Evidence map›Paper›PMID 29471680›Full record

ArticleConnective tissue research2018

Proteomic profiling of extracellular vesicles released from vascular smooth muscle cells during initiation of phosphate-induced mineralization.

Sandeep C Chaudhary, Sana Khalid, Victoria Smethurst, Daisy Monier, James Mobley, Alexis Huet, James F Conway, Dobrawa Napierala

Abstract read
In one paragraph

Article in Connective tissue research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Considerations on the Development of Therapeutics in Vascular Calcification.Journal of cardiovascular development and disease · 2025
    Review
  2. Similarities and Differences of Vascular Calcification in Diabetes and Chronic Kidney Disease.Diabetes, metabolic syndrome and obesity : targets and therapy · 2024
    Review
  3. Review
  4. Review
  5. Extracellular vesicles in vascular remodeling.Acta pharmacologica Sinica · 2022
    Review
  6. Review
  7. Review
  8. Article
  9. Article
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  11. Review
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

8 authors.

Sandeep C Chaudharya Department of Dermatology , University of Alabama at Birmingham , Birmingham , AL , USA.
Sana Khalidb Department of Oral Biology, Center for Craniofacial Regeneration , University of Pittsburgh School of Dental Medicine , Pittsburgh , PA , USA.
Victoria Smethurstb Department of Oral Biology, Center for Craniofacial Regeneration , University of Pittsburgh School of Dental Medicine , Pittsburgh , PA , USA.
Daisy Monierb Department of Oral Biology, Center for Craniofacial Regeneration , University of Pittsburgh School of Dental Medicine , Pittsburgh , PA , USA.
James Mobleyc Department of Surgery , University of Alabama at Birmingham , Birmingham , AL , USA.
Alexis Huetd Department of Structural Biology , University of Pittsburgh School of Medicine , Pittsburgh , PA , USA.
James F Conwayd Department of Structural Biology , University of Pittsburgh School of Medicine , Pittsburgh , PA , USA.
Dobrawa Napieralab Department of Oral Biology, Center for Craniofacial Regeneration , University of Pittsburgh School of Dental Medicine , Pittsburgh , PA , USA.

Funding

XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Robert S Welner · 1985 to 2026
$165.9M
Transcriptional Regulation of Dentin MineralizationR01DE023083 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI NAPIERALA, DOBRAWA · 2014 to 2018
$1.9M
NCI NIH HHS P30 CA013148NIDCR NIH HHS R01 DE023083
6 · The paper itself

Abstract

Purpose/Aim: Elevated serum phosphate is one of the major factors contributing to vascular calcification. Studies suggested that extracellular vesicles released from vascular smooth muscle cells significantly contribute to the initiation and progression of this pathology. Recently, we have demonstrated that elevated phosphate stimulates release of extracellular vesicles from osteogenic cells at the initiation of the mineralization process. Here, we used MOVAS cell line as an in vitro model of vascular calcification to examine whether vascular smooth muscle cells respond to high phosphate levels in a similar way and increase formation of extracellular vesicles. MATERIALS AND

methodsVesicles residing in extracellular matrix as well as vesicles released to culture medium were evaluated by nanoparticle tracking analyses. In addition, using mass spectrometry and protein profiling, protein composition of extracellular vesicles released by MOVAS cells under standard growth conditions and upon exposure to high phosphate was compared.

resultsSignificant increase of the number of extracellular vesicles was detected after 72 h of exposure of cells to high phosphate. Elevated phosphate levels also affected protein composition of extracellular vesicles released from MOVAS cells. Finally, the comparative analyses of proteins in extracellular vesicles isolated from extracellular matrix and from conditioned medium identified significant differences in protein composition in these two groups of extracellular vesicles.

conclusionsResults of this study demonstrate that exposure of MOVAS cells to high phosphate levels stimulates the release of extracellular vesicles and changes their protein composition.

Indexed as

Extracellular VesiclesGene Expression ProfilingHumansMuscle, Smooth, VascularMyocytes, Smooth MusclePhosphatesProteomicsVascular CalcificationPhosphatesExtracellular vesiclesmatrix vesiclesmineralizationphosphateproteomics

Identifiers

PMID29471680
PMCPMC6414064

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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.