Regulation of Autophagy and Tumorigenesis by Bif-1

Bif-1 对自噬和肿瘤发生的调节

• 批准号: 8215872
• 负责人: HONG-GANG WANG
• 金额: $ 31.22万
• 依托单位: PENNSYLVANIA STATE UNIV HERSHEY MED CTR
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-04-01 至 2014-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8215872
• 关键词: 1-Phosphatidylinositol 3-Kinase; Ablation; Amino Acids; Apoptosis; Apoptotic; Autoimmune Diseases; Autophagocytosis; Autophagosome; Binding; Binding Proteins; Biogenesis; Birth; Carcinoma; Cells; Cellular Stress; Charge; Coiled-Coil Domain; Colon; Complex; Development; Digestion; Disease; Docking; Eating; Embryo; Family member; Frequencies; Generations; Genes; Genetic Screening; Haploidy; Health; Hela Cells; Hepatic Lymphoma; Homeostasis; Homologous Gene; Human; In Vitro; Knock-out; Knockout Mice; Lipid Binding; Liposomes; Lymphoma; Lysosomes; Malignant Neoplasms; Malignant neoplasm of lung; Malignant neoplasm of ovary; Mantle Cell Lymphoma; Mediating; Membrane; Microscopy; Mitochondria; Modeling; Molecular; Mus; N-terminal; Neonatal; Neurodegenerative Disorders; Nude Mice; Nutrient; Organelles; Phenotype; Phosphotransferases; Play; Prevention strategy; Primary carcinoma of the liver cells; Process; Proline-Rich Domain; Prostate; Protein Family; Proteins; Recruitment Activity; Regulation; Reporting; Retrieval; Role; Shapes; Staging; Starvation; Stimulus; Stomach; Structure; System; Testing; Time; Tissues; Tumor Suppressor Proteins; Vesicle; Wild Type Mouse; Yeasts; age related; amphiphysin; cancer cell; cancer therapy; chemotherapy; deprivation; dimer; driving force; implementation research; insight; malignant breast neoplasm; member; microbial; mutant; novel; pathogen; response; tumor; tumor growth; tumor progression; tumorigenesis

DESCRIPTION (provided by applicant): The overall objective of this project is to determine the molecular mechanisms by which Bif-1 activates autophagy and suppresses tumorigenesis. Autophagy, an evolutionarily conserved "self- eating" process, is activated in response to environmental and cellular stresses and plays a fundamental role in maintaining normal cellular homeostasis by delivering unfolded proteins, damaged organelles, and microbial pathogens to lysosomes for degradation. Dysregulation of this cellular self-digestion process can have profound consequences and most likely plays a major role in many types of diseases, including cancer, autoimmune diseases, and neurodegenerative disorders. To date, many autophagy-related (Atg) genes have been identified by independent genetic screens for autophagy-defective mutants in yeast; however, the molecular machinery required for the biogenesis of autophagosomes in mammalian systems has yet to be determined. We have recently discovered that Bif-1 interacts with Beclin 1 through UVRAG and is required for the biogenesis of autophagosomes. Bif-1, also known as SH3GLB1 or endophilin B1, was originally discovered as a Bax-binding protein that contains an amino-terminal N-BAR domain and a carboxy-terminal SH3 domain and demonstrates membrane binding and bending activities. Although the SH3 domain of Bif-1 is sufficient for binding to UVRAG, the N-BAR domain is indispensable for Bif-1 to induce autophagosome formation. Therefore, it is possible that Bif-1 interacts with Beclin 1 through UVRAG at the isolation membrane, or phagophore, during autophagy to regulate vesicle nucleation by inducing membrane curvature through its N- BAR domain. Specific Aim 1 will test this possibility. While our in vitro studies clearly demonstrated the vital role Bif-1 plays in autophagosome formation, the majority of Bif-1 knockout mice, unlike Atg-deficient mice, developed normally. This phenotypic discrepancy suggests that an unknown factor(s) exists in specific tissues that functionally compensate for the lack of Bif-1 during embryonic and neonatal development. A possible candidate is the Bif-1 homologue endophilin B2. Our preliminary results revealed that endophilin B2 also interacts with Beclin 1 as well as UVRAG and can restore autophagosome formation in Bif-1 deficient cells. Specific Aim 2 will examine whether endophilin B2 shares a function redundant with Bif-1 in the control of autophagy. Moreover, we found that Bif-1 ablation significantly enhances the development of spontaneous tumors in mice. Since loss of Bif-1 also suppresses Bax/Bak activation and mitochondrial apoptosis, Specific Aim 3 will determine whether Bif-1 induces autophagosome formation and suppresses tumorigenesis independently of its interaction with Bax. We believe that successful implementation of this research will not only gain novel insight into the origin of isolation membranes and the molecular mechanism responsible for autophagic vesicle nucleation and expansion, but will also contribute to the establishment of new strategies for the prevention and treatment of cancer through manipulation of autophagy. PUBLIC HEALTH RELEVANCE: We believe that successful implementation of this research will not only gain novel insight into the origin of isolation membranes and the molecular mechanism responsible for autophagic vesicle nucleation and expansion, but will also contribute to the establishment of new strategies for the prevention and treatment of cancer through manipulation of autophagy.

描述（由申请人提供）：本项目的总体目标是确定Bif-1激活自噬和抑制肿瘤发生的分子机制。自噬是一种进化上保守的“自食”过程，其响应于环境和细胞应激而被激活，并且通过将未折叠的蛋白质、受损的细胞器和微生物病原体递送至溶酶体进行降解而在维持正常的细胞内稳态中起基本作用。这种细胞自我消化过程的失调可能会产生深远的后果，并且很可能在许多类型的疾病中发挥重要作用，包括癌症，自身免疫性疾病和神经退行性疾病。迄今为止，许多自噬相关（Atg）基因已被确定为独立的遗传筛选酵母中的自噬缺陷突变体，然而，在哺乳动物系统中的自噬体的生物合成所需的分子机制尚未确定。我们最近发现Bif-1通过UVRAG与Beclin 1相互作用，并且是自噬体生物发生所必需的。Bif-1，也被称为SH 3GLB 1或endophilin B1，最初被发现是一种包含氨基末端N-BAR结构域和羧基末端SH 3结构域的膜结合蛋白，并显示膜结合和弯曲活性。虽然Bif-1的SH 3结构域足以与UVRAG结合，但N-BAR结构域对于Bif-1诱导自噬体形成是必不可少的。因此，在自噬过程中，Bif-1可能通过UVRAG在隔离膜或吞噬细胞上与Beclin 1相互作用，从而通过其N-BAR结构域诱导膜弯曲来调节囊泡成核.具体目标1将测试这种可能性。虽然我们的体外研究清楚地证明了Bif-1在自噬体形成中的重要作用，但与Atg缺陷小鼠不同，大多数Bif-1敲除小鼠发育正常。这种表型差异表明，在胚胎和新生儿发育过程中，特定组织中存在一种未知的因子，在功能上弥补了Bif-1的缺乏。一个可能的候选者是Bif-1同源物内亲和素B2。我们的初步研究结果表明，内啡肽B2也与Beclin 1以及UVRAG相互作用，并可以恢复Bif-1缺陷细胞中自噬体的形成。具体目标2将检查在控制自噬中，内嗜蛋白B2是否与Bif-1共享冗余功能。此外，我们发现Bif-1消融显著增强了小鼠自发性肿瘤的发展。由于Bif-1的缺失也抑制Bax/巴克活化和线粒体凋亡，特异性目的3将确定Bif-1是否诱导自噬体形成并抑制肿瘤发生，而不依赖于其与Bax的相互作用。我们相信，这项研究的成功实施不仅将获得新的见解的起源隔离膜和负责自噬囊泡成核和扩张的分子机制，但也将有助于建立新的战略，预防和治疗癌症通过操纵自噬。公共卫生相关性：我们相信，这项研究的成功实施不仅将获得新的见解的起源隔离膜和负责自噬囊泡成核和扩张的分子机制，但也将有助于建立新的战略，预防和治疗癌症通过操纵自噬。