Evidence map›Paper›PMID 37802039›Full record

ArticleCell stem cell2023

Tissue morphology influences the temporal program of human brain organoid development.

Ilaria Chiaradia, Ivan Imaz-Rosshandler, Benedikt S Nilges, Jerome Boulanger, Laura Pellegrini, Richa Das, Nachiket D Kashikar, Madeline A Lancaster

Open access · hybridAbstract read
In one paragraph

Article in Cell stem cell, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 1 pooled it
13.1field-weighted citation impact, top 1% 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

59 citing papers in PubMed, 1 synthesis or guideline pooled it, 85 citations in OpenAlex.

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  18. Spatial architecture of development and disease.Nature reviews. Genetics · 2026
    Review
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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

8 authors at 1 institution in 1 country.

Ilaria ChiaradiaMRC Laboratory of Molecular Biology, Cambridge Biomedical Campus, Cambridge, UK.
Ivan Imaz-RosshandlerMRC Laboratory of Molecular Biology, Cambridge Biomedical Campus, Cambridge, UK.
Benedikt S NilgesResolve Biosciences GmbH, Alfred-Nobel-Strasse 10, 40789 Monheim am Rhein, Germany.
Jerome BoulangerMRC Laboratory of Molecular Biology, Cambridge Biomedical Campus, Cambridge, UK.
Laura PellegriniMRC Laboratory of Molecular Biology, Cambridge Biomedical Campus, Cambridge, UK.
Richa DasResolve Biosciences GmbH, Alfred-Nobel-Strasse 10, 40789 Monheim am Rhein, Germany.
Nachiket D KashikarResolve Biosciences GmbH, Alfred-Nobel-Strasse 10, 40789 Monheim am Rhein, Germany.
Madeline A LancasterMRC Laboratory of Molecular Biology, Cambridge Biomedical Campus, Cambridge, UK; Wellcome-MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK. Electronic address: madeline.lancaster@mrc-lmb.cam.ac.uk.
MRC Laboratory of Molecular Biology · GB

Funding

European Research Council
6 · The paper itself

Abstract

Progression through fate decisions determines cellular composition and tissue architecture, but how that same architecture may impact cell fate is less clear. We took advantage of organoids as a tractable model to interrogate this interaction of form and fate. Screening methodological variations revealed that common protocol adjustments impacted various aspects of morphology, from macrostructure to tissue architecture. We examined the impact of morphological perturbations on cell fate through integrated single nuclear RNA sequencing (snRNA-seq) and spatial transcriptomics. Regardless of the specific protocol, organoids with more complex morphology better mimicked in vivo human fetal brain development. Organoids with perturbed tissue architecture displayed aberrant temporal progression, with cells being intermingled in both space and time. Finally, encapsulation to impart a simplified morphology led to disrupted tissue cytoarchitecture and a similar abnormal maturational timing. These data demonstrate that cells of the developing brain require proper spatial coordinates to undergo correct temporal progression.

Indexed as

BrainOrganoidsCell DifferentiationHumansSequence Analysis, RNAbraincell fatecytoarchitecturedevelopmentdifferentiationmorphologyneurogenesisorganoidsspatial transcriptomicsstem cells

Identifiers

PMID37802039
PMCPMC10765088
OpenAlexW4387364595

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.