Busca avançada
Ano de início
Entree
(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Titanium-released from dental implant enhances pre-osteoblast adhesion by ROS modulating crucial intracellular pathways

Texto completo
Autor(es):
Rossi, M. C. [1] ; Bezerra, F. J. B. [1] ; Silva, R. A. [1] ; Crulhas, B. P. [1] ; Fernandes, C. J. C. [1] ; Nascimento, A. S. [1] ; Pedrosa, V. A. [1] ; Padilha, P. [1] ; Zambuzzi, W. F. [1]
Número total de Autores: 9
Afiliação do(s) autor(es):
[1] State Univ Sao Paulo UNESP, Dept Chem & Biochem, Biosci Inst, Campus Botucatu, POB 510, BR-18618970 Botucatu, SP - Brazil
Número total de Afiliações: 1
Tipo de documento: Artigo Científico
Fonte: Journal of Biomedical Materials Research Part A; v. 105, n. 11, p. 2968-2976, NOV 2017.
Citações Web of Science: 11
Resumo

It is important to understand the cellular and molecular events that occur at the cell-material interface of implants used for bone repair. The mechanisms involved in the initial stages of osteoblast interactions with the surface of the implant material must be decisive for cell fating surrounding them. In order to address this issue, we decided to investigate if conditioned medium for dental implants was able to modulate murine pre-osteoblast metabolism. First, we determined the concentration of titanium (Ti)-containing conditioned medium and found that it was 2-fold increased (p<0.0001). We have reported that this conditioned medium significantly up-modulated pre-osteoblast adhesion up to 24 h (p<0.0001). In parallel, our results showed that both phosphorylations of FAK (focal adhesion kinase) at Y397 (p<0.0011) and Cofilin at Ser03 (p<0.0053) were also up-modulated, as well as for Rac1 expression (p<0.0175); both of them are involved with cell adaptation by rearranging cytoskeleton actin filaments. Thereafter, Ti-containing medium stimulated ROS (reactive oxygen species) production by pre-osteoblast cells, and it is very possible that ROS compromised PTP-1B (protein tyrosine phosphatase 1B) activation since PTP1B was down-phosphorylated (p<0.0148). The low PTP activity guarantees the phosphorylation of FAK at Y-residue, causing better pre-osteoblast adhesion in response to Ti-containing medium. Altogether, these data indicate that ROS indirectly modulate FAK phosphorylation in response to Ti-released from dental implants. Taken the results in account, these data showed for the first time that the implanted dental device is able to dynamically affect surrounding tissues, mainly by promoting a better performance of the pre-osteoblast cells. (c) 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 105A: 2968-2976, 2017. (AU)

Processo FAPESP: 14/22689-3 - Sinalização parácrina mediada por microvesículas e proteínas entre células ósseas e endoteliais durante o desenvolvimento e regeneração do tecido ósseo
Beneficiário:Willian Fernando Zambuzzi
Modalidade de apoio: Auxílio à Pesquisa - Jovens Pesquisadores