The effects of metal ions released from orthopedic implants on nearby bone cells remain largely unknown. The purpose of this study was to examine the acute toxicity of metal ions on osteogenic cells derived from bone marrow. Bone marrow stromal cells were cultured with metal ions found in commonly u
Effects of sublethal metal ion concentrations on osteogenic cells derived from bone marrow stromal cells
β Scribed by Gary J. Thompson; David A. Puleo
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1995
- Tongue
- English
- Weight
- 876 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1045-4861
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Ions released from implant surfaces are suspected of playing some role in osteolysis surrounding metal prostheses. To understand how ions may affect osteogenesis, previous work exposed osteogenic cells to metal ions to study acute cytotoxic responses. The purpose of this study was to assess the longβterm effects of sublethal ion concentrations on osteogenic cell proliferation and function. Bone marrow stromal cells were harvested from juvenile rats and exposed to solutions of ions associated with CoβCrβMo and Tiβ6Alβ4V implants. Cells were cultured for up to 4 weeks and assayed for total protein, alkaline phosphatase, osteocalcin, and calcium. Other than V^+5^, none of the ions affected cell proliferation, indicating that the chosen concentrations were sublethal as desired. V^+5^ elicited delayed gross toxicity not previously observed during acute experiments. At the chosen concentrations, Co^+2^, Cr^+6^, Mo^+6^, and CoβCrβMo alloy elicited little effect on cell proliferation and moderate effects on matrix mineralization. Cultures exposed to Ti^+4^, Al^+3^, and Tiβ6Alβ4V alloy also showed no decrease in cell number, but did show near total suppression of osteocalcin secretion and matrix mineralization. These results suggest that ions released from Ti alloy implants may interfere with osteoblastic cell differentiation, contributing to periprosthetic osteolysis by impairing normal osteogenesis. Β© 1995 John Wiley & Sons, Inc.
π SIMILAR VOLUMES
## Abstract Bioactive glass (BG) is an effective synthetic bone graft material. BG granules of narrow size range (300β355 ΞΌm) have the ability to form new bone tissue inside excavations produced by __in vivo__ resorption. Previously, we demonstrated that BG stimulates the differentiation of culture
## Abstract Hyaluronan (HA) plays a predominant role in tissue morphogenesis, cell migration, proliferation, and cell differentiation. The aims of the present study were to investigate whether (i) prolonged presence of high concentration (4.0 mg/mL) 800 KDa HA and (ii) pretreatment with HA can modi
## Abstract This study aims to investigate the effect of culturing conditions (static and flow perfusion) on the proliferation and osteogenic differentiation of rat bone marrow stromal cells seeded on two novel scaffolds exhibiting distinct porous structures. Specifically, scaffolds based on SEVAβC
## Abstract Coculturing scaffolds with seeded cells __in vitro__ is an indispensable process for construction of engineered tissues. It is essential to understand effects of the constituent particles of scaffold on seeded cells. In this study, we investigated the influence of nanoβsized hydroxyapat