Regulation and Function of Kallikreins in Spinal Cord Injury and Repair

激肽释放酶在脊髓损伤和修复中的调节和功能

• 批准号: 7456686
• 负责人: ISOBEL A SCARISBRICK
• 金额: $ 33.97万
• 依托单位: MAYO CLINIC ROCHESTER
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-04-01 至 2013-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7456686
• 关键词: Acute; Address; Affect; Animal Model; Apoptosis; Astrocytes; Attenuated; Automobile Driving; Axon; Behavioral; Biological; Biological Assay; Blocking Antibodies; Cell Culture System; Cell surface; Cells; Chronic; Cicatrix; Cleaved cell; Clinical; Clip; Cytoskeletal Proteins; Data; Demyelinations; Development; Disease; Elevation; Encephalomyelitis; Endopeptidases; Environment; Enzymes; Event; Exhibits; Experimental Autoimmune Encephalomyelitis; Extracellular Matrix Proteins; Failure; Family; Gene Family; Goals; Growth; Homologous Gene; Human; Human Glandular Kallikrein 2; Hydrolysis; Immune; In Situ Hybridization; Infiltration; Inflammation; Inflammatory; Injection of therapeutic agent; Injury; Kininogenase; Knockout Mice; Laboratories; Laminin; Locomotor Recovery; MAPK11 gene; MAPK8 gene; Mediating; Mediator of activation protein; Messenger RNA; Methods; Mitogen-Activated Protein Kinases; Modeling; Modification; Monomeric GTP-Binding Proteins; Motor; Mus; Myelin; Myelin Proteins; Natural regeneration; Nerve; Nerve Regeneration; Neurites; Neurons; PAR-1 Receptor; Pathogenesis; Pattern; Peptide Hydrolases; Peptides; Phosphorylation; Play; Polymerase Chain Reaction; Positioning Attribute; Process; Prostate-Specific Antigen; Proteinase-Activated Receptors; Proteolysis; Protocols documentation; Public Health; Range; Receptor Activation; Recombinants; Recovery; Recovery of Function; Regulation; Research; Rodent; Role; Secondary to; Serine Protease; Signal Pathway; Signal Transduction; Site; Specificity; Spinal Cord; Spinal Cord Diseases; Spinal cord injury; Spinal cord injury patients; Techniques; Testing; Therapeutic; Therapeutic Intervention; Time; Tissues; Trauma; Trypsin; Urinary Kallikrein; aggrecan; astrogliosis; axon regeneration; base; cell behavior; human KLK15 protein; injury and repair; insight; interest; kallikrein 4; macrophage; member; nerve injury; neurobehavioral; novel; novel therapeutics; prevent; receptor; release of sequestered calcium ion into cytoplasm; repaired; research study; response; spinal cord white matter

DESCRIPTION (provided by applicant): The objective of this proposal is to investigate the activity and potential mechanism of action of kallikreins in traumatic spinal cord injury with a focus on their roles in mediating axon injury, astrogliosis, and alteration of the environment available for nerve regeneration. Preliminary studies of all 15 members of this newly identified gene family show select kallikreins are differentially expressed across the CNS-immune axis and therein are differentially regulated by injury. We are particularly interested in the activity of kallikrein 6 (K6) since we have shown that: 1) K6 is up regulated in resident spinal cord cells and infiltrating macrophages at acute and chronic time points post-injury in both animal models and cases of human traumatic spinal cord injury; 2) K6 is a trypsin-like enzyme that rapidly hydrolyzes myelin and extracellular matrix proteins; 3) K6 hydrolyzes growth facilitatory substrates such as laminin to inhibit neurite outgrowth, while hydrolysis of inhibitory substrates, such as aggrecan, promote neurite extension; 4) K6-function blocking antibodies attenuate clinical and pathological disease in murine models of inflammatory spinal cord injury. Further, preliminary data demonstrate that kallikreins may exert their effects not only at the level of the substrate, but in addition may cleave select protease activate receptors (PARs) to trigger intracellular signaling cascades including calcium flux and Erk- phosphorylation, which may directly contribute to altered neurite outgrowth and astrogliosis. Based on these results, we hypothesize that kallikrein-mediated proteolysis plays fundamental roles in the response of the spinal cord to injury, including secondary tissue destructive events and modification of the capacity for nerve regeneration. To test this hypothesis, we intend to fulfill the following specific aims: 1) determine the dynamics and cellular specificity of expression of all 15 kallikreins in human and murine traumatic spinal cord injury; 2) using cell culture systems compare the consequences of elevations in the level of 2 kallikreins, K1 or K6, on axon integrity and neurite outgrowth, astrogliosis, and the potential mechanism of action; 3) determine the range of action of K1 and K6 in spinal cord pathogenesis and whether their effects are mediated by PAR following direct injection into the spinal cord of wild-type or PAR-deficient mice; and 4) determine whether altering the activity of K1, K6, or PAR at the time of SCI, alone or in combination, alters secondary tissue destruction and promotes locomotor recovery in a murine clip compression model. Our long-term goal is to understand the role and possible mechanisms by which kallikreins participate in events secondary to spinal cord trauma, including failure of axon regeneration. This study should generate new and important information providing the impetus for development of novel therapeutic regimes to promote recovery in cases of SCI. PUBLIC HEALTH RELEVANCE: The goal of this project is to delineate novel pathophysiologic mechanisms mediated by a family of proteases referred to as kallikreins, in human traumatic spinal cord injury, to model these in mice, and to determine whether altering their activity promotes neurobehavioral recovery. These studies have the potential to identify new therapeutic interventions for SCI patients with both acute and more chronic injuries.

描述（由申请人提供）：本提案的目的是研究激肽释放酶在创伤性脊髓损伤中的活性和潜在作用机制，重点是其在介导轴突损伤、星形胶质细胞增生和改变神经再生环境中的作用。对这个新鉴定的基因家族的所有15个成员的初步研究表明，选择的激肽释放酶在CNS-免疫轴上差异表达，并且其中受到损伤的差异调节。我们对激肽释放酶6（K6）的活性特别感兴趣，因为我们已经表明：1）在动物模型和人类创伤性脊髓损伤的病例中，在损伤后的急性和慢性时间点，K6在驻留的脊髓细胞和浸润的巨噬细胞中上调; 2）K6是快速水解髓鞘和细胞外基质蛋白的胰蛋白酶样酶; 3）K6水解生长促进底物如层粘连蛋白以抑制神经突生长，而水解抑制性底物如聚集蛋白聚糖促进神经突延伸; 4）K6功能阻断抗体减轻炎性脊髓损伤的鼠模型中的临床和病理疾病。此外，初步数据表明，激肽释放酶不仅可以在底物水平发挥其作用，而且还可以切割选择的蛋白酶激活受体（PAR）以触发细胞内信号传导级联，包括钙通量和Erk-磷酸化，这可能直接有助于改变的神经突生长和星形胶质细胞增生。基于这些结果，我们假设激肽释放酶介导的蛋白水解在脊髓对损伤的反应中起着重要作用，包括继发性组织破坏事件和神经再生能力的改变。为了验证这一假设，我们打算实现以下具体目标：1）确定人和鼠创伤性脊髓损伤中所有15种激肽释放酶表达的动力学和细胞特异性; 2）使用细胞培养系统比较2种激肽释放酶（K1或K6）水平升高对轴突完整性和神经突生长、星形胶质细胞增生的后果，以及潜在的作用机制; 3）确定K1和K6在脊髓发病机制中的作用范围，以及在直接注射到野生型或PAR缺陷型小鼠的脊髓中后，它们的作用是否由PAR介导;和4）确定在SCI时单独或联合改变K1、K6或PAR的活性，在鼠夹压迫模型中改变继发性组织破坏并促进运动恢复。我们的长期目标是了解激肽释放酶参与脊髓创伤继发事件的作用和可能机制，包括轴突再生失败。这项研究应该产生新的和重要的信息，为发展新的治疗方案，以促进恢复的情况下，SCI提供动力。 公共卫生相关性：该项目的目标是描绘新的病理生理机制介导的蛋白酶家族被称为激肽释放酶，在人类创伤性脊髓损伤，这些在小鼠模型，并确定是否改变其活动促进神经行为恢复。这些研究有可能为急性和慢性损伤的SCI患者确定新的治疗干预措施。