Regulation of cellular cytoskeleton by the soluble LDL receptor family with the application for novel anti-atherosclerosis therapy
Regulation of cellular cytoskeleton by the soluble LDL receptor family with the application for novel anti-atherosclerosis therapy
批准号:
21390277
负责人:
BUJO Hideaki
金额:
$11.07万
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:
2009
资助国家:
日本
项目状态:
已结题
起止时间:
2009 至 2011
中文摘要
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英文摘要
Soluble form of LR11, a member of LDL receptor family, plays an important role in the pathological phenotypic conversion of intimal smooth muscle cells. The aim of study was to clarify the mechanism underlying the regulation of cytoskeleton reorganization to achieve the acceleration of cellular migration and adhesion through the LR11-mediated pathways, the involvement of sLR11 in various diseases, and the basic significance for the development of novel therapy against atherosclerosis. The results obtained from the cell-biological, animal or patient analysis has shown that soluble LR11 is important for the common mechanism underlying the migration for floating cells as well as attached cells, the differentiation of adipocytes, and the development of vascular injury. These results suggested that the target regulation focused on the molecule contributes to the development of novel therapy to regulate the cell migration in the fields of atherosclerosis and also in other diseases.
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Interrelations between CSF soluble APP, amyloid-b 1-42, SORL1, and tau levels in Alzheimer's disease
阿尔茨海默病中脑脊液可溶性 APP、淀粉样蛋白-b 1-42、SORL1 和 tau 水平之间的相互关系
DOI:
--
发表时间:
2011
期刊:
J Alzheimers Dis
影响因子:
4
作者:
[Alexopoulos P, Luo L-H, Tsolakidou A, Kratzer M, Grimmer T, Westerteicher C, Jiang M, Bujo H, Diehl-Schmid J, Kurz A, Perneczky R]
通讯作者:
Perneczky R
DOI:
10.1007/s00406-012-0295-x
发表时间:
2012-09-01
期刊:
EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE
影响因子:
4.7
作者:
[Guo, Liang-Hao, Westerteicher, Christine, Perneczky, Robert]
通讯作者:
Perneczky, Robert
Enhanced circulating solubule LR11 in patients with coronary organic stenosis.
冠状动脉器质性狭窄患者循环可溶性 LR11 增强。
DOI:
--
发表时间:
2010
期刊:
Atherosclerosis
影响因子:
5.3
作者:
[Takahashi M, Bujo H, Jiang M, Noike H, Saito Y, Shirai K.]
通讯作者:
Shirai K.
DOI:
10.1016/j.yexcr.2011.10.007
发表时间:
2012-01-01
期刊:
EXPERIMENTAL CELL RESEARCH
影响因子:
3.7
作者:
[Aoyagi, Yasuyuki, Kuroda, Masayuki, Bujo, Hideaki]
通讯作者:
Bujo, Hideaki
Crystallization and preliminary crystallographic anal-ysis of human LR11 Vps10p domain
人LR11 Vps10p结构域的结晶及初步晶体学分析
DOI:
10.1107/s1744309110048153
发表时间:
2011
期刊:
Acta Crystallogr Sect F Struct Biol Cryst Commun
影响因子:
--
作者:
[Nakata Z, Nagae M, Yasui N, Bujo H, Nogi T, Takagi J]
通讯作者:
Takagi J
共 12 条
Examinational significance and production mechanism of a circulating soluble receptor for the diagnosis of activated adipocytes to prevent diabetes
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批准号:16H05231
-
项目类别:Grant-in-Aid for Scientific Research (B)
-
资助金额:$11.56万
-
财政年份:2016
-
负责人:BUJO Hideaki
-
依托单位:
Identification of the pathologically-transited immature cells diagnosed by soluble LR11
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批准号:15K15198
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项目类别:Grant-in-Aid for Challenging Exploratory Research
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资助金额:$2.41万
-
财政年份:2015
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负责人:BUJO Hideaki
-
依托单位:
Molecular clarification of trans-differentiation to brown adipocytes through the action of soluble receptor LR11
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批准号:24390231
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项目类别:Grant-in-Aid for Scientific Research (B)
-
资助金额:$9.48万
-
财政年份:2012
-
负责人:BUJO Hideaki
-
依托单位:
Amelioration of pathological phenotypes of vascular smooth muscle cells by the sLR11 regulation
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批准号:19591036
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.91万
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财政年份:2007
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负责人:BUJO Hideaki
-
依托单位:
Molecular analysis and clinical application of LR11 in SMCs.
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批准号:17590917
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.24万
-
财政年份:2005
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负责人:BUJO Hideaki
-
依托单位:
Functional analysis of LR11 in vascular smooth muscle cells
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批准号:12835002
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.37万
-
财政年份:2000
-
负责人:BUJO Hideaki
-
依托单位:
Functional analysis of the brain-specific LDL receptor family memners
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批准号:09671027
-
项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$2.05万
-
财政年份:1997
-
负责人:BUJO Hideaki
-
依托单位:
海外基金