Cytotoxicity of glass ionomer cement on human exfoliated deciduous teeth stem cells correlates with released fluoride, strontium and aluminum ion concentrations
Stem cells from human exfoliated deciduous teeth (SHED) can be used as a cell-based therapy in regenerative medicine and in immunomodulation. Pulp from human deciduous teeth can be stored as a source of SHED. Glass ionomer cements (GICs) are commonly used in restorative dentistry and in cav...
Main Authors: | , , , , , |
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Format: | Article |
Language: | English |
Published: |
University of Belgrade, University of Novi Sad
2015-01-01
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Series: | Archives of Biological Sciences |
Subjects: | |
Online Access: | http://www.doiserbia.nb.rs/img/doi/0354-4664/2015/0354-46641500022K.pdf |
Summary: | Stem cells from human exfoliated deciduous teeth (SHED) can be used as a
cell-based therapy in regenerative medicine and in immunomodulation. Pulp
from human deciduous teeth can be stored as a source of SHED. Glass ionomer
cements (GICs) are commonly used in restorative dentistry and in cavity
lining. GICs have lower biocompatibility and are cytotoxic for dental pulp
cells. In this study, seven commonly used GICs were tested for their
cytotoxic effects on SHED, for their potential to arrest mitosis in cells and
induce chromosome aberrations, and were compared with the effects of
composite. Fuji II, Fuji VIII, Fuji IX, Fuji plus and Vitrebond had
significantly higher cytotoxic effects on SHED than composite. Only SHEDs
that have been treated with Fuji I, Fuji IX, Fuji plus and composite
recovered the potential for proliferation, but no chromosome aberrations were
found after treatment with GICs. The cytotoxic effects of GICs on SHEDs were
in strong correlation with combined concentrations of released fluoride,
aluminum and strontium ions. Fuji I exhibited the lowest activity towards
SHEDs; it did not interrupt mitosis and did not induce chromosome
aberrations, and was accompanied by the lowest levels of released F, Al and
Sr ions. Projekat Ministarstva nauke Republike Srbije, br. ON175069, br.
ON175071 i br. ON175103] |
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ISSN: | 0354-4664 1821-4339 |