Evidence map›Paper›PMID 28196918›Full record

ArticleJournal of neurointerventional surgery2018

M1 macrophages are required for murine cerebral aneurysm formation.

Kamil W Nowicki, Koji Hosaka, Frank J Walch, Edward W Scott, Brian L Hoh

Open access · greenAbstract read
In one paragraph

Article in Journal of neurointerventional surgery, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 2 pooled it
1.3field-weighted citation impact, top 21% 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

38 citing papers in PubMed, 2 syntheses or guidelines pooled it, 50 citations in OpenAlex.

  1. Pooled it
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  13. Peripheral macrophages in the development and progression of structural cerebrovascular pathologies.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2024
    Review
  14. Article
  15. A Future Blood Test to Detect Cerebral Aneurysms.Cellular and molecular neurobiology · 2023
    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

5 authors at 3 institutions in 1 country.

Kamil W NowickiDepartment of Neurosurgery, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
Koji HosakaDepartment of Neurosurgery, University of Florida, Gainesville, Florida, USA.
Frank J WalchDepartment of Neurosurgery, University of Colorado, Denver, Colorado, USA.
Edward W ScottDepartment of Molecular Genetics and Microbiology, University of Florida, Gainesville, Florida, USA.
Brian L HohDepartment of Neurosurgery, University of Florida, Gainesville, Florida, USA.
University of Florida · USUniversity of Colorado Denver · USUniversity of Pittsburgh Medical Center · US

Funding

Inflammation and Cerebral Aneurysm Formation: Targets for Modulation and VascularK08NS067058 · NINDS · UNIVERSITY OF FLORIDA · PI HOH, BRIAN LIM · 2009 to 2013
$856k
NINDS NIH HHS K08 NS067058
6 · The paper itself

Abstract

introductionMacrophages and neutrophils have been separately implicated in cerebral aneurysm formation. The interactions between different myeloid subsets and the contributions of macrophage phenotypes in these lesions over time are not known. The purpose of the study was to examine macrophage phenotypic changes in cerebral aneurysms.

methodsWe induced aneurysm formation in C57BL/6 mice and quantified contributions of M1 and M2 macrophages in aneurysm specimens with or without neutrophil blockade. In our aneurysm model, the left common carotid and right renal arteries were ligated, and mice were placed on a hypertensive high fat diet. One week later, stereotactic injection with elastase solution into the basal cisterns was performed. An angiotensin II secreting osmotic pump was implanted. The mice were then treated with anti-CXCL1 antibody or IgG control antibody. Animals were euthanized at 3 days, or 1 or 2 weeks. The circle of Willis was analyzed using immunohistochemistry for M1 and M2 macrophage phenotype contributions.

resultsProinflammatory M1/M2 ratio increased in cerebral aneurysm formation over time, from 0.56 at 3 days to 1.75 at 2 weeks (p<0.0001). In contrast, anti-CXCL1 antibody blockade led to polarization towards an anti-inflammatory phenotype with an M1/M2 ratio of 0.95 at 2 weeks compared with IgG treated mice (p=0.0007).

conclusionsCXCL1 dependent neutrophil inflammation appears to have an important role in macrophage polarization to M1 phenotype in cerebral aneurysm development.

Indexed as

AnimalsAnti-Inflammatory AgentsChemokine CXCL1FemaleImmunoglobulin GImmunoglobulins, IntravenousIntracranial AneurysmMacrophagesMiceMice, Inbred C57BLPhenotypeAnti-Inflammatory AgentsChemokine CXCL1Cxcl1 protein, mouseImmunoglobulin GImmunoglobulins, IntravenousAneurysmBrainInflammationInflammatory Response

Identifiers

PMID28196918
PMCPMC7814362
OpenAlexW2589022407

What OpenQuestion holds

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LicenceTDM
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.