Vitamin D Promotes MSC Osteogenic Differentiation Stimulating Cell Adhesion and αVβ3 Expression

Author:

Posa Francesca12ORCID,Di Benedetto Adriana1,Cavalcanti-Adam Elisabetta A.2,Colaianni Graziana3ORCID,Porro Chiara1,Trotta Teresa1,Brunetti Giacomina4ORCID,Lo Muzio Lorenzo1ORCID,Grano Maria3ORCID,Mori Giorgio1ORCID

Affiliation:

1. Department of Clinical and Experimental Medicine, Medical School, University of Foggia, Foggia, Italy

2. Institute of Physical Chemistry, Department of Biophysical Chemistry, University of Heidelberg and Max Planck Institute for Intelligent Systems, Stuttgart, Germany

3. Department of Emergency and Organ Transplantation, University of Bari, Bari, Italy

4. Department of Basic and Medical Sciences, Neurosciences and Sense Organs, University of Bari, Bari, Italy

Abstract

Vitamin D (Vit D) by means of its biological active form, 1α,25-dihydroxyvitamin D3 (1,25(OH)2D3), has a protective effect on the skeleton by acting on calcium homeostasis and bone formation. Furthermore, Vit D has a direct effect on mesenchymal stem cells (MSCs) in stimulating their osteogenic differentiation. In this work, we present for the first time the effect of 1,25(OH)2D3 on MSC adhesion. Considering that cell adhesion to the substrate is fundamental for cell commitment and differentiation, we focused on the expression of αVβ3 integrin, which has a key role in the commitment of MSCs to the osteoblastic lineage. Our data indicate that Vit D increases αVβ3 integrin expression inducing the formation of focal adhesions (FAs). Moreover, we assayed MSC commitment in the presence of the extracellular matrix (ECM) glycoprotein fibronectin (FN), which is able to favor cell adhesion on surfaces and also to induce osteopontin (OPN) expression: this suggests that Vit D and FN synergize in supporting cell adhesion. Taken together, our findings provide evidence that Vit D can promote osteogenic differentiation of MSCs through the modulation of αVβ3 integrin expression and its subcellular organization, thus favoring binding with the matrix protein (FN).

Funder

Fondo di Sviluppo e Coesione

Publisher

Hindawi Limited

Subject

Cell Biology,Molecular Biology

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