Osteoblast adhesion dynamics: a possible role for ROS and LMW-PTP

Gustavo V. O. Fernandes, Alexandre D. M. Cavagis, Carmen V. Ferreira, Beni Olej, Maurício de Souza Leão, Cláudia L. Yano, Maikel Peppelenbosch, José Mauro Granjeiro, Willian F. Zambuzzi*

*Autor correspondente para este trabalho

Resultado de pesquisarevisão de pares

29 Citações (Scopus)

Resumo

Reactive oxygen species (ROS) modulate a variety of intracellular events, but their role in osteoblast adhesion and spreading remains unclear. ROS is a very-known physiological modulators of Protein Tyrosine Phosphatases activities, mainly to low molecular weight protein tyrosine phosphatase (LMW-PTP) activity. As this biological mechanism is not clear in osteoblast adhesion, we decided to investigate ROS levels and phosphorylations of FAK and Src, identifying these proteins as potential substrates to LMW-PTP activity. Our results showed that during osteoblast adhesion/spreading (30 min and 2 h of seeding) the intracellular ROS content (hydrogen peroxide) is finely regulated by an effective anti-oxidant system [catalase and Superoxide Dismutase (SOD) activities were evaluated]. During the first 30 min of adhesion, there was an increase in ROS production and a concomitant increase in focal adhesion kinase (FAK) activity after its phosphorylation at Tyrosine 397 (Y397). Moreover, after 2 h there was a decrease in ROS content and FAK phosphorylation. There was no significant change in LMW-PTP expression at 30 min or 2 h. In order to validate our hypothesis that LMW-PTP is able to control FAK activity by modulating its phosphorylation status, we decided to overexpress and silence LMW-PTP in this context. Our results showed that FAK phosphorylation at Y 397 was increased and decreased in osteoblasts with silenced or overexpressed LMW-PTP, respectively. Together, these data show that ROS modulate FAK phosphorylation by an indirect way, suggesting that a LMW-PTP/FAK supra-molecular complex is involved in transient responses during osteoblast adhesion and spreading.
Idioma originalEnglish
Páginas (de-até)1063-1069
Número de páginas7
RevistaJournal of Cellular Biochemistry
Volume115
Número de emissão6
DOIs
Estado da publicaçãoPublicado - jun 2014
Publicado externamenteSim

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