Evidence map›Paper›PMID 41066163›Full record

ArticleAlzheimer's & dementia : the journal of the Alzheimer's Association2025

Alzheimer's disease-associated PLCG2 variants alter microglial state and function in human induced pluripotent stem cell-derived microglia-like cells.

Logan M Bedford, Kaylee D Tutrow, Karly Hooper, Evan J Messenger, Melody Hernandez, Bruce T Lamb, Jason S Meyer, Timothy I Richardson, Stephanie J Bissel

Abstract read
In one paragraph

Article in Alzheimer's & dementia : the journal of the Alzheimer's Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Neuroinflammation in glaucoma: a myriad of cellular pathways and players.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Review
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  6. PreoperativeFrontiers in bioinformatics · 2026
    Review
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Logan M BedfordStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Kaylee D TutrowStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Karly HooperDepartment of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Evan J MessengerStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Melody HernandezDepartment of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Bruce T LambStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Jason S MeyerStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Timothy I RichardsonStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Stephanie J BisselStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, Indiana, USA.ORCID 0000-0002-7376-2327

Funding

Structural Biology CoreU54AG065181 · NIA · INDIANA UNIVERSITY INDIANAPOLIS · PI Timothy I Richardson · 2019 to 2026
$61.3M
Training Grant on Alzheimer's Disease and ADRD at Indiana UniversityT32AG071444 · NIA · INDIANA UNIVERSITY INDIANAPOLIS · PI GARY E. LANDRETH, Bruce T Lamb · 2021 to 2026
$2.8M
Impact of PLCG2 Alzheimer's Disease Risk Variants on Microglia Biology and Disease PathogenesisRF1AG074566 · NIA · INDIANA UNIVERSITY INDIANAPOLIS · PI BISSEL, STEPHANIE J, LAMB, BRUCE T · 2021 to 2021
$2.3M
Impact of PLCG2 Alzheimer's Disease Risk Variants on Microglia Biology and Disease PathogenesisR01AG074566 · NIA · INDIANA UNIVERSITY INDIANAPOLIS · PI BISSEL, STEPHANIE J, LAMB, BRUCE T · 2024 to 2025
$1.5M
Investigating the role of the fractalkine axis in Alzheimer's Disease pathology using human induced pluripotent stem cellsF30AG084304 · NIA · INDIANA UNIVERSITY INDIANAPOLIS · PI Kaylee Tutrow · 2024 to 2026
$128k
Validating PLCG2 as a target for the treatment of Alzheimer's Disease through cell biology and pharmacological toolsF31AG089990 · NIA · INDIANA UNIVERSITY INDIANAPOLIS · PI BEDFORD, LOGAN · 2024 to 2025
$74k
NIA NIH HHS F30 AG084304NIA NIH HHS F30AG084304NIA NIH HHS F31 AG089990NIA NIH HHS F31AG089990NIA NIH HHS R01 AG074566NIA NIH HHS R01AG074566NIA NIH HHS RF1 AG074566NIA NIH HHS T32 AG071444NIA NIH HHS T32AG071444NIA NIH HHS U54 AG065181NIA NIH HHS U54AG065181
6 · The paper itself

Abstract

introductionVariants of phospholipase C gamma 2 (PLCG2), a key microglial immune signaling protein, are genetically linked to Alzheimer's disease (AD) risk. Understanding how PLCG2 variants alter microglial function is critical for identifying mechanisms that drive neurodegeneration or resiliency in AD.

methodsInduced pluripotent stem cell (iPSC) -derived microglia carrying the protective PLCG2

resultsProtective PLCG2 DISCUSSION: These findings demonstrate that PLCG2 variants drive distinct microglia transcriptomes that influence microglial functional responses that could contribute to AD risk and protection. Targeting PLCG2-mediated signaling may represent a powerful therapeutic strategy to modulate neuroinflammation. HIGHLIGHTS: The impact of Alzheimer's disease protective- and risk-associated variants of phospholipase C gamma 2 (PLCG2) on the transcriptome and function of induced pluripotent stem cell (iPSC) -derived microglia was investigated. PLCG2 risk variant microglia exhibited a basal transcriptional profile similar to PLCG2-deficient microglia but significantly different from isotype control and the transcriptionally similar PLCG2 protective variant microglia. PLCG2 risk variant and PLCG2-deficient microglia show decreased levels of triggering receptor expressed on myeloid cells 2 (TREM2). The differential transcriptional pathways of protective and risk-associated PLCG2 variant microglia functionally affect proliferation, apoptosis, and immune response. Protective PLCG2 microglia show resilience to apoptosis and increased cytokine/chemokine secretion upon exposure to lipopolysaccharide (LPS).

Indexed as

Alzheimer DiseaseInduced Pluripotent Stem CellsMicrogliaPhospholipase C gammaHumansMembrane GlycoproteinsReceptors, ImmunologicTranscriptomeMembrane GlycoproteinsPhospholipase C gammaPLCG2 protein, humanReceptors, ImmunologicTREM2 protein, humanAlzheimer's diseaseapoptosiscell deathcell proliferationgenetic predisposition to diseasegenetic variantsinduced pluripotent stem cellsmicrogliaphenotypePLCG2RNA: sequence analysis, RNA

Identifiers

PMID41066163
PMCPMC12510136

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Registered trials

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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.