Neointimal formation in the earotid artery of in IP3^R knock out mouse
IP3^R 敲除小鼠耳动脉中的新内膜形成
基本信息
- 批准号:14571129
- 负责人:
- 金额:$ 2.05万
- 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:2002
- 资助国家:日本
- 起止时间:2002 至 2003
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Vascular remodeling with neointimal formation was studied in 1P3-R knock out mouse. IP3-R type1 hetero knock out mouse (n=10)、 IP-3 type2 homo knock out mouse (n=9)、 IP-3 type3 homo knock out mouse (n=11) and control mouse (n=10) were used in the carotid ligation model. The animals were anesthetized, and the left common carotid artery was exposed through a small midline incision in the neck. The artery was completely ligated just proximal to the carotid bifurcation to disrupt blood flow. Left carotids were snap-frozen at days 28 after ligation. Neointima area/medial area ratio was calculated. The maximum ratio of IP3-type1 and type2 homo knock out mouse group was significantly smaller than that of control. The average ratio of IP-3 type2 and type3 homo knock out mouse group was significantly smaller than that of control. In this study, intimal hyperplasia in the carotid ligation model was suppressed in IP3-R knockout mouse.
研究了1P3-R基因敲除小鼠血管重塑与新生内膜形成的关系。颈动脉结扎模型采用IP3-R型异源基因敲除小鼠(n=10)、、IP-3型基因敲除小鼠(n=9)、、IP-3型基因敲除小鼠(n=11)和对照组(n=10)。动物麻醉后,通过颈部正中小切口暴露左侧颈总动脉。动脉被完全结扎在颈动脉分叉处的近端,以扰乱血流。结扎后第28天快速冰冻左侧颈总动脉。计算新生内膜面积/中膜面积比值。IP3-type1和type2基因敲除小鼠的最大比值显著小于对照组。IP-3型2和3型基因敲除小鼠的平均比例显著低于对照组。在本研究中,IP3-R基因敲除小鼠颈动脉结扎模型中的内膜增生受到抑制。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
NAKAZAWA Tatsu其他文献
NAKAZAWA Tatsu的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
相似海外基金
RII Track-4: NSF: Developing 3D Models of Live-Endothelial Cell Dynamics with Application Appropriate Validation
RII Track-4:NSF:开发活内皮细胞动力学的 3D 模型并进行适当的应用验证
- 批准号:
2327466 - 财政年份:2024
- 资助金额:
$ 2.05万 - 项目类别:
Standard Grant
CAREER: Modulating endothelial cell function using targeted electrical stimulation
职业:使用靶向电刺激调节内皮细胞功能
- 批准号:
2338949 - 财政年份:2024
- 资助金额:
$ 2.05万 - 项目类别:
Continuing Grant
ERI: Biological Effects of Low-Frequency, Low-Intensity Ultrasound on Endothelial Cell and Macrophage Co-Culture
ERI:低频、低强度超声对内皮细胞和巨噬细胞共培养的生物学效应
- 批准号:
2347558 - 财政年份:2024
- 资助金额:
$ 2.05万 - 项目类别:
Standard Grant
Control of endothelial cell mechanics and blood vessel remodeling by blood flow
通过血流控制内皮细胞力学和血管重塑
- 批准号:
23K23887 - 财政年份:2024
- 资助金额:
$ 2.05万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Reverse translarional research based on cultured human corneal endothelial cell injection therapy
基于培养人角膜内皮细胞注射疗法的反向翻译研究
- 批准号:
23H03062 - 财政年份:2023
- 资助金额:
$ 2.05万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Endothelial Cell Reprogramming in Familial Intracranial Aneurysm
家族性颅内动脉瘤的内皮细胞重编程
- 批准号:
10595404 - 财政年份:2023
- 资助金额:
$ 2.05万 - 项目类别:
General Capillary to Arterial Endothelial Cell Transition in Pulmonary Arterial Hypertension
肺动脉高压中毛细血管内皮细胞向动脉内皮细胞的转变
- 批准号:
10716738 - 财政年份:2023
- 资助金额:
$ 2.05万 - 项目类别:
Role of endothelial cell senescence in age-related cardiomyopathy
内皮细胞衰老在年龄相关性心肌病中的作用
- 批准号:
10726050 - 财政年份:2023
- 资助金额:
$ 2.05万 - 项目类别:
Altered microglia states and microglia-endothelial cell axis in relation to white matter disease progression in VCID
VCID 中小胶质细胞状态和小胶质细胞内皮细胞轴的改变与白质疾病进展相关
- 批准号:
10738860 - 财政年份:2023
- 资助金额:
$ 2.05万 - 项目类别:
MLL1 drives collaborative leukocyte-endothelial cell signaling and thrombosis after coronavirus infection
MLL1在冠状病毒感染后驱动白细胞-内皮细胞信号传导和血栓形成
- 批准号:
10748433 - 财政年份:2023
- 资助金额:
$ 2.05万 - 项目类别: