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M0LECULAR MECHANISIM AND BIOMARKER OF AORTIC DISSECTION

M0LECULAR MECHANISIM AND BIOMARKER OF AORTIC DISSECTION
主动脉夹层的分子机制和生物标志物
批准号:
22591535
负责人:
SATO Akira
金额:
$2.91万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2010
资助国家:
日本
项目状态:
已结题
起止时间:
2010 至 2012

项目摘要

项目成果

SATO Akira的其他基金

相关文献

中文摘要
翻译
我们评估了42例B型急性主动脉夹层(AD)患者,血清TN-C水平在第7天显著升高,然后在第28天逐渐下降到正常范围。7天血清TN-C水平与入院时c反应蛋白峰值水平、FDP水平、d -二聚体水平和主动脉夹层最大直径呈正相关。3例死亡患者入院时血清TN-C水平明显高于存活患者。血清TN-C水平在急性期显著升高,可能是预测B型急性AD患者预后的一种新的生物标志物。在小鼠模型中,TN-C在主动脉壁夹层高表达,且与α-SMA染色的血管平滑肌细胞(VSMCs)面积一致。在tnc报告基因敲入LacZ的小鼠中,主动脉壁夹层被β-gal染色,α sma阳性细胞β-gal也呈阳性。我们发现产生TN-C的细胞是主动脉壁夹层的VSMCs。
英文摘要
We evaluated 42 patients with type B acute aortic dissection (AD), andserum TN-C levels significantly increased at 7 days and then gradually decreased to normal range at 28 days. Serum TN-C levels at 7 days correlated positively with peak C-reactive protein levels, FDP levels, D-dimer levels, and maximum aortic diameter at the dissection level on admission. Serum TN-C levels of 3 dead patients on admission were significantly higher than those of surviving patients. Serum TN-C levels were significantly elevated during acute stage and might be a novel biomarker to predict patient prognosis of type B acute AD.In mouse model, TN-C was highly expressed in the medial layer of the dissected aortic wall, andwas concordant with the area of the vascular smooth muscle cells (VSMCs) stained by α-SMA. In the TN-C reporter mouse knock-in with LacZ, the medial layer of the dissected aortic wall was stained by the β-gal, and furthermore αSMA-positive cells were also positive in β-gal. We found that the producing cells of TN-C were VSMCs in the dissected aortic wall.
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会议论文
テネイシンCは大動脈解離を予防する分子的ショックアブソーバーである
Tenascin-C 是一种分子减震器,可预防主动脉夹层
DOI: --
发表时间: 2011
期刊:
影响因子: --
作者: [片山雄三, 横山詩子, 根元寛子, 笠間啓一郎, 鈴木伸一, 磯松尚幸, 内田敬二, 井元清隆, 石川義弘, 益田宗孝, 木村泰三,吉村耕一,青木浩樹,今中恭子,吉田利通,青沼和隆,廣江道昭,今泉勉,松崎益徳]
通讯作者: 木村泰三,吉村耕一,青木浩樹,今中恭子,吉田利通,青沼和隆,廣江道昭,今泉勉,松崎益徳
大動脈瘤分子病態における細胞外マトリックステネイシンCの役割の解明
阐明细胞外基质腱蛋白-C 在主动脉瘤分子病理学中的作用
DOI: --
发表时间: 2010
期刊:
影响因子: --
作者: [鈴木伸一、益田宗孝、磯松尚幸、笠間啓一郎、片山雄三、根元寛子、井元清隆、内田敬二、南智行、堺温哉, 松本直通, 木村泰三,佐藤 明,青沼和隆]
通讯作者: 木村泰三,佐藤 明,青沼和隆
DOI: 10.1111/j.1440-1827.2011.02699.x
发表时间: 2011-10-01
期刊: PATHOLOGY INTERNATIONAL
影响因子: 2.2
作者: [Kimura, Taizo, Yoshimura, Koichi, Matsuzaki, Masunori]
通讯作者: Matsuzaki, Masunori
A Study on the development of structure for mutual learning and support in the area to encourage proactive social participation among elderly with special needs.
  • 批准号:
    15K03952
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 资助金额:
    $1.08万
  • 财政年份:
    2015
  • 负责人:
    SATO Akira
  • 依托单位:
Development of the macro-micro fluid and fracture evaluation methods by hybrid X-ray CT method.
  • 批准号:
    23560987
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 资助金额:
    $3.41万
  • 财政年份:
    2011
  • 负责人:
    SATO Akira
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Identification of novel kinases in Wnt signaling
  • 批准号:
    22770127
  • 项目类别:
    Grant-in-Aid for Young Scientists (B)
  • 资助金额:
    $2.75万
  • 财政年份:
    2010
  • 负责人:
    SATO Akira
  • 依托单位:
Molecular mechanisms in two cell death-types, necrosis and apoptosis, induced by 5-fluoro-2'-deoxyuridine
  • 批准号:
    21790078
  • 项目类别:
    Grant-in-Aid for Young Scientists (B)
  • 资助金额:
    $2.75万
  • 财政年份:
    2009
  • 负责人:
    SATO Akira
  • 依托单位: