17 research outputs found

    Nigrostriatal overabundance of alpha-synuclein leads to decreased vesicle density and deficits in dopamine release that correlate with reduced motor activity

    Get PDF
    alpha-Synuclein (alpha-syn) is a presynaptic protein present at most nerve terminals, but its function remains largely unknown. The familial forms of Parkinson's disease associated with multiplications of the alpha-syn gene locus indicate that overabundance of this protein might have a detrimental effect on dopaminergic transmission. To investigate this hypothesis, we use adeno-associated viral (AAV) vectors to overexpress human alpha-syn in the rat substantia nigra. Moderate overexpression of either wild-type (WT) or A30P alpha-syn differs in the motor phenotypes induced, with only the WT form generating hemiparkinsonian impairments. Wild-type alpha-syn causes a reduction of dopamine release in the striatum that exceeds the loss of dopaminergic neurons, axonal fibers, and the reduction in total dopamine. At the ultrastructural level, the reduced dopamine release corresponds to a decreased density of dopaminergic vesicles and synaptic contacts in striatal terminals. Interestingly, the membrane-binding-deficient A30P mutant does neither notably reduce dopamine release nor it cause ultrastructural changes in dopaminergic axons, showing that alpha-syn's membrane-binding properties are critically involved in the presynaptic defects. To further determine if the affinity of the protein for membranes determines the extent of motor defects, we compare three forms of alpha-syn in conditions leading to pronounced degeneration. While membrane-binding alpha-syns (wild-type and A53T) induce severe motor impairments, an N-terminal deleted form with attenuated affinity for membranes is inefficient in inducing motor defects. Overall, these results demonstrate that alpha-syn overabundance is detrimental to dopamine neurotransmission at early stages of the degeneration of nigrostriatal dopaminergic axons

    PGC-1 alpha activity in nigral dopamine neurons determines vulnerability to alpha-synuclein

    No full text
    Introduction: Mitochondrial dysfunction and oxidative stress are critical factors in the pathogenesis of age-dependent neurodegenerative diseases. PGC-1 alpha, a master regulator of mitochondrial biogenesis and cellular antioxidant defense, has emerged as a possible therapeutic target for Parkinson's disease, with important roles in the function and survival of dopaminergic neurons in the substantia nigra. The objective of this study is to determine if the loss of PGC-1 alpha activity contributes to alpha-synuclein-induced degeneration. Results: We explore the vulnerability of PGC-1 alpha null mice to the accumulation of human alpha-synuclein in nigral neurons, and assess the neuroprotective effect of AAV-mediated PGC-1 alpha expression in this experimental model. Using neuronal cultures derived from these mice, mitochondrial respiration and production of reactive oxygen species are assessed in conditions of human alpha-synuclein overexpression. We find ultrastructural evidence for abnormal mitochondria and fragmented endoplasmic reticulum in the nigral dopaminergic neurons of PGC-1 alpha null mice. Furthermore, PGC-1 alpha null nigral neurons are more prone to degenerate following overexpression of human alpha-synuclein, an effect more apparent in male mice. PGC-1 alpha overexpression restores mitochondrial morphology, oxidative stress detoxification and basal respiration, which is consistent with the observed neuroprotection against alpha-synuclein toxicity in male PGC-1 alpha null mice. Conclusions: Altogether, our results highlight an important role for PGC-1 alpha in controlling the mitochondrial function of nigral neurons accumulating alpha-synuclein, which may be critical for gender-dependent vulnerability to Parkinson's disease

    Close Packing of Nitroxide Radicals in Stable Organic Radical Polymeric Materials

    No full text
    The relationship between the polymer network and electronic transport properties for stable radical polymeric materials has come under investigation owing to their potential application in electronic devices. For the radical polymer poly­(2,2,6,6-tetramethylpiperidine-4-yl-1-oxyl methacrylate), it is unclear whether the radical packing is optimal for charge transport partially because the relationship between radical packing and molecular structure is not well-understood. Using the paramagnetic nitroxide radical as a probe of the polymer and synthetic techniques to control the radical concentration on the methyl methacrylate backbone, we investigate the dependence of radical concentration on molecular structure. The electron paramagnetic resonance data indicate that radicals in the PTMA assume a closest approach distance to each other when more than 60% of the backbone is populated with radical pendant groups. Below 60% coverage, the polymer rearranges to accommodate larger radical–radical spacing. These findings are consistent with theoretical calculations and help explain some experimentally determined electron-transport properties

    Solar thermoelectricity via advanced latent heat storage

    No full text
    We report on a new modular, dispatchable, and cost-effective solar electricity-generating technology. Solar ThermoElectricity via Advanced Latent heat Storage (STEALS) integrates several state-of-the-art technologies to provide electricity on demand. In the envisioned STEALS system, concentrated sunlight is converted to heat at a solar absorber. The heat is then delivered to either a thermoelectric (TE) module for direct electricity generation, or to charge a phase change material for thermal energy storage, enabling subsequent generation during off-sun hours, or both for simultaneous electricity production and energy storage. The key to making STEALS a dispatchable technology lies in the development of a “thermal valve,” which controls when heat is allowed to flow through the TE module, thus controlling when electricity is generated. The current project addresses each of the three major subcomponents, (i) the TE module, (ii) the thermal energy storage system, and (iii) the thermal valve. The project also includes system-level and techno- economic modeling of the envisioned integrated system and will culminate in the demonstration of a laboratory-scale STEALS prototype capable of generating 3kWe
    corecore