ABSTRACT
Spike timing-dependent plasticity, related to differential Hebb-rules, has become a leading paradigm in neuronal learning, because weights can grow or shrink depending on the timing of pre- and post-synaptic signals. Here we use this paradigm to reduce unwanted (acoustic) noise. Our system relies on heterosynaptic differential Hebbian learning and we show that it can efficiently eliminate noise by up to -140 dB in multi-microphone setups under various conditions. The system quickly learns, most often within a few seconds, and it is robust with respect to different geometrical microphone configurations, too. Hence, this theoretical study demonstrates that it is possible to successfully transfer differential Hebbian learning, derived from the neurosciences, into a technical domain.
Subject(s)
Learning , Neuronal Plasticity , Learning/physiology , Mathematics , Models, Neurological , Neuronal Plasticity/physiology , Neurons/physiology , Noise , Synapses/physiologyABSTRACT
We investigated the biotransformation of very small superparamagnetic iron oxide nanoparticles (VSOP) in atherosclerotic LDLR-/- mice. Transmission electron microscopy revealed an uptake of VSOP not only by macrophages but also by endothelial cells in liver, spleen, and atherosclerotic lesions and their accumulation in the lysosomal compartment. Using magnetic particle spectroscopy (MPS), we show that the majority of VSOP's superparamagnetic iron was degraded within 28â¯days. MPS spectrum shape indicated changes in the magnetic properties of VSOP during the biodegradation process. Experiments with primary murine bone marrow derived macrophages, primary murine liver sinusoidal endothelial cells, and primary human aortic endothelial cells demonstrated that loading with VSOP induced a differential response of cellular iron homeostasis mechanisms with increased levels of ferritin and iron transport proteins in macrophages and increased levels of ferritin in endothelial cells.
Subject(s)
Atherosclerosis/metabolism , Ferric Compounds/chemistry , Ferric Compounds/metabolism , Magnetite Nanoparticles/administration & dosage , Receptors, LDL/physiology , Animals , Aorta/cytology , Aorta/metabolism , Atherosclerosis/physiopathology , Capillaries/cytology , Capillaries/metabolism , Cell Proliferation , Cells, Cultured , Endothelium, Vascular/cytology , Endothelium, Vascular/metabolism , Ferritins/metabolism , Humans , Macrophages/cytology , Macrophages/metabolism , Magnetite Nanoparticles/chemistry , Male , Mice , Mice, KnockoutABSTRACT
In vivo tracking of nanoparticle-labeled cells by magnetic resonance imaging (MRI) crucially depends on accurate determination of cell-labeling efficacy prior to transplantation. Here, we analyzed the feasibility and accuracy of magnetic particle spectroscopy (MPS) for estimation of cell-labeling efficacy in living THP-1 cells incubated with very small superparamagnetic iron oxide nanoparticles (VSOP). Cell viability and proliferation capacity were not affected by the MPS measurement procedure. In VSOP samples without cell contact, MPS enabled highly accurate quantification. In contrast, MPS constantly overestimated the amount of cell associated and internalized VSOP. Analyses of the MPS spectrum shape expressed as harmonic ratio A5/A3 revealed distinct changes in the magnetic behavior of VSOP in response to cellular uptake. These changes were proportional to the deviation between MPS and actual iron amount, therefore allowing for adjusted iron quantification. Transmission electron microscopy provided visual evidence that changes in the magnetic properties correlated with cell surface interaction of VSOP as well as with alterations of particle structure and arrangement during the phagocytic process. Altogether, A5/A3-adjusted MPS enables highly accurate, cell-preserving VSOP quantification and furthermore provides information on the magnetic characteristics of internalized VSOP.
