Evidence map›Paper›PMID 41566372›Full record

ArticleJournal of translational medicine2026

Single-cell transcriptome analysis reveals mechanisms by which hippocampal deep brain stimulation promotes neurorepair and microglial subpopulation remodeling in ischemic stroke.

Xuyu Zhao, Yiyang Cao, Xiao Li, Peiru Wu, Jianxin Zhou, Qing Zou, Huanle Hong, Jingying Huang, Rabia Sultan, Jiao Wang

Abstract read
In one paragraph

Article in Journal of translational medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Xuyu Zhao *Laboratory of Molecular Neural Biology, Shanghai Key Laboratory of Bio-Energy Crops, School of Life Sciences, Shanghai University, Shanghai, 200444, China.
Yiyang Cao *Laboratory of Molecular Neural Biology, Shanghai Key Laboratory of Bio-Energy Crops, School of Life Sciences, Shanghai University, Shanghai, 200444, China.
Xiao Li *Shanghai Key Laboratory of Psychotic Disorders, Brain Health Institute, National Center for Mental Disorders, Shanghai Mental Health Center, Shanghai Jiaotong University School of Medicine, Shanghai, 200030, China.
Peiru WuLaboratory of Molecular Neural Biology, Shanghai Key Laboratory of Bio-Energy Crops, School of Life Sciences, Shanghai University, Shanghai, 200444, China.
Jianxin ZhouLaboratory of Molecular Neural Biology, Shanghai Key Laboratory of Bio-Energy Crops, School of Life Sciences, Shanghai University, Shanghai, 200444, China.
Qing ZouLaboratory of Molecular Neural Biology, Shanghai Key Laboratory of Bio-Energy Crops, School of Life Sciences, Shanghai University, Shanghai, 200444, China.
Huanle HongLaboratory of Molecular Neural Biology, Shanghai Key Laboratory of Bio-Energy Crops, School of Life Sciences, Shanghai University, Shanghai, 200444, China.
Jingying HuangLaboratory of Molecular Neural Biology, Shanghai Key Laboratory of Bio-Energy Crops, School of Life Sciences, Shanghai University, Shanghai, 200444, China.
Rabia SultanLaboratory of Molecular Neural Biology, Shanghai Key Laboratory of Bio-Energy Crops, School of Life Sciences, Shanghai University, Shanghai, 200444, China.
Jiao WangLaboratory of Molecular Neural Biology, Shanghai Key Laboratory of Bio-Energy Crops, School of Life Sciences, Shanghai University, Shanghai, 200444, China. jo717@shu.edu.cn.ORCID 0000-0001-9875-5425

Funding

Basic Research Program of Shanghai 20JC1412200Basic Research Program of Shanghai 24JS2810400Basic Research Program of Shanghai 25J22800700National Key Research and Development Program of China 2020YFA0113000
6 · The paper itself

Abstract

backgroundIn patients with ischemic stroke, the hippocampus is one of the most severely damaged regions of the brain; however, the optimal parameters for hippocampal deep brain stimulation in these patients remain unknown. The underlying mechanism of hippocampal deep brain stimulation in the treatment of ischemic stroke is not fully understood.

objectiveTo investigate the effect and underlying mechanisms by which hippocampal deep brain stimulation enhances the repair of brain damage from ischemic stroke.

methodsWe utilized multi-channel electrode arrays to record local field potentials and to monitor motor symptoms in mice with ischemic stroke during deep brain stimulation in hippocampus. Using 10x single-cell transcriptome sequencing and RNA-seq in stroke mice with and without electrostimulation treatment, we explored the underlying mechanisms.

resultsAfter being treated with hippocampal deep brain stimulation, the stroke mice showed significant improvements in motor ability, neuronal function, and behaviors related to anxiety/depression. Bioinformatics analysis and subsequent investigations revealed a significant increase in the quantity of excitatory neurons and astrocytes in the hippocampus following deep brain stimulation while the number of oligodendrocytes, microglia and inhibitory neurons was markedly diminished. The microglia subset 5 showed a significant increase following deep brain stimulation treatment, while subsets 3 and 4 experienced a significant reduction. Within subset 5, markers such as Cd93, Ccr2, Emilin2, Pirb, Lgals3, Thbs1, Gpnmb, and Ccr1 were associated with immune inflammation and angiogenesis.

conclusionCollectively, our findings imply that hippocampal deep brain stimulation is highly effective for treating ischemic stroke and offer deeper insights into the potential mechanisms by which hippocampal deep brain stimulation improves stroke symptoms. These findings support hippocampal deep brain stimulation as a promising novel therapeutic approach for stroke and offer valuable insights for the treatment of other neurological disorders.

Indexed as

Brain IschemiaDeep Brain StimulationGene Expression ProfilingHippocampusIschemic StrokeMicrogliaSingle-Cell AnalysisAnimalsMaleMiceMice, Inbred C57BLNeuronsSingle-Cell Gene Expression AnalysisBrain injury repairDeep brain stimulationIschemic strokeMicrogliaNeural regeneration

Identifiers

PMID41566372
PMCPMC12822071

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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.