LRP-1 is a multifunctional regulator during peripheral nerve injury and pain.

LRP-1 是周围神经损伤和疼痛期间的多功能调节剂。

• 批准号: 8206801
• 负责人: WENDY M. CAMPANA
• 金额: $ 33.12万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN DIEGO
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-01-15 至 2013-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8206801
• 关键词: Applications Grants; Astrocytes; Axon; Behavior; Biological Models; Brain-Derived Neurotrophic Factor; C Fiber; Cell Death; Cellular biology; Collaborations; Communication; Complex; Data; Development; Extracellular Signal Regulated Kinases; Foundations; Goals; Hand; Immunoblot Analysis; Immunoblotting; In Situ Nick-End Labeling; In Vitro; Inflammatory; Injection of therapeutic agent; Injury; LDL-Receptor Related Protein 1; Label; Letters; Ligand Binding; Ligands; Lipoprotein Receptor; Maintenance; Mediator of activation protein; Membrane; Messenger RNA; Modeling; Molecular; Mus; Myelin; Nerve; Nerve Pain; Nervous System Trauma; Neuroglia; Neurons; Neuropathy; Neuropeptides; Outcome; Pain; Pathway interactions; Peptide Hydrolases; Peripheral Nervous System; Peripheral nerve injury; Phagocytosis; Procedures; Process; Proteins; Published Comment; Rattus; Regulation; Reporting; Research; Research Project Grants; Resources; Role; Sampling; Schwann Cells; Series; Signal Pathway; Signal Transduction; Site; Spinal; Spinal Ganglia; Study Section; TNF gene; Technology; Therapeutic; Time; Vesicle; Work; caspase-3; central sensitization; chronic neuropathic pain; chronic pain; cytokine; design; dorsal horn; extracellular; flexibility; gain of function; in vivo; injured; insight; loss of function; mitogen-activated protein kinase p38; nerve injury; neuronal excitability; novel; novel strategies; novel therapeutics; painful neuropathy; palliation; prevent; programs; public health relevance; receptor; receptor binding; receptor mediated endocytosis; research study; response; sciatic nerve; spontaneous pain; success; time use

DESCRIPTION (provided by applicant): Direct injury to the sciatic nerve and other major nerves in the peripheral nervous system (PNS) may cause chronic neuropathic pain. Multiple mechanisms are involved in the development and maintenance of neuropathic pain. These mechanisms involve neurons and glia at the site of injury, in the dorsal root ganglia, and in the spinal dorsal horn. At the injury site, diverse extracellular mediators, including cytokines and proteases, provide communication between damaged axons, Schwann cells, and preserved C-fibers, which may be very important in pain processing. We hypothesize that receptors which regulate the extracellular microenviron- ment within the injured nerve may regulate neuropathic pain. The low-density lipoprotein receptor related pro- tein-1 (LRP-1) is a multifunctional receptor that binds numerous extracellular mediators implicated in the res- ponse to PNS injury. Ligand-binding to LRP-1 results in receptor-mediated endocytosis and also in cell-signaling. We have demonstrated for the first time that Schwann cells express LRP-1 and that LRP-1 expression is increased in Schwann cells by nerve injury. LRP-1 expresses activities that may be important in nerve in- jury, including regulation of Schwann cell activation and survival, regulation of the response to inflammatory cytokines, and management of myelin debris. LRP-1 also appears to regulate spontaneous and evoked pain- related behavior. The goal of this research program is to elucidate the function of membrane-anchored LRP-1 and the shed form of the receptor in peripheral nerve injury. In Aim 1, we will apply a series of "loss of function" and "gain of function" approaches to study the activity of LRP-1 as a regulator of Schwann cell biology in vitro, in sciatic nerve injury in vivo, and in the development of neuropathic pain. In Aim 2, we will study LRP-1 ligands, which may be essential in triggering LRP-1-dependent cell-signaling pathways that regulate the res- ponse to PNS injury. Finally, in Aim 3, we will elucidate the role of LRP-1 in the clearance of myelin debris in the injured sciatic nerve. Overall, these studies will offer insight into novel mechanisms that may control the progression of peripheral nerve injury and the development and maintenance of neuropathic pain. We hope to elucidate novel pathways by which Schwann cells regulate neuropathic pain. Furthermore, these studies offer the opportunity for developing novel strategies to treat or prevent neuropathic pain.7. PUBLIC HEALTH RELEVANCE: Direct injury to nerves in the peripheral nervous system may cause chronic pain. Currently, most of the therapeutics for chronic pain treatment are not effective. This grant application seeks to understand the molecular mechanisms underlying peripheral nerve injury and with that understanding, build a foundation in which we can develop novel therapeutics for chronic pain.

描述（由申请人提供）：周围神经系统（PNS）中坐骨神经和其他主要神经的直接损伤可能导致慢性神经性疼痛。神经病理性疼痛的发生和维持涉及多种机制。这些机制涉及损伤部位、背根神经节和脊髓背角的神经元和神经胶质。在损伤部位，不同的细胞外介质，包括细胞因子和蛋白酶，提供受损轴突，雪旺细胞和保存的C纤维之间的通信，这可能是非常重要的疼痛处理。我们推测，调节受损神经内细胞外微环境的受体可能调节神经病理性疼痛。低密度脂蛋白受体相关蛋白-1（LRP-1）是一种多功能受体，可结合许多参与PNS损伤反应的细胞外介质。配体与LRP-1的结合导致受体介导的内吞作用以及细胞信号传导。我们已经证明了第一次，雪旺细胞表达LRP-1和LRP-1的表达增加雪旺细胞神经损伤。LRP-1表达在神经损伤中可能重要的活性，包括调节雪旺细胞活化和存活、调节对炎性细胞因子的应答和管理髓磷脂碎片。LRP-1似乎还调节自发性和诱发性疼痛相关行为。本研究的目的是阐明膜锚定LRP-1的功能和周围神经损伤中受体的脱落形式。在目标1中，我们将应用一系列“功能丧失”和“功能获得”方法来研究LRP-1作为体外雪旺细胞生物学调节剂、在体内坐骨神经损伤中以及在神经性疼痛的发展中的活性。在目标2中，我们将研究LRP-1配体，其可能在触发LRP-1依赖性细胞信号传导通路调节对PNS损伤的反应中是必需的。最后，在目标3中，我们将阐明LRP-1在损伤的坐骨神经中髓鞘碎片的清除中的作用。总的来说，这些研究将提供新的机制，可以控制周围神经损伤的进展和神经性疼痛的发展和维持的见解。我们希望阐明雪旺细胞调节神经病理性疼痛的新途径。此外，这些研究为开发治疗或预防神经性疼痛的新策略提供了机会。 公共卫生相关性：周围神经系统神经的直接损伤可能导致慢性疼痛。目前，大多数用于慢性疼痛治疗的疗法是无效的。这项拨款申请旨在了解周围神经损伤的分子机制，并通过这种理解，建立一个基础，我们可以开发新的治疗慢性疼痛的方法。

项目成果

The hemopexin domain of matrix metalloproteinase-9 activates cell signaling and promotes migration of schwann cells by binding to low-density lipoprotein receptor-related protein.

• DOI: 10.1523/jneurosci.3053-08.2008
• 发表时间: 2008-11-05
• 期刊: The Journal of neuroscience : the official journal of the Society for Neuroscience
• 作者: Mantuano E;Inoue G;Li X;Takahashi K;Gaultier A;Gonias SL;Campana WM
• 通讯作者: Campana WM