Macrophage Induced Effect of Particulate Silica on Rat Mesenchymal Stem Cells In Vitro

Article Preview

Abstract:

The role of silica and macrophages in fibrosis is well documented, but in bone formation it is relatively unknown despite decades of research with bioactive glasses. In this study macrophages were isolated from rat peritoneal and then cultured for five days in the presence of two types of silica microparticles with different solubilities. After the fifth day the culture medium was collected, purified and used as an additive in bone marrow derived rat stem cell cultures. The stem cells were cultured for five days in α-mem containing only 0,5% of FCS, enabling cell survival but disrupting their proliferation. As controls, stem cells were also cultured in α-mem containing silica microparticles. At days one and five the amount of soluble collagen was assayed from the culture medium and the cells were counted. All stem cell cultures with macrophage medium additives were found to be proliferative, with statistically significant difference to controls. However, collagen was only produced in cultures containing medium from macrophages cultured with fast-dissolving silica microparticles. This suggests that silica can induce cell proliferation and extra cellular matrix protein secretion which is mediated by macrophages, and that the solubility of silica is also a major factor in this reaction.

You might also be interested in these eBooks

Info:

Periodical:

Key Engineering Materials (Volumes 396-398)

Pages:

123-126

Citation:

Online since:

October 2008

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2009 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] M. Aalto and E. Kulonen. Acta Pathol Microbiol Scand. Vol. 87 (1979) pp.241-50.

Google Scholar

[2] R. Rago, J. Mitchen and G Wilding. Anal Biochem. Vol. 191 (1990) pp.31-4.

Google Scholar

[3] C.J. Brinker and G.W. Scherer: Sol-Gel Science: The Physics and Chemistry of Sol-Gel Processing (Academic Press Inc. San Diego, USA 1990).

DOI: 10.1080/10426919308934843

Google Scholar

[4] J. Paul, in: Cell and Tissue Culture 5th edn, 221 (Churchill Livingstone, New York, 1975).

Google Scholar

[5] VV. Yurovsky. Am J Respir Cell Mol Biol. Vol. 28 (2003) pp.225-31. Soluble Collagen 0, 0 2, 0 4, 0 6, 0 8, 0 10, 0 12, 0 Fast dissolving SiO2 Slow dissolving SiO2 No SiO2 ug/ml Control Macrophage-treated.

Google Scholar