# CD38 Inhibition Ameliorates Age-Related CognitiveDecline via a Choroid Plexus–Cerebrospinal Fluid–Hippocampus Axis

**Authors:** Eric Verdin, Jingqi Fang, Rebeccah Riley, Kevin Schneider, Rosalba Perrone, Prasanna Kumaar, Christina King, Grant Kauwe, Andrea Roberts, Genesis Vega Hormazabal, Yini Zhang, Ethan Millard, Xinran Liu, Wendy Jara, Carlos Galicia Aguirre, Harrison Baker, Natalia Murad, Ben Ambrose, Tommy Tran, Nicolas Martin, Ran Zhang, Durai Sellegounder, Simon Melov, David Furman, Tara Tracy, Akos Gerencser, Birgit Schilling, Lisa Ellerby

PMC · DOI: 10.21203/rs.3.rs-8330519/v1 · Research Square · 2026-01-06

## TL;DR

Blocking CD38, an enzyme linked to aging, improves cognitive function in old mice by boosting brain energy and reducing inflammation.

## Contribution

CD38 inhibition is shown to rejuvenate brain aging via choroid plexus–CSF–hippocampus signaling and a new brain-penetrant inhibitor is introduced.

## Key findings

- CD38 inhibition restores NAD+ levels and suppresses senescence in choroid plexus pericytes.
- CSF proteomic/metabolomic profiles improve with CD38 inhibition, reducing inflammation and enhancing neurotrophic support.
- CD38 inhibition reverses age-related hippocampal transcriptional changes and enhances synaptic plasticity and cognition.

## Abstract

Age-related cognitive decline represents a major and unresolved challenge of human aging. Here, we identify the NAD+-consuming enzyme CD38 as a central regulator of cognitive aging acting through a choroid plexus–cerebrospinal fluid (CSF)–hippocampus axis. CD38 expression increases with age and localizes primarily to pericytes in the choroid plexus, where it depletes NAD+, impairs mitochondrial function, and promotes cellular senescence. Genetic ablation or pharmacological inhibition of CD38 restores NAD+ levels, suppresses senescence markers, and improves choroid plexus function, resulting in a rejuvenated CSF proteomic and metabolomic profile characterized by reduced inflammatory signaling and enhanced neurotrophic support. These changes propagate to the hippocampus, reversing age-related transcriptional signatures and enhancing synaptic plasticity. A novel, brain-penetrant CD38 inhibitor, NTX-748, reproduced the benefits of CD38 deficiency—elevating systemic and brain NAD+ levels, improving long-term potentiation, and enhancing multiple domains of cognition in aged mice. Collectively, these findings identify the choroid plexus as a metabolic gatekeeper of brain aging and establish CD38 inhibition as a promising therapeutic strategy to promote cognitive resilience and healthy brain aging.

## Linked entities

- **Genes:** CD38 (CD38 molecule) [NCBI Gene 952]
- **Chemicals:** NAD+ (PubChem CID 5892)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Sirt3 (sirtuin 3) [NCBI Gene 64384] {aka 2310003L23Rik, Sir2l3}, Cdkn1a (cyclin dependent kinase inhibitor 1A) [NCBI Gene 12575] {aka CAP20, CDKI, CIP1, Cdkn1, P21, SDI1}, Rbfox3 (RNA binding protein, fox-1 homolog (C. elegans) 3) [NCBI Gene 52897] {aka Fox-3, Hrnbp3, NeuN, Neuna60}, Fgg (fibrinogen gamma chain) [NCBI Gene 99571] {aka 3010002H13Rik}, Nr1h3 (nuclear receptor subfamily 1, group H, member 3) [NCBI Gene 22259] {aka LXR, RLD1, Unr1}, Gem (GTP binding protein overexpressed in skeletal muscle) [NCBI Gene 14579], Serpind1 (serine (or cysteine) peptidase inhibitor, clade D, member 1) [NCBI Gene 15160] {aka HC-II, HCII, Hcf2}, Ctss (cathepsin S) [NCBI Gene 13040] {aka Cats}, Serpina1d (serine (or cysteine) peptidase inhibitor, clade A, member 1D) [NCBI Gene 20703] {aka AAT, DOM-7, Dom1, Dom4, PI4, Serpina1a}, Csf2 (colony stimulating factor 2 (granulocyte-macrophage)) [NCBI Gene 12981] {aka CSF, Csfgm, GMCSF, Gm-CSf, MGI-IGM}, C1qb (complement component 1, q subcomponent, beta polypeptide) [NCBI Gene 12260] {aka Adia}, Cd38 (CD38 antigen) [NCBI Gene 12494] {aka ADPRC 1, Cd38-rs1, I-19}, Pdgfrb (platelet derived growth factor receptor, beta polypeptide) [NCBI Gene 18596] {aka CD140b, PDGFR-1, Pdgfr}, Gapdh (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 14433] {aka Gapd}, C4b (complement C4B (Chido blood group)) [NCBI Gene 12268] {aka C4, Ss}, Hmgb1 (high mobility group box 1) [NCBI Gene 15289] {aka HMG-1, Hmg1, SBP-1, p30}, Cdh1 (cadherin 1) [NCBI Gene 12550] {aka ARC-1, E-cad, Ecad, L-CAM, UVO, Um}, Pecam1 (platelet/endothelial cell adhesion molecule 1) [NCBI Gene 18613] {aka Cd31, PECAM-1, Pecam}, TRPM2 (transient receptor potential cation channel subfamily M member 2) [NCBI Gene 7226] {aka EREG1, KNP3, LTRPC2, LTrpC-2, NUDT9H, NUDT9L1}, Ttr (transthyretin) [NCBI Gene 22139] {aka prealbumin}, Anpep (alanyl aminopeptidase, membrane) [NCBI Gene 16790] {aka AP-M, AP-N, Apn, Cd13, P150}, CD38 (CD38 molecule) [NCBI Gene 952] {aka ADPRC 1, ADPRC1, cADPR1}, Serping1 (serine (or cysteine) peptidase inhibitor, clade G, member 1) [NCBI Gene 12258] {aka C1 Inh, C1INH., C1Inh, C1nh}, Serpina3k (serine (or cysteine) peptidase inhibitor, clade A, member 3K) [NCBI Gene 20714] {aka 1300001I07Rik, D12Rp54, MMCM2, MMSpi2, RP54, Spi-2}, Cfh (complement component factor h) [NCBI Gene 12628] {aka Mud-1, NOM, Sas-1, Sas1}
- **Diseases:** Age (MESH:D019588), choroid plexus dysfunction (MESH:D020288), neuroinflammation (MESH:D000090862), neurodegenerative (MESH:D019636), mitochondrial dysfunction (MESH:D028361), infection (MESH:D007239), Anxiety (MESH:D001007), inflammation (MESH:D007249), metabolic dysfunction (MESH:D008659), intracranial hemorrhage (MESH:D020300), brain dysfunction (MESH:D001927), Cognitive Decline (MESH:D003072), AD (MESH:D000544)
- **Chemicals:** antimycin A (MESH:D000968), xylene (MESH:D014992), TBS (MESH:D013725), Cysteine (MESH:D003545), MgSO4 (MESH:D008278), ACN (MESH:C032159), MgCl2 (MESH:D015636), Alexa Fluor (-), methionine (MESH:D008715), L-glutamine (MESH:D005973), TBS-T (MESH:C027647), NAM (MESH:D009536), phosphoric acid (MESH:C030242), Glucose (MESH:D005947), methanol (MESH:D000432), DAPI (MESH:C007293), ammonium hydroxide (MESH:D064753), FA (MESH:C030544), pyruvate (MESH:D019289), HCl (MESH:D006851), nitrogen (MESH:D009584), Formalin (MESH:D005557), DEPC (MESH:D004047), SDS (MESH:D012967), C600 (MESH:C040656), calcium (MESH:D002118), TEAB (MESH:C041737), glutamate (MESH:D018698), iodoacetamide (MESH:D007460), NaCl (MESH:D012965), ammonium acetate (MESH:C018824), KCl (MESH:D011189), water (MESH:D014867), trypan blue (MESH:D014343), HEPES (MESH:D006531), formamide (MESH:C031066), cADPR (MESH:D036563), xylazine (MESH:D014991), cholesterol (MESH:D002784), Nicotinamide 1,N6-ethenoadenine dinucleotide (MESH:C011038), dithiothreitol (MESH:D004229), paraffin (MESH:D010232), NAD+ (MESH:D009243), CO2 (MESH:D002245), Sucrose (MESH:D013395), rotenone (MESH:D012402), oligomycin (MESH:D009840), ATP (MESH:D000255), acetic acid (MESH:D019342), nicotinamide riboside (MESH:C018613), O2 (MESH:D010100), EtOH (MESH:D000431), EDTA (MESH:D004492), NaHCO3 (MESH:D017693), CaCl2 (MESH:D002122), ADP-ribose (MESH:D000246), paraformaldehyde (MESH:C003043), FCCP (MESH:D002259), Tween-20 (MESH:D011136), NMN (MESH:D009537)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090], Ovis aries (domestic sheep, species) [taxon 9940], Rattus norvegicus (brown rat, species) [taxon 10116]
- **Cell lines:** /6J — Homo sapiens (Human), Cutaneous melanoma, Cancer cell line (CVCL_W797)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12803333/full.md

## References

94 references — full list in the complete paper: https://tomesphere.com/paper/PMC12803333/full.md

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Source: https://tomesphere.com/paper/PMC12803333