Effects of nicotine on cell growth, migration, and production of inflammatory cytokines and reactive oxygen species by cementoblasts

Background/purpose: Cigarette smoking is an important risk factor in the pathogenesis of periodontal disease. However, little is known about the effect of nicotine, the major component of cigarette smoke, on cementoblasts. The aim of this study was to investigate the pathological effects of nicotine...

Full description

Bibliographic Details
Main Authors: Chun-San Chen, Shiuan-Shinn Lee, Hui-Chieh Yu, Fu-Mei Huang, Yu-Chao Chang
Format: Article
Language:English
Published: Elsevier 2015-06-01
Series:Journal of Dental Sciences
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1991790214000403
_version_ 1819296073610428416
author Chun-San Chen
Shiuan-Shinn Lee
Hui-Chieh Yu
Fu-Mei Huang
Yu-Chao Chang
author_facet Chun-San Chen
Shiuan-Shinn Lee
Hui-Chieh Yu
Fu-Mei Huang
Yu-Chao Chang
author_sort Chun-San Chen
collection DOAJ
description Background/purpose: Cigarette smoking is an important risk factor in the pathogenesis of periodontal disease. However, little is known about the effect of nicotine, the major component of cigarette smoke, on cementoblasts. The aim of this study was to investigate the pathological effects of nicotine on the murine immortalized cementoblast cell line (OCCM.30). Materials and methods: Cell viability was judged by using the Alamar Blue reduction assay. Cell migration was evaluated by transwell and wound-healing assays. The protein concentrations of interleukin-6 (IL-6) and tumor necrosis factor alpha (TNF-α) were measured by using enzyme linked immunosorbent assay (ELISA). The semiquantitative 2′,7′-dichlorfluorescein-diacetate (DCFH-DA) fluorescence technique was used to detect the intracellular level of reactive oxygen species (ROS). Results: Concentrations of nicotine > 1.5mM demonstrated cytotoxicity to cementoblasts (P < 0.05). Nicotine attenuated cell migration in a dose-dependent manner (P < 0.05). In addition, nicotine augmented the production of IL-6 and TNF-α in a dose-dependent manner (P < 0.05). The concentration of 1mM nicotine enhanced the generation of intracellular ROS in a time-dependent manner (P < 0.05). Conclusion: Taken together, these results suggest that nicotine could inhibit the growth and migration of cementoblasts. In addition, nicotine could also induce the generation of inflammatory cytokines and ROS by cementoblasts.
first_indexed 2024-12-24T04:52:19Z
format Article
id doaj.art-40f4ebf4384a497cb0fac39fffc13cf9
institution Directory Open Access Journal
issn 1991-7902
language English
last_indexed 2024-12-24T04:52:19Z
publishDate 2015-06-01
publisher Elsevier
record_format Article
series Journal of Dental Sciences
spelling doaj.art-40f4ebf4384a497cb0fac39fffc13cf92022-12-21T17:14:30ZengElsevierJournal of Dental Sciences1991-79022015-06-0110215416010.1016/j.jds.2014.04.002Effects of nicotine on cell growth, migration, and production of inflammatory cytokines and reactive oxygen species by cementoblastsChun-San Chen0Shiuan-Shinn Lee1Hui-Chieh Yu2Fu-Mei Huang3Yu-Chao Chang4School of Dentistry, Chung Shan Medical University, Taichung, TaiwanSchool of Public Health, Chung Shan Medical University, Taichung, TaiwanSchool of Dentistry, Chung Shan Medical University, Taichung, TaiwanSchool of Dentistry, Chung Shan Medical University, Taichung, TaiwanSchool of Dentistry, Chung Shan Medical University, Taichung, TaiwanBackground/purpose: Cigarette smoking is an important risk factor in the pathogenesis of periodontal disease. However, little is known about the effect of nicotine, the major component of cigarette smoke, on cementoblasts. The aim of this study was to investigate the pathological effects of nicotine on the murine immortalized cementoblast cell line (OCCM.30). Materials and methods: Cell viability was judged by using the Alamar Blue reduction assay. Cell migration was evaluated by transwell and wound-healing assays. The protein concentrations of interleukin-6 (IL-6) and tumor necrosis factor alpha (TNF-α) were measured by using enzyme linked immunosorbent assay (ELISA). The semiquantitative 2′,7′-dichlorfluorescein-diacetate (DCFH-DA) fluorescence technique was used to detect the intracellular level of reactive oxygen species (ROS). Results: Concentrations of nicotine > 1.5mM demonstrated cytotoxicity to cementoblasts (P < 0.05). Nicotine attenuated cell migration in a dose-dependent manner (P < 0.05). In addition, nicotine augmented the production of IL-6 and TNF-α in a dose-dependent manner (P < 0.05). The concentration of 1mM nicotine enhanced the generation of intracellular ROS in a time-dependent manner (P < 0.05). Conclusion: Taken together, these results suggest that nicotine could inhibit the growth and migration of cementoblasts. In addition, nicotine could also induce the generation of inflammatory cytokines and ROS by cementoblasts.http://www.sciencedirect.com/science/article/pii/S1991790214000403cementoblastscytotoxicityinflammatory cytokinesmigrationnicotineROS generation
spellingShingle Chun-San Chen
Shiuan-Shinn Lee
Hui-Chieh Yu
Fu-Mei Huang
Yu-Chao Chang
Effects of nicotine on cell growth, migration, and production of inflammatory cytokines and reactive oxygen species by cementoblasts
Journal of Dental Sciences
cementoblasts
cytotoxicity
inflammatory cytokines
migration
nicotine
ROS generation
title Effects of nicotine on cell growth, migration, and production of inflammatory cytokines and reactive oxygen species by cementoblasts
title_full Effects of nicotine on cell growth, migration, and production of inflammatory cytokines and reactive oxygen species by cementoblasts
title_fullStr Effects of nicotine on cell growth, migration, and production of inflammatory cytokines and reactive oxygen species by cementoblasts
title_full_unstemmed Effects of nicotine on cell growth, migration, and production of inflammatory cytokines and reactive oxygen species by cementoblasts
title_short Effects of nicotine on cell growth, migration, and production of inflammatory cytokines and reactive oxygen species by cementoblasts
title_sort effects of nicotine on cell growth migration and production of inflammatory cytokines and reactive oxygen species by cementoblasts
topic cementoblasts
cytotoxicity
inflammatory cytokines
migration
nicotine
ROS generation
url http://www.sciencedirect.com/science/article/pii/S1991790214000403
work_keys_str_mv AT chunsanchen effectsofnicotineoncellgrowthmigrationandproductionofinflammatorycytokinesandreactiveoxygenspeciesbycementoblasts
AT shiuanshinnlee effectsofnicotineoncellgrowthmigrationandproductionofinflammatorycytokinesandreactiveoxygenspeciesbycementoblasts
AT huichiehyu effectsofnicotineoncellgrowthmigrationandproductionofinflammatorycytokinesandreactiveoxygenspeciesbycementoblasts
AT fumeihuang effectsofnicotineoncellgrowthmigrationandproductionofinflammatorycytokinesandreactiveoxygenspeciesbycementoblasts
AT yuchaochang effectsofnicotineoncellgrowthmigrationandproductionofinflammatorycytokinesandreactiveoxygenspeciesbycementoblasts