Age and pathology-induced alteration of G protein-coupled receptor signaling

年龄和病理诱导的 G 蛋白偶联受体信号传导改变

基本信息

批准号：
7591988
负责人：
Stuart Maudsley
金额：
$ 62.54万
依托单位：
NATIONAL INSTITUTE ON AGING
依托单位国家：
美国
项目类别：
财政年份：
资助国家：
美国
起止时间：
至
项目状态：
未结题

来源：
https://reporter.nih.gov/project-details/7591988
关键词：
Acetylcholine Acute Affect Affinity Age Aging-Related Process Alzheimer&apos s Disease Amyloid beta-Protein Antibodies Area Bees Biological Assay Butyric Acid Butyric Acids Cell Line Cell membrane Cell surface Cells Chemicals Chromosome Pairing Clathrin Condition Confocal Microscopy Dendritic Spines Disease Disease model Environment Epitopes Face Focal Adhesions G Protein-Coupled Receptor Signaling G protein coupled receptor kinase G-Protein-Coupled Receptors Gated Ion Channel Glucose Glutamates Hemagglutinin Human Huntington Disease Hydrogen Peroxide Immune Sera In Vitro Integral Membrane Protein Investigation Life Ligands Link Mediating Membrane Membrane Microdomains Modeling Multiprotein Complexes Muscarinic Acetylcholine Receptor Muscarinics Nature Neuraxis Neurodegenerative Disorders Neurons Neurotransmitters Numbers Oxidative Stress Parkinson Disease Pathology Pharmacology Phase Process Production Protein Isoforms Protein Overexpression Proteins Proteomics Receptor Activation Receptor Cell Receptor Mediated Signal Transduction Recruitment Activity Research Scaffolding Protein Sepharose Serum Signal Transduction Signaling Protein Site Structure Synapses Synaptic Transmission System Techniques Technology Therapeutic Thinking Tissues Transcript Work animal tissue base beta-arrestin coated pit deprivation desensitization gamma secretase human RIPK1 protein mimetics neurotransmitter release normal aging novel programs receptor receptor function scaffold spinophilin stoichiometry stressor tandem mass spectrometry therapeutic target

项目摘要

Research Summary My proposed study involves investigation of age- and disease-dependent alteration of three distinct levels of receptor-mediated signal transduction control. These three levels of control are: receptor accessory protein modulation of signal transduction; scaffolding protein functionality in neuronal cells; receptor microdomain environment and its impact on receptor function. To these multiple ends myself and my research fellows have been undertaking the following research to illuminate these areas. Receptor Accessory protein modulation We have generated two sets of stably expressing human neuronal cell lines (SH-SY5Y) expressing an epitope-tagged (3x haemagglutinins) human m1 and m2 muscarinic acetylcholine G protein-coupled receptors (GPCRs). These receptors have been chosen as they represent one of the most important and tractable therapeutic targets for the treatment of Alzheimers disease (AD), e.g. the only currently prescribed AD therapeutic, AriceptTM, works by facilitating stimulation of these targets. We have chosen 24 clones of each of these cell lines and have been employing these for proteomic research. Our need to generate these clones resides in the purification techniques required to isolate large amounts of the receptor proteins so that their associated accessory proteins can be identified by tandem mass spectrometry. Using conventional antibody-based techniques using sera directed against functional regions of the receptor it is likely that subtle ultrastructural changes between receptor isoforms may be disregarded. Our hypothesis is that during aging and disease there are changes of the stoichiometry of the receptor with its accessory proteins and that this then affects the interaction of the receptor with its cognate ligand. Therefore our need to unambiguously purify transmembrane receptors was paramount. We have successfully purified high numbers of muscarinic receptors and demonstrated that large numbers of accessory proteins can associate with the GPCR. We intend now to compare these associated proteins to the groups of proteins that interact with the receptor in a disease state model, i.e. addition of exogenous amyloid beta peptide or oxidative stress in the form of either hydrogen peroxide addition or glucose deprivation. Scaffolding protein functionality modulation Scaffolding proteins are large proteins often associated with GPCRs at the cell surface but also with cytoskeletal entities. These proteins assemble multiple signaling factors into coherent cascades of functional relevance. These scaffolding proteins are thought to be the basis of GPCR selectivity of function. The ability of these scaffolding proteins to still function in the face of disease-mimicking stressors (see above) has yet to the thoroughly investigated. We have been developing technologies to isolate and purify these scaffolding molecules both from clonal human neuronal cells and also from primary animal tissue from disease models. The two GPCR-interacting scaffolding proteins we have been investigating are the G protein coupled receptor kinase-interacting transcript (GIT) and spinophilin. The first protein has been demonstrated to link GPCR desensitization to the ability of the stimulated receptor to affect cytoskeletal dynamics. This will be of great importance at the functional synapse. We are currently generating stable SH-SY5Y cell lines expressing epitope tagged (FLAG and haemagglutinin) and GFP-tagged forms of these proteins for live confocal microscopy. In addition we have created our own affinity matrix purification systems to isolated specifically large amounts of GIT from cells and tissues through chemical combination of GIT antisera to an immobilized agarose phase. This process has also bee repeated for the second scaffolding protein, spinophilin. This protein, specifically enriched in the dendritic spines of neurons (of particular importance for control of synaptic transmission) also can act as a novel scaffolding protein than becomes recruited to the GPCR upon ligand activation. We are currently analyzing the functional signaling proteins that interact with these scaffolding factors in the presence or absence of disease mimetics. Receptor microdomain study The interactions that GPCRs make with other functional transmembrane proteins are primarily controlled via their association with microdomain regions of the plasma membrane. Such microdomain regions include focal adhesions, clathrin-coated pits and lipid rafts. We have begun studying how GPCR-interacting proteins, such as the beta-arrestins, can control the presence of GPCRs in these microdomains is affected by neurodegenerative disorders such as AD. To this end we are in the process of generating SH-SY5Y cell lines overexpressing various forms of the beta-arrestin molecules. With purification of both clathrin pits and lipid raft structures we are intending to identify how the presence of the GPCRs in various different plasma membrane compartments can affect their pharmacology, with respect to ligand interaction and also their downstream signaling ability. In addition to this we have been elucidating the nature of the connection between GPCR activity and the enzymatic function of the gamma-secretase complex that is specifically enriched in the same compartment as many GPCRs, e.g. the lipid raft. We have been employing both proteomic identification and in vitro enzymatic assays to demonstrate how acute receptor stimulation may control minute-to-minute beta amyloid production.