Alzheimer's disease (AD) is characterized by progressive neurodegeneration and build-up of A? peptides, amyloid plaques, and neurofibrillary tau tangles. Current strategies to prevent A? formation or secretion are not successful. Preventing A? build-up while enhancing A? uptake and clearance is an alternative approach to minimize the effect of A? peptides. A critical barrier to progress in the development of novel drugs that prevent A? build-up and improve clearance is the lack of a thorough understanding of how A? amyloid plaques are nucleated and proliferate instead of A? being taken up and cleared by glial cells. Our goal is to interrupt amyloid plaque nucleation and propagation to enhance A? clearance and delay the onset and reduce neurodegeneration in AD. Our central hypothesis is that ceramide-enriched exosomes secreted by astrocytes form complexes with A? (A?/Exos) that function as seeds to catalyze nucleation and propagation of neurotoxic plaques instead of facilitating A? transport and clearance by microglia. Secretion, aggregation, and neurotoxicity of A?/Exos is enhanced by elevation of ceramide levels, in particular by neutral sphingomyelinase 2 (nSMase2), an enzyme generating ceramide when activated by A?. Drug (e.g., nSMase2 inhibitor)-induced reduction of ceramide will prevent A?/Exo build-up/spreading and protect neurons, which is a novel treatment option for AD. Our objectives are to 1) test key regulatory factors that control secretion of exosomes and their association with A?; 2) test a novel molecular mechanism by which A?/Exos induce plaque formation, tau hyperphosphorylation, and neuronal cell death; 3) test pharmacological drugs that prevent exosome secretion, A?/Exo-induced plaque formation, tau hyperphosphorylation, and neuronal cell death in vitro and in vivo; and 4) test if A?/Exos in serum and cerebrospinal fluid from AD model mice and AD patients can be used as a novel diagnostic tool for monitoring plaque and tangle build-up, and treatment success. Our expected outcomes include 1) determining an exosome composition that induces association with A?, plaque nucleation and propagation, tau hyperphosphorylation, and neuronal cell death; 2) identifying ceramide- modulating drugs that prevent A?/Exo-induced plaque formation, tau hyperphosphorylation, and neuronal cell death; and 3) defining a level of A?/Exos in serum that indicates severity of AD and success of treatment. The impact of this project on public health will include knowledge needed for the development of new strategies and treatments that could delay and reduce the onset of progressive neurodegeneration in AD. We will test by which mechanism ceramide promotes association and aggregation of A?42 (Aim 1), how A?42/Exos induce plaque formation and neurodegeneration (Aim 2), and which treatment prevents exosome-induced amyloid aggregation, plaque formation, and AD pathology (Aim 3).
Development of novel drugs to treat Alzheimer's disease (AD) by preventing amyloid plaque formation and neurodegeneration is being impeded by lack of knowledge of how neurotoxic plaques are nucleated and propagated. Our goal is to interrupt amyloid plaque nucleation and propagation to enhance amyloid peptide clearance and delay the onset and reduce neurodegeneration in AD. The impact of this project on public health will include knowledge needed for the development of new strategies and treatments that could delay and/or reduce the onset of progressive neurodegeneration in Alzheimer's disease.
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|Zhong, Liansheng; Kong, Ji Na; Dinkins, Michael B et al. (2018) Increased liver tumor formation in neutral sphingomyelinase-2-deficient mice. J Lipid Res 59:795-804|
|Elsherbini, Ahmed; Bieberich, Erhard (2018) Ceramide and Exosomes: A Novel Target in Cancer Biology and Therapy. Adv Cancer Res 140:121-154|
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|Wang, Guanghu; Bieberich, Erhard (2018) Sphingolipids in neurodegeneration (with focus on ceramide and S1P). Adv Biol Regul 70:51-64|
|Bieberich, Erhard (2018) Sphingolipids and lipid rafts: Novel concepts and methods of analysis. Chem Phys Lipids 216:114-131|
|Wang, Guanghu; Spassieva, Stefka D; Bieberich, Erhard (2018) Ceramide and S1P Signaling in Embryonic Stem Cell Differentiation. Methods Mol Biol 1697:153-171|
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|Yue, Hai-Yuan; Bieberich, Erhard; Xu, Jianhua (2017) Promotion of endocytosis efficiency through an ATP-independent mechanism at rat calyx of Held terminals. J Physiol 595:5265-5284|
|Burgert, Anne; Schlegel, Jan; Bécam, Jérôme et al. (2017) Characterization of Plasma Membrane Ceramides by Super-Resolution Microscopy. Angew Chem Int Ed Engl 56:6131-6135|
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