Evidence map›Paper›PMID 22550136›Full record

ArticleJournal of lipid research2012

Evidence for the importance of OxPAPC interaction with cysteines in regulating endothelial cell function.

James R Springstead, B Gabriel Gugiu, Sangderk Lee, Seung Cha, Andrew D Watson, Judith A Berliner

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

17 citing papers in PubMed, 31 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

James R SpringsteadDepartment of Medicine and University of California at Los Angeles, Los Angeles, CA 90095, USA.
B Gabriel Gugiu
Sangderk Lee
Seung Cha
Andrew D Watson
Judith A Berliner
University of California, Los Angeles · US

Funding

ULTRASTRUCTURE OF THE INTIMA IN EARLY LESION FORMATIONP01HL030568 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI FOGELMAN, ALAN M · 1985 to 2019
$55.2M
Vascular Biology Training GrantT32HL069766 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LUSIS, ALDONS JAKE · 2002 to 2022
$7.4M
ENDOTHELIAL ACTIVATION BY AN ISOPROSTANE PHOSPHOLIPIDR01HL064731 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BERLINER, JUDITH ANNE · 2000 to 2011
$3.2M
Role of MP-HBEGF-EGFR signaling for inflammatory action of oxidized phospholipidsR00HL105577 · NHLBI · UNIVERSITY OF KENTUCKY · PI LEE, SANGDERK · 2013 to 2015
$718k
Role of MP-HBEGF-EGFR signaling for inflammatory action of oxidized phospholipidsK99HL105577 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LEE, SANGDERK · 2011 to 2012
$180k
NHLBI NIH HHS 1K99-HL-105577NHLBI NIH HHS HL-064731NHLBI NIH HHS HL-30568NHLBI NIH HHS K99 HL105577NHLBI NIH HHS P01 HL030568NHLBI NIH HHS R00 HL105577NHLBI NIH HHS R01 HL064731NHLBI NIH HHS T32 HL069766NHLBI NIH HHS T32-HL-69766
6 · The paper itself

Abstract

Oxidation products of 1-palmitoyl-2-arachidonoyl-sn-glycerol-3-phosphatidylcholine (PAPC), referred to as OxPAPC, and an active component, 1-palmitoyl-2-(5,6-epoxyisoprostane E₂)-sn-glycero-3-phosphatidylcholine (PEIPC), accumulate in atherosclerotic lesions and regulate over 1,000 genes in human aortic endothelial cells (HAEC). We previously demonstrated that OxPNB, a biotinylated analog of OxPAPC, covalently binds to a number of proteins in HAEC. The goal of these studies was to gain insight into the binding mechanism and determine whether binding regulates activity. In whole cells, N-acetylcysteine inhibited gene regulation by OxPAPC, and blocking cell cysteines with N-ethylmaleimide strongly inhibited the binding of OxPNB to HAEC proteins. Using MS, we demonstrate that most of the binding of OxPAPC to cysteine is mediated by PEIPC. We also show that OxPNB and PEIPE-NB, the analog of PEIPC, bound to a model protein, H-Ras, at cysteines previously shown to regulate activity in response to 15-deoxy-Δ12,14-prostaglandin J2 (15dPGJ₂). This binding was observed with recombinant protein and in cells overexpressing H-Ras. OxPAPC and PEIPC compete with OxPNB for binding to H-Ras. 15dPGJ₂ and OxPAPC increased H-Ras activity at comparable concentrations. Using microarray analysis, we demonstrate a considerable overlap of gene regulation by OxPAPC, PEIPC, and 15dPGJ₂ in HAEC, suggesting that some effects attributed to 15dPGJ₂ may also be regulated by PEIPC because both molecules accumulate in inflammatory sites. Overall, we provide evidence for the importance of OxPAPC-cysteine interactions in regulating HAEC function.

Indexed as

Binding SitesCells, CulturedCysteineEndothelial CellsEthylmaleimideHumansIsoprostanesPhosphatidylcholinesProstaglandin D215-deoxyprostaglandin J21-palmitoyl-2-(epoxyisoprostane-E2)-sn-glycero-3-phosphocholineCysteineEthylmaleimideIsoprostanesoxidized-L-alpha-1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphorylcholinePhosphatidylcholinesProstaglandin D2

Identifiers

PMID22550136
PMCPMC3371242
OpenAlexW2126862630

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.