Evidence map›Paper›PMID 39856551›Full record

ArticleBMC genomics2025

Integrated analysis of chromatin and transcriptomic profiling of the striatum after cerebral hypoperfusion in mice.

Shijia Le, Fengyiyang Xu, Zhi Luo, Weihao Shi, Shuangshuang Lu, Zengyu Zhang, Zimin Guo, Wenshi Xu, Mingqi Yang, Tianyi Li and 3 more

Abstract read
In one paragraph

Article in BMC genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Shijia Le *Shanghai Medical College, Fudan University, Shanghai, 200032, China.
Fengyiyang Xu *Shanghai Medical College, Fudan University, Shanghai, 200032, China.
Zhi Luo *Department of Surgery, Shanghai Deji Hospital, Qingdao University, Shanghai, 200331, China.
Weihao ShiDepartment of Vascular Surgery, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Shuangshuang LuDepartment of Radiology, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Zengyu ZhangShanghai Medical College, Fudan University, Shanghai, 200032, China.
Zimin GuoShanghai Medical College, Fudan University, Shanghai, 200032, China.
Wenshi XuShanghai Medical College, Fudan University, Shanghai, 200032, China.
Mingqi YangShanghai Medical College, Fudan University, Shanghai, 200032, China.
Tianyi LiShanghai Medical College, Fudan University, Shanghai, 200032, China.
Xu LiDepartment of Vascular Surgery, Zhongshan Hospital, Institute of Vascular Surgery, National Clinical Research Center for Interventional Medicine, Fudan University, Shanghai, 200032, China. lixu007qq@163.com.
Kun LiangDepartment of Vascular Surgery, Huashan Hospital, Fudan University, Shanghai, 200040, China. kuhn.leung@outlook.com.
Lei ZhuDepartment of Vascular Surgery, Huashan Hospital, Fudan University, Shanghai, 200040, China. julian.lei.zhu@fudan.edu.cn.

Funding

Shanghai Development Center SHDC2023CRS025
6 · The paper itself

Abstract

backgroundVascular cognitive impairment (VCI) is a significant contributor to dementia, yet the precise mechanisms underlying the cognitive decline associated with chronic cerebral hypoperfusion (CCH) remain unclear. This study investigated the molecular and epigenetic changes in the striatum, a brain region critical for motor function and cognition, following chronic hypoperfusion using a bilateral common carotid artery stenosis (BCAS) model in mice.

methodsRNA-seq was utilized to identify differentially expressed genes (DEGs) associated with hypoperfusion. In parallel, ATAC-seq was used to assess changes in chromatin accessibility within the striatum, providing insight into the epigenome and potential regulatory mechanisms. The integration of these datasets allowed us to correlate chromatin accessibility with transcriptional activity and to identify key transcription factors driving the observed gene expression changes.

resultsAnalysis of striatum-specific transcriptome revealed significant upregulation of immune response genes, particularly type II interferon signaling, and downregulation of neural activation pathways. Analysis of striatum-specific epigenome showed increased chromatin accessibility at promoters of immune-related genes. Integrated analysis highlighted PU.1 as a key transcription factor in upregulated pathways, while neural pathways lacked epigenetic regulation, revealing distinct molecular responses in the striatum following chronic hypoperfusion.

conclusionsOur findings indicate that upregulated pathways in the striatum following BCAS-induced CCH are driven by epigenetic changes, while downregulated pathways occur independently of these modifications. Additionally, PU.1 plays a critical role in mediating immune responses, offering a potential target for therapeutic intervention.

Indexed as

ChromatinCorpus StriatumGene Expression ProfilingTranscriptomeAnimalsDisease Models, AnimalEpigenesis, GeneticMaleMiceMice, Inbred C57BLChromatinATAC-seqBilateral carotid artery stenosisChronic cerebral hypoperfusionRNA-seqStriatum

Identifiers

PMID39856551
PMCPMC11762485

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.