Application of Green Tea Catechin for Inducing the Osteogenic Differentiation of Human Dedifferentiated Fat Cells in Vitro

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Application of Green Tea Catechin for Inducing the Osteogenic Differentiation of Human Dedifferentiated Fat Cells in Vitro

Persistent ID (NDL): info:ndljp/pid/12071636

Material type: 博士論文

Author: 海田, 浩治

Publisher: -

Date granted: 2016-03-11

Material Format: Digital

Capacity, size, etc.: -

Degree grantor and degree: 大阪歯科大学,博士（歯学）

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Note (General)：: Despite the advances in stem cell biology, there are few effective techniques to promote the osteogenic differentiation of human primary dedifferentia...

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Material Type: 博士論文
Title: Application of Green Tea Catechin for Inducing the Osteogenic Differentiation of Human Dedifferentiated Fat Cells in Vitro
Author/Editor: 海田, 浩治
Author Heading: 海田, 浩治
Publication Date: 2016-03-11
Publication Date (W3CDTF): 2016-03-11
Alternative Title: ヒト脱分化脂肪細胞の骨芽細胞分化誘導にむけたin vitroでの緑茶カテキンの応用
Degree Grantor: 大阪歯科大学
Date Granted: 2016-03-11
Date Granted (W3CDTF): 2016-03-11
Dissertation Number: 甲第774号
Degree Type: 博士（歯学）
Conferring No. (Dissertation): 甲第774号
Text Language Code: eng
Subject Heading: Human Dedifferentiated Fat Cells
Catechin
Osteogenic
Target Audience: 一般
Note (General): Despite the advances in stem cell biology, there are few effective techniques to promote the osteogenic differentiation of human primary dedifferentiated fat (DFAT) cells. We attempted to investigate whether epigallocatechin-3-gallate (EGCG), which is the main component of green tea catechin, facilitates early osteogenic differentiation and mineralization on DFAT cells in vitro. DFAT cells were treated with EGCG (1.25–10 μM) in two osteogenic media with or without 100 nM dexamethasone [OM, OM(DEX)] for 12 days. Supplementation of 1.25 μM EGCG to both the media effectively increased the mRNA expression of collagen 1 (Col1A1) and runt-related transcription factor 2 (RUNX2), and also increased proliferation and mineralization. Compared with OM(DEX) with EGCG, OM with EGCG induced earlier COL1A1 and RUNX2 expression at day 1 and resulted in lower alkaline phosphatase staining at day 6, but higher mineralization at day 12. OM (DEX) with 10 μM EGCG remarkably hampered the proliferation of the DFAT cells. These results suggest that OM without DEX might be a preferable medium to promote proliferation and to induce osteoblast differentiation of DFAT cells. Our findings provide evidence for the potential use of EGCG and DFAT cells for bone regeneration and stem cell-based therapy.
2015
機関リポジトリ記載の権利情報: CC BY-NC-ND
Persistent ID (NDL): info:ndljp/pid/12071636
https://dl.ndl.go.jp/pid/12071636
Collection: 障害者向け資料
Collection (Materials For Handicapped People:1): テキストデータ
Collection (particular): 国立国会図書館デジタルコレクション > デジタル化資料 > 博士論文
https://dl.ndl.go.jp/collections/A00014
Acquisition Basis: 博士論文（自動収集）
Date Accepted (W3CDTF): 2022-02-06T04:33:19+09:00
Format (IMT): application/pdf
Access Restrictions: 国立国会図書館内限定公開
Service for the Digitized Contents Transmission Service: 図書館・個人送信対象外
Availability of remote photoduplication service: 可
Periodical Title (URI): http://id.nii.ac.jp/1392/00000095/
Data Provider (Database): 国立国会図書館 : 国立国会図書館デジタルコレクション
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