The role of cell death signals in retinal ischemia

细胞死亡信号在视网膜缺血中的作用

• 批准号: 8035310
• 负责人: Dmitry V Ivanov
• 金额: $ 18.36万
• 依托单位: UNIVERSITY OF MIAMI SCHOOL OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-04-01 至 2012-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8035310
• 关键词: Affect; Animals; Anterior Ischemic Optic Neuropathy; Anti-Inflammatory Agents; Anti-inflammatory; Apoptosis; Apoptotic; Area; Blindness; Brain; Cell Death; Cell Death Signaling Process; Cells; Clinical; Data; Diabetic Retinopathy; Functional disorder; Glaucoma; Infarction; Inflammatory; Injury; Ischemia; Laboratories; Lead; Lesion; Literature; Mediating; Necrosis; Neurons; Optic Nerve Injuries; Outcome; Pathology; Patients; Phagocytes; Pharmaceutical Preparations; Phase; Platelet Factor 4; Predisposition; Reaction; Recovery; Refuse Disposal; Reperfusion Injury; Research; Research Personnel; Retina; Retinal; Retinopathy of Prematurity; Role; Series; Severities; Signal Transduction; Stress; Testing; Tissues; Toxic effect; Validation; Visual impairment; base; excitotoxicity; improved; innovation; interest; neuron loss; novel; preference; prevent; public health relevance; research study; retinal ischemia

DESCRIPTION (provided by applicant): Ischemia has been widely studied in the retina, because of its proposed role in glaucoma, anterior ischemic optic neuropathy (AION), retinal and choroidal vessel occlusions, diabetic retinopathy, retinopathy of prematurity (ROP) and traumatic optic neuropathy. Thus studying the basic mechanisms underlying retinal ischemia is of substantial clinical interest. In retinal ischemia, energy depletion leads to necrotic cell death in the most severely affected areas, whereas apoptotic neurons are concentrated in the area of the ischemic territory, where the insult is milder. Necrosis of tissue leads to inflammatory and toxic activation of professional phagocytes, whereas the elimination of apoptotic cells by phagocytes stimulates the synthesis of anti- inflammatory and protective factors. Hence, the combination of different types of dead cells in tissue can determine the predominance of either toxicity or protection derived from phagocytes. The predominance of necrotic over apoptotic cells in ischemic tissue can mediate additional inflammatory stress in ischemic tissue. Our preliminary data and the literature suggest that such inflammatory stress can be responsible for a significantly greater amount of neuronal damage after retinal ischemia. We hypothesize that cell death related inflammatory stress makes a statistically significant contribution to the pathology of retinal ischemia. This hypothesis will be tested in a series of experiments outlined in the following specific aims: 1) To determine whether the predominance of necrotic over apoptotic signals influences the increased severity of post-ischemic damage in the retina; 2) To determine whether the predisposition of cells to necrosis governs the increased severity of post ischemic damage in the retina; 3) To determine the role of phagocyte interactions with dead cells on the increased severity of post-ischemic damage in the retina. Validation of our hypotheses will generate a potentially new list of targets for novel drugs which are aimed at reducing damage following retinal ischemia. PUBLIC HEALTH RELEVANCE: Retinal ischemia is a common cause of visual impairment and blindness. Predisposition to cell death via necrosis or apoptosis as a result of retinal ischemia could mediate inflammatory stress and consequently affect lesion size and the potential for recovery. The studies outlined in the specific aims will provide a better understanding of the effects of necrotic and apoptotic signals in the pathology of retinal ischemia and can stimulate the discovery of innovative strategies to help prevent the loss of vision in patients with ischemic injury.

描述（由申请人提供）：由于其在青光眼、前部缺血性视神经病变（AION）、视网膜和脉络膜血管闭塞、糖尿病性视网膜病变、早产儿视网膜病变（ROP）和创伤性视神经病变中的作用，已在视网膜中广泛研究了缺血。因此，研究视网膜缺血的基本机制具有重要的临床意义。在视网膜缺血中，能量消耗导致受影响最严重的区域中的坏死细胞死亡，而凋亡神经元集中在损伤较轻的缺血区域中。组织坏死导致专职吞噬细胞的炎性和毒性活化，而吞噬细胞对凋亡细胞的清除刺激抗炎和保护因子的合成。因此，组织中不同类型的死细胞的组合可以决定来自吞噬细胞的毒性或保护的优势。缺血组织中坏死细胞相对于凋亡细胞的优势可以介导缺血组织中的额外炎性应激。我们的初步数据和文献表明，这种炎症应激可能是视网膜缺血后神经元损伤显著增加的原因。我们假设细胞死亡相关的炎症应激对视网膜缺血的病理学有统计学意义的贡献。该假设将在以下具体目的中概述的一系列实验中进行检验：1）确定坏死信号相对于凋亡信号的优势是否影响视网膜中缺血后损伤的严重性增加; 2）确定细胞坏死的倾向是否支配视网膜中缺血后损伤的严重性增加; 3）确定吞噬细胞与死细胞的相互作用对视网膜缺血后损伤严重程度增加的作用。我们的假设的验证将产生一个潜在的新的目标清单，为新的药物，旨在减少视网膜缺血后的损害。 公共卫生相关性：视网膜缺血是视力损害和失明的常见原因。视网膜缺血导致的细胞坏死或凋亡倾向可介导炎症应激，从而影响病变大小和恢复潜力。具体目标中概述的研究将更好地了解视网膜缺血病理学中坏死和凋亡信号的影响，并可以刺激创新策略的发现，以帮助预防缺血性损伤患者的视力丧失。