Evidence map›Paper›PMID 26244942›Full record

ArticlePloS one2015

An Engineered N-Cadherin Substrate for Differentiation, Survival, and Selection of Pluripotent Stem Cell-Derived Neural Progenitors.

Amranul Haque, Nihad Adnan, Ali Motazedian, Farhima Akter, Sharif Hossain, Koichi Kutsuzawa, Kakon Nag, Eiry Kobatake, Toshihiro Akaike

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 25 citations in OpenAlex.

  1. Incubator-Free Organoid Culture in a Sealed Recirculatory System.bioRxiv : the preprint server for biology · 2025
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  4. Review
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  11. Detachment of Chain-Forming Neuroblasts by Fyn-Mediated Control of cell-cell Adhesion in the Postnatal Brain.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  12. 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

9 authors at 1 institution in 1 country.

Amranul HaqueDepartment of Biomolecular Engineering, Tokyo Institute of Technology, Yokohama, Japan.
Nihad AdnanDepartment of Biomolecular Engineering, Tokyo Institute of Technology, Yokohama, Japan.
Ali MotazedianDepartment of Biomolecular Engineering, Tokyo Institute of Technology, Yokohama, Japan.
Farhima AkterDepartment of Biological Information, Tokyo Institute of Technology, Yokohama, Japan.
Sharif HossainDepartment of Biomolecular Engineering, Tokyo Institute of Technology, Yokohama, Japan.
Koichi KutsuzawaDepartment of Biomolecular Engineering, Tokyo Institute of Technology, Yokohama, Japan.
Kakon NagDepartment of Biomolecular Engineering, Tokyo Institute of Technology, Yokohama, Japan.
Eiry KobatakeDepartment of Biological Information, Tokyo Institute of Technology, Yokohama, Japan.
Toshihiro AkaikeDepartment of Biomolecular Engineering, Tokyo Institute of Technology, Yokohama, Japan.
Tokyo Institute of Technology · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

For stem cell-based treatment of neurodegenerative diseases a better understanding of key developmental signaling pathways and robust techniques for producing neurons with highest homogeneity are required. In this study, we demonstrate a method using N-cadherin-based biomimetic substrate to promote the differentiation of mouse embryonic stem cell (ESC)- and induced pluripotent stem cell (iPSC)-derived neural progenitor cells (NPCs) without exogenous neuro-inductive signals. We showed that substrate-dependent activation of N-cadherin reduces Rho/ROCK activation and β-catenin expression, leading to the stimulation of neurite outgrowth and conversion into cells expressing neural/glial markers. Besides, plating dissociated cells on N-cadherin substrate can significantly increase the differentiation yield via suppression of dissociation-induced Rho/ROCK-mediated apoptosis. Because undifferentiated ESCs and iPSCs have low affinity to N-cadherin, plating dissociated cells on N-cadherin-coated substrate increase the homogeneity of differentiation by purging ESCs and iPSCs (~30%) from a mixture of undifferentiated cells with NPCs. Using this label-free cell selection approach we enriched differentiated NPCs plated as monolayer without ROCK inhibitor. Therefore, N-cadherin biomimetic substrate provide a powerful tool for basic study of cell-material interaction in a spatially defined and substrate-dependent manner. Collectively, our approach is efficient, robust and cost effective to produce large quantities of differentiated cells with highest homogeneity and applicable to use with other types of cells.

Indexed as

Animalsbeta CateninBlotting, WesternCadherinsCell Culture TechniquesCell DifferentiationCell LineCell SurvivalEmbryonic Stem CellsGene ExpressionImmunoglobulin Fc FragmentsInduced Pluripotent Stem CellsMiceMicroscopy, ConfocalNeural Stem CellsNeuritesbeta CateninCadherinsImmunoglobulin Fc FragmentsRecombinant Fusion Proteinsrho-Associated Kinasesrho GTP-Binding Proteins

Identifiers

PMID26244942
PMCPMC4526632
OpenAlexW1908287103

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.