Evidence map›Paper›PMID 38558012›Full record

ArticleTranslational stroke research2025

Development of a 3D Brain Model to Study Sex-Specific Neuroinflammation After Hemorrhagic Stroke.

Rezwanul Islam, Hadi Hasan Choudhary, Hritik Mehta, Feng Zhang, Tudor G Jovin, Khalid A Hanafy

Open access · hybridAbstract read
In one paragraph

Article in Translational stroke research, 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
1.2field-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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Toll like receptor 4 (TLR4) in neuroinflammation: From acute hemorrhagic stroke to chronic neurodegeneration.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2026
    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

6 authors at 2 institutions in 1 country.

Rezwanul Islam *Department of Biomedical Sciences, Cooper Medical School at Rowan University, Camden, NJ, USA.
Hadi Hasan Choudhary *Department of Biomedical Sciences, Cooper Medical School at Rowan University, Camden, NJ, USA.
Hritik MehtaDepartment of Biomedical Sciences, Cooper Medical School at Rowan University, Camden, NJ, USA.
Feng ZhangDepartment of Biomedical Sciences, Cooper Medical School at Rowan University, Camden, NJ, USA.
Tudor G JovinDepartment of Biomedical Sciences, Cooper Medical School at Rowan University, Camden, NJ, USA.
Khalid A HanafyDepartment of Biomedical Sciences, Cooper Medical School at Rowan University, Camden, NJ, USA. hanafy@rowan.edu.
Cooper Medical School of Rowan University · USCooper University Health Care · US

Funding

Modulation of the TLR4-Lyn interaction in SAHR01NS109174 · NINDS · ROWAN UNIVERSITY · PI HANAFY, KHALID A. · 2019 to 2023
$2.4M
NIH HHS R01NS109174NINDS NIH HHS R01 NS109174
6 · The paper itself

Abstract

Subarachnoid hemorrhage (SAH) accounts for 5% of stroke, with women having a decreased inflammatory response compared to men; however, this mechanism has yet to be identified. One hurdle in SAH research is the lack of human brain models. Studies in murine models are helpful, but human models should be used in conjunction for improved translatability. These observations lead us to develop a 3D system to study the sex-specific microglial and neuroglial function in a novel in vitro human SAH model and compare it to our validated in vivo SAH model. Our lab has developed a 3D, membrane-based in vitro cell culture system with human astrocytes, microglia, and neurons from both sexes. The 3D cultures were incubated with male and female cerebrospinal fluid from SAH patients in the Neuro-ICU. Furthermore, microglial morphology, erythrophagocytosis, microglial inflammatory cytokine production, and neuronal apoptosis were studied and compared with our murine SAH models. The human 3D system demonstrated intercellular interactions and proportions of the three cell types similar to the adult human brain. In vitro and in vivo models of SAH showed concordance in male microglia being more inflammatory than females via morphology and flow cytometry. On the contrary, both in vitro and in vivo models revealed that female microglia were more phagocytic and less prone to damaging neurons than males. One possible explanation for the increased phagocytic ability of female microglia was the increased expression of CD206 and MerTK. Our in vitro, human, 3D cell culture SAH model showed similar results to our in vivo murine SAH model with respect to microglial morphology, inflammation, and phagocytosis when comparing the sexes. A human 3D brain model of SAH may be a useful adjunct to murine models to improve translation to SAH patients.

Indexed as

BrainHemorrhagic StrokeNeuroinflammatory DiseasesSex CharacteristicsSubarachnoid HemorrhageAnimalsAstrocytesCells, CulturedDisease Models, AnimalFemaleHumansMaleMiceMice, Inbred C57BLMicrogliaNeurons3D cell cultureAstrocytesCerebrospinal fluidMicrogliaNeuroinflammationNeuronsSex-specificSubarachnoid hemorrhage

Identifiers

PMID38558012
PMCPMC12045812
OpenAlexW4393386072

What Socratic holds

Textmetadata
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 Socratic graph.