OSCR

Promoting donor microglial replacement through augmented conditioning or radiation sensitivity.

Overview

Authors: Troy C Lund1, Willa Durose1, Emma Schindhelm1, Megan M Constans1, Erin E Nolan1, Ashish O Gupta1, Kai Braaten1, Paul J Orchard1
  1. Department of Pediatrics, Division of Pediatric Blood and Marrow Transplantation & Cellular Therapy, Minneapolis, MN 55455, USA
Dates: received 17 September 2025; accepted 2 April 2026; published online 12 April 2026; in print 1 July 2026
Type: Brief report · Language: English
License: CC BY-NC-ND
Identifiers: DOI 10.1016/j.ymthe.2026.04.012 · PMID 41968582 · PMCID PMC13330021 · OpenAlex W7153802326
Open access: hybrid, a free copy (OpenAlex)
Status: code on request
Categories: mouse (organism), cellular / molecular (subfield)
Methods: Evoked potentials
Keywords: hematopoietic cell transplantation, microglia, brain, radiation, DNA damage
MeSH: Hematopoietic Stem Cell Transplantation*, Microglia*, Radiation Tolerance*, Transplantation Conditioning*, Animals, Brain, Busulfan, Graft Survival, Mice, Mice, Inbred C57BL, Myeloid Cells (* major topic)
Topic: Neuroinflammation and Neurodegeneration Mechanisms (Neurology, Neuroscience), according to OpenAlex
Citations: cited by 1 paper (Europe PMC); 25 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 says that its authors' code is available on request: it was not published with the paper, so there is nothing to verify.

The paper's code and data availability statement is in the Data section.

Tracing map

A tracing map links a paper to the code its authors published: this paper has none (its code is available on request), so it has no map.

Data

No dataset and no data link were found in the paper.

Code and data availability statement

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

  • it says that the data are available on request
  • it says that the code is available on request

Read it in the paper: doi.org/10.1016/j.ymthe.2026.04.012.

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, 29 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 8 authors, 5 keywords, 11 MeSH terms, 25 references.

Cite

This paper

Lund, T. C., Durose, W., Schindhelm, E., Constans, M. M., Nolan, E. E., Gupta, A. O., Braaten, K., & Orchard, P. J. (2026). Promoting donor microglial replacement through augmented conditioning or radiation sensitivity. Molecular therapy : the journal of the American Society of Gene Therapy, 34(7), 3756-3762. https://doi.org/10.1016/j.ymthe.2026.04.012

BibTeX

@article{lund2026promoting,
author = {Lund, Troy C and Durose, Willa and Schindhelm, Emma and Constans, Megan M and Nolan, Erin E and Gupta, Ashish O and Braaten, Kai and Orchard, Paul J},
title = {{Promoting donor microglial replacement through augmented conditioning or radiation sensitivity}},
journal = {Molecular therapy : the journal of the American Society of Gene Therapy},
year = {2026},
month = apr,
volume = {34},
number = {7},
pages = {3756--3762},
publisher = {American Society of Gene \& Cell Therapy},
issn = {1525-0016},
doi = {10.1016/j.ymthe.2026.04.012},
url = {https://doi.org/10.1016/j.ymthe.2026.04.012},
pmid = {41968582},
pmcid = {PMC13330021}
}

RIS

TY - JOUR
AU - Lund, Troy C
AU - Durose, Willa
AU - Schindhelm, Emma
AU - Constans, Megan M
AU - Nolan, Erin E
AU - Gupta, Ashish O
AU - Braaten, Kai
AU - Orchard, Paul J
TI - Promoting donor microglial replacement through augmented conditioning or radiation sensitivity
T2 - Molecular therapy : the journal of the American Society of Gene Therapy
J2 - Mol Ther
PY - 2026
DA - 2026/04/12
VL - 34
IS - 7
SP - 3756
EP - 3762
SN - 1525-0016
PB - American Society of Gene & Cell Therapy
DO - 10.1016/j.ymthe.2026.04.012
UR - https://doi.org/10.1016/j.ymthe.2026.04.012
LA - en
ER -

CSL-JSON

{
"id": "10.1016/j.ymthe.2026.04.012",
"type": "article-journal",
"title": "Promoting donor microglial replacement through augmented conditioning or radiation sensitivity",
"container-title": "Molecular therapy : the journal of the American Society of Gene Therapy",
"author": [
{
"family": "Lund",
"given": "Troy C"
},
{
"family": "Durose",
"given": "Willa"
},
{
"family": "Schindhelm",
"given": "Emma"
},
{
"family": "Constans",
"given": "Megan M"
},
{
"family": "Nolan",
"given": "Erin E"
},
{
"family": "Gupta",
"given": "Ashish O"
},
{
"family": "Braaten",
"given": "Kai"
},
{
"family": "Orchard",
"given": "Paul J"
}
],
"container-title-short": "Mol Ther",
"volume": "34",
"issue": "7",
"page": "3756-3762",
"DOI": "10.1016/j.ymthe.2026.04.012",
"PMID": "41968582",
"PMCID": "PMC13330021",
"ISSN": "1525-0016",
"publisher": "American Society of Gene & Cell Therapy",
"URL": "https://doi.org/10.1016/j.ymthe.2026.04.012",
"language": "en",
"issued": {
"date-parts": [
[
2026,
4,
12
]
]
}
}

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/s12974-026-03809-z
Ependymal cell inflammatory activation in response to intracerebral hemorrhage.
Journal: Journal of neuroinflammation
In common: mouse, cellular / molecular, 1 reference
[2] doi:10.1093/brain/awag080 [code]
Early glymphatic failure in AppNL-F knock-in mice is linked to parenchymal border macrophages loss.
Journal: Brain : a journal of neurology
In common: mouse, cellular / molecular, 1 reference
[3] doi:10.1186/s13073-026-01687-x
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
In common: mouse, cellular / molecular, 1 reference
[4] doi:10.1016/j.isci.2026.116563
Microglia and its P2RY12 receptors regulate seizure severity.
Journal: iScience
In common: mouse, cellular / molecular, 1 reference
[5] 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, 1 reference
[6] doi:10.1186/s13024-026-00948-y
Dual orexin receptor antagonism with lemborexant enhances microglial clearance of β-amyloid in mice.
Journal: Molecular neurodegeneration
In common: mouse, cellular / molecular, 1 reference
[7] doi:10.1002/ctm2.70683 [code]
Niacin promotes motor function recovery after spinal cord injury via Hcar2-dependent microglia immunometabolic regulation.
Journal: Clinical and translational medicine
In common: mouse, cellular / molecular, 1 reference
[8] doi:10.1016/j.omta.2026.201824
GAA engineered to improve cellular uptake enhances correction in a preclinical hematopoietic stem cell gene therapy model of Pompe disease.
Journal: Molecular therapy. Advances
In common: mouse, 1 reference
[9] doi:10.1002/advs.202519669
Mr BMT Achieves Systemic Macrophage Replacement With Preservation of Tissue Homeostasis.
Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)
In common: cellular / molecular, 1 reference
[10] doi:10.1084/jem.20251801
Identification of secondary microglial formation centers in the human fetal brain.
Journal: The Journal of experimental medicine
In common: cellular / molecular, 1 reference

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.