Matrix Metalloproteinases and Regenerative Plasticity Following Brain Injury

脑损伤后的基质金属蛋白酶和再生可塑性

• 批准号: 7462891
• 负责人: Linda L. Phillips
• 金额: $ 32.11万
• 依托单位: VIRGINIA COMMONWEALTH UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2002
• 资助国家: 美国
• 起止时间: 2002-05-15 至 2012-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7462891
• 关键词: Accounting; Activities of Daily Living; Acute; Agrin; American; Antibodies; Astrocytes; Attenuated; Bilateral; Binding; Biological Assay; Brain; Brain Injuries; Cholera Toxin; Chromosome Pairing; Complex; Condition; Craniocerebral Trauma; Cytolysis; Cytoskeleton; Deafferentation procedure; Diffuse; Dose; Drug or chemical Tissue Distribution; Electrophysiology (science); Environment; Enzymes; Excitatory Postsynaptic Potentials; Exposure to; Extracellular Matrix; Extracellular Matrix Proteins; FN-439; Fostering; Functional disorder; Gelatin Zymography; Gelatinase A; Gelatinases; Glial Fibrillary Acidic Protein; Growth Cones; Health; Hippocampus (Brain); Immunohistochemistry; Individual; Infusion procedures; Inhibition of Matrix Metalloproteinases Pathway; Injury; Label; Lesion; Link; Liquid substance; Localized; Long-Term Potentiation; MMP3 gene; Matrix Metalloproteinase Inhibitor; Matrix Metalloproteinases; Measures; Mediating; Membrane; Methods; Microglia; Modeling; N-Cadherin; Nature; Neurodegenerative Disorders; Neurons; Outcome; Outcome Measure; Pathology; Pathway interactions; Percussion; Phase; Phosphorylation; Physiological; Presynaptic Terminals; Principal Investigator; Process; Property; Protein Dephosphorylation; Protein Tyrosine Phosphatase; Proteins; Public Health; Recovery; Recovery of Function; Role; Signal Transduction; Site; Slice; Small Interfering RNA; Source; Spatial Distribution; Stroke; Stromelysin 1; Structure; Synapses; Synapsins; Synaptic plasticity; Synaptophysin; Techniques; Tenascin; Testing; Tissues; Trauma; Traumatic Brain Injury; Tyrosine; Vertebral column; Western Blotting; axon growth; axonal sprouting; base; bisperoxo(1,10-phenanthroline)oxovanadate(1-); day; density; dentate gyrus; enzyme activity; enzyme substrate; functional status; genetic manipulation; human PTPRT protein; improved; in vivo; indexing; injured; janusin; knock-down; mRNA Expression; new growth; novel strategies; phosphatase inhibitor; postsynaptic; presynaptic; programs; protein function; research study; response; synaptogenesis; treatment effect

DESCRIPTION (provided by applicant): Millions of Americans are victims of traumatic brain injury (TBI), making it a serious health challenge. TBI often involves significant axonal injury with attendant neuronal deafferentation and synaptic loss. While the brain has an inherent capacity for synaptic reorganization, this plasticity often fails after TBI, resulting in serious functional deficits. We have examined the role of extracellular matrix (ECM) proteins during reactive synaptogenesis induced by TBI. Certain ECM proteins and their regulatory matrix metalloproteinases (MMPs) appear to influence the extent of recovery achieved after TBI. Our initial studies contrasted ECM/MMP response in a recovering adaptive injury (unilateral entorhinal cortical lesion or UEC) and a non-recovering maladaptive insult (fluid percussion TBI + bilateral entorhinal cortical lesion or TBI+BEC). Two gelatinases (MMPs 2,9), stromelysin-1 (MMP 3) and the membrane bound MT-5 MMP all showed change in expression and function which correlated with different phases of reactive synaptogenesis. ECM shifts in agrin, tenascin, RPTP-2 and N-cadherin occurred during postinjury recovery as well. We also found that aberrant MMP activation was linked with failed plasticity after TBI+BEC. When MMP inhibitors were applied, plasticity was altered either positively or negatively depending upon dosing and complexity of injury. Given these results, we now posit that specific matrix enzyme/substrate pairs mediate different phases of pre and postsynaptic recovery, as well as the subsequent synapse stabilization. By contrasting profiles of these matrix proteins after adaptive UEC and maladaptive TBI+BEC, we will determine if individual protein dysfunction at specific phases of synaptogenesis can account for the extent of recovery achieved. We will test the facilitative role of MMP3/agrin during the axonal sprouting phase of synaptic recovery, tenascin/RPTP-2/2-catenin during the synaptogenic period, and MT-5MMP/N-cadherin at synapse maturation. For each molecule we will document protein/mRNA expression, synaptic distribution and, when applicable, binding interactions. Finally, we will manipulate MMP3, RPTP-2 and MT-5MMP by either pharmacological inhibition or siRNA knockdown and examine recovery using structural and physiological indices of synaptic plasticity. These studies will better define matrix role in TBI-induced synaptic plasticity and provide new treatment strategies. PUBLIC HEALTH RELEVANCE: Common feature of head injury is poor recovery of damaged brain connections. The proposed studies will determine the role of extracellular matrix proteins during this recovery and identify matrix manipulations which would improve recovery.

描述（由申请人提供）：数百万美国人是创伤性脑损伤（TBI）的受害者，使其成为严重的健康挑战。TBI通常涉及显著的轴突损伤，伴随着神经元去传入和突触丢失。虽然大脑具有突触重组的固有能力，但这种可塑性在TBI后通常会失败，导致严重的功能缺陷。我们已经研究了细胞外基质（ECM）蛋白在TBI诱导的反应性突触发生过程中的作用。某些ECM蛋白及其调节性基质金属蛋白酶（MMP）似乎影响TBI后恢复的程度。我们最初的研究对比了ECM/MMP在恢复适应性损伤（单侧内嗅皮质病变或UEC）和非恢复适应不良损伤（液压冲击TBI +双侧内嗅皮质病变或TBI+BEC）中的反应。两种明胶酶（MMPs 2，9），基质溶解素-1（MMPs 3）和膜结合型MT-5 MMP的表达和功能的变化与反应性突触发生的不同阶段相关。细胞外基质中聚集蛋白、腱生蛋白、RPTP-2和N-cadherin在损伤后恢复过程中也发生了变化。我们还发现异常的MMP激活与TBI+BEC后可塑性失败有关。当应用MMP抑制剂时，可塑性根据剂量和损伤的复杂性而被积极或消极地改变。鉴于这些结果，我们现在证明，特定的基质酶/底物对介导突触前和突触后恢复的不同阶段，以及随后的突触稳定。通过对比自适应UEC和适应不良TBI+BEC后这些基质蛋白的概况，我们将确定在突触发生的特定阶段的单个蛋白功能障碍是否可以解释所实现的恢复程度。我们将测试MMP 3/聚集蛋白在突触恢复的轴突发芽阶段的促进作用，腱生蛋白/RPTP-2/2-连环蛋白在突触形成期间，和MT-5 MMP/N-cadherin在突触成熟。对于每个分子，我们将记录蛋白质/mRNA表达，突触分布和结合相互作用（如适用）。最后，我们将操纵MMP 3，RPTP-2和MT-5 MMP通过药理学抑制或siRNA敲低，并使用突触可塑性的结构和生理指标检查恢复。这些研究将更好地确定基质在TBI诱导的突触可塑性中的作用，并提供新的治疗策略。公共卫生相关性：头部损伤的共同特征是受损的大脑连接恢复不良。拟议的研究将确定细胞外基质蛋白在恢复过程中的作用，并确定可以改善恢复的基质操作。