Evidence map›Paper›PMID 41903542›Full record

ArticleCell reports methods2026

Electrophysiological development and functional plasticity in dissociated human cerebral organoids across multiple cell lines.

Adam Pavlinek, Sara Guerrisi, Kara O'Driscoll, Lucia Dutan Polit, Roland Nagy, APEX consortium, Madeline A Lancaster, Anthony C Vernon, Deepak P Srivastava

Abstract read
In one paragraph

Article in Cell reports methods, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

9 authors.

Adam PavlinekDepartment of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 9RT, UK; MRC Centre for Neurodevelopmental Disorders, King's College London, London, UK. Electronic address: ap2025@cantab.ac.uk.
Sara GuerrisiDepartment of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 9RT, UK; MRC Centre for Neurodevelopmental Disorders, King's College London, London, UK.
Kara O'DriscollDepartment of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 9RT, UK; MRC Centre for Neurodevelopmental Disorders, King's College London, London, UK.
Lucia Dutan PolitDepartment of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 9RT, UK; MRC Centre for Neurodevelopmental Disorders, King's College London, London, UK.
Roland NagyDepartment of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 9RT, UK; MRC Centre for Neurodevelopmental Disorders, King's College London, London, UK.
APEX consortium
Madeline A LancasterMRC Laboratory of Molecular Biology, Cambridge, UK.
Anthony C VernonDepartment of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 9RT, UK; MRC Centre for Neurodevelopmental Disorders, King's College London, London, UK.
Deepak P SrivastavaDepartment of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 9RT, UK; MRC Centre for Neurodevelopmental Disorders, King's College London, London, UK; Dementia Research Institute, King's College London, London, UK. Electronic address: deepak.srivastava@kcl.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microelectrode arrays (MEAs) are increasingly used to profile the development of synchronized activity in neural organoids, yet no organoid study has reported on the consistency of electrophysiological development across cell lines. Here, we used dissociated neural organoids derived from six cell lines on MEAs to characterize functional synapse development using multiple parameters across time. The dissociated organoids demonstrated increasing functional connectivity and network activity over time across all cell lines and plasticity in response to synaptic-like stimulation. Like the organoids they were derived from, dissociated organoid cultures contained a diverse mixture of cell types. These results demonstrate that dissociated cerebral organoids can generate functional neurons, akin to primary neuronal cultures from brain tissue, providing a scalable model for studies of neurodevelopment and synaptic function. Consistent with unguided differentiation, we observed variability in activity parameters linked to donor cell line and batch effects, which must be considered in experimental design.

Indexed as

BrainElectrophysiological PhenomenaNeuronal PlasticityOrganoidsCell DifferentiationCell LineHumansMicroelectrodesNeurodevelopmentNeuronscerebral organoidsCP: stem cellelectrophysiologyestradiolfunctional connectivityhuman induced pluripotent stem cellsMEAmicro-electrode arraysnetwork dynamicsneuronal culturessynaptic plasticity

Identifiers

PMID41903542
PMCPMC13107059

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.