2011 Fiscal Year Final Research Report
Analysis of regeneration ability of periodontal ligament by ADAMTSL4 and development of novel therapeutic for conservative dentistry
Project/Area Number |
21390509
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Conservative dentistry
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Research Institution | Tokyo University of Science |
Principal Investigator |
SAITO Masahiro 東京理科大学, 基礎工学部・生物工学科, 准教授 (40215562)
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Co-Investigator(Kenkyū-buntansha) |
TERANAKA Toshio 神奈川歯科大学, 歯学部, 教授 (60104460)
TSUJI Takashi 東京理科大学, 基礎工学部・生物工学科, 教授 (50339131)
須田 直人 明海大学, 歯学部形態機能成育学講座歯科矯正学, 教授 (90302885)
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Project Period (FY) |
2009 – 2011
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Keywords | 保存修復学 |
Research Abstract |
Marfan's syndrome(MFS) is a systemic disorder of the connective tissues including periodontal ligament(PDL) by insufficiency of fibrillin-1 microfibril formation and can cause severe periodontal disease. ADAMTSL6β, a microfibril-associated extracellular matrix protein that has been implicated in fibrillin-1 microfibril assembly is able to improve microfibril insufficiency of PDL in MFS mice model. These findings suggest ADAMTSL6β-mediated fibrillin-1 microfibril assembly develop as a new therapeutic of conservative dentistry for the treatment of periodontal disease in MFS.
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[Journal Article] Role of epithelial-stem cell interactions during dental cell differentiation2012
Author(s)
M. Arakaki, M. Ishikawa, T. Nakamura, T. Iwamoto, A. Yamada, E. Fukumoto, M. Saito, K. Otsu, H. Harada, Y. Yamada, and S. Fukumoto
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Journal Title
J Biol Chem
Volume: 287(13)
Pages: 10590-601
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[Journal Article] ADAMTSL6β rescues fibrillin-1 microfibril disorder in Marfan syndrome mouse model through the promotion of fibrillin-1 assembly2011
Author(s)
M. Saito, M. Kurokawa, M. Oda, M. Oshima, K. Tsutsui, K. Kosaka, K. Nakao, M. Ogawa, R. Manabe, N. Suda, G. Ganjargal, Y. Hada, T. Noguchi, T. Teranaka, K. Sekiguchi, T. Yoneda and T. Tsuji
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Journal Title
J Biol Chem
Volume: 286(44)
Pages: 38602-38613
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[Journal Article] Functional tooth regeneration using a bioengineered tooth unit as a mature organ replacement regenerative therapy2011
Author(s)
M. Oshima, M. Mizuno, A. Imamura, M. Ogawa, M. Yasukawa, H. Yamazaki, R. Morita, E. Ikeda, K. Nakao, T. Takano-Yamamoto, S. Kasugai, M. Saito and T. Tsuji
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Journal Title
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[Journal Article] Regulation of endoplasmic reticulum stress response by a BBF2H7-mediated Sec23a pathway is essential for chondrogenesis2009
Author(s)
A. Saito, S. Hino, T. Murakami, S. Kanemoto, S. Kondo, M. Saito, R. Nishimura, T. Yoneda, T. Furuichi, S. Ikegawa, M. Ikawa, M. Okabe, K. Imaizumi
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Journal Title
Nat Cell Biol.
Volume: 11(10)
Pages: 1197-1204
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[Journal Article] Signalling mediated by the endoplasmic reticulum stress transducer OASIS is involved in bone formation2009
Author(s)
T. Murakami, A. Saito, S. Hino, S. Kondo, S. Kanemoto, K. Chihara, H. Sekiya, K. Tsumagari, K. Ochiai, K. Yoshinaga, M. Saito, R. Nishimura, T. Yoneda, I. Kou, T. Furuichi, S. Ikegawa, M. Ikawa, M. Okabe, A. Wanaka, K. Imaizumi
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Journal Title
Nat Cell Biol.
Volume: 11(10)
Pages: 1205-1211
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[Remarks] 発表者、齋藤正寛、辻孝、発表内容、マルファン症候群の歯周病、歯根再生の治療法を発見、発表先、朝日新聞、発表年2011
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[Remarks] 発表者、齋藤正寛、辻孝、発表内容、体の弾力を調節する微細線維の成分「ADAMTSL6β」が、遺伝病のマルファン症候群の症状を改善する、発表先、日本歯科新聞、発表年2011
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[Remarks] 発表者、齋藤正寛、辻孝、発表内容、マルファン症候群の新薬期待?組織強化たんぱく発見-、発表先、ASAHI. com、発表年2011
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[Remarks] 発表者、齋藤正寛、辻孝、発表内容、マルファン症候群の新薬期待?組織強化たんぱく発見-、発表先、時事通信、発表年2011
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[Remarks] 発表者、齋藤正寛、辻孝、発表内容、微細線維のADAMTSL6βがマルファン症候群の症状改善、アンチエイジングにも寄与、発表先、日経バイオテクOnline、発表年2011
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