Ascorbate-induced osteoblast differentiation recruits distinct MMP-inhibitors: RECK and TIMP-2


Autoria(s): ZAMBUZZI, Willian F.; YANO, Claudia L.; CAVAGIS, Alexandre D. M.; PEPPELENBOSCH, Maikel P.; GRANJEIRO, Jose Mauro; FERREIRA, Carmen V.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2009

Resumo

The bone formation executed by osteoblasts represents an interesting research field both for basic and applied investigations. The goal of this work was to evaluate the molecular mechanisms involved during osteoblast differentiation in vitro. Accordingly, we demonstrated that, during the osteoblastic differentiation, TIMP-2 and RECK presented differential expressions, where RECK expression was downregulated from the 14th day in contrast with an increase in TIMP-2. Concomitantly, our results showed a temporal regulation of two major signaling cascades during osteoblast differentiation: proliferation cascades in which RECK, PI3 K, and GSK-3 beta play a pivotal role and latter, differentiation cascades with participation of Ras, Rho, Rac-1, PKC alpha/beta, and TIMP-2. Furthermore, we observed that phosphorylation level of paxillin was downregulated while FAK(125) remained unchangeable, but active during extracellular matrix (ECM) remodeling. Concluding, our results provide evidences that RECK and TIMP-2 are involved in the control of ECM remodeling in distinct phases of osteoblast differentiation by modulating MMP activities and a multitude of signaling proteins governs these events.

FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo[04/14906-2]

Identificador

MOLECULAR AND CELLULAR BIOCHEMISTRY, v.322, n.1/Fev, p.143-150, 2009

0300-8177

http://producao.usp.br/handle/BDPI/26155

10.1007/s11010-008-9951-x

http://dx.doi.org/10.1007/s11010-008-9951-x

Idioma(s)

eng

Publicador

SPRINGER

Relação

Molecular and Cellular Biochemistry

Direitos

closedAccess

Copyright SPRINGER

Palavras-Chave #Osteoblast differentiation #RECK #TIMP-2 #MMP #Signal transduction #PROTEIN-TYROSINE-PHOSPHATASE #MATRIX METALLOPROTEINASES #TISSUE INHIBITORS #MC3T3-E1 CELLS #IN-VITRO #BONE #EXPRESSION #ANGIOGENESIS #STRESS #KINASE #Cell Biology
Tipo

article

original article

publishedVersion