Publication: Regulation of DNA methylation levels in the process of oral mucosal regeneration of oral ulcer model.
Authors
Akiyama, Naotaro ; Fukuda, Tomomi Yamamoto ; Yoshikawa, Mamoru ; Kojima, Hiromi
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Publisher
Universidad de Murcia, Departamento de Biologia Celular e Histiologia
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DOI
https://doi.org/10.14670/HH-18-147
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info:eu-repo/semantics/article
Description
Abstract
DNA methylation is an important epigenetic
mechanism for cellular maintenance. However, the
methylation pattern and the key molecule regulated
epigenetically in oral mucosal regeneration is unclear. In
this study, we generated a rat oral ulcer model and
investigated the cell proliferative activities and DNA
methylation patterns immunohistochemically. We also
performed immunohistochemical analysis of a regulator
of epithelial stem/progenitor cell differentiation in the rat
model.
We demonstrated immunohistochemistry using
antibodies for the molecules as follows: Ki-67, a marker
of cellular proliferation; 5-methylcytosine (5-mC), a
marker of DNA methylation; 5-hydroxymethylcytosine
(5-hmC), a marker of DNA demethylation; Dnmt1, a
maintenance DNA methyltransferase; Dnmt3a and
Dnmt3b, de novo DNA methyltransferases; and Wnt5a, a
regulator of stem/progenitor cell differentiation.
In this model, re-epithelialization was completed at
Day 4 after ulceration. Regenerating mucosal
hypertrophy reached a peak at Day 5 and appeared
normal at Day 14. Ki-67-positive cells increased at Day
2 and returned to normal at Day 6 after ulceration. The
ratio of the expression level of 5-mC to 5-hmC declined
at Day 5 and returned to normal at Day 6. The
expression level of Dnmt1 had not changed compared to
the normal control at every time point. On the other
hand, the expression levels of Dnmt3a and Dnmt3b had
decreased significantly at Day 5 and returned to normal
at Day 6. Moreover, Wnt5a-positive cells increased at
Day 5.
In conclusion, oral mucosal regeneration was strictly
regulated by DNA methylation. Moreover, Wnt5a might
play a critical role in oral mucosal regeneration.
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Citation
Histology and Histopathology Vol. 35, nº 3 (2020)
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