Palmieri Annalisa, Pezzetti Furio, Brunelli Giorgio, Scapoli Luca, Lo Muzio Lorenzo, Scarano Antonio, Martinelli Marcella, Carinci Francesco
Institute of Histology, University of Bologna and Center of Molecular Genetics, CARISBO Foundation, Bologna, Italy.
J Biomed Mater Res B Appl Biomater. 2008 Feb;84(2):369-74. doi: 10.1002/jbm.b.30880.
Calcium sulfate (CaS) is a highly biocompatible material and enhances bone formation in vivo. However, how CaS alters osteoblast activity to promote bone formation is incompletely understood. We therefore investigated the translation regulation in osteoblasts exposed to CaS by using microRNA microarray techniques. Transduction, transcription, and translation are the three levels of regulation of cell activity. Recently, a new type of translation regulation has been identified: RNA interference (RNAi). RNAi is a process in which microRNA, (miRNA), that is, noncoding RNAs of 19-23 nucleotides can induce sequence-specific mRNA degradation and/or translational repression. The human genome encodes a few hundred miRNAs that can post-transcriptionally repress thousands of genes. The miRNA oligonucleotide microarray provides a novel method of carrying out genome-wide miRNA profiling in human samples. By using miRNA microarrays containing 329 probes designed from Human miRNA sequences, we identified in osteoblast-like cells line (MG-63) cultured with CaS (Surgiplaster, Classimplant, Roma, Italy) several miRNA whose expression is significantly modified. The data reported are, to our knowledge, the first study on translation regulation in osteoblasts exposed to CaS. They could be relevant to a better understanding of the molecular mechanism of bone regeneration and as a model for comparing other materials with similar clinical effects.
硫酸钙(CaS)是一种具有高度生物相容性的材料,可增强体内骨形成。然而,CaS如何改变成骨细胞活性以促进骨形成尚不完全清楚。因此,我们使用微小RNA微阵列技术研究了暴露于CaS的成骨细胞中的翻译调控。转导、转录和翻译是细胞活性调控的三个层面。最近,一种新型的翻译调控已被确定:RNA干扰(RNAi)。RNAi是一个过程,其中微小RNA(miRNA),即19 - 23个核苷酸的非编码RNA,可诱导序列特异性mRNA降解和/或翻译抑制。人类基因组编码数百种miRNA,它们可在转录后抑制数千个基因。miRNA寡核苷酸微阵列提供了一种在人类样本中进行全基因组miRNA谱分析的新方法。通过使用包含从人类miRNA序列设计的329个探针的miRNA微阵列,我们在与CaS(Surgiplaster,Classimplant,罗马,意大利)一起培养的成骨样细胞系(MG - 63)中鉴定出几种表达显著改变的miRNA。据我们所知,所报道的数据是关于暴露于CaS的成骨细胞中翻译调控的首次研究。它们可能有助于更好地理解骨再生的分子机制,并作为比较具有类似临床效果的其他材料的模型。