Evidence map›Paper›PMID 28768823›Full record

ArticleMolecular biology of the cell2017

Manganese-induced trafficking and turnover of GPP130 is mediated by sortilin.

Swati Venkat, Adam D Linstedt

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Golgi Drivers of Cancer.Sub-cellular biochemistry · 2026
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  5. Protein quality control in the secretory pathway.The Journal of cell biology · 2019
    Review
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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 1 institution in 1 country.

Swati VenkatDepartment of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA 15213.
Adam D LinstedtDepartment of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA 15213 linstedt@cmu.edu.
Carnegie Mellon University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Elevated, nontoxic doses of manganese (Mn) protect against Shiga toxin-1-induced cell death via down-regulation of GPP130, a cycling Golgi membrane protein that serves as an endosome-to-Golgi trafficking receptor for the toxin. Mn binds to GPP130 in the Golgi and causes GPP130 to oligomerize/aggregate, and the complexes are diverted to lysosomes. In fact, based on experiments using the self-interacting FM domain, it appears generally true that aggregation of a Golgi protein leads to its lysosomal degradation. How such oligomers are selectively sorted out of the Golgi is unknown. Here we provide evidence that Mn-induced exit of GPP130 from the

Indexed as

Adaptor Proteins, Vesicular TransportEndosomesGolgi ApparatusHeLa CellsHumansLysosomesManganeseMembrane GlycoproteinsMembrane ProteinsPhosphoproteinsProtein TransportShiga Toxin 1Sortilintrans-Golgi NetworkVesicular Transport ProteinsAdaptor Proteins, Vesicular TransportGOLIM4 protein, humanManganeseMembrane GlycoproteinsMembrane ProteinsPhosphoproteinsShiga Toxin 1SortilinVesicular Transport Proteins

Identifiers

PMID28768823
PMCPMC5597328
OpenAlexW2741057028

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.