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1000 Titel
  • Use of in vitro bone models to screen for altered bone metabolism, osteopathies, and fracture healing: challenges of complex models
1000 Autor/in
  1. Ehnert, Sabrina |
  2. Rinderknecht, Helen |
  3. Aspera-Werz, Romina H. |
  4. Häussling, Victor |
  5. Nussler, Andreas |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-09-10
1000 Erschienen in
1000 Quellenangabe
  • 94(12):3937-3958
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00204-020-02906-z |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7655582/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Approx. every third hospitalized patient in Europe suffers from musculoskeletal injuries or diseases. Up to 20% of these patients need costly surgical revisions after delayed or impaired fracture healing. Reasons for this are the severity of the trauma, individual factors, e.g, the patients' age, individual lifestyle, chronic diseases, medication, and, over 70 diseases that negatively affect the bone quality. To investigate the various disease constellations and/or develop new treatment strategies, many in vivo, ex vivo, and in vitro models can be applied. Analyzing these various models more closely, it is obvious that many of them have limits and/or restrictions. Undoubtedly, in vivo models most completely represent the biological situation. Besides possible species-specific differences, ethical concerns may question the use of in vivo models especially for large screening approaches. Challenging whether ex vivo or in vitro bone models can be used as an adequate replacement for such screenings, we here summarize the advantages and challenges of frequently used ex vivo and in vitro bone models to study disturbed bone metabolism and fracture healing. Using own examples, we discuss the common challenge of cell-specific normalization of data obtained from more complex in vitro models as one example of the analytical limits which lower the full potential of these complex model systems.
1000 Sacherschließung
lokal Endothelial Cells/pathology [MeSH]
lokal Bone Diseases/metabolism [MeSH]
lokal Osteoclasts/metabolism [MeSH]
lokal Bone Remodeling [MeSH]
lokal Cell Communication [MeSH]
lokal Osteoblasts/metabolism [MeSH]
lokal Ex vivo bone cultures
lokal Osteoclasts/pathology [MeSH]
lokal 2D/3D
lokal Bone Diseases/pathology [MeSH]
lokal Disease Models, Animal [MeSH]
lokal Fracture Healing [MeSH]
lokal Osteoclast
lokal Bone and Bones/metabolism [MeSH]
lokal Endothelial Cells/metabolism [MeSH]
lokal Bone and Bones/physiopathology [MeSH]
lokal Humans [MeSH]
lokal Review Article
lokal Animals [MeSH]
lokal Osteoblast/osteocyte
lokal Osteocytes/metabolism [MeSH]
lokal Osteocytes/pathology [MeSH]
lokal Tissue Culture Techniques [MeSH]
lokal Endothelial cells
lokal Bone Diseases/physiopathology [MeSH]
lokal Osteoblasts/pathology [MeSH]
lokal Bone and Bones/pathology [MeSH]
lokal Cell Culture Techniques [MeSH]
lokal Co-culture
lokal Cells, Cultured [MeSH]
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0003-4347-1702|https://frl.publisso.de/adhoc/uri/UmluZGVya25lY2h0LCBIZWxlbg==|https://frl.publisso.de/adhoc/uri/QXNwZXJhLVdlcnosIFJvbWluYSBILg==|https://frl.publisso.de/adhoc/uri/SMOkdXNzbGluZywgVmljdG9y|https://orcid.org/0000-0002-6666-6791
1000 Hinweis
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1000 Erstellt am 2023-11-16T22:24:54.999+0100
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1000 Zuletzt bearbeitet 2023-12-01T04:06:23.351+0100
1000 Objekt bearb. Fri Dec 01 04:06:23 CET 2023
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