Evidence map›Paper›PMID 23526941›Full record

ArticlePloS one2013

Rab3D is critical for secretory granule maturation in PC12 cells.

Tanja Kögel, Rüdiger Rudolf, Erlend Hodneland, John Copier, Romano Regazzi, Sharon A Tooze, Hans-Hermann Gerdes

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

  1. Membrane trafficking alterations in breast cancer progression.Frontiers in cell and developmental biology · 2024
    Review
  2. Article
  3. Article
  4. Endosomal Rab GTPases regulate secretory granule maturation inCommunicative & integrative biology · 2021
    Article
  5. Article
  6. ImprovedThe Journal of biological chemistry · 2019
    Article
  7. Article
  8. Article
  9. Article
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 4 institutions in 4 countries.

Tanja KögelDepartment of Biomedicine, University of Bergen, Bergen, Norway.
Rüdiger Rudolf
Erlend Hodneland
John Copier
Romano Regazzi
Sharon A Tooze
Hans-Hermann Gerdes
University of Bergen · NOThe Honourable Society of Lincoln's Inn · GBHeidelberg University · DEUniversity of Lausanne · CH

Funding

Cancer Research UK 15153
6 · The paper itself

Abstract

Neuropeptide- and hormone-containing secretory granules (SGs) are synthesized at the trans-Golgi network (TGN) as immature secretory granules (ISGs) and complete their maturation in the F-actin-rich cell cortex. This maturation process is characterized by acidification-dependent processing of cargo proteins, condensation of the SG matrix and removal of membrane and proteins not destined to mature secretory granules (MSGs). Here we addressed a potential role of Rab3 isoforms in these maturation steps by expressing their nucleotide-binding deficient mutants in PC12 cells. Our data show that the presence of Rab3D(N135I) decreases the restriction of maturing SGs to the F-actin-rich cell cortex, blocks the removal of the endoprotease furin from SGs and impedes the processing of the luminal SG protein secretogranin II. This strongly suggests that Rab3D is implicated in the subcellular localization and maturation of ISGs.

Indexed as

ActinsAnimalsFurinMutant ProteinsNeuroendocrine CellsPC12 Cellsrab3 GTP-Binding ProteinsRatsSecretogranin IISecretory VesiclesActinsFurinMutant ProteinsRab3d protein, ratrab3 GTP-Binding Proteinssecretogranin 2, ratSecretogranin II

Identifiers

PMID23526941
PMCPMC3602456
OpenAlexW2094821916

What OpenQuestion holds

Textmetadata
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.