Evidence map›Paper›PMID 28238793›Full record

ArticleStem cell reports2017

Differential Maturation of the Two Regulated Secretory Pathways in Human iPSC-Derived Neurons.

Javier Emperador Melero, Aishwarya G Nadadhur, Desiree Schut, Jan V Weering, Vivi M Heine, Ruud F Toonen, Matthijs Verhage

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2017. 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
0.8field-weighted citation impact, top 34% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. 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

7 authors at 2 institutions in 1 country.

Javier Emperador MeleroDepartments of Functional Genomics and Clinical Genetics, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, Vrije Universiteit (VU) Amsterdam and VU Medical Center, de Boelelaan 1087, 1081 HV Amsterdam, the Netherlands.
Aishwarya G NadadhurDepartments of Functional Genomics and Clinical Genetics, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, Vrije Universiteit (VU) Amsterdam and VU Medical Center, de Boelelaan 1087, 1081 HV Amsterdam, the Netherlands.
Desiree SchutDepartments of Functional Genomics and Clinical Genetics, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, Vrije Universiteit (VU) Amsterdam and VU Medical Center, de Boelelaan 1087, 1081 HV Amsterdam, the Netherlands.
Jan V WeeringDepartments of Functional Genomics and Clinical Genetics, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, Vrije Universiteit (VU) Amsterdam and VU Medical Center, de Boelelaan 1087, 1081 HV Amsterdam, the Netherlands.
Vivi M HeineDepartments of Functional Genomics and Clinical Genetics, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, Vrije Universiteit (VU) Amsterdam and VU Medical Center, de Boelelaan 1087, 1081 HV Amsterdam, the Netherlands; Department of Pediatrics/Child Neurology, Amsterdam Neuroscience, VU Medical Center, 1081 HV Amsterdam, the Netherlands; Department of Complex Trait Genetics, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, the Netherlands.
Ruud F ToonenDepartments of Functional Genomics and Clinical Genetics, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, Vrije Universiteit (VU) Amsterdam and VU Medical Center, de Boelelaan 1087, 1081 HV Amsterdam, the Netherlands. Electronic address: ruud.toonen@cncr.vu.nl.
Matthijs VerhageDepartments of Functional Genomics and Clinical Genetics, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, Vrije Universiteit (VU) Amsterdam and VU Medical Center, de Boelelaan 1087, 1081 HV Amsterdam, the Netherlands. Electronic address: matthijs@cncr.vu.nl.
Amsterdam Neuroscience · NLVrije Universiteit Amsterdam · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurons communicate by regulated secretion of chemical signals from synaptic vesicles (SVs) and dense-core vesicles (DCVs). Here, we investigated the maturation of these two secretory pathways in micro-networks of human iPSC-derived neurons. These micro-networks abundantly expressed endogenous SV and DCV markers, including neuropeptides. DCV transport was microtubule dependent, preferentially anterograde in axons, and 2-fold faster in axons than in dendrites. SV and DCV secretion were strictly Ca

Indexed as

Cell DifferentiationSecretory PathwayAnimalsAxonsBiological TransportBiomarkersCalciumDendritesHumansInduced Pluripotent Stem CellsMiceMicrotubulesNeuronsSecretory VesiclesSNARE ProteinsSynapsesBiomarkersCalciumSNARE Proteinsdense-core vesicleshuman iPSC-derived neuronsneuropeptidesregulated neurosecretionsynaptic transmission

Identifiers

PMID28238793
PMCPMC5355645
OpenAlexW2590090116

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.