Evidence map›Paper›PMID 29046341›Full record

ArticleJournal of lipid research2017

Influence of the membrane environment on cholesterol transfer.

Jeffrey Michael Breidigan, Natalie Krzyzanowski, Yangmingyue Liu, Lionel Porcar, Ursula Perez-Salas

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 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
1.0field-weighted citation impact, top 24% 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, 25 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Molecular Transport and Growth of Lipid Vesicles Exposed to Antimicrobial Peptides.Langmuir : the ACS journal of surfaces and colloids · 2022
    Article
  7. Article
  8. 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

5 authors at 2 institutions in 2 countries.

Jeffrey Michael BreidiganDepartment of Physics, University of Illinois at Chicago, Chicago, IL 60607.
Natalie KrzyzanowskiDepartment of Physics, University of Illinois at Chicago, Chicago, IL 60607.
Yangmingyue LiuDepartment of Physics, University of Illinois at Chicago, Chicago, IL 60607.
Lionel PorcarLarge Scale Structures Group, Institut Laue-Langevin, F-38042 Grenoble CEDEX 9, France.
Ursula Perez-SalasDepartment of Physics, University of Illinois at Chicago, Chicago, IL 60607 ursulaps@uic.edu.
University of Illinois Chicago · USInstitut Laue-Langevin · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cholesterol, an essential component in biological membranes, is highly unevenly distributed within the cell, with most localized in the plasma membrane while only a small fraction is found in the endoplasmic reticulum, where it is synthesized. Cellular membranes differ in lipid composition and protein content, and these differences can exist across their leaflets too. This thermodynamic landscape that cellular membranes impose on cholesterol is expected to modulate its transport. To uncover the role the membrane environment has on cholesterol inter- and intra-membrane movement, we used time-resolved small angle neutron scattering to study the passive movement of cholesterol between and within membranes with varying degrees of saturation content. We found that cholesterol moves systematically slower as the degree of saturation in the membranes increases, from a palmitoyl oleyl phosphotidylcholine membrane, which is unsaturated, to a dipalmitoylphosphatidylcholine (DPPC) membrane, which is fully saturated. Additionally, we found that the energetic barrier to move cholesterol in these phosphatidylcholine membranes is independent of their relative lipid composition and remains constant for both flip-flop and exchange at ∼100 kJ/mol. Further, by replacing DPPC with the saturated lipid palmitoylsphingomyelin, an abundant saturated lipid of the outer leaflet of the plasma membrane, we found the rates decreased by a factor of two. This finding is in stark contrast with recent molecular dynamic simulations that predict a dramatic slow-down of seven orders of magnitude for cholesterol flipping in membranes with a similar phosphocholine and SM lipid composition.

Indexed as

1,2-DipalmitoylphosphatidylcholineBiological TransportCholesterolKineticsPhosphatidylcholinesSphingomyelinsThermodynamicsUnilamellar Liposomes1,2-Dipalmitoylphosphatidylcholine1,2-oleoylphosphatidylcholine1-palmitoyl-2-oleoylphosphatidylcholineCholesterolpalmitoylsphingomyelinPhosphatidylcholinesSphingomyelinsUnilamellar Liposomescholesterol exchangecholesterol flip-floplipid exchangelipid flip-floplipid vesiclesspontaneous lipid transporttime resolved SANS

Identifiers

PMID29046341
PMCPMC5711489
OpenAlexW2765138878

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.