Evidence map›Paper›PMID 30797003›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2019

Modulating smooth muscle cell response by the release of TGFβ2 from tubular scaffolds for vascular tissue engineering.

D C Ardila, E Tamimi, T Doetschman, W R Wagner, J P Vande Geest

Open access · greenAbstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.9field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Electrospun fibre diameter and its effects on vascular smooth muscle cells.Journal of materials science. Materials in medicine · 2021
    Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. 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 3 institutions in 1 country.

D C ArdilaDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, PA 15213, USA.
E TamimiDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, PA 15213, USA.
T DoetschmanDepartment of Cellular and Molecular Medicine, The University of Arizona, Tucson, AZ 85721, USA; BIO5 Institute, The University of Arizona, Tucson, AZ 85724, USA.
W R WagnerDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, PA 15213, USA; McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, PA 15213, USA; Department of Surgery, University of Pittsburgh, Pittsburgh, PA 15213, USA.
J P Vande GeestDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, PA 15213, USA; McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, PA 15213, USA; Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, PA 15219, USA. Electronic address: jpv20@pitt.edu.
University of Pittsburgh · USMcGowan Institute for Regenerative Medicine · USUniversity of Arizona · US

Funding

Cellular Approaches to Tissue Engineering/RegenerationT32EB001026 · NIBIB · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DUNCAN, ANDREW W, MONGA, SATDARSHAN SINGH · 2003 to 2024
$5.5M
Preclinical assessment of a compliance matched biopolymer vascular graftR56HL136517 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI VANDE GEEST, JONATHAN PIETER · 2017 to 2017
$673k
NHLBI NIH HHS R56 HL136517NIBIB NIH HHS T32 EB001026
6 · The paper itself

Abstract

Tissue engineering has gained considerable attention in the development of small diameter tissue engineered vascular grafts (TEVGs) for treating coronary heart disease. A properly designed acellular and biodegradable TEVG must encourage the infiltration and growth of vascular smooth muscle cells (SMCs). Our group has previously shown that increasing levels of TGFβ2 can differentially modulate SMC migration and proliferation. In this study, tubular electrospun scaffolds loaded with TGFβ2 were fabricated using various ratios of gelatin/polycaprolactone (PCL), resulting in scaffolds with porous nano-woven architecture suitable for tissue ingrowth. Scaffold morphology, degradation rate, TGβ2 release kinetics, and bioactivity were assessed. TGFβ2 was successfully integrated into the electrospun biomaterial that resulted in a differential release profile depending on the gelatin/PCL ratio over the course of 42 days. Higher TGFβ2 elution was obtained in scaffolds with higher gelatin content, which may be related to the biodegradation of gelatin in culture media. The biological activity of the released TGFβ2 was evaluated by its ability to affect SMC proliferation as a function of its concentration. SMCs seeded on TGFβ2-loaded scaffolds also showed higher densities and infiltration after 5 days in culture as compared to scaffolds without TGFβ2. Our results demonstrate that the ratio of synthetic and natural polymers in electrospun blends can be used to tune the release of TGFβ2. This method can be used to intelligently modulate the SMC response in gelatin/PCL scaffolds making the TGFβ2-loaded conduits attractive for cardiovascular tissue engineering applications.

Indexed as

AnimalsBiocompatible MaterialsCell ProliferationCells, CulturedDrug CarriersGelatinHumansMyocytes, Smooth MuscleRecombinant ProteinsSwineTissue EngineeringTissue ScaffoldsTransforming Growth Factor betaBiocompatible MaterialsDrug CarriersGelatinRecombinant ProteinsTransforming Growth Factor betaElectrospinningGelatinPolycaprolactoneSmooth muscle cellsTGFβ2 releaseVascular tissue engineering

Identifiers

PMID30797003
PMCPMC6430660
OpenAlexW2917450941

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.