Evidence map›Paper›PMID 30650592›Full record

ReviewJournal of developmental biology2019

Crosstalk of Intercellular Signaling Pathways in the Generation of Midbrain Dopaminergic Neurons In Vivo and from Stem Cells.

Claude Brodski, Sandra Blaess, Juha Partanen, Nilima Prakash

Open access · goldAbstract readReview
In one paragraph

Review in Journal of developmental biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

21 citing papers in PubMed, 27 citations in OpenAlex.

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  13. Acquisition of the Midbrain Dopaminergic Neuronal Identity.International journal of molecular sciences · 2020
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  16. Midbrain Dopaminergic Neuron Development at the Single Cell Level:Frontiers in cell and developmental biology · 2020
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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 4 institutions in 3 countries.

Claude BrodskiDepartment of Physiology and Cell Biology, Zlotowski Center for Neuroscience, Faculty of Health Sciences, Ben-Gurion University of the Negev, Be'er Sheva 84105, Israel. claude@bgu.ac.il.
Sandra BlaessInstitute of Reconstructive Neurobiology, University of Bonn Medical Center, 53127 Bonn, Germany. sandra.blaess@uni-bonn.de.
Juha PartanenFaculty of Biological and Environmental Sciences, FIN00014-University of Helsinki, P.O. Box 56, Viikinkaari 9, FIN-00014 Helsinki, Finland. juha.m.partanen@helsinki.fi.
Nilima PrakashDepartment Hamm 2, Hamm-Lippstadt University of Applied Sciences, 59063 Hamm, Germany. Nilima.Prakash@hshl.de.ORCID 0000-0002-0568-6262
Ben-Gurion University of the Negev · ILHamm-Lippstadt University of Applied Sciences · DEUniversity of Bonn · DEUniversity of Helsinki · FI

Funding

Deutsche Forschungsgemeinschaft 408031320Deutsche Forschungsgemeinschaft 417960915Deutsche Forschungsgemeinschaft BL 767/2-1Deutsche Forschungsgemeinschaft BL 767/3-1Israel Science Foundation grant 1391/11United States - Israel Binational Science Foundation grant 2015356
6 · The paper itself

Abstract

Dopamine-synthesizing neurons located in the mammalian ventral midbrain are at the center stage of biomedical research due to their involvement in severe human neuropsychiatric and neurodegenerative disorders, most prominently Parkinson's Disease (PD). The induction of midbrain dopaminergic (mDA) neurons depends on two important signaling centers of the mammalian embryo: the ventral midline or floor plate (FP) of the neural tube, and the isthmic organizer (IsO) at the mid-/hindbrain boundary (MHB). Cells located within and close to the FP secrete sonic hedgehog (SHH), and members of the wingless-type MMTV integration site family (WNT1/5A), as well as bone morphogenetic protein (BMP) family. The IsO cells secrete WNT1 and the fibroblast growth factor 8 (FGF8). Accordingly, the FGF8, SHH, WNT, and BMP signaling pathways play crucial roles during the development of the mDA neurons in the mammalian embryo. Moreover, these morphogens are essential for the generation of stem cell-derived mDA neurons, which are critical for the modeling, drug screening, and cell replacement therapy of PD. This review summarizes our current knowledge about the functions and crosstalk of these signaling pathways in mammalian mDA neuron development in vivo and their applications in stem cell-based paradigms for the efficient derivation of these neurons in vitro.

Indexed as

BMPdopamineFGF8iPSCneuronParkinson’s diseasepluripotent stem cellsSHHWNT

Identifiers

PMID30650592
PMCPMC6473842
OpenAlexW2909154945

What OpenQuestion holds

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LicenceCC BY
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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.