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Activin Receptor-Like Kinase-2 in Cardiac Morphogenesis

Activin Receptor-Like Kinase-2 in Cardiac Morphogenesis
心脏形态发生中的激活素受体样激酶 2
批准号:
6844624
负责人:
VESA M KAARTINEN
金额:
$29.76万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-02-01 至 2008-01-31

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中文摘要
翻译
描述(由申请人提供):心血管系统畸形是人类最常见的先天缺陷之一。进化保守的tgf - β分泌生长因子超家族成员已被证明在正常心脏发育过程中发挥重要作用。它们都通过几种不同的I型受体(称为激活素受体样激酶;Alks)发出信号,这些受体是信号特异性的主要决定因素。在这些受体中,AIk2是特别有趣的,因为AIk2似乎同时介导BMP、激活素和tgf - β信号。AIk2在心脏中强烈表达,我们的初步实验表明,AIk2是正常心脏发育所必需的。
英文摘要
DESCRIPTION (provided by applicant): Malformations of the cardiovascular system are among the most common birth defects in humans. Members of the evolutionary conserved TGF-beta superfamily of secreted growth factors have been shown to play important roles during normal heart development. They all signal through several different type I receptors (called Activin Receptor-Like Kinases; Alks), which are the primary determinants of signaling specificity. Among these receptors AIk2 is of particular interest, since it appears that AIk2 mediates both BMP, Activin and TGFbeta signals. AIk2 is strongly expressed in the heart, and our preliminary experiments demonstrate that AIk2 is required for normal cardiac development. Therefore, we hypothesize that AIk2 plays a key role in cardiac outflow tract development by regulating differentiation, proliferation and/or survival of cardiac neural crest cells. We will test this hypothesis by three Specific Aims by utilizing a genetically manipulated mouse strain we recently developed that allows inactivation of AIk2 specifically in neural crest cells. In Aim 1, defects in valves, septa and outflow tracts will be analyzed in detail. In Aim 2, we will define the specific process controlled by AIk2 during cardiac outflow tract morphogenesis, and in Aim 3 we will identify the relevant downstream signaling molecules, Smads, and transcriptional targets in the AIk2-mediated pathway. Our experimental strategy will allow us to determine the biological role of AIk2 in cardiac outflow tract development. The results of these studies are likely to be of critical importance in attempting to reach our long-term goal to understand the molecular basis of life-threatening congenital heart defects in humans.
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