Evidence map›Paper›PMID 28821816›Full record

ArticleScientific reports2017

An expandable embryonic stem cell-derived Purkinje neuron progenitor population that exhibits in vivo maturation in the adult mouse cerebellum.

Gustavo A Higuera, Grazia Iaffaldano, Meiwand Bedar, Guy Shpak, Robin Broersen, Shashini T Munshi, Catherine Dupont, Joost Gribnau, Femke M S de Vrij, Steven A Kushner and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–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

12 citing papers in PubMed.

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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

11 authors.

Gustavo A HigueraDepartment of Neuroscience, Erasmus MC Rotterdam, NL-3015 GE, Rotterdam, The Netherlands. g.higuerasierra@erasmusmc.nl.
Grazia IaffaldanoDepartment of Neuroscience, Erasmus MC Rotterdam, NL-3015 GE, Rotterdam, The Netherlands.
Meiwand BedarDepartment of Neuroscience, Erasmus MC Rotterdam, NL-3015 GE, Rotterdam, The Netherlands.
Guy ShpakDepartment of Psychiatry, Erasmus MC Rotterdam, NL-3015 GE, Rotterdam, The Netherlands.
Robin BroersenDepartment of Neuroscience, Erasmus MC Rotterdam, NL-3015 GE, Rotterdam, The Netherlands.
Shashini T MunshiDepartment of Psychiatry, Erasmus MC Rotterdam, NL-3015 GE, Rotterdam, The Netherlands.
Catherine DupontDepartment of Endocrinology & Reproduction, Erasmus MC Rotterdam, NL-3015 GE, Rotterdam, The Netherlands.
Joost GribnauDepartment of Endocrinology & Reproduction, Erasmus MC Rotterdam, NL-3015 GE, Rotterdam, The Netherlands.
Femke M S de VrijDepartment of Psychiatry, Erasmus MC Rotterdam, NL-3015 GE, Rotterdam, The Netherlands.
Steven A KushnerDepartment of Psychiatry, Erasmus MC Rotterdam, NL-3015 GE, Rotterdam, The Netherlands.ORCID 0000-0002-9777-3338
Chris I De ZeeuwDepartment of Neuroscience, Erasmus MC Rotterdam, NL-3015 GE, Rotterdam, The Netherlands. c.dezeeuw@erasmusmc.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The directed differentiation of patient-derived induced pluripotent stem cells into cell-type specific neurons has inspired the development of therapeutic discovery for neurodegenerative diseases. Many forms of ataxia result from degeneration of cerebellar Purkinje cells, but thus far it has not been possible to efficiently generate Purkinje neuron (PN) progenitors from human or mouse pluripotent stem cells, let alone to develop a methodology for in vivo transplantation in the adult cerebellum. Here, we present a protocol to obtain an expandable population of cerebellar neuron progenitors from mouse embryonic stem cells. Our protocol is characterized by applying factors that promote proliferation of cerebellar progenitors. Cerebellar progenitors isolated in culture from cell aggregates contained a stable subpopulation of PN progenitors that could be expanded for up to 6 passages. When transplanted into the adult cerebellum of either wild-type mice or a strain lacking Purkinje cells (L7cre-ERCC1 knockout), GFP-labeled progenitors differentiated in vivo to establish a population of calbindin-positive cells in the molecular layer with dendritic trees typical of mature PNs. We conclude that this protocol may be useful for the generation and maturation of PNs, highlighting the potential for development of a regenerative medicine approach to the treatment of cerebellar neurodegenerative diseases.

Indexed as

Cell DifferentiationAction PotentialsAge FactorsAnimalsBiomarkersCell Culture TechniquesCells, CulturedCerebellumCulture MediaEmbryonic Stem CellsFemaleFluorescent Antibody TechniqueGene ExpressionGenes, ReporterImmunophenotypingMaleBiomarkersCulture Media

Identifiers

PMID28821816
PMCPMC5562837

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Registered trials

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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.