| Literature DB >> 27012556 |
Simona Martinotti1, Mauro Patrone2, Marcello Manfredi2,3, Fabio Gosetti2, Marco Pedrazzi4, Emilio Marengo2, Elia Ranzato2.
Abstract
High mobility group box protein-1 (HMGB1) is released from cells under various pathological conditions and it plays a pivotal role as an alarmin signaling tissue damage. Little is known about the impact of HMGB1 in bone repair and remodeling. To this aim, we focused on HMGB1-induced effects on the in vitro osteoblast model SaOS-2. Cell proliferation was stimulated with a maximum at concentration of 2.5 nM, and such a dose also stimulated cell migration and scratch wound healing. We then characterized the modulatory effect of HMGB1 on bone biology, by using osteogenesis/mineralization assays, a PCR array, and the analysis of a series of osteogenic markers. We performed also a proteomic screening using SWATH-MS on SaOS-2 cell exposed to HMGB1 and we provide evidence for proteins modulated in HMGB1 exposed cells. Taken together, our data demonstrate that SaOS-2 cell proliferation, migration, and osteogenic differentiation were increased by HMGB1. We, therefore, propose that HMGB1 could be a potent bone-remodeling signal but the physiological meaning of this property remains to be more ascertained. J. Cell. Biochem. 117: 2559-2569, 2016.Entities:
Keywords: HMGB1; MIGRATION; OSTEOGENESIS; PCR ARRAY; SCRATCH WOUND ASSAY; SWATH-MS; SaOS-2
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Year: 2016 PMID: 27012556 DOI: 10.1002/jcb.25549
Source DB: PubMed Journal: J Cell Biochem ISSN: 0730-2312 Impact factor: 4.429