Evidence map›Paper›PMID 42068248›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2026

Quantification of SARM1 NADase Activity in Human Peripheral Blood Mononuclear Cells.

Lila F Dabill, Ivana R Shen, Jennifer M Brazill, Alicia Neiner, Yo Sasaki, Erica L Scheller

Abstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Lila F DabillDivision of Bone and Mineral Diseases, Washington University School of Medicine, St. Louis, Missouri, USA.
Ivana R ShenDivision of Bone and Mineral Diseases, Washington University School of Medicine, St. Louis, Missouri, USA.
Jennifer M BrazillDivision of Bone and Mineral Diseases, Washington University School of Medicine, St. Louis, Missouri, USA.
Alicia NeinerDepartment of Genetics, Washington University School of Medicine, St. Louis, Missouri, USA.
Yo SasakiDepartment of Genetics, Washington University School of Medicine, St. Louis, Missouri, USA.
Erica L SchellerDivision of Bone and Mineral Diseases, Washington University School of Medicine, St. Louis, Missouri, USA.ORCID https://orcid.org/0000-0002-1551-3816

Funding

HHS | National Institutes of Health (NIH) U24-DK115255
6 · The paper itself

Abstract

SARM1 (sterile α and TIR motif-containing protein-1) is an NADase enzyme that serves as the central executioner of Wallerian axon degeneration. Given this, SARM1 is of high interest as a candidate therapeutic target, and SARM1 inhibitors are currently in clinical trials for treatment of neurodegeneration. Beyond neuroscience, emerging studies reveal that SARM1 may also drive aspects of bone fragility, liver pathology, adipose expansion, and insulin resistance in metabolic disease. However, we lack methods to quantify SARM1 activation in humans to better define patients at high risk of SARM1-mediated tissue damage. Unlike neurons, peripheral blood mononuclear cells (PBMCs) represent an easily accessible population for clinical screening. While SARM1 gene expression has been identified in PBMCs, it is less known whether functional SARM1 NADase is present. We hypothesized that by pairing activators and inhibitors of SARM1 with analysis of downstream changes in cellular metabolites, we could identify and quantify both basal SARM1 activity and the SARM1 activation potential of human PBMCs. Our results reveal that SARM1 agonist pyrinuron, also known as Vacor, activates a dose-dependent increase in cAPDR and the cADPR:ADPR ratio that is arrested when paired with SARM1 inhibitor DSRM-3716. Changes in secondary metabolites including NAD+, NMN, NaMN, ATP, AMP, IMP, inosine, and succinyl adenosine were also characterized and used to generate a working model of PBMC SARM1 activation. Overall, these findings demonstrate that human PBMCs have detectable SARM1 activation potential and could be leveraged as a clinical readout of SARM1 expression and activity across diverse disease contexts.

Indexed as

Armadillo Domain ProteinsCytoskeletal ProteinsLeukocytes, MononuclearNAD+ NucleosidaseHumansArmadillo Domain ProteinsCytoskeletal ProteinsNAD+ NucleosidaseSARM1 protein, human

Identifiers

PMID42068248
PMCPMC13135277

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.