The roles of PLZF transcription factor in osteogenesis and chondrogenesis.
Project/Area Number |
25870785
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Morphological basic dentistry
General anatomy (including histology/embryology)
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Research Institution | Nihon University |
Principal Investigator |
NAITO Masako 日本大学, 歯学部, 准教授 (40436803)
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Project Period (FY) |
2013-04-01 – 2016-03-31
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Project Status |
Completed (Fiscal Year 2015)
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Budget Amount *help |
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2015: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2013: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
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Keywords | 軟骨細胞分化 / 骨芽細胞分化 / 脂肪細胞分化 / 転写因子 / グルココルチコイド / 軟骨細胞 / glucocorticoid / 細胞周期 / 分化 / 軟骨基質 / CDK inhibitor / 骨芽細胞 / 間葉系前駆細胞 / Glucocorticoid |
Outline of Final Research Achievements |
Transcription factor PLZF is involved in various biological processes, including cell proliferation and differentiation. However, the role of PLZF in chondrogenesis is not well understood. In this study, we investigated PLZF expression during chondrocyte differentiation by using a chondrogenic progenitor cell line ATDC5. Our results indicated that PLZF expression was upregulated during chondrocyte differentiation. To elucidate the role of PLZF in chondrogenesis, we transfected ATDC5 cells with the gene encoding PLZF or a shRNA against the gene encoding PLZF. PLZF overexpression suppressed the proliferation and promoted the differentiation of ATDC5 cells into hypertrophic chondrocytes. In contrast, transfection of ATDC5 cells with the shRNA against the gene encoding PLZF suppressed their differentiation into hypertrophic chondrocytes and promoted cell cycle progression. These results suggested that PLZF promoted hypertrophic phenotypes by regulating cell cycle progression.
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Report
(4 results)
Research Products
(6 results)
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[Journal Article] Low-intensity pulsed ultrasound-induced ATP increases bone formation via the P2X7 receptor in osteoblast-like MC3T3E1 cells.2015
Author(s)
Manaka S, Tanabe N, Kariya T, Naito M, Takayama T, Nagao M, Liu D, Ito K, Maeno M, Suzuki N, Miyazaki M
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Journal Title
FEBS Letters
Volume: 589
Issue: 3
Pages: 310-318
DOI
Related Report
Peer Reviewed / Open Access / Acknowledgement Compliant
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