课题基金 / 基金详情

项目摘要

项目成果

Deborah Ann Ferrington的其他基金

相似基金

相关文献

中文摘要
翻译
这一申请是为了回应作为2009年美国复苏和再投资法案一部分的两年潜在支持。具体目标已从最初的建议修改为适合2年的资金。蛋白酶体复合物在细胞生存过程中发挥着重要作用,如细胞周期调节,信号转导和基因表达的控制,氧化和错误折叠蛋白的降解。两种类型的蛋白酶体,组成型蛋白酶体和免疫蛋白酶体,已经被描述。本研究探讨了影响视网膜细胞中两种蛋白酶体亚型之间平衡的因素,并测试了有关视网膜稳态依赖于免疫蛋白酶体功能的特定假设。潜在的假设是免疫蛋白酶体的功能
英文摘要
This application is in response to potential support for two years as part of the American Recovery and Reinvestment Act of 2009. The Specific Aims have been modified from the original proposal to fit 2 years of funding. The proteasome complex plays a fundamental role in processes essential for cell viability, such as cell cycle regulation, control of signal transduction and gene expression, and the degradation of oxidized and misfolded proteins. Two types of proteasomes, the constitutive and immunoproteasomes, have been described. The proposed work investigates factors that influence the balance between the two proteasome subtypes in cells of the retina, and tests specific hypotheses regarding the dependence of retinal homeostasis on immunoproteasome function. The underlying hypothesis is that immunoproteasome performs functions that are vital to cells under stress; this hypothesis links the immunoproteasome to the innate immune system, and its role in tissue homeostasis, but does not limit it to immunological functions. Aim 1 tests the hypothesis that immunoproteasome is critical for maintaining a healthy retina under normal conditions in vivo. The approach is to use immunoproteasome-deficient mice lacking two (lmp7/-/mecl-r/-) catalytic subunits of immunoproteasome (L7Ml mice) to determine the consequences of inhibiting immunoproteasome expression by comparing age-matched WT and L7Ml mice, ages 1 to 24 months. Aim 2 tests the hypothesis that the inability to make immunoproteasome sensitizes the retina to more adverse outcomes following extraordinary stress. The extent of damage in WT and L7Ml mice after two distinct types of injury models (constant light and optic nerve crush) will be tested. Results from these experiments will help verify that immunoproteasome is an essential component of the retinal stress response and plays a fundamental role in maintaining retinal health.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Deciphering the mechanisms associated with high-risk AMD genotypes for ARMS2/HTRA1 andComplement Factor H
  • 批准号:
    10581822
  • 项目类别:
  • 资助金额:
    $41.89万
  • 财政年份:
    2022
  • 负责人:
    Deborah Ann Ferrington
  • 依托单位:
Deciphering the mechanisms associated with high-risk AMD genotypes for ARMS2/HTRA1 andComplement Factor H
  • 批准号:
    10707245
  • 项目类别:
  • 资助金额:
    $38.21万
  • 财政年份:
    2022
  • 负责人:
    Deborah Ann Ferrington
  • 依托单位:
Immunoproteasome: A key component of the cellular stress response
  • 批准号:
    7510560
  • 项目类别:
  • 资助金额:
    $14.72万
  • 财政年份:
    2008
  • 负责人:
    Deborah Ann Ferrington
  • 依托单位:
Training Grant: Functional Protemics of Aging
  • 批准号:
    8850365
  • 项目类别:
  • 资助金额:
    $28.26万
  • 财政年份:
    2008
  • 负责人:
    Deborah Ann Ferrington
  • 依托单位:
海外基金