Evidence map›Paper›PMID 36105132›Full record

ArticleInternational journal of bioprinting2022

Bone Sialoprotein Immobilized in Collagen Type I Enhances Bone Regeneration In vitro and In vivo.

Anja Kriegel, Christian Schlosser, Tanja Habeck, Christoph Dahmen, Hermann Götz, Franziska Clauder, Franz Paul Armbruster, Andreas Baranowski, Philipp Drees, Pol Maria Rommens and 1 more

Open access · diamondAbstract read
In one paragraph

Article in International journal of bioprinting, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

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  7. The role of bone sialoprotein in bone healing.Journal of structural biology · 2024
    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

11 authors at 1 institution in 1 country.

Anja KriegelDepartment of Orthopedics and Traumatology, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany.
Christian SchlosserDepartment of Orthopedics and Traumatology, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany.
Tanja HabeckDepartment of Orthopedics and Traumatology, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany.
Christoph DahmenDepartment of Orthopedics and Traumatology, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany.
Hermann GötzCell Biology Unit, PKZI, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany.
Franziska ClauderImmundiagnostik AG, Bensheim, Germany.
Franz Paul ArmbrusterImmundiagnostik AG, Bensheim, Germany.
Andreas BaranowskiDepartment of Orthopedics and Traumatology, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany.
Philipp DreesDepartment of Orthopedics and Traumatology, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany.
Pol Maria RommensDepartment of Orthopedics and Traumatology, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany.
Ulrike RitzDepartment of Orthopedics and Traumatology, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany.
Johannes Gutenberg University Mainz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The use of bioactive molecules is a promising approach to enhance the bone healing properties of biomaterials. The aim of this study was to define the role of bone sialoprotein (BSP) immobilized in collagen type I in various settings. In vitro studies with human primary osteoblasts in mono- or in co-culture with endothelial cells demonstrated a slightly increased gene expression of osteogenic markers as well as an increased proliferation rate in osteoblasts after application of BSP immobilized in collagen type I. Two critical size bone defect models were used to analyze bone regeneration. BSP incorporated in collagen type I increased bone regeneration only marginally at one concentration in a calvarial defect model. To induce the mechanical stability, three-dimensional printing was used to produce a stable porous cylinder of polylactide. The cylinder was filled with collagen type I and immobilized BSP and implanted into a femoral defect of critical size in rats. This hybrid material was able to significantly induce bone regeneration. Our study clearly shows the osteogenic effect of BSP when combined with collagen type I as carrier and thereby offers various approaches and options for its use as bioactive molecule in bone substitute materials.

Indexed as

3D printingBone regenerationIn vivo critical size defectsOsteogenesisPolylactide

Identifiers

PMID36105132
PMCPMC9469197
OpenAlexW4288060867

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.