Effects of exogenous phosphorus and silicon on osteoblast differentiation at the interface with bioactive ceramics
✍ Scribed by Gautam Gupta; Sreenatha Kirakodu; Ahmed El-Ghannam
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 741 KB
- Volume
- 95A
- Category
- Article
- ISSN
- 1549-3296
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✦ Synopsis
Abstract
In this study, we have investigated the effects of dissolved phosphorus and silicon on osteoblast differentiation in vitro. Neonatal rat calvarial osteoblasts were seeded on silica–calcium phosphate composites (SCPCS), hydroxyapatite (HA‐200), and tissue culture polystyrene (TCPS) and incubated over 4 days in media containing 0 {minimal essential medium [MEM] (−)} or 3 m__M__ β‐glycerophosphate [MEM (+)]. Inductively coupled plasma analysis showed that P‐content in original MEM (+) was 225% higher than that in MEM (−). Moreover, P‐content in MEM (+) significantly increased to 3.4–4.4 m__M__ and 3.6–4.7 m__M__ after 2 and 4 days incubation with SCPC, respectively, owing to material dissolution and exogenous phosphate supplementation. In contrast, P‐content in MEM (+) showed no change upon incubation with HA or TCPS. The P‐content in MEM (−) incubated with SCPC was considerably lower than that in MEM (+). SCPC exhibited controlled Si‐release in cell culture media [MEM (−) or MEM (+)], with Si‐rich SCPC showing a significantly greater dissolution than Si‐poor SCPC. Moreover, SCPC, unlike HA, demonstrated a cell‐ and solution‐mediated dissolution over 4 days. Quantitative real‐time PCR showed that in MEM (−), osteocalcin and osteopontin mRNA expression on Si‐rich SCPC was significantly greater than that on HA, suggesting that Si plays an important role in enhancing bone‐cell differentiation. However, osteoblast phenotypic expression on SCPC was significantly decreased after 4 days incubation in MEM (+), indicating that sustained exposure to elevated P‐levels in the media can downregulate osteoblast function. Our results demonstrate that the controlled dissolution of SCPC provides a natural stimulus for bone‐cell differentiation in vitro and could obviate the need of exogenous phosphate supplementation. © 2010 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2010.