Evidence map›Paper›PMID 39159174›Full record

ArticleJournal of cellular and molecular medicine2024

A2 reactive astrocyte-derived exosomes alleviate cerebral ischemia-reperfusion injury by delivering miR-628.

Yingju Wang, He Li, Hanwen Sun, Chen Xu, Hongxue Sun, Wan Wei, Jihe Song, Feihong Jia, Di Zhong, Guozhong Li

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2024. 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
–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

11 citing papers in PubMed.

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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

10 authors.

Yingju WangDepartment of Neurology, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, People's Republic of China.
He LiDepartment of Neurology, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, People's Republic of China.
Hanwen SunDepartment of Emergency, Rui Jin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, People's Republic of China.
Chen XuDepartment of Neurology, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, People's Republic of China.
Hongxue SunDepartment of Neurology, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, People's Republic of China.
Wan WeiDepartment of Neurology, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, People's Republic of China.
Jihe SongDepartment of Neurology, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, People's Republic of China.
Feihong JiaDepartment of Neurology, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, People's Republic of China.
Di ZhongDepartment of Neurology, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, People's Republic of China.
Guozhong LiDepartment of Neurology, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, People's Republic of China.ORCID 0000-0002-5482-393X

Funding

Heilongjiang Province Key R&D Program GA21C005Heilongjiang Province Key R&D Program GY2022ZB0104
6 · The paper itself

Abstract

Ischemia and hypoxia activate astrocytes into reactive types A1 and A2, which play roles in damage and protection, respectively. However, the function and mechanism of A1 and A2 astrocyte exosomes are unknown. After astrocyte exosomes were injected into the lateral ventricle, infarct volume, damage to the blood-brain barrier (BBB), apoptosis and the expression of microglia-related proteins were measured. The dual luciferase reporter assay was used to detect the target genes of miR-628, and overexpressing A2-Exos overexpressed and knocked down miR-628 were constructed. qRT-PCR, western blotting and immunofluorescence staining were subsequently performed. A2-Exos obviously reduced the infarct volume, damage to the BBB and apoptosis and promoted M2 microglial polarization. RT-PCR showed that miR-628 was highly expressed in A2-Exos. Dual luciferase reporter assays revealed that NLRP3, S1PR3 and IRF5 are target genes of miR-628. After miR-628 was overexpressed or knocked down, the protective effects of A2-Exos increased or decreased, respectively. A2-Exos reduced pyroptosis and BBB damage and promoted M2 microglial polarization through the inhibition of NLRP3, S1PR3 and IRF5 via the delivery of miR-628. This study explored the mechanism of action of A2-Exos and provided new therapeutic targets and concepts for treating cerebral ischemia.

Indexed as

AstrocytesBlood-Brain BarrierBrain IschemiaExosomesMicroRNAsReperfusion InjuryAnimalsApoptosisMaleMiceMicrogliaMicroRNAsA2 astrocyteblood–brain barriercerebral ischemiaIRF5microglial polarizationmiR‐628NLRP3pyroptosisS1PR3

Identifiers

PMID39159174
PMCPMC11332600

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.