Evidence map›Paper›PMID 40346597›Full record

ArticleStem cell research & therapy2025

Electrophysiological characterisation of intranigral-grafted hiPSC-derived dopaminergic neurons in a mouse model of Parkinson's disease.

Bérengère Ballion, Marie-Laure Bonnet, Sébastien Brot, Afsaneh Gaillard

Abstract read
In one paragraph

Article in Stem cell research & therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
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

4 authors.

Bérengère BallionLaboratoire des neurosciences expérimentales et cliniques (LNEC), Université de Poitiers- INSERM 1084, Poitiers Cedex 9, 86073, France. berengere.ballion@univ-poitiers.fr.
Marie-Laure BonnetLaboratoire des neurosciences expérimentales et cliniques (LNEC), Université de Poitiers- INSERM 1084, Poitiers Cedex 9, 86073, France.
Sébastien BrotLaboratoire des neurosciences expérimentales et cliniques (LNEC), Université de Poitiers- INSERM 1084, Poitiers Cedex 9, 86073, France.
Afsaneh GaillardLaboratoire des neurosciences expérimentales et cliniques (LNEC), Université de Poitiers- INSERM 1084, Poitiers Cedex 9, 86073, France. afsaneh.gaillard@univ-poitiers.fr.ORCID http://orcid.org/0000-0002-9375-6506

Funding

Fondation de France 66517Fondation pour la Recherche Médicale Victor and Erminia Mescle price
6 · The paper itself

Abstract

backgroundParkinson's disease (PD) is a complex neurological disorder characterized by the progressive degeneration of midbrain dopaminergic (mDA) neurons in the substantia nigra (SN). This degeneration disrupts the basal ganglia loops, leading to both motor and non-motor dysfunctions. Cell therapy for PD aims to replace lost mDA neurons to restore the DA neurotransmission in the denervated forebrain targets. In clinical trials for PD, mDA neurons are implanted into the target area, the striatum, and not in the SN where they are normally located. This ectopic localisation of cells may affect the functionality of transplanted neurons due to the absence of appropriate host afferent regulation. We recently demonstrated that human induced pluripotent stem cells (hiPSCs) derived mDA progenitors grafted into the substantia nigra pars compacta (SNpc) in a mouse model of PD, differentiated into mature mDA neurons, restored the degenerated nigrostriatal pathway, and induced motor recovery. The objective of the present study was to evaluate the long-term functionality of these intranigral-grafted mDA neurons by assessing their electrophysiological properties.

methodsWe performed intranigral transplantation of hiPSC-derived mDA progenitors in a 6-hydroxydopamine RAG2-KO mouse model of PD. We recorded in vivo unit extracellular activity of grafted mDA neurons in anesthetised mice from 9 to 12 months post-transplantation. Their electrophysiological properties, including firing rates, patterns and spike characteristics, were analysed and compared with those of native nigral dopaminergic neurons from control mice.

resultsWe demonstrated that these grafted mDA neurons exhibited functional characteristics similar to those of native nigral dopaminergic neurons, such as large bi- or triphasic spike waveforms, low firing rates, pacemaker-like properties, and two single-spike firing patterns. Although grafted mDA neurons also displayed low discharge frequencies below 10 Hz, their mean frequency was significantly lower than that of nigral mDA neurons, with a differential pattern distribution.

conclusionsOur findings indicate that grafted mDA neurons exhibit dopaminergic-like functional properties, including intrinsic membrane potential oscillations leading to regular firing patterns. Additionally, they demonstrated irregular and burst firing patterns, suggesting they receive modulatory inputs. However, grafted mDA neurons displayed distinct properties, potentially related to their human origin or the incomplete maturation one year after transplantation.

Indexed as

Dopaminergic NeuronsInduced Pluripotent Stem CellsParkinson DiseaseAnimalsCell DifferentiationDisease Models, AnimalElectrophysiological PhenomenaHumansMiceSubstantia NigraCell therapyElectrophysiologyHiPSCIntranigral transplantationIn vivoMouseParkinson’s disease

Identifiers

PMID40346597
PMCPMC12065326

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.