Evidence map›Paper›PMID 24596093›Full record

ArticleThe Journal of biological chemistry2014

Tracking the subcellular fate of 20(s)-hydroxycholesterol with click chemistry reveals a transport pathway to the Golgi.

Sara M Peyrot, Sigrid Nachtergaele, Giovanni Luchetti, Laurel K Mydock-McGrane, Hideji Fujiwara, David Scherrer, Andrew Jallouk, Paul H Schlesinger, Daniel S Ory, Douglas F Covey and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Pathways and Mechanisms of Cellular Cholesterol Efflux-Insight From Imaging.Frontiers in cell and developmental biology · 2022
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Ketamine: NMDA Receptors and Beyond.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
  9. Article
  10. Article
  11. 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

11 authors at 2 institutions in 1 country.

Sara M PeyrotDepartments of Medicine and Stanford University School of Medicine, Stanford, California 94305.
Sigrid NachtergaeleBiochemistry, Stanford University School of Medicine, Stanford, California 94305, and.
Giovanni LuchettiBiochemistry, Stanford University School of Medicine, Stanford, California 94305, and.
Laurel K Mydock-McGraneDepartments of Developmental Biology, Washington University in St. Louis School of Medicine, St. Louis, Missouri 63110.
Hideji FujiwaraThe Diabetic Cardiovascular Research Center, and Washington University in St. Louis School of Medicine, St. Louis, Missouri 63110.
David ScherrerThe Diabetic Cardiovascular Research Center, and Washington University in St. Louis School of Medicine, St. Louis, Missouri 63110.
Andrew JalloukDepartments of Cell Biology and Physiology, Washington University in St. Louis School of Medicine, St. Louis, Missouri 63110.
Paul H SchlesingerDepartments of Cell Biology and Physiology, Washington University in St. Louis School of Medicine, St. Louis, Missouri 63110.
Daniel S OryThe Diabetic Cardiovascular Research Center, and Washington University in St. Louis School of Medicine, St. Louis, Missouri 63110.
Douglas F CoveyDepartments of Developmental Biology, Washington University in St. Louis School of Medicine, St. Louis, Missouri 63110; Departments ofAnesthesiology, and Washington University in St. Louis School of Medicine, St. Louis, Missouri 63110; Departments of Psychiatry, Washington University in St. Louis School of Medicine, St. Louis, Missouri 63110; The Taylor Family Institute for Innovative Psychiatric Research, Washington University in St. Louis School of Medicine, St. Louis, Missouri 63110.
Rajat RohatgiDepartments of Medicine and Stanford University School of Medicine, Stanford, California 94305; Biochemistry, Stanford University School of Medicine, Stanford, California 94305, and. Electronic address: rrohatgi@stanford.edu.
Washington University in St. Louis · USStanford University · US

Funding

Supplement to Enhance Wellness and Resiliency in the Graduate EnvironmentT32GM007276 · NIGMS · STANFORD UNIVERSITY · PI MORRISON, ASHBY J. · 1985 to 2023
$32.9M
WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI Jennifer Lynn Powers Carson · 2013 to 2026
$27.1M
STRUCTURE/ACTIVITY STUDIES OF NEUROSTEROID ANALOGUESP01GM047969 · NIGMS · WASHINGTON UNIVERSITY · PI COVEY, DOUGLAS F · 1992 to 2011
$18.7M
Post-lysosomal cholesterol trafficking networksR01HL067773 · NHLBI · WASHINGTON UNIVERSITY · PI SCHAFFER, JEAN E. · 2002 to 2021
$6.3M
CARDIOVASCULAR SYSTEM--FUNCTION/REGULATION/PHARMACOLOGYT32HL007275 · NHLBI · WASHINGTON UNIVERSITY · PI NERBONNE, JEANNE M. · 1985 to 2013
$6.0M
Signal Transduction by OxysterolsR01GM106078 · NIGMS · STANFORD UNIVERSITY · PI COVEY, DOUGLAS F, ROHATGI, RAJAT · 2014 to 2017
$1.6M
Biochemical Mechanisms of Hedgehog SignalingR00CA129174 · NCI · STANFORD UNIVERSITY · PI ROHATGI, RAJAT · 2009 to 2011
$1.0M
NCI NIH HHS R00 CA129174NHLBI NIH HHS 5 T32 HL007275NHLBI NIH HHS HL67773NHLBI NIH HHS R01 HL067773NHLBI NIH HHS T32 HL007275NIDDK NIH HHS P30 DK020579NIGMS NIH HHS GM47969NIGMS NIH HHS P01 GM047969NIGMS NIH HHS R01 GM106078NIGMS NIH HHS T32 GM007276
6 · The paper itself

Abstract

Oxysterols, oxidized metabolites of cholesterol, are endogenous small molecules that regulate lipid metabolism, immune function, and developmental signaling. Although the cell biology of cholesterol has been intensively studied, fundamental questions about oxysterols, such as their subcellular distribution and trafficking pathways, remain unanswered. We have therefore developed a useful method to image intracellular 20(S)-hydroxycholesterol with both high sensitivity and spatial resolution using click chemistry and fluorescence microscopy. The metabolic labeling of cells with an alkynyl derivative of 20(S)-hydroxycholesterol has allowed us to directly visualize this oxysterol by attaching an azide fluorophore through cyclo-addition. Unexpectedly, we found that this oxysterol selectively accumulates in the Golgi membrane using a pathway that is sensitive to ATP levels, temperature, and lysosome function. Although previous models have proposed nonvesicular pathways for the rapid equilibration of oxysterols between membranes, direct imaging of oxysterols suggests that a vesicular pathway is responsible for differential accumulation of oxysterols in organelle membranes. More broadly, clickable alkynyl sterols may represent useful tools for sterol cell biology, both to investigate the functions of these important lipids and to decipher the pathways that determine their cellular itineraries.

Indexed as

Click ChemistryFluorescent DyesHydroxycholesterolsAnimalsBiological Transport, ActiveCHO CellsCricetinaeCricetulusGolgi ApparatusIntracellular MembranesMiceMicroscopy, FluorescenceNIH 3T3 CellsFluorescent DyesHydroxycholesterolsImagingLipidsLysosomesOxysterolSignalingTrafficking

Identifiers

PMID24596093
PMCPMC4036249
OpenAlexW2083760146

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.