| 2011 |
NT5E/CD73 converts AMP to adenosine; loss-of-function mutations (nonsense p.S221X, missense p.C358Y, frameshift p.V537fsX7) abolish this enzyme activity and cause arterial and joint calcifications. Cultured fibroblasts from affected patients showed markedly reduced CD73 protein, absent enzyme activity, elevated alkaline phosphatase, and accumulated calcium phosphate crystals. Genetic rescue with wild-type NT5E normalized CD73 and alkaline phosphatase activity; adenosine treatment reduced alkaline phosphatase levels and calcification. |
Western blotting, enzyme activity assays, in vitro calcification assays, transduction rescue experiments, SNP analysis, targeted gene sequencing |
The New England journal of medicine |
High |
21288095
|
| 2014 |
Disease-causing NT5E mutations (p.S221X, p.C358Y, p.V537fsX7) result in mistrafficking of NT5E protein away from the plasma membrane: mutant proteins accumulate in the cell synthetic apparatus (ER/vesicles) rather than reaching the cell surface, with reduced ER retention and absent NT5E enzymatic activity at the cell surface. |
Confocal microscopy, western blot of fractionated cell constituents, enzyme histochemistry (Malachite green assay), heterologous expression of DsRed-tagged wild-type and mutant NT5E in COS-7 cells |
PloS one |
High |
24887587
|
| 1997 |
CD73 functions as a costimulatory molecule for T cell activation independently of its enzymatic activity and independently of its GPI anchor (demonstrated using a Jurkat T cell transfection model); however, expression of p56lck, CD45, and the T cell receptor are required for CD73-mediated T cell activation in vitro. |
Jurkat T cell transfection with CD73 cDNA constructs (enzymatic-activity-null and GPI-anchorless mutants), functional T cell activation assays |
Cellular signalling |
Medium |
9113412
|
| 2012 |
CD73-generated adenosine promotes osteoblast differentiation via A2B adenosine receptor (A2BAR) signaling. CD73-deficient mice show osteopenia with reduced osteoblastic markers but normal osteoclastic markers. Overexpression of CD73 in MC3T3-E1 cells enhanced osteocalcin and bone sialoprotein expression, an effect blocked by an A2BAR antagonist but not an A2AAR antagonist. |
CD73-knockout mouse bone phenotyping, in vitro osteoblast differentiation assays, CD73 overexpression in MC3T3-E1 cells, pharmacological receptor antagonism |
Journal of cellular physiology |
High |
21882189
|
| 2011 |
NT5E (CD73) and PAP are the principal ectonucleotidases generating adenosine in spinal nociceptive circuits. AMP hydrolysis was nearly abolished in dorsal root ganglia and spinal cord lamina II of Pap/Nt5e double-knockout mice. NT5E rapidly converts AMP to adenosine within seconds in lamina II (measured by fast-scan cyclic voltammetry), and the resulting adenosine inhibits nociception via the A1 adenosine receptor. |
Histochemical AMP hydrolysis, fast-scan cyclic voltammetry in spinal lamina II, behavioral nociception assays, Pap/Nt5e double-knockout mice, pharmacological A1 receptor analysis |
Molecular pain |
High |
22011440
|
| 2015 |
CD73-generated adenosine induces cortical actin polymerization in endometrial epithelial cells via adenosine A1 receptor (A1R) activation of a Rho GTPase CDC42-dependent conformational change of the N-WASP subunit of the ARP2/3 complex. This cortical F-actin elevation increases membrane E-cadherin, β-catenin, and Na+K+ ATPase, maintaining epithelial integrity. Loss of CD73 reduces endometrial epithelial barrier function and increases migration/invasion. |
CD73 pharmacological inhibition, CD73 knockout mouse model, in vitro migration/invasion assays, co-localization of CD73 with cell-cell contacts and filopodia, A1R antagonism, Rho GTPase and ARP2/3 pathway analysis |
The Journal of clinical investigation |
High |
26642367
|
| 2019 |
CD73-derived adenosine activates adenosine A2A receptor (A2AR) in a feed-forward manner in microglia, upregulating CD73 and A2AR to promote neuroinflammation in Parkinson's disease models. CD73 inactivation attenuated LPS-induced pro-inflammatory responses, enhanced microglial process extension and movement, and suppressed microglia-mediated neuroinflammation. A2AR-mediated pro-inflammation was restored by exogenous adenosine analogues. |
CD73 inactivation in MPTP mouse model, LPS-stimulated microglia assays, laser injury model, pharmacological adenosine replenishment, morphological analysis of microglia |
Brain : a journal of neurology |
Medium |
30689733
|
| 2017 |
CD73 regulates anti-inflammatory signaling between apoptotic cells and endotoxin-conditioned macrophages. Adenosine generated by CD73 (AMP→adenosine) but not CD39 (ATP→AMP) is required for apoptotic cell-driven suppression of TNF in LPS-conditioned macrophages, acting through the adenosine A2a receptor (Adora2a). In mice, CD73 was required to limit neutrophil influx in a peritonitis model. |
Enzymatic depletion of adenosine, pharmacological A2a receptor inhibition, CD73-knockout macrophages, RAW264.7 ectopic co-expression of A2a and CD73, in vivo peritonitis model |
Cell death and differentiation |
High |
28060378
|
| 2020 |
Tumor-infiltrating NK cells transport CD73 in intracellular vesicles to the cell surface and extracellular space via actin polymerization-dependent exocytosis, triggered by engagement of 4-1BBL on tumor cells. CD73-positive NK cells undergo transcriptional reprogramming with upregulated IL-10 production via STAT3 transcriptional activity, suppressing CD4+ T cell proliferation and IFN-γ production. |
Flow cytometry, live cell imaging of CD73-vesicle trafficking, cytokine assays, STAT3 inhibition, functional T cell suppression assays |
The Journal of clinical investigation |
Medium |
31770109
|
| 2019 |
CD73 on glioblastoma endothelial cells promotes tumor invasiveness through A2B adenosine receptor (A2B AR) signaling, which induces matrix metalloproteinase-2 (MMP-2) expression. Inhibition of A2B AR signaling decreased multidrug resistance transporter expression (P-gp and MRP1) and potentiated temozolomide-induced cell death. The CD73-FLK mouse model demonstrated that endothelial CD73 drives tumor invasiveness and brain morphology distortion. |
CD73-knockout and CD73-FLK transgenic mouse GBM models, A2B AR inhibition, immunohistochemistry, tumor growth/vessel density measurement |
The Journal of neuroscience |
Medium |
30926752
|
| 2023 |
TRIM21 is an E3 ubiquitin ligase that targets CD73 for ubiquitin-mediated proteolytic degradation. Lysine residues K133, K208, K262, and K321 on CD73 are required for TRIM21-mediated ubiquitylation and degradation. Loss of TRIM21 stabilizes CD73, enhancing CD73-catalyzed adenosine production and suppressing CD8+ T cell function, promoting tumor growth. |
Co-immunoprecipitation, ubiquitylation assays, site-directed mutagenesis of CD73 lysine residues, TRIM21 knockout/overexpression, CD8+ T cell functional assays |
Science advances |
High |
36608132
|
| 2023 |
CD73 deficiency in pancreatic tumor cells leads to increased DNA damage and activation of the cGAS-STING pathway. cGAS expression in tumor cells was required for the antitumor activity of the CD73 inhibitor AB680 in vivo, linking CD73 to suppression of innate immune sensing of tumor DNA damage. |
CRISPR/genetic CD73 deletion in mouse KPC tumor cells, cGAS knockout, in vivo tumor models, pharmacogenomic analysis of human PDAC cell lines |
Cancer immunology research |
Medium |
36409930
|
| 2023 |
CD73 significantly enhances tumor cell mitochondrial respiration, oxidative phosphorylation (OXPHOS), glycolytic reserve, and aspartate biosynthesis. Rescuing aspartate biosynthesis was sufficient to restore proliferation of CD73-deficient tumors in immune-deficient mice. Targeting CD73 decreased metabolic fitness, increased genomic instability, and suppressed PARP activity. |
Metabolomics, Seahorse analysis of large panel of mouse and human tumor cell lines, CD73-deficient tumor implantation in immune-deficient mice, aspartate rescue experiments |
eLife |
High |
37261423
|
| 2023 |
NT5E/CD73 directly interacts with Aurora kinase A (AURKA) and inhibits AURKA ubiquitination. This interaction, confirmed by co-immunoprecipitation and molecular docking, downregulates p53 signaling and regulates hepatic stellate cell senescence and activation, thereby promoting alcohol-related liver fibrosis. |
Co-immunoprecipitation, molecular docking, KEGG pathway analysis, CD73 overexpression/knockdown in stellate cells, proteomic analysis |
International journal of biological sciences |
Medium |
36778123
|
| 2019 |
CD73 perivascular cell expression (Foxd1+ lineage pericytes/fibroblasts) is required to suppress inflammation and prevent kidney fibrosis after ischemia-reperfusion injury. Conditional deletion of CD73 from perivascular cells increased collagen deposition, proinflammatory markers, and PDGFR-β immunoreactivity. Fibrosis and dysfunction were rescued by administration of soluble CD73 or by macrophage deletion. |
Conditional CD73 knockout (Foxd1Cre × CD73fl/fl), unilateral ischemia-reperfusion injury, folic acid nephropathy model, soluble CD73 rescue, macrophage depletion |
American journal of physiology. Renal physiology |
Medium |
31364375
|
| 2013 |
CD73 promotes tumor angiogenesis through both enzymatic (adenosine-dependent) and non-enzymatic functions. Tumor-derived CD73 enhances VEGF production by tumor cells; host-derived CD73 is required for in vivo angiogenic responses; endothelial cells require CD73 expression for tube formation and migration. Anti-CD73 monoclonal antibody treatment significantly decreased tumor VEGF levels and suppressed angiogenesis in vivo. |
Mouse breast cancer model with CD73-deficient host cells, in vitro tube formation and migration assays with CD73-knockdown endothelial cells, VEGF ELISA, anti-CD73 antibody treatment |
International journal of cancer |
Medium |
23982901
|
| 2006 |
Ecto-5'-nucleotidase (CD73) in melanoma cells is catalytically active and is located in lipid rafts. Concanavalin A-induced clustering of CD73 causes its redistribution to heavier cytoskeletal fractions along with co-expressed integrins (αv, α5, β1, β3), caveolin-1, and CD44. Tenascin C inhibits CD73 activity and adenosine generation. Knockdown of CD73 in WM9 cells significantly reduces cell adhesion to tenascin C, indicating a CD73 role in adhesion to extracellular matrix independent of adenosine generation. |
Density gradient centrifugation, enzyme activity assays, concanavalin A clustering, siRNA knockdown of CD73, cell adhesion assay on ECM proteins |
Melanoma research |
Medium |
16718268
|
| 2022 |
CD73 deficiency on Foxp3+ regulatory T cells impairs their tissue tropism and immunosuppressive function during cardiac healing post-myocardial infarction. CD73-deficient Tregs showed impaired ability to inhibit inflammatory cytokine production in effector T cells. CD73 on Tregs was found to bind to FoxP3- effector T cells directly. |
CD73-knockout Treg adoptive transfer, flow cytometry, permanent coronary ligation mouse model, cytokine assays, IL-2/anti-IL-2 complex Treg expansion |
Theranostics |
Medium |
35401839
|
| 2023 |
Hypoxic conditioning increases the frequency of CD73+ CD4+ T cells and promotes HIV latency. CD73 or adenosine receptor blockade facilitates latent HIV reactivation in vitro, mechanistically linking CD73-mediated adenosine signaling to viral quiescence. CD73+ CD4+ T cells harbor a functional HIV reservoir and can reinitiate productive infection ex vivo. |
Systems transcriptomics, hypoxic culture, CD73/adenosine receptor blockade, ex vivo HIV reactivation assay, tissue imaging of lymph nodes from HIV-infected individuals |
Cell reports |
Medium |
37910505
|
| 2022 |
CD73 expression defines CD73+CD104+ epithelial progenitor cells in the esophagus with enhanced organoid-forming capacity. Knockdown of CD73 decreases organoid formation rate, demonstrating a functional role of CD73 in esophageal epithelial stem cell self-renewal. IL-4 and IL-13 (via STAT6 signaling) deplete the CD73+CD104+ population, which is associated with basal cell hyperplasia in eosinophilic esophagitis. |
Fluorescence-activated cell sorting of CD73+CD104+ vs CD73-CD104+ populations, organoid formation assays, RNA interference knockdown of CD73, single-cell RNA sequencing, STAT6 inhibition |
Cellular and molecular gastroenterology and hepatology |
Medium |
35108658
|
| 2022 |
CD73 knockdown in pancreatic cancer cells inhibited ERK/STAT3 pathway activation and activated the E-cadherin pathway, leading to inhibition of cell growth, migration, and G1 cell cycle arrest. A CRISPR/Cas9 protein kinase library screen identified Pbk, Fastk, Cdk19, Adck5, Trim28, and Pfkp as potential regulators of CD73. |
CRISPR/Cas9 CD73 knockout in human and murine pancreatic cancer cell lines, flow cytometry cell cycle analysis, migration assay, western blotting of ERK/STAT3 and E-cadherin pathways, kinase library CRISPR screen |
Cancers |
Medium |
37835536
|
| 2022 |
CD73 in lung adenocarcinoma cells physically interacts with EGFR (demonstrated by immunoprecipitation) and promotes activation of the AKT/mTOR signaling pathway, driving proliferation, migration, and invasion. |
Immunoprecipitation of CD73-EGFR interaction, siRNA knockdown and overexpression of CD73 in A549 cells, western blotting of AKT/mTOR pathway, proliferation, colony formation, wound healing, and Transwell invasion assays |
BioMed research international |
Low |
35813221
|
| 2019 |
CD73 knockdown in pancreatic ductal adenocarcinoma inhibited cell growth and induced G1 phase arrest via the AKT/ERK/cyclin D signaling pathway. TNFR2 was identified as involved in CD73-induced AKT and ERK signaling pathway activation in PDAC cells. |
CD73 knockdown, cell cycle analysis, western blotting of AKT/ERK/cyclin D, TNFR2 inhibition experiments |
Journal of molecular medicine |
Low |
30927045
|
| 2021 |
Structure-based design of methylenephosphonic acid CD73 inhibitors exploited key binding interactions of the known inhibitor AMPCP with human CD73, demonstrating that the catalytic site of CD73 can accommodate this class of competitive inhibitors with high potency and selectivity against related ectonucleotidases. |
Structure-based drug design using hCD73 crystal structure with AMPCP, in vitro enzymatic inhibition assays, selectivity profiling against related ectonucleotidases, pharmacokinetic analysis |
Journal of medicinal chemistry |
Medium |
33399453
|
| 2014 |
CD73 catalytic activity (AMP to adenosine conversion) can be harnessed to instruct supramolecular hydrogelation: CD73 dephosphorylation of AMP precursors triggers self-assembly of nanofibers forming hydrogels, demonstrating that CD73 enzymatic activity can be coupled to materials formation. |
Enzymatic supramolecular hydrogelation assay, nanofiber characterization |
Journal of colloid and interface science |
Low |
25524006
|
| 2022 |
AHR promotes TET2 expression by binding to the TET2 promoter (kynurenine-dependent), and TET2 in turn regulates NT5E promoter methylation status to control CD73 expression on regulatory T cells. Downregulation of the AHR/TET2/NT5E axis in SLE Tregs is associated with reduced CD73 expression and impaired immunosuppressive function. |
ChIP assay (AHR binding to TET2 promoter), methylation-specific analysis of NT5E promoter, kynurenine treatment of Tregs and Jurkat T cells, flow cytometry, adenosine receptor pathway analysis |
Immunology |
Medium |
36314527
|