Evidence map›Paper›PMID 26979533›Full record

ArticleStem cell research & therapy2016

Intraspinal bone-marrow cell therapy at pre- and symptomatic phases in a mouse model of amyotrophic lateral sclerosis.

Fernanda Gubert, Ana B Decotelli, Igor Bonacossa-Pereira, Fernanda R Figueiredo, Camila Zaverucha-do-Valle, Fernanda Tovar-Moll, Luísa Hoffmann, Turan P Urmenyi, Marcelo F Santiago, Rosalia Mendez-Otero

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.2field-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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Preclinical studies of mesenchymal stem cells transplantation in amyotrophic lateral sclerosis: a systemic review and metaanalysis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2021
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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 at 3 institutions in 1 country.

Fernanda GubertInstituto de Biofísica Carlos Chagas Filho, Centro de Ciências da Saúde, Sala G2-028, Universidade Federal do Rio de Janeiro, Cidade Universitária, RJ 21941-902, Rio de Janeiro, Brazil. fegubert@biof.ufrj.br.
Ana B DecotelliInstituto de Biofísica Carlos Chagas Filho, Centro de Ciências da Saúde, Sala G2-028, Universidade Federal do Rio de Janeiro, Cidade Universitária, RJ 21941-902, Rio de Janeiro, Brazil.
Igor Bonacossa-PereiraInstituto de Biofísica Carlos Chagas Filho, Centro de Ciências da Saúde, Sala G2-028, Universidade Federal do Rio de Janeiro, Cidade Universitária, RJ 21941-902, Rio de Janeiro, Brazil.
Fernanda R FigueiredoInstituto de Biofísica Carlos Chagas Filho, Centro de Ciências da Saúde, Sala G2-028, Universidade Federal do Rio de Janeiro, Cidade Universitária, RJ 21941-902, Rio de Janeiro, Brazil.
Camila Zaverucha-do-ValleEvandro Chagas National Institute of Infectious Diseases (INI), Oswaldo Cruz Foundation, Avenida Brasil 4365, Maguinhos, RJ 21040-900, Rio de Janeiro, Brazil.
Fernanda Tovar-MollInstitute of Biomedical Sciences and National Center of Structural Biology and Bioimaging, CENABIO, Centro de Ciências da Saúde, Universidade Federal do Rio de Janeiro, Cidade Universitária, RJ 21941-902, Rio de Janeiro, Brazil.
Luísa HoffmannInstituto de Biofísica Carlos Chagas Filho, Centro de Ciências da Saúde, Sala G2-028, Universidade Federal do Rio de Janeiro, Cidade Universitária, RJ 21941-902, Rio de Janeiro, Brazil.
Turan P UrmenyiInstituto de Biofísica Carlos Chagas Filho, Centro de Ciências da Saúde, Sala G2-028, Universidade Federal do Rio de Janeiro, Cidade Universitária, RJ 21941-902, Rio de Janeiro, Brazil.
Marcelo F SantiagoInstituto de Biofísica Carlos Chagas Filho, Centro de Ciências da Saúde, Sala G2-028, Universidade Federal do Rio de Janeiro, Cidade Universitária, RJ 21941-902, Rio de Janeiro, Brazil.
Rosalia Mendez-OteroInstituto de Biofísica Carlos Chagas Filho, Centro de Ciências da Saúde, Sala G2-028, Universidade Federal do Rio de Janeiro, Cidade Universitária, RJ 21941-902, Rio de Janeiro, Brazil.
Universidade Federal do Rio de Janeiro · BRFundação Oswaldo Cruz · BRNational Institute of Science and Technology for Structural Biology and Bioimaging · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAmyotrophic lateral sclerosis (ALS) is a progressive neurological disease that selectively affects the motor neurons. The details of the mechanisms of selective motor-neuron death remain unknown and no effective therapy has been developed. We investigated the therapy with bone-marrow mononuclear cells (BMMC) in a mouse model of ALS (SOD1(G93A) mice).

methodsWe injected 10(6) BMMC into the lumbar portion of the spinal cord of SOD1(G93A) mice in presymptomatic (9 weeks old) and symptomatic (14 weeks old) phases. In each condition, we analyzed the progression of disease and the lifespan of the animals.

resultsWe observed a mild transitory delay in the disease progression in the animals injected with BMMC in the presymptomatic phase. However, we observed no increase in the lifespan. When we injected BMMC in the symptomatic phase, we observed no difference in the animals' lifespan or in the disease progression. Immunohistochemistry for NeuN showed a decrease in the number of motor neurons during the course of the disease, and this decrease was not affected by either treatment. Using different strategies to track the BMMC, we noted that few cells remained in the spinal cord after transplantation. This observation could explain why the BMMC therapy had only a transitory effect.

conclusionThis is the first report of intraspinal BMMC therapy in a mouse model of ALS. We conclude this cellular therapy has only a mild transitory effect when performed in the presymptomatic phase of the disease.

Indexed as

Bone Marrow TransplantationAmyotrophic Lateral SclerosisAnimalsAnterior Horn CellsAsymptomatic DiseasesCell MovementCell SurvivalCell TrackingFemaleInjections, SpinalLumbosacral RegionMaleMice, Inbred C57BLMice, TransgenicMicrogliaMotor ActivitySod1 protein, mouseSuperoxide DismutaseSuperoxide Dismutase-1Amyotrophic lateral sclerosisBone marrow cell therapyNeuronal degeneration

Identifiers

PMID26979533
PMCPMC4791786
OpenAlexW2299689687

What OpenQuestion holds

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LicenceCC BY
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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.