Evidence map›Paper›PMID 36936782›Full record

ArticleiScience2023

Microglia-containing cerebral organoids derived from induced pluripotent stem cells for the study of neurological diseases.

Yiling Hong, Xu Dong, Lawrence Chang, Chen Xie, Mariann Chang, Jose S Aguilar, Jimmy Lin, Juncheng Lin, Qingshun Q Li

Open access · goldAbstract read
In one paragraph

Article in iScience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 2 pooled it
5.0field-weighted citation impact, top 4% 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

29 citing papers in PubMed, 2 syntheses or guidelines pooled it, 41 citations in OpenAlex.

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  8. Human Brain Organoids: Development and Applications.Journal of microbiology and biotechnology · 2025
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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

9 authors at 1 institution in 1 country.

Yiling HongCollege of Veterinary Medicine, Western University of Health Sciences, Pomona, CA 91766-1854, USA.
Xu DongGraduate College of Biomedical Sciences, Western University of Health Sciences, Pomona, CA 91766-1854, USA.
Lawrence ChangGraduate College of Biomedical Sciences, Western University of Health Sciences, Pomona, CA 91766-1854, USA.
Chen XieCollege of Veterinary Medicine, Western University of Health Sciences, Pomona, CA 91766-1854, USA.
Mariann ChangCollege of Veterinary Medicine, Western University of Health Sciences, Pomona, CA 91766-1854, USA.
Jose S AguilarCollege of Veterinary Medicine, Western University of Health Sciences, Pomona, CA 91766-1854, USA.
Jimmy LinGraduate College of Biomedical Sciences, Western University of Health Sciences, Pomona, CA 91766-1854, USA.
Juncheng LinGraduate College of Biomedical Sciences, Western University of Health Sciences, Pomona, CA 91766-1854, USA.
Qingshun Q LiGraduate College of Biomedical Sciences, Western University of Health Sciences, Pomona, CA 91766-1854, USA.
Western University of Health Sciences · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microglia play an important role in neuroinflammation and neurodegeneration. Here, we report an approach for generating microglia-containing cerebral organoids derived from human pluripotent stem cells involving the supplementation of growth factors (FGF, EGF, heparin) and 10% CO2 culture conditions. Using this platform, Western Pacific Amyotrophic Lateral Sclerosis and Parkinsonism-Dementia Complex (ALS-PDC) cerebral organoids were generated from patient-derived induced pluripotent stem cells (iPSCs). These ALS-PDC-affected organoids had more reactive astrocytes and M1 microglia, and had fewer M2 microglia than their unaffected counterparts, leading to impaired microglia-mediated phagocytosis. RNA-seq analysis of ALS-PDC and control organoids indicated that the most significant changes were microglia- and astrocyte-related genes (IFITM1/2, TGF-β, and GFAP). The most significantly downregulated pathway was type I interferon signaling. Interferon-gamma supplementation increased IFITM expression, enhanced microglia-mediated phagocytosis, and reduced beta-amyloid accumulation in ALS-PDC-affected network. The results demonstrated the feasibility of using microglia-containing organoids for the study of neurodegenerative diseases.

Indexed as

Cell biologyImmunologyNeuroscienceStem cells research

Identifiers

PMID36936782
PMCPMC10014280
OpenAlexW4321764338

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.