Evidence map›Paper›PMID 31784595›Full record

ArticleScientific reports2019

Functional maturation of human neural stem cells in a 3D bioengineered brain model enriched with fetal brain-derived matrix.

Disha Sood, Dana M Cairns, Jayanth M Dabbi, Charu Ramakrishnan, Karl Deisseroth, Lauren D Black, Sabato Santaniello, David L Kaplan

Abstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing 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

38 citing papers in PubMed.

  1. Article
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  6. Modelling human brain development and disease with organoids.Nature reviews. Molecular cell biology · 2025
    Review
  7. Article
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  12. Article
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  17. Advances in currentFrontiers in bioengineering and biotechnology · 2023
    Review
  18. Review
  19. Article
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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.

Disha SoodDepartment of Biomedical Engineering, Tufts University, Medford, MA, 02155, USA.
Dana M CairnsDepartment of Biomedical Engineering, Tufts University, Medford, MA, 02155, USA.
Jayanth M DabbiDepartment of Biomedical Engineering, Tufts University, Medford, MA, 02155, USA.
Charu RamakrishnanDepartment of Bioengineering, Stanford University, Stanford, CA, 94305, USA.
Karl DeisserothDepartment of Bioengineering, Stanford University, Stanford, CA, 94305, USA.
Lauren D BlackDepartment of Biomedical Engineering, Tufts University, Medford, MA, 02155, USA.
Sabato SantanielloNeural Systems Engineering and Control Laboratory, University of Connecticut, CT, 06269, USA.
David L KaplanDepartment of Biomedical Engineering, Tufts University, Medford, MA, 02155, USA. David.kaplan@tufts.edu.

Funding

National Institutes of Health, United States R01NS092847National Institutes of Health, United States S10OD021624
6 · The paper itself

Abstract

Brain extracellular matrix (ECM) is often overlooked in vitro brain tissue models, despite its instructive roles during development. Using developmental stage-sourced brain ECM in reproducible 3D bioengineered culture systems, we demonstrate enhanced functional differentiation of human induced neural stem cells (hiNSCs) into healthy neurons and astrocytes. Particularly, fetal brain tissue-derived ECM supported long-term maintenance of differentiated neurons, demonstrated by morphology, gene expression and secretome profiling. Astrocytes were evident within the second month of differentiation, and reactive astrogliosis was inhibited in brain ECM-enriched cultures when compared to unsupplemented cultures. Functional maturation of the differentiated hiNSCs within fetal ECM-enriched cultures was confirmed by calcium signaling and spectral/cluster analysis. Additionally, the study identified native biochemical cues in decellularized ECM with notable comparisons between fetal and adult brain-derived ECMs. The development of novel brain-specific biomaterials for generating mature in vitro brain models provides an important path forward for interrogation of neuron-glia interactions.

Indexed as

Models, BiologicalAstrocytesBiocompatible MaterialsBioengineeringCalcium SignalingCell Culture TechniquesCell DifferentiationChondroitin SulfatesCluster AnalysisExtracellular MatrixGene ExpressionHumansNeural Stem CellsNeurogliaNeuronsBiocompatible MaterialsChondroitin Sulfates

Identifiers

PMID31784595
PMCPMC6884597

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.