Evidence map›Paper›PMID 33836143›Full record

ArticleStem cell reports2021

Efficient conversion of human induced pluripotent stem cells into microglia by defined transcription factors.

Shih-Wei Chen, Yu-Sheng Hung, Jong-Ling Fuh, Nien-Jung Chen, Yeh-Shiu Chu, Shu-Cian Chen, Ming-Ji Fann, Yu-Hui Wong

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
7.3field-weighted citation impact, top 2% of its field
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

42 citing papers in PubMed, 81 citations in OpenAlex.

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  18. Accelerating Diverse Cell-Based Therapies Through Scalable Design.Annual review of chemical and biomolecular engineering · 2024
    Review
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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

8 authors at 1 institution in 1 country.

Shih-Wei ChenBrain Research Center, National Yang Ming Chiao Tung University, Taipei 112, Taiwan (ROC); Department of Life Sciences and Institute of Genome Sciences, School of Life Sciences, National Yang Ming Chiao Tung University, Taipei 112, Taiwan (ROC).
Yu-Sheng HungDepartment of Life Sciences and Institute of Genome Sciences, School of Life Sciences, National Yang Ming Chiao Tung University, Taipei 112, Taiwan (ROC).
Jong-Ling FuhBrain Research Center, National Yang Ming Chiao Tung University, Taipei 112, Taiwan (ROC); Division of General Neurology, Neurological Institute, Taipei Veterans General Hospital, Taipei 112, Taiwan (ROC).
Nien-Jung ChenInstitute of Microbiology and Immunology, School of Life Sciences, National Yang Ming Chiao Tung University, Taipei 112, Taiwan (ROC).
Yeh-Shiu ChuBrain Research Center, National Yang Ming Chiao Tung University, Taipei 112, Taiwan (ROC).
Shu-Cian ChenBrain Research Center, National Yang Ming Chiao Tung University, Taipei 112, Taiwan (ROC).
Ming-Ji FannBrain Research Center, National Yang Ming Chiao Tung University, Taipei 112, Taiwan (ROC); Department of Life Sciences and Institute of Genome Sciences, School of Life Sciences, National Yang Ming Chiao Tung University, Taipei 112, Taiwan (ROC).
Yu-Hui WongBrain Research Center, National Yang Ming Chiao Tung University, Taipei 112, Taiwan (ROC); Department of Life Sciences and Institute of Genome Sciences, School of Life Sciences, National Yang Ming Chiao Tung University, Taipei 112, Taiwan (ROC). Electronic address: yuhui.wong@nycu.edu.tw.
National Yang Ming Chiao Tung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microglia, the immune cells of the central nervous system, play critical roles in brain physiology and pathology. We report a novel approach that produces, within 10 days, the differentiation of human induced pluripotent stem cells (hiPSCs) into microglia (iMG) by forced expression of both SPI1 and CEBPA. High-level expression of the main microglial markers and the purity of the iMG cells were confirmed by RT-qPCR, immunostaining, and flow cytometry analyses. Whole-transcriptome analysis demonstrated that these iMGs resemble human fetal/adult microglia but not human monocytes. Moreover, these iMGs exhibited appropriate physiological functions, including various inflammatory responses, ADP/ATP-evoked migration, and phagocytic ability. When co-cultured with hiPSC-derived neurons, the iMGs respond and migrate toward injured neurons. This study has established a protocol for the rapid conversion of hiPSCs into functional iMGs, which should facilitate functional studies of human microglia using different disease models and also help with drug discovery.

Indexed as

Cell DifferentiationAdenosine DiphosphateAdenosine TriphosphateBiomarkersCalcium SignalingCell MovementCulture MediaGene Expression ProfilingGene Expression RegulationHumansInduced Pluripotent Stem CellsMicrogliaTranscription FactorsAdenosine DiphosphateAdenosine TriphosphateBiomarkersCulture MediaTranscription FactorsCEBPAinduced microgliainduced pluripotent stem cellsreprogrammingSPI1/PU.1

Identifiers

PMID33836143
PMCPMC8185376
OpenAlexW3148088325

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.