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Bone Morphogenetic Proteins in Arterial Remodeling

Bone Morphogenetic Proteins in Arterial Remodeling
动脉重塑中的骨形态发生蛋白
批准号:
6724915
负责人:
Raul J. Guzman
金额:
$11.84万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-04-01 至 2007-03-31

项目摘要

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中文摘要
翻译
描述(由申请人提供): 本指导K 08提案描述了一个为期5年的培训计划,博士。 古兹曼在血管领域向科学独立的转变 生物学 候选人是外科系的助理教授 和细胞生物学 他现在将扩展他的科学技能和知识 基地通过多学科的互动与博士布里吉德L霍根,一个高级 我们的细胞生物学系成员和理查德胡佛博士,从 病理学系和范德比尔特血管生物学主任 培训计划。 古兹曼博士还寻求了一位顾问的帮助, 一个由德高望重的科学家组成的委员会, 职业建议 他们包括杰弗里·巴瑟博士、芭芭拉·梅里克博士和 道格拉斯沃恩。 细胞生物学系为这次培训提供了理想的环境 程序。 它结合了来自广泛学科的专业知识, 广泛的资源,可以用来支持年轻的教师。 在 除了直接在霍根博士的实验室工作外,古兹曼博士还将 有一个专门的实验室空间,位于靠近霍根博士的 实验室和属于细胞生物学系的实验室走廊里。 古兹曼得到了他的处长和部门主席的全力支持, 他将75%的时间用于追求他的学术研究目标, 奖期。 古兹曼博士的近期目标是获得必要的培训和经验 成为一名独立的科学家 研究计划的重点是 骨形态发生蛋白(BMPs)在病理性动脉重构中的作用这 细胞外信号蛋白家族属于TGF-β超家族 并且其在血管疾病中的作用尚未被表征。 背景 初步数据表明,这些蛋白质可能是重要的调节因子, 通过其对血管平滑肌细胞迁移的影响, 增殖 根据他的初步数据,古兹曼博士假设, BMP受体可能是基因导向策略控制肿瘤的理想靶点。 内膜增生 具体目标包括:1)时间特征化 病理性动脉粥样硬化中Bmp表达的过程和细胞分布 在小鼠中重塑。 2)确定剪切应力在诱导 体外内皮细胞BMP 4表达。 3)评价IA型BMP的效果 和IB受体激活对损伤诱导的SMC增殖和内膜增殖的影响 体内积累。 4)检测BMP IA型和IB型受体的作用 激活对SMC迁移、侵袭和增殖的影响。 为了 为了实现这些具体目标,古兹曼博士概述了他的研究生涯。 发展计划,其中包括在实验室的重点培训期, 霍根博士沿着在相关领域的课程工作。 在此期间,他将 学习进行原位杂交和双杂交技术, 免疫荧光染色。 他还将学习基本技术 参与转基因和基因敲除小鼠品系的开发。 博士 古兹曼的长期目标是为我们的 了解病理性动脉重塑。 预计在 在此期间,古兹曼博士将朝着成为一名 独立科学调查员。
英文摘要
DESCRIPTION (provided by applicant): This Mentored K08 proposal describes a 5 year training program for Dr. Guzman's transition to scientific independence in the field of vascular biology. The candidate is an Assistant Professor in the Department of Surgery and Cell Biology. He will now expand on his scientific skills and knowledge base through a multidisciplinary interaction with Dr. Brigid L Hogan, a senior member of our Department of Cell Biology and Dr. Richard Hoover, from the Department of Pathology and the director of the Vanderbilt Vascular Biology Training Program. Dr. Guzman has also enlisted the help of an advisory committee of-highly-respected scientists who will provide scientific and career advice. They include Dr. Jeffrey Balser, Dr. Barbara Meyrick and Dr. Douglas Vaughan. The Department of Cell Biology provides an ideal environment for this training prograrn. It incorporates expertise from a broad array of disciplines and has extensive resources that can be used to support young faculty members. In addition to working directly in the laboratory of Dr. Hogan, Dr. Guzman will have a dedicated lab space that is located in close proximity to Dr. Hogan's lab and in a corridor of labs belonging to the Department of Cell Biology. Guzman has the full support of his Division Chief and Departmental Chair to devote 75 percent of his time to pursuing his academic research goals during the award period. Dr. Guzman's immediate goal is to obtain the training and experience necessary to become an independent scientist. The research plan focuses on the role of the Bone Morphogenetic Proteins (BMPs) in pathologic arterial remodeling. This family of extracellular signaling proteins belongs to the TGF-P superfamily and its role in vascular disease has not been characterized. The background and preliminary data suggest that these proteins may be important regulators of restenosis via their effects on vascular smooth muscle cell migration and proliferation. Based on his preliminary data, Dr. Guzman hypothesizes that BMP receptors may be ideal targets for gene-directed strategies to control intinial hyperplasia. The specific aims include: 1) Characterize the time course and cellular distribution of Bmp expression during pathologic arterial remodeling in mice. 2) Determine the role of shear stress in inducing endothelial BMP4 expression in-vitro. 3) Evaluate the effect of BMP type IA and IB receptor activation on injury-induced SMC proliferation and intinial accumulation in vivo. 4) Examine the effect of BMP type IA and IB receptor activation on SMC migration, invasion, and proliferation in vitro. In order to perform these specific aims, Dr. Guzman has outlined a research career development plan that includes a focused training period in the laboratory of Dr. Hogan along with course work in relevant areas. During this time he will learn to perform the techniques of in situ hybridization and double immunofluorescent staining. He will also learn fundamental techniques involved in the development of transgenic and knockout mouse strains. Dr. Guzman's long term goal is to make significant contributions to our understanding of pathologic arterial remodeling. It is expected that during this award period, Dr. Guzman will progress toward his goal of becoming an independent scientific investigator.
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Role of MMPs in arterial calcification
  • 批准号:
    10004162
  • 项目类别:
  • 资助金额:
    $46.35万
  • 财政年份:
    2019
  • 负责人:
    Raul J. Guzman
  • 依托单位:
Role of Arterial Calcification in Restenosis
Role of Arterial Calcification in Restenosis
Role of Arterial Calcification in Restenosis
  • 批准号:
    8383478
  • 项目类别:
  • 资助金额:
    $17.11万
  • 财政年份:
    2010
  • 负责人:
    Raul J. Guzman
  • 依托单位:
海外基金