Evidence map›Paper›PMID 31738018›Full record

ReviewStem cells translational medicine2020

Adult tissue-derived neural crest-like stem cells: Sources, regulatory networks, and translational potential.

Pihu Mehrotra, Georgios Tseropoulos, Marianne E Bronner, Stelios T Andreadis

Open access · goldAbstract readReview
In one paragraph

Review in Stem cells translational medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
5.2field-weighted citation impact, top 3% 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

33 citing papers in PubMed, 60 citations in OpenAlex.

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  15. The amazing and anomalous axolotls as scientific models.Developmental dynamics : an official publication of the American Association of Anatomists · 2022
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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

4 authors at 2 institutions in 1 country.

Pihu MehrotraDepartment of Chemical and Biological Engineering, University at Buffalo, Buffalo, New York.ORCID 0000-0001-9369-5013
Georgios TseropoulosDepartment of Chemical and Biological Engineering, University at Buffalo, Buffalo, New York.
Marianne E BronnerDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, California.
Stelios T AndreadisDepartment of Chemical and Biological Engineering, University at Buffalo, Buffalo, New York.
University at Buffalo, State University of New York · USCalifornia Institute of Technology · US

Funding

Direct reprogramming of epidermal cells to neural crest derivatives for cell therapiesR01EB023114 · NIBIB · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI ANDREADIS, STELIOS THEOHARIS · 2016 to 2019
$1.7M
NIBIB NIH HHS R01 EB023114
6 · The paper itself

Abstract

Neural crest (NC) cells are a multipotent stem cell population that give rise to a diverse array of cell types in the body, including peripheral neurons, Schwann cells (SC), craniofacial cartilage and bone, smooth muscle cells, and melanocytes. NC formation and differentiation into specific lineages takes place in response to a set of highly regulated signaling and transcriptional events within the neural plate border. Premigratory NC cells initially are contained within the dorsal neural tube from which they subsequently emigrate, migrating to often distant sites in the periphery. Following their migration and differentiation, some NC-like cells persist in adult tissues in a nascent multipotent state, making them potential candidates for autologous cell therapy. This review discusses the gene regulatory network responsible for NC development and maintenance of multipotency. We summarize the genes and signaling pathways that have been implicated in the differentiation of a postmigratory NC into mature myelinating SC. We elaborate on the signals and transcription factors involved in the acquisition of immature SC fate, axonal sorting of unmyelinated neuronal axons, and finally the path toward mature myelinating SC, which envelope axons within myelin sheaths, facilitating electrical signal propagation. The gene regulatory events guiding development of SC in vivo provides insights into means for differentiating NC-like cells from adult human tissues into functional SC, which have the potential to provide autologous cell sources for the treatment of demyelinating and neurodegenerative disorders.

Indexed as

Gene Regulatory NetworksHumansNeural CrestSchwann CellsStem Cellsdemyelinating disordersgene regulatory networkneural crestSchwann cells

Identifiers

PMID31738018
PMCPMC7031649
OpenAlexW2987429763

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.