Evidence map›Paper›PMID 30117633›Full record

ReviewDevelopmental dynamics : an official publication of the American Association of Anatomists2019

Compartmentalized Devices as Tools for Investigation of Human Brain Network Dynamics.

Joseph A Fantuzzo, Ronald P Hart, Jeffrey D Zahn, Zhiping P Pang

Abstract readReview
In one paragraph

Review in Developmental dynamics : an official publication of the American Association of Anatomists, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Frontiers in immunology · 2025
    Review
  5. Beyond a Transmission Cable-New Technologies to Reveal the Richness in Axonal Electrophysiology.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Long-distance regressive signaling in neural development and disease.Wiley interdisciplinary reviews. Developmental biology · 2021
    Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. 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

4 authors.

Joseph A FantuzzoChild Health Institute of New Jersey, Robert Wood Johnson Medical School, New Brunswick, New Jersey.
Ronald P HartDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, New Jersey.
Jeffrey D ZahnDepartment of Biomedical Engineering, Rutgers University, Piscataway, New Jersey.
Zhiping P PangChild Health Institute of New Jersey, Robert Wood Johnson Medical School, New Brunswick, New Jersey.

Funding

Deciphering the neural basis of alcohol use disorders using human and mouse neuronsR01AA023797 · NIAAA · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI ZHIPING P. PANG · 2016 to 2026
$4.8M
Developing an In Vitro Neurocircuitry Model of Addiction using Risk-Associated HuR21DA035594 · NIDA · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI HART, RONALD P, PANG, ZHIPING P. · 2013 to 2014
$409k
High throughput multicompartment culture chambers to develop neurocircuit models of addiction riskR21DA039686 · NIDA · RUTGERS, THE STATE UNIV OF N.J. · PI HART, RONALD P, PANG, ZHIPING P. · 2015 to 2016
$382k
NIAAA NIH HHS R01 AA023797NIDA NIH HHS R21 DA035594NIDA NIH HHS R21 DA039686
6 · The paper itself

Abstract

Neuropsychiatric disorders have traditionally been difficult to study due to the complexity of the human brain and limited availability of human tissue. Induced pluripotent stem (iPS) cells provide a promising avenue to further our understanding of human disease mechanisms, but traditional 2D cell cultures can only provide a limited view of the neural circuits. To better model complex brain neurocircuitry, compartmentalized culturing systems and 3D organoids have been developed. Early compartmentalized devices demonstrated how neuronal cell bodies can be isolated both physically and chemically from neurites. Soft lithographic approaches have advanced this approach and offer the tools to construct novel model platforms, enabling circuit-level studies of disease, which can accelerate mechanistic studies and drug candidate screening. In this review, we describe some of the common technologies used to develop such systems and discuss how these lithographic techniques have been used to advance our understanding of neuropsychiatric disease. Finally, we address other in vitro model platforms such as 3D culture systems and organoids and compare these models with compartmentalized models. We ask important questions regarding how we can further harness iPS cells in these engineered culture systems for the development of improved in vitro models. Developmental Dynamics 248:65-77, 2019. © 2018 Wiley Periodicals, Inc.

Indexed as

Models, BiologicalAnimalsBrainCell CompartmentationCell Culture TechniquesHumansInduced Pluripotent Stem CellsNeuronsOrganoidsPrinting, Three-Dimensional3D cultureaxonal transportcompartmentalizationHuntington's Diseaseinduced neuronsmicrofluidicsneurocircuitryneuropsychiatric disordersorganoidsstem cells

Identifiers

PMID30117633
PMCPMC6312734

What OpenQuestion holds

Textmetadata
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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.