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PINK1 mediated mitophagy attenuates early apoptosis of gingival epithelial cells induced by high glucose

BACKGROUND: Oxidative stress mediated by hyperglycemia damages cell-reparative processes such as mitophagy. Down-regulation of mitophagy is considered to be a susceptible factor for diabetes mellitus (DM) and its complications. However, the role of mitophagy in DM-associated periodontitis has not be...

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Autores principales: Zhu, Chunhui, Zhao, Ying, Pei, Dandan, Liu, Zhongbo, Liu, Jin, Li, Ye, Yu, Shuchen, Ma, Lingyan, Sun, Junyi, Li, Ang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9044577/
https://www.ncbi.nlm.nih.gov/pubmed/35473620
http://dx.doi.org/10.1186/s12903-022-02167-5
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author Zhu, Chunhui
Zhao, Ying
Pei, Dandan
Liu, Zhongbo
Liu, Jin
Li, Ye
Yu, Shuchen
Ma, Lingyan
Sun, Junyi
Li, Ang
author_facet Zhu, Chunhui
Zhao, Ying
Pei, Dandan
Liu, Zhongbo
Liu, Jin
Li, Ye
Yu, Shuchen
Ma, Lingyan
Sun, Junyi
Li, Ang
author_sort Zhu, Chunhui
collection PubMed
description BACKGROUND: Oxidative stress mediated by hyperglycemia damages cell-reparative processes such as mitophagy. Down-regulation of mitophagy is considered to be a susceptible factor for diabetes mellitus (DM) and its complications. However, the role of mitophagy in DM-associated periodontitis has not been fully elucidated. Apoptosis of human gingival epithelial cells (hGECs) is one of the representative events of DM-associated periodontitis. Thus, this study aimed to investigate PTEN-induced putative kinase 1 (PINK1)-mediated mitophagy activated in the process of high glucose (HG)-induced hGECs apoptosis. METHODS: For dose–response studies, hGECs were incubated in different concentrations of glucose (5.5, 15, 25, and 50 mmol/L) for 48 h. Then, hGECs were challenged with 25 mmol/L glucose for 12 h and 48 h, respectively. Apoptosis was detected by TdT-mediated dUTP nick end labeling (TUNEL), caspase 9 and mitochondrial membrane potential (MMP). Subsequently, autophagy was evaluated by estimating P62, LC3 II mRNA levels, LC3 fluorescent puncta and LC3-II/I ratio. Meanwhile, the involvement of PINK1-mediated mitophagy was assessed by qRT-PCR, western blotting and immunofluorescence. Finally, hGECs were transfected with shPINK1 and analyzed by MMP, caspase 9 and annexin V-FITC apoptosis. RESULTS: The number of TUNEL-positive cells and caspase 9 protein were significantly increased in cells challenged with HG (25 mmol/L) for 48 h (HG 48 h). MMP was impaired both at HG 12 h and HG 48 h, but the degree of depolarization was more serious at HG 48 h. The autophagy improved as the amount of LC3 II increased and p62 decreased in HG 12 h. During this process, HG 12 h treatment induced PINK1-mediated mitophagy. PINK1 silencing with HG 12 h resulted in MMP depolarization and cell apoptosis. CONCLUSIONS: These results suggested that loss of the PINK1 gene may cause mitochondrial dysfunction and increase sensitivity to HG-induced apoptosis of hGECs at the early stage. PINK1 mediated mitophagy attenuates early apoptosis of gingival epithelial cells induced by high glucose. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12903-022-02167-5.
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spelling pubmed-90445772022-04-28 PINK1 mediated mitophagy attenuates early apoptosis of gingival epithelial cells induced by high glucose Zhu, Chunhui Zhao, Ying Pei, Dandan Liu, Zhongbo Liu, Jin Li, Ye Yu, Shuchen Ma, Lingyan Sun, Junyi Li, Ang BMC Oral Health Research BACKGROUND: Oxidative stress mediated by hyperglycemia damages cell-reparative processes such as mitophagy. Down-regulation of mitophagy is considered to be a susceptible factor for diabetes mellitus (DM) and its complications. However, the role of mitophagy in DM-associated periodontitis has not been fully elucidated. Apoptosis of human gingival epithelial cells (hGECs) is one of the representative events of DM-associated periodontitis. Thus, this study aimed to investigate PTEN-induced putative kinase 1 (PINK1)-mediated mitophagy activated in the process of high glucose (HG)-induced hGECs apoptosis. METHODS: For dose–response studies, hGECs were incubated in different concentrations of glucose (5.5, 15, 25, and 50 mmol/L) for 48 h. Then, hGECs were challenged with 25 mmol/L glucose for 12 h and 48 h, respectively. Apoptosis was detected by TdT-mediated dUTP nick end labeling (TUNEL), caspase 9 and mitochondrial membrane potential (MMP). Subsequently, autophagy was evaluated by estimating P62, LC3 II mRNA levels, LC3 fluorescent puncta and LC3-II/I ratio. Meanwhile, the involvement of PINK1-mediated mitophagy was assessed by qRT-PCR, western blotting and immunofluorescence. Finally, hGECs were transfected with shPINK1 and analyzed by MMP, caspase 9 and annexin V-FITC apoptosis. RESULTS: The number of TUNEL-positive cells and caspase 9 protein were significantly increased in cells challenged with HG (25 mmol/L) for 48 h (HG 48 h). MMP was impaired both at HG 12 h and HG 48 h, but the degree of depolarization was more serious at HG 48 h. The autophagy improved as the amount of LC3 II increased and p62 decreased in HG 12 h. During this process, HG 12 h treatment induced PINK1-mediated mitophagy. PINK1 silencing with HG 12 h resulted in MMP depolarization and cell apoptosis. CONCLUSIONS: These results suggested that loss of the PINK1 gene may cause mitochondrial dysfunction and increase sensitivity to HG-induced apoptosis of hGECs at the early stage. PINK1 mediated mitophagy attenuates early apoptosis of gingival epithelial cells induced by high glucose. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12903-022-02167-5. BioMed Central 2022-04-26 /pmc/articles/PMC9044577/ /pubmed/35473620 http://dx.doi.org/10.1186/s12903-022-02167-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Zhu, Chunhui
Zhao, Ying
Pei, Dandan
Liu, Zhongbo
Liu, Jin
Li, Ye
Yu, Shuchen
Ma, Lingyan
Sun, Junyi
Li, Ang
PINK1 mediated mitophagy attenuates early apoptosis of gingival epithelial cells induced by high glucose
title PINK1 mediated mitophagy attenuates early apoptosis of gingival epithelial cells induced by high glucose
title_full PINK1 mediated mitophagy attenuates early apoptosis of gingival epithelial cells induced by high glucose
title_fullStr PINK1 mediated mitophagy attenuates early apoptosis of gingival epithelial cells induced by high glucose
title_full_unstemmed PINK1 mediated mitophagy attenuates early apoptosis of gingival epithelial cells induced by high glucose
title_short PINK1 mediated mitophagy attenuates early apoptosis of gingival epithelial cells induced by high glucose
title_sort pink1 mediated mitophagy attenuates early apoptosis of gingival epithelial cells induced by high glucose
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9044577/
https://www.ncbi.nlm.nih.gov/pubmed/35473620
http://dx.doi.org/10.1186/s12903-022-02167-5
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