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中文摘要
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描述(由申请人提供):支持被要求为基石研讨会会议题为自噬:疾病的基础,由克里斯蒂娜H。Eng,丹尼尔J. Klionsky,Guido Kroemer and Li Yu.会议将于2014年5月23日至28日在德克萨斯州奥斯汀举行。自噬是一个基本的细胞过程,在基础和细胞或环境应激条件下协调蛋白质,脂质和细胞器的降解。自噬曾经被认为只发生在营养有限的时期,但显然在发育和病理情况下都起着重要作用。随着自噬在多种疾病中的重要性日益显现,需要深入了解自噬的主要和替代途径,以充分理解和有效调控自噬。本次会议将重点介绍自噬研究的前沿,从基本的机制见解和信号传导到自噬在多个疾病领域中的作用以及治疗靶向的前景。讨论的关键领域将包括自噬体膜的来源,对macroautophagy和mitophagy的新机制见解,以及自噬在正常和疾病情况下的关键作用,如癌症,神经退行性疾病,克罗恩病,溶酶体贮积病,心肌病和衰老。检查自噬在疾病中的作用将使我们能够了解自噬调节可能有益的背景,并确定控制自噬的核心过程将使我们能够确定调节途径的工具。这次会议将汇集各种研究人员探索自噬的不同方面,他们的相互作用将扩大我们对不同背景下的基本自噬机制及其在生理和病理环境中的关键功能的了解。
英文摘要
DESCRIPTION (provided by applicant): Support is requested for a Keystone Symposia meeting entitled Autophagy: Fundamentals to Disease, organized by Christina H. Eng, Daniel J. Klionsky, Guido Kroemer and Li Yu. The meeting will be held in Austin, Texas from May 23-28, 2014. Autophagy is a fundamental cellular process that orchestrates the degradation of proteins, lipids and organelles during both basal and cellular or environmental stress conditions. Once thought to occur only during times of nutrient limitation, autophagy clearly plays major roles in both developmental and pathological situations. As the importance of autophagy in a variety of diseases is emerging, an in-depth knowledge of primary and alternative autophagic pathways is required to fully understand and effectively modulate it. The forefront of autophagy research will be highlighted at this meeting, from basic mechanistic insights and signaling to the role autophagy plays in multiple disease areas and prospects for therapeutic targeting. Key areas of discussion will include the source of the autophagosomal membrane, new mechanistic insights into both macroautophagy and mitophagy, and the critical roles of autophagy in normal and disease situations such as cancer, neurodegenerative diseases, Crohn's disease, lysosomal storage diseases, cardiomyopathy and aging. Examining the role of autophagy in disease will enable us to understand in contexts in which modulation of autophagy may be beneficial, and identifying the core processes that control autophagy will enable us to identify tools to modulate the pathway. This meeting will bring together a variety of investigators exploring different facets of autophagy, and their interactions will expand our knowledge of fundamental autophagic mechanisms in different contexts and their critical functions in physiological and pathological settings.
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会议论文
Fibrosis: From Basic Mechanisms to Targeted Therapies
  • 批准号:
    9039836
  • 项目类别:
  • 资助金额:
    $1.5万
  • 财政年份:
    2016
  • 负责人:
    DAVID L. WOODLAND
  • 依托单位:
Stem Cells and Cancer
  • 批准号:
    8985625
  • 项目类别:
  • 资助金额:
    $0.5万
  • 财政年份:
    2016
  • 负责人:
    DAVID L. WOODLAND
  • 依托单位:
Microglia in the Brain
  • 批准号:
    9125542
  • 项目类别:
  • 资助金额:
    $1.08万
  • 财政年份:
    2016
  • 负责人:
    DAVID L. WOODLAND
  • 依托单位:
Chromatin and Epigenetics
  • 批准号:
    9106870
  • 项目类别:
  • 资助金额:
    $0.4万
  • 财政年份:
    2016
  • 负责人:
    DAVID L. WOODLAND
  • 依托单位:
海外基金