Evidence map›Paper›PMID 30769337›Full record

ArticleBiofabrication2019

Bioprinted osteon-like scaffolds enhance in vivo neovascularization.

Charlotte Piard, Hannah Baker, Timur Kamalitdinov, John Fisher

Abstract read
In one paragraph

Article in Biofabrication, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing 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

40 citing papers in PubMed.

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  16. Research progress of vascularization strategies of tissue-engineered bone.Frontiers in bioengineering and biotechnology · 2023
    Review
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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

4 authors.

Charlotte PiardFischell Department of Bioengineering, University of Maryland, 3121 A James Clark Hall, College Park, MD 20742, United States of America.ORCID 0000-0001-7874-1499
Hannah BakerFischell Department of Bioengineering, University of Maryland, 3121 A James Clark Hall, College Park, MD 20742, United States of America.
Timur KamalitdinovFischell Department of Bioengineering, University of Maryland, 3121 A James Clark Hall, College Park, MD 20742, United States of America.ORCID 0000-0001-7120-8915
John FisherFischell Department of Bioengineering, University of Maryland, 3121 A James Clark Hall, College Park, MD 20742, United States of America.

Funding

Training and Dissemination CoreP41EB023833 · NIBIB · UNIV OF MARYLAND, COLLEGE PARK · PI FISHER, JOHN P · 2017 to 2021
$6.2M
Studies in Translational Regenerative MedicineT32EB014836 · NIBIB · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ANTHONY ATALA, Victoria Weis · 2013 to 2026
$1.7M
Three-Dimensional Image-Guided Development and Optimization of Molecular Regulating Bone Regenerative ScaffoldsR01EB014946 · NIBIB · UNIV OF MARYLAND, COLLEGE PARK · PI CHEN, YU · 2015 to 2018
$1.3M
NIBIB NIH HHS P41 EB023833NIBIB NIH HHS R01 EB014946NIBIB NIH HHS T32 EB014836
6 · The paper itself

Abstract

Bone tissue engineers are facing a daunting challenge when attempting to fabricate bigger constructs intended for use in the treatment of large bone defects, which is the vascularization of the graft. Cell-based approaches and, in particular, the use of in vitro coculture of human umbilical vein endothelial cells (HUVECs) and human mesenchymal stem cells (hMSCs) has been one of the most explored options. We present in this paper an alternative method to mimic the spatial pattern of HUVECs and hMSCs found in native osteons based on the use of extrusion-based 3D bioprinting (3DP). We developed a 3DP biphasic osteon-like scaffold, containing two separate osteogenic and vasculogenic cell populations encapsulated in a fibrin bioink in order to improve neovascularization. To this end, we optimized the fibrin bioink to improve the resolution of printed strands and ensure a reproducible printing process; the influence of printing parameters on extruded strand diameter and cell survival was also investigated. The mechanical strength of the construct was improved by co-printing the fibrin bioink along a supporting PCL carrier scaffold. Compressive mechanical testing showed improved mechanical properties with an average compressive modulus of 131 ± 23 MPa, which falls in the range of cortical bone. HUVEC and hMSC laden fibrin hydrogels were printed in osteon-like patterns and cultured in vitro. A significant increase in gene expression of angiogenic markers was observed for the biomimetic scaffolds. Finally, biphasic scaffolds were implanted subcutaneously in rats. Histological analysis of explanted scaffolds showed a significant increase in the number of blood vessels per area in the 3D printed osteon-like scaffolds. The utilization of these scaffolds in constructing biomimetic osteons for bone regeneration demonstrated a promising capacity to improve neovascularization of the construct. These results indicates that proper cell orientation and scaffold design could play a critical role in neovascularization.

Indexed as

BioprintingNeovascularization, PhysiologicAnimalsCattleCell LineFibrinHaversian SystemHumansHuman Umbilical Vein Endothelial CellsInkMesenchymal Stem CellsMiceRats, Sprague-DawleySwineTissue ScaffoldsFibrin

Identifiers

PMID30769337
PMCPMC7195919

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.