Evidence map›Paper›PMID 36401768›Full record

ArticleTissue engineering and regenerative medicine2023

Tailoring Hydrogel Composition and Stiffness to Control Smooth Muscle Cell Differentiation in Bioprinted Constructs.

Zongzhe Xuan, Qiuyue Peng, Thomas Larsen, Leonid Gurevich, Jesper de Claville Christiansen, Vladimir Zachar, Cristian Pablo Pennisi

Open access · greenAbstract read
In one paragraph

Article in Tissue engineering and regenerative medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 20 citations in OpenAlex.

  1. 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

7 authors at 1 institution in 1 country.

Zongzhe XuanRegenerative Medicine Group, Department of Health Science and Technology, Aalborg University, Frederik Bajers Vej 3B, 9220, Aalborg Ø, Denmark.
Qiuyue PengRegenerative Medicine Group, Department of Health Science and Technology, Aalborg University, Frederik Bajers Vej 3B, 9220, Aalborg Ø, Denmark.
Thomas LarsenMaterials Science and Engineering Group, Department of Materials and Production, Aalborg University, Pontoppidanstræde 103, 9220, Aalborg, Denmark.
Leonid GurevichMaterials Science and Engineering Group, Department of Materials and Production, Aalborg University, Pontoppidanstræde 103, 9220, Aalborg, Denmark.
Jesper de Claville ChristiansenMaterials Science and Engineering Group, Department of Materials and Production, Aalborg University, Pontoppidanstræde 103, 9220, Aalborg, Denmark.
Vladimir ZacharRegenerative Medicine Group, Department of Health Science and Technology, Aalborg University, Frederik Bajers Vej 3B, 9220, Aalborg Ø, Denmark.
Cristian Pablo PennisiRegenerative Medicine Group, Department of Health Science and Technology, Aalborg University, Frederik Bajers Vej 3B, 9220, Aalborg Ø, Denmark. cpennisi@hst.aau.dk.ORCID 0000-0002-7716-1182
Aalborg University · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundReliable in vitro cellular models are needed to study the phenotypic modulation of smooth muscle cells (SMCs) in health and disease. The aim of this study was to optimize gelatin methacrylate (GelMA)/alginate hydrogels for bioprinting three-dimensional (3D) SMC constructs.

methodsFour different hydrogel groups were prepared by mixing different concentrations (% w/v) of GelMA and alginate: G1 (5/1.5), G2 (5/3), G3 (7.5/1.5), and G4 (7.5/3). GelMA 10% was used as control (G5). A circular structure containing human bladder SMCs was fabricated by using an extrusion-based bioprinter. The effects of the mixing ratios on printability, viability, proliferation, and differentiation of the cells were investigated.

resultsRheological analysis showed that the addition of alginate significantly stabilized the change in mechanical properties with temperature variations. The group with the highest GelMA and alginate concentrations (G4) exhibited the highest viscosity, resulting in better stability of the 3D construct after crosslinking. Compared to other hydrogel compositions, cells in G4 maintained high viability (> 80%), exhibited spindle-shaped morphology, and showed a significantly higher proliferation rate within an 8-day period. More importantly, G4 provided an optimal environment for the induction of a SMC contractile phenotype, as evidenced by significant changes in the expression of marker proteins and morphological parameters.

conclusionAdjusting the composition of GelMA/alginate hydrogels is an effective means of controlling the SMC phenotype. These hydrogels support bioprinting of 3D models to study phenotypic smooth muscle adaptation, with the prospect of using the constructs in the study of therapies for the treatment of urethral strictures.

Indexed as

BioprintingHydrogelsAlginatesCell DifferentiationGelatinHumansMethacrylatesMuscle, SmoothAlginatesGelatinHydrogelsMethacrylatesBiomechanical phenomenaBioprintingHydrogelSmooth muscle myocytesUrethral stricture

Identifiers

PMID36401768
PMCPMC10070577
OpenAlexW4309413000

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Registered trials

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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.