OSCR

Infiltrating monocyte-derived macrophages does not survive long term in stroke brain despite their dominance in the acute ischemic core and myeloid derived IGF-1 play dichotomous roles in stroke recovery.

Overview

Authors: Hongli Ma1, Nicolas Hugues1, Kirsten Voice1, Joshua Peter1, Aleksandr Taranov1, Christina Thapa2, Krishna Roskin3,4, Yu Luo1,4
  1. Department of Molecular and Cellular Biosciences, University of Cincinnati,Cincinnati, OH 45229 USA
  2. Center for Psychiatric Genetics, NorthShore University HealthSystem,Evanston, IL 60201 USA
  3. Divisions of Biomedical Informatics, Cincinnati Children’s Hospital Medical Center, University of Cincinnati College of Medicine,Cincinnati, OH 45229 USA
  4. Division of Immunobiology, Cincinnati Children’s Hospital Medical Center, University of Cincinnati College of Medicine,Cincinnati, OH 45229 USA
Institutions: University of Cincinnati (United States); Endeavor Health (United States)
Journal: Genome medicine, volume 18, issue 1, article 122
Dates: received 23 January 2026; accepted 2 June 2026; published online 10 June 2026
Type: Research article · Language: English
License: CC BY-NC-ND
Identifiers: DOI 10.1186/s13073-026-01687-x · PMID 42271455 · PMCID PMC13474826 · OpenAlex W7164120728
Open access: gold, a free copy (OpenAlex)
Status: data only
Categories: genetics / omics (modality), mouse (organism), stroke (population), cellular / molecular (subfield)
Methods: Statistics, Smoothing, state filtering, decompositions
Keywords: Microglia, Infiltration of monocytes-derived macrophages (iMM), Ischemic stroke, Igf1, Single-cell RNA sequencing
MeSH: Brain*, Brain Ischemia*, Insulin-Like Growth Factor I*, Macrophages*, Monocytes*, Stroke*, Animals, Disease Models, Animal, Male, Mice, Microglia, Transcriptome (* major topic)
Topic: Neuroinflammation and Neurodegeneration Mechanisms (Neurology, Neuroscience), according to OpenAlex
Funding: NIH grants (R01NS125074)
Citations: cited by 2 papers (Europe PMC); 89 references in the paper

Abstract

The abstract is not reproduced here: the paper's license (CC BY-NC-ND) does not allow it. Read it in the paper, at the publisher or on Europe PMC.

Code

The paper links to its data, not to its authors' code: see the Data section.

Tracing map

A tracing map links a paper to the code its authors published: this paper has none, so it has no map.

Data

Datasets cited

Data availability statement

The paper has a data availability statement. Its license (CC BY-NC-ND) does not allow reproducing it here; in short, from what the harvester recognized in it:

Read it in the paper: doi.org/10.1186/s13073-026-01687-x.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 8 authors, 5 keywords, 12 MeSH terms, 1 funder, 88 references.

Cite

This paper

Ma, H., Hugues, N., Voice, K., Peter, J., Taranov, A., Thapa, C., Roskin, K., & Luo, Y. (2026). Infiltrating monocyte-derived macrophages does not survive long term in stroke brain despite their dominance in the acute ischemic core and myeloid derived IGF-1 play dichotomous roles in stroke recovery. Genome medicine, 18(1), 122. https://doi.org/10.1186/s13073-026-01687-x

BibTeX

@article{ma2026infiltrating,
author = {Ma, Hongli and Hugues, Nicolas and Voice, Kirsten and Peter, Joshua and Taranov, Aleksandr and Thapa, Christina and Roskin, Krishna and Luo, Yu},
title = {{Infiltrating monocyte-derived macrophages does not survive long term in stroke brain despite their dominance in the acute ischemic core and myeloid derived IGF-1 play dichotomous roles in stroke recovery}},
journal = {Genome medicine},
year = {2026},
month = jun,
volume = {18},
number = {1},
pages = {122},
publisher = {BMC},
issn = {1756-994X},
doi = {10.1186/s13073-026-01687-x},
url = {https://doi.org/10.1186/s13073-026-01687-x},
pmid = {42271455},
pmcid = {PMC13474826}
}

RIS

TY - JOUR
AU - Ma, Hongli
AU - Hugues, Nicolas
AU - Voice, Kirsten
AU - Peter, Joshua
AU - Taranov, Aleksandr
AU - Thapa, Christina
AU - Roskin, Krishna
AU - Luo, Yu
TI - Infiltrating monocyte-derived macrophages does not survive long term in stroke brain despite their dominance in the acute ischemic core and myeloid derived IGF-1 play dichotomous roles in stroke recovery
T2 - Genome medicine
J2 - Genome Med
PY - 2026
DA - 2026/06/10
VL - 18
IS - 1
SP - 122
SN - 1756-994X
PB - BMC
DO - 10.1186/s13073-026-01687-x
UR - https://doi.org/10.1186/s13073-026-01687-x
LA - en
ER -

CSL-JSON

{
"id": "10.1186/s13073-026-01687-x",
"type": "article-journal",
"title": "Infiltrating monocyte-derived macrophages does not survive long term in stroke brain despite their dominance in the acute ischemic core and myeloid derived IGF-1 play dichotomous roles in stroke recovery",
"container-title": "Genome medicine",
"author": [
{
"family": "Ma",
"given": "Hongli"
},
{
"family": "Hugues",
"given": "Nicolas"
},
{
"family": "Voice",
"given": "Kirsten"
},
{
"family": "Peter",
"given": "Joshua"
},
{
"family": "Taranov",
"given": "Aleksandr"
},
{
"family": "Thapa",
"given": "Christina"
},
{
"family": "Roskin",
"given": "Krishna"
},
{
"family": "Luo",
"given": "Yu"
}
],
"container-title-short": "Genome Med",
"volume": "18",
"issue": "1",
"page": "122",
"DOI": "10.1186/s13073-026-01687-x",
"PMID": "42271455",
"PMCID": "PMC13474826",
"ISSN": "1756-994X",
"publisher": "BMC",
"URL": "https://doi.org/10.1186/s13073-026-01687-x",
"language": "en",
"issued": {
"date-parts": [
[
2026,
6,
10
]
]
}
}

Similar papers

The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.

[1] doi:10.1186/s12974-026-03885-1 [code]
Shared transcriptomic signatures in perilesional and contralesional cortex after ischemic stroke.
Journal: Journal of neuroinflammation
In common: stroke, genetics / omics, mouse, 1 other category, 5 references
[2] doi:10.1186/s13062-026-00912-2
Integrated analysis of single-cell transcriptome identifies a glial-neurovascular signaling trajectory in brain repair after ischemia.
Journal: Biology direct
In common: stroke, genetics / omics, mouse, 1 other category, 5 references
[3] doi:10.1186/s12974-026-03794-3
Single-cell omics and flow cytometry identify distinct immune states of dural and brain-infiltrating IL-17-producing γδ T cells after experimental stroke.
Journal: Journal of neuroinflammation
In common: stroke, genetics / omics, mouse, 1 other category, 5 references
[4] doi:10.1155/humu/4033506
SELL Marks an Effector-Deficient CD8<sup>+</sup> T Cell Subset That Promotes Intracerebral Hemorrhage and Responds to Rutin Therapy.
Journal: Human mutation
In common: stroke, genetics / omics, mouse, 5 references
[5] doi:10.1016/j.isci.2026.117228 [code]
Single-nucleus transcriptomics reveals cell type-specific remodeling and epilepsy-associated microglia.
Journal: iScience
In common: genetics / omics, cellular / molecular, 5 references
[6] doi:10.1016/j.celrep.2026.117411
Enhancing the specificity of microglia genetic targeting using a CSF1R inhibitor.
Journal: Cell reports
In common: mouse, cellular / molecular, 4 references
[7] doi:10.1038/s41467-026-74904-1
FcγR- and CD9-dependent synapse-engulfing microglia in the thalamus drive cognitive impairment following cortical brain damage in mice.
Journal: Nature communications
In common: mouse, cellular / molecular, 4 references
[8] doi:10.1007/s10565-026-10177-0
Multi-omics analysis and experimental validation reveal the IRF7-CXCL10 axis as a master regulator of microglial PCD in ischemic stroke.
Journal: Cell biology and toxicology
In common: stroke, genetics / omics, mouse, 1 other category, 3 references
[9] doi:10.1016/j.isci.2026.116257
Decoding neuron-specific lineage to identify diagnostic biomarkers and therapeutic targets for ischemic stroke.
Journal: iScience
In common: stroke, genetics / omics, 3 references
[10] doi:10.1126/sciadv.adz6517 [code]
Corticosterone-linked microglial activity underpins sexually dimorphic neuroplasticity after ketamine anesthesia.
Journal: Science advances
In common: mouse, cellular / molecular, 3 references

Contribute

The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.

Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.

Request its removal

To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).

Discussion, reproductions, activity

Discussion: questions and error reports about this paper and its code, from signed-in readers and its authors. It opens with sign-in.

Reproductions: reports from readers who ran the authors' code: what they reproduced, with which environment, commit and data. It opens with sign-in.

Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.