Evidence map›Paper›PMID 23922881›Full record

ArticlePloS one2013

PIMT prevents the apoptosis of endothelial cells in response to glycated low density lipoproteins and protective effects of grape seed procyanidin B2.

Xiao-li Li, Bao-ying Li, Mei Cheng, Fei Yu, Wen-bin Yin, Qian Cai, Zhen Zhang, Jian-hua Zhang, Jun-fu Wang, Rui-hai Zhou and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

9 citing papers in PubMed, 21 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

11 authors at 2 institutions in 2 countries.

Xiao-li LiKey Laboratory of Cardiovascular Proteomics of Shandong Province, Department of Geriatric Endocrinology, Qi-Lu Hospital of Shandong University, Jinan, China.
Bao-ying Li
Mei Cheng
Fei Yu
Wen-bin Yin
Qian Cai
Zhen Zhang
Jian-hua Zhang
Jun-fu Wang
Rui-hai Zhou
Hai-qing Gao
Qilu Hospital of Shandong University · CNUniversity of North Carolina at Chapel Hill · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe development of diabetic angiopathy is associated with profound vascular endothelial cells (VEC) dysfunction and apoptosis. Glycated low density lipoproteins (gly-LDL) continuously produced in the setting of diabetic patients play an important role in causing VEC dysfunction and apoptosis. However, the underlying molecular mechanism remains largely elusive. Protein L-isoaspartyl methyltransferase (PIMT) is a widely expressed protein repair enzyme by multiple cell types of arterial wall including VEC. Our previous proteomic studies showed that the expression of PIMT was significantly decreased in the aorta of diabetic rats as compared with control rats and treatment with grape seed procyanidin extracts significantly increased the PIMT expression in diabetic rats. We hypothesized that PIMT plays a critical role in gly-LDL induced VEC apoptosis; grape seed procyanidin B2 (GSPB2) protect against gly-LDL induced VEC apoptosis through PIMT regulation. METHODS AND

resultsHUVEC transfected negative control and PIMT siRNA were treated with or without GSPB2 (10 µmol/L) for 48 h. Moreover, HUVEC of PIMT overexpression were stimulated by gly-LDL (50 µg/ml) in the presence or absence of GSPB2 (10 µmol/L) for 48 h. Our results showed that gly-LDL downregulated PIMT expression and PIMT overexpression or GSPB2 significantly attenuated gly-LDL induced VEC apoptosis. PIMT siRNA increased VEC apoptosis with up-regulation of p53, cytochrome c release, caspase-9 and caspase-3 activation. Mechanistically, overexpression of PIMT or GSPB2 increased the phosphorylation of ERK1/2 and GSK3β in the gly-LDL induced VEC.

conclusionIn summary, our study identified PIMT as a key player responsible for gly-LDL induced VEC apoptosis and GSPB2 protect against gly-LDL induced VEC apoptosis by PIMT up-regulation. Targeting PIMT including use of GSPB2 could be turned into clinical application in the fighting against diabetic vascular complications.

Indexed as

AnimalsApoptosisBiflavonoidsCaspase 3Caspase 9CatechinCell SurvivalCytochromes cCytosolExtracellular Signal-Regulated MAP KinasesGlucoseGlycated ProteinsGlycation End Products, AdvancedGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaGrape Seed ExtractBiflavonoidsCaspase 3Caspase 9CatechinCytochromes cExtracellular Signal-Regulated MAP KinasesGlucoseglycated lipoproteins, LDLGlycated ProteinsGlycation End Products, AdvancedGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaGrape Seed ExtractGrape Seed ProanthocyanidinsGSK3B protein, humanGsk3b protein, ratLipoproteins, LDLProanthocyanidinsprocyanidin B2Protective AgentsProtein D-Aspartate-L-Isoaspartate MethyltransferaseRNA, Small InterferingTumor Suppressor Protein p53

Identifiers

PMID23922881
PMCPMC3724603
OpenAlexW1988765884

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.