Evidence map›Paper›PMID 24758724›Full record

ArticleBiochemistry2014

Side-chain oxysterols modulate cholesterol accessibility through membrane remodeling.

Agata A Bielska, Brett N Olsen, Sarah E Gale, Laurel Mydock-McGrane, Kathiresan Krishnan, Nathan A Baker, Paul H Schlesinger, Douglas F Covey, Daniel S Ory

Open access · bronzeAbstract read
In one paragraph

Article in Biochemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

25 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Oxysterols in Infectious Diseases.Advances in experimental medicine and biology · 2024
    Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Pathways and Mechanisms of Cellular Cholesterol Efflux-Insight From Imaging.Frontiers in cell and developmental biology · 2022
    Review
  13. Oxysterols protect bovine endometrial cells against pore-forming toxins from pathogenic bacteria.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

9 authors at 2 institutions in 1 country.

Agata A BielskaDiabetic Cardiovascular Disease Center, Washington University School of Medicine , St. Louis, Missouri 63110, United States.
Brett N Olsen
Sarah E Gale
Laurel Mydock-McGrane
Kathiresan Krishnan
Nathan A Baker
Paul H Schlesinger
Douglas F Covey
Daniel S Ory
Washington University in St. Louis · USPacific Northwest National Laboratory · US

Funding

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
Regulation of Cellular Cholesterol Through Oxysterol-Membrane InteractionsF30HL097563 · NHLBI · WASHINGTON UNIVERSITY · PI BIELSKA, AGATA AGNIESZKA · 2010 to 2011
$73k
NCRR NIH HHS P41 RR0860516NHLBI NIH HHS F30 HL97563NHLBI NIH HHS HL067773NHLBI NIH HHS R01 HL067773NHLBI NIH HHS T32HL007275
6 · The paper itself

Abstract

Side-chain oxysterols, such as 25-hydroxycholesterol (25-HC), are key regulators of cholesterol homeostasis. New evidence suggests that the alteration of membrane structure by 25-HC contributes to its regulatory effects. We have examined the role of oxysterol membrane effects on cholesterol accessibility within the membrane using perfringolysin O (PFO), a cholesterol-dependent cytolysin that selectively binds accessible cholesterol, as a sensor of membrane cholesterol accessibility. We show that 25-HC increases cholesterol accessibility in a manner dependent on the membrane lipid composition. Structural analysis of molecular dynamics simulations reveals that increased cholesterol accessibility is associated with membrane thinning, and that the effects of 25-HC on cholesterol accessibility are driven by these changes in membrane thickness. Further, we find that the 25-HC antagonist LY295427 (agisterol) abrogates the membrane effects of 25-HC in a nonenantioselective manner, suggesting that agisterol antagonizes the cholesterol-homeostatic effects of 25-HC indirectly through its membrane interactions. These studies demonstrate that oxysterols regulate cholesterol accessibility, and thus the availability of cholesterol to be sensed and transported throughout the cell, by modulating the membrane environment. This work provides new insights into how alterations in membrane structure can be used to relay cholesterol regulatory signals.

Indexed as

Bacterial ToxinsCell MembraneCholestanolsCholesterolHemolysin ProteinsHomeostasisHydroxycholesterolsLiposomesMembrane LipidsMolecular Dynamics SimulationStructure-Activity Relationship25-hydroxycholesterolBacterial ToxinsCholestanolsCholesterolClostridium perfringens theta-toxinHemolysin ProteinsHydroxycholesterolsLiposomesLY 295427Membrane Lipids

Identifiers

PMID24758724
PMCPMC4020583
OpenAlexW2049069397

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.