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A chemical screen to identify molecular mechanisms of rod outer segment renewal

用于识别棒外节更新分子机制的化学筛选

基本信息

批准号：
8828697
负责人：
ABIGAIL M JENSEN
金额：
$ 19.48万
依托单位：
UNIVERSITY OF MASSACHUSETTS AMHERST
依托单位国家：
美国
项目类别：
财政年份：
2014
资助国家：
美国
起止时间：
2014-04-01 至 2017-03-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8828697
关键词：
Affect Animal Model Animals Biological Assay Biological Sciences Candidate Disease Gene Cell Maintenance Cells Cellular biology Chemicals Cilia Digestion Dimethyl Sulfoxide Disease Distal Eye FDA approved Fertilization Goals Growth Health Heat-Shock Response Human Label Laboratories Larva Laser Scanning Confocal Microscopy Length Libraries Life Light Maintenance Mammals Measures Molecular Molecular Genetics Molecular Target Morphogenesis Morphology Mus Neurons Organelles Pathway interactions Phagocytosis Pharmaceutical Preparations Photons Photoreceptors Process Research Research Project Grants Retina Retinal Retinal Degeneration Retinal Photoreceptors Rhodopsin Rod Outer Segments Signal Transduction Staging Structure Structure of retinal pigment epithelium Testing Transgenic Organisms Vertebrate Photoreceptors Vision Zebrafish design genetic approach mouse model mutant offspring photoreceptor degeneration red fluorescent protein retinal rods reverse genetics rod outer segment disc screening small molecule libraries trafficking tv watching

项目摘要

DESCRIPTION (provided by applicant): The long-term goal of this research is to identify and define the molecular pathways and cellular mechanisms that regulate retinal photoreceptor maintenance. Retinal photoreceptors are unique cells in that they are continually renewing a part of themselves - their outer segments, the light receptive organelle. Although this renewal process is central to the function of photoreceptors we still know very little about how these cell renew their outer segments. It is observed that the outer segments of photoreceptors progressively shorten before photoreceptors die during photoreceptor degeneration diseases and the question remains as to whether these cells might be dying because they lose their outer segments. This proposal focuses primarily on identifying the molecular mechanisms that control rod photoreceptor outer segment renewal. This proposal has one specific aim: perform a high content screen to identify compounds and molecular pathways affecting rod outer segment renewal, phagocytosis and digestion of shed rod outer segment material by the neighboring retinal pigmented epithelium, rod outer segment disc integrity, Rhodopsin trafficking and localization, and rod differentiation and morphogenesis. This project will use chemical libraries, containing many chemical compounds with known molecular targets. Although the primary objective of the proposal is to identify chemical compounds that stimulate outer segment growth, the design of the screen offers the unique and rich opportunity to identify compounds that affect additional aspects of rod photoreceptor cell biology and maintenance. This project will use young zebrafish larvae as a model organism. Zebrafish rod photoreceptors have the same morphology as mammalian species and similarly renew their outer segments. Zebrafish offers several advantages for this research. For example, this proposed screen requires large numbers of double transgenic larvae that also are homozygous mutants (albino) and large numbers of zebrafish offspring can be produced from a small number of matings. Rods are already maintaining their outer segments through renewal as soon as 6 days after fertilization, in comparison, it takes several weeks after fertilization for mouse rods to reach the same stage. In addition, unlike mammals, the retina continues to grow in zebrafish, which means that we also can examine new rods in the retinal margin to identify regulators of photoreceptor differentiation and initial photoreceptor morphogenesis, such as inner and outer segment formation at the same time that we screen for regulators of outer segment renewal, phagocytosis and digestion of shed rod outer segment material by the neighboring retinal pigmented epithelium, rod outer segment disc integrity, Rhodopsin trafficking and localization. If, as expected, chemical compounds are discovered that lengthen outer segments by either stimulating growth or suppressing shedding, these can then be tested in zebrafish and mouse models of human retinal degeneration disease for their ability to maintain outer segments, promote photoreceptor survival and prolong vision.

描述（由申请人提供）：本研究的长期目标是确定和定义调节视网膜感光细胞维持的分子途径和细胞机制。视网膜光感受器是一种独特的细胞，因为它们不断更新自己的一部分-它们的外节，光感受器。尽管这种更新过程是光感受器功能的核心，但我们对这些细胞如何更新其外节仍然知之甚少。据观察，在光感受器变性疾病期间，光感受器的外节在光感受器死亡之前逐渐缩短，并且问题仍然是这些细胞是否可能因为失去外节而死亡。这项建议主要集中在确定控制视杆细胞外节更新的分子机制。该提议具有一个特定目的：进行高内容筛选以鉴定影响视杆外段更新、邻近视网膜色素上皮细胞对脱落视杆外段材料的吞噬作用和消化、视杆外段椎间盘完整性、视紫红质运输和定位以及视杆分化和形态发生的化合物和分子途径。该项目将使用化学库，其中包含许多具有已知分子靶点的化合物。虽然该提案的主要目的是确定刺激外节生长的化合物，但屏幕的设计提供了独特且丰富的机会来确定影响视杆细胞生物学和维护的其他方面的化合物。该项目将使用年轻的斑马鱼幼虫作为模式生物。斑马鱼杆状光感受器具有与哺乳动物物种相同的形态，并且类似地更新它们的外节。斑马鱼为这项研究提供了几个优势。例如，这种提出的筛选需要大量的双转基因幼虫，它们也是纯合突变体（白化病），并且可以从少量的交配中产生大量的斑马鱼后代。受精后6天，杆状体就已经通过更新维持其外节，相比之下，小鼠杆状体在受精后需要几周才能达到相同的阶段。此外，与哺乳动物不同，斑马鱼的视网膜继续生长，这意味着我们也可以检查视网膜边缘的新视杆细胞，以确定感光细胞分化和初始感光细胞形态发生的调节因子，例如内外段形成，同时我们筛选外段更新的调节因子，通过邻近的视网膜色素上皮细胞对脱落的视杆外段材料的吞噬和消化、视杆外段盘的完整性、视紫红质运输和定位。如果像预期的那样，发现通过刺激生长或抑制脱落来延长外节的化合物，那么可以在斑马鱼和人类视网膜变性疾病的小鼠模型中测试它们维持外节，促进感光细胞存活和延长视力的能力。