Evidence map›Paper›PMID 40388609›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Imaging a concussion and the ensuing immune response at the blood-brain barrier.

Rita H Nguyen, Michelle Newton, Rachel M Kratofil, Brittney N V Scott, Fernanda Castanheira, Jung-Seok Kim, Florent Ginhoux, Steffen Jung, Paul Kubes

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
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.

Rita H NguyenDepartment of Pharmacology and Physiology, University of Calgary, Calgary T2N1N4, AB, Canada.ORCID 0009-0004-0795-8016
Michelle NewtonDepartment of Pharmacology and Physiology, University of Calgary, Calgary T2N1N4, AB, Canada.
Rachel M KratofilDepartment of Pharmacology and Physiology, University of Calgary, Calgary T2N1N4, AB, Canada.ORCID 0000-0003-3927-2508
Brittney N V ScottDepartment of Pharmacology and Physiology, University of Calgary, Calgary T2N1N4, AB, Canada.
Fernanda CastanheiraDepartment of Pharmacology and Physiology, University of Calgary, Calgary T2N1N4, AB, Canada.
Jung-Seok KimDepartment of Immunology and Biological Regeneration, Weizmann Institute of Science, Rehovot 76100, Israel.ORCID 0000-0003-0284-1658
Florent GinhouxShanghai Institute of Immunology, Department of Immunology and Microbiology, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.ORCID 0000-0002-2857-7755
Steffen JungDepartment of Immunology and Biological Regeneration, Weizmann Institute of Science, Rehovot 76100, Israel.ORCID 0000-0003-4290-5716
Paul KubesDepartment of Pharmacology and Physiology, University of Calgary, Calgary T2N1N4, AB, Canada.ORCID 0000-0002-2835-4244

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Concussions can cause debilitating symptoms despite no evidence of structural changes on diagnostic imaging. The cellular events occurring in the brain parenchyma following concussion, especially repetitive concussion, are not well elucidated. We developed a concussion model to induce a confined area of injury without causing frank hemorrhage. Using intravital microscopy, we observe activation of the vasculature that supported neutrophil rolling and platelet adhesion but no overt cellular recruitment from blood into brain parenchyma. Activated resident, not monocyte-derived, macrophages relocated to the injury site via Cx3cr1 and phagocytosed dysfunctional/detached astrocytes via scavenger receptors and TLR4, particularly after repetitive concussion. Additionally, microglia sealed areas of blood-brain barrier (BBB) disruption via purinergic pathways. Using a splitCre approach to dissect microglia and perivascular macrophages, we show that microglial invasion into the injury site is key to reducing BBB disruption. Our data suggest that microglia repair the BBB following concussion, but in doing so significantly alter the cellular ultrastructure of the brain milieu.

Indexed as

Blood-Brain BarrierBrain ConcussionAnimalsAstrocytesBrainCX3C Chemokine Receptor 1Disease Models, AnimalMacrophagesMaleMiceMice, Inbred C57BLMicrogliaToll-Like Receptor 4CX3C Chemokine Receptor 1Cx3cr1 protein, mouseToll-Like Receptor 4astrocytesblood–brain barrierconcussionmicrogliatraumatic brain injury

Identifiers

PMID40388609
PMCPMC12130861

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Registered trials

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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.