Targeting Daxx-mediated complex for autoimmune diseases

靶向 Daxx 介导的复合物治疗自身免疫性疾病

• 批准号: 8728728
• 负责人: JIANKE ZHANG
• 金额: $ 23.25万
• 依托单位: THOMAS JEFFERSON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-09-01 至 2016-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8728728
• 关键词: Ablation; Affect; Apoptosis; Apoptotic; Autoimmune Diseases; Autoimmune Process; Binding; Binding Proteins; CD95 Antigens; Cell Death; Cell Nucleus; Cell Proliferation; Cells; Cessation of life; Complex; Cytoplasm; Data; Death Domain; Defect; Development; Disease; Disease model; Embryo; Family; Family member; Genes; Genetic; Germ Cells; Homeostasis; Human; Immune; Immune system; In Vitro; Knockout Mice; Lead; Lymphocyte; Lymphoproliferative Disorders; MDM2 gene; Mature T-Lymphocyte; Mediating; Mediator of activation protein; Membrane; Modeling; Molecular; Mus; Mutant Strains Mice; Mutation; Nature; Necrosis; Oncogene Proteins; Pathway interactions; Play; Prevention Measures; Process; Protein Binding; Protein p53; Proteins; RIPK3 gene; Recruitment Activity; Resistance; Role; Signal Transduction; Stimulus; T-Cell Receptor; T-Lymphocyte; TNFRSF6 gene; Testing; Therapeutic; Transactivation; Tumor Cell Line; Yeasts; apoptosis in lymphocytes; autoimmune lymphoproliferative syndrome; caspase-10; caspase-8; design; in vivo; insight; knock-down; member; mutant; novel; public health relevance; response; yeast two hybrid system

DESCRIPTION (provided by applicant): The focus of this project is to investigate the molecular mechanism involved in a novel function of Daxx, which can be explored in developing strategies for autoimmune diseases. The multifunctional protein Daxx was originally identified as a potential mediator of Fas-induced apoptosis. Mutations in the Fas gene lead to an autoimmune-lymphoproliferative syndrome (ALPS), due to impaired apoptosis in lymphocytes and other immune cells. While Fas-induced cell death is initiated at the membrane, Daxx is present not only in the cytoplasm but also in the nucleus. Many potential Daxx-binding proteins have been identified, including the tumor suppressor p53 family members as well as the oncoprotein MDM2. However, the in vivo function of Daxx is poorly defined, as deletion of Daxx in germ cells leads to early embryonic lethality. During lymphocyte development and function, cell proliferation, survival and death are tightly regulated by various genes. Dysregulation in these processes may lead to autoimmune diseases. We and others identified the Fas- associated death domain (FADD) protein as a critical adaptor for Fas to recruit and activate the initiator caspase 8 during apoptotic signaling. Interestingly, FADD deficiency also has an embryonic lethal effect. Whereas lymphocytes in lymphocyte-specific FADD-deficient mice are resistant to Fas-induced apoptosis, these conditional FADD knockout mice do not develop autoimmune diseases, unlike that in Fas mutant mice. This paradox is explained by our recent study which reveals a potent, RIP1-dependent necrotic pathway unleashed in the absence of FADD. Our preliminary data show that deletion of RIP3, a member of the RIP1 family, restores normal development in FADD-deficient mice. Importantly, the resulting RIP3-/- FADD-/- double knockout (DKO) mice develop progressive autoimmune diseases, similar to that in Fas mutant mice. These data contrast a model suggesting that Daxx promotes FADD-independent apoptosis in the Fas pathway. Indeed, our preliminary data shows that Daxx-deficient T cells from conditional Daxx knockout mice have no defect in Fas-induced apoptosis. Unexpectedly, Daxx-/- T cells are hypersensitive to activation-induced cell death (AICD) when stimulated through the T cell antigen receptor (TCR). We hypothesize that in primary lymphocytes, there is an additional death pathway which is independent of the Fas-FADD-Caspase 8 axis, and is suppressed by Daxx. Therefore, targeting Daxx would promote cell death and serves as a strategy for autoimmune disease therapy. However, the molecular mechanism of this novel function of Daxx in the immune system is unclear. Therefore, we propose: 1) to elucidate the cell death pathway(s) in primary lymphocytes that is inhibited by Daxx; 2) to test for the effect o genetic and pharmacological ablation of Daxx function on suppressing autoimmune diseases. Successful completion of these specific aims will provide new insight into the mechanisms of the action by Daxx and lead to better design of measures for prevention and treatment of autoimmune and related diseases.

项目描述（由申请人提供）：本项目的重点是研究Daxx的一种新功能的分子机制，该功能可用于开发自身免疫性疾病的策略。多功能蛋白Daxx最初被确定为fas诱导的细胞凋亡的潜在介质。由于淋巴细胞和其他免疫细胞的凋亡受损，Fas基因突变可导致自身免疫淋巴细胞增生性综合征（ALPS）。虽然fas诱导的细胞死亡始于细胞膜，但Daxx不仅存在于细胞质中，也存在于细胞核中。许多潜在的daxx结合蛋白已被确定，包括肿瘤抑制因子p53家族成员以及癌蛋白MDM2。然而，Daxx在体内的功能尚不明确，因为生殖细胞中Daxx的缺失会导致早期胚胎死亡。在淋巴细胞的发育和功能过程中，细胞的增殖、存活和死亡受到多种基因的严格调控。这些过程的失调可能导致自身免疫性疾病。我们和其他人发现Fas相关死亡结构域（FADD）蛋白是Fas在凋亡信号传导过程中募集和激活启动物caspase 8的关键接头。有趣的是，FADD缺陷也有胚胎致死效应。尽管淋巴细胞特异性FADD缺陷小鼠的淋巴细胞对Fas诱导的细胞凋亡具有抗性，但与Fas突变小鼠不同，这些条件FADD敲除小鼠不会发生自身免疫性疾病。我们最近的研究解释了这一悖论，该研究揭示了在没有FADD的情况下释放的一种有效的、依赖rip1的坏死途径。我们的初步数据表明，RIP3 （RIP1家族的一员）的缺失可以恢复fadd缺陷小鼠的正常发育。重要的是，由此产生的RIP3-/- FADD-/-双敲除（DKO）小鼠发展为进行性自身免疫性疾病，类似于Fas突变小鼠。这些数据对比了一个模型，表明Daxx促进Fas通路中与fadd无关的细胞凋亡。事实上，我们的初步数据显示，来自条件Daxx基因敲除小鼠的Daxx缺陷T细胞在fas诱导的凋亡中没有缺陷。出乎意料的是，当通过T细胞抗原受体（TCR）刺激时，Daxx-/- T细胞对活化诱导的细胞死亡（AICD）非常敏感。我们推测，在原发性淋巴细胞中，存在一个独立于Fas-FADD-Caspase 8轴的额外死亡途径，该途径被Daxx抑制。因此，靶向Daxx可促进细胞死亡，并可作为自身免疫性疾病治疗的策略。然而，Daxx在免疫系统中这种新功能的分子机制尚不清楚。因此，我们提出：1)阐明Daxx抑制原代淋巴细胞的细胞死亡途径；2)检测基因和药理学消融Daxx功能对自身免疫性疾病的抑制作用。成功完成这些特定目标将为Daxx的作用机制提供新的见解，并导致更好地设计预防和治疗自身免疫及相关疾病的措施。