Evidence map›Paper›PMID 20053687›Full record

ArticleMolecular biology of the cell2010

Glycolipid trafficking in Drosophila undergoes pathway switching in response to aberrant cholesterol levels.

Ralf Hortsch, Esther Lee, Nandanan Erathodiyil, Sarita Hebbar, Steffen Steinert, Jun Yu Lee, Doreen See Kin Chua, Rachel Kraut

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. The Journal of pharmacology and experimental therapeutics · 2019
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  14. Golgi glycosylation and human inherited diseases.Cold Spring Harbor perspectives in biology · 2011
    Review
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

8 authors at 2 institutions in 1 country.

Ralf HortschInstitute of Bioengineering and Nanotechnology, Agency for Science, Technology, and Research, Singapore.
Esther Lee
Nandanan Erathodiyil
Sarita Hebbar
Steffen Steinert
Jun Yu Lee
Doreen See Kin Chua
Rachel Kraut
Agency for Science, Technology and Research · SGNanyang Technological University · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In lipid storage diseases, the intracellular trafficking of sphingolipids is altered by conditions of aberrant cholesterol accumulation. Drosophila has been used recently to model lipid storage diseases, but the effects of sterol accumulation on sphingolipid trafficking are not known in the fly, and the trafficking of sphingolipids in general has not been studied in this model organism. Here, we examined the uptake and intracellular distribution of a fluorescent glycolipid analog, BODIPY-lactosyl-ceramide, in Drosophila neurons. The uptake mechanism and intracellular trafficking route of this simple glycolipid are largely conserved. Our principle finding is that cholesterol steers trafficking of the glycolipid between Golgi, lysosome, and recycling compartments. Our analyses support the idea that cholesterol storage in Drosophila triggers a switch in glycolipid trafficking from the biosynthetic to the degradative endolysosomal pathway, whereas cholesterol depletion eliminates recycling of the glycolipid. Unexpectedly, we observe a novel phenomenon we term "hijacking," whereby lactosyl-ceramide diverts the trafficking pathway of an endocytic cargo, dextran, completely away from its lysosomal target. This work establishes that glycolipid trafficking in Drosophila undergoes changes similar to those seen in mammalian cells under conditions of cholesterol storage and therefore validates Drosophila as a suitable model organism in which to study lipid storage diseases.

Indexed as

AnimalsAntigens, CDBoron CompoundsCholesterolDrosophila melanogasterEndocytosisGlycolipidsGolgi ApparatusGreen Fluorescent ProteinsLactosylceramidesLipidsLysosomesMicroscopy, FluorescenceModels, BiologicalModels, ChemicalNeurons4,4-difluoro-4-bora-3a,4a-diaza-s-indaceneAntigens, CDBoron CompoundsCDw17 antigenCholesterolGlycolipidsGreen Fluorescent ProteinsLactosylceramidesLipids

Identifiers

PMID20053687
PMCPMC2828964
OpenAlexW2156779401

What OpenQuestion holds

Textmetadata
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.