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Advanced Dental Care 2018

Dentistry and Craniofacial Research

ISSN: 2576-392X

Page 40

October 08-09, 2018

Moscow, Russia

26

th

International Conference on

Advanced Dental Care

Background:

Predictable regeneration of alveolar bone

defects has always been an important therapeutic challenge

in implant dentistry. Allografts including FDBA and DFDBA are

some substitutes being widely used and reported as having

osteoinductive activities with some degrees of controversy.

Aim:

The aim of this study is to determine the effect of growth

factors (GFs) on osteoinductive activities of different bone

materials.

Materials & Methods:

MG-63 cells were exposed to 60 mg

amounts of four different commercially available freeze-dried

bone allografts with or without 5 ng/mL of two growth factors

(singular or in combination). After 24 and 72 hours of incubation,

the effect of water-soluble allograft released materials and

soluble growth factors on cell viability and proliferation was

assessed using methyl thiazol tetrazolium (MTT) assay. Cell

differentiation and mineralization was respectively assessed by

real-time quantitative reverse transcription PCR (qRT-PCR) and

alizarin red staining after 72 hours of exposure.

Results:

The effect of different GFs on cell/allograft containing

plates was affected by the allograft type. Early proliferative and

late osteoinductive effects of GFs were more consistent in TGF-β

rather than PDGF. PDGF only showed limited osteoinductivity in

terms of accelerating BSP and OC genes.

Conclusions:

Based on the results of this study, TGF-β can have

additional osteoinductive effect on allografts/cells combination

and its application may be beneficial in

in vitro

and clinical

regenerative studies.

ivsure1@gmail.com

Effects of different bone allografts with and

without growth factors on proliferation,

osteogenic differentiation and mineralization of

MG-63 osteoblast-like cells

Surena Vahabi, M Torshaby and A Esmailnejad

Shahid Beheshti Medical University, Iran

Dent Craniofac Res 2018, Volume 3

DOI: 10.21767/2576-392X-C4-012