Evidence map›Paper›PMID 32407317›Full record

ArticlePloS one2020

Neurons from human mesenchymal stem cells display both spontaneous and stimuli responsive activity.

Nihal Karakaş, Sadık Bay, Nezaket Türkel, Nurşah Öztunç, Merve Öncül, Hülya Bilgen, Khalid Shah, Fikrettin Şahin, Gürkan Öztürk

Abstract 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 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.

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  7. Huntington's Disease: Complex Pathogenesis and Therapeutic Strategies.International journal of molecular sciences · 2024
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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

9 authors.

Nihal KarakaşMedical Biology Department, School of Medicine, İstanbul Medipol University, İstanbul, Turkey.ORCID 0000-0002-9096-1512
Sadık BayRegenerative and Restorative Medicine Research Center (REMER), Research Institute for Health Sciences and Technologies (SABITA), İstanbul Medipol University, İstanbul, Turkey.ORCID 0000-0001-8089-1330
Nezaket TürkelGenetics and Bioengineering Department, Faculty of Engineering, Yeditepe University, İstanbul, Turkey.
Nurşah ÖztunçRegenerative and Restorative Medicine Research Center (REMER), Research Institute for Health Sciences and Technologies (SABITA), İstanbul Medipol University, İstanbul, Turkey.
Merve ÖncülRegenerative and Restorative Medicine Research Center (REMER), Research Institute for Health Sciences and Technologies (SABITA), İstanbul Medipol University, İstanbul, Turkey.
Hülya BilgenCenter for Bone Marrow Transplantation, İstanbul Medipol University Hospital, İstanbul, Turkey.
Khalid ShahCenter for Stem Cell Therapeutics and Imaging, Brigham and Woman's Hospital, Harvard Medical School, Boston, Massachusetts, United States of America.
Fikrettin ŞahinGenetics and Bioengineering Department, Faculty of Engineering, Yeditepe University, İstanbul, Turkey.
Gürkan ÖztürkRegenerative and Restorative Medicine Research Center (REMER), Research Institute for Health Sciences and Technologies (SABITA), İstanbul Medipol University, İstanbul, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cells have the ability to transdifferentiate into neurons and therefore one of the potential adult stem cell source for neuronal tissue regeneration applications and understanding neurodevelopmental processes. In many studies on human mesenchymal stem cell (hMSC) derived neurons, success in neuronal differentiation was limited to neuronal protein expressions which is not statisfactory in terms of neuronal activity. Established neuronal networks seen in culture have to be investigated in terms of synaptic signal transmission ability to develop a culture model for human neurons and further studying the mechanism of neuronal differentiation and neurological pathologies. Accordingly, in this study, we analysed the functionality of bone marrow hMSCs differentiated into neurons by a single step cytokine-based induction protocol. Neurons from both primary hMSCs and hMSC cell line displayed spontaneous activity (≥75%) as demonstrated by Ca++ imaging. Furthermore, when electrically stimulated, hMSC derived neurons (hMd-Neurons) matched the response of a typical neuron in the process of maturation. Our results reveal that a combination of neuronal inducers enhance differentiation capacity of bone marrow hMSCs into high yielding functional neurons with spontaneous activity and mature into electrophysiologically active state. Conceptually, we suggest these functional hMd-Neurons to be used as a tool for disease modelling of neuropathologies and neuronal differentiation studies.

Indexed as

Adult Stem CellsBone Marrow CellsCell DifferentiationCell LineageCells, CulturedElectrophysiological PhenomenaHumansMesenchymal Stem CellsMesenchymal Stem Cell TransplantationNeurons

Identifiers

PMID32407317
PMCPMC7224507

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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.