Evidence map›Paper›PMID 32455791›Full record

ArticleInternational journal of molecular sciences2020

ASC-Exosomes Ameliorate the Disease Progression in SOD1(G93A) Murine Model Underlining Their Potential Therapeutic Use in Human ALS.

Roberta Bonafede, Ermanna Turano, Ilaria Scambi, Alice Busato, Pietro Bontempi, Federica Virla, Lorenzo Schiaffino, Pasquina Marzola, Bruno Bonetti, Raffaella Mariotti

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed, 2 pooled it
6.5field-weighted citation impact, top 2% 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

87 citing papers in PubMed, 2 syntheses or guidelines pooled it, 136 citations in OpenAlex.

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27 more citing papers are in PubMed but not listed here.

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 at 2 institutions in 1 country.

Roberta BonafedeDepartment of Neuroscience, Biomedicine and Movement Sciences, University of Verona, 37134 Verona, Italy.
Ermanna TuranoDepartment of Neuroscience, Biomedicine and Movement Sciences, University of Verona, 37134 Verona, Italy.ORCID 0000-0002-0760-1787
Ilaria ScambiDepartment of Neuroscience, Biomedicine and Movement Sciences, University of Verona, 37134 Verona, Italy.
Alice BusatoDepartment of Computer Sciences, University of Verona, 37134 Verona, Italy.
Pietro BontempiDepartment of Computer Sciences, University of Verona, 37134 Verona, Italy.
Federica VirlaDepartment of Neuroscience, Biomedicine and Movement Sciences, University of Verona, 37134 Verona, Italy.
Lorenzo SchiaffinoDepartment of Neuroscience, Biomedicine and Movement Sciences, University of Verona, 37134 Verona, Italy.
Pasquina MarzolaDepartment of Computer Sciences, University of Verona, 37134 Verona, Italy.
Bruno BonettiNeurology Unit, Azienda Ospedaliera Universitaria Integrata Verona, 37126 Verona, Italy.ORCID 0000-0002-3944-4165
Raffaella MariottiDepartment of Neuroscience, Biomedicine and Movement Sciences, University of Verona, 37134 Verona, Italy.
University of Verona · ITAzienda Ospedaliera Universitaria Integrata Verona · IT

Funding

AriSLA FGBR_7/2016Brain Research Fondation Verona Onlus Grant 2017
6 · The paper itself

Abstract

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by progressive degeneration of motoneurons. To date, there is no effective treatment available. Exosomes are extracellular vesicles that play important roles in intercellular communication, recapitulating the effect of origin cells. In this study, we tested the potential neuroprotective effect of exosomes isolated from adipose-derived stem cells (ASC-exosomes) on the in vivo model most widely used to study ALS, the human SOD1 gene with a G93A mutation (SOD1(G93A)) mouse. Moreover, we compared the effect of two different routes of exosomes administration, intravenous and intranasal. The effect of exosomes administration on disease progression was monitored by motor tests and analysis of lumbar motoneurons and glial cells, neuromuscular junction, and muscle. Our results demonstrated that repeated administration of ASC-exosomes improved the motor performance; protected lumbar motoneurons, the neuromuscular junction, and muscle; and decreased the glial cells activation in treated SOD1(G93A) mice. Moreover, exosomes have the ability to home to lesioned ALS regions of the animal brain. These data contribute by providing additional knowledge for the promising use of ASC-exosomes as a therapy in human ALS.

Indexed as

Adipose TissueAmyotrophic Lateral SclerosisAnimalsCells, CulturedExosomesMesenchymal Stem Cell TransplantationMiceMice, Inbred C57BLMotor NeuronsMovementMutation, MissenseNeuromuscular JunctionSuperoxide Dismutase-1Superoxide Dismutase-1amyotrophic lateral sclerosisextracellular vesicleshomingmotoneuronsMRIneuromuscular junctionstem cells

Identifiers

PMID32455791
PMCPMC7279464
OpenAlexW3026155598

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.