Abstract
This study aims to define the function of Slug transcription factor in human normal osteoblasts (hOBs). To date, Slug is considered exclusively a marker of malignancy in bone tissue. Here, we identified, for the first time, a role for Slug in hOBs using a knockdown approach. We demonstrated that Slug is positively correlated with osteoblast markers, including Runx2, osteopontin, osteocalcin, Collagen type 1, Wnt/β-catenin signaling mediators, and mineral deposition. At the same time, Slug silencing potentiates the expression of Sox-9, a factor indispensable for chondrogenic development. These data, with the finding that Slug is in vivo recruited by the promoters of Runx2 and Sox-9 genes, suggest that, in hOBs, Slug may act both as positive and negative transcriptional regulator of Runx2 and Sox-9 genes, respectively. In summary, our results support the hypothesis that Slug functions as a novel regulator of osteoblast activity and may be considered a new factor required for osteoblast maturation.
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Acknowledgments
This research was supported by grants from MIUR COFIN-2007, Regione Emilia Romagna, Programma di Ricerca Regione Universita’ 2007–2009, the Fondazione Cassa di Risparmio di Padova e Rovigo. E.L. is a recipient of a fellowship from the Fondazione Cassa di Risparmio di Cento.
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Lambertini, E., Lisignoli, G., Torreggiani, E. et al. Slug gene expression supports human osteoblast maturation. Cell. Mol. Life Sci. 66, 3641–3653 (2009). https://doi.org/10.1007/s00018-009-0149-5
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DOI: https://doi.org/10.1007/s00018-009-0149-5