Histological and molecular analysis of developmental process of the midline facial skeleton
Project/Area Number |
25460254
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
General anatomy (including histology/embryology)
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Research Institution | Tokyo University of Science |
Principal Investigator |
Wada Naoyuki 東京理科大学, 理工学部, 教授 (50267449)
|
Project Period (FY) |
2013-04-01 – 2016-03-31
|
Project Status |
Completed (Fiscal Year 2015)
|
Budget Amount *help |
¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2015: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2014: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2013: ¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
|
Keywords | 顎顔面発生 / 頭蓋底軟骨 / 鼻中隔 / 神経堤細胞 / 発生系譜 / 糖鎖 / 頭顔面発生 / 軟骨分化 / レクチン |
Outline of Final Research Achievements |
The developmental process and origin of the anterior part of skull base cartilage has not been unclear. In this project, we analyzed the origin of the cartilage by focusing on the expression of a novel carbohydrate chain, PNA-BM (peanut-agglutinin lectin binding molecule). Two molecules were detected by PNA-lectin blotting analysis. Fate mapping analysis and tissue removal experiment of cranial neural crest cells showed that expression of PNA-BM correlated to the origin of the cartilage. The expression was weak in the cells of paired rod-like cartilage, the trabecular cartilage (TC), whereas strong expression of it was observed in the cells of inter-trabecular cartilage (ITC), which connects the anterior end of TC. In TC cells, actin polymerization was unclear, while in PNA-BM positive ITC cells, the polymerization was apparent. These results suggest that cells in TC and ITC have distinct properties, although both are histologically designated as chondrocytes.
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Report
(4 results)
Research Products
(12 results)
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[Journal Article] Short-term feeding at the wrong time is sufficient to desynchronize peripheral clocks and induce obesity with hyperphagia, physical inactivity and metabolic disorders in mice2016
Author(s)
Yasumoto Y, Hashimoto C, Nakao R, Yamazaki H, Hiroyama H, Nemoto T, Yamamoto S, Sakurai M, Oike H, Wada N, Yoshida-Noro C, Oishi K
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Journal Title
Metabolism
Volume: 65
Issue: 5
Pages: 714-727
DOI
Related Report
Peer Reviewed / Open Access / Int'l Joint Research
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[Journal Article] Distinct populations within Isl1 lineages contribute to appendicular and facial skeletogenesis through the β-catenin pathway2014
Author(s)
Akiyama, R., Kawakami, H., Taketo, M. M., Evans, S. M., Wada, N., Petryk. A., Kawakami, Y.
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Journal Title
Developmental Biology
Volume: 387
Issue: 1
Pages: 37-48
DOI
Related Report
Peer Reviewed
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[Journal Article] GTP hydrolysis of TC10 promotes neurite outgrowth through exocytic fusion of Rab11- and L1-containing vesicles by releasing exocyst component Exo70.2013
Author(s)
2. Fujita, A., Koinuma, S., Yasuda, S., Nagai, H., Kamiguchi, H., Wada, N., and Nakamura, T.
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Journal Title
PLoS One
Volume: 8
Issue: 11
Pages: 9593-9601
DOI
Related Report
Peer Reviewed
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