Evidence map›Paper›PMID 32540123›Full record

ReviewSeminars in cell & developmental biology2021

Bioengineering tissue morphogenesis and function in human neural organoids.

Nikolai J Fedorchak, Nisha Iyer, Randolph S Ashton

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in cell & developmental biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Article
  3. Modelling human brain development and disease with organoids.Nature reviews. Molecular cell biology · 2025
    Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. RosetteArraybioRxiv : the preprint server for biology · 2024
    Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Advances in neural organoid systems and their application in neurotoxicity testing of environmental chemicals.Genes and environment : the official journal of the Japanese Environmental Mutagen Society · 2021
    Review
  14. Review
  15. Review
  16. Toward Studying Cognition in a Dish.Trends in cognitive sciences · 2021
    Review
  17. Review
  18. Review
  19. 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

3 authors at 2 institutions in 1 country.

Nikolai J FedorchakWisconsin Institute for Discovery, University of Wisconsin-Madison, Madison, WI 53715, United States.
Nisha IyerWisconsin Institute for Discovery, University of Wisconsin-Madison, Madison, WI 53715, United States.
Randolph S AshtonWisconsin Institute for Discovery, University of Wisconsin-Madison, Madison, WI 53715, United States; Department of Biomedical Engineering, University of Wisconsin-Madison, Madison, WI 53706, United States. Electronic address: rashton2@wisc.edu.
University of Wisconsin–Madison · USWisconsin Institutes for Discovery · US

Funding

Human Microphysiological Model of Afferent Nociceptive SignalingUG3TR003150 · NCATS · TULANE UNIVERSITY OF LOUISIANA · PI ASHTON, RANDOLPH S, MOORE, MICHAEL J · 2019 to 2019
$1.2M
High-Throughput Modeling of ALS Using iPSC-Derived Neural Tube MicroarraysR33NS082618 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI ASHTON, RANDOLPH S · 2017 to 2018
$779k
High-Throughput Modeling of ALS Using iPSC-Derived Neural Tube MicroarraysR21NS082618 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI ASHTON, RANDOLPH S · 2014 to 2015
$348k
Regionalized Human Motor Neuron TherapiesF32NS106740 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI IYER, NISHA · 2018 to 2021
$222k
NCATS NIH HHS UG3 TR003150NINDS NIH HHS F32 NS106740NINDS NIH HHS R21 NS082618NINDS NIH HHS R33 NS082618
6 · The paper itself

Abstract

Over the last decade, scientists have begun to model CNS development, function, and disease in vitro using human pluripotent stem cell (hPSC)-derived organoids. Using traditional protocols, these 3D tissues are generated by combining the innate emergent properties of differentiating hPSC aggregates with a bioreactor environment that induces interstitial transport of oxygen and nutrients and an optional supportive hydrogel extracellular matrix (ECM). During extended culture, the hPSC-derived neural organoids (hNOs) obtain millimeter scale sizes with internal microscale cytoarchitectures, cellular phenotypes, and neuronal circuit behaviors mimetic of those observed in the developing brain, eye, or spinal cord. Early studies evaluated the cytoarchitectural and phenotypical character of these organoids and provided unprecedented insight into the morphogenetic processes that govern CNS development. Comparisons to human fetal tissues revealed their significant similarities and differences. While hNOs have current disease modeling applications and significant future promise, their value as anatomical and physiological models is limited because they fail to form reproducibly and recapitulate more mature in vivo features. These include biomimetic macroscale tissue morphology, positioning of morphogen signaling centers to orchestrate appropriate spatial organization and intra- and inter-connectivity of discrete tissue regions, maturation of physiologically relevant neural circuits, and formation of vascular networks that can support sustained in vitro tissue growth. To address these inadequacies scientists have begun to integrate organoid culture with bioengineering techniques and methodologies including genome editing, biomaterials, and microfabricated and microfluidic platforms that enable spatiotemporal control of cellular differentiation or the biochemical and biophysical cues that orchestrate organoid morphogenesis. This review will examine recent advances in hNO technologies and culture strategies that promote reproducible in vitro morphogenesis and greater biomimicry in structure and function.

Indexed as

BioengineeringBrainCell DifferentiationEndothelial CellsExtracellular MatrixHumansModels, BiologicalMorphogenesisNeovascularization, PhysiologicNeural Stem CellsNeurogenesisNeurogliaNeuronsOrganoidsPluripotent Stem CellsTissue EngineeringAssembloidsCircuit formationMorphogenetic patterningNetwork maturationSignaling centersTissue morphologyVascularization

Identifiers

PMID32540123
PMCPMC8755418
OpenAlexW3035460345

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.