Evidence map›Paper›PMID 40023165›Full record

ArticleCell reports. Medicine2025

Outer radial glia promotes white matter regeneration after neonatal brain injury.

Hideo Jinnou, Lauren M Rosko, Satoshi Yamashita, Soichiro Henmi, Jaya Prasad, Van K Lam, Artur Agaronyan, Tsang-Wei Tu, Yuka Imamura, Kazuya Kuboyama and 4 more

Abstract read
In one paragraph

Article in Cell reports. Medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
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

14 authors.

Hideo JinnouCenter for Neuroscience Research, Children's National Research Institute, Children's National Hospital, Washington, DC 20010, USA; Department of Pediatrics and Neonatology, Nagoya City University, Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Lauren M RoskoCenter for Neuroscience Research, Children's National Research Institute, Children's National Hospital, Washington, DC 20010, USA.
Satoshi YamashitaCenter for Neuroscience Research, Children's National Research Institute, Children's National Hospital, Washington, DC 20010, USA.
Soichiro HenmiCenter for Neuroscience Research, Children's National Research Institute, Children's National Hospital, Washington, DC 20010, USA.
Jaya PrasadCenter for Neuroscience Research, Children's National Research Institute, Children's National Hospital, Washington, DC 20010, USA.
Van K LamCenter for Neuroscience Research, Children's National Research Institute, Children's National Hospital, Washington, DC 20010, USA.
Artur AgaronyanMolecular Imaging Laboratory, Department of Radiology, Howard University, Washington, DC 20059, USA.
Tsang-Wei TuMolecular Imaging Laboratory, Department of Radiology, Howard University, Washington, DC 20059, USA.
Yuka ImamuraDepartments of Pharmacology and Biochemistry and Molecular Biology, Pennsylvania State University College of Medicine, Hershey, PA 17033, USA.
Kazuya KuboyamaDepartment of Developmental and Regenerative Neurobiology, Institute of Brain Science, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Kazunobu SawamotoDepartment of Developmental and Regenerative Neurobiology, Institute of Brain Science, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Kazue Hashimoto-ToriiCenter for Neuroscience Research, Children's National Research Institute, Children's National Hospital, Washington, DC 20010, USA; Department of Pediatrics, Pharmacology and Physiology, George Washington University School of Medicine and Health Sciences, Washington, DC 20037, USA.
Nobuyuki IshibashiCenter for Neuroscience Research, Children's National Research Institute, Children's National Hospital, Washington, DC 20010, USA; Department of Pediatrics, Pharmacology and Physiology, George Washington University School of Medicine and Health Sciences, Washington, DC 20037, USA. Electronic address: nishibas@childrensnational.org.
Vittorio GalloCenter for Neuroscience Research, Children's National Research Institute, Children's National Hospital, Washington, DC 20010, USA; Department of Pediatrics, Pharmacology and Physiology, George Washington University School of Medicine and Health Sciences, Washington, DC 20037, USA; Seattle Children's Research Institute, Seattle Children's Hospital, Seattle, WA 98101, USA; Department of Pediatrics, University of Washington, Seattle, WA 98105, USA. Electronic address: vittorio.gallo@seattlechildrens.org.

Funding

Cell Therapy for Neuroprotection in Congenital Heart DiseaseR01HL139712 · NHLBI · CHILDREN'S RESEARCH INSTITUTE · PI Nobuyuki Ishibashi · 2018 to 2026
$5.7M
White Matter Protection in the Fetus with Congenital Heart DiseaseR01HL146670 · NHLBI · CHILDREN'S RESEARCH INSTITUTE · PI ISHIBASHI, NOBUYUKI · 2020 to 2023
$3.3M
In vivo MRI Measures of Brain Metabolism in Traumatic Brain InjuryR01NS123442 · NINDS · HOWARD UNIVERSITY · PI Tsang-Wei Tu · 2022 to 2026
$1.9M
NHLBI NIH HHS R01 HL139712NHLBI NIH HHS R01 HL146670NINDS NIH HHS R01 NS123442
6 · The paper itself

Abstract

The developing gyrencephalic brain contains a large population of neural stem cells in the ventricular zone and outer subventricular zone (OSVZ), the latter populated by outer radial glia (oRG). The role of oRG during postnatal development is not well understood. We show that oRG cells increase proliferative capacity and contribute to oligodendrocyte precursor cell (OPC) production following brain injury in human infants and neonatal piglets, whose brains resemble the human brain in structure and development. RNA sequencing revealed oRG-specific transcriptional responses to injury in piglets and showed that the activating transcription factor 5 (ATF5) pathway positively regulates oRG proliferation. Intranasal activation of ATF5 using salubrinal enhanced OSVZ-derived oligodendrogenesis in the injured periventricular white matter and improved functional recovery. These results reveal a key role for postnatal oRG in brain injury recovery and identify ATF5 as a potential therapeutic target for treating white matter injury in infants.

Indexed as

Brain InjuriesEpendymoglial CellsNeurogliaRegenerationWhite MatterActivating Transcription FactorsAnimalsAnimals, NewbornCell ProliferationCinnamatesHumansInfant, NewbornMaleNeural Stem CellsOligodendrocyte Precursor CellsOligodendrogliaActivating Transcription FactorsCinnamatessalubrinalThioureaATF5diffusion tensor imaginggait behaviorMCL1neural stem cellsoligodendrocyte precursor cellsouter radial gliaouter subventricular zonepiglet brainwhite matter regeneration

Identifiers

PMID40023165
PMCPMC11970391

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.