Evidence map›Paper›PMID 34847707›Full record

ArticleStroke2022

Postischemic Neuroprotection Associated With Anti-Inflammatory Effects by Mesenchymal Stromal Cell-Derived Small Extracellular Vesicles in Aged Mice.

Chen Wang, Verena Börger, Ayan Mohamud Yusuf, Tobias Tertel, Oumaima Stambouli, Florian Murke, Nico Freund, Christoph Kleinschnitz, Josephine Herz, Matthias Gunzer and 4 more

Abstract read
In one paragraph

Article in Stroke, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing 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

45 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

14 authors.

Chen WangDepartment of Neurology (C.W., A.M.Y., C.K., D.M.H.), University Hospital Essen, Germany.ORCID 0000-0002-0213-9642
Verena BörgerInstitute of Transfusion Medicine (V.B., T.T., O.S., F.M., N.F., B.G.), University Hospital Essen, Germany.ORCID 0000-0002-8230-2218
Ayan Mohamud YusufDepartment of Neurology (C.W., A.M.Y., C.K., D.M.H.), University Hospital Essen, Germany.ORCID 0000-0001-6863-7612
Tobias TertelInstitute of Transfusion Medicine (V.B., T.T., O.S., F.M., N.F., B.G.), University Hospital Essen, Germany.ORCID 0000-0001-8659-8610
Oumaima StambouliInstitute of Transfusion Medicine (V.B., T.T., O.S., F.M., N.F., B.G.), University Hospital Essen, Germany.ORCID 0000-0003-1686-0323
Florian MurkeInstitute of Transfusion Medicine (V.B., T.T., O.S., F.M., N.F., B.G.), University Hospital Essen, Germany.
Nico FreundInstitute of Transfusion Medicine (V.B., T.T., O.S., F.M., N.F., B.G.), University Hospital Essen, Germany.ORCID 0000-0002-7053-5532
Christoph KleinschnitzDepartment of Neurology (C.W., A.M.Y., C.K., D.M.H.), University Hospital Essen, Germany.
Josephine HerzDepartment of Pediatrics I (J.H.), University Hospital Essen, Germany.
Matthias GunzerInstitute of Experimental Immunology and Imaging (M.G.), University Hospital Essen, Germany.ORCID 0000-0002-5534-6055
Aurel Popa-WagnerCenter of Experimental and Clinical Medicine, University of Medicine and Pharmacy, Craiova, Romania (A.P.-W.).ORCID 0000-0003-4574-8605
Thorsten R DoeppnerDepartment of Neurology, University Medicine Göttingen, Germany (T.R.D.).
Bernd GiebelInstitute of Transfusion Medicine (V.B., T.T., O.S., F.M., N.F., B.G.), University Hospital Essen, Germany.ORCID 0000-0003-2446-948X
Dirk M HermannDepartment of Neurology (C.W., A.M.Y., C.K., D.M.H.), University Hospital Essen, Germany.ORCID 0000-0003-0198-3152

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeSmall extracellular vesicles (sEVs) obtained from mesenchymal stromal cells (MSCs) were shown to induce ischemic neuroprotection in mice by modulating the brain infiltration of leukocytes and, specifically polymorphonuclear neutrophils. So far, effects of MSC-sEVs were only studied in young ischemic rodents. We herein examined the effects of MSC-sEVs in aged mice.

methodsMale and female C57Bl6/j mice (8-10 weeks or 15-24 months) were exposed to transient intraluminal middle cerebral artery occlusion. Vehicle or sEVs (equivalent of 2×10

resultsMSC-sEV delivery reduced neurological deficits, infarct volume, brain edema, and neuronal injury in young and aged mice of both sexes, when delivered immediately postreperfusion or with 6 hours delay. MSC-sEVs decreased leukocyte and specifically polymorphonuclear neutrophil, monocyte, and macrophage infiltrates in ischemic brains of aged mice. In peripheral blood, the number of monocytes and activated T cells was significantly reduced by MSC-sEVs.

conclusionsMSC-sEVs induce postischemic neuroprotection and anti-inflammation in aged mice.

Indexed as

AgingAnimalsBrainDisease Models, AnimalExtracellular VesiclesFemaleHumansInfarction, Middle Cerebral ArteryMaleMesenchymal Stem CellsMiceMice, Inbred C57BLNeuronsNeuroprotectionexosomesinflammationischemic strokemacrophagesneutrophils

Identifiers

PMID34847707
PMCPMC8700303

What OpenQuestion holds

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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.