Evidence map›Paper›PMID 40121230›Full record

ArticleNature communications2025

Radial glia integrin avb8 regulates cell autonomous microglial TGFβ1 signaling that is necessary for microglial identity.

Gabriel L McKinsey, Nicolas Santander, Xiaoming Zhang, Kilian L Kleemann, Lauren Tran, Aditya Katewa, Kaylynn Conant, Matthew Barraza, Kian Waddell, Carlos O Lizama and 10 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors.

Gabriel L McKinseyUniversity of California San Francisco, Department of Pediatrics and Newborn Brain Research Institute, San Francisco, CA, USA. gabriel.mckinsey@ucsf.edu.ORCID http://orcid.org/0000-0002-5503-2830
Nicolas SantanderInstituto de Ciencias de la Salud, Universidad de O´Higgins, Rancagua, Chile.ORCID http://orcid.org/0000-0001-8919-833X
Xiaoming ZhangCenter for Translational Neurodegeneration and Regenerative Therapy, Tongji Hospital affiliated to Tongji University School of Medicine, Shanghai, China.
Kilian L KleemannAnn Romney Center for Neurologic Diseases, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0002-2753-6804
Lauren TranUniversity of California San Francisco, Department of Pediatrics and Newborn Brain Research Institute, San Francisco, CA, USA.
Aditya KatewaUniversity of California San Francisco, Department of Pediatrics and Newborn Brain Research Institute, San Francisco, CA, USA.
Kaylynn ConantUniversity of California San Francisco, Department of Pediatrics and Newborn Brain Research Institute, San Francisco, CA, USA.ORCID http://orcid.org/0000-0002-8114-4318
Matthew BarrazaNorthwestern University, Department of Neuroscience, Chicago, IL, USA.
Kian WaddellSidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, PA, USA.
Carlos O LizamaUniversity of California San Francisco, Cardiovascular Research Institute, San Francisco, CA, USA.ORCID http://orcid.org/0000-0002-0471-8525
Marie La RussaStanford University, Department of Bioengineering, Stanford, CA, USA.
Ji Hyun KooUniversity of California San Francisco, Department of Pediatrics and Newborn Brain Research Institute, San Francisco, CA, USA.
Hyunji LeeUniversity of California San Francisco, Department of Pediatrics and Newborn Brain Research Institute, San Francisco, CA, USA.
Dibyanti MukherjeeUniversity of California San Francisco, Department of Pediatrics and Newborn Brain Research Institute, San Francisco, CA, USA.
Helena PaidassiCIRI Centre International de Recherche en Infectiologie, Univ Lyon Inserm U1111 Université Claude Bernard Lyon 1 CNRS UMR5308 ENS de Lyon, F-69007, Lyon, France.ORCID http://orcid.org/0000-0001-9915-4365
E S AntonUniversity of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Kamran AtabaiUniversity of California San Francisco, Cardiovascular Research Institute, San Francisco, CA, USA.ORCID http://orcid.org/0000-0001-8170-7881
Dean SheppardUniversity of California San Francisco, Cardiovascular Research Institute, San Francisco, CA, USA.ORCID http://orcid.org/0000-0002-6277-2036
Oleg ButovskyAnn Romney Center for Neurologic Diseases, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0003-0186-8867
Thomas D ArnoldUniversity of California San Francisco, Department of Pediatrics and Newborn Brain Research Institute, San Francisco, CA, USA. thomas.arnold@ucsf.edu.ORCID http://orcid.org/0000-0002-7310-5597

Funding

Translational InformaticsP30CA082103 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Kate Taylor Shumate · 1999 to 2026
$209.7M
Rapid-Prototyping and Design CoreP30EY002162 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LAMBA, DEEPAK ASHOK · 1985 to 2024
$16.8M
DEFINING MECHANISMS OF PROGENITOR BALANCE AND NEURONAL CONNECTIVITYR35NS116859 · NINDS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI EVA S ANTON · 2020 to 2026
$4.1M
Defective heme transport in the development of congenital hydrocephalusR01NS123168 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ARNOLD, THOMAS DARMODY · 2021 to 2025
$3.1M
Primary Cilia: A Novel Signaling Gateway To Neural Circuit ModulationRF1MH132710 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ANTON, EVA S, LICHTMAN, JEFF W · 2025 to 2025
$2.2M
NCI NIH HHS P30 CA082103NEI NIH HHS P30 EY002162NIMH NIH HHS RF1 MH132710NINDS NIH HHS R01 NS123168NINDS NIH HHS R35 NS116859
6 · The paper itself

Abstract

Microglial diversity arises from the interplay between inherent genetic programs and external environmental signals. However, the mechanisms by which these processes develop and interact within the growing brain are not yet fully understood. Here, we show that radial glia-expressed integrin beta 8 (ITGB8) activates microglia-expressed TGFβ1 to drive microglial development. Domain-restricted deletion of Itgb8 in these progenitors results in regionally restricted and developmentally arrested microglia that persist into adulthood. In the absence of autocrine TGFβ1 signaling, microglia adopt a similar phenotype, leading to neuromotor symptoms almost identical to Itgb8 mutant mice. In contrast, microglia lacking the canonical TGFβ signal transducers Smad2 and Smad3 have a less polarized dysmature phenotype and correspondingly less severe neuromotor dysfunction. Our study describes the spatio-temporal regulation of TGFβ activation and signaling in the brain necessary to promote microglial development, and provides evidence for the adoption of microglial developmental signaling pathways in brain injury or disease.

Indexed as

Ependymoglial CellsIntegrin beta ChainsMicrogliaTransforming Growth Factor beta1AnimalsBrainMaleMiceMice, Inbred C57BLMice, KnockoutSignal TransductionSmad2 ProteinSmad3 Proteinintegrin beta8Integrin beta ChainsSmad2 ProteinSmad2 protein, mouseSmad3 ProteinSmad3 protein, mouseTgfb1 protein, mouseTransforming Growth Factor beta1

Identifiers

PMID40121230
PMCPMC11929771

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.