Modulation of lysosomal function for the treatment of neuronal ceroid lipofuscino

调节溶酶体功能治疗神经元蜡样脂褐质

基本信息

  • 批准号:
    9103210
  • 负责人:
  • 金额:
    $ 34.41万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2012
  • 资助国家:
    美国
  • 起止时间:
    2012-09-30 至 2017-07-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): Neuronal ceroid lipofuscinoses (NCLs) are among the most devastating inherited disorders of childhood and the most common cause of neurodegeneration in children in the U.S. There is currently no cure for these disorders, and treatments remain largely supportive. NCLs are characterized by the progressive intralysosomal accumulation of ceroid lipopigment; this accumulation is thought to result from defects in lysosomal metabolism or trafficking, but could itself contribute to pathogenesis. We hypothesize that enhancing clearance processes will counteract disease progression in NCLs, even if the primary defect remains uncorrected. To test this hypothesis, we will boost lysosomal function by using genetic (Tfeb) and chemical (trehalose) enhancers of clearance processes in two mouse models of NCLs. In Aim 1 we will generate and characterize transgenic mice that conditionally express either a normal or constitutively active form of the transcription factor EB (TFEB), a master modulator of lysosomal and autophagic pathways. We will also perform molecular genetic analyses that will enable us to map the TFEB targetome, a crucial step in understanding its activities in health and disease. In Aim 2 we will cross these transgenics with Cln3 ex7/8 and Cln8mnd mice, two well-characterized models of NCLs, to investigate the effects of genetic TFEB enhancement on disease course. Importantly, we use models of NCL caused by mutations in two distinct genes in order to rigorously test whether TFEB- mediated clearance can indeed mitigate disease regardless of the underlying defect. In Aim 3 we will study the metabolism of trehalose, a putative inducer of autophagic pathways, which our data indicate activates TFEB; we will test the effect of trehalose on disease course in the two NCL models. Results from this project will show whether genetically or chemically induced lysosomal enhancement is able to counteract disease progression in NCLs and impact health and life span of affected animals. Positive results from this study will be the foundation for the development of a therapy for these devastating disorders. In addition, any knowledge gained from studies on NCLs could, in principle, be applicable to other neurodegenerative disorders caused by defects in lysosome-mediated cellular clearance.
描述(由申请人提供):神经元蜡样脂褐质病(NCL)是儿童期最具破坏性的遗传性疾病之一,也是美国儿童神经退行性疾病的最常见原因。目前,这些疾病无法治愈,治疗方法在很大程度上仍然是支持性的。NCL的特征在于蜡样脂肪色素的进行性溶酶体内蓄积;这种蓄积被认为是由溶酶体代谢或运输缺陷引起的,但其本身可能有助于发病机制。我们假设,增强清除过程将抵消NCL的疾病进展,即使原发性缺陷仍未纠正。为了验证这一假设,我们将通过在两种NCL小鼠模型中使用清除过程的遗传(Tfeb)和化学(海藻糖)增强剂来增强溶酶体功能。在目标1中,我们将产生和表征转基因小鼠,条件性表达正常或组成型活性形式的转录因子EB(TFEB),溶酶体和自噬途径的主调节剂。我们还将进行分子遗传分析,这将使我们能够绘制TFEB靶组,这是了解其在健康和疾病中的活动的关键一步。在目标2中,我们将这些转基因小鼠与Cln 3 ex 7/8和Cln 8 mnd小鼠(两种充分表征的NCL模型)杂交,以研究遗传TFEB增强对疾病进程的影响。重要的是,我们使用由两种不同基因中的突变引起的NCL模型,以严格测试TFEB介导的清除是否确实可以减轻疾病,而不管潜在的缺陷如何。在目标3中,我们将研究海藻糖的代谢,海藻糖是一种假定的自噬途径诱导剂,我们的数据表明其激活TFEB;我们将在两种NCL模型中检测海藻糖对病程的影响。该项目的结果将显示遗传或化学诱导的溶酶体增强是否能够抵消NCL的疾病进展并影响受影响动物的健康和寿命。这项研究的积极成果将成为发展的基础, 治疗这些毁灭性疾病的方法此外,从NCL研究中获得的任何知识原则上都适用于溶酶体介导的细胞清除缺陷引起的其他神经退行性疾病。

项目成果

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会议论文数量(0)
专利数量(0)

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Marco Sardiello其他文献

Marco Sardiello的其他文献

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{{ truncateString('Marco Sardiello', 18)}}的其他基金

TFEB-mediated lysosome-to-nucleus signaling in aging and lifespan regulation
TFEB 介导的溶酶体到细胞核信号传导在衰老和寿命调节中的作用
  • 批准号:
    10172235
  • 财政年份:
    2021
  • 资助金额:
    $ 34.41万
  • 项目类别:
TFEB-mediated lysosome-to-nucleus signaling in aging and lifespan regulation
TFEB 介导的溶酶体到细胞核信号传导在衰老和寿命调节中的作用
  • 批准号:
    10413974
  • 财政年份:
    2021
  • 资助金额:
    $ 34.41万
  • 项目类别:
TFEB-mediated lysosome-to-nucleus signaling in aging and lifespan regulation
TFEB 介导的溶酶体到细胞核信号传导在衰老和寿命调节中的作用
  • 批准号:
    10583543
  • 财政年份:
    2021
  • 资助金额:
    $ 34.41万
  • 项目类别:
Mechanisms Of Er-To-Golgi Transport Of Lysosomal Enzymes
溶酶体酶从 Er 到高尔基体的转运机制
  • 批准号:
    10345430
  • 财政年份:
    2019
  • 资助金额:
    $ 34.41万
  • 项目类别:
Mechanisms Of Er-To-Golgi Transport Of Lysosomal Enzymes
溶酶体酶从 Er 到高尔基体的转运机制
  • 批准号:
    10376728
  • 财政年份:
    2019
  • 资助金额:
    $ 34.41万
  • 项目类别:
Mechanisms Of Er-To-Golgi Transport Of Lysosomal Enzymes
溶酶体酶从 Er 到高尔基体的转运机制
  • 批准号:
    10094001
  • 财政年份:
    2019
  • 资助金额:
    $ 34.41万
  • 项目类别:
Modulation of lysosomal function for the treatment of Batten disease
调节溶酶体功能治疗巴顿病
  • 批准号:
    10317363
  • 财政年份:
    2012
  • 资助金额:
    $ 34.41万
  • 项目类别:
Modulation of lysosomal function for the treatment of Batten disease
调节溶酶体功能治疗巴顿病
  • 批准号:
    10247068
  • 财政年份:
    2012
  • 资助金额:
    $ 34.41万
  • 项目类别:
Modulation of lysosomal function for the treatment of neuronal ceroid lipofuscino
调节溶酶体功能治疗神经元蜡样脂褐质
  • 批准号:
    8660355
  • 财政年份:
    2012
  • 资助金额:
    $ 34.41万
  • 项目类别:
Modulation of lysosomal function for the treatment of neuronal ceroid lipofuscino
调节溶酶体功能治疗神经元蜡样脂褐质
  • 批准号:
    8843982
  • 财政年份:
    2012
  • 资助金额:
    $ 34.41万
  • 项目类别:

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