MG63 and MC3T3-E1 Osteoblastic Cell Lines Response to Raloxifene

Bone resorption in edentulous regions often results in inadequate ridge for implant osseointegration. In order to overcome this problem, the use of osteoconductive biomaterials has been proposed as a carrier for different types of pharmacological molecules. Since raloxifene, a drug used in osteoporo...

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Published in:European journal of inflammation Vol. 11; no. 3; pp. 797 - 804
Main Authors: Muzio, L. Lo, Santarelli, A., Orsini, G., Memè, L., Mattioli-Belmonte, M., De Florio, I., Gatto, R., Gallusi, G., Nocini, P.F., Bertossi, D., Emanuelli, M., Putignano, A., Bambini, F.
Format: Journal Article
Language:English
Published: London, England SAGE Publications 01-09-2013
SAGE PUBLICATIONS, INC
SAGE Publishing
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Summary:Bone resorption in edentulous regions often results in inadequate ridge for implant osseointegration. In order to overcome this problem, the use of osteoconductive biomaterials has been proposed as a carrier for different types of pharmacological molecules. Since raloxifene, a drug used in osteoporosis therapy, inhibits the osteoclast, but not osteoblast functions, it has been suggested to improve recovery during implant surgery. The present work evaluated in vitro the effect of raloxifene on two different cell populations: the human osteoblast-like cells (MG63) and osteoblasts derived from rat calvaria (MC3T3-E1). The morpho-functional investigations carried out showed a different behavior of the two cell lines. Raloxifene showed a stimulatory effect towards MG63 cell proliferation with a significant increase in cell viability after 7 days of culture. On the contrary, MC3T3-E1 cells showed a significant reduction in cell viability, when compared with the same cells at 72 h, or with the control cell population. The predominantly proliferative effect of raloxifene on MG63 cells is partly confirmed by the reduction of alkaline phosphatase activity, an early marker of osteoblast differentiation. The different effect of raloxifene on osteoblastic population in relationship to the type and age of the cell is an issue that needs further investigation.
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ISSN:2058-7392
1721-727X
2058-7392
DOI:10.1177/1721727X1301100322