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Effects of Metal Ion Exposure from Joint Prostheses on Organ Systems

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Toxicology".

Deadline for manuscript submissions: closed (31 December 2018) | Viewed by 3479

Special Issue Editor


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Guest Editor
Department of Oncology and Metabolism, University of Sheffield, Sheffield, UK
Interests: joint replacement; epidemiology of implant–host interactions; genetics of musculoskeletal disease; disease biomarkers; metabolic bone disease
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

All metal-containing joint replacement prostheses release metal debris into the local and systemic tissue environments. This debris arises as a result of wear and corrosion at the prosthesis surfaces. Local adverse tissue responses to this released metal have resulted in a substantially higher prosthesis failure rate in prostheses using cobalt–chromium at the bearing surfaces and other modular interfaces. Case reports of severe systemic illness involving cardiac, neurological, and other distant organ systems have also been associated with excessive wear or corrosion of cobalt–chromium alloy-containing prostheses. Despite this burden of clinical disease associated with metal ion exposure, the magnitude of the underlying risk associated with metal-on-metal bearings and interfaces remains unclear and the relevant molecular pathways are poorly characterized.

This Special Issue of the International Journal of Molecular Sciences will focus on recent advances in our understanding of “Adverse Reactions to Metal Debris”, including new insights into the epidemiology as it relates to disease mechanisms, pathogenesis, and molecular biology of ARMD. The issue will include articles addressing both adverse responses at the local tissue level and those addressing the effects at distant organ sites. Topics will include those exploring the relationship between magnitude of exposure and disease burden, the spectrum of organ systems that may be implicated, toxicology, disease biomarkers, and the biological mechanisms that underpin the observed pathologies.

Prof. Dr. Mark Wilkinson
Guest Editor

Manuscript Submission Information

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Keywords

  • cobalt
  • chromium
  • exposure
  • adverse response to metal debris
  • epidemiology
  • pathogenesis
  • biomarker
  • toxicology

Published Papers (1 paper)

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Research

16 pages, 2065 KiB  
Article
Differential Effect of Cobalt and Chromium Ions as Well as CoCr Particles on the Expression of Osteogenic Markers and Osteoblast Function
by Andreas Drynda, Susanne Drynda, Jörn Kekow, Christoph Hubertus Lohmann and Jessica Bertrand
Int. J. Mol. Sci. 2018, 19(10), 3034; https://doi.org/10.3390/ijms19103034 - 05 Oct 2018
Cited by 18 | Viewed by 3262
Abstract
The balance of bone formation and resorption is the result of a regulated crosstalk between osteoblasts, osteoclasts, and osteocytes. Inflammation, mechanical load, and external stimuli modulate this system. Exposure of bone cells to metal ions or wear particles are thought to cause osteolysis [...] Read more.
The balance of bone formation and resorption is the result of a regulated crosstalk between osteoblasts, osteoclasts, and osteocytes. Inflammation, mechanical load, and external stimuli modulate this system. Exposure of bone cells to metal ions or wear particles are thought to cause osteolysis via activation of osteoclasts and inhibition of osteoblast activity. Co2+ ions have been shown to impair osteoblast function and the expression of the three transforming growth factor (TGF)-β isoforms. The current study was performed to analyze how Co2+ and Cr3+ influence the expression, proliferation, and migration profile of osteoblast-like cells. The influence of Co2+, Cr3+, and CoCr particles on gene expression was analyzed using an osteogenesis PCR Array. The expression of different members of the TGF-β signaling cascade were down-regulated by Co2+, as well as several TGF-β regulated collagens, however, Cr3+ had no effect. CoCr particles partially affected similar genes as the Co2+treatment. Total collagen production of Co2+ treated osteoblasts was reduced, which can be explained by the reduced expression levels of various collagens. While proliferation of MG63 cells appears unaffected by Co2+, the migration capacity was impaired. Our data may improve the knowledge of changes in gene expression patterns, and the proliferation and migration effects caused by artificial materials. Full article
(This article belongs to the Special Issue Effects of Metal Ion Exposure from Joint Prostheses on Organ Systems)
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