Evidence map›Paper›PMID 23500015›Full record

Trial reportBiochimica et biophysica acta2013

Effect of lyso-phosphatidylcholine and Schnurri-3 on osteogenic transdifferentiation of vascular smooth muscle cells to calcifying vascular cells in 3D culture.

Fernando Castro-Chavez, Kasey C Vickers, Jae Sam Lee, Ching-Hsuan Tung, Joel D Morrisett

Abstract readClinical Trial
In one paragraph

Trial report in Biochimica et biophysica acta, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Magnetic-Based Human Tissue 3D Cell Culture: A Systematic Review.International journal of molecular sciences · 2022
    Pooled it
  2. Article
  3. Article
  4. Article
  5. Imaging Approaches to the Diagnosis of Vascular Diseases.Current atherosclerosis reports · 2022
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. 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

5 authors at 2 institutions in 1 country.

Fernando Castro-ChavezDepartment of Medicine, Baylor College of Medicine, Houston, TX, USA.
Kasey C Vickers
Jae Sam Lee
Ching-Hsuan Tung
Joel D Morrisett
Baylor College of Medicine · USMethodist Hospital · US

Funding

ATHEROSCLEROSIS AND VASCULAR BIOLOGY TRAINING CENTERT32HL007812 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI BALLANTYNE, CHRISTIE MITCHELL · 1997 to 2012
$3.4M
LESION QUANTIFICATION IN HUMAN CAROTID ATHEROSCLEROSISR01HL063090 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI MORRISETT, JOEL DAVID · 2002 to 2005
$1.3M
Intramural NIH HHS Z99 HL999999NHLBI NIH HHS HL-07812NHLBI NIH HHS HL-63090NHLBI NIH HHS R01 HL063090NHLBI NIH HHS T32 HL007812
6 · The paper itself

Abstract

backgroundIn vitro cell culture is a widely used technique for investigating a range of processes such as stem cell behavior, regenerative medicine, tissue engineering, and drug discovery. Conventional cell culture is performed in Petri dishes or flasks where cells typically attach to a flat glass or plastic surface as a cell monolayer. However, 2D cell monolayers do not provide a satisfactory representation of in vivo conditions. A 3D culture could be a much better system for representing the conditions that prevail in vivo. METHODS AND

resultsTo simulate 3D conditions, vascular smooth muscle cells (VSMCs) were loaded with gold-polyvmer-iron oxide hydrogel, enabling levitation of the cells by using spatially varying magnetic fields. These magnetically levitated 3D cultures appeared as freely suspended, clustered cells which proliferated 3-4 times faster than cells in conventional 2D cultures. When the levitated cells were treated with 10nM lysophosphatidylcholine (LPC), for 3days, cell clusters exhibited translucent extensions/rods 60-80μm wide and 200-250μm long. When 0.5μg/μl Schnurri-3 was added to the culture containing LPC, these extensions were smaller or absent. When excited with 590-650nm light, these extensions emitted intrinsic fluorescence at >667nm. When the 3D cultures were treated with a fluorescent probe specific for calcium hydroxyapatite (FITC-HABP-19), the cell extensions/rods emitted intensely at 518nm, the λmax for FITC emission. Pellets of cells treated with LPC were more enriched in calcium, phosphate, and glycosaminoglycans than cells treated with LPC and Schnurri-3.

conclusionsIn 3D cultures, VSMCs grow more rapidly and form larger calcification clusters than cells in 2D cultures. Transdifferentiation of VSMC into calcifying vascular cells is enhanced by LPC and attenuated by Schnurri-3. GENERAL SIGNIFICANCE: The formation of calcified structures in 3D VSMC cultures suggests that similar structures may be formed in vivo.

Indexed as

CalcinosisCell Culture TechniquesCell LineCell TransdifferentiationDNA-Binding ProteinsHumansLysophosphatidylcholinesMaleMuscle, Smooth, VascularMyocytes, Smooth MuscleOsteogenesisDNA-Binding ProteinsHIVEP3 protein, humanLysophosphatidylcholines

Identifiers

PMID23500015
PMCPMC4383529
OpenAlexW2005803450

What OpenQuestion holds

Textmetadata
LicenceTDM
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.