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dc.contributor.authorManzano-Moreno, Francisco Javier
dc.contributor.authorMedina Huertas, Rosa María
dc.contributor.authorRamos Torrecillas, Javier 
dc.contributor.authorGarcía Martínez, Olga 
dc.contributor.authorRuiz Rodríguez, Concepción 
dc.date.accessioned2024-09-04T10:49:16Z
dc.date.available2024-09-04T10:49:16Z
dc.date.issued2015-11
dc.identifier.urihttps://hdl.handle.net/10481/93925
dc.description.abstractObjectives: The objective of this study was to determine the effect of LLDL therapy on the gene expression of osteoblast markers of growth and differentiation. Materials and methods: The MG-63 cell line was exposed to diode laser (ezLase) of 940 nm at 1-1.5 W and 3-4 J, and gene expressions (Runx-2, alkaline phosphatase [ALP], type I collagen [Col-I], osterix [OSX], osteocalcin [OSC], osteoprotegerin [OPG], bone morphogenetic protein [BMP]-2 and -7, transforming growth factor-β1 [TGF-β1], and TGF-β receptors [TGF-β R1, TGF-β R2; TGF-β R3]) were evaluated by quantitative RT-PCR. Results: LLDL treatment stimulated the expression of osteoblast differentiation markers ALP, Col-I, Runx-2, and OSX in relation to the doses applied (P < 0.05), but no changes were detected in OSC, OPG, or BMP-7 at any study dose. This effect may be mediated by TGF-β1 and BMP-2, given that the treatment increased their expression and that of TGF-β receptors R1, R2, and R3 (P < 0.001). Conclusion: These results suggest that the biostimulatory effect of laser therapy on osteoblasts may be attributable to the release of autocrine factors in response to the irradiation. A clinical trial is warranted to test its therapeutic usefulness in bone tissue regeneration and to define a treatment protocol.es_ES
dc.language.isoenges_ES
dc.rightsAttribution-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nd/4.0/*
dc.subjectBiostimulatory effectes_ES
dc.subjectGene expressiones_ES
dc.subjectLow-level diode laser therapyes_ES
dc.titleThe effect of low-level diode laser therapy on early differentiation of osteoblast via BMP-2/TGF-β1 and its receptorses_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.1016/j.jcms.2015.08.026
dc.type.hasVersionAMes_ES


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Attribution-NoDerivatives 4.0 Internacional
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