| Literature DB >> 28621452 |
Viviana Costa1, Valeria Carina1, Simona Fontana2, Angela De Luca1, Francesca Monteleone2, Stefania Pagani3, Maria Sartori4, Stefania Setti5, Cesare Faldini6, Riccardo Alessandro2, Milena Fini3,4, Gianluca Giavaresi1,3.
Abstract
Low-intensity pulsed ultrasound (LIPUS) as an adjuvant therapy in in vitro and in vivo bone engineering has proven to be extremely useful. The present study aimed at investigating the effect of 30 mW/cm2 LIPUS stimulation on commercially available human mesenchymal stem cells (hMSCs) cultured in basal or osteogenic medium at different experimental time points (7, 14, 21 days). The hypothesis was that LIPUS would improve the osteogenic differentiation of hMSC and guarantying the maintenance of osteogenic committed fraction, as demonstrated by cell vitality and proteomic analysis. LIPUS stimulation (a) regulated the balance between osteoblast commitment and differentiation by specific networks (activations of RhoA/ROCK signaling and upregulation of Ribosome constituent/Protein metabolic process, Glycolysis/Gluconeogenesis, RNA metabolic process/Splicing and Tubulins); (b) allowed the maintenance of a few percentage of osteoblast precursors (21 days CD73+/CD90+: 6%; OCT-3/4+/NANOG+/SOX2+: 10%); (c) induced the activation of osteogenic specific pathways shown by gene expression (early: ALPL, COL1A1, late: RUNX2, BGLAP, MAPK1/6) and related protein release (COL1a1, OPN, OC), in particular in the presence of osteogenic soluble factors able to mimic bone microenvironment. To summarize, LIPUS might be able to improve the osteogenic commitment of hMSCs in vitro, and, at the same time, enhance their osteogenic differentiation.Entities:
Keywords: low-intensity pulsed ultrasound; mesenchymal stem cells; osteoblast differentiation; osteogenic commitment; proteomic analysis
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Year: 2017 PMID: 28621452 DOI: 10.1002/jcp.26058
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384