Calcium sulfate: Analysis of MG63 osteoblast-like cell response by means of a microarray technology

被引:37
作者
Carinci, F
Piattelli, A
Stabellini, G
Palmieri, A
Scapoli, L
Laino, G
Caputi, S
Pezzetti, F
机构
[1] Univ Ferrara, I-44100 Ferrara, Italy
[2] Univ G dAnnunzio, Dent Clin, I-66100 Chieti, Italy
[3] Univ Milan, Inst Histol, I-20133 Milan, Italy
[4] Univ Ferrara, Dept Morphol & Embryol, I-44100 Ferrara, Italy
[5] Univ Naples Federico II, Dent Clin, I-80138 Naples, Italy
[6] Univ Bologna, Inst Histol, I-40126 Bologna, Italy
[7] CARISBO Fdn, Ctr Mol Genet, I-40126 Bologna, Italy
关键词
calcium sulfate; DNA microarray; gene expression; gene profiling;
D O I
10.1002/jbm.b.30133
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
Calcium sulfate (CaS) is an highly biocompatible material that has the characteristic of being one of the simplest as well as one of the synthetic bone-like graft with the longest clinical history, spanning more than 100 years. Solidified or crystallized CaS is very osteogenic in vivo. As the surface CaS dissolves in body fluid, the calcium ions form calcium phosphate that reprecipitates on the surface forming an osteoblast "friendly" environment. How this "friendly" environment alters osteoblast activity to promote bone formation is poorly understood. We therefore attempted to address this question by using microarray techniques to identified genes that are differently regulated in osteoblasts exposed to CaS. By using DNA microarrays containing 19,200 genes, we identified in osteoblast-like cells line (MG-63) cultured with CaS (Surgiplaster, Classimplant, Roma, Italy) several genes that expression was significantly upregulated. The differentially expressed genes cover a broad range of functional activities: (a) immunity, (b) lysosomal enzymes production, (c) cell cycle regulation, (d) and signaling transduction. It was also possible to detect some genes whose function is unknown. The data reported are, to our knowledge, the first genetic portrait of CaS effects. They can be relevant to better understand the molecular mechanism of bone regeneration and as a model for comparing other materials with similar clinical effects. (C) 2004 Wiley Periodicals, Inc.
引用
收藏
页码:260 / 267
页数:8
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