Characterizing the metabolomes of microglia, astrocytes and neurons in ageing and Alzheimer's brains.
A correction to this paper has been published: the notice, 42680904, from Europe PMC.
Overview
13 affiliations
- Department of Neurology, First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China
- Chinese Institute for Brain Research, Beijing (CIBR), Beijing, China
- Beijing Institute for Brain Research, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China
- State Key Laboratory of Cognitive Neuroscience and Learning, Faculty of Psychology, Beijing Normal University, Beijing, China
- College of Life Sciences, Nankai University, Tianjin, China
- Institute of Biophysics, Chinese Academy of Sciences, Beijing, China
- School of Industry–Education Integration, University of Chinese Academy of Sciences, Beijing, China
- Changping Laboratory, Beijing, China
- Children’s Research Institute, University of Texas Southwestern Medical Center, Dallas, TX USA
- Eugene McDermott Center for Human Growth and Development, University of Texas Southwestern Medical School, Texas, TX USA
- Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX USA
- Institute of Blood Transfusion, Chinese Academy of Medical Sciences, Chengdu, China
- School of Basic Medical Sciences, Capital Medical University, Beijing, China
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
- geo:GSE316928, at NCBI GEO; found in “Data availability”
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:
- it points to a dataset: NCBI GEO GSE316928
- it says that the data are available on request
Read it in the paper: doi.org/10.1038/s41556-026-01910-2.
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, 30 September 2026: the first record
Recorded: type, language, journal, volume, issue, pages, dates, 18 authors, 3 keywords, 16 MeSH terms, 2 funders, 115 references, 1 integrity notice.
Cite
This paper
Yu, J., Li, F., Chen, X.-j., Mou, C., Yao, D., Bi, Z., Chen, X., Du, L., Feng, Z., Zhang, X., Yu, X., Zacharias, L. G., DeBerardinis, R. J., Zhang, L., Li, Z., Luo, B., Hu, X.-L., & Ge, W.-p. (2026). Characterizing the metabolomes of microglia, astrocytes and neurons in ageing and Alzheimer's brains. Nature cell biology, 28(5), 1031-1048. https://
BibTeX
@article{yu2026character
author = {Yu, Jie and Li, Fengzhi and Chen, Xing-jun and Mou, Chenye and Yao, Di and Bi, Zhanying and Chen, Xiaoli and Du, Lulu and Feng, Ziyan and Zhang, Xinshuang and Yu, Xiaoqian and Zacharias, Lauren G and DeBerardinis, Ralph J and Zhang, Li and Li, Zhen and Luo, Benyan and Hu, Xiao-Ling and Ge, Woo-ping},
title = {{Characterizing the metabolomes of microglia, astrocytes and neurons in ageing and Alzheimer's brains}},
journal = {Nature cell biology},
year = {2026},
month = apr,
volume = {28},
number = {5},
pages = {1031--1048},
publisher = {Nature Portfolio},
issn = {1465-7392},
doi = {10.1038/
url = {https://
pmid = {42062482},
pmcid = {PMC13179133}
}
RIS
TY - JOUR
AU - Yu, Jie
AU - Li, Fengzhi
AU - Chen, Xing-jun
AU - Mou, Chenye
AU - Yao, Di
AU - Bi, Zhanying
AU - Chen, Xiaoli
AU - Du, Lulu
AU - Feng, Ziyan
AU - Zhang, Xinshuang
AU - Yu, Xiaoqian
AU - Zacharias, Lauren G
AU - DeBerardinis, Ralph J
AU - Zhang, Li
AU - Li, Zhen
AU - Luo, Benyan
AU - Hu, Xiao-Ling
AU - Ge, Woo-ping
TI - Characterizing the metabolomes of microglia, astrocytes and neurons in ageing and Alzheimer's brains
T2 - Nature cell biology
J2 - Nat Cell Biol
PY - 2026
DA - 2026/
VL - 28
IS - 5
SP - 1031
EP - 1048
SN - 1465-7392
PB - Nature Portfolio
DO - 10.1038/
UR - https://
LA - en
ER -
CSL-JSON
{
"id": "10.1038/
"type": "article-journal",
"title": "Characterizing the metabolomes of microglia, astrocytes and neurons in ageing and Alzheimer's brains",
"container-title": "Nature cell biology",
"author": [
{
"family": "Yu",
"given": "Jie"
},
{
"family": "Li",
"given": "Fengzhi"
},
{
"family": "Chen",
"given": "Xing-jun"
},
{
"family": "Mou",
"given": "Chenye"
},
{
"family": "Yao",
"given": "Di"
},
{
"family": "Bi",
"given": "Zhanying"
},
{
"family": "Chen",
"given": "Xiaoli"
},
{
"family": "Du",
"given": "Lulu"
},
{
"family": "Feng",
"given": "Ziyan"
},
{
"family": "Zhang",
"given": "Xinshuang"
},
{
"family": "Yu",
"given": "Xiaoqian"
},
{
"family": "Zacharias",
"given": "Lauren G"
},
{
"family": "DeBerardinis",
"given": "Ralph J"
},
{
"family": "Zhang",
"given": "Li"
},
{
"family": "Li",
"given": "Zhen"
},
{
"family": "Luo",
"given": "Benyan"
},
{
"family": "Hu",
"given": "Xiao-Ling"
},
{
"family": "Ge",
"given": "Woo-ping"
}
],
"container-title-short":
"volume": "28",
"issue": "5",
"page": "1031-1048",
"DOI": "10.1038/
"PMID": "42062482",
"PMCID": "PMC13179133",
"ISSN": "1465-7392",
"publisher": "Nature Portfolio",
"URL": "https://
"language": "en",
"issued": {
"date-parts": [
[
2026,
4,
30
]
]
}
}
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:10.1126/sciadv.adt2527
- NPAS3-regulated astrocyte mitochondrial bioenergetics is required for cognition.Journal: Science advancesIn common: mouse, cellular / molecular, 6 references
- [2] doi:10.1126/sciadv.adx0731 [code]
- Targeting glial PD-1/
PD-L1 restores microglial homeostasis and reduces neuronal hyperactivity in an Alzheimer's disease model. Journal: Science advancesIn common: Alzheimer's / dementia, mouse, cellular / molecular, 4 references - [3] doi:10.1126/sciadv.aed6825
- SORLA up-regulation suppresses pathological effects in aged tauopathy mouse brain.Journal: Science advancesIn common: Alzheimer's / dementia, genetics / omics, mouse, 1 other category, 4 references
- [4] doi:10.1186/s12967-026-08108-y [code]
- An explainable multimodal machine learning model for diagnosing disorders of consciousness: evidence from a large multicenter Chinese cohort.Journal: Journal of translational medicineIn common: 1 reference, author Benyan Luo
- [5] doi:10.1038/s41593-026-02348-3
- Microglial TDP-43 mediates myelin refinement and represses Tyrobp cryptic exon inclusion in mice.Journal: Nature neuroscienceIn common: mouse, cellular / molecular, 5 references
- [6] doi:10.1186/s40035-026-00567-z
- Transaldolase 1 contributes to pentose phosphate pathway disruption and synaptic dysfunction in Alzheimer's disease.Journal: Translational neurodegenerationIn common: Alzheimer's / dementia, genetics / omics, mouse, 1 other category, 3 references
- [7] doi:10.1016/j.isci.2026.116092
- Sigma-1 receptor promotes glycolysis in neuronal systems by suppressing GRIM19.Journal: iScienceIn common: mouse, cellular / molecular, 4 references
- [8] doi:10.1111/acel.70653
- Distinct Transposable Element Transcript Patterns in Microglia Across Aging and Alzheimer's Disease.Journal: Aging cellIn common: Alzheimer's / dementia, genetics / omics, mouse, 1 other category, 4 references
- [9] doi:10.1007/s00401-026-03036-z
- Mechanisms of increased Alzheimer's disease pathology with R47H and R62H TREM2 variants.Journal: Acta neuropathologicaIn common: Alzheimer's / dementia, genetics / omics, cellular / molecular, 3 references
- [10] doi:10.1038/s41467-026-74253-z
- Disruption of the brain-spleen axis impairs monocyte-microglia communication and accelerates disease progression in a mouse model of amyloidosis.Journal: Nature communicationsIn common: Alzheimer's / dementia, 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.
Claim this paper
Correct its record
Say what each link of this record is, remove the ones that are not the paper's, add the ones that are missing. The correction becomes a new version of the record, in its Versions section.
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.
