Anti-inflammaging effects of vitamin D in human gingival fibroblasts with advanced glycation end product stimulation

Background/purpose: :Both periodontal disease and diabetes mellitus (DM) are long-term inflammatory disorders that are highly prevalent and have a significant health impact. Inflammaging, a state of pre-aging and hyperinflammatory state has been acknowledged for its role in DM patients to have heigh...

Full description

Bibliographic Details
Main Authors: Hung-Chieh Lu, Taichen Lin, Min Yee Ng, Chang-Wei Hsieh, Yi-Wen Liao, Chun-Cheng Chen, Cheng-Chia Yu, Chun-Jung Chen
Format: Article
Language:English
Published: Elsevier 2023-04-01
Series:Journal of Dental Sciences
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1991790222002550
_version_ 1797862208028278784
author Hung-Chieh Lu
Taichen Lin
Min Yee Ng
Chang-Wei Hsieh
Yi-Wen Liao
Chun-Cheng Chen
Cheng-Chia Yu
Chun-Jung Chen
author_facet Hung-Chieh Lu
Taichen Lin
Min Yee Ng
Chang-Wei Hsieh
Yi-Wen Liao
Chun-Cheng Chen
Cheng-Chia Yu
Chun-Jung Chen
author_sort Hung-Chieh Lu
collection DOAJ
description Background/purpose: :Both periodontal disease and diabetes mellitus (DM) are long-term inflammatory disorders that are highly prevalent and have a significant health impact. Inflammaging, a state of pre-aging and hyperinflammatory state has been acknowledged for its role in DM patients to have heightened risk of periodontitis. Numerous evidences revealed that inflammaging contributed by cell senescence, acceleration of inflammation and oxidative stress participates in the destruction of periodontium in DM. Abilities of vitamin D in suppressing inflammation and oxidative stress have been revealed in a range of tissues, however in DM’s gingival cells, the effect remain undefined. Materials and methods: : Under the stimulation of advanced glycation end-products (AGEs), we assessed the cell proliferation in human gingival fibroblast (HGF), IL-6 and IL-8 secretions, cellular senescence expression and generation of reactive oxygen species (ROS) with or without vitamin D intervention. Following that, we examined the expression of Nrf2 and HO-1 to see if vitamin D was able to modulate the anti-oxidant signaling. A knockdown experiment was then conducted to proof the participation of Nrf2 on the secretion of pro-inflammatory IL-6 and IL-8. Results: : Following the treatment of vitamin D, AGEs-elicited IL-6 and IL-8 production and cell senescence were dose-dependently repressed. Moreover, vitamin D attenuated AGEs-induced ROS in a dose-dependent pattern. Results from qRT-PCR demonstrated vitamin D reversed the suppression of Nrf2 and HO-1 induced by AGEs. Our findings revealed that the anti-inflammatory and anti-oxidant effect in vitamin D was mediated via the upregulation of Nrf2 expression. Conclusion: : These data showed that high levels of AGEs in the gingiva lead to inflammaging reflected by increased pro-inflammatory cytokines, cell senescence expression and oxidative stress. Vitamin D supplementation can reduce oxidative stress and inflammation via the upregulation of Nrf2 signaling and hence, may be a potential approach for treatment of diabetes-associated periodontitis.
first_indexed 2024-04-09T22:15:32Z
format Article
id doaj.art-cf35421663f941d18ea62a52c9040260
institution Directory Open Access Journal
issn 1991-7902
language English
last_indexed 2024-04-09T22:15:32Z
publishDate 2023-04-01
publisher Elsevier
record_format Article
series Journal of Dental Sciences
spelling doaj.art-cf35421663f941d18ea62a52c90402602023-03-23T04:35:05ZengElsevierJournal of Dental Sciences1991-79022023-04-01182666673Anti-inflammaging effects of vitamin D in human gingival fibroblasts with advanced glycation end product stimulationHung-Chieh Lu0Taichen Lin1Min Yee Ng2Chang-Wei Hsieh3Yi-Wen Liao4Chun-Cheng Chen5Cheng-Chia Yu6Chun-Jung Chen7School of Dentistry, Chung Shan Medical University, Taichung, TaiwanSchool of Dentistry, Chung Shan Medical University, Taichung, Taiwan; Department of Dentistry, Chung Shan Medical University Hospital, Taichung, TaiwanSchool of Dentistry, Chung Shan Medical University, Taichung, TaiwanDepartment of Food Science and Biotechnology, National Chung Hsing University, Taichung, TaiwanDepartment of Medical Research, Chung Shan Medical University Hospital, Taichung, Taiwan; Institute of Oral Sciences, Chung Shan Medical University, Taichung, TaiwanSchool of Dentistry, Chung Shan Medical University, Taichung, Taiwan; Department of Dentistry, Chung Shan Medical University Hospital, Taichung, TaiwanSchool of Dentistry, Chung Shan Medical University, Taichung, Taiwan; Department of Dentistry, Chung Shan Medical University Hospital, Taichung, Taiwan; Institute of Oral Sciences, Chung Shan Medical University, Taichung, Taiwan; Corresponding author. Institute of Oral Sciences, Chung Shan Medical University, No.110, Sec.1, Jianguo N. Rd., Taichung 40201, Taiwan.School of Dentistry, Chung Shan Medical University, Taichung, Taiwan; Division of Periodontics, Department of Dentistry, Chi Mei Medical Center, Tainan, Taiwan; Corresponding author. Division of Periodontics, Department of Dentistry, Chi Mei Medical Center, No. 901, Zhonghua Rd. Yongkang Dist., Tainan 71004, Taiwan.Background/purpose: :Both periodontal disease and diabetes mellitus (DM) are long-term inflammatory disorders that are highly prevalent and have a significant health impact. Inflammaging, a state of pre-aging and hyperinflammatory state has been acknowledged for its role in DM patients to have heightened risk of periodontitis. Numerous evidences revealed that inflammaging contributed by cell senescence, acceleration of inflammation and oxidative stress participates in the destruction of periodontium in DM. Abilities of vitamin D in suppressing inflammation and oxidative stress have been revealed in a range of tissues, however in DM’s gingival cells, the effect remain undefined. Materials and methods: : Under the stimulation of advanced glycation end-products (AGEs), we assessed the cell proliferation in human gingival fibroblast (HGF), IL-6 and IL-8 secretions, cellular senescence expression and generation of reactive oxygen species (ROS) with or without vitamin D intervention. Following that, we examined the expression of Nrf2 and HO-1 to see if vitamin D was able to modulate the anti-oxidant signaling. A knockdown experiment was then conducted to proof the participation of Nrf2 on the secretion of pro-inflammatory IL-6 and IL-8. Results: : Following the treatment of vitamin D, AGEs-elicited IL-6 and IL-8 production and cell senescence were dose-dependently repressed. Moreover, vitamin D attenuated AGEs-induced ROS in a dose-dependent pattern. Results from qRT-PCR demonstrated vitamin D reversed the suppression of Nrf2 and HO-1 induced by AGEs. Our findings revealed that the anti-inflammatory and anti-oxidant effect in vitamin D was mediated via the upregulation of Nrf2 expression. Conclusion: : These data showed that high levels of AGEs in the gingiva lead to inflammaging reflected by increased pro-inflammatory cytokines, cell senescence expression and oxidative stress. Vitamin D supplementation can reduce oxidative stress and inflammation via the upregulation of Nrf2 signaling and hence, may be a potential approach for treatment of diabetes-associated periodontitis.http://www.sciencedirect.com/science/article/pii/S1991790222002550PeriodontitisAdvanced glycation end productsVitamin D
spellingShingle Hung-Chieh Lu
Taichen Lin
Min Yee Ng
Chang-Wei Hsieh
Yi-Wen Liao
Chun-Cheng Chen
Cheng-Chia Yu
Chun-Jung Chen
Anti-inflammaging effects of vitamin D in human gingival fibroblasts with advanced glycation end product stimulation
Journal of Dental Sciences
Periodontitis
Advanced glycation end products
Vitamin D
title Anti-inflammaging effects of vitamin D in human gingival fibroblasts with advanced glycation end product stimulation
title_full Anti-inflammaging effects of vitamin D in human gingival fibroblasts with advanced glycation end product stimulation
title_fullStr Anti-inflammaging effects of vitamin D in human gingival fibroblasts with advanced glycation end product stimulation
title_full_unstemmed Anti-inflammaging effects of vitamin D in human gingival fibroblasts with advanced glycation end product stimulation
title_short Anti-inflammaging effects of vitamin D in human gingival fibroblasts with advanced glycation end product stimulation
title_sort anti inflammaging effects of vitamin d in human gingival fibroblasts with advanced glycation end product stimulation
topic Periodontitis
Advanced glycation end products
Vitamin D
url http://www.sciencedirect.com/science/article/pii/S1991790222002550
work_keys_str_mv AT hungchiehlu antiinflammagingeffectsofvitamindinhumangingivalfibroblastswithadvancedglycationendproductstimulation
AT taichenlin antiinflammagingeffectsofvitamindinhumangingivalfibroblastswithadvancedglycationendproductstimulation
AT minyeeng antiinflammagingeffectsofvitamindinhumangingivalfibroblastswithadvancedglycationendproductstimulation
AT changweihsieh antiinflammagingeffectsofvitamindinhumangingivalfibroblastswithadvancedglycationendproductstimulation
AT yiwenliao antiinflammagingeffectsofvitamindinhumangingivalfibroblastswithadvancedglycationendproductstimulation
AT chunchengchen antiinflammagingeffectsofvitamindinhumangingivalfibroblastswithadvancedglycationendproductstimulation
AT chengchiayu antiinflammagingeffectsofvitamindinhumangingivalfibroblastswithadvancedglycationendproductstimulation
AT chunjungchen antiinflammagingeffectsofvitamindinhumangingivalfibroblastswithadvancedglycationendproductstimulation