Inducible mechanism and role of novel aggrecanase in early stage of arthritis and its therapeutic application
Inducible mechanism and role of novel aggrecanase in early stage of arthritis and its therapeutic application
批准号:
18390416
负责人:
HIROHATA Satoshi
金额:
$11.0万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
2006
资助国家:
日本
项目状态:
已结题
起止时间:
2006 至 2007
中文摘要
1侵袭的诱导机制取新生大鼠膝关节,分离软骨细胞。施加机械应力,检测血管紧张素转换酶的表达。ADAMTS5不受机械应力的影响,而ADAMTS1、4和ADAMTS9的mRNAs随着机械应力的增加而增加。2 ADAMTS9在软骨中的分布我们建立了Wistar大鼠骨关节炎模型。当软骨破坏不是很严重时,ADAMTS9已经被诱导表达。然后检测ADAMTS9在发育膝关节中的表达。分别于出生后0、7、14周取ICR小鼠膝关节。ADAMTS9在成熟软骨细胞层(部分)和肥大带有表达。这些实验表明,ADAMTS9与膝关节软骨细胞的成熟有关。
英文摘要
1 Inducible mechanism for aggrecanaseChondrocytes were isolated from new born rat knee joint. Mechanical stress was performed and the expressions of aggrecanases were examined. ADAMTS5 was not increased by mechanical stress, while mRNAs of ADAMTS1,4, and ADAMTS9 were increased by mechanical stress. Then, the2 Distribution of ADAMTS9 in cartilageWe produced osteoarthritis model in Wister rats. When the cartilage destruction was not so severe, the expression of ADAMTS9 was already induced. Then we examined the expression of ADAMTS9 in developmental knee joint. The knee joint was taken at 0, 7, and 14 weeks after birth in ICR mice, respectively. The expression of ADAMTS9 was observed in mature chondrocyte layer (partially) as well as hypertrophic zone. From these experiments, it is suggested that ADAMTS9 is related to the maturation of chondrocytes in knee joint.
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Expression of ADAMTS9 gene in chondrocytes and its regulation.
ADAMTS9基因在软骨细胞中的表达及其调控。
DOI:
--
发表时间:
2007
期刊:
影响因子:
--
作者:
[Saio, M., Bai, J., Umemura, N., Nonaka, K., Okada, M., Kito, Y., Suwa, T., Ohe, N., Takami, T., Hirohata S]
通讯作者:
Hirohata S
Tumor-specific expression of the RGD-alpha3(IV)NC1 domain suppresses endothelial tube formation and tumor growth in mice
RGD-α3(IV)NC1 结构域的肿瘤特异性表达抑制小鼠内皮管形成和肿瘤生长
DOI:
--
发表时间:
2006
期刊:
FASEB 20 (11)
影响因子:
--
作者:
[Miyoshi, T., et. al.]
通讯作者:
et. al.
DOI:
10.1016/j.joca.2007.10.014
发表时间:
2008-06-01
期刊:
OSTEOARTHRITIS AND CARTILAGE
影响因子:
7
作者:
[Nasu, Y., Nishida, K., Ozaki, T.]
通讯作者:
Ozaki, T.
DOI:
10.1016/j.jaut.2007.05.004
发表时间:
2007-09-01
期刊:
JOURNAL OF AUTOIMMUNITY
影响因子:
12.8
作者:
[Okada, Tomoyuki, Ayada, Kiyoshi, Oguma, Keiji]
通讯作者:
Oguma, Keiji
Coronary pressure measurement to identify the lesion requiring percutaneous coronary intervention in equivocal tandem lesions
测量冠状动脉压力以识别可疑串联病变中需要经皮冠状动脉介入治疗的病变
DOI:
--
发表时间:
2006
期刊:
Coron Artery Dis 17(2)
影响因子:
--
作者:
[Yamasaki K, Setoguchi T, Takenouchi T, Yone K, Komiya S, Sakamoto Y, Hirota M]
通讯作者:
Hirota M
The role of endocytosis in oateoarhthritis
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批准号:26670665
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项目类别:Grant-in-Aid for Challenging Exploratory Research
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资助金额:$2.33万
-
财政年份:2014
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负责人:HIROHATA Satoshi
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依托单位:
Regulatory mechanism of transcriptional factors and microRNA in arthritis
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批准号:23390366
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$12.23万
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财政年份:2011
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负责人:HIROHATA Satoshi
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依托单位:
Aggrecanase regulation system in osteoarthritis and strategy for early diagnosis and therapy for osteoarthritis
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批准号:20390399
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$12.56万
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财政年份:2008
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负责人:HIROHATA Satoshi
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依托单位:
Toe role of novel aggrecanase in rheumatoid arthritis and its diagnostic potential
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批准号:15390459
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$9.6万
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财政年份:2003
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负责人:HIROHATA Satoshi
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依托单位:
Identifying new aggrecanase and producing antibody and gene-targeting mouse
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批准号:13470312
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$8.96万
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财政年份:2001
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负责人:HIROHATA Satoshi
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依托单位:
国内基金
海外基金
Aggrecan和Aggrecanase的基因多态性对腰椎间盘突出症易感性的影响及其机制研究
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批准号:81201419
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项目类别:青年科学基金项目
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资助金额:23.0万元
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批准年份:2012
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负责人:丛琳
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依托单位: