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Mechanical forces-induced human osteoblasts differentiation involves MMP-2/MMP-13/MT1-MMP proteolytic cascade
Authors:Barthelemi Stéphane  Robinet Julien  Garnotel Roselyne  Antonicelli Frank  Schittly Estelle  Hornebeck William  Lorimier Sandrine
Affiliation:1. Unité INSERM UMRS‐926, “Interface Biomatériaux/Tissus H?tes”, Institut “Biomolécules” (IFR53), Faculté d'Odontologie, Université de Reims Champagne‐Ardenne, 1 Rue du Maréchal Juin, 51095 Reims Cedex, France;2. Faculté d'Odontologie, Université de Reims Champagne‐Ardenne, 2 Rue du Général Koenig, 51095 Reims Cedex, France;3. Unité CNRS UMR 6237, “Matrice Extracellulaire et Dynamique Cellulaire”, Institut “Biomolécules” (IFR53), Faculté de Médecine, 51 Rue Cognac Jay, 51095 Reims Cedex, France
Abstract:
Matrix metalloproteinase (MMP) family proteins play diverse roles in many aspects of cellular processes such as osteoblastic differentiation. Besides, mechanical forces that occur in 3D collagen gel promote the osteoblastic phenotype and accelerate matrix mineralization. Although MMPs have been involved in bone differentiation, the proteolytic cascades triggered by mechanical forces are still not well characterized. In this study, we have investigated the contribution of both proteolytic cascades, MMP-3/MMP-1 and MMP-2/MMP-13/MT1-MMP in the differentiation of human osteoblasts cultured in a floating type I collagen lattice (FL) versus an attached collagen lattice (AL). Compared to AL, contraction of human osteoblasts-populated FL led to a fast (1 day) induction of alkaline phosphatase (ALP), bone sialoprotein (BSP), osteoprotegerin (OPG), and Runx-2 expression. At day 4, osteocalcin (OC) overexpression preceded the formation of calcium-containing nodule formation as assessed by X-ray analyses. MMP-1 and MMP-3 were produced to similar extent by cells cultured in FL and AL, whereas contraction of collagen lattices triggered both mRNA overexpression of MMP-2, MMP-13, and MT1-MMP (i.e., MMP-14), and their activation as evidenced by Western blotting or zymographic analyses. Down-regulating MT1-MMP expression or activity either by siRNA transfection or supplementation of culture medium with TIMP-1 or TIMP-2 highlighted the contribution of that enzyme in OC, ALP, and OPG expression. MMP-2 and MMP-13 were more directly involved in BSP expression. So, these results suggest that the main proteolytic cascade, MMP-2/MMP-13/MT1-MMP, and more particularly, its initial regulator MT1-MMP is involved in osteoblast differentiation through mechanical forces.
Keywords:OSTEOBLAST  COLLAGEN LATTICES  MATRIX METALLOPROTEINASES  DIFFERENTIATION MARKERS  BONE MINERALIZATION
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