Evidence map›Paper›PMID 28122218›Full record

ArticleBiophysical journal2017

Molecular-Scale Biophysical Modulation of an Endothelial Membrane by Oxidized Phospholipids.

Manuela A A Ayee, Elizabeth LeMaster, Tzu Pin Shentu, Dev K Singh, Nicolas Barbera, Dheeraj Soni, Chinnaswamy Tiruppathi, Papasani V Subbaiah, Evgeny Berdyshev, Irina Bronova and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

23 citing papers in PubMed, 47 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 1 country.

Manuela A A AyeeDivision of Pulmonary, Critical Care, Sleep and Allergy, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois.
Elizabeth LeMasterDivision of Pulmonary, Critical Care, Sleep and Allergy, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois.
Tzu Pin ShentuDivision of Pulmonary, Critical Care, Sleep and Allergy, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois.
Dev K SinghDivision of Pulmonary, Critical Care, Sleep and Allergy, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois.
Nicolas BarberaDivision of Pulmonary, Critical Care, Sleep and Allergy, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois.
Dheeraj SoniDepartment of Pharmacology, University of Illinois at Chicago, Chicago, Illinois.
Chinnaswamy TiruppathiDepartment of Pharmacology, University of Illinois at Chicago, Chicago, Illinois.
Papasani V SubbaiahDivision of Endocrinology, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois.
Evgeny BerdyshevNational Jewish Health, Denver, Colorado.
Irina BronovaNational Jewish Health, Denver, Colorado.
Michael ChoDepartment of Bioengineering, University of Illinois at Chicago, Chicago, Illinois.
Belinda S AkpaDepartment of Molecular Biomedical Sciences, North Carolina State University, Raleigh, North Carolina.
Irena LevitanDivision of Pulmonary, Critical Care, Sleep and Allergy, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois. Electronic address: levitan@uic.edu.
University of Illinois Chicago · USNational Jewish Health · USNorth Carolina State University · US

Funding

Cholesterol Regulation of Endothelial K+ ChannelsR01HL073965 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI LEVITAN, IRENA · 2004 to 2024
$7.3M
Impact of dyslipidemia on endothelial biomechanicsR01HL083298 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI LEVITAN, IRENA, MINSHALL, RICHARD D · 2007 to 2021
$7.0M
Pulmonary and Critical Care Post-Doctoral Research Training ProgramT32HL082547 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI FINN, PATRICIA W · 2007 to 2017
$2.7M
Endothelial Cell Deubiquitinase A20 Signals Repair of Lung Vascular InjuryR01HL128359 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI TIRUPPATHI, CHINNASWAMY · 2015 to 2018
$1.6M
Endothelial TAK1 Signaling and Resolution of Pulmonary Edema in SepsisR01GM117028 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI TIRUPPATHI, CHINNASWAMY · 2016 to 2019
$1.3M
Purchase of AB Sciex QTRAP 5500 SystemS10OD010660 · OD · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SUBBAIAH, PAPASANI V · 2012 to 2012
$440k
Molecular Form of Dietary DHA and its Bioavailability for the BrainR21AT008457 · NCCIH · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SUBBAIAH, PAPASANI V · 2014 to 2015
$431k
NCCIH NIH HHS R21 AT008457NHLBI NIH HHS R01 HL073965NHLBI NIH HHS R01 HL083298NHLBI NIH HHS R01 HL128359NHLBI NIH HHS T32 HL082547NIGMS NIH HHS R01 GM117028NIH HHS S10 OD010660
6 · The paper itself

Abstract

The influence of two bioactive oxidized phospholipids on model bilayer properties, membrane packing, and endothelial cell biomechanics was investigated computationally and experimentally. The truncated tail phospholipids, 1-palmitoyl-2-(5-oxovaleroyl)-sn-glycero-3-phosphocholine (POVPC) and 1-palmitoyl-2-glutaroyl-sn-glycero-3-phosphocholine (PGPC), are two major oxidation products of the unsaturated phospholipid 1-palmitoyl-2-arachidonoyl-sn-glycero-phosphocholine. A combination of coarse-grained molecular dynamics simulations, Laurdan multiphoton imaging, and atomic force microscopy microindentation experiments was used to determine the impact of POVPC and PGPC on the structure of a multicomponent phospholipid bilayer and to assess the consequences of their incorporation on membrane packing and endothelial cell stiffness. Molecular simulations predicted differential bilayer perturbation effects of the two oxidized phospholipids based on the chemical identities of their truncated tails, including decreased bilayer packing, decreased bilayer bending modulus, and increased water penetration. Disruption of lipid order was consistent with Laurdan imaging results indicating that POVPC and PGPC decrease the lipid packing of both ordered and disordered membrane domains. Computational predictions of a larger membrane perturbation effect by PGPC correspond to greater stiffness of PGPC-treated endothelial cells observed by measuring cellular elastic moduli using atomic force microscopy. Our results suggest that disruptions in membrane structure by oxidized phospholipids play a role in the regulation of overall endothelial cell stiffness.

Indexed as

AnimalsBiomechanical PhenomenaCattleCell MembraneEndothelial CellsLipid BilayersMechanical PhenomenaMolecular ConformationMolecular Dynamics SimulationPhospholipid Ethers1-palmitoyl-2-(5-oxovaleroyl)-sn-glycero-3-phosphorylcholine1-palmitoyl-2-glutaroyl-sn-glycero-3-phosphorylcholineLipid BilayersPhospholipid Ethers

Identifiers

PMID28122218
PMCPMC5266087
OpenAlexW2582141824

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.