Evidence map›Paper›PMID 32231396›Full record

ArticlePloS one2020

All-trans retinoic acid induces reprogramming of canine dedifferentiated cells into neuron-like cells.

Rei Nakano, Taku Kitanaka, Shinichi Namba, Nanako Kitanaka, Masaki Sato, Yoshiyuki Shibukawa, Yoshikazu Masuhiro, Koichiro Kano, Taro Matsumoto, Hiroshi Sugiya

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. 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
1.3field-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, 10 citations in OpenAlex.

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  6. Biology · 2023
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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

10 authors at 2 institutions in 1 country.

Rei NakanoLaboratory for Cellular Function Conversion Technology, RIKEN Center for Integrative Medical Sciences (IMS), Yokohama, Kanagawa, Japan.ORCID 0000-0003-0255-6347
Taku KitanakaLaboratory of Veterinary Biochemistry, College of Bioresource Sciences, Nihon University, Fujisawa, Kanagawa, Japan.
Shinichi NambaLaboratory of Veterinary Biochemistry, College of Bioresource Sciences, Nihon University, Fujisawa, Kanagawa, Japan.
Nanako KitanakaLaboratory of Veterinary Biochemistry, College of Bioresource Sciences, Nihon University, Fujisawa, Kanagawa, Japan.
Masaki SatoDepartment of Biology, Tokyo Dental College, Tokyo, Japan.
Yoshiyuki ShibukawaDepartment of Physiology, Tokyo Dental College, Tokyo, Japan.
Yoshikazu MasuhiroLaboratory of Molecular and Cellular Physiology, College of Bioresource Sciences, Nihon University, Fujisawa, Kanagawa, Japan.
Koichiro KanoLaboratory of Cell and Tissue Biology, College of Bioresource Sciences, Nihon University, Fujisawa, Kanagawa, Japan.
Taro MatsumotoDivision of Cell Regeneration and Transplantation, Department of Functional Morphology, Nihon University School of Medicine, Tokyo, Japan.
Hiroshi SugiyaLaboratory of Veterinary Biochemistry, College of Bioresource Sciences, Nihon University, Fujisawa, Kanagawa, Japan.ORCID 0000-0003-4795-7806
Nihon University · JPTokyo Dental College · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The specification of cell identity depends on the exposure of cells to sequences of bioactive ligands. All-trans retinoic acid (ATRA) affects neuronal development in the early stage, and it is involved in neuronal lineage reprogramming. We previously established a fibroblast-like dedifferentiated fat cells (DFATs) derived from highly homogeneous mature adipocytes, which are more suitable for the study of cellular reprogramming. Canine cognitive dysfunction is similar to human cognitive dysfunction, suggesting that dogs could be a pathological and pharmacological model for human neuronal diseases. However, the effect of ATRA on neuronal reprogramming in dogs has remained unclear. Therefore, in this study, we investigated the effect of ATRA on the neuronal reprogramming of canine DFATs. ATRA induced the expression of neuronal marker mRNA/protein. The neuron-like cells showed Ca2+ influx with depolarization (50 mM KCl; 84.75 ± 4.05%) and Na+ channel activation (50 μM veratridine; 96.02 ± 2.02%). Optical imaging of presynaptic terminal activity and detection of neurotransmitter release showed that the neuron-like cells exhibited the GABAergic neuronal property. Genome-wide RNA-sequencing analysis shows that the transcriptome profile of canine DFATs is effectively reprogrammed towards that of cortical interneuron lineage. Collectively, ATRA can produce functional GABAergic cortical interneuron-like cells from canine DFATs, exhibiting neuronal function with > 80% efficiency. We further demonstrated the contribution of JNK3 to ATRA-induced neuronal reprogramming in canine DFATs. In conclusion, the neuron-like cells from canine DFATs could be a powerful tool for translational research in cell transplantation therapy, in vitro disease modeling, and drug screening for neuronal diseases.

Indexed as

AnimalsCell DedifferentiationCell DifferentiationCellular ReprogrammingDogsNeurogenesisNeuronsRNA, MessengerSynapsesTretinoinRNA, MessengerTretinoin

Identifiers

PMID32231396
PMCPMC7108708
OpenAlexW3013894205

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.