Evidence map›Paper›PMID 28599598›Full record

ArticleExperimental biology and medicine (Maywood, N.J.)2017

Uniform neural tissue models produced on synthetic hydrogels using standard culture techniques.

Christopher Barry, Matthew T Schmitz, Nicholas E Propson, Zhonggang Hou, Jue Zhang, Bao K Nguyen, Jennifer M Bolin, Peng Jiang, Brian E McIntosh, Mitchell D Probasco and 5 more

Abstract read
In one paragraph

Article in Experimental biology and medicine (Maywood, N.J.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Brain organoid protocols and limitations.Frontiers in cellular neuroscience · 2024
    Review
  8. Review
  9. Three-DimensionalFrontiers in toxicology · 2021
    Review
  10. Article
  11. Review
  12. Article
  13. Materials for blood brain barrier modelingMaterials science & engineering. R, Reports : a review journal · 2020
    Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Teratogen screening with human pluripotent stem cells.Integrative biology : quantitative biosciences from nano to macro · 2018
    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

15 authors.

Christopher Barry1 Morgridge Institute for Research, Madison, WI 53705, USA.
Matthew T Schmitz1 Morgridge Institute for Research, Madison, WI 53705, USA.
Nicholas E Propson1 Morgridge Institute for Research, Madison, WI 53705, USA.
Zhonggang Hou1 Morgridge Institute for Research, Madison, WI 53705, USA.
Jue Zhang1 Morgridge Institute for Research, Madison, WI 53705, USA.
Bao K Nguyen1 Morgridge Institute for Research, Madison, WI 53705, USA.
Jennifer M Bolin1 Morgridge Institute for Research, Madison, WI 53705, USA.
Peng Jiang1 Morgridge Institute for Research, Madison, WI 53705, USA.
Brian E McIntosh1 Morgridge Institute for Research, Madison, WI 53705, USA.
Mitchell D Probasco1 Morgridge Institute for Research, Madison, WI 53705, USA.
Scott Swanson1 Morgridge Institute for Research, Madison, WI 53705, USA.
Ron Stewart1 Morgridge Institute for Research, Madison, WI 53705, USA.
James A Thomson1 Morgridge Institute for Research, Madison, WI 53705, USA.
Michael P Schwartz5 Center for Sustainable Nanotechnology, Department of Chemistry, University of Wisconsin-Madison, Madison, WI 53706, USA.
William L Murphy6 Department of Biomedical Engineering, University of Wisconsin-Madison, Madison, WI 53705, USA.

Funding

Retinal tissue chips for ocular disease modelingUH3TR000506 · NCATS · MORGRIDGE INSTITUTE FOR RESEARCH, INC. · PI THOMSON, JAMES ALEXANDER · 2014 to 2016
$6.2M
Biomaterials for local regulation of growth factor signalingR01HL093282 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI MURPHY, WILLIAM L. · 2009 to 2018
$3.3M
Human iPS/ES Cell-Based Models for Predictive Neural Toxicity and TeratogenicityUH2TR000506 · NCATS · MORGRIDGE INSTITUTE FOR RESEARCH, INC. · PI THOMSON, JAMES ALEXANDER · 2012 to 2013
$2.4M
CIHRNCATS NIH HHS UH2 TR000506NCATS NIH HHS UH3 TR000506NHLBI NIH HHS R01 HL093282
6 · The paper itself

Abstract

The aim of the present study was to test sample reproducibility for model neural tissues formed on synthetic hydrogels. Human embryonic stem (ES) cell-derived precursor cells were cultured on synthetic poly(ethylene glycol) (PEG) hydrogels to promote differentiation and self-organization into model neural tissue constructs. Neural progenitor, vascular, and microglial precursor cells were combined on PEG hydrogels to mimic developmental timing, which produced multicomponent neural constructs with 3D neuronal and glial organization, organized vascular networks, and microglia with ramified morphologies. Spearman's rank correlation analysis of global gene expression profiles and a comparison of coefficient of variation for expressed genes demonstrated that replicate neural constructs were highly uniform to at least day 21 for samples from independent experiments. We also demonstrate that model neural tissues formed on PEG hydrogels using a simplified neural differentiation protocol correlated more strongly to in vivo brain development than samples cultured on tissue culture polystyrene surfaces alone. These results provide a proof-of-concept demonstration that 3D cellular models that mimic aspects of human brain development can be produced from human pluripotent stem cells with high sample uniformity between experiments by using standard culture techniques, cryopreserved cell stocks, and a synthetic extracellular matrix. Impact statement Pluripotent stem (PS) cells have been characterized by an inherent ability to self-organize into 3D "organoids" resembling stomach, intestine, liver, kidney, and brain tissues, offering a potentially powerful tool for modeling human development and disease. However, organoid formation must be quantitatively reproducible for applications such as drug and toxicity screening. Here, we report a strategy to produce uniform neural tissue constructs with reproducible global gene expression profiles for replicate samples from multiple experiments.

Indexed as

Models, BiologicalBrainCell Culture TechniquesCell DifferentiationCells, CulturedHumansHydrogelsNeural Stem CellsPluripotent Stem CellsPolyethylene GlycolsTissue EngineeringHydrogelsPolyethylene GlycolsBiomaterialdevelopmentmatrixneurotoxicologyorganoidscreening

Identifiers

PMID28599598
PMCPMC5786368

What OpenQuestion holds

Textmetadata
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.