Evidence map›Paper›PMID 28467503›Full record

ArticlePloS one2017

Zebrafish GDNF and its co-receptor GFRα1 activate the human RET receptor and promote the survival of dopaminergic neurons in vitro.

Tuulia Saarenpää, Konstantin Kogan, Yulia Sidorova, Arun Kumar Mahato, Igor Tascón, Heidi Kaljunen, Liying Yu, Jukka Kallijärvi, Jaana Jurvansuu, Mart Saarma and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
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  6. TheDevelopment (Cambridge, England) · 2018
    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

11 authors at 2 institutions in 2 countries.

Tuulia SaarenpääDepartment of Biochemistry, Faculty of Biological and Environmental Sciences, University of Helsinki, Helsinki, Finland.
Konstantin KoganDepartment of Biochemistry, Faculty of Biological and Environmental Sciences, University of Helsinki, Helsinki, Finland.
Yulia SidorovaInstitute of Biotechnology, University of Helsinki, Helsinki, Finland.
Arun Kumar MahatoInstitute of Biotechnology, University of Helsinki, Helsinki, Finland.
Igor TascónDepartment of Biochemistry, Faculty of Biological and Environmental Sciences, University of Helsinki, Helsinki, Finland.
Heidi KaljunenDepartment of Biochemistry, Faculty of Biological and Environmental Sciences, University of Helsinki, Helsinki, Finland.
Liying YuInstitute of Biotechnology, University of Helsinki, Helsinki, Finland.
Jukka KallijärviInstitute of Biotechnology, University of Helsinki, Helsinki, Finland.
Jaana JurvansuuInstitute of Biotechnology, University of Helsinki, Helsinki, Finland.
Mart SaarmaInstitute of Biotechnology, University of Helsinki, Helsinki, Finland.
Adrian GoldmanDepartment of Biochemistry, Faculty of Biological and Environmental Sciences, University of Helsinki, Helsinki, Finland.ORCID http://orcid.org/0000-0001-8032-9700
University of Helsinki · FIUniversity of Leeds · GB

Funding

Parkinson's UK K-1408
6 · The paper itself

Abstract

Glial cell line-derived neurotrophic factor (GDNF) is a ligand that activates, through co-receptor GDNF family receptor alpha-1 (GFRα1) and receptor tyrosine kinase "RET", several signaling pathways crucial in the development and sustainment of multiple neuronal populations. We decided to study whether non-mammalian orthologs of these three proteins have conserved their function: can they activate the human counterparts? Using the baculovirus expression system, we expressed and purified Danio rerio RET, and its binding partners GFRα1 and GDNF, and Drosophila melanogaster RET and two isoforms of co-receptor GDNF receptor-like. Our results report high-level insect cell expression of post-translationally modified and dimerized zebrafish RET and its binding partners. We also found that zebrafish GFRα1 and GDNF are comparably active as mammalian cell-produced ones. We also report the first measurements of the affinity of the complex to RET in solution: at least for zebrafish, the Kd for GFRα1-GDNF binding RET is 5.9 μM. Surprisingly, we also found that zebrafish GDNF as well as zebrafish GFRα1 robustly activated human RET signaling and promoted the survival of cultured mouse dopaminergic neurons with comparable efficiency to mammalian GDNF, unlike E. coli-produced human proteins. These results contradict previous studies suggesting that mammalian GFRα1 and GDNF cannot bind and activate non-mammalian RET and vice versa.

Indexed as

Amino Acid SequenceAnimalsCell SurvivalDopamineGlial Cell Line-Derived Neurotrophic FactorGlial Cell Line-Derived Neurotrophic Factor ReceptorsHumansNeuronsPhosphorylationProto-Oncogene Proteins c-retSequence Homology, Amino AcidZebrafishDopamineGlial Cell Line-Derived Neurotrophic FactorGlial Cell Line-Derived Neurotrophic Factor ReceptorsProto-Oncogene Proteins c-ret

Identifiers

PMID28467503
PMCPMC5415192
OpenAlexW2611264810

What OpenQuestion holds

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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.