Evidence map›Paper›PMID 41262332›Full record

ArticleFrontiers in bioinformatics2025

Cellf-deception: human microglia clone 3 (HMC3) cells exhibit more astrocyte-like than microglia-like gene expression.

Kylee K Rahm, Branden S Kinghorn, Myanna J Moody, Ben C Stone, Kenton C Strong, Brian S Kim, Yen Jou Chang, Samantha N Sleight, Alyssa A Nitz, David V Hansen and 1 more

Abstract read
In one paragraph

Article in Frontiers in bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

11 authors.

Kylee K Rahm *Department of Microbiology and Molecular Biology, Brigham Young University, Provo, UT, United States.
Branden S KinghornDepartment of Biology, Brigham Young University, Provo, UT, United States.
Myanna J MoodyDepartment of Biology, Brigham Young University, Provo, UT, United States.
Ben C StoneDepartment of Biology, Brigham Young University, Provo, UT, United States.
Kenton C StrongComputer Science Department, Brigham Young University, Provo, UT, United States.
Brian S KimDepartment of Biology, Brigham Young University, Provo, UT, United States.
Yen Jou ChangDepartment of Chemistry and Biochemistry, Brigham Young University, Provo, UT, United States.
Samantha N SleightDepartment of Chemistry and Biochemistry, Brigham Young University, Provo, UT, United States.
Alyssa A NitzDepartment of Biology, Brigham Young University, Provo, UT, United States.
David V HansenDepartment of Chemistry and Biochemistry, Brigham Young University, Provo, UT, United States.
Matthew H Bailey *Department of Biology, Brigham Young University, Provo, UT, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Recent advances in Alzheimer's research suggest that the brain's immune system plays a critical role in the development and progression of this devastating disease. Microglial cells are vital as immune cells in the brain's defense system. Human Microglia Clone 3 (HMC3) is a cell line developed as a promising experimental model to understand the role of microglial cells in human diseases including Alzheimer's and other neurodegenerative diseases. The frequency of HMC3 cell usage has increased in recent years, with the idea that this cell line could serve as a convenient model for human microglial cell functions. Methods: We utilized gene-pair ratios from bulk and single-cell RNA sequencing (scRNA-seq) expression data to create predictive models of cell-type origins. Results: Our model reveals that the HMC3 cell line represents various cell types, with the highest cell similarity score relating to astrocytes, not microglia. Discussion: These findings suggest that the HMC3 cell line is not a reliable human microglia model and that extreme caution should be taken when interpreting the results of studies using the HMC3 cell line.

Indexed as

Alzheimer’s diseaseastrocytescell-type classificationHMC3 cellsiPSC-derived microglia (iMG)microglia

Identifiers

PMID41262332
PMCPMC12623408

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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.