Evidence map›Paper›PMID 24324574›Full record

ArticlePloS one2013

Impact of simulated microgravity on oligodendrocyte development: implications for central nervous system repair.

Araceli Espinosa-Jeffrey, Pablo M Paez, Veronica T Cheli, Vilma Spreuer, Ina Wanner, Jean de Vellis

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 26% 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, 19 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

6 authors at 1 institution in 1 country.

Araceli Espinosa-JeffreySemel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine at UCLA, Intellectual and Developmental Disabilities Research Center, Los Angeles, California, United States of America.
Pablo M Paez
Veronica T Cheli
Vilma Spreuer
Ina Wanner
Jean de Vellis
Intel (United States) · US

Funding

Stem CellsP30HD004612 · NICHD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BOOKHEIMER, SUSAN Y · 1985 to 2014
$19.5M
Early intervention to restore OL and myelin development in leukodystrophy modelR03HD057560 · NICHD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DE VELLIS, JEAN · 2008 to 2009
$154k
NICHD NIH HHS HD-04612NICHD NIH HHS P30 HD004612NICHD NIH HHS R03 HD057560
6 · The paper itself

Abstract

We have recently established a culture system to study the impact of simulated microgravity on oligodendrocyte progenitor cells (OPCs) development. We subjected mouse and human OPCs to a short exposure of simulated microgravity produced by a 3D-Clinostat robot. Our results demonstrate that rodent and human OPCs display enhanced and sustained proliferation when exposed to simulated microgravity as assessed by several parameters, including a decrease in the cell cycle time. Additionally, OPC migration was examined in vitro using time-lapse imaging of cultured OPCs. Our results indicated that OPCs migrate to a greater extent after stimulated microgravity than in normal conditions, and this enhanced motility was associated with OPC morphological changes. The lack of normal gravity resulted in a significant increase in the migration speed of mouse and human OPCs and we found that the average leading process in migrating bipolar OPCs was significantly longer in microgravity treated cells than in controls, demonstrating that during OPC migration the lack of gravity promotes leading process extension, an essential step in the process of OPC migration. Finally, we tested the effect of simulated microgravity on OPC differentiation. Our data showed that the expression of mature oligodendrocyte markers was significantly delayed in microgravity treated OPCs. Under conditions where OPCs were allowed to progress in the lineage, simulated microgravity decreased the proportion of cells that expressed mature markers, such as CC1 and MBP, with a concomitant increased number of cells that retained immature oligodendrocyte markers such as Sox2 and NG2. Development of methodologies aimed at enhancing the number of OPCs and their ability to progress on the oligodendrocyte lineage is of great value for treatment of demyelinating disorders. To our knowledge, this is the first report on the gravitational modulation of oligodendrocyte intrinsic plasticity to increase their progenies.

Indexed as

AnimalsAnimals, NewbornAntigensAutophagy-Related ProteinsBiomarkersCell CycleCell DifferentiationCell MovementCentral Nervous SystemChondroitin Sulfate Proteoglycan 4Gene ExpressionHumansIntracellular Signaling Peptides and ProteinsMiceMyelin Basic ProteinNerve RegenerationAntigensAutophagy-Related ProteinsBiomarkersChondroitin Sulfate Proteoglycan 4Intracellular Signaling Peptides and ProteinsMyelin Basic ProteinProteoglycansRb1cc1 protein, mouseSOX2 protein, humanSOXB1 Transcription Factors

Identifiers

PMID24324574
PMCPMC3850904
OpenAlexW1988105413

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.