Advanced Search

Home > Journals > Minerva Stomatologica > Past Issues > Minerva Stomatologica 2010 May;59(5) > Minerva Stomatologica 2010 May;59(5):259-70

ISSUES AND ARTICLES   MOST READ   eTOC

CURRENT ISSUEMINERVA STOMATOLOGICA

A Journal on Dentistry and Maxillofacial Surgery

Official Journal of the Italian Society of Odontostomatology and Maxillofacial Surgery
Indexed/Abstracted in: CAB, EMBASE, Index to Dental Literature, PubMed/MEDLINE, Scopus, Emerging Sources Citation Index

Frequency: Bi-Monthly

ISSN 0926-4970

Online ISSN 1827-174X

 

Minerva Stomatologica 2010 May;59(5):259-70

    ORIGINAL ARTICLES

In vitro expression of osteoblastic phenotype on titanium surfaces

Ramaglia L. 1, Capece G. 1, Di Spigna G. 2, Esposito D. 1, Postiglione L. 2

1 Department of Dental and Maxillofacial Surgery Federico II University, Naples, Italy;
2 Department of Biology and Cellular and Molecular Pathology, Federico II University, Naples, Italy

AIM: Differentiation toward the osteoblastic phenotype is a complex phenomenon regulated by means of several factors. Numerous studies in vitro et in vivo showed that surface properties of titanium dental implants modulate cell proliferation and osteoblastic differentiation, affecting bone healing processes. Optimal superficial morphology is still controversial. The aim of the present study was to evaluate in vitro the effects of two different titanium surfaces on biological behaviour of human osteoblast-like cells SaOS-2 with regard to production of extra-cellular matrix (ECM) proteins.
MEHODS: Human osteoblast-like cells SaOS-2, cultured on commercially pure titanium disks with two different surface topographies, smooth and microstructured with sand-blasting and acid-etching treatment, were evaluated by investigating adhesion, proliferation and deposition of extra-cellular matrix (ECM) proteins Fibronectin, Tenascin and Collagen I.
RESULTS: The different values of cellular adhesion at three hours and the increase of SaOS-2 proliferation values at the different experimental times on both evaluated surfaces didn’t result statistically significant. ECM deposition analysis showed that Fibronectin, Tenascin and Collagen I were gradually produced, with not statistically significant differences for Fibrone-ctin and Tenascin and statistically significant differences for Collagen I.
CONCLUSION: Implant surface properties modulate in vitro the biological behavior of osteoblasts-like cells SaOS-2. SaOS-2 cells proliferate on both evaluated surfaces, showing a more organized differentiation towards an osteoblastic phenotype in ECM proteins production when cultured on microstructured surface.

language: English, Italian


FULL TEXT  REPRINTS

top of page