Evidence map›Paper›PMID 35241178›Full record

ArticleStem cell research & therapy2022

EPC-EXs improve astrocyte survival and oxidative stress through different uptaking pathways in diabetic hypoxia condition.

Manasi Suchit Halurkar, Jinju Wang, Shuzhen Chen, Ji Chen Bihl

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 26 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

4 authors at 2 institutions in 1 country.

Manasi Suchit HalurkarDepartment of Pharmacology and Toxicology, Boonshoft School of Medicine, Wright State University, Dayton, OH, 45435, USA.
Jinju WangDepartment of Biomedical Sciences, Joan C Edwards School of Medicine, Marshall University, Huntington, WV, 25755, USA.
Shuzhen ChenDepartment of Biomedical Sciences, Joan C Edwards School of Medicine, Marshall University, Huntington, WV, 25755, USA.
Ji Chen BihlDepartment of Biomedical Sciences, Joan C Edwards School of Medicine, Marshall University, Huntington, WV, 25755, USA. bihlj@marshall.edu.ORCID 0000-0003-2404-1782
Marshall University · USWright State University · US

Funding

West Virginia IDEA-CTRU54GM104942 · NIGMS · WEST VIRGINIA UNIVERSITY · PI Sally Lynn Hodder · 2012 to 2026
$81.0M
Exosomes from miR-primed endothelial progenitor cells for treating ischemic strokeR01NS102720 · NINDS · WRIGHT STATE UNIVERSITY · PI BIHL, JI CHEN · 2018 to 2022
$1.6M
NIGMS NIH HHS U54 GM104942NINDS NIH HHS R01 NS102720
6 · The paper itself

Abstract

backgroundHyperglycemia contributes to cardiovascular complications in patients with type 2 diabetes. We confirmed that high glucose (HG) induces endothelial dysfunction and cerebral ischemic injury is enlarged in diabetic mice. Stem cell-released exosomes have been shown to protect the brain from ischemic stroke. We have previously shown that endothelial progenitor cells (EPCs)-released exosomes (EPC-EXs) can protect endothelial cells from hypoxia/reoxygenation (H/R) and HG-induced injury. Here, we aim to investigate the effects of EPC-EXs on astrocytes under H/R and HG-induced injury and whether miR-126 enriched EPC-EXs (miR126-EPC-EXs) have enhanced efficacy.

methodsEPC-EX uptake and co-localization were measured by fluorescent microscopy using PKH26 and DAPI staining. miR-126 enrichment was achieved by transfecting with miR-126 mimics and quantified with real-time PCR. After co-incubation, cell death or injury was measured by using LDH (Lactate Dehydrogenase) assay. Oxidative stress/ROS (reactive oxygen species) generation was measured by DHE (Dihydroethidium) staining and lipid peroxidation assay.

resultsThe EPC-EXs were effectively taken up by the astrocytes in a concentration as well as time-dependent manners and were co-localized within the nucleus as well as the cytoplasm. Pathway uptake inhibitors revealed that the EPC-EXs are effectively taken up by the clathrin-mediated, caveolin-dependent, and micropinocytosis via PI3K/Akt pathway. H/R and HG-induced a cell injury which could be protected by EPC-EXs evidenced by decreased cell cytotoxicity, oxidative stress, and lipid peroxidation. Moreover, miR-126 overexpression could increase the level of miR-126 in astrocytes and enhance the protective effects of EPC-EXs.

conclusionsThese results collectively indicate that the EPC-EXs could protect astrocytes against the HG plus H/R-induced damage.

Indexed as

Diabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2Endothelial Progenitor CellsMicroRNAsAnimalsApoptosisAstrocytesHumansHypoxiaMiceOxidative StressPhosphatidylinositol 3-KinasesMicroRNAsMIRN126 microRNA, mousePhosphatidylinositol 3-KinasesAstrocytesEndothelial progenitor cellsExosomesHigh glucoseHypoxiamicroRNAs

Identifiers

PMID35241178
PMCPMC8896364
OpenAlexW4214850803

What OpenQuestion holds

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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 OpenQuestion graph.