Evidence map›Paper›PMID 37378751›Full record

ArticleTranslational stroke research2024

The Transcriptional Landscape of Pericytes in Acute Ischemic Stroke.

Carolina Buizza, Andreas Enström, Robert Carlsson, Gesine Paul

Open access · hybridAbstract read
In one paragraph

Article in Translational stroke research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Single-cell RNA sequencing in stroke and traumatic brain injury: Current achievements, challenges and future perspectives on transcriptomic profiling.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2026
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  13. Brain repair mechanisms after cell therapy for stroke.Brain : a journal of neurology · 2024
    Review
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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

4 authors at 2 institutions in 1 country.

Carolina BuizzaTranslational Neurology Group, Department of Clinical Science, Lund University, 22184, Lund, Sweden.ORCID 0000-0001-8398-2385
Andreas EnströmTranslational Neurology Group, Department of Clinical Science, Lund University, 22184, Lund, Sweden.ORCID 0000-0001-8792-8028
Robert CarlssonTranslational Neurology Group, Department of Clinical Science, Lund University, 22184, Lund, Sweden.ORCID 0000-0001-5955-2916
Gesine PaulTranslational Neurology Group, Department of Clinical Science, Lund University, 22184, Lund, Sweden. gesine.paul-visse@med.lu.se.ORCID 0000-0002-6806-2254
Lund University · SEScania (Sweden) · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The current treatment options for ischemic stroke aim to achieve reperfusion but are time critical. Novel therapeutic approaches that can be given beyond the limited time window of 3-4.5 h are still an unmet need to be addressed to improve stroke outcomes. The lack of oxygen and glucose in the area of ischemic injury initiates a pathological cascade leading to blood-brain barrier (BBB) breakdown, inflammation, and neuronal cell death, a process that may be intercepted to limit stroke progression. Pericytes located at the blood/brain interface are one of the first responders to hypoxia in stroke and therefore a potential target cell for early stroke interventions. Using single-cell RNA sequencing in a mouse model of permanent middle cerebral artery occlusion, we investigated the temporal differences in transcriptomic signatures in pericytes at 1, 12, and 24 h after stroke. Our results reveal a stroke-specific subcluster of pericytes that is present at 12 and 24 h and characterized by the upregulation of genes mainly related to cytokine signaling and immune response. This study identifies temporal transcriptional changes in the acute phase of ischemic stroke that reflect the early response of pericytes to the ischemic insult and its secondary consequences and may constitute potential future therapeutic targets.

Indexed as

Ischemic StrokePericytesAnimalsBlood-Brain BarrierBrain IschemiaDisease Models, AnimalInfarction, Middle Cerebral ArteryMaleMiceMice, Inbred C57BLTranscriptomeInterleukin 11Ischemic strokePericytesSingle-cell RNA sequencing

Identifiers

PMID37378751
PMCPMC11226519
OpenAlexW4382344406

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.