The role of focal adhesion kinase in CNS myelination

粘着斑激酶在中枢神经系统髓鞘形成中的作用

• 批准号: 7791409
• 负责人: Audrey D Lafrenaye
• 金额: $ 1.25万
• 依托单位: VIRGINIA COMMONWEALTH UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-01-15 至 2010-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7791409
• 关键词: Address; Alleles; Axon; Cell membrane; Cell surface; Cells; Cytoskeleton; DNA Sequence Rearrangement; Data; Development; Electric Capacitance; Event; Extracellular Matrix; Fiber; Focal Adhesion Kinase 1; Focal Adhesions; Goals; Human; In Vitro; Injection of therapeutic agent; Investigation; Knock-out; Knockout Mice; Lead; Molecular; Morphology; Multiple Sclerosis; Mus; Mutation; Myelin; Myelin Sheath; Neuraxis; Neurons; Oligodendroglia; Patients; Phosphorylation; Phosphotransferases; Play; Process; Proteins; Proteolipids; Rattus; Regulation; Role; Signal Transduction; Signaling Protein; Site; Staging; System; Tamoxifen; Time; Transgenic Mice; Tyrosine; base; cell type; central nervous system demyelinating disorder; disability; in vivo; interest; myelination; postnatal; promoter; repaired; research study; therapeutic target

DESCRIPTION (provided by applicant): The formation of the myelin sheath is a crucial step during development allowing for efficient conduction velocities to occur in the limited space of the mammalian central nervous system (CNS). During this event, oligodendrocytes (OLGs), the myelinating cells of the CMS, send out numerous processes that associate with axonal segments and ultimately enwrap them. For the maturation of OLG processes into myelin sheaths, interactions between the OLG plasma membrane and the extracellular matrix (ECM) are of vital importance. Therefore, the long term goal of this study is to investigate the role of OLG-ECM interactions during process outgrowth and myelination. The protein focal adhesion kinase (FAK) plays a central role in plasma membrane-ECM interactions. In addition, FAK protein and phosphorylation levels are altered during myelination. To further investigate the role of FAK for myelination we generated conditional FAK knockout mice, by using transgenic mice that express a tamoxifen-inducible Cre protein under the control of the proteolipid protein (PLP) promoter (PLP/CreERT) and mice that harbor homologous recombined FAK alleles in which the second kinase domain of FAK is flanked by loxP sites (FAKflox/flox). This system allows for an OLG-specific FAK knockout at a time point when OLGs are sending out processes before interacting with axons and beginning myelination. Based on our preliminary observations and the role of focal adhesion constituents for proper OLG process outgrowth, we hypothesize that FAK and in particular its phosphorylation state at the tyrosine 925 residue regulates OLG process outgrowth/remodeling and myelination. In particular our investigations proposed here will determine the role of FAK in 1) OLG myelination and myelin morphology in vivo and 2) OLG process outgrowth/remodeling in vitro. Improper myelination in pathological conditions, such as is seen in Multiple Sclerosis (MS) patients, results in persistent disabilities. Unfortunately repair of the myelin sheath under these conditions is limited and no curative treatment is currently available. Thus, a better understanding of the molecular mechanisms regulating OGL process outgrowth/remodeling and myelination will aid in identifying possible therapeutic targets to stimulate remyelination in such pathological conditions.

描述（由申请人提供）：髓鞘的形成是发育过程中的关键步骤，允许在哺乳动物中枢神经系统（CNS）的有限空间中发生有效的传导速度。在此过程中，CMS的髓鞘形成细胞少突胶质细胞（OLG）发出许多与轴突节段相关的突起，并最终包裹它们。对于OLG过程成熟为髓鞘，OLG质膜和细胞外基质（ECM）之间的相互作用是至关重要的。因此，本研究的长期目标是研究OLG-ECM相互作用在过程生长和髓鞘形成过程中的作用。黏着斑激酶（FAK）在细胞膜与细胞外基质的相互作用中起着重要的作用。此外，FAK蛋白和磷酸化水平在髓鞘形成期间改变。为了进一步研究FAK对髓鞘形成的作用，我们通过使用在蛋白脂质蛋白（PLP）启动子（PLP/CreERT）的控制下表达他莫昔芬诱导型Cre蛋白的转基因小鼠和携带同源重组FAK等位基因的小鼠（FAK的第二激酶结构域侧翼为loxP位点（FAKflox/flox）），产生了条件性FAK敲除小鼠。该系统允许在OLG在与轴突相互作用并开始髓鞘形成之前发出过程的时间点进行OLG特异性FAK敲除。基于我们的初步观察和粘着斑成分对适当的OLG过程生长的作用，我们假设FAK，特别是其在酪氨酸925残基的磷酸化状态调节OLG过程生长/重塑和髓鞘形成。特别地，我们在此提出的研究将确定FAK在1）体内OLG髓鞘形成和髓鞘形态和2）体外OLG过程生长/重塑中的作用。病理条件下的髓鞘形成不当，如多发性硬化症（MS）患者中所见，会导致持续性残疾。不幸的是，在这些条件下髓鞘的修复是有限的，目前没有治愈性治疗。因此，更好地理解调节OGL过程生长/重塑和髓鞘形成的分子机制将有助于确定可能的治疗靶点，以刺激这种病理条件下的髓鞘再生。