Genetic Analysis of Autophagy in the Drosophila Nervous System

果蝇神经系统自噬的遗传分析

• 批准号: 7676136
• 负责人: KIM D. FINLEY
• 金额: $ 15.88万
• 依托单位: SAN DIEGO STATE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-09-01 至 2011-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7676136
• 关键词: Adult; Affect; Age; Aging; Alzheimer' s Disease; Animal Model; Animals; Autophagocytosis; Biological Assay; Brain; Cell Culture Techniques; Clinical Trials; Complementary DNA; Complex; Defect; Degenerative Disorder; Development; Disease; Drosophila genus; Electron Microscopy; Employee Strikes; Eukaryotic Cell; Excision; Eye; Future; Gene Expression; Genes; Genetic; Genetic Models; Genetic Research; Goals; Head; Health; Human; Huntington Disease; Image; Immunofluorescence Immunologic; Individual; Inherited; Laboratories; Link; Location; Longevity; Lysosomes; Maintenance; Messenger RNA; Modeling; Mutation; Nerve Degeneration; Nervous system structure; Neurodegenerative Disorders; Neurons; Neurophysiology - biologic function; Oxidative Stress; Parkinson Disease; Pathology; Pathway interactions; Pattern; Peptides; Phenotype; Phosphorus; Play; Premature aging syndrome; Process; Proteins; Reagent; Relative (related person); Research; Research Proposals; Role; Severities; Sirolimus; System; Techniques; Time; Tissues; Toxic effect; Transgenic Organisms; Transport Vesicles; Ubiquitin; Western Blotting; Work; age related; biological adaptation to stress; cDNA Expression; cytotoxic; design; design and construction; expression vector; fly; gain of function; genetic analysis; human disease; human tissue; insight; loss of function; loss of function mutation; member; mutant; neuron loss; neuronal patterning; normal aging; oxidant stress; polyglutamine; prevent; protein aggregate; relating to nervous system; response; trafficking

DESCRIPTION (provided by applicant): During normal aging and in the progression of common neurodegenerative disorders such as Alzheimer's and Parkinson's disease, both intra-cellular and extra-cellular protein aggregates containing ubiquitin can accumulate in neurons and neural tissues of humans. The underlying cellular pathways that prevent or suppress this accumulation from occurring are not well understood but a growing body of evidence indicates the macroautophagy pathway (autophagy) is involved with the removal of age-related cellular damage and protein aggregates. Autophagy is a highly conserved lysosomal trafficking pathway that functions by sequestering damaged cellular components or aggregated proteins into new vesicles that are transported to the lysosome for degradation. Using Drosophila genetics, we have shown that mutations in autophagy genes result in progressive neural degeneration that is accompanied by the accumulation of ubiquitinated protein aggregates. We also demonstrate that increasing the expression levels of individual autophagy genes in the mature CNS can dramatically extend adult lifespan. In this research proposal we will we continue our phenotypic characterization of new autophagy mutant strains for reduced longevity and the development of progressive neural defects. To determine which members of the autophagic pathway are essential for neuronal maintenance we will use genetic and transgenic techniques (Gal4/UAS) to suppress (UAS- dsRNAi) or enhance (UAS-cDNA) the expression levels of autophagy genes in the adult fly brain. Adult longevity profiles, formation of neural aggregates and accumulation insoluble ubiquitinated proteins (IUP) will be used as assays to detect changes in aging patterns, response to environmental stress (oxidant exposure) and the suppression of cytotoxic phenotypes by aggregate prone proteins (PolyQ). Immunofluorescence imaging and electron microscopy studies will be used to determine the timing and location of ubiquitinated inclusion formation in the CNS and the type and severity of intracellular trafficking defects occurring in neurons. The goal of this proposal is to determine the role that individual autophagy genes and the pathway in general has on neuronal aging and the elimination of cellular damage from neurons. The implications for human health are significant since defects in autophagic trafficking are found in many neural degenerative disorders and that upregulating the pathway by rapamycin treatment is being used in clinical trials on Huntington's disease patients.Relevance: The accumulation of age-dependent damage and the formation of neural aggregates are associated with degenerative disorders affecting millions of people. Recent genetic research in fruit flies has shown a cellular pathway that removes cellular damage from nerve cells can significantly affect longevity by protecting the aging nervous system. Insight from this genetic model of neural degeneration and protection it affords the nervous system will enhance our understanding of complex processes that occur in people and will direct future research that is designed to promote human health and longevity.

描述（由申请人提供）：在正常衰老期间和在常见神经变性疾病如阿尔茨海默氏病和帕金森氏病的进展中，含有泛素的细胞内和细胞外蛋白质聚集体均可在人的神经元和神经组织中积累。阻止或抑制这种积累发生的潜在细胞途径尚未得到很好的理解，但越来越多的证据表明，大自噬途径（自噬）与年龄相关的细胞损伤和蛋白质聚集体的去除有关。自噬是一种高度保守的溶酶体运输途径，其通过将受损的细胞组分或聚集的蛋白质隔离到新的囊泡中而发挥作用，所述新的囊泡被运输到溶酶体进行降解。利用果蝇遗传学，我们已经表明，自噬基因的突变导致进行性神经变性，伴随着泛素化蛋白质聚集体的积累。我们还证明，增加成熟CNS中单个自噬基因的表达水平可以显着延长成年人的寿命。在这项研究计划中，我们将继续对新的自噬突变株进行表型表征，以减少寿命和发展进行性神经缺陷。为了确定自噬途径的哪些成员对于神经元维持是必不可少的，我们将使用遗传和转基因技术（Gal 4/UAS）来抑制（UAS-dsRNAi）或增强（UAS-cDNA）自噬基因在成蝇脑中的表达水平。成年人寿命曲线、神经聚集体的形成和不溶性泛素化蛋白（IUP）的积累将被用作检测衰老模式变化、对环境应激（氧化剂暴露）的反应以及聚集倾向蛋白（PolyQ）对细胞毒性表型的抑制的试验。免疫荧光成像和电子显微镜研究将用于确定CNS中泛素化包涵体形成的时间和位置以及神经元中发生的细胞内运输缺陷的类型和严重程度。该提案的目标是确定单个自噬基因和途径在神经元老化和消除神经元细胞损伤中的作用。对人类健康的影响是显着的，因为在许多神经退行性疾病中发现了自噬运输的缺陷，并且通过雷帕霉素治疗上调途径正在用于亨廷顿氏病patients.Relevance的临床试验：年龄依赖性损伤的积累和神经聚集体的形成与影响数百万人的退行性疾病有关。最近对果蝇的遗传研究表明，一种从神经细胞中去除细胞损伤的细胞途径可以通过保护衰老的神经系统来显着影响寿命。从这种神经变性的遗传模型及其对神经系统的保护中获得的见解将增强我们对人类复杂过程的理解，并将指导未来旨在促进人类健康和长寿的研究。

项目成果

Treatment with Bacterial Biologics Promotes Healthy Aging and Traumatic Brain Injury Responses in Adult Drosophila, Modeling the Gut-Brain Axis and Inflammation Responses.

• DOI: 10.3390/cells10040900
• 发表时间: 2021-04-14
• 期刊: Cells
• 影响因子: 6
• 作者: Molina B;Mastroianni J;Suarez E;Soni B;Forsberg E;Finley K
• 通讯作者: Finley K

Aging and Intermittent Fasting Impact on Transcriptional Regulation and Physiological Responses of Adult Drosophila Neuronal and Muscle Tissues.

衰老和间歇性禁食对成年果蝇神经元和肌肉组织的转录调节和生理反应的影响。

• DOI: 10.3390/ijms19041140
• 发表时间: 2018
• 期刊: International journal of molecular sciences
• 影响因子: 5.6
• 作者: Zhang,Sharon;Ratliff,EricP;Molina,Brandon;El-Mecharrafie,Nadja;Mastroianni,Jessica;Kotzebue,RoxanneW;Achal,Madhulika;Mauntz,RuthE;Gonzalez,Arysa;Barekat,Ayeh;Bray,WilliamA;Macias,AndrewM;Daugherty,Daniel;Harris,GregL;Edwa
• 通讯作者: Edwa

A pilot study: Innate immune modulation reduces F2-Isoprostanes and improves psychological health in a chronically stressed cohort.

• DOI: 10.1002/hsr2.289
• 发表时间: 2021-06
• 期刊: Health science reports
• 影响因子: 2
• 作者: Finley KD;Marcellus JE;Jones BA
• 通讯作者: Jones BA

Assessing Basal and Acute Autophagic Responses in the Adult Drosophila Nervous System: The Impact of Gender, Genetics and Diet on Endogenous Pathway Profiles.

• DOI: 10.1371/journal.pone.0164239
• 发表时间: 2016
• 期刊: PloS one
• 影响因子: 3.7
• 作者: Ratliff EP;Kotzebue RW;Molina B;Mauntz RE;Gonzalez A;Barekat A;El-Mecharrafie N;Garza S;Gurney MA;Achal M;Linton PJ;Harris GL;Finley KD
• 通讯作者: Finley KD