NAD+ supplementation has significant benefits in compromised settings, acting largely through improved mitochondrial function and DNA repair. Elevating NAD+ to physiological levels has been shown to improve the function of some adult stem cells, with implications that these changes will lead to sustained improvement of the tissue or system. Here, we examined the effect of elevating NAD+ levels in models with reduced hematopoietic stem cell (HSC) potential, ATM-deficient and aged WT mice, and showed that supplementation of nicotinamide riboside (NR), a NAD+ precursor, improved lymphoid lineage potential during supplementation. In aged mice, this improved lymphoid potential was maintained in competitive transplants and was associated with transcriptional repression of myeloid gene signatures in stem and lineage-committed progenitor cells after NR treatment. However, the altered transcriptional priming of the stem cells toward lymphoid lineages was not sustained in the aged mice after NR removal. These data characterize significant alterations to the lineage potential of functionally compromised HSCs after short-term exposure to NR treatment.
Nicotinamide adenine dinucleotide (oxidized form, NAD+) is a critical coenzyme with broad physiological functions, including the regulation of metabolism and DNA repair. Decreased levels of NAD+ are often associated with impaired conditions, such as those found in models of cancer, metabolic disorders, neurodegeneration, as well as physiological and accelerated aging processes1,2,3,4. Recent studies have highlighted significant improvements of compromised systems after NAD+ levels have been elevated through supplementation with NAD+ precursors including nicotinic acid, nicotinamide, nicotinamide mononucleotide, or nicotinamide riboside (NR)5,6,7,8.
We recently examined the role of NAD+ supplementation in models of ataxia–telangiectasia (A–T), which is a disorder caused by mutations (ATM)9,10,11. A–T is a rare autosomal recessive disease with patients showing uncoordinated movement, telangiectasia, radiosensitivity, severe cerebellar atrophy, and distinct features of accelerated aging12. Murine models of ATM loss show defects in DNA damage repair associated with mitochondrial dysfunction13 and loss of hematopoietic stem cell (HSC) potential14. Supplementation of NR in models of A–T led to significantly improved lifespan and healthspan, mediated by improvement of both DNA damage repair and mitophagy in the tissues examined1,11,15. However, the role of NR supplementation on the hematopoietic system and stem cell compartment has not yet been explored in this model.
The hematopoietic system includes the cells that give rise to and reside in the blood. Blood cells can be divided into three lineages: myeloid, lymphoid, and erythroid. Myeloid cells have roles in innate immunity and include neutrophils, megakaryocytes, and macrophages. Lymphoid cells, including B and T cells, are responsible for adaptive immunity. Erythroid cells, or red blood cells, are key for the oxygen transport to cells throughout the body and deliver carbon dioxide to the lungs. Alterations in the balance of these cell types can lead to compromised function of the blood system. HSCs are responsible for maintaining homeostasis of the system and providing the capacity for repair and restoration after injury or stress. It is thought that some aberrant phenotypes within the hematopoietic system may be attributed to functional alterations of the stem cell compartment. Conversely, restoration of potential to dysfunctional HSCs may lead to long-term improvements of the hematopoietic system given HSCs’ unique self-renewal potential and ability to give rise to all cells within the hematopoietic system.
Here, we investigate the effects of supplementation of the NAD+ precursor NR on dysfunctional HSC compartments, from Atm−/− and normal aged mice, to examine possible improvement of HSC potential. Our results showed significant alterations in lineage commitment of HSCs after NR treatment, with enhanced lymphoid potential. This correlated with changes in inflammatory cytokines and transcriptional alterations of the HSCs. While transplantation of aged NR-treated HSCs reproduced the enhanced lymphoid output seen in the transcriptional profiles, the changes in potential are not sustained after NR withdrawal in the aged mice, and the rebound phenotype appear to exacerbate aging phenotypes. Our results highlight the importance of the duration of NR exposure and the timing of initial exposure to derive robust, balanced lineage outputs from HSCs.
NR supplementation increases lymphoid-progenitor cell frequencies in young Atm −/− bone marrow
Given the robust improvement in life and healthspan after NR treatment in models of A–T1,11,15, we first investigated the response of the hematopoietic system after supplementing Atm−/− mice (ATM) and littermate Atm+/+ controls (WT) with a precursor of NAD+. Examination of hematopoietic progenitor cells in whole bone marrow (WBM) showed that NR-treated Atm−/− mice had significantly increased common lymphoid-progenitor (CLP) frequency compared to the nontreated Atm−/− mice (Fig. 1a and Supplementary Fig. 1). While NR treatment did not drive significant changes in the frequencies of the LSK (Lin−Sca1+cKit+) and HSC compartments of Atm−/− mice, we did see significant aging-like phenotypes (increases) in these compartments in the Atm−/− mice compared to WT (Fig. 1b, c). Consistent with the increased frequency of CLP in NR-treated Atm−/− mice, MPPFlk2+ (including lymphoid-primed multipotent progenitors (LMPPs)16 and similar to MPP417,18) frequency was also significantly increased compared to untreated Atm−/− mice (Fig. 1d).
Changes of the lymphoid lineage progenitors in NR-treated Atm−/− mice could be driven by differentiation choices of the earliest progenitor cells or through improved systemic environments supporting lymphoid-primed cell types. To determine if there were changes in the frequency of lineage-biased HSCs, we used CD150/Slamf1 to subfractionate the LSKCD34−Flk2− cells19. We did not observe changes in the composition of the HSC compartment, with similar frequencies of balanced (Slamf1Low) and myeloid-biased (Slamf1High) HSCs both before and after NR treatment (Fig. 1e). However, the myeloid-biased HSCs contribute only modestly to the young WT and Atm−/− HSC compartments, while the majority of HSCs already can robustly contribute to lymphoid output and NR effects may not be readily reflected in changes of these HSC compartments.
NR supplementation improves HSC lymphoid potential in aged mice
Given that Atm−/− mice display many physiologic aging phenotypes and supplementing the Atm−/− mice with NR led to increased lymphoid-progenitor cells (Fig. 1), we wanted to examine if NAD+ supplementation could have similar positive effects on aged wild-type mice. Analysis of progenitor cells from marrow of young and old C57BL/6J mice showed the expected decrease in frequencies of lymphoid progenitors (CLPs) in the old untreated mice (O-WT) compared to young mice (Y-WT)20. After NR treatment (O-NR) the CLP compartment frequency increased but did not return to levels in young mice (Y-WT) (Fig. 2a). NR treatment of old mice did not significantly decrease compartments that expand with age, including LSK (Supplementary Fig. 2a, b), HSC (Fig. 2b), or Slamf1High (Supplementary Fig. 2c) cells, and NR did not show any effect on the young bone marrow compartments examined (Fig. 2 and Supplementary Fig. 2).
Though there were modest changes to the frequencies of the stem cells, we sought to address if NR supplementation affects the functional potential of HSCs from different ages with competitive transplants. Flow cytometric analysis of peripheral blood 4 months post transplant showed the expected decrease in old HSC donor contribution but there were no significant differences in chimerism derived from old HSCs after NR treatment (Fig. 2c). However, analysis of the lineage contribution from donor HSCs demonstrated old NR-treated HSCs have a more balanced lineage output, with a significant reduction in the frequency of the myeloid cells compared to untreated old HSCs (Fig. 2d and Supplementary Fig. 3).
NR treatment reduces inflammation in old C57BL/6 mice
To examine if the number of myeloid cells also decreases in the aged animals after NR supplementation, we examined complete blood cell counts in treated and untreated mice. The results showed the expected increase in neutrophils in the aged blood compared to young blood, but in aged, NR-treated mice there was a trend toward decreased neutrophil count (Fig. 3a). Examination of the distribution of myeloid lineage cells with flow cytometry showed a significant reduction in the frequency of neutrophils, yet an increase in inflammatory monocytes21,22 when comparing O-NR to O-WT mice (Fig. 3b).
Neutrophils and monocytes are implicated in the context of diverse inflammatory responses and also can be functionally involved though the intermediate of cytokine production23,24. Given the intimate association between inflammation, myeloid cells, and aging23, we wanted to examine if NR treatment in aged mice might affect inflammatory signals. Using a commercially available immunoassay of murine inflammatory cytokines, we show old mice have higher levels of inflammatory cytokines compared to young mice, with 7 of the 13 cytokines examined significantly elevated in circulation of aged mice. Notably, after NR treatment in old mice, there was a significant decrease in the levels of 11 of the 13 examined inflammatory cytokines compared to old untreated mice (Fig. 3c). These data suggest short-term NR treatment in inflamed environments, such as aged mice, leads to a significant reduction in inflammatory signals, corresponding to a decrease of granulocytes yet a significant increase in the inflammatory monocytes.
Previous studies have shown inflammatory cytokines such as IL-1β and TNFα can affect HSCs by promoting myeloid differentiation at the expense of lymphoid differentiation25,26,27,28, thus we wanted to examine if global decreases in inflammatory cytokines are necessary to drive alterations in lineage potential of the aged HSCs or if direct NR supplementation could drive lineage potential alterations seen when NR-treated HSCs were transplanted. To address this, we performed ex vivo culture assays with conditions promoting B-cell differentiation. Three independent experiments were performed with a minimum of 6 replicates per condition (average of 12 replicates). Analysis of total B220+ cells derived from young and aged HSCs showed reduced B220+ cell output from the aged HSCs compared to young HSCs (Fig. 3d); however, direct supplementation of NR in vitro did not contribute to significantly improved B-cell output from HSCs. Notably, in vitro supplementation of NR to CLPs had significantly negative effects on the B-cell output of both young and old cells (Fig. 3d).
NR supplementation leads to transcriptional alterations in aged HSCs
Given the positive effects of improved lymphoid output appear to require additional endogenous signals and that different progenitor cells responded differently to NR ex vivo (Fig. 3d), we wanted to examine if there were cell-intrinsic alterations in the aged progenitors after NR treatment in vivo. Transcriptional changes were evaluated by generating total RNA sequencing (RNA-seq) datasets of HSC, CLPs, and granulocyte–monocyte progenitors (GMPs) isolated from old WT (O-WT) and NR-treated (O-NR) mice. Principle component analysis (PCA) showed that specific progenitors cells cluster together, supporting the reproducibility of the data (Fig. 4a). These data also showed each of the cell types had changes in their transcriptional landscape after NR treatment (Fig. 4a). The progenitor cells with the greatest differences in transcription were the HSCs (Fig. 4a, b). The majority of the significant transcriptional changes were decreases in expression in all progenitors: HSC-NR: 403, CLP-NR: 232, and GMP-NR: 121. Overall, the transcription of myeloid progenitors was least affected by the NR treatment (Fig. 4b and Supplementary Table 1). Gene set enrichment analysis (GSEA) revealed that the glycolysis pathway was repressed in all NR-treated progenitor cells (Fig. 4c), similar to human muscle cells after NR29. The upregulated oxidative phosphorylation and mitophagy pathways, together with downregulated hypoxia and inflammatory response pathways, indicate a reduced stress state30 (Fig. 4c), which is consistent with the observation that NR treatment reduces the level of inflammatory cytokines in aged mice (Fig. 3c). To address if these transcriptional changes correlated with differences in mitochondrial potential, we stained HSCs, LSKs, lineage negative (Lin−) and positive (Lin+) cells with TMRM, and the efflux pump inhibitor, verapamil. We saw HSCs had more robust mitochondrial potential than differentiated cells, but there were no significant alterations in potential after NR treatment in any population we assayed (Fig. 4d).
Looking for specific enrichment of pathways relevant to hematopoiesis, we found that after NR treatment the stem and progenitor cells decreased expression of genes robustly expressed in myeloid progenitor cells compared to lymphoid-progenitor cells (Fig. 4e and Supplementary Fig. 4, GSE37301_CLP_VS_GMP_Down). These data further support the intrinsic alterations of stem and progenitor cells contributing the shift from myeloid toward more lymphoid lineage after NR treatment.
Alterations driven by NR supplementation are not sustained after NR withdrawal
Given the improved lymphoid output in NR-treated aged HSCs, we also wanted to evaluate if these NR-driven phenotypes could be sustained after NAD+ supplement removal in an aged environment. We analyzed old mice treated with NR that received a 2-month washout period. NR supplement-directed changes in frequency seen in the primitive compartments (CLP and HSC) were significantly reversed after withdrawal of NR (O-NR-RC: Fig. 5a, b). The same rebounding effect was also seen in the myeloid cell compartment of the peripheral blood (Fig. 5c), in which the neutrophil compartment (reduced after NR treatment) becomes the predominant population after NR withdrawal. Given these striking reversals of progenitor cell and peripheral blood composition after supplement removal, we purified HSCs from the old NR-RC mice and performed RNA-seq analysis. PCA clustering among the three groups of isolated HSCs shows the O-WT separate furthest away from both the O-NR and O-NR-RC groups (Fig. 5d). Further, the O-NR-RC HSCs do not revert back toward the O-WT HSCs on two main component axes (PC1 or PC2), but instead move away from O-NR HSCs in a different trajectory. We found 107 significantly upregulated and 126 significantly downregulated transcripts between O-NR and O-NR-RC HSCs (Fig. 5e). Pathways previously implicated in NR benefits and examined in Fig. 4c were evaluated in HSCs after the removal of NR (Fig. 5f). We see in these pathways the NR-RC HSCs do not revert back toward WT expression. For both OxPhos and mitophagy, after NR, there is an enhancement of transcripts involved in those pathways. After removal of NR, there is decreased expression of these pathways, and reversion of expression is to an extent that is even lower that what was seen originally in old-WT HSCs (NRRC < WT < NR). Similarly, the increased expression of genes involved in the inflammatory pathway in O-NR-RC HSCs overshoot the expression levels of these genes in old WT HSCs (NR < WT < NRRC). NR-RC transcripts involved in hematopoietic specific comparisons (GMP vs CLP) as well as hypoxia were at intermediate levels, between the NR and WT conditions (NR < NRRC < WT). Finally, for genes associated with glycolysis, instead of reversion toward or beyond the expression levels in the WT HSCs, their expression in O-NRRC HSCs is even lower than in the NR-treated old HSCs (NR-RC < NR < WT). These data suggest that removal of the supplement does not lead to direct reversion back toward untreated states, but instead may have exaggerated negative effects on the hematopoietic system.
To examine hematopoietic signatures in the NR-treated HSC and after NR removal, we used CellRadar31 to compare genes up- and downregulated in the HSC transcriptomes against published lineage associated genes. After NR treatment, compared to WT, the NR HSCs are enriched for profiles associated with lymphoid-progenitor cells including CLPs and LMPPs, while depleted for profiles associated with HSCs or myeloid cells (Fig. 5g). These expression profiles mirror the lineage output of the NR-treated mice as well as the change in lineage potential during HSC transplant paradigms (Fig. 2). After the washout period, the NRRC HSCs have a more HSC-centric profile and elevated expression of genes associated with myeloid and erythroid progenitor populations (Fig. 5g). The NRRC HSCs also show repressed monocyte signatures (Fig. 5g), which corresponds with cell composition changes seen in the hematopoietic system after withdrawal of the supplement (Fig. 5a–c). Together, these data suggest that cell-intrinsic alterations contributing to improved lymphoid potential in the aged environment are not sustained after NR withdrawal, and that withdrawal in an aged environment may lead to more severe myeloid skewing compared to normal aging.
The improved lymphoid lineage potential in mice with compromised hematopoietic systems after NR treatment suggests that elevated NAD+ levels could provide a more favorable systemic environment for these cells and/or promote differentiation toward lymphoid cell types. In both the Atm−/− and aged environments, there is an associated loss of NAD+ levels compared to young, healthy mice32,33, and global administration of the NR likely has a direct effect not only on stem cells, but on all hematopoietic cells. In anecdotal data, NAD+ levels were elevated in bulk bone marrow cells after oral administration at concentrations used in our experiments. Of note, many hematopoietic cells express the NAD+ glycohydrolases CD38, CD157 (BST-1), and RT-6 (with robust expression on many lymphoid cell types)34,35,36 and elevating circulating levels of NAD+ may improve substrate availability to those cells. However, improved environmental stimuli cannot be the only contributing factor driving the altered lineage potential seen in the impaired systems after NAD+ supplementation, as transplants of purified HSCs from the NR-treated aged mice show long-term phenotypes of improved lymphoid output (Fig. 2d).
While investigating the environmental contribution to the altered lineage potential, we detected a general decline in inflammatory cytokines in the circulation of NR-treated old mice (Fig. 3c). Of particular interest, regarding the function of HSCs, is the reduction of the IL-1 cytokine level, which has been shown to play a critical role in driving HSC myeloid differentiation28. This decline in myeloid differentiation potential may be contributing to the decreased numbers of neutrophils (Fig. 3a, b). As neutrophils are mediators of inflammation, responding to signals and producing cytokines and other inflammatory factors regulating inflammation37,38, reduction of these cells would dampen the feedback loop of increased inflammatory cytokines and increased myeloid cell production. However, this decrease in neutrophils is also associated with an increase in frequency of inflammatory monocytes, but CBC data show the numbers of monocytes remains lower in NR-treated mice (data not shown). This global decrease in myeloid differentiation could then allow for increased frequencies of lymphoid progenitors and decreased overall inflammation, mitigating two major negative features in aged hematopoiesis. We also noted that the decline in inflammatory factors we see after short-term NR supplementation in both the aged (Fig. 3c) and Atm−/− mice39 overlapped with those reported (IL-6 and TNF-α) in a study of oral NR supplementation in humans29.
We were unable to reproduce the improved lymphoid potential of either HSCs or CLPs with direct exposure to NR in ex vivo culture conditions (Fig. 3d) though the improved lymphoid potential of old HSCs was maintained in transplanted young, irradiated recipients (Fig. 2d). This is possibly due to suboptimal differentiation conditions ex vivo or the inability to reproduce the systemic changes of NR supplementation that may contribute to the altered potential of the primitive cells. To characterize the lasting effects of NR exposure in the aged mouse, we provided a 2-month washout. We saw that the improved lymphoid output seen after NR was not sustained in the aged environment after supplement removal. Together, this suggests that the transcriptional changes of the progenitor cells are augmented by environmental stimuli—associated either with a young-recipient environment or NAD+ supplemented aged environment—and the combination is required to sustain the improved lymphoid lineage output.
Using transcriptome analysis to address changes in progenitor cells that could contribute to functional alterations in the treated HSCs, we did not see striking differences in genes implicated in other studies of NAD+ repletion, such as the sirtuin genes, Parp1, or even Cd38 when comparing NR-treated old HSCs to untreated old HSCs (data not shown). We also did not see significant changes in overall mitochondrial DNA content after NR treatment (data not shown) or in mitochondrial membrane potential associated with the improved functional potential of HSCs after NR (Fig. 4d). One potential caveat is that we did not directly measure HSCs’ mitochondrial function, and we did see a minor increase in the expression of PGC-1α, which encodes the protein PGC-1α, a master regulator of mitochondrial biogenesis, in O-NR HSCs compared to O-WT. This expression change, however, did not reach our minimal significance threshold of FDR < 0.05. Since NAD+ coordinates both mitochondrial biogenesis (e.g., via PGC-1α) and the elimination of damaged mitochondria via mitophagy, it may lead paradoxical reports on either increased or reduced mitochondrial content by NAD+ in different conditions2,4,40.
Though we see improvement after NR supplementation in the deficient (Atm−/− or old) HSCs, we did not see the recently reported improved HSC potential after 1 week of NR treatment in young mice41. These differences could be due, in part, to the duration of treatment, the vehicle for administration of NR, gender differences (male vs female), and potentially background strain differences between the groups. Thus, it will be important to further examine some of these key differences, with particular focus on duration of NR treatment and effects on robust versus compromised hematopoietic environments.
While more than seven phase I clinical trials have shown NR supplementation drives elevated NAD+ levels in the blood and is well tolerated in middle and old aged individuals4,42, potential translation of benefits from NAD+ supplementation in human hematopoiesis remain unresolved. Our data suggest that NR administration in compromised hematopoietic systems (NAD+ depleted system) drives cell-intrinsic changes of the HSC compartment together with an overall reduction in circulating inflammatory cytokines. However, once the aged system has been exposed to NR, the effects of removing the supplementation may have undesirable consequences. Thus, once a deficient system is exposed to NAD+ supplementation, to maintain the benefits we have demonstrated, the regimen may need to be sustained long-term.
The ATM heterozygous strain (B6;129S4-Atmtm1bal/J) was purchased from The Jackson Laboratory and bred at the NIA facility. After weaning, Atm−/− mice and Atm+/+ littermates were given NR (12 mM) from ChromaDex in drinking water. Mice used in the aging studies were C57BL/6 males: young (3–4 months) and old (24–29 months). NR was supplemented for 4–6 weeks11. In condition of NR supplementation, water bottles were changed twice a week. All animal experiments were performed under protocols approved by NIA Institutional Animal Care and Use Committees. Transplant recipient and competitor cells were young female B6.SJL-Ptprca Pepcb/BoyJ (CD45.1) from The Jackson Laboratory.
Purification of cells
For HSC sorting, bone marrow was first selected as c-Kit positive (PE-cKit antibody and EasySep™ PE Positive Selection Kit II). Enriched cells were stained with antibodies against lineage (Ter119 (BioLegend, 116232, 1/200), B220 (BioLegend, 103227, 1/200), Mac1 (BioLegend, 101224, 1/200), CD3 (BioLegend, 100214, 1/200), Gr1 (BioLegend, 108434, 1/200), IL-7Rα (BioLegend, 135024, 1/200)), cKit (BioLegend, 105808, 1/200), Sca1 (BioLegend, 108126, 1/200), CD34 (eBioscience, 11-0341-85, 1/50), Flk2 (BioLegend, 135310, 1/50), CD150 (BioLegend, 115914, 1/200), and PI and sorted as PI-Lin-cKit+Sca1+CD34-Flk2-CD150+.
A total of 200 HSCs pooled from donor mice were transplanted into lethally irradiated (9.56 Gy) recipients against 2 × 105 competitor (CD45.1) WBM cells. Peripheral blood analysis was performed at 4-week intervals post transplantation.
Peripheral blood analysis
CBC data collected using a Hemavet 950FS and frequencies of populations were generated using flow cytometry after ACK treatment and staining with for Ter119 (BioLegend, 116228, 1/100), B220 (BioLegend, 103224, 1/100), Mac1 (BioLegend, 101216, 1/100), CD3 (BioLegend, 100244, 1/100), and Gr1 (BioLegend, 108406, 1/100) and PI (Supplementary Table 2). CD45.1 (BioLegend, 110714, 1/100) and CD45.2 (BioLegend, 109820, 1/100) antibodies were included in transplant blood analysis.
Bone marrow cells were ACK treated and then stained with antibodies Ter119 (BioLegend, 116204, 1/100), B220 (BioLegend, 103204, 1/100), Mac1 (BioLegend, 101204, 1/100), CD3 (BioLegend, 100244, 1/100), Gr1 (BioLegend, 108404, 1/100) (Lin), cKit, Sca1, CD34, Flk2, CD150, IL-7Rα FcγRα (eBioscience, 45-0161-82, 1/100), and PI (Supplementary Table 2). Biotinylated antibodies were stained using Streptavidin-Pacific Orange (Thermo Fisher Scientific) before staining PI. Posttransplant marrow was stained with antibodies Ter119, B220, Mac1, CD3, Gr1, IL-7Rα (Lin), cKit, Sca1, CD34, Flk2, CD150, FcγRα, CD45.1 (BioLegend, 110728, 1/100), CD45.2, and PI.
Serum cytokine assays
Blood was collected by cardiac puncture at the time of sacrifice. After 15 min room temperature incubation, samples were centrifuged at 500 × g for 15 min at 4 °C. The sera were collected and stored at −25 °C. Serum cytokines were assayed using LEGENDplexTM (BioLegend) according to the manufacturer’s instructions. For data acquisition and analysis, a CytoFLEX (Beckman Coulter) and LEGENDplex v.8 data analysis software were used, respectively.
Ex vivo culture analysis
A total of 100 HSCs were cultured in 0.2 mL of αMEM supplemented with 10 ng/mL of Flt3L, 5 ng/mL of IL-3, 20 ng/mL of IL-7, 50 ng/mL of SCF, 100 mM of β-MEM, 20% of FBS, and NR (0.0 or 2.5 mM) in 96-well flat bottom plates precoated with OP9 cells (ATCC) at 4 × 104 cells/well. A total of 100 CLPs were cultured in 0.2 mL of ExVivo15 with 100 ng/mL of Flt3L, 20 ng/mL of IL-7 and SCF, 50 mM of β-MEM, 1% of BSA, and NR (0.0 or 2.5 mM) in 96-well round bottom plates. After 48 h with NR, the media were replaced with fresh media excluding NR. The media were replaced every 3–4 days. After 14 days (HSC) or 10 days (CLP) of culture, cells were analyzed by flow cytometry for the differentiation to B cells (B220+). Culture plates were maintained at 5% CO2 and O2 at 37° C. Recombinant mouse cytokines were purchased from Peprotech.
Mitochondrial membrane potential assay
Sorted cells were incubated with 2 nM tetramethylrhodamine, methyl ester, perchlorate (TMRM) in StemSPAN SFEM supplemented with 50 ng/mL SCF and TPO, and 50 µM verapamil for 60 min at 37° C followed by a wash. PI with 2 nM TMRM was used for dead cell exclusion and data were collected on a FACSAria Fusion. Flow data analysis was performed using FlowJo.
RNA-seq and analysis
RNA was purified with TRIzol™ Reagent and Direct-zol RNA Microprep. RNA-seq libraries were constructed using SMARTer Stranded Total RNA-Seq Kit v2 - Pico Input Mammalian according to the manufacturer’s protocol. Sequencing was done on Illumina HiSeq 2500 instrument using 2 × 105 bp reads.
A total of 2.2 billion sequencing reads were used, with an average of 62 million reads per sample. For analysis of transcriptome datasets, we built an index sequence for STAR using the Gencode M22 reference feature including protein-coding and noncoding genes. Prior to sequence alignment, we applied trim galore (version 0.4.3) with cutadapt package (version 1.12)43 to remove any unnecessary genomic fragments (e.g., adapter dimers) and low-quality nucleotide sequences from the raw reads. We mapped adapter trimmed sequencing reads to the mouse reference genome (mm10) using STAR aligner44 and calculated the raw count using featureCounts package (gene level)45. Differentially expressed transcripts (DETs) lists were generated with edgeR using cutoff: fold change > 1.5, CPM > 3, FDR < 0.05, or p value < 0.0146. GSEA was performed for pathway analysis47. Visualization of the DET profiles in HSCs was performed using software CellRadar31.
Prism software (GraphPad) was used for statistical analyses. Statistical analysis used in this study was Kruskal–Wallis test or two-way ANOVA. Data are presented as mean ± S.E.M. and q value (Kruskal–Wallis test) or p value (two-way ANOVA) < 0.05 were the minimal threshold for statistical significance. The statistical parameters and number of samples can be found in the figure legends.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
RNA-seq data are available on GEO with accession number GSE147662.
No new code was generated or used in this manuscript and RNA-seq analysis code is publicly available at https://github.com/Zhang-lab/TaRGET-II-RNAseq-pipeline.
Fang, E. F. et al. NAD(+) in aging: molecular mechanisms and translational implications. Trends Mol. Med. 23, 899–916 (2017).
Fang, E. F. et al. Defective mitophagy in XPA via PARP-1 hyperactivation and NAD(+)/SIRT1 reduction. Cell 157, 882–896 (2014).
Das, A. et al. Impairment of an endothelial NAD(+)-H2S signaling network is a reversible cause of vascular. Aging Cell 173, 74–89 (2018).
Lautrup, S., Sinclair, D. A., Mattson, M. P. & Fang, E. F. NAD(+) in brain aging and neurodegenerative disorders. Cell Metab. 30, 630–655 (2019).
Verdin, E. NAD(+) in aging, metabolism, and neurodegeneration. Science 350, 1208–1213 (2015).
Rajman, L., Chwalek, K. & Sinclair, D. A. Therapeutic potential of NAD-boosting molecules: the in vivo evidence. Cell Metab. 27, 529–547 (2018).
Imai, S. & Guarente, L. NAD+ and sirtuins in aging and disease. Trends Cell Biol. 24, 464–471 (2014).
Johnson, S. & Imai, S. I. NAD (+) biosynthesis, aging, and disease. F1000Res 7, 132 (2018).
Barlow, C. et al. Atm-deficient mice: a paradigm of ataxia telangiectasia. Cell 86, 159–171 (1996).
Savitsky, K. et al. A single ataxia telangiectasia gene with a product similar to PI-3 kinase. Science 268, 1749–1753 (1995).
Fang, E. F. et al. NAD(+) replenishment improves lifespan and healthspan in ataxia telangiectasia models via mitophagy and DNA repair. Cell Metab. 24, 566–581 (2016).
Shiloh, Y. & Lederman, H. M. Ataxia-telangiectasia (A-T): an emerging dimension of premature ageing. Ageing Res. Rev. 33, 76–88 (2017).
Valentin-Vega, Y. A. et al. Mitochondrial dysfunction in ataxia-telangiectasia. Blood 119, 1490–1500 (2012).
Ito, K. et al. Regulation of oxidative stress by ATM is required for self-renewal of haematopoietic stem cells. Nature 431, 997–1002 (2004).
Fang, E. F. & Bohr, V. A. NAD(+): the convergence of DNA repair and mitophagy. Autophagy 13, 442–443 (2017).
Adolfsson, J. et al. Identification of Flt3+ lympho-myeloid stem cells lacking erythro-megakaryocytic potential a revised road map for adult blood lineage commitment. Cell 121, 295–306 (2005).
Wilson, A. et al. Hematopoietic stem cells reversibly switch from dormancy to self-renewal during homeostasis and repair. Cell 135, 1118–1129 (2008).
Pietras, E. M. et al. Functionally distinct subsets of lineage-biased multipotent progenitors control blood production in normal and regenerative conditions. Cell Stem Cell 17, 35–46 (2015).
Beerman, I. et al. Functionally distinct hematopoietic stem cells modulate hematopoietic lineage potential during aging by a mechanism of clonal expansion. Proc. Natl Acad. Sci. USA 107, 5465–5470 (2010).
Rossi, D. J. et al. Cell intrinsic alterations underlie hematopoietic stem cell aging. Proc. Natl Acad. Sci. USA 102, 9194–9199 (2005).
Rose, S., Misharin, A. & Perlman, H. A novel Ly6C/Ly6G-based strategy to analyze the mouse splenic myeloid compartment. Cytom. A 81, 343–350 (2012).
Kratofil, R. M., Kubes, P. & Deniset, J. F. Monocyte conversion during inflammation and injury. Arterioscler Thromb. Vasc. Biol. 37, 35–42 (2017).
Soehnlein, O., Steffens, S., Hidalgo, A. & Weber, C. Neutrophils as protagonists and targets in chronic inflammation. Nat. Rev. Immunol. 17, 248–261 (2017).
Tecchio, C., Micheletti, A. & Cassatella, M. A. Neutrophil-derived cytokines: facts beyond expression. Front. Immunol. 5, 508 (2014).
Ueda, Y., Yang, K., Foster, S. J., Kondo, M. & Kelsoe, G. Inflammation controls B lymphopoiesis by regulating chemokine CXCL12 expression. J. Exp. Med. 199, 47–58 (2004).
Nagaoka, H., Gonzalez-Aseguinolaza, G., Tsuji, M. & Nussenzweig, M. C. Immunization and infection change the number of recombination activating gene (RAG)-expressing B cells in the periphery by altering immature lymphocyte production. J. Exp. Med. 191, 2113–2120 (2000).
Yamashita, M. & Passegue, E. TNF-alpha coordinates hematopoietic stem cell survival and myeloid regeneration. Cell Stem Cell 25, 357–372 (2019).
Pietras, E. M. et al. Chronic interleukin-1 exposure drives haematopoietic stem cells towards precocious myeloid differentiation at the expense of self-renewal. Nat. Cell Biol. 18, 607–618 (2016).
Elhassan, Y. S. et al. Nicotinamide riboside augments the aged human skeletal muscle NAD(+) metabolome and induces transcriptomic and anti-inflammatory signatures. Cell Rep. 28, 1717–1728 (2019). e1716.
Nakamura-Ishizu, A., Ito, K. & Suda, T. Hematopoietic stem cell metabolism during development and aging. Dev. Cell 54, 239–255 (2020).
Dhapola, P. E. et al. Nabo—a framework to define leukemia-initiating cells and differentiation in single-cell RNA-sequencing data. bioRxiv (2020).
Qian, M. et al. Boosting ATM activity alleviates aging and extends lifespan in a mouse model of progeria. Elife 7, e34836 (2018).
Mouchiroud, L. et al. The NAD(+)/sirtuin pathway modulates longevity through activation of mitochondrial UPR and FOXO signaling. Cell 154, 430–441 (2013).
Howard, M. et al. Formation and hydrolysis of cyclic ADP-ribose catalyzed by lymphocyte antigen CD38. Science 262, 1056–1059 (1993).
Dong, C., Wang, J., Neame, P. & Cooper, M. D. The murine BP-3 gene encodes a relative of the CD38/NAD glycohydrolase family. Int. Immunol. 6, 1353–1360 (1994).
Thiele, H. G. Rat Thy-1 antigen and its relation to RT-6. Immunol. Ser. 45, 149–170 (1989).
Nauseef, W. M. & Borregaard, N. Neutrophils at work. Nat. Immunol. 15, 602–611 (2014).
Scapini, P. & Cassatella, M. A. Social networking of human neutrophils within the immune system. Blood 124, 710–719 (2014).
Yang, B. et al. NAD(+) supplementation prevents STING-induced senescence in ataxia telangiectasia by improving mitophagy. Aging Cell 20, e13329 (2021).
Li, P. et al. NCoR repression of LXRs restricts macrophage biosynthesis of insulin-sensitizing omega 3 fatty acids. Cell 155, 200–214 (2013).
Vannini, N. et al. The NAD-booster nicotinamide riboside potently stimulates hematopoiesis through increased mitochondrial clearance. Cell Stem Cell 24, 405–418 (2019).
Gilmour, B. C. et al. Targeting NAD(+) in translational research to relieve diseases and conditions of metabolic stress and ageing. Mech. Ageing Dev. 186, 111208 (2020).
Martin, M. Cutadapt removes adapter sequences from high-throughput sequencing reads. EMBnet. journal 17, 10–12 (2011).
Dobin, A. et al. STAR: ultrafast universal RNA-seq aligner. Bioinformatics 29, 15–21 (2013).
Liao, Y., Smyth, G. K. & Shi, W. featureCounts: an efficient general purpose program for assigning sequence reads to genomic features. Bioinformatics 30, 923–930 (2014).
Risso, D., Ngai, J., Speed, T. P. & Dudoit, S. Normalization of RNA-seq data using factor analysis of control genes or samples. Nat. Biotechnol. 32, 896–902 (2014).
Subramanian, A. et al. Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles. Proc. Natl Acad. Sci. USA 102, 15545–15550 (2005).
The authors would like to thank all members of the Epigenetic and Stem Cell Unit and Experimental Gerontology Section of the NIA. The authors would also like to acknowledge the support of William Wood and all of the Genetics and Genomics Core at the NIA for their assistance. I.B. and V.A.B. were supported by the Intramural Research Program of the NIH, National Institute on Aging. The authors would like to specially thank Elizabeth Beerman for editing efforts. E.F.F. was supported by HELSE Sør-Øst (#2017056), The Research Council of Norway (#262175), Rosa Sløyfe & Norwegian Breast Cancer Society (#207819), and NSFC (#81971327). M.T.-Y. was supported by the Intramural Research Program of NIA and Japan Society for the Promotion of Science Research Fellowship for Japanese Biomedical and Behavioral Researchers at NIH.
E.F.F. has CRADA arrangements with ChromaDex and is a consultant to Aladdin Healthcare Technologies and the Vancouver Dementia Prevention Centre. The remaining authors declare no competing interests.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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Zong, L., Tanaka-Yano, M., Park, B. et al. NAD+ augmentation with nicotinamide riboside improves lymphoid potential of Atm−/− and old mice HSCs. npj Aging Mech Dis 7, 25 (2021). https://doi.org/10.1038/s41514-021-00078-3
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