Evidence map›Paper›PMID 25463485›Full record

ArticleActa biomaterialia2015

Manipulation of cellular spheroid composition and the effects on vascular tissue fusion.

T R Olsen, B Mattix, M Casco, A Herbst, C Williams, A Tarasidis, D Simionescu, R P Visconti, F Alexis

Open access · greenAbstract read
In one paragraph

Article in Acta biomaterialia, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
  2. Review
  3. Multiscale Construction, Evaluation, and Application of Organoids.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  4. Article
  5. Article
  6. Development and Validation of a Scaffold-Free Human Multilineage Spheroid Model for Early Stage Cholangiopathies Driven by Cholangiocyte Senescence.Liver international : official journal of the International Association for the Study of the Liver · 2025
    Article
  7. Article
  8. Review
  9. Remotely Controlled 3D-Engineered Scaffolds for Biomimetic In Vitro Investigations on Brain Cell Cocultures.Advanced intelligent systems (Weinheim an der Bergstrasse, Germany) · 2024
    Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Progress in scaffold-free bioprinting for cardiovascular medicine.Journal of cellular and molecular medicine · 2018
    Review
  17. Review
  18. Review
  19. Article
  20. Article
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

9 authors at 2 institutions in 1 country.

T R OlsenDepartment of Bioengineering, Clemson University, 301 Rhodes Research Center, Clemson, SC 29634, USA.
B MattixDepartment of Bioengineering, Clemson University, 301 Rhodes Research Center, Clemson, SC 29634, USA.
M CascoDepartment of Bioengineering, Clemson University, 301 Rhodes Research Center, Clemson, SC 29634, USA.
A HerbstDepartment of Bioengineering, Clemson University, 301 Rhodes Research Center, Clemson, SC 29634, USA.
C WilliamsDepartment of Bioengineering, Clemson University, 301 Rhodes Research Center, Clemson, SC 29634, USA.
A TarasidisDepartment of Bioengineering, Clemson University, 301 Rhodes Research Center, Clemson, SC 29634, USA.
D SimionescuDepartment of Bioengineering, Clemson University, 301 Rhodes Research Center, Clemson, SC 29634, USA. Electronic address: dsimion@clemson.edu.
R P ViscontiDepartment of Regenerative Medicine and Cell Biology, Medical University of South Carolina, 173 Ashley Avenue - BSB 601, Charleston, SC 29425, USA. Electronic address: visconrp@musc.edu.
F AlexisDepartment of Bioengineering, Clemson University, 301 Rhodes Research Center, Clemson, SC 29634, USA; Institute of Biological Interfaces of Engineering, Department of Bioengineering, Clemson University, 401-2 Rhodes Engineering Research Center, Clemson, SC 29634, USA. Electronic address: falexis@clemson.edu.
Clemson University · USMedical University of South Carolina · US

Funding

UBIQUITIN CARBOXYL TERMINAL HYDROLASE L1 (UCH-L1) AND VASCULAR LESION FORMATIONP20RR016434 · NCRR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MARKWALD, ROGER R · 2001 to 2011
$24.8M
Targeted Nano-therapeutics for Neural RegenerationP20GM103444 · NIGMS · CLEMSON UNIVERSITY · PI MARKWALD, ROGER R, VYAVAHARE, NAREN R · 2012 to 2018
$14.9M
SC COBRE for Developmentally Based Cardiovascular DiseasesP30GM103342 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI ARGRAVES, WILLIAM SCOTT · 2012 to 2016
$5.5M
UNDERSTANDING AND CONTROLLING TISSUE-SPECIFIC VASCULAR PATTERNINGP20RR021949 · NCRR · CLEMSON UNIVERSITY · PI MARKWALD, ROGER R · 2009 to 2011
$5.2M
NCRR NIH HHS P20 RR016434NCRR NIH HHS P20 RR021949NIGMS NIH HHS P20 GM103444NIGMS NIH HHS P30 GM103342
6 · The paper itself

Abstract

Cellular spheroids were investigated as tissue-engineered building blocks that can be fused to form functional tissue constructs. While spheroids can be assembled using passive contacts for the fusion of complex tissues, physical forces can be used to promote active contacts to improve tissue homogeneity and accelerate tissue fusion. Understanding the mechanisms affecting the fusion of spheroids is critical to fabricating tissues. Here, manipulation of the spheroid composition was used to accelerate the fusion process mediated by magnetic forces. The Janus structure of magnetic cellular spheroids spatially controls iron oxide magnetic nanoparticles (MNPs) to form two distinct domains: cells and extracellular MNPs. Studies were performed to evaluate the influence of extracellular matrix (ECM) content and cell number on the fusion of Janus magnetic cellular spheroids (JMCSs). Results showed that the integration of iron oxide MNPs into spheroids increased the production of collagen over time when compared to spheroids without MNPs. The results also showed that ring tissues composed of JMCSs with high ECM concentrations and high cell numbers fused together, but exhibited less contraction when compared to their lower concentration counterparts. Results from spheroid fusion in capillary tubes showed that low ECM concentrations and high cell numbers experienced more fusion and cellular intermixing over time when compared to their higher counterparts. These findings indicate that cell-cell and cell-matrix interactions play an important role in regulating fusion, and this understanding sets the rationale of spheroid composition to fabricate larger and more complex tissue-engineered constructs.

Indexed as

Magnetite NanoparticlesAnimalsCapillariesCells, CulturedCollagenMuscle, Smooth, VascularMyocytes, Smooth MuscleRatsSpheroids, CellularTissue EngineeringCollagenMagnetite NanoparticlesMagnetic nanoparticlesMagnetic patterningSpheroidsTissue engineeringTissue fusion

Identifiers

PMID25463485
PMCPMC4737648
OpenAlexW2024027536

What OpenQuestion holds

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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.