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Critical analysis of glycosphingolipid pathways in aging and Parkinsons disease

衰老和帕金森病中鞘糖脂通路的批判性分析

基本信息

批准号：
9278296
负责人：
PENELOPE Jane HALLETT
金额：
$ 31.11万
依托单位：
MCLEAN HOSPITAL
依托单位国家：
美国
项目类别：
财政年份：
2015
资助国家：
美国
起止时间：
2015-08-15 至 2019-05-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/9278296
关键词：
Acids Affect Aging Biochemical Biological Markers Brain Catabolism Cell membrane Cell physiology Cells Characteristics Corpus striatum structure Data Development Disease model Endosomes Enzymes Epoxy Compounds Fibroblasts Functional disorder Gaucher Disease Gene Mutation Genes Genetic Glucosylceramides Glycosphingolipids Grant Health Hippocampus (Brain)Homeostasis Human Hydrolase Hydrolysis In Vitro Knowledge Link Lipids Lysosomal Storage Diseases Lysosomes Measures Membrane Metabolism Midbrain structure Modeling Modification Mus Mutation Nerve Degeneration Neurodegenerative Disorders Neuronal Dysfunction Neurons Parkinson Disease Parkinsonian Disorders Pathology Pathway interactions Patients Predisposition Rattus Reporting Risk Factors Rodent Model Role Testing Therapeutic Toxic effect Transgenic Mice Validation alpha synuclein design disease stressor dopaminergic neuron experimental study gene therapy genetic risk factor glucosylceramidase glucosylsphingosine improved in vitro testing in vivo in vivo Model induced pluripotent stem cell inhibitor/antagonist neuropathology neurotoxic normal aging novel novel therapeutics overexpression pharmacodynamic biomarker prevent public health relevance stressor synucleinopathy

项目摘要

DESCRIPTION (provided by applicant): Glycosphingolipids are essential for many cellular processes, are enriched in membranes, and undergo catabolism in endosomes and lysosomes through the action of acid hydrolases. GBA encodes the lysosomal enzyme glucocerebrosidase (GCase), which is responsible for the hydrolysis of the glycosphingolipid substrates glucosylceramide (GluCer) and glucosylsphingosine (GluSph). GBA gene mutations are the highest known genetic risk factor for developing Parkinson's disease (PD) and related α-synucleinopathies. Our preliminary data shows that levels of GluSph are increased in the human brain in sporadic PD. Moreover, we show that GCase activity is reduced, and glycosphingolipid levels are increased in the brain in normal aging. The consequences of increased glycosphingolipid levels on neuronal health in aging and in sporadic PD are not known. In this R01 application I have designed experiments to test the relevance of elevated glycosphingolipids in neural cells in aging and PD. In Specific Aim 1 we hypothesize that altered levels of glycosphingolipids induce neuronal dysfunction and susceptibility to degeneration. We will modulate levels of GluSph in mouse and human neurons in vitro to determine whether neuronal vulnerability to PD-stressors, including increased α-synuclein loads, is altered. We will also establish whether reduced GCase and increased GluSph levels are detected in human PD patient fibroblasts and neurons as such alterations may represent novel bio- and pharmacodynamic- markers for PD. In Specific Aim 2 we hypothesize that reducing the accumulation of glycosphingolipids in aging and PD can prevent the aggregation and toxicity of α-synuclein. We will determine how the homeostasis of glycosphingolipid pathways are altered in two rodent models of α-synucleinopathy, and we will measure the effect of manipulating glycosphingolipid pathways by increasing neuronal GCase levels, in these same in vivo models. These experiments will provide critical analysis of the role of glycosphingolipid pathways in PD and related α-synucleinopathies, and should provide new targets for the development of novel therapeutics to improve glycosphingolipid metabolism and prevent neurodegeneration.