−/− mice.
Although most data in this study were derived from mice, transcriptional insights from the mouse liver transcriptome are largely confirmed by data derived from co-expressed genes of the NAMPT gene in human prenatal and pediatric liver samples (Figures 6a–d and Supplementary Table 9). These results strongly indicate that our findings are applicable to human studies. NAMPT has been implicated in the pathogenesis or therapeutic targets of a number of human diseases or conditions,4 such as acute respiratory distress syndrome,26 aging,27 cancer,28 coronary artery disease,29 diabetes, nonalcoholic fatty liver disease and obesity,30 rheumatoid arthritis, and sepsis.31 Recently, a small chemical molecule, P7C3 and its derivatives, has been found to exert neuroprotective activity in animal models of Parkinson’s disease, amyotrophic lateral sclerosis, and concussive injury.32 This compound was identified as an allosteric activator of NAMPT.33 Our study contributes global metabolic and transcriptional insights into Nampt’s essential roles and also provides potential leads to Nampt’s pleiotropic physiological functions and pathological roles applicable to disease in humans.
Materials and Methods
Generation of Nampt+/− mice and their timed pregnancy
A mouse (129/Ola) embryonic stem (ES) cell line (RRR084) harboring characterized insertional mutation in the intron-7 of mouse Nampt gene via gene-trap vector inactivation was obtained from BayGenomics (http://baygenomics.ucsf.edu), a consortium of research groups in the San Francisco Bay Area funded as part of the NHLBI's Programs for Genomic Applications.34 The verified RRR084 clone was injected into C57BL/6N (NCI) blastocysts to generate chimeras in the Johns Hopkins University School of Medicine (Baltimore, MD, USA) transgenic facility. The generated chimeric Nampt+/− mice were genotyped by PCR of their tail DNAs. The chimeric Nampt+/− mice were backcrossed with C57BL/6J for 10 generations before their usage. All mice were fed an AIN-76 A diet and water ad libitum. They were housed under controlled conditions (25±2 °C; 12 h light–dark periods). All mouse experiments were conducted in accordance with the NIH guidelines and were approved by the University of Missouri Kansas City Animal Care and Use Committee.
The early stages of Nampt gene mutant mouse embryos were obtained by timed pregnancy after breeding between Nampt+/− male and Nampt+/− female mice. Visual observation of a vaginal plug in female Nampt+/− mice after the mating was counted 0.5 days post coitum (d.p.c.). Mouse embryos at 8.5 or 11.5 d.p.c. were harvested and fixed in 4% paraformaldehyde for 24 h. The genotyping of mouse embryos was done by PCR amplification of yolk sac DNA. Mouse embryos at 8.5 d.p.c. were also subjected to β-Gal staining.
Generation of Nampt gene exon 2 floxed (NamptF/F) and Nampt−/− mice
A Nampt gene target vector prepared in our lab, in which the exon 2 of Nampt gene was floxed, was electroporated into a B6-White Murine ES Cell Line (cat. no. SCR011, EMD Millipore, Billerica, MA, USA) and injected into C57BL/6J mouse blastocysts in The Transgenic Animal Core, University of Missouri, Columbia, USA. The generated chimeric NamptF/F mice were verified by PCR analyses of their tail DNAs.
Adult Nampt−/− mice were generated by mating NamptF/F mice with B6.Cg-Tg(CAG-cre/Esr1*)5Amc/J(Stock No:004682, Jax Lab, Bar Harbor, ME, USA) followed by administering tamoxifen induction.
Histological examination of mouse intestinal tissues
Formalin-fixed mouse intestinal tissue samples were embedded in paraffin, and 5-micron-thick sections were cut. Replicate sections were stained with hematoxylin and eosin (H & E) according to standard methods.
Mass Spec analysis of mouse serum lipid levels
The serum samples were collected and stored at −80 °C until analyzed. The samples were extracted and subjected to the ultra-high performance liquid chromatography – high resolution mass spectrometry UHPLC-HRMS procedure as outlined by Oliver Fiehn’s group35 and (http://www.metabolomicsworkbench.org/protocols/getprotocol.php?file_id=163). The analysis was conducted on a Waters Acquity UPLC coupled to a Waters Xevo G2-qTOF (quadrupole time-of-flight) mass spectrometer. The samples were analyzed in positive electrospray mode, and the data were acquired using the MSe acquisition format with a scan rate of 2 Hz. High-energy MSe scans were ramped from 15 eV to 30 eV. A leucine enkaphlin (2 μg/ml) solution was used as lockspray solution. Data processing, including chromatographic alignment and peak picking occurred in Progenesis QI 2.0. Potential markers were identified by matching the molecular ion (5 p.p.m. error) and fragment ions (50 p.p.m. error) to the lipidblast database using the database search feature within progenesis QI. Further processing occurred by exporting the data to EZinfo 3.0.
Mouse liver RNA isolation
Total mouse liver RNA was isolated from either the wild-type mice or Nampt−/− mice using the MirVana kit (cat. no. AM1560, ThermoFisher Scientific, Grand Island, NY, USA) according to the manufacturer's instructions.
RNA sequencing of mouse liver transcriptomes
RNA-seq of mouse liver RNAs was carried out in the Core of Genetic Research, Children’s Mercy, Kansas City, KS, USA, according to the previously published protocol36 except that sequencing library from 1 μg total mouse liver RNA of each sample was prepared using the Illumina TruSeq Stranded Total RNA Sample Prep Kit (cat. No. RS-122-2201) and 2 × 101 paired-end sequencing of high output run mode was performed using the HiSeq 1500 instrument. Each sample was sequenced to an average depth of ~63 million reads with >80% of bases above Q30. The resulting base calling (.bcl) files were converted to FASTQ files using Illumina’s bcl2fastq v220.127.116.11 software. Mapping of RNA-seq reads and transcript assembly and abundance estimation were conducted using Tuxedo Suite pipeline (TopHat v1.3.0/Bowtie v0.12.7/Cufflinks v1.0.3) and reported in Fragments Per Kilobase of exon per Million fragments mapped (FPKM).
Functional analysis of differentially expressed gene lists using Ingenuity Pathway Analysis
The pathway analysis of differentially expressed gene lists in Nampt−/− mice were analyzed using DAVID (https://david.ncifcrf.gov/)37 and Ingenuity Pathway Analysis (IPA, Ingenuity Systems, Inc., Redwood City, CA, USA) as we described before.38, 39 Briefly, genes with a significant expression change (P<0.05) in mouse liver expression in Nampt−/− mice versus wild-type mice were loaded into IPA and they were associated with various pathways in Ingenuity's Knowledge Base for the analysis. The significance of the association between the data set and any pathway was measured in two ways: (i) the ratio of the number of molecules from the data set that map to the pathway divided by the total number of molecules that map to the pathway, and (ii) Fisher's exact test was used to calculate a P-value determining the probability that the association between the genes in the data set and the pathway in IPA is explained by chance alone. Transcription factor prediction database (DBD)40 and Database of Essential Genes (DEG)41 were used to annotate mouse transcript factors and essential genes for differentially expressed gene list.
Human pediatric liver samples and RNA-seq analysis
Forty-eight, anonymized pediatric liver samples, ages 0 days to 17 years, were received from the following sources: the NICHD Brain and Tissue Bank at the University of Maryland (funded by NIH contract HHSN275200900011C, Ref. No. #N01-HD-9-0011); the Liver Tissue Cell Distribution System (funded by NIH Contract #N01-DK-7-0004/HHSN267200700004C); and six samples were received from XenoTech, LLC (Lenexa, KS, USA), to whom we are grateful for their generous gift of tissue samples. Thirty-four prenatal human liver samples (57–196 days, post-conception) were received from an additional NICHD-funded tissue retrieval center, the Central Laboratory for Human Embryology (University of Washington, Seattle, WA, USA). All tissues were flash frozen and maintained at −80 °C before isolation of DNA and RNA. All the samples were from anonymous, deceased donors, and the use of these tissues was declared as nonhuman subjects research by the University of Missouri-Kansas City Pediatric Health Sciences Review Board.
RNA-seq analyses of human pediatric liver samples were carried out as described above for mouse liver transcriptome analyses.
Measurement of mouse liver and jejunum NAD+/NADH levels
Mouse liver and jejunum tissues (10–30 mg) were homogenized and the supernatants were applied for NAD+/NADH assays using a Fluorimetric NAD+/NADH assay kit (Cat. No. 15263; AAT Bioquest. Inc. Sunnyvale, CA, USA).
Statistical analyses were performed using the Sigma Stat (ver 13.0, Systat Software, Inc., San Jose, CA, USA). Results are expressed as means±S.D. of more than three samples for each group from at least two independent experiments. Two group comparisons were done by unpaired t-test. Three or more group comparisons were carried out using ANOVA followed by a Holm–Sidak test, P<0.05 was considered statistically significant.
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We thank Marianne N Nsumu and Suman Chaudhary for excellent technical assistance. Our research has been in part supported by National Institutes of Health Grant HL 080042 (SQY), the start-up fund and William R Brown/Missouri Endowment of The Children’s Mercy Hospitals and University of Missouri at Kansas City (SQY).
LQZ, SQY, D-YL, and JSL conceived the project. LQZ, DPH, MX, DNG, LG, CB, and SQY analyzed the data and wrote the manuscript. LQZ, DPH, LVH, PH, XJ, and RG performed the experiments. GW, LL, and MW had inputs on the experimental designs and critically read the manuscript.
The authors declare no conflict of interest.
Edited by Shui Qing Ye
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Zhang, L., Van Haandel, L., Xiong, M. et al. Metabolic and molecular insights into an essential role of nicotinamide phosphoribosyltransferase. Cell Death Dis 8, e2705 (2017). https://doi.org/10.1038/cddis.2017.132
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