Studies of the Fate of the Osteoclast

破骨细胞命运的研究

• 批准号: 6868161
• 负责人: Brendan F Boyce
• 金额: $ 31.19万
• 依托单位: UNIVERSITY OF ROCHESTER
• 依托单位国家: 美国
• 财政年份: 1995
• 资助国家: 美国
• 起止时间: 1995-06-01 至 2009-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6868161
• 关键词: AP1 protein; biological signal transduction; cell growth regulation; cytokine; developmental genetics; fos protein; genetically modified animals; interferon beta; laboratory mouse; nuclear factor kappa beta; osteoclast activating factor; osteoclasts; pathologic bone resorption; protooncogene; tissue /cell culture; transfection

DESCRIPTION (provided by applicant): Bone loss is associated with a variety of conditions in which increased production of pro-inflammatory cytokines promotes bone loss by increasing osteoclast formation, activation and survival. Most published data indicate that these effects are mediated mainly indirectly through stromal cell production of M-CSF and RANKL, which bind to their receptors on osteoclasts and activate c-Fos/AP-1, NFkappaB, and NFAT2, expression of each of which is required for osteoclast formation. However, osteoclasts express receptors for a growing list of agents, including pro-inflammatory cytokines, suggesting that direct and indirect effects of cytokines on osteoclasts could combine to induce bone loss. Our over-riding hypothesis is that in disease states, osteoclast numbers may be regulated by direct effects of cytokines on cells in the osteoclast lineage that can lead to self perpetuating, up-regulatory cycles within these cells and subsequently to bone loss. However, the precise mechanisms and the signaling molecules involved remain to be fully elucidated. We plan to investigate the direct effects of cytokines on osteoclasts and their precursors and to determine the roles of c-Fos/AP-1, NFkappaB and NFAT2 signaling in this process using NFkappaB dKO, TNF transgenic and wild-type mice. We propose the following Specific Aims: 1. To fully characterize the effects of cytokines and retroviral transfer of c-Fos/AP-1 genes to wt and NFkB dKO splenocytes and to determine if other osteoclast stimulating factors induce osteoclast formation directly when c-Fos is expressed; 2. To determine the mechanisms whereby retroviral transfer of c-Fos and cytokines induce osteoclast formation directly and to examine the role of NFkB in this process; 3. To examine if cytokine and c-Fos/AP-1 expression are up-regulated in osteoclasts and their precursors in models of cytokine-mediated bone disease. These studies will better define the roles of key signaling pathways and advance our understanding of the mechanisms that directly regulate osteoclast formation and survival. Ultimately they should lead to the development of specific therapeutic agents to prevent and treat common bone diseases associated with increased osteoclast activity.

描述（由申请人提供）：骨丢失与多种病症相关，其中促炎细胞因子的产生增加通过增加破骨细胞的形成、活化和存活来促进骨丢失。 大多数已发表的数据表明，这些作用主要是通过基质细胞产生M-CSF和RANKL间接介导的，M-CSF和RANKL与破骨细胞上的受体结合并激活c-Fos/AP-1、NF κ B和NFAT 2，每种蛋白的表达都是破骨细胞形成所必需的。 然而，破骨细胞表达越来越多的试剂，包括促炎细胞因子的受体，表明细胞因子对破骨细胞的直接和间接作用可能联合收割机诱导骨丢失。 我们的主要假设是，在疾病状态下，破骨细胞数量可能受到细胞因子对破骨细胞谱系细胞的直接影响的调节，这可能导致这些细胞内的自我延续、上调周期，随后导致骨丢失。 然而，确切的机制和涉及的信号分子仍有待充分阐明。 我们计划使用NFkappaB dKO、TNF转基因和野生型小鼠来研究细胞因子对破骨细胞及其前体的直接影响，并确定c-Fos/AP-1、NFkappaB和NFAT 2信号传导在这一过程中的作用。 我们提出以下具体目标：1。充分表征细胞因子和逆转录病毒转移c-Fos/AP-1基因到wt和NFkB dKO脾细胞的作用，并确定当c-Fos表达时，其他破骨细胞刺激因子是否直接诱导破骨细胞形成; 2.探讨逆转录病毒介导c-Fos和细胞因子直接诱导破骨细胞形成的机制，以及NF κ B在此过程中的作用。目的：研究在姜黄素介导的骨疾病模型中，破骨细胞及其前体细胞中细胞因子和c-Fos/AP-1的表达是否上调。 这些研究将更好地确定关键信号通路的作用，并促进我们对直接调节破骨细胞形成和存活的机制的理解。 最终，它们将导致特异性治疗剂的开发，以预防和治疗与破骨细胞活性增加相关的常见骨疾病。