Evidence map›Paper›PMID 32221280›Full record

ArticleNature communications2020

Human iPSC-derived mature microglia retain their identity and functionally integrate in the chimeric mouse brain.

Ranjie Xu, Xiaoxi Li, Andrew J Boreland, Anthony Posyton, Kelvin Kwan, Ronald P Hart, Peng Jiang

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 129 papers.

0numbers the graph read from it
0cells of the map it votes in
129citing papers in PubMed
11.5field-weighted citation impact, top 1% 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

129 citing papers in PubMed, 201 citations in OpenAlex.

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  12. Exploration (Beijing, China) · 2026
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69 more citing papers are in PubMed but not listed here.

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

7 authors at 1 institution in 2 countries.

Ranjie XuDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ, 08854, USA.
Xiaoxi LiDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ, 08854, USA.
Andrew J BorelandDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ, 08854, USA.
Anthony PosytonDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ, 08854, USA.
Kelvin KwanDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ, 08854, USA.ORCID http://orcid.org/0000-0002-8617-5543
Ronald P HartDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ, 08854, USA.ORCID http://orcid.org/0000-0003-4836-8712
Peng JiangDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ, 08854, USA. peng.jiang@rutgers.edu.ORCID http://orcid.org/0000-0002-2650-3082
Rutgers, The State University of New Jersey · US

Funding

Subject CollectionU10AA008401 · NIAAA · SUNY DOWNSTATE MEDICAL CENTER · PI JESSICA E SALVATORE · 1989 to 2026
$162.7M
X-RAY STRUCTURE OF RIFM PROTEIN FROM THE BIOSYNTHESIS PATHWAY OF THE ANSAMYCIN AP41RR012408 · NCRR · BROOKHAVEN SCIENCE ASSOC-BROOKHAVEN LAB · PI ORVILLE, ALLEN M · 1998 to 2011
$32.2M
UMDNJ TRAINING GRANT IN BIOTECHNOLOGYT32GM008339 · NIGMS · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI YARMUSH, MARTIN L · 1989 to 2019
$6.1M
Deciphering the neural basis of alcohol use disorders using human and mouse neuronsR01AA023797 · NIAAA · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI ZHIPING P. PANG · 2016 to 2026
$4.8M
Mechanism of Gene Environment Interactions in Alzheimer's DiseaseR01ES026057 · NIEHS · NORTHEAST OHIO MEDICAL UNIVERSITY · PI RICHARDSON, JASON R · 2016 to 2020
$2.4M
Novel Functions of OLIG2 in Regulating Human Interneuron Production in Health and DiseaseR01NS102382 · NINDS · RUTGERS, THE STATE UNIV OF N.J. · PI JIANG, PENG · 2018 to 2022
$1.6M
Developing an Astroglial Model for Down SyndromeR21HD091512 · NICHD · RUTGERS, THE STATE UNIV OF N.J. · PI JIANG, PENG · 2017 to 2018
$426k
NCRR NIH HHS P41 RR012408NIAAA NIH HHS R01 AA023797NIAAA NIH HHS U10 AA008401NICHD NIH HHS R21 HD091512NIEHS NIH HHS R01 ES026057NIGMS NIH HHS T32 GM008339NINDS NIH HHS R01 NS102382
6 · The paper itself

Abstract

Microglia, the brain-resident macrophages, exhibit highly dynamic functions in neurodevelopment and neurodegeneration. Human microglia possess unique features as compared to mouse microglia, but our understanding of human microglial functions is largely limited by an inability to obtain human microglia under homeostatic states. Here, we develop a human pluripotent stem cell (hPSC)-based microglial chimeric mouse brain model by transplanting hPSC-derived primitive macrophage progenitors into neonatal mouse brains. Single-cell RNA-sequencing of the microglial chimeric mouse brains reveals that xenografted hPSC-derived microglia largely retain human microglial identity, as they exhibit signature gene expression patterns consistent with physiological human microglia and recapitulate heterogeneity of adult human microglia. Importantly, the engrafted hPSC-derived microglia exhibit dynamic response to cuprizone-induced demyelination and species-specific transcriptomic differences in the expression of neurological disease-risk genes in microglia. This model will serve as a tool to study the role of human microglia in brain development and degeneration.

Indexed as

Cell DifferentiationAnimalsBrainCell LineChimeraCuprizoneDemyelinating DiseasesFemaleHumansImaging, Three-DimensionalInduced Pluripotent Stem CellsMiceMicrogliaRNA-SeqSingle-Cell AnalysisTranscriptomeCuprizone

Identifiers

PMID32221280
PMCPMC7101330
OpenAlexW3013671437

What OpenQuestion holds

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LicenceCC BY
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.