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O Umino

Publications and source records attributed to O Umino.

11 recordsLinked to original sources
PubMed2000

Image processing experiments for computer-based three-dimensional reconstruction of neurones from electron micrographs from serial ultrathin sections.

This study examined an image processing technique that uses a computer to reconstruct a three-dimensional image of neurones from electron micrographs of serial ultrathin sections. The major problems involved were: (a) a distortion of features in electron micrographs; (b) a significant change of cross-section features of neurones in electron micrographs of neighbouring sections; and (c) disagreement between the electron microscopic section face and the coordinate plane desired for the reconstruction. Electron micrographs of a retinal bipolar cell stained with a biotinylated tracer were used. We corrected the distortion of features by means of a warp, a widely used algorithm in morphing image processing. The change of features between neighbouring electron micrographs was minimized by filling the gaps with an interpolated image produced by a dissolve, another algorithm in morphing, as well as the warp. The distortion of the three-dimensional reconstructed image made by piling up features was corrected by making the image with a wire frame model. Furthermore, in order to estimate a closed contour of features, an active contour model, Snakes, was applied to the electron microscope features. Snakes successfully detected the contour of the target feature, but in some electron microscope images broke into the target feature.

Algorithms↗
PubMed1998

Spatio-temporal receptive fields in carp retinal horizontal cells.

1. The dynamics of the receptive fields of retinal horizontal cells were examined by applying a spatio-temporal modulated light signal to the retina. 2. The spatio-temporal receptive fields of both cone- and rod-driven horizontal cells, estimated through cross-correlation between the modulated light signal and the cells' responses, showed their receptive fields (the space-dependent component) to be reduced in size with time. 3. In cone-driven horizontal cells, the reduction in receptive field size was initially small but then rapidly became prominent with time. The time to peak of the time-dependent component of spatio-temporal receptive fields did not depend on the distance from the centre. 4. Application of a small amount of Co2+, an agent blocking the cone-driven horizontal cells' feedback action on cones, or GABA, resulted in a reversal of the time-dependent shrinkage of receptive fields to time-dependent expansion. 5. In rod-driven horizontal cells, the receptive field shrinkage was slow. The time to peak of the time-dependent component decreased with the distance from the centre. 6. Image processing experiments examining the response pattern in the horizontal cell layer (neural image) to a moving square of light showed smudging of the neural image when the time-dependent receptive field expansion was present, while there was essentially no smudging under conditions of receptive field shrinkage.

Animals↗
PubMed1997

Syncytial integration by a network of coupled bipolar cells in the retina.

A model system for syncytial integration is the outer vertebrate retina, where graded signals or electrotonic potentials interact laterally via gap junctions to form an integrated response that is relayed by chemical synapses to the next layer of interconnected cells. Morphological and physiological experiments confirm that bipolar cells form quasisyncytial lattices, and so this review will aim to address two important issues: the function of coupling in visual information processing and the construction of a robust mathematical model that can adequately simulate signal spread in the bipolar cell syncytium. It is shown that the role of coupling in bipolar cells differs from that associated in the presynaptic networks, namely, loss in spatial resolution in order to increase the signal-to-noise ratio. The intrinsic membrane properties of bipolar cells which give rise to voltage-dependent currents are inactive over the normal in vivo operating range of membrane potential and may be shunted as a direct result of electrotonic coupling, suppressing any possibility of action potential propagation in the bipolar cell syncytium. It is therefore speculated that the mechanisms underlying processing of information in bipolar networks are dependent on the structure of bipolar cells and in particular, on the presence of gap junctions. It is proposed that a three-dimensional model which incorporates the spatial properties of each bipolar cell in the network in the form of a leaky cable is the most likely model to simulate signal spread in the bipolar cell syncytium in vivo. This is because discrete network models represent each bipolar cell in the syncytium as isopotential units without any spatial structure, and thus are unable to reproduce the temporal characteristics of electrotonic potential spread within the central receptive field of bipolar cells.

Animals↗
PubMed1993

Lateral gap junction connections between retinal amacrine cells summating sustained responses.

Vertebrate retinal amacrine cells produce transient or sustained responses. Sustained depolarizing amacrine cells in the dace retina were identified by their intracellularly recorded responses to light flashes. The response amplitude produced a notable spatial summation which exceeded that of individual dendritic arbors. When sustained type amacrine cells were intracellularly injected with Lucifer Yellow and biocytin, there was extensive transfer of biocytin, but not Lucifer Yellow, to surrounding cells with similar cellular morphology. Ultrastructural analysis of the interconnections by electron microscopy revealed the presence of gap junctions at the contact area, which did not include conventional synapses. Present results demonstrate that sustained response amacrine cells make direct electrical connections between the cells of the same type and electrical coupling may contribute to extension of their receptive fields.

Animals↗
PubMed1991

Effects of light stimuli on the release of dopamine from interplexiform cells in the white perch retina.

Interplexiform cells are centrifugal neurons in the retina carrying information from the inner to the outer plexiform layers. In teleost fish, interplexiform cells appear to release dopamine in the outer plexiform layer after prolonged darkness that modulates the receptive-field size and light responsiveness of horizontal cells (Mangel & Dowling, 1985; Yang et al., 1988a, b). It has been proposed that interplexiform cells may also release dopamine upon steady illumination because horizontal cells' receptive fields shrink in the light (Shigematsu & Yamada, 1988). Here, we report the shrinkage of the receptive fields of horizontal cells seen in the presence of background illumination is not blocked by dopamine antagonists, indicating that dopamine does not underlie the receptive-field size changes observed during steady illumination. Flickering light, however, does appear to stimulate the release of dopamine from the interplexiform cells, resulting in a marked reduction of horizontal cell receptive-field size. Taken together, experiments on horizontal cells indicate that dopamine is released from interplexiform cells in the teleost retina after prolonged darkness and during flickering light, but that dopamine release from interplexiform cells during steady retinal illumination is minimal.

Animals↗
PubMed1991

Dopamine release from interplexiform cells in the retina: effects of GnRH, FMRFamide, bicuculline, and enkephalin on horizontal cell activity.

In teleost fish, dopaminergic interplexiform cells provide an intraretinal centrifugal pathway from the inner to the outer plexiform layer, where they make abundant synapses on cone-related horizontal cells. The interplexiform cells receive all their input in the inner plexiform layer from centrifugal fibers and amacrine cells. In fish, centrifugal fibers contain gonadotropin hormone-releasing hormone (GnRH)-like and FMRFamide-like peptides (Munz et al., 1982; Stell et al., 1984), whereas amacrine cells contain a variety of neuroactive substances, including a number of peptides. In this study, we examined the effects of GnRH, FMRFamide, bicuculline, and enkephalin on horizontal cell activity in the white perch retina in an attempt to understand the synaptic inputs to the interplexiform cells. When the retina was superfused with Ringer's solution containing GnRH, horizontal cells depolarized (approximately 10 mV), and their responses to small spots increased, whereas their responses to full-field lights decreased. Thus, GnRH closely mimicked the effects of dopamine on horizontal cells. The GnRH antagonist [D-Phe2, Pro3, D-Phe6]-GnRH blocked the effects of GnRH, as did haloperidol. GnRH also had no effect on horizontal cells in retinas treated with 6-hydroxydopamine. The results indicate that GnRH acts by stimulating the release of dopamine from interplexiform cells. FMRFamide alone produced no changes on either the membrane potential or light responses of horizontal cells, but it did suppress the effects of GnRH on horizontal cells in some experiments. FRMFamide also reversed the effects of prolonged darkness on horizontal cell responses. When bicuculline was applied to the retina, horizontal cells also depolarized (approximately 10 mV), responses to full-field illumination decreased, and responses to small spots increased. Most of the effects of bicuculline were suppressed by haloperidol, indicating that bicuculline also stimulates the release of dopamine from interplexiform cells. Similar results were obtained when [D-Ala2]-met-enkephalinamide was applied to the retina; horizontal cells depolarized (approximately 10 mV), responses to full-field stimuli decreased, and responses to the light spots increased. On the other hand, [D-Ala2]-leuenkephalinamide and [D-Ala2, D-Leu5]-enkephalin had no effects on horizontal cells. Both haloperidol and naloxone blocked the effects of [D-Ala2]-met-enkephalinamide on horizontal cells, indicating that [D-Ala2]-met-enkephalinamide stimulates dopamine release from interplexiform cells via specific opiate receptors.

Animals↗
PubMed1989

Neural mechanisms of chromatic adaptation in L-type cone horizontal cells of the carp retina.

When a background light is delivered, the responsiveness of horizontal cells to light stimulus initially lowers but subsequently recovers gradually as shown by the increase in response amplitude to test light. These changes of responsiveness are observed when white or close wavelengths are used for both the background and test lights. However, the response amplitude to blue-green test light was initially enhanced but decreased and reached a steady state after the onset of red background illumination. The mechanism causing such a change of test responses was studied in the luminosity-type cone horizontal cells. The initial response enhancement was accompanied by an increase of the slope of hyperpolarizing phase, while the subsequent decrease of response amplitude was caused by the advancement of the recovery phase. The advancement of the recovery phase was eliminated by gamma-aminobutyric acid (GABA) or Co2+ (50 microM), which blocks GABA-induced currents in cone terminals. Dopamine, which inhibits GABA release from horizontal cells, stimulated the advancement of the recovery phase. The time course of the hyperpolarizing phase was not affected by these agents. The enhancement and the subsequent decrease of test responses were also observed in 6-hydroxydopamine-treated retinae. The results suggest that the GABAergic feedback pathway from horizontal cells to cones advances the recovery phase of response to test light. It appears, therefore, that the feedback modifies the responsiveness of horizontal cells to light stimulus under a red background illumination. The mechanism enhancing response amplitude will be also discussed.

Adaptation, Physiological↗
PubMed1987

Decline of blocking effect of cobalt ions on transmission from photoreceptors to horizontal cells during its prolonged application.

In high-Mg2+ medium, luminosity-type cone horizontal cells (L-cells) hyperpolarized and lost their photoresponses at a full membrane hyperpolarization of about -80 mV. These effects of high-Mg2+ are attributed to the blockade of transmitter release from photoreceptors. Application of Co2+ hyperpolarized the L-cells at first and the photoresponses disappeared at full membrane hyperpolarization. After a little while, however, the membrane potential began to depolarize and the light stimuli again evoked responses. The recovery of the membrane potential and photoresponses indicates that prolonged application of Co2+ weakens its ability to block transmission from photoreceptors to L-cells.

Animals↗
PubMed1983

Information processing in the system from light to horizontal cell response of the carp retina.

In this paper, two types of experiments in the carp retina are presented. One is the analysis of responses to white-noise-modulated light at different average mean intensity levels recorded from L-type horizontal cells. For weak light, the responses fluctuated symmetrically around mean values. For brighter light, however, the distribution of amplitude of the response departed from the normal distribution. The deviation from the normal distribution was characterized in terms of symmetry rather than peakedness. The deviation also implies the existence of a nonlinearity in the system. The other type is with barium ion. Ba2+ produced dramatic effects on the spectral response patterns of horizontal cells; the depolarizing response to long wavelength light of the R/G cell and the hyperpolarizing response to deep red light of the Y/RB cell were eliminated in Ba2+-containing solutions. The response of the L cell to white-noise-modulated light was also changed by application of Ba2+. In Ba2+-containing solution, the response became larger as well as slower than that in normal solution. The results of Ba2+ are discussed in relation to the interactions between cone and horizontal cells.

Animals↗
PubMedDate not supplied

The network properties of bipolar-bipolar cell coupling in the retina of teleost fishes.

Retinal bipolar cells exhibit a center-surround antagonistic receptive field to a light stimulus (Werblin & Dowling, 1969; Kaneko, 1970), and thus constitute an early stage of spatial information processing. We injected Lucifer Yellow and a small biotinylated tracer, biocytin, into bipolar cells of the teleost retina to examine electrical coupling in these cells. Lucifer-Yellow coupling was observed in one of 55 stained bipolar cells; the coupling pattern was one injected bipolar cell and three surrounding cells. Biocytin coupling was observed in 16 of 55 stained bipolar cells, six of which were ON center and ten OFF center. Although biocytin usually coupled to three to six bipolar cells, some OFF-center bipolar cells showed strong coupling to more than 20 cells. The biocytin-coupled bipolar cells were morphologically homologous. Membrane appositions resembling gap junctions were found between dendrites and between axon terminals of neighboring bipolar cells. In the strongest biocytin-coupled bipolar cells, the contacts between bipolar cells and cone photoreceptor cells were examined after reconstruction of the dendritic trees of five well-stained, serially sectioned OFF-center bipolar cells. Each of these bipolar cells was in contact with different numbers of cones: 11 to 20 for twin cones and two to four for single cones. This implies that, although these bipolar cells belong to the same category, the signal inputs differ among bipolar cells. Numerical simulation conducted on a hexagonal array network model demonstrated that the electrical coupling of bipolar cells can decrease the difference in input (approximately 80%) without causing significant loss of spatial resolution. Our results suggest that electrical coupling of bipolar cells has the advantage of decreasing the dispersion of input signals from cones, and permits bipolar cells of the same class to respond to light with similar properties.

Animals↗