RESUMEN
Multimodal integration facilitates object recognition and response to sensory cues. This depends on spatiotemporal coincidence of sensory information, recruitment of NMDA-type glutamate receptors and inhibitory feedback. Shepherd's crook neurons (SCNs) in the avian optic tectum (TeO) are an ideal model for studying cellular mechanism of multimodal integration. They receive different sensory modalities through spatially segregated dendrites, are important for stimulus selection and have an axon-carrying dendrite (AcD). We performed whole-cell patch-clamp experiments in chicken midbrain slices of both sexes. We emulated visual and auditory input in vitro by stimulating presynaptic afferents electrically. Simultaneous stimulation enhanced responses inversely depending on stimulation amplitude demonstrating the principle of inverse effectiveness. Contribution of NMDA-type glutamate receptors prolonged postsynaptic events for visual inputs only, causing a strong modality-specific difference in synaptic efficacy. We designed a multicompartment model to study the effect of morphological and physiological parameters on multimodal integration by varying the distance between soma and axonal origin and the amount of NMDA receptor (NMDAR) contribution. These parameters changed the preference of the model for one input channel and adjusted the range of input rates at which multimodal enhancement occurred on naturalistic stimulation. Thus, the unique morphology and synaptic features of SCNs shape the integration of input at different dendrites and generates an enhanced multimodal response.SIGNIFICANCE STATEMENT Multimodal integration improves perception and responses to objects. The underlying cellular mechanism depends on a balance between excitation and inhibition, and NMDA-type glutamate receptors that are involved in the multiplicative nature of enhancement following the principle of inverse effectiveness. Based on a detailed analysis of an identified multimodal cell type in the vertebrate midbrain, we studied the influence of cellular morphology and unimodal synaptic properties on multimodal integration. We can show that the combination of cellular morphology and modality-specific synaptic properties including NMDA receptor (NMDAR) contribution is optimal for nonlinear, multimodal enhancement and determines the dynamic response range of the integrating neuron. Our findings mechanistically explain how synaptic properties and cellular morphology of a midbrain neuron contribute to multimodal enhancement.
Asunto(s)
Neuronas , Colículos Superiores , Animales , Axones , Dendritas/fisiología , Femenino , Masculino , Neuronas/fisiología , Receptores de N-Metil-D-Aspartato/fisiología , Colículos Superiores/fisiologíaRESUMEN
The incorporation of colloidal nanocrystals in a high crystalline quality semiconductor matrix, the efficient carrier injection into the embedded nanocrystals and the fast optical response are key features for the fabrication of novel optoelectronic nanodevices based on colloidal nanostructures as active optical material. Using a novel growth approach, colloidal bare CdSe and core-shell CdSe/ZnS nanocrystals were monolithically incorporated in pseudomorphic ZnSe/ZnMgSe quantum wells in order to control and enhance the carrier transfer into the nanocrystals. The photoluminescence for bare CdSe nanocrystals incorporated in ZnSe/ZnMgSe quantum well structures is substantially enhanced in comparison to nanocrystals sandwiched in ZnSe epilayers, which we attribute to increased carrier injection into the embedded nanocrystals via the quantum well, resembling the function of a wetting layer in Stranski-Krastanov-grown quantum dots. Core-shell CdSe/ZnS nanocrystals embedded in quantum well structures do not show considerable PL modifications because the ZnS shell prevents the efficient carrier migration between the nanocrystal and the matrix. Systematic investigations of structural and optical properties by high-resolution x-ray diffraction, temperature-dependent photoluminescence and time-resolved emission are presented.
RESUMEN
The emission of light in the blue-green region from cubic InxGa1-xN alloys grown by molecular beam epitaxy is observed at room temperature and 30 K. By using selective resonant Raman spectroscopy (RRS) we demonstrate that the emission is due to quantum confinement effects taking place in phase-separated In-rich quantum dots formed in the layers. RRS data show that the In content of the dots fluctuates across the volume of the layers. We find that dot size and alloy fluctuation determine the emission wavelengths.
RESUMEN
We present a growth technique which combines wet-chemical growth and molecular beam epitaxy (MBE) to create complex semiconductor nanostructures with nanocrystals as active optical material. The obtained results show that wet-chemically prepared semiconductor nanocrystals can be incorporated in an epitaxally grown crystalline cap layer. As an exemplary system we chose CdSe nanorods and CdSe(ZnS) core-shell nanocrystals in ZnSe and discuss the two limits of thin (d approximately 2R) and thick (d>2R) ZnSe cap layers of thickness d for CdSe nanorods and nanodots of radii R between 2 and 4 nm. In contrast to the strain-induced CdSe/ZnSe Stranski-Krastanow growth of a quantum dot layer in a semiconductor heterostructure, the technique proposed here does not rely on strain and thus results in additional degrees of freedom for choosing composition, concentration, shape, and size of the nanocrystals. Transmission electron microscopy and X-ray diffractometry show that the ZnSe cap layer is of high crystalline quality and provides all parameters for a consecutive growth of Bragg structures, waveguides, or diode structures for electrical injection.
Asunto(s)
Compuestos de Cadmio/química , Cristalización/métodos , Nanoestructuras/química , Nanoestructuras/ultraestructura , Compuestos de Selenio/química , Semiconductores , Compuestos de Zinc/química , Compuestos de Cadmio/análisis , Coloides/química , Diseño de Equipo , Análisis de Falla de Equipo , Ensayo de Materiales , Conformación Molecular , Nanoestructuras/análisis , Tamaño de la Partícula , Compuestos de Selenio/análisis , Integración de Sistemas , Compuestos de Zinc/análisisRESUMEN
The synthesis of bile acid oligodeoxynucleotide conjugates via the 3-OH group of the bile acids is described. When used in vivo in rats, covalent conjugation of an oligodeoxynucleotide via a linker to cholic acid resulted in an increased biliary excretion of bile acid-oligodeoxynucleotide conjugates compared to unconjugated oligodeoxynucleotides.