FGF Receptors in Myelin Function and Disease

FGF 受体在髓磷脂功能和疾病中的作用

• 批准号: 6906406
• 负责人: RASHMI BANSAL
• 金额: $ 34.44万
• 依托单位: UNIVERSITY OF CONNECTICUT SCH OF MED/DNT
• 依托单位国家: 美国
• 财政年份: 1999
• 资助国家: 美国
• 起止时间: 1999-07-05 至 2008-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6906406
• 关键词: SDS polyacrylamide gel electrophoresis; biological signal transduction; cell differentiation; cell growth regulation; electron microscopy; fibroblast growth factor; genetic regulation; genetically modified animals; growth factor receptors; immunocytochemistry; laboratory mouse; laboratory rat; mass spectrometry; myelin; myelination; neurogenesis; oligodendroglia; protein structure function; receptor expression; tissue /cell culture; western blottings

DESCRIPTION (provided by applicant): Fibroblast Growth Factor (FGF) Receptors (R) R1, R2 and R3 are important regulators of oligodendrocytes (OL) differentiation. Further, R2 is targeted into the myelin membrane, where it may play a role in myelin-axon signaling. The expression of R1, R3 and R2 is carefully regulated during OL differentiation. We hypothesize that the observed multiple responses of OLs to FGF are due to multi-receptor phenomena involving R1, R2 and R3, each of which contributes a subset of the overall phenotype at each stage of the lineage. In AIM I we will examine the role of R2 in an R2-null mouse model we have developed using cre/Iox technology, in which R2 expression is deleted specifically in myelinating cells. We propose that FGF signaling via R2 plays a role in both the regulation of OL terminal differentiation and myelin biogenesis, maintenance and function, including axoglial signaling. Preliminary data indicate that these mice have significant alterations in OL differentiation and myelin-axon interactions. In AIM II we investigate the functional significance of regulated FGF Receptor expression during OL development, applying new tools including FGFs that activate specific FGF receptors, OL cultured from R3- and R2-deficient mice, and SH2 profiling to identify likely down-stream targets of specific FGF receptor activation. In AIM III we note that OL development in vivo is a balanced orchestration of multiple factors produced by multiple cell types. We propose to study the role of FGF in vivo in the context of signaling through all its receptors acting in concert, by either hypostimulating or hyperstimulating the FGF receptors. Against the background of these studies, we then propose to introduce focal demyelination in R2- and R3- null mice in order to study the role of these receptors in remyelination and repair. The long term goal of this project is to understand the functional significance of the rigorously controlled developmental expression of FGF receptors both during OL differentiation leading to myelin biogenesis, as well as in myelin membrane function, maintenance and repair, and to apply this knowledge to an informed intervention in the treatment of demyelinating diseases such as Multiple Sclerosis.

描述（由申请人提供）：成纤维细胞生长因子（FGF）受体（R）R1、R2和R3是少突胶质细胞（OL）分化的重要调节因子。此外，R2靶向髓磷脂膜，在那里它可能在髓磷脂-轴突信号传导中发挥作用。在OL分化过程中，R1、R3和R2的表达受到精心调控。我们假设，所观察到的OL对FGF的多重反应是由于涉及R1、R2和R3的多受体现象，其中每一个都在谱系的每个阶段贡献了整体表型的一个子集。在AIM I中，我们将研究R2在我们使用CRE/Iox技术开发的R2缺失小鼠模型中的作用，其中R2表达在髓鞘形成细胞中特异性缺失。我们建议，FGF信号通过R2在OL终末分化和髓鞘的生物发生，维持和功能，包括轴突信号的调节中发挥作用。初步数据表明，这些小鼠在OL分化和髓鞘-轴突相互作用方面有显著改变。在AIM II中，我们研究了在OL发育过程中调节FGF受体表达的功能意义，应用新工具，包括激活特定FGF受体的FGF，从R3和R2缺陷小鼠培养的OL，以及SH 2分析，以确定特定FGF受体激活的可能下游靶点。在AIM III中，我们注意到OL在体内的发育是由多种细胞类型产生的多种因子的平衡协调。我们建议研究FGF在体内的作用，通过其所有的受体在音乐会上发挥作用的背景下，无论是hypostimulating或hyperstimulating的FGF受体的信号。在这些研究的背景下，我们建议在R2和R3缺失小鼠中引入局灶性脱髓鞘，以研究这些受体在髓鞘再生和修复中的作用。该项目的长期目标是了解在导致髓鞘生物发生的OL分化期间以及在髓鞘膜功能、维护和修复中FGF受体的严格控制的发育表达的功能意义，并将这些知识应用于治疗脱髓鞘疾病如多发性硬化症的知情干预。