Evidence map›Paper›PMID 31283381›Full record

ReviewAnnual review of cell and developmental biology2019

Architecture and Dynamics of the Neuronal Secretory Network.

Matthew J Kennedy, Cyril Hanus

Open access · bronzeAbstract readReview
In one paragraph

Review in Annual review of cell and developmental biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

44 citing papers in PubMed, 62 citations in OpenAlex.

  1. Late Endosome Transport by RILP-RAB7A Promotes Dendrite Arborization Independently of Degradation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
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  3. ER discontinuities are common inbioRxiv : the preprint server for biology · 2026
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  8. Late endosome transport by RILP-RAB7A promotes dendrite arborization.bioRxiv : the preprint server for biology · 2025
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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

2 authors at 2 institutions in 2 countries.

Matthew J KennedyDepartment of Pharmacology, University of Colorado School of Medicine, Aurora, Colorado 80045, USA; email: matthew.kennedy@ucdenver.edu.
Cyril HanusInstitute for Psychiatry and Neurosciences of Paris, Institut National de la Santé et de la Recherche Médicale (INSERM), Université de Paris, 75014 Paris, France; email: cyril.hanus@inserm.fr.
Université Paris Cité · FRUniversity of Colorado Denver · US

Funding

Validating and extending optical tools for extended neural silencingUF1NS107710 · NINDS · UNIVERSITY OF COLORADO DENVER · PI FORD, CHRISTOPHER PETER, KENNEDY, MATTHEW J · 2018 to 2018
$2.0M
Mechanisms of dendritic exocytosisR01NS082271 · NINDS · UNIVERSITY OF COLORADO DENVER · PI KENNEDY, MATTHEW J · 2013 to 2017
$1.7M
Investigating Unconventional Secretory Trafficking in Neuronal DendritesR01NS107554 · NINDS · UNIVERSITY OF COLORADO DENVER · PI KENNEDY, MATTHEW J · 2018 to 2019
$680k
Mechanisms of beta-amyloid induced synaptic dysfunctionR21AG058005 · NIA · UNIVERSITY OF COLORADO DENVER · PI KENNEDY, MATTHEW J · 2018 to 2019
$423k
PDGF CELL CYCLE CONTROL IN NEURONAL DIFFERENTIATIONF32NS010755 · NINDS · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI TONG, BETTY · 1998 to 2000
$29k
NIA NIH HHS R21 AG058005NINDS NIH HHS F32 NS010755NINDS NIH HHS R01 NS082271NINDS NIH HHS R01 NS107554NINDS NIH HHS UF1 NS107710
6 · The paper itself

Abstract

Regulated synthesis and movement of proteins between cellular organelles are central to diverse forms of biological adaptation and plasticity. In neurons, the repertoire of channel, receptor, and adhesion proteins displayed on the cell surface directly impacts cellular development, morphology, excitability, and synapse function. The immensity of the neuronal surface membrane and its division into distinct functional domains present a challenging landscape over which proteins must navigate to reach their appropriate functional domains. This problem becomes more complex considering that neuronal protein synthesis is continuously refined in space and time by neural activity. Here we review our current understanding of how integral membrane and secreted proteins important for neuronal function travel from their sites of synthesis to their functional destinations. We discuss how unique adaptations to the function and distribution of neuronal secretory organelles may facilitate local protein trafficking at remote sites in neuronal dendrites to support diverse forms of synaptic plasticity.

Indexed as

AnimalsCell CompartmentationCell MembraneDendritesEndoplasmic ReticulumEndosomesGolgi ApparatusMembrane ProteinsNeuronal PlasticityNeuronsProtein TransportSynapsesMembrane Proteinsdendriteendoplasmic reticulumGolgi apparatusintermediate compartmentrecycling endosomesynapse

Identifiers

PMID31283381
PMCPMC6935261
OpenAlexW2958571635

What OpenQuestion holds

Textmetadata
LicenceTDM
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.