Evidence map›Paper›PMID 28567004›Full record

ArticleFrontiers in cellular neuroscience2017

Differentiation of Human Induced Pluripotent Stem Cell (hiPSC)-Derived Neurons in Mouse Hippocampal Slice Cultures.

Toshimitsu Hiragi, Megumi Andoh, Toshihiro Araki, Takayuki Shirakawa, Takashi Ono, Ryuta Koyama, Yuji Ikegaya

Abstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Frontiers in molecular neuroscience · 2022
    Article
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  7. Review
  8. 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

7 authors.

Toshimitsu HiragiLaboratory of Chemical Pharmacology, Graduate School of Pharmaceutical Sciences, University of TokyoTokyo, Japan.
Megumi AndohLaboratory of Chemical Pharmacology, Graduate School of Pharmaceutical Sciences, University of TokyoTokyo, Japan.
Toshihiro ArakiAdvanced Drug Research Laboratories, Mitsubishi Tanabe Pharma CorporationYokohama, Japan.
Takayuki ShirakawaAdvanced Drug Research Laboratories, Mitsubishi Tanabe Pharma CorporationYokohama, Japan.
Takashi OnoAdvanced Drug Research Laboratories, Mitsubishi Tanabe Pharma CorporationYokohama, Japan.
Ryuta KoyamaLaboratory of Chemical Pharmacology, Graduate School of Pharmaceutical Sciences, University of TokyoTokyo, Japan.
Yuji IkegayaLaboratory of Chemical Pharmacology, Graduate School of Pharmaceutical Sciences, University of TokyoTokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Potential clinical applications of neurons derived from human induced pluripotent stem cells (hiPSC-neurons) for drug screening and transplantation therapies have received considerable attention. However, it remains unclear whether and how transplanted hiPSC-neurons are incorporated into pre-existing neural circuits. Here we developed a co-culture system of hiPSC-neurons and mouse hippocampal slices to examine the differentiation of hiPSC-neurons in pre-existing neural circuits. hiPSC-neurons transplanted in mouse hippocampal slices expressed the hippocampal neuron-specific markers HuB and Prox1 after 7 days of culture, while those markers were scarcely expressed in hiPSC-neurons cultured on glass dishes. Furthermore, hiPSC-neurons transplanted in the dentate gyrus (DG) of slice cultures grew to exhibit dentate granule cell-like morphologies, including besom-shaped dendrites. Similarly, hiPSC-neurons transplanted in the CA1 region of slice cultures grew to exhibit CA1 pyramidal cell-like morphologies, including primary apical and multiple basal dendrites with synaptic spines. Additionally, these cells projected axons toward the entorhinal cortex (EC) as observed

Indexed as

hippocampusiPS cellsneural differentiationslice culturetransplantation

Identifiers

PMID28567004
PMCPMC5434115

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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.