Evidence map›Paper›PMID 31162801›Full record

ArticleJournal of cellular and molecular medicine2019

Transplantation of mesenchymal stem cells overexpressing interleukin-10 induces autophagy response and promotes neuroprotection in a rat model of TBI.

Panchanan Maiti, Sarah Peruzzaro, Nivya Kolli, Melissa Andrews, Abeer Al-Gharaibeh, Julien Rossignol, Gary L Dunbar

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

37 citing papers in PubMed, 55 citations in OpenAlex.

  1. Review
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  7. Mitochondrial-targeted therapies in traumatic brain injury: From bench to bedside.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
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  17. Neuroprotective effects of interleukin 10 in spinal cord injury.Frontiers in molecular neuroscience · 2023
    Review
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4 · The record

Corrections and comments

  • Erratum issued
    2022
5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Panchanan MaitiField Neurosciences Institute of Laboratory for Restorative Neurology, Central Michigan University, Mt. Pleasant, Michigan.ORCID 0000-0003-3213-8015
Sarah PeruzzaroField Neurosciences Institute of Laboratory for Restorative Neurology, Central Michigan University, Mt. Pleasant, Michigan.
Nivya KolliField Neurosciences Institute of Laboratory for Restorative Neurology, Central Michigan University, Mt. Pleasant, Michigan.
Melissa AndrewsField Neurosciences Institute of Laboratory for Restorative Neurology, Central Michigan University, Mt. Pleasant, Michigan.
Abeer Al-GharaibehField Neurosciences Institute of Laboratory for Restorative Neurology, Central Michigan University, Mt. Pleasant, Michigan.
Julien RossignolField Neurosciences Institute of Laboratory for Restorative Neurology, Central Michigan University, Mt. Pleasant, Michigan.
Gary L DunbarField Neurosciences Institute of Laboratory for Restorative Neurology, Central Michigan University, Mt. Pleasant, Michigan.
Central Michigan University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy, including mitophagy, is critical for neuroprotection in traumatic brain injury (TBI). Transplantation of mesenchymal stem cells (MSCs) provides neuroprotection and induces autophagy by increasing anti-inflammatory cytokines, such as interleukin-10 (IL-10). To evaluate these effects of IL10 that are released by MSCs, we genetically engineered MSCs to overexpress IL10 and compared their effects to unaltered MSCs following transplantation near the site of induced TBIs in rats. Adult, male Sprague-Dawley rats were divided into four groups: Sham + vehicle, TBI + vehicle, TBI + MSCs-IL-10 and TBI + MSCs-GFP. Thirty-six hours post-TBI, the first two groups received vehicle (Hanks balance salt solution), whereas last two groups were transplanted with MSCs-IL-10 or MSCs-GFP. Three weeks after transplantation, biomarkers for neurodegenerative changes, autophagy, mitophagy, cell death and survival markers were measured. We observed a significant increase in the number of dead cells in the cortex and hippocampus in TBI rats, whereas transplantation of MSCs-IL-10 significantly reduced their numbers in comparison to MSCs alone. MSCs-IL-10 rats had increased autophagy, mitophagy and cell survival markers, along with decreased markers for cell death and neuroinflammation. These results suggest that transplantation of MSCs-IL-10 may be an effective strategy to protect against TBI-induced neuronal damage.

Indexed as

Mesenchymal Stem Cell TransplantationAnimalsAutophagyBiomarkers, TumorBrain Injuries, TraumaticCell SurvivalDisease Models, AnimalHippocampusHumansInflammationInterleukin-10Mesenchymal Stem CellsMitophagyNeuronsNeuroprotectionRatsBiomarkers, TumorInterleukin-10autophagy markersIL-10 overexpressed MSCsneuroinflammationTBI

Identifiers

PMID31162801
PMCPMC6653779
OpenAlexW2948435134

What OpenQuestion 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 OpenQuestion graph.