Evidence map›Paper›PMID 28299779›Full record

ArticleThe Journal of comparative neurology2017

The related neuronal endosomal proteins NEEP21 (Nsg1) and P19 (Nsg2) have divergent expression profiles in vivo.

Kelly Barford, Chan Choo Yap, Noelle D Dwyer, Bettina Winckler

Abstract read
In one paragraph

Article in The Journal of comparative neurology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

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  10. Schizophrenia-Linked Protein tSNARE1 Regulates Endosomal Trafficking in Cortical Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    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

4 authors.

Kelly BarfordDepartment of Cell Biology, University of Virginia, Charlottesville, Virginia.ORCID http://orcid.org/0000-0002-8999-9580
Chan Choo YapDepartment of Cell Biology, University of Virginia, Charlottesville, Virginia.
Noelle D DwyerDepartment of Cell Biology, University of Virginia, Charlottesville, Virginia.
Bettina WincklerDepartment of Cell Biology, University of Virginia, Charlottesville, Virginia.

Funding

Organization and Function of Neuronal EndosomesR01NS083378 · NINDS · UNIVERSITY OF VIRGINIA · PI Bettina R Winckler · 2013 to 2026
$5.2M
Roles of Cytokinesis in Polarized Neural Stem Cell Divisions and Brain GrowthR01NS076640 · NINDS · UNIVERSITY OF VIRGINIA · PI DWYER, NOELLE D · 2013 to 2017
$1.7M
Novel Endosomal Pathways Underlying NGF/TrkA Dependent Dendrite DevelopmentF31NS098621 · NINDS · UNIVERSITY OF VIRGINIA · PI BARFORD, KELLY ANN · 2016 to 2018
$44k
NINDS NIH HHS F31 NS098621NINDS NIH HHS R01 NS076640NINDS NIH HHS R01 NS083378
6 · The paper itself

Abstract

Endosomal maturation and transport constitutes a complex trafficking system present in all cell types. Neurons have adapted their endosomal system to meet their unique and complex needs. These adaptations include repurposing existing proteins to diversify endocytosis and trafficking, as well as preferential expression of certain regulators more highly in neurons than other cell types. These neuronal regulators include the family of Neuron-Specific Gene family members (Nsg), NEEP21 (Nsg1), and P19 (Nsg2). NEEP21/Nsg1 plays a role in the trafficking of multiple receptors, including the cell adhesion molecule L1/NgCAM, the neurotransmitter receptor GluA2, and β-APP. Recently, we showed that NEEP2/Nsg1 and P19/Nsg2 are not expressed in all neuronal cell types in vitro. However, it is not known where and when NEEP21/Nsg1 and P19/Nsg2 are expressed in vivo, and whether both proteins are always coexpressed. Here, we show that NEEP21/Nsg1 and P19/Nsg2 are present in both overlapping and distinct cell populations in the hippocampus, neocortex, and cerebellum during development. NEEP21/Nsg1 and P19/Nsg2 levels are highest during embryonic development, and expression persists in the juvenile mouse brain. In particular, a subset of layer V cortical neurons retains relatively high expression of both NEEP21/Nsg1 and P19/Nsg2 at postnatal day 16 as well as in the CA1-3 regions of the hippocampus. In the cerebellum, NEEP21/Nsg1 expression becomes largely restricted to Purkinje neurons in adulthood whereas P19/Nsg2 expression strikingly disappears from the cerebellum with age. This divergent and restricted expression likely reflects differential needs for this class of trafficking regulators in different neurons during different stages of maturation.

Indexed as

AnimalsBrainCarrier ProteinsEndosomesGene Expression ProfilingImmunohistochemistryMiceMice, Inbred C57BLMice, KnockoutNerve Tissue ProteinsNeurogenesisNeuronsProtein TransportTranscriptomeCarrier ProteinsNerve Tissue ProteinsNsg2 protein, mouseKEYWORDS endosomeneural-specific geneneurodevelopmentPurkinje neuronRRID: AB_10896795RRID: AB_11205592RRID: AB_2138173RRID: AB_2286684RRID: AB_2314065RRID: AB_2340462RRID: AB_2340686RRID: AB_2534017RRID: AB_2534102RRID: AB_2535788RRID: AB_2536181RRID: AB_2571866RRID: AB_477329RRID: AB_882455RRID: RGD_737891RRID: SCR_007318

Identifiers

PMID28299779
PMCPMC5663458

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Registered trials

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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.