Evidence map›Paper›PMID 39103424›Full record

ArticleScientific reports2024

Exosomal miR-486 derived from bone marrow mesenchymal stem cells promotes angiogenesis following cerebral ischemic injury by regulating the PTEN/Akt pathway.

Hangyang Bao, Shihui Mao, Xiaowei Hu, Lin Li, Hongmiao Tao, Jie Zhou, Lanxi Xu, Yan Fang, Yani Zhang, Lisheng Chu

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
–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

28 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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.

Hangyang Bao *School of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, 310053, China.
Shihui Mao *School of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, 310053, China.
Xiaowei Hu *School of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, 310053, China.
Lin LiSchool of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, 310053, China.
Hongmiao TaoMedical College, Jinhua Polytechnic, Jinhua, 321017, China.
Jie ZhouSchool of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, 310053, China.
Lanxi XuSchool of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, 310053, China.
Yan FangSchool of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, 310053, China.
Yani ZhangSchool of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, 310053, China.
Lisheng ChuSchool of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, 310053, China. cls2004@zcmu.edu.cn.

Funding

National Natural Science Foundation of China 81274113Natural Science Foundation of Zhejiang Province 2016C33185
6 · The paper itself

Abstract

Bone marrow mesenchymal stem cell-derived exosomes (BMSC-Exos) have been shown to promote angiogenesis after ischemic stroke, in which microRNAs (miRs) are believed to play an important role in exosome-mediated therapeutic effects, though the mechanism is still not clear. In this study, a series of molecular biological and cellular assays, both in vitro and in vivo, were performed to elucidate the role of exosomal miR-486 in angiogenesis following cerebral ischemic and its molecular mechanisms. Our results revealed that BMSC-Exos significantly improved neurological function and increased microvessel density in ischemic stroke rats. In vitro assays showed that BMSC-Exos promoted the proliferation, migration, and tube formation ability of oxygen-glucose deprivation/reoxygenation (OGD/R) injured rat brain microvascular endothelial cells (RBMECs). Importantly, BMSC-Exos increased the expression of miR-486 and phosphorylated protein kinase B (p-Akt) and down-regulated the protein level of phosphatase and tensin homolog (PTEN) in vivo and in vitro. Mechanistic studies demonstrated that transfection with miR-486 mimic enhanced RBMECs angiogenesis and increased p-Akt expression, while inhibited PTEN expression. On the other hand, the miR-486 inhibitor induced an opposite effect, which could be blocked by PTEN siRNA. It was thus concluded that exosomal miR-486 from BMSCs may enhance the functional recovery by promoting angiogenesis following cerebral ischemic injury, which might be related to its regulation of the PTEN/Akt pathway.

Indexed as

ExosomesMesenchymal Stem CellsMicroRNAsNeovascularization, PhysiologicProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseSignal TransductionAngiogenesisAnimalsBrain IschemiaCell MovementCell ProliferationDisease Models, AnimalEndothelial CellsMaleRatsMicroRNAsProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePten protein, rat

Identifiers

PMID39103424
PMCPMC11300871

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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.