Evidence map›Paper›PMID 36523152›Full record

ArticleCNS neuroscience & therapeutics2023

Chemokine receptor 7 mediates miRNA-182 to regulate cerebral ischemia/reperfusion injury in rats.

Qi Wang, Sifan Xu, Bin Wang, Yu Qin, Yachen Ji, Qian Yang, Yang Xu, Zhiming Zhou

Open access · goldAbstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
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

11 citing papers in PubMed, 13 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Qi WangDepartment of Neurology, The First Affiliated Hospital of Wannan Medical College, Yijishan Hospital, Wuhu, China.
Sifan XuDepartment of Neurology, The First Affiliated Hospital of Wannan Medical College, Yijishan Hospital, Wuhu, China.
Bin WangDepartment of Anesthesiology, The First Affiliated Hospital of Wannan Medical College, Yijishan Hospital, Wuhu, China.
Yu QinDepartment of Neurology, The First Affiliated Hospital of Wannan Medical College, Yijishan Hospital, Wuhu, China.
Yachen JiDepartment of Neurology, The First Affiliated Hospital of Wannan Medical College, Yijishan Hospital, Wuhu, China.
Qian YangDepartment of Neurology, The First Affiliated Hospital of Wannan Medical College, Yijishan Hospital, Wuhu, China.
Yang XuDepartment of Neurology, The First Affiliated Hospital of Wannan Medical College, Yijishan Hospital, Wuhu, China.
Zhiming ZhouDepartment of Neurology, The First Affiliated Hospital of Wannan Medical College, Yijishan Hospital, Wuhu, China.ORCID 0000-0002-0851-3930
First Affiliated Hospital of Wannan Medical College · CNWannan Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsChemokine receptor 7 (CXCR7) exerts protective effects on the brain. MicroRNAs (miRNAs) are involved in cerebral ischemia/reperfusion (I/R) injury, but their involvement in CXCR7-mediated brain protection is unknown. In this study, we investigated the role of miRNAs in CXCR7-mediated brain protection.

methodsCXCR7 levels in peripheral blood samples from patients with acute ischemic stroke (AIS) and ischemic penumbra area brain tissues from middle cerebral artery occlusion (MCAO) rats after recanalization were measured. An miRNA microarray analysis was performed to examine the expression of miRNAs caused by CXCR7 knockdown in ischemic penumbra area brain tissue in middle cerebral artery occlusion-reperfusion rats and to predict corresponding downstream target genes. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis revealed the most enriched pathways. A dual-luciferase reporter assay confirmed the direct regulation of miR-182 on the target gene TCF7L2. The correlation between TCF7L2 and CXCR7/miR-182 was verified using rescue assays.

resultsCXCR7 expression was upregulated in MCAO rats and mechanical thrombectomy patients with AIS compared to that in controls. The motor and sensory functions of MCAO rats with CXCR7 knockdown further decreased, and the infarct volume and cerebral edema increased. miRNA microarray data showed that seven miRNAs were differentially expressed after shRNA-CXCR7 treatment. The dual-luciferase reporter assay confirmed that miR-182 directly targeted the TCF7L2 gene. Rescue assays confirmed that TCF7L2 is downstream of CXCR7/miR-182. KEGG pathway analysis showed that the Hippo pathway may be a key pathway in CXCR7 upregulation and plays a role in protecting the brain after interventional surgery. Animal experiments have shown that CXCR7-mediated cerebral I/R injury promotes the phosphorylation of key molecules YAP and TAZ in the Hippo pathway.

conclusionCXCR7 protects against cerebral I/R injury, possibly via the miR-182/TCF7L2/Hippo pathway. These results indicate that CXCR7 affects cerebral ischemia-reperfusion injury through miRNA regulation and downstream pathways.

Indexed as

Brain IschemiaIschemic StrokeMicroRNAsReceptors, CXCRReperfusion InjuryAnimalsInfarction, Middle Cerebral ArteryRatsRats, Sprague-DawleyMicroRNAsMIRN182 microRNA, ratReceptors, CXCRcerebral ischemia/reperfusion injurychemokine receptor 7hippo pathwaymicroRNA

Identifiers

PMID36523152
PMCPMC9873520
OpenAlexW4311668567

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Registered trials

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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.