Evidence map›Paper›PMID 11416186›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2001

Sorting and directed transport of membrane proteins during development of hippocampal neurons in culture.

M A Silverman, S Kaech, M Jareb, M A Burack, L Vogt, P Sonderegger, G Banker

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing 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

49 citing papers in PubMed.

  1. Article
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  7. Imaging Intracellular Trafficking in Neurons of C. elegans.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  8. Article
  9. Spatial control of membrane traffic in neuronal dendrites.Molecular and cellular neurosciences · 2020
    Review
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  15. 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.

M A SilvermanCenter for Research on Occupational and Environmental Toxicology, Oregon Health Sciences University, Portland, OR 97201, USA.
S Kaech
M Jareb
M A Burack
L Vogt
P Sonderegger
G Banker

Funding

THE DEVELOPMENT OF HIPPOCAMPAL NEURONS IN CULTURER01NS017112 · NINDS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI BANKER, GARY A · 1985 to 2008
$2.6M
NINDS NIH HHS NS17112NINDS NIH HHS R01 NS017112
6 · The paper itself

Abstract

Hippocampal neurons in culture develop morphological polarity in a sequential pattern; axons form before dendrites. Molecular differences, particularly those of membrane proteins, underlie the functional polarity of these domains, yet little is known about the temporal relationship between membrane protein polarization and morphological polarization. We took advantage of viral expression systems to determine when during development the polarization of membrane proteins arises. All markers were unpolarized in neurons before axonogenesis. In neurons with a morphologically distinguishable axon, even on the first day in culture, both axonal and dendritic proteins were polarized. The degree of polarization at these early stages was somewhat less than in mature cells and varied from cell to cell. The cellular mechanism responsible for the polarization of the dendritic marker protein transferrin receptor (TfR) in mature cells centers on directed transport to the dendritic domain. To examine the relationship between cell surface polarization and transport, we assessed the selectivity of transport by live cell imaging. TfR-green fluorescent protein-containing vesicles were already preferentially transported into dendrites at 2 days, the earliest time point we could measure. The selectivity of transport also varied somewhat among cells, and the amount of TfR-green fluorescent protein fluorescence on intracellular structures within the axon correlated with the amount of cell surface expression. This observation implies that selective microtubule-based transport is the primary mechanism that underlies the polarization of TfR on the cell surface. By 5 days in culture, the extent of polarization on the cell surface and the selectivity of transport reached mature levels.

Indexed as

AnimalsAxonsCell PolarityCells, CulturedDendritesEmbryo, MammalianGenes, ReporterGreen Fluorescent ProteinsHippocampusLuminescent ProteinsMembrane ProteinsMicroscopy, VideoNerve Tissue ProteinsNeuritesNeuronsProtein TransportGreen Fluorescent ProteinsLuminescent ProteinsMembrane ProteinsNerve Tissue ProteinsReceptors, LDLReceptors, TransferrinRecombinant Proteins

Identifiers

PMID11416186
PMCPMC34621

What OpenQuestion holds

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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.