Identification of sUA as an endogenous inhibitor for CD38.

(A) Preliminary screening of 8-OG binding proteins by mass spectrum (MS)-based proteomics, and effect of 8-OG (50 μM) on CD38 activity (n = 3 experiments/technical replicates).

(B) Hydrolase and cyclase activities of recombinant human CD38 (hCD38) in the presence of sUA, using nicotinamide 1, N6-ethenoadenine dinucleotide (ε-NAD+), and nicotinamide guanine dinucleotide (NGD) as substrates, respectively (n = 3 experiments/technical replicates).

(C and D) Effect of different substrate concentrations on sUA inhibition of recombinant hCD38 hydrolase (C) and cyclase (D) activities (n = 3 experiments/technical replicates).

(E) Effect of different sUA concentrations on hydrolase and cyclase activities (FU/min/μg protein) in tissues from 8- to 12-week-old WT mice (n = 3 mice).

(F and G) Reversibility of inhibition of recombinant hCD38 hydrolase (F) and cyclase

(G) activities by sUA. After 30-min pre-incubation as indicated, samples were diluted 100-fold in reaction buffer with or without 500 μM sUA for enzyme assay (n = 3-5 experiments/technical replicates).

Data are mean ± s.d. (B-E) or mean ± s.e.m. (A, F, and G).

CD38 inhibition is restricted to sUA in purine metabolism.

(A and B) Effect of sUA and its precursors and metabolite on hydrolase and cyclase activities of recombinant hCD38 (n = 3 experiments/technical replicates for each ligand).

(C) Major pathways of purine metabolism.

(D) Effect of different analogs on hydrolase and cyclase activities (n = 3 experiments/technical replicates). THP-1 cells were used to detect the effects of oxypurinol, caffeine, 1-MU, and 1,3-DMU on hydrolase activity, recombinant hCD38 was used in the remaining detections.

(E) Effect of uracil and 1,3-dihydroimidazol-2-one (1,3-DHI-2-one) on hydrolase and cyclase activities of recombinant hCD38 (n = 3 experiments/technical replicates).

(F) A structural comparison reveals the functional group for CD38 inhibition. The concentrations of all ligands are from 5 to 500 μM. Data are mean ± s.e.m.

sUA physiologically limits NAD+ degradation via CD38 inhibition.

WT and CD38 KO mice (10- to 12-week-old) received oral administration of saline, OA, or OA plus inosine (Ino) twice (1-day moderate sUA supplementation).

(A-D) Effect of 1-day sUA supplementation on whole blood NAD+ (A), NMN (B), cADPR (C), and plasma sUA (D) levels in WT and CD38 KO mice (WT-Saline: n = 8 mice, WT-OA: n = 9 mice, WT-OA + Ino: n = 9 mice, KO-Saline: n = 6 mice, KO-OA: n = 8 mice, KO-OA + Ino: n = 8 mice).

(E) Effect of 1-day or 3-day release on whole blood NAD+, NMN, cADPR, and plasma sUA levels in WT mice that received 1-day supplementation (WT-Saline: n = 6 mice, WT-OA: n = 8 mice, WT-OA + Ino: n = 8 mice).

(F) Effect of sUA (100, 200, or 500 μM) and other ligands (analogs at 500 μM, 78c, a CD38 inhibitor, at 0.5 μM) on NAD+ degradation by recombinant hCD38 (n = 5 independent samples).

Data are mean ± s.e.m. Significance was tested using 2-way ANOVA (A-D), Kruskal-Wallis test or 1-way ANOVA with Tukey’s multiple comparisons test (E and F). NS, not significant. Statistic difference (A-D) between OA and OA + Ino groups in WT or KO mice (saline alone group excluded) was also analyzed by unpaired two-sided t-test or Mann Whitney test; WT mice: P = 0.0056 (A), 0.0351 (B), or P < 0.0001 (D); KO mice: P = 0.0003 (D).

sUA physiologically prevents excessive inflammation by interacting with CD38.

WT and CD38 KO mice (10- to 12-week-old) received 1-day moderate sUA supplementation, plasma sUA was increased to the minimum physiological levels of humans in OA plus inosine (Ino) groups. Then, the mice were stimulated with cLPS (2 mg/kg) or MSU crystals (2 mg/mouse) for 6 h.

(A-C) Effect of sUA at physiological levels on serum levels of IL-1β (A), IL-18 (B), and TNF-α (C) in mice with cLPS-induced systemic inflammation (WT-OA: n = 6 mice, WT-OA + cLPS: n = 11 mice, WT-OA + Ino + cLPS: n = 12 mice, KO-OA: n = 6 mice, KO-OA + cLPS: n = 8 mice, KO-OA + Ino + cLPS: n = 8 mice).

(D-H) Effect of sUA at physiological levels on IL-1β (D), IL-6 (E), and CXCL1 (F) levels and recruitment of viable cells (red blood cells excluded) (G) and neutrophils (H) in peritoneal lavage fluid from the mice with MSU crystal-induced peritonitis (WT-OA: n = 6 mice, WT-OA+MSU: n = 12 mice, WT-OA + Ino + MSU: n = 13 mice, KO-OA: n = 6 mice, KO-OA+MSU: n = 10 mice, KO-OA + Ino + MSU: n = 10 mice).

Data are mean ± s.e.m. Significance was tested using 2-way ANOVA with Tukey’s multiple comparisons test. NS, not significant. Statistic difference between OA + cLPS/MSU and OA + Ino + cLPS/MSU groups in WT or KO mice (OA alone group excluded) was also analyzed by unpaired two-sided t-test (with Welch’s correction when applicable) or Mann Whitney test; WT mice: P = 0.0398 (A), 0.0383 (B), 0.0407 (D), 0.0417 (E), 0.0222 (G), or 0.0205 (H).

sUA inhibition of CD38 and reversibility in THP-1 and A549 cells.

(A) Hydrolase activity of THP-1 cells in the presence of sUA (0 to 500 μM) (n = 3 experiments/technical replicates).

(B) Effect of different ε-NAD+ concentrations on sUA inhibition of hydrolase activity of THP-1 cells (n = 3 experiments/technical replicates).

(C and D) Reversibility of inhibition of hydrolase (A549 cells) (C) and cyclase (THP-1 cells) (D) by sUA (n = 3 experiments/technical replicates).

Data are mean ± s.d. (A and B) or mean ± s.e.m. (C and D).

Comparison between Ki values and mean levels of sUA in different tissues.

Ki values were also shown in Figure 1E, and serum and tissue sUA levels were from WT mice that received 1-day treatment of saline (also shown in Figure 3D and Figure 3-figure supplement 5A).

Endogenous sUA concentrations in the final reaction buffer for enzyme assays.

sUA levels in initial homogenate or membrane fractions were measured, then the endogenous sUA concentrations in the final reaction buffer were calculated based on loading dilution (n = 3 biologically independent samples).

Data are mean ± s.e.m.

Effect of sUA, sUA precursors and metabolite, and other derivates on CD38 activity in cells and tissues.

(A-C) Effect of sUA and its precursors and metabolite on hydrolase (A and B) and cyclase (C) activities. (n = 3 experiments/technical replicates)

(D and E) Effect of uracil and 1,3-dihydroimidazol-2-one (1,3-DHI-2-one) on hydrolase and cyclase activities of WT lung tissues. (n = 3 experiments/technical replicates)

Data are mean ± s.e.m.

Effect of sUA on intracellular NAD+ levels in A549 and THP-1 cells.

(A) Effect of sUA on intracellular NAD+ levels of A549 cells (n = 5 biologically independent samples).

(B) Effect of sUA pre-incubation on intracellular NAD+ levels of THP-1 cells. Naïve THP-1 cells were incubated with sUA (0-10 mg/dL) for 2h, then the cells were washed twice with sterile PBS and stimulated with MSU crystals (200 μg/mL), cLPS (20 μg/mL), zymosan (50 μg/mL) or ATP (2 mM) for 6 h (n = 6 biologically independent samples).

Data are mean ± s.e.m. Significance was tested using 1-way ANOVA with Dunnett’s multiple comparisons test (A and B) or Kruskal-Wallis test (cLPS groups in B).

Effect of sUA and its precursors and metabolite on NAMPT and PARP activities.

(A and B) NAMPT activity. (n = 4 experiments/technical replicates)

(C and D) PARP activity. 3-Aminobenzamide is a PARP inhibitor. (n = 4 experiments/technical replicates)

Data are mean ± s.d. (A and C) or mean ± s.e.m. (B and D).

Effect of OA on CD38 activity and plasma sUA levels.

(A and B) Hydrolase and cyclase activities of lung tissues from WT mice in the presence of OA (0 to 5 mM) (n = 3 experiments/technical replicates).

(C) Effect of OA administration on plasma sUA levels in WT mice (10- to 12-week-old) that received oral administration of inosine. In saline group, the mice received oral administration and intraperitoneal injection of saline. In OA p.o. group, the mice received oral administration of inosine (1.5 g/kg) and OA (1.5 g/kg) (the same treatment in our models), and intraperitoneal injection of saline. In OA i.p. group, the mice received oral administration of inosine (1.5 g/kg), and intraperitoneal injection of OA (0.25 g/kg). Four hours after treatment, plasma sUA was measured (n = 5-8 mice per group).

Data are mean ± s.d. (A and B) or mean ± s.e.m. (C). Significance was tested using Brown-Forsythe and Welch ANOVA tests (C).

Effect of sUA at physiological levels on NAD+ degradation under inflammatory conditions.

(A-D) Effect of 1-day sUA supplementation on plasma sUA (A) and whole blood NAD+(B), NMN (C), and cADPR (D) levels in WT and CD38 KO mice (10- to 12-week-old) under inflammatory conditions. The mice received 1-day sUA supplementation. Two hours after the last treatment, the mice were intraperitoneally stimulated with sterile PBS or cLPS (2 mg/kg) for 6 h (WT-OA: n = 6 mice, WT-OA + cLPS: n = 11 mice, WT-OA + Ino + cLPS: n = 12 mice, KO-OA: n = 6 mice, KO-OA + cLPS: n = 8 mice, KO-OA + Ino + cLPS: n = 8 mice).

(E-H) Effect of 1-day treatment of OA or inosine (Ino) on plasma sUA (E) and whole blood NAD+ (F), NMN (G), and cADPR (H) levels in WT mice (10- to 12-week-old) under inflammatory conditions. The mice received 1-day treatment of OA or Ino (from the evening of day 0 to the morning of day 1). Two hours after the last treatment, the mice were intraperitoneally stimulated with sterile PBS or cLPS (2 mg/kg) for 6 h (n = 6 mice in Saline + cLPS group, n = 5 mice in other groups).

Data are mean ± s.e.m. Significance was tested using 2-way ANOVA with Tukey’s multiple comparisons test (A-D), or 1-way ANOVA with Tukey’s multiple comparisons test (E-H). Statistic difference (A-D) between OA + cLPS and OA + Ino + cLPS groups in WT or KO mice (OA alone group excluded) was also analyzed by unpaired two-sided t-test (with Welch’s correction when applicable) or Mann Whitney test; WT mice: P < 0.0001 (A), or P = 0.0092 (B), 0.0221 (D); KO mice: P = 0.0004 (A).

Effect of 1-day, 3-day, and 7-day moderate sUA supplementation on NAD+, NMN, and sUA levels in whole blood and tissues.

WT and CD38 KO mice (10- to 12-week-old) received oral administration of saline, OA, or OA plus inosine (Ino) twice daily for 1, 3, or 7 days. Four hours after the last treatment, the mice were sacrificed. In 1-day model, the mice were treated from the evening of day 0 to the morning of day 1.

(A) Effect of 1-day sUA supplementation on tissue NAD+, NMN, and sUA levels (n = 5 male mice per group).

(B) Effect of 3-day sUA supplementation on tissue NAD+, NMN, and sUA levels (n = 5 male mice per group).

(C-F) Effect of 3-day sUA supplementation on plasma sUA (C), whole blood NAD+ (D), NMN (E), and cADPR (F) levels (WT-Saline: n = 6 mice, WT-OA: n = 8 mice, WT-OA + Ino: n = 8 mice, KO-Saline: n = 6 mice, KO-OA: n = 8 mice, KO-OA + Ino: n = 8 mice).

(G-I) Effect of 7-day sUA supplementation on tissue NAD+ and sUA levels (n = 5 male mice per group).

Data are mean ± s.e.m. Significance was tested using 2-way ANOVA with Tukey’s multiple comparisons test (A-H), Kruskal-Wallis test or 1-way ANOVA with Dunnett’s multiple comparisons test (I). Statistic difference (C-H) between OA and OA + Ino groups in WT or KO mice (saline alone group excluded) was also analyzed by unpaired two-sided t-test; WT mice: P < 0.0001 (C), or P = 0.0058 (D), 0.0453 (E), 0.0083 (G, left panel), 0.0036 (H, left panel); KO mice: P = 0.0004 (C).

No effect of 1- to 7-day sUA supplementation on serum IL-1β production.

Four hours after the last treatment, serum was collected for IL-1β measurement (n = 5 mice per group).

sUA limits NMN degradation via CD38 inhibition.

(A) Effect of sUA on recombinant hCD38-mediated NMN (200 μM) degradation in medium (n = 8 independent samples).

(B) Effect of sUA (100, 200, and 500 μM) or 78c (0.5 μM) on intracellular NAD+ levels of WT BMDMs treated with NMN. WT BMDMs were primed with100 ng/mL ultrapure LPS for 8 h (n = 6 biologically independent samples).

(C-E) Effect of sUA on extracellular NMN degradation in WT (C) or CD38 KO BMDMs in the absence (D) or presence (E) of recombinant hCD38 (10 ng/mL). BMDMs were primed with 100 ng/mL ultrapure LPS for 8 h before metabolic assays. (n = 6 biologically independent samples in C and D, n = 8 biologically independent samples in E)

Data are mean ± s.e.m. Significance was tested using 1-way ANOVA with Tukey’s multiple comparisons test.

Effect of CD38 KO and sUA pre-incubation on IL-1β release in primed BMDMs.

(A) Effect of CD38 KO on IL-1β release in primed BMDMs. WT and KO BMDMs were primed with 100 ng/mL ultrapure LPS for 4 h, then primed BMDMs were challenged by ATP (5 mM, 30min), nigericin (3 μM, 2 h), MSU crystals (200 μg/mL, 6 h), cLPS (20 μg/mL, 6 h), and zymosan (50 μg/mL, 4 h). US means unstimulated. (n = 8 biologically independent samples in ATP and nigericin groups, n = 6 biologically independent samples in other groups)

(B-D) Effect of sUA pre-incubation on IL-1β release and intracellular sUA levels in primed BMDMs. WT BMDMs were primed with 100 ng/mL ultrapure LPS for 4 h. (B) The cells were pre-incubated with or without sUA (100 or 200 μM) for 2 h. Then, the cells were washed twice with sterile PBS and were stimulated with nigericin (3 μM, 2 h), MSU crystals (200 μg/mL, 4 h), or cLPS (1 μg/mL, 4 h). (C and D) Primed BMDMs were directly incubated with sUA (100, 200, and 500 μM) or MSU crystals (100 μg/mL) for 6 h in C, 2 or 15 h in D. US means unstimulated. (n = 6 biologically independent samples in B and C, n = 3 biologically independent samples in D)

Data are mean ± s.e.m. Significance was tested using two-tailed unpaired t-test and Mann-Whitney test (ATP and Zymosan) (A), or 1-way ANOVA with Dunnett’s multiple comparisons test (B-D).

Effect of sUA pre-incubation and CD38 blockade on IL-1β release in primed THP-1 cells.

THP-1 cells were primed with 0.5 μM PMA for 3 h the day before stimulation.

(A) Primed THP-1 cells were pre-incubated with sUA (0-10 mg/dL) for 2 h, then the cells were washed twice with sterile PBS and challenged by MSU crystals (200 μg/mL), cLPS (20 μg/mL), zymosan (50 μg/mL), and ATP (2 mM) for 4 h (n = 6 biologically independent samples).

(B and C) Primed THP-1 cells were treated without or with 2 μM 78c (CD38 blockade by the highly specific and potent inhibitor of CD38) for 2 h. Then the cells were pre-incubated with blank medium or sUA for 2 h. The cells were washed twice with sterile PBS. The washed cells were challenged by MSU crystals (200 μg/mL, 4 h) for IL-1β measurement (B) or were directly used for sUA uptake measurement without MSU crystal stimulation (C). 78c was used in all steps for CD38 blockade groups, including sUA pre-incubation and MSU crystal stimulation (n = 6 biologically independent samples).

Data are mean ± s.e.m. Significance was tested using Kruskal-Wallis test (ATP groups in A), 1-way ANOVA with Dunnett’s multiple comparisons test (A), or 2-way ANOVA with Tukey’s multiple comparisons test (B).

Crystal precipitation in high-concentration sUA stock solutions after long-term storage.

sUA stock solutions in NaOH were prepared without pH adjustment. Crystals were immediately precipitated after dissolution in 50 mg/mL tube. Visible crystals were observed in 5 mg/mL tube after 2-month storage at 4 ℃ (before taking the picture, the tube was slightly shaken to resuspend the crystals on the bottom).

Moderate sUA supplementation fails to prevent high-dose cLPS-induced systemic inflammation.

WT mice (10- to 12-week-old) received 1-day treatment of OA or OA plus inosine (Ino), 2 h after the last treatment, the mice were intraperitoneally stimulated with sterile PBS or cLPS (20 mg/kg) for 4 h (n = 5 mice per group).

(A-C) Serum IL-1β (A), IL-18 (B), and TNF-α (C) were measured.

(D-G) Plasma sUA (D), whole blood NAD+ (E), NMN (F), and cADPR (G) levels were measured.

Data are mean ± s.e.m. Significance was tested using 1-way ANOVA with Tukey’s multiple comparisons test (A, and C-G) or Kruskal-Wallis test (B).

OA or inosine alone does not limit cLPS-induced systemic inflammation and MSU crystal-induced peritonitis.

WT mice (10- to 12-week-old) received 1-day oral administration of saline, OA, or inosine (Ino), 2 h after the last treatment, the mice were intraperitoneally stimulated with sterile PBS, cLPS (2 mg/kg), or MSU crystals (2 mg/mouse) for 6 h.

(A-C) Serum IL-1β (A), IL-18 (B), and TNF-α (C) levels in mice with cLPS-induced systemic inflammation were measured (n = 6 mice in Saline + cLPS group, n = 5 mice in other groups).

(D-H) IL-1β (D), IL-6 (E), CXCL1 (F), and the number of viable cells (red blood cells excluded) (G) and neutrophils (H) in peritoneal lavage fluid from the mice with MSU crystal-induced peritonitis were measured (n = 5 mice per group).

Data are mean ± s.e.m. Significance was tested using 1-way ANOVA with Tukey’s (A, C-H) multiple comparisons test, or Kruskal-Wallis test (B).

Potential mechanism of the paradox in gout therapy (urate-lowering therapy).