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Fracture Healing Research-Shift towards In Vitro Modeling?

作者信息

Pfeiffenberger Moritz, Damerau Alexandra, Lang Annemarie, Buttgereit Frank, Hoff Paula, Gaber Timo

机构信息

Department of Rheumatology and Clinical Immunology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, 10117 Berlin, Germany.

German Rheumatism Research Centre Berlin (DRFZ), The Leibniz Institute, 10117 Berlin, Germany.

出版信息

Biomedicines. 2021 Jun 28;9(7):748. doi: 10.3390/biomedicines9070748.


DOI:10.3390/biomedicines9070748
PMID:34203470
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8301383/
Abstract

Fractures are one of the most frequently occurring traumatic events worldwide. Approximately 10% of fractures lead to bone healing disorders, resulting in strain for affected patients and enormous costs for society. In order to shed light into underlying mechanisms of bone regeneration (habitual or disturbed), and to develop new therapeutic strategies, various in vivo, ex vivo and in vitro models can be applied. Undeniably, in vivo models include the systemic and biological situation. However, transferability towards the human patient along with ethical concerns regarding in vivo models have to be considered. Fostered by enormous technical improvements, such as bioreactors, on-a-chip-technologies and bone tissue engineering, sophisticated in vitro models are of rising interest. These models offer the possibility to use human cells from individual donors, complex cell systems and 3D models, therefore bridging the transferability gap, providing a platform for the introduction of personalized precision medicine and finally sparing animals. Facing diverse processes during fracture healing and thus various scientific opportunities, the reliability of results oftentimes depends on the choice of an appropriate model. Hence, we here focus on categorizing available models with respect to the requirements of the scientific approach.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acdb/8301383/469c127d9262/biomedicines-09-00748-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acdb/8301383/469c127d9262/biomedicines-09-00748-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acdb/8301383/469c127d9262/biomedicines-09-00748-g001.jpg

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本文引用的文献

[1]
Functional Scaffold-Free Bone Equivalents Induce Osteogenic and Angiogenic Processes in a Human In Vitro Fracture Hematoma Model.

J Bone Miner Res. 2021-6

[2]
Effect of platelet-rich plasma on fracture healing.

Injury. 2021-6

[3]
Ex vivo Bone Models and Their Potential in Preclinical Evaluation.

Curr Osteoporos Rep. 2021-2

[4]
A Human Osteochondral Tissue Model Mimicking Cytokine-Induced Key Features of Arthritis In Vitro.

Int J Mol Sci. 2020-12-24

[5]
Fibro-porous PLLA/gelatin composite membrane doped with cerium oxide nanoparticles as bioactive scaffolds for future angiogenesis.

J Mater Chem B. 2020-9-15

[6]
Immobilizing magnesium ions on 3D printed porous tantalum scaffolds with polydopamine for improved vascularization and osteogenesis.

Mater Sci Eng C Mater Biol Appl. 2020-12

[7]
The osteoporosis treatment gap in patients at risk of fracture in European primary care: a multi-country cross-sectional observational study.

Osteoporos Int. 2021-2

[8]
Vascular endothelial growth factor for in vivo bone formation: A systematic review.

J Orthop Translat. 2020-6-7

[9]
Macroscale mesenchymal condensation to study cytokine-driven cellular and matrix-related changes during cartilage degradation.

Biofabrication. 2020-8-10

[10]
The in vitro human fracture hematoma model - a tool for preclinical drug testing.

ALTEX. 2020

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