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ID 67183
フルテキストURL
fulltext.pdf 3.97 MB
著者
Mu, Xindi Department of Molecular Biology and Biochemistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Ono, Mitsuaki Department of Molecular Biology and Biochemistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Kaken ID researchmap
Nguyen, Ha Thi Thu Department of Molecular Biology and Biochemistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Wang, Ziyi Department of Molecular Biology and Biochemistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Zhao, Kun Department of Molecular Biology and Biochemistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Komori, Taishi Department of Oral Rehabilitation and Regenerative Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Yonezawa, Tomoko Department of Molecular Biology and Biochemistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Kaken ID publons researchmap
Kuboki, Takuo Department of Oral Rehabilitation and Implantology, Okayama University Hospital ORCID Kaken ID publons researchmap
Oohashi, Toshitaka Department of Molecular Biology and Biochemistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences ORCID Kaken ID publons researchmap
抄録
The oral mucosa functions as a physico-chemical and immune barrier to external stimuli, and an adequate width of the keratinized mucosa around the teeth or implants is crucial to maintaining them in a healthy and stable condition. In this study, for the first time, bulk RNA-seq analysis was performed to explore the gene expression of laser microdissected epithelium and lamina propria from mice, aiming to investigate the differences between keratinized and non-keratinized oral mucosa. Based on the differentially expressed genes (DEGs) and Gene Ontology (GO) Enrichment Analysis, bone morphogenetic protein 2 (BMP-2) was identified to be a potential regulator of oral mucosal keratinization. Monoculture and epithelial-mesenchymal cell co-culture models in the air-liquid interface (ALI) indicated that BMP-2 has direct and positive effects on epithelial keratinization and proliferation. We further performed bulk RNA-seq of the ALI monoculture stimulated with BMP-2 in an attempt to identify the downstream factors promoting epithelial keratinization and proliferation. Analysis of the DEGs identified, among others, IGF2, ID1, LTBP1, LOX, SERPINE1, IL24, and MMP1 as key factors. In summary, these results revealed the involvement of a well-known growth factor responsible for bone development, BMP-2, in the mechanism of oral mucosal keratinization and proliferation, and pointed out the possible downstream genes involved in this mechanism.
キーワード
cell differentiation
epithelia
growth factor(s)
bioinformatics
extracellular matrix (ECM)
mucocutaneous disorders
発行日
2024-05-09
出版物タイトル
Cells
13巻
10号
出版者
MDPI
開始ページ
807
ISSN
2073-4409
資料タイプ
学術雑誌論文
言語
英語
OAI-PMH Set
岡山大学
著作権者
© 2024 by the authors.
論文のバージョン
publisher
PubMed ID
DOI
Web of Science KeyUT
関連URL
isVersionOf https://doi.org/10.3390/cells13100807
ライセンス
https://creativecommons.org/licenses/by/4.0/
Citation
Mu, X.; Ono, M.; Nguyen, H.T.T.; Wang, Z.; Zhao, K.; Komori, T.; Yonezawa, T.; Kuboki, T.; Oohashi, T. Exploring the Regulators of Keratinization: Role of BMP-2 in Oral Mucosa. Cells 2024, 13, 807. https://doi.org/10.3390/cells13100807
助成機関名
Japan Society for the Promotion of Science
助成番号
JP22K10100
JP22H03280
JP19H03841
JP22KF0265