Evidence map›Paper›PMID 28562594›Full record

ArticleNature biotechnology2017

Guided self-organization and cortical plate formation in human brain organoids.

Madeline A Lancaster, Nina S Corsini, Simone Wolfinger, E Hilary Gustafson, Alex W Phillips, Thomas R Burkard, Tomoki Otani, Frederick J Livesey, Juergen A Knoblich

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Nature biotechnology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 448 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
448citing papers in PubMed, 1 pooled it
28.9field-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

448 citing papers in PubMed, 1 synthesis or guideline pooled it, 785 citations in OpenAlex.

  1. Pooled it
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  5. Using Brain Organoids to Explore Human Neurobiology.Cellular and molecular neurobiology · 2026
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388 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Madeline A LancasterIMBA-Institute of Molecular Biotechnology of the Austrian Academy of Science, Vienna, Austria.ORCID http://orcid.org/0000-0003-2324-8853
Nina S CorsiniIMBA-Institute of Molecular Biotechnology of the Austrian Academy of Science, Vienna, Austria.
Simone WolfingerIMBA-Institute of Molecular Biotechnology of the Austrian Academy of Science, Vienna, Austria.
E Hilary GustafsonIMBA-Institute of Molecular Biotechnology of the Austrian Academy of Science, Vienna, Austria.ORCID http://orcid.org/0000-0003-3978-8088
Alex W PhillipsMRC Laboratory of Molecular Biology, Cambridge Biomedical Campus, Cambridge, UK.
Thomas R BurkardIMBA-Institute of Molecular Biotechnology of the Austrian Academy of Science, Vienna, Austria.
Tomoki OtaniGurdon Institute and Department of Biochemistry, University of Cambridge, Tennis Court Road, Cambridge, UK.
Frederick J LiveseyGurdon Institute and Department of Biochemistry, University of Cambridge, Tennis Court Road, Cambridge, UK.
Juergen A KnoblichIMBA-Institute of Molecular Biotechnology of the Austrian Academy of Science, Vienna, Austria.
Institute of Molecular Biotechnology · ATUniversity of Cambridge · GBMRC Laboratory of Molecular Biology · GB

Funding

Medical Research Council MC_UP_1201/9Medical Research Council MR/L023784/1Medical Research Council MR/L023784/2
6 · The paper itself

Abstract

Three-dimensional cell culture models have either relied on the self-organizing properties of mammalian cells or used bioengineered constructs to arrange cells in an organ-like configuration. While self-organizing organoids excel at recapitulating early developmental events, bioengineered constructs reproducibly generate desired tissue architectures. Here, we combine these two approaches to reproducibly generate human forebrain tissue while maintaining its self-organizing capacity. We use poly(lactide-co-glycolide) copolymer (PLGA) fiber microfilaments as a floating scaffold to generate elongated embryoid bodies. Microfilament-engineered cerebral organoids (enCORs) display enhanced neuroectoderm formation and improved cortical development. Furthermore, reconstitution of the basement membrane leads to characteristic cortical tissue architecture, including formation of a polarized cortical plate and radial units. Thus, enCORs model the distinctive radial organization of the cerebral cortex and allow for the study of neuronal migration. Our data demonstrate that combining 3D cell culture with bioengineering can increase reproducibility and improve tissue architecture.

Indexed as

Batch Cell Culture TechniquesCells, CulturedGuided Tissue RegenerationHumansNeural Stem CellsNeurogenesisOrgan Culture TechniquesOrganoidsProsencephalonTissue Engineering

Identifiers

PMID28562594
PMCPMC5824977
OpenAlexW2617770907

What OpenQuestion holds

Textmetadata
LicenceTDM
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.