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High Glucose Induces Late Differentiation and Death of Human Oral Keratinocytes
Keratinocytes are essential cells for wound repair. Impaired oral wound healing is common in diabetic patients with periodontal disease. High glucose, or hyperglycemia, impairs the cellular function of different cell types. However, it is unknown whether high glucose has a detrimental effect on the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9498150/ https://www.ncbi.nlm.nih.gov/pubmed/36135187 http://dx.doi.org/10.3390/cimb44090275 |
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author | Shi, Junhe Han, Chen Chen, Dandan Trivedi, Harsh M. Bangash, Hiba I. Chen, Lin |
author_facet | Shi, Junhe Han, Chen Chen, Dandan Trivedi, Harsh M. Bangash, Hiba I. Chen, Lin |
author_sort | Shi, Junhe |
collection | PubMed |
description | Keratinocytes are essential cells for wound repair. Impaired oral wound healing is common in diabetic patients with periodontal disease. High glucose, or hyperglycemia, impairs the cellular function of different cell types. However, it is unknown whether high glucose has a detrimental effect on the functions of oral keratinocytes. In the current study, a human gingival keratinocyte cell line, telomerase immortalized gingival keratinocytes (TIGK), was treated with high glucose (24 and 48 mM) for up to 120 h. Proliferation, migration, cell viability, and production of markers of differentiation, growth factors and enzymatic antioxidants were assessed after high glucose treatment. The results showed that high glucose significantly inhibited TIGK proliferation and migration. High glucose also induced significant cell death through apoptosis and necrosis as determined by flow cytometry, especially at 120 h after high glucose treatment. Necrosis was the dominant form of cell death induced. Real-time PCR showed that high glucose treatment upregulated mRNA expression of late keratinocyte differentiation makers, such as keratin 1, 10, 13 and loricrin, and downregulated enzymatic antioxidants, including superoxide dismutase 1, catalase, nuclear factor erythroid 2 -related factor 2, heme oxygenase 1. In conclusion, high glucose impairs the proliferation and migration of oral keratinocytes and likely induces cell death through the promotion of late cell differentiation and down-regulation of enzymatic antioxidants. |
format | Online Article Text |
id | pubmed-9498150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94981502022-09-23 High Glucose Induces Late Differentiation and Death of Human Oral Keratinocytes Shi, Junhe Han, Chen Chen, Dandan Trivedi, Harsh M. Bangash, Hiba I. Chen, Lin Curr Issues Mol Biol Article Keratinocytes are essential cells for wound repair. Impaired oral wound healing is common in diabetic patients with periodontal disease. High glucose, or hyperglycemia, impairs the cellular function of different cell types. However, it is unknown whether high glucose has a detrimental effect on the functions of oral keratinocytes. In the current study, a human gingival keratinocyte cell line, telomerase immortalized gingival keratinocytes (TIGK), was treated with high glucose (24 and 48 mM) for up to 120 h. Proliferation, migration, cell viability, and production of markers of differentiation, growth factors and enzymatic antioxidants were assessed after high glucose treatment. The results showed that high glucose significantly inhibited TIGK proliferation and migration. High glucose also induced significant cell death through apoptosis and necrosis as determined by flow cytometry, especially at 120 h after high glucose treatment. Necrosis was the dominant form of cell death induced. Real-time PCR showed that high glucose treatment upregulated mRNA expression of late keratinocyte differentiation makers, such as keratin 1, 10, 13 and loricrin, and downregulated enzymatic antioxidants, including superoxide dismutase 1, catalase, nuclear factor erythroid 2 -related factor 2, heme oxygenase 1. In conclusion, high glucose impairs the proliferation and migration of oral keratinocytes and likely induces cell death through the promotion of late cell differentiation and down-regulation of enzymatic antioxidants. MDPI 2022-09-04 /pmc/articles/PMC9498150/ /pubmed/36135187 http://dx.doi.org/10.3390/cimb44090275 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Shi, Junhe Han, Chen Chen, Dandan Trivedi, Harsh M. Bangash, Hiba I. Chen, Lin High Glucose Induces Late Differentiation and Death of Human Oral Keratinocytes |
title | High Glucose Induces Late Differentiation and Death of Human Oral Keratinocytes |
title_full | High Glucose Induces Late Differentiation and Death of Human Oral Keratinocytes |
title_fullStr | High Glucose Induces Late Differentiation and Death of Human Oral Keratinocytes |
title_full_unstemmed | High Glucose Induces Late Differentiation and Death of Human Oral Keratinocytes |
title_short | High Glucose Induces Late Differentiation and Death of Human Oral Keratinocytes |
title_sort | high glucose induces late differentiation and death of human oral keratinocytes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9498150/ https://www.ncbi.nlm.nih.gov/pubmed/36135187 http://dx.doi.org/10.3390/cimb44090275 |
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