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Toxic mechanisms of Roth801, Canals, microparticles and nanoparticles of ZnO on MG-63 osteoblasts.

Identifieur interne : 000002 ( Main/Exploration ); précédent : 000001; suivant : 000003

Toxic mechanisms of Roth801, Canals, microparticles and nanoparticles of ZnO on MG-63 osteoblasts.

Auteurs : Mei-Chi Chang [Taïwan] ; Chia-Mei Tang [Taïwan] ; Yu-Heng Lin [Taïwan] ; Hsin-Cheng Liu [Taïwan] ; Tong-Mei Wang [Taïwan] ; Wen-Chien Lan [Taïwan] ; Ru-Hsiu Cheng [Taïwan] ; Yan-Ru Lin [Taïwan] ; Hsiao-Hua Chang [Taïwan] ; Jiiang-Huei Jeng [Taïwan]

Source :

RBID : pubmed:33321673

Descripteurs français

English descriptors

Abstract

ZnO eugenol-based materials are widely used for restoration of caries cavity, apical retrograde filling and root canal sealer. Their effects on apical bone healing await investigation. The toxic mechanisms of ZnO particles and nanoparticles to MG-63 osteoblastic cells were studied. We found the different morphology and size of various particles as observed by scanning electron microscope. Particles of Canals and Roth801 were larger than ZnO-205532 microparticles and ZnO-677450 nanoparticles. Four ZnO particles showed cytotoxicity (>25 μg/ml) as analyzed by MTT. Transmission electron microscope found intracellular vacuoles with particle content. Exposure to ZnO particles induced ROS production and cell cycle arrest as studied by DCF and propidium iodide flow cytometry. ZnO particles activated ATM, ATR, Chk1, Chk2, γ-H2AX, ERK and p38 phosphorylation as detected by immunofluorescent staining and western blotting. The protein expression of cdc2, cyclin B1 and cdc25C were decreased, whereas GADD45α and hemeoxygenase-1 (HO-1) were stimulated. ZnO particles' cytotoxicity to MG63 cells was prevented by N-acetylcysteine (NAC), but not CGK733, AZD7762, U0126 and SB203580. ZnO showed little effect on IL-8 and sICAM-1 secretion. These results indicated that ZnO particles are toxic to osteoblasts. ZnO particles' toxicity were related to ROS, and DNA damage responses, checkpoint kinases, cell cycle arrest, ERK and p38 signaling, but not IL-8 and ICAM-1. These results were useful for materials' development and promote apical healing. Dentists should avoid of extruding ZnO-based sealers excessively over root apex and prevent residual ZnO-based retrograde filling materials in apical area during endodontic practice.

DOI: 10.1016/j.msec.2020.111635
PubMed: 33321673


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<div type="abstract" xml:lang="en">ZnO eugenol-based materials are widely used for restoration of caries cavity, apical retrograde filling and root canal sealer. Their effects on apical bone healing await investigation. The toxic mechanisms of ZnO particles and nanoparticles to MG-63 osteoblastic cells were studied. We found the different morphology and size of various particles as observed by scanning electron microscope. Particles of Canals and Roth801 were larger than ZnO-205532 microparticles and ZnO-677450 nanoparticles. Four ZnO particles showed cytotoxicity (>25 μg/ml) as analyzed by MTT. Transmission electron microscope found intracellular vacuoles with particle content. Exposure to ZnO particles induced ROS production and cell cycle arrest as studied by DCF and propidium iodide flow cytometry. ZnO particles activated ATM, ATR, Chk1, Chk2, γ-H2AX, ERK and p38 phosphorylation as detected by immunofluorescent staining and western blotting. The protein expression of cdc2, cyclin B1 and cdc25C were decreased, whereas GADD45α and hemeoxygenase-1 (HO-1) were stimulated. ZnO particles' cytotoxicity to MG63 cells was prevented by N-acetylcysteine (NAC), but not CGK733, AZD7762, U0126 and SB203580. ZnO showed little effect on IL-8 and sICAM-1 secretion. These results indicated that ZnO particles are toxic to osteoblasts. ZnO particles' toxicity were related to ROS, and DNA damage responses, checkpoint kinases, cell cycle arrest, ERK and p38 signaling, but not IL-8 and ICAM-1. These results were useful for materials' development and promote apical healing. Dentists should avoid of extruding ZnO-based sealers excessively over root apex and prevent residual ZnO-based retrograde filling materials in apical area during endodontic practice.</div>
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<AbstractText>ZnO eugenol-based materials are widely used for restoration of caries cavity, apical retrograde filling and root canal sealer. Their effects on apical bone healing await investigation. The toxic mechanisms of ZnO particles and nanoparticles to MG-63 osteoblastic cells were studied. We found the different morphology and size of various particles as observed by scanning electron microscope. Particles of Canals and Roth801 were larger than ZnO-205532 microparticles and ZnO-677450 nanoparticles. Four ZnO particles showed cytotoxicity (>25 μg/ml) as analyzed by MTT. Transmission electron microscope found intracellular vacuoles with particle content. Exposure to ZnO particles induced ROS production and cell cycle arrest as studied by DCF and propidium iodide flow cytometry. ZnO particles activated ATM, ATR, Chk1, Chk2, γ-H2AX, ERK and p38 phosphorylation as detected by immunofluorescent staining and western blotting. The protein expression of cdc2, cyclin B1 and cdc25C were decreased, whereas GADD45α and hemeoxygenase-1 (HO-1) were stimulated. ZnO particles' cytotoxicity to MG63 cells was prevented by N-acetylcysteine (NAC), but not CGK733, AZD7762, U0126 and SB203580. ZnO showed little effect on IL-8 and sICAM-1 secretion. These results indicated that ZnO particles are toxic to osteoblasts. ZnO particles' toxicity were related to ROS, and DNA damage responses, checkpoint kinases, cell cycle arrest, ERK and p38 signaling, but not IL-8 and ICAM-1. These results were useful for materials' development and promote apical healing. Dentists should avoid of extruding ZnO-based sealers excessively over root apex and prevent residual ZnO-based retrograde filling materials in apical area during endodontic practice.</AbstractText>
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<Keyword MajorTopicYN="N">Nanoparticles</Keyword>
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<Keyword MajorTopicYN="N">Signal transduction</Keyword>
<Keyword MajorTopicYN="N">Toxicity</Keyword>
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<Year>2020</Year>
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<ArticleId IdType="pubmed">33321673</ArticleId>
<ArticleId IdType="pii">S0928-4931(20)33553-0</ArticleId>
<ArticleId IdType="doi">10.1016/j.msec.2020.111635</ArticleId>
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<li>Taïwan</li>
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<name sortKey="Chang, Mei Chi" sort="Chang, Mei Chi" uniqKey="Chang M" first="Mei-Chi" last="Chang">Mei-Chi Chang</name>
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<name sortKey="Chang, Hsiao Hua" sort="Chang, Hsiao Hua" uniqKey="Chang H" first="Hsiao-Hua" last="Chang">Hsiao-Hua Chang</name>
<name sortKey="Cheng, Ru Hsiu" sort="Cheng, Ru Hsiu" uniqKey="Cheng R" first="Ru-Hsiu" last="Cheng">Ru-Hsiu Cheng</name>
<name sortKey="Jeng, Jiiang Huei" sort="Jeng, Jiiang Huei" uniqKey="Jeng J" first="Jiiang-Huei" last="Jeng">Jiiang-Huei Jeng</name>
<name sortKey="Lan, Wen Chien" sort="Lan, Wen Chien" uniqKey="Lan W" first="Wen-Chien" last="Lan">Wen-Chien Lan</name>
<name sortKey="Lin, Yan Ru" sort="Lin, Yan Ru" uniqKey="Lin Y" first="Yan-Ru" last="Lin">Yan-Ru Lin</name>
<name sortKey="Lin, Yu Heng" sort="Lin, Yu Heng" uniqKey="Lin Y" first="Yu-Heng" last="Lin">Yu-Heng Lin</name>
<name sortKey="Liu, Hsin Cheng" sort="Liu, Hsin Cheng" uniqKey="Liu H" first="Hsin-Cheng" last="Liu">Hsin-Cheng Liu</name>
<name sortKey="Tang, Chia Mei" sort="Tang, Chia Mei" uniqKey="Tang C" first="Chia-Mei" last="Tang">Chia-Mei Tang</name>
<name sortKey="Wang, Tong Mei" sort="Wang, Tong Mei" uniqKey="Wang T" first="Tong-Mei" last="Wang">Tong-Mei Wang</name>
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