Mechanism of 4-1BBL-mediated sustained inflammation: target of anti-inflammation

4-1BBL介导的持续炎症机制：抗炎靶点

• 批准号: 7992860
• 负责人: Young Jun Kang
• 金额: $ 37.98万
• 依托单位: SCRIPPS RESEARCH INSTITUTE, THE
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-05-05 至 2015-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7992860
• 关键词: Adaptor Signaling Protein; Anti-Inflammatory Agents; Anti-inflammatory; Arthritis; Binding; Biological; Biological Models; Biological Response Modifiers; Cell Surface Proteins; Cell surface; Cells; Complex; Cytoplasmic Tail; Development; Disease; Endotoxins; Equilibrium; Event; Genes; Genetic Transcription; Goals; Hour; Immune; Immune response; Immune system; In Vitro; Infection; Inflammation; Inflammatory; Inflammatory Bowel Diseases; Inflammatory Response; Injection of therapeutic agent; Injury; Knowledge; Lead; Ligands; Lipopolysaccharides; MAP Kinase Gene; MAP3K7 gene; MAP3K7IP1 gene; Macrophage Activation; Mediating; Messenger RNA; Microbe; Modeling; Modification; Molecular; Monitor; Mus; Mutation; Operative Surgical Procedures; Organ; Pathway interactions; Pattern; Phase; Play; Point Mutation; Post-Transcriptional Regulation; Production; Recruitment Activity; Regulation; Resistance; Rest; Role; Sepsis; Septic Shock; Signal Pathway; Signal Transduction; Signaling Molecule; Small Interfering RNA; Specificity; Staging; Surface; System; TLR2 gene; TLR4 gene; TNF gene; TRAF2 gene; TRAF6 gene; Techniques; Testing; Therapeutic; Time; Tissues; Trauma; Tumor Necrosis Factor Receptor; cell injury; chemical release; cytokine; expression vector; in vivo; mRNA Stability; macrophage; member; microbial; mutant; novel; novel strategies; protein expression; public health relevance; receptor; research study; response; response to injury; transcription factor

DESCRIPTION (provided by applicant): Inflammation is a beneficial response in limiting cellular and organ damages to protect a body from an infection or to remove the damaged tissues, and that a breakdown in the regulation of the inflammatory responses may result in a wide range of inflammatory disorders. Innate immune cells immediately respond to initiate the inflammatory responses to microbial infection and cellular injury, and the responses can be prolonged for duration of time. Sustained cytokine production by macrophages contributes to the prolonged inflammation in vivo. Our preliminary study shows that induction of cell surface 4-1BB ligand (4-1BBL) is essentially required for the sustained TNF production in macrophages. This signaling mechanism occurs sequentially; 4-1BBL is induced in TLR pathway-dependent manner at the initial phase and translocates to the cell surface to form a complex with TLRs at the later phase to activate downstream signaling. Inhibition of the later phase secondary signaling pathway resulted in the reduction of inflammatory responses, and this indicates that 4-1BBL signaling is the potential target of anti-inflammation treatment. However, there are still missing steps in the initial and secondary signaling pathways which control TNF production and its relevance in inflammatory disorder is unclear. We therefore hypothesized that 4-1BBL, expression of which is mediated by TLR-specific signaling pathways, induces a novel second signaling mechanism to sustain the inflammatory response. We propose following specific aims to test our hypothesis. In Aim 1, we will investigate the signaling mechanism of 4-1BBL-mediated TNF production focusing such as the involvement and interaction of signaling molecules in 4-1BBL-mediated secondary signaling pathway. In Aim 2, we will investigate the expression mechanism of 4-1BBL in TLR-mediated signaling pathway to define the specificity of 4-1BBL in inflammatory responses in TLR signaling. Aim 3 is focused on the suppression of inflammatory responses by blocking 4- 1BBL signaling by targeting the 4-1BBL-mediated signaling to reduce the sustained inflammatory response. The studies in this proposal will answer the fundamental question of how inflammation is regulated. The knowledge obtained from these studies will be extended to biological studies and will help to develop new strategies of novel anti-inflammatory therapeutics. PUBLIC HEALTH RELEVANCE: This project is aimed at understanding the molecular mechanism of sustained cytokine production in macrophages and its application to anti-inflammation treatment. We will determine the 4-1BBL-mediated signaling pathways underlying the signaling events that are essential for sustained cytokine production. The information obtained from this study will help to develop new strategies to treat inflammatory diseases.

描述（由申请人提供）：炎症是限制细胞和器官损伤以保护身体免受感染或去除受损组织的有益反应，并且炎症反应调节的破坏可导致广泛的炎性病症。先天免疫细胞立即响应以启动对微生物感染和细胞损伤的炎症反应，并且该反应可以延长一段时间。巨噬细胞持续产生细胞因子导致体内炎症延长。我们的初步研究表明，诱导细胞表面的4-1BB配体（4-1BBL）是必需的持续产生TNF在巨噬细胞。这种信号传导机制依次发生; 4-1BBL在初始阶段以TLR途径依赖性方式被诱导，并在后期易位至细胞表面与TLR形成复合物以激活下游信号传导。抑制后相次级信号通路导致炎症反应的减轻，这表明4-1BBL信号通路是抗炎治疗的潜在靶点。然而，在控制TNF产生的初始和次级信号传导途径中仍然缺少步骤，并且其在炎症性疾病中的相关性尚不清楚。因此，我们假设，4-1BBL，其表达介导的TLR特异性信号通路，诱导一种新的第二信号机制，以维持炎症反应。我们提出以下具体目标来检验我们的假设。目的一：研究4- 1BBL介导的TNF产生的信号转导机制，重点研究4- 1BBL介导的次级信号转导途径中信号分子的参与和相互作用。目的二：研究4-1BBL在TLR介导的信号通路中的表达机制，明确4-1BBL在TLR信号通路中炎症反应的特异性。目标3的重点是通过靶向4 - 1BBL介导的信号传导来阻断4 - 1BBL信号传导以减少持续的炎症反应，从而抑制炎症反应。这项提案中的研究将回答炎症如何调节的基本问题。从这些研究中获得的知识将扩展到生物学研究，并将有助于开发新的抗炎疗法的新策略。 公共卫生相关性：本项目旨在了解巨噬细胞持续产生细胞因子的分子机制及其在抗炎治疗中的应用。我们将确定4- 1BBL介导的信号通路，这些信号通路是持续细胞因子产生所必需的信号事件的基础。从这项研究中获得的信息将有助于开发治疗炎症性疾病的新策略。