Evidence map›Paper›PMID 38138649›Full record

ArticleMaterials (Basel, Switzerland)2023

In Vitro Investigation of Gelatin/Polycaprolactone Nanofibers in Modulating Human Gingival Mesenchymal Stromal Cells.

Zhiwei Tian, Zhongqi Zhao, Marco Aoqi Rausch, Christian Behm, Hassan Ali Shokoohi-Tabrizi, Oleh Andrukhov, Xiaohui Rausch-Fan

Open access · goldAbstract read
In one paragraph

Article in Materials (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

5 citing papers in PubMed, 3 citations in OpenAlex.

  1. Electrospun Fibers EncapsulatingMolecules (Basel, Switzerland) · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. 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

7 authors at 1 institution in 1 country.

Zhiwei TianCompetence Center for Periodontal Research, University Clinic of Dentistry, Medical University of Vienna, 1090 Wien, Austria.ORCID 0009-0008-7662-2945
Zhongqi ZhaoCompetence Center for Periodontal Research, University Clinic of Dentistry, Medical University of Vienna, 1090 Wien, Austria.ORCID 0000-0002-9801-8713
Marco Aoqi RauschCompetence Center for Periodontal Research, University Clinic of Dentistry, Medical University of Vienna, 1090 Wien, Austria.
Christian BehmCompetence Center for Periodontal Research, University Clinic of Dentistry, Medical University of Vienna, 1090 Wien, Austria.ORCID 0000-0002-3065-3200
Hassan Ali Shokoohi-TabriziCore Facility Applied Physics, Laser and CAD/CAM Technology, University Clinic of Dentistry, Medical University of Vienna, 1090 Wien, Austria.ORCID 0000-0002-1816-3436
Oleh AndrukhovCompetence Center for Periodontal Research, University Clinic of Dentistry, Medical University of Vienna, 1090 Wien, Austria.ORCID 0000-0002-0485-2142
Xiaohui Rausch-FanCenter for Clinical Research, University Clinic of Dentistry, Medical University of Vienna, 1090 Wien, Austria.
Medical University of Vienna · AT

Funding

Neo Modulus (Suzhou) Medical Sci-Tech Co., Ltd 2023050560
6 · The paper itself

Abstract

The aesthetic constancy and functional stability of periodontium largely depend on the presence of healthy mucogingival tissue. Soft tissue management is crucial to the success of periodontal surgery. Recently, synthetic substitute materials have been proposed to be used for soft tissue augmentation, but the tissue compatibility of these materials needs to be further investigated. This study aims to assess the in vitro responses of human gingival mesenchymal stromal cells (hG-MSCs) cultured on a Gelatin/Polycaprolactone prototype (GPP) and volume-stable collagen matrix (VSCM). hG-MSCs were cultured onto the GPP, VSCM, or plastic for 3, 7, and 14 days. The proliferation and/or viability were measured by cell counting kit-8 assay and resazurin-based toxicity assay. Cell morphology and adhesion were evaluated by microscopy. The gene expression of collagen type I, alpha1 (COL1A1), α-smooth muscle actin (α-SMA), fibroblast growth factor (FGF-2), vascular endothelial growth factor A (VEGF-A), transforming growth factor beta-1 (TGF-β1), focal adhesion kinase (FAK), integrin beta-1 (ITG-β1), and interleukin 8 (IL-8) was investigated by RT-qPCR. The levels of VEGF-A, TGF-β1, and IL-8 proteins in conditioned media were tested by ELISA. GPP improved both cell proliferation and viability compared to VSCM. The cells grown on GPP exhibited a distinct morphology and attachment performance. COL1A1, α-SMA, VEGF-A, FGF-2, and FAK were positively modulated in hG-MSCs on GPP at different investigation times. GPP increased the gene expression of TGF-β1 but had no effect on protein production. The level of ITG-β1 had no significant changes in cells seeded on GPP at 7 days. At 3 days, notable differences in VEGF-A, TGF-β1, and α-SMA expression levels were observed between cells seeded on GPP and those on VSCM. Meanwhile, GPP showed higher COL1A1 expression compared to VSCM after 14 days, whereas VSCM demonstrated a more significant upregulation in the production of IL-8. Taken together, our data suggest that GPP electrospun nanofibers have great potential as substitutes for soft tissue regeneration in successful periodontal surgery.

Indexed as

collagenelectrospinninggelatinhuman gingival mesenchymal stromal cellsperiodontal tissuepolycaprolactone

Identifiers

PMID38138649
PMCPMC10744501
OpenAlexW4389346956

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.