Overexpression of Nerve Growth Factors

神经生长因子的过度表达

• 批准号: 6500062
• 负责人: BRIAN M DAVIS
• 金额: $ 40.74万
• 依托单位: UNIVERSITY OF PITTSBURGH AT PITTSBURGH
• 依托单位国家: 美国
• 财政年份: 1993
• 资助国家: 美国
• 起止时间: 1993-05-01 至 2005-07-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6500062
• 关键词: afferent nerve; animal genetic material tag; developmental genetics; developmental neurobiology; gene expression; genetically modified animals; laboratory mouse; nerve injury; neurogenesis; neurogenetics; neurotrophic factors; neutralizing antibody; peripheral nervous system; ventral column; wound healing

Sensory neurons responsive to painful stimuli, called nociceptors, are crucial for the health of an organism as they are responsible for initiating behavioral responses that prevent or limit tissue damage. Under normal circumstances pain is an important sensation. However, following injury or disease, pain can become persistent, seriously disrupting the lives of those affected. Development and maintenance of nociceptors is known to be dependent on two growth factors, nerve growth factor (NGF) and glial-line derived neurotrophic factor (GDNF). Furthermore, it has been proposed that NGF and GDNF support two different populations of nociceptors and that these two populations are responsible for different types of persistent pain. In addition, changes in nociceptor function induced by NGF and GDNF also modulate nociceptive processing in the adult spinal cord, suggesting a multi-level, growth factor-driven plasticity in the somatosensory system. In our previous studies we determined that NGF plays a dramatic role in determining the "comprehensive phenotype" of nociceptors, influencing physiological, anatomical and functional properties of NGF-dependent nociceptors. The next step is to determine how GDNF affects nociceptors, how changes in NGF and GDNF affect spinal cord neurons receiving nociceptive input, and what affects these changes have on persistent pain. This proposal consists of three Specific Aims employing a "genes to behavior" approach. Specific Aim 1 examines how increases in the level of GDNF affects the comprehensive phenotype of nociceptors. This data will be compared with the results from the NGF studies to provide a complete analysis of the role of growth factors in nociceptor development. Specific Aim 2 examines how NGF- and GDNF- induced changes in nociceptors affects dorsal horn anatomy and neurochemistry. Analysis of spinal cord is crucial because alteration in spinal cord homeostasis can exacerbate or compensate for persistent pain. Specific Aim 3 examines how mice with hypertrophied NGF and GDNF phenotypes respond in two models of persistent pain. Whole animal behavior, nociceptor physiology and changes in dorsal horn neurochemistry will be examined. Upon completion of these specific aims, we anticipate that the differences between NGF- dependent and GDNF-dependent nociceptors will be understood with respect to their anatomical, physiological and neurochemical traits. In addition, it should be possible to identify how these two classes of nociceptors affect dorsal horn development and function. Finally, we will gain insight into how these two classes of nociceptors and their spinal cord targets, respond to induction of persistent pain.

对疼痛刺激有反应的感觉神经元，称为伤害感受器，对生物体的健康至关重要，因为它们负责启动防止或限制组织损伤的行为反应。 在正常情况下，疼痛是一种重要的感觉。 然而，在受伤或疾病之后，疼痛可能会变得持久，严重扰乱受影响者的生活。 已知伤害感受器的发育和维持依赖于两种生长因子，神经生长因子（NGF）和胶质细胞源性神经营养因子（GDNF）。 此外，已经提出NGF和GDNF支持两种不同的伤害感受器群体，并且这两种群体负责不同类型的持续性疼痛。 此外，由NGF和GDNF诱导的伤害感受器功能的变化也调节成年脊髓中的伤害性处理，这表明躯体感觉系统中的多水平、生长因子驱动的可塑性。 在我们以前的研究中，我们确定了神经生长因子在决定伤害感受器的“综合表型”中起着重要作用，影响神经生长因子依赖的伤害感受器的生理、解剖和功能特性。 下一步是确定GDNF如何影响伤害感受器，NGF和GDNF的变化如何影响接受伤害性输入的脊髓神经元，以及这些变化对持续性疼痛的影响。该提案包括三个具体目标，采用“基因到行为”的方法。 具体目标1检查GDNF水平的增加如何影响伤害感受器的综合表型。 这些数据将与NGF研究的结果进行比较，以提供生长因子在伤害感受器发育中的作用的完整分析。 特异性目标2研究了NGF和GDNF诱导的伤害感受器变化如何影响背角解剖学和神经化学。 脊髓的分析是至关重要的，因为脊髓内稳态的改变可以加剧或补偿持续性疼痛。具体目标3检查了具有肥大的NGF和GDNF表型的小鼠在两种持续性疼痛模型中的反应。 将检查整个动物行为、伤害感受器生理学和背角神经化学变化。 在完成这些特定目标后，我们预期将了解NGF依赖性和GDNF依赖性伤害感受器之间在解剖学、生理学和神经化学特征方面的差异。 此外，应该可以确定这两类伤害感受器如何影响背角的发育和功能。 最后，我们将深入了解这两类伤害感受器及其脊髓靶点如何对持续性疼痛的诱导作出反应。