课题基金 / 基金详情

Temporal and spatial regulation of caspases in development and metamorphosis

Temporal and spatial regulation of caspases in development and metamorphosis
发育和变态过程中半胱天冬酶的时空调节
批准号:
nhmrc : 250349
负责人:
Prof Sharad Kumar
金额:
$31.56万
依托单位:
依托单位国家:
澳大利亚
项目类别:
NHMRC Project Grants
财政年份:
2003
资助国家:
澳大利亚
项目状态:
已结题
起止时间:
2003-01-01 至 2005-12-31

项目摘要

项目成果

Prof Sharad Kumar的其他基金

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中文摘要
翻译
细胞死亡通过一种称为细胞凋亡的特殊过程,是从体内删除不需要和有害细胞的一种手段。在胎儿发育期间发生广泛的细胞凋亡,这是去除胚胎生长期间产生的许多多余细胞所必需的。选择性细胞凋亡对于发育中的胎儿的不同组织和器官的形成也是必不可少的。在成年人中,细胞凋亡是免疫系统正常运作所必需的,以清除病毒感染和癌细胞,并在一般情况下保持体内细胞的正确数量。因此,失调的细胞凋亡与多种疾病的发病机制相关,例如自身免疫性疾病、许多形式的癌症和神经退行性疾病(例如阿尔茨海默病和帕金森病)、心脏病、局部缺血和其他病症。为了理解、管理和治疗由异常细胞凋亡引起的疾病,我们需要在分子和细胞水平上了解细胞凋亡是如何产生的,以及它是如何调节的。多年来,我们一直在详细研究这些过程。细胞凋亡执行细胞死亡的中心是一组蛋白酶,其靶向许多细胞蛋白进行特异性切割。这些蛋白酶的激活是启动细胞凋亡的关键步骤,因此每个细胞都开发了复杂的方法来控制这一过程。在目前的建议中,我们的目标是研究参与发育性细胞凋亡的半胱天冬酶的调节。此外,我们计划确定负责调节caspase激活的蛋白质。
英文摘要
Cell death by a special process called apoptosis is a means of deleting unwanted and harmful cells from the body. Extensive apoptosis occurs during foetal development which is required to get rid of many excess cells produced during the growth of the embryo. Selective apoptosis is also essential for the formation of different tissues and organs in developing foetus. In the adult, apoptosis is required for proper functioning of the immune system, to remove virus infected and cancer cells and in general to maintain the correct number of cells in the body. As such, misregulated apoptosis is associated with the pathogenesis of a wide array of diseases such as autoimmune diseases, many forms of cancer and neurodegenerative disorders (such as Alzheimer's and Parkinson's diseases), heart disease, ischaemia and other conditions. To understand, manage and treat disorders that result from aberrant apoptosis, we need to know at molecular and cellular level, how apoptosis is brought about and how it is regulated. We have been studying these processes in detail for several years. Central to the apoptotic execution of cell death are a group of proteases that target many cellular proteins for specific cleavage. The activation of these proteases is the crucial step in the initiation of apoptosis and therefore each cell has developed complex ways to control this process. In the present proposal, we aim to study regulation of caspases that are involved in developmental apoptosis. Furthermore, we plan to identify proteins that are responsible for the regulation of caspase activation.
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