The Role of BMP-10 in Cardiac Development

BMP-10 在心脏发育中的作用

基本信息

  • 批准号:
    6623300
  • 负责人:
  • 金额:
    $ 33.53万
  • 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
  • 起止时间:
    2002-04-01 至 2006-03-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): During the midgestation of mammalian embryonic development (E9.5-E15.5), the newly formed embryonic heart is required to grow rapidly in cell number and size and undergoes a series of morphological and functional changes in response to the increasing volume of circulating blood. The proliferating cardiomyocytes form a distinct loose interwoven meshwork of myocardial fibers, the so-called ventricular trabeculae, in E9.5 ventricular chambers. By E14.5, these trabecular structures become more compact toward the epicardial surface, and the intertrabecular recesses are reduced to capillaries. The significant reduction of trabeculation is closely associated with the myocardium growth arrest that leads to an early embryonic lethality. On the other hand, the abnormal enhancement of growth activity of myocardium leads to the failure of myocardial compaction, which is likely the cause of a severe pediatric cardiac disease, Noncompaction of the Ventricular Myocardium, in humans. However, there is little known about the underlying molecular and cellular mechanism. Recently, we found that a member of transforming growth factor beta superfamily, Bone Morphogenetic Protein-10 (BMP10), may be a novel peptide growth factor involved in the cardiac ventricular trabeculation and compaction during the midgestation stages. This proposal is designed to test our hypothesis that BMP-l0 is critical to the cardiac growth and ventricular trabeculation-compaction using both in vitro and in vivo analyses. We propose to: 1) Assess the role of BMP-10 in enhancing embryonic cardiomyocyte proliferation using two cardiomyocyte growth assays in vitro; 2) Determine the BMP-10 dependency of cardiomyocyte proliferation; 3) Analyze the role of BMP-10 in cardiac development by generating BMP-10- deficient mice; 4) Further define the role of BMP-10 using a transgenic approach. We believe that our effort will shed light on further understanding of cardiac development and some forms of congenital cardiac defects.
描述(由申请人提供):哺乳动物妊娠中期

项目成果

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WEINIAN SHOU其他文献

WEINIAN SHOU的其他文献

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{{ truncateString('WEINIAN SHOU', 18)}}的其他基金

Deciphering the mechanisms of c-kit+ cells in heart repair
破译c-kit细胞在心脏修复中的机制
  • 批准号:
    10166901
  • 财政年份:
    2018
  • 资助金额:
    $ 33.53万
  • 项目类别:
The role of Smyd4 in regulating cardioprogenitor specification.
Smyd4 在调节心脏祖细胞规格中的作用。
  • 批准号:
    10495951
  • 财政年份:
    2017
  • 资助金额:
    $ 33.53万
  • 项目类别:
Molecular Pathway in Myocardium Development
心肌发育的分子途径
  • 批准号:
    7793581
  • 财政年份:
    2007
  • 资助金额:
    $ 33.53万
  • 项目类别:
Molecular Pathway in Myocardium Development
心肌发育的分子途径
  • 批准号:
    7305004
  • 财政年份:
    2007
  • 资助金额:
    $ 33.53万
  • 项目类别:
Molecular Pathway in Myocardium Development
心肌发育的分子途径
  • 批准号:
    7469412
  • 财政年份:
    2007
  • 资助金额:
    $ 33.53万
  • 项目类别:
Molecular Pathway in Myocardium Development
心肌发育的分子途径
  • 批准号:
    7617155
  • 财政年份:
    2007
  • 资助金额:
    $ 33.53万
  • 项目类别:
Role of FKBP52 in androgen signaling and hypospadias
FKBP52 在雄激素信号传导和尿道下裂中的作用
  • 批准号:
    7339838
  • 财政年份:
    2006
  • 资助金额:
    $ 33.53万
  • 项目类别:
Role of FKBP52 in androgen signaling and hypospadias
FKBP52 在雄激素信号传导和尿道下裂中的作用
  • 批准号:
    7540934
  • 财政年份:
    2006
  • 资助金额:
    $ 33.53万
  • 项目类别:
Role of FKBP52 in androgen signaling and hypospadias
FKBP52 在雄激素信号传导和尿道下裂中的作用
  • 批准号:
    7017512
  • 财政年份:
    2006
  • 资助金额:
    $ 33.53万
  • 项目类别:
Role of FKBP52 in androgen signaling and hypospadias
FKBP52 在雄激素信号传导和尿道下裂中的作用
  • 批准号:
    7172662
  • 财政年份:
    2006
  • 资助金额:
    $ 33.53万
  • 项目类别:

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