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R Weiler

Publications and source records attributed to R Weiler.

89 records · Page 5Linked to original sources
PubMed1982

The photoresponses of structurally identified amacrine cells in the turtle retina.

Intracellular recordings were obtained from amacrine cells afterwards identified morphologically by horseradish peroxidase injection. There is a correlation between the time course of the photoresponses and the distribution of the cell processes across the inner plexiform layer (i.p.l.). Cells producing the shortest duration, transient 'on-off' photoresponses branched in a single, narrow stratum of the i.p.l. (3-7 microns across). Transient photoresponses with a longer time course were recorded from cells branching in a thicker stratum of i.p.l. (up to 20 microns), or from bistratified cells. Amacrine cells producing sustained centre-on or centre-off photoresponses were radially diffused across the whole i.p.l.; therefore this type of photoresponse need not be associated with a specific cellular stratification within the i.p.l. It is concluded that the two main functional types of amacrine cell, i.e. transient on-off and sustained centre-on and centre-off, are subject to different structural organization of inputs than are the homologous physiological types of ganglion cells in this species, in the cat and in the carp. In a summary diagram the observed characteristics of the photoresponses are tentatively explained in terms of a non-homogeneous distribution of bipolar synaptic inputs along amacrine cell processes.

Animals↗
PubMed1981

The ramification pattern of amacrine cells within the inner plexiform layer of the carp retina.

The morphology of amacrine cells in the retina of the carp is described using the Golgi technique. The ramification pattern of these cells was analyzed in flat-mounts of retinas, Based on these observations classification into five groups was made. Cells possessing one principal process leaving the soma were subdivided into starburst A-neurons and radiate neurons. Cells having two or more principal processes were subdivided into starburst B-neutrons and spindle-shaped soma neurons. Small, diffuse amacrine cells form the fifth group. With respect to the shape of the field of arborization, the following cell types could be distinguished: (i) uniform cells, (ii) cells with a preferential direction, and (iii) cells with a marked edge, i.e., cells that lack processes in one direction. The latter form rarely occurs among starburst neurons; most of the spindle-shaped soma cells possess processes with a preferred direction, and cells with a marked edge are mainly found among the radiate neurons. All five cell types are found throughout the retina. The size of the cells varies within each group, and there is no correlation between size and distance from the optic nerve. The radial arborization pattern of each cell was examined in serial transverse sections. Starburst A-neurons ramify in the middle of the inner plexiform layer (IPL), radiate neurons in the inner half, and spindle-shaped soma neurons without overlapping processes (type B) as well as starburst B-neurons in the outer half. The ramification can be monostratified (narrow or broad), bistratified or multistratified. Small, diffuse amacrine cells and spindle-shaped soma neurons with overlapping process (type A) ramify throughout the entire IPL.

Animals↗
PubMed1981

Morphology of horizontal cells in the frog retina.

Two types of horizontal cells, H1 and H2, were classified using the Golgi technique on flat mounts of the retina of the frog. Cell type H1 possesses rather short, thick dendrites; the diameter of its dendritic field ranges from 40-90 micrometers. H2-cell displays long and thin dendrites; the diameter of its dendritic field is 70-160 micrometers. H1-cells possess an axon running horizontally within the outer plexiform layer. The axon terminals are slight swellings emitting fine processes that end in the outer plexiform layer. H2-cells do not have a discernible axon.

Animals↗
PubMed1980

Intracellular analysis and structural correlates of the organization of inputs to ganglion cells in the retina of the turtle.

Intracellular recording from the ganglion cells of the retina of the turtle Pseudemys scripta elegans shows that the photoresponses are characterized by either of two reversal potentials. These have been related to the bipolar and amacrine cell inputs to ganglion cells. Of the recorded ganglion cells, 33% (type A) are driven predominantly by one type of input, attributed to bipolar cells. Other ganglion cells (66%, type B) receive a mixed input from bipolar and amacrine cells. Type A ganglion cells show a higher conduction velocity (up to 3 m/s) and a higher firing frequency (up to 160 spikes per second) than type B cells. By injecting Procion yellow into bipolar, amacrine and ganglion cells it may be observed that type A ganglion cells ramify only in those regions of the inner plexiform layer that contain cell processes originating exclusively from the bipolar cell type predicted from the recordings. Type B ganglion cells ramify throughout the inner plexiform layer in either a multi-stratified or a diffuse fashion.

Action Potentials↗
PubMed1978

Horizontal cells of the carp retina: Golgi impregnation and Procion-Yellow injection.

Application of two methods for the selective staining of neurons, Golgi impregnation and intracellular marking with Procion Yellow, has revealed the anatomical arrangements of the horizontal cells in the carp retina. There are two basic horizontal-cell types, those with axons and these without. The former can be subdivided into three groups on the basis of the pattern of branching of the dendrites. These three structural groups are also functionally distinct, as shown by the electrical recordings made during Procion-Yellow injection. The axons of these three types of cell project into the proximal part of the inner nuclear layer, where they expand to form morphologically indistinguishable terminals. Fine horizontal processes leave the surfaces of these axon terminals. The functional behavior of a terminal resembles that of the associated soma. The horizontal cells lacking axons vary in morphological appearance, but they are similar functionally.

Animals↗
PubMedDate not supplied

Short-term effects of dopamine on photoreceptors, luminosity- and chromaticity-horizontal cells in the turtle retina.

The effects of dopamine on luminosity-type horizontal cells have been documented in different vertebrate retinas, both in vivo and in vitro. Some of these effects may reflect direct action of dopamine onto these cells, but indirect effects mediated by presynaptic neurons cannot be ruled out. Furthermore, direct effects of dopamine on horizontal cells may affect other, postsynaptic neurons in the outer plexiform layer. To test these possibilities, we studied the effects of dopamine on photoreceptors and all types of horizontal cells in the turtle (Pseudemys scripta elegans) retina. Receptive-field properties, responsiveness to light, and time course of light responses were monitored with intracellular recordings. Dopamine at a concentration of 40 microM exerted effects with two different time courses. "Short-term" effects were fully developed after 3 min of dopamine application and reversed within 30 min of washout of the drug. "Long-term" effects were fully developed after about 7-10 min and could not be washed out during the course of our experiments. Only the "short-term" effects were studied in detail in this paper. These were expressed in a reduction of the receptive-field size of all types of horizontal cells studied; L1 and L2 luminosity types as well as Red/Green and Yellow/Blue chromaticity types. The L1 horizontal cells did not exhibit signs of reduced responsiveness to light under dopamine, while in the L2 cells and the two types of chromaticity cells responsiveness decreased. None of the rods, long-wavelength-sensitive, or medium-wavelength-sensitive cones exhibited any apparent reduction in their receptive-field sizes or responsiveness to light. The present results suggest that the "short-term" effects of dopamine are not mediated by photoreceptors and are probably due to direct action of dopamine on horizontal cells.

Animals↗
PubMedDate not supplied

Dark-suppression and light-sensitization of horizontal cell responses in the hybrid bass retina.

The responsiveness of luminosity-type horizontal cells, recorded intracellularly from isolated hybrid bass retinas, decreased after superfusion for 2 h in constant darkness. Responsiveness was subsequently increased (light-sensitized) up to 10-fold after exposure to several short (approximately 0.5 min) periods of continuous illumination. The increase in horizontal cell responsiveness following light-sensitization was due to an increase of peak response amplitude rather than a reduction of peak response time. The increased responsiveness after light-sensitization was intensity-dependent with brighter sensitizing stimuli causing a greater increase than dimmer stimuli. The extent of LHC dark-suppression was affected by the time of day, being greater when induced during the night than during the day. However, there was no significant difference in horizontal cell responsiveness after light-sensitization in retinas studied during the night compared to those studied during the day. The responsiveness of light-sensitized horizontal cells from isolated hybrid bass retinas was found to be suppressed by relatively brief periods of darkness. The responsiveness of horizontal cells, that were first light-sensitized, decreased by more than 50% following only 5 min of darkness. Suppression of light-sensitized horizontal cell responsiveness after such a short time in the dark has not been described in other teleost retinas. The suppression of light-sensitized horizontal cell responsiveness in hybrid bass retinas may be rapid in comparison to other teleosts.

Adaptation, Ocular↗
PubMedDate not supplied

Modulation of endogenous dopamine release in the turtle retina: effects of light, calcium, and neurotransmitters.

In the turtle retina, dopamine has been observed in a small population of amacrine cells. Whereas the effect of dopamine has been intensively studied, knowledge about the release of this transmitter and the neuronal control of its release are still poorly understood. We therefore decided to study the release of endogenous dopamine. Isolated retinas were superfused with Ringer's solutions and stimulated with increased potassium, light, or drugs which interfere with neurotransmitter systems. Dopamine was analyzed by using aluminum-oxide extraction and high-pressure liquid chromatography (HPLC) with electrochemical detection. Increased potassium (25 mM) caused a five-fold increase in the basal release. When calcium was replaced by cobalt, no increase was induced by 25 mM potassium. Flickering light increased the basal release of endogenous dopamine by a factor of three. The effect of flickering light was greater in the presence of additional steady background illumination. Kainate (10 microM), an agonist for excitatory amino acids, doubled the basal dopamine release. Bicuculline (10 microM), a gamma-amino butyric acid (GABA) antagonist, increased the release to about six times the basal level. Naloxone (10 microM), an opiate antagonist, increased the release to eight times the basal level. These findings suggest that dopamine is released from amacrine cells in the turtle retina in a calcium-dependent manner, which is most likely a vesicular release. Dopamine release is induced by flickering light vs. darkness and vs. steady background illumination. A moderate background illumination alone does not significantly increase basal dopamine release.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMedDate not supplied

Modulation of endogenous dopamine release in the fish retina by light and prolonged darkness.

The effect of light stimuli and prolonged darkness on the release of endogenous dopamine was measured in the white perch and hybrid bass retinas. Isolated retinas were superfused and released dopamine was measured using extraction and high-pressure liquid chromatography separation techniques. Potassium-induced release did not depend on the background illumination nor on the period of previous darkness. Steady white light did not affect release, but flickering light of 2 Hz increased release about two-fold. During prolonged darkness, the release of dopamine increased steadily over the test period of 2 h, but only if the experiments were performed at night. During the day such an increase was not observed. The increased release during prolonged darkness at night was turned off by a short period of steady white light. The release patterns obtained from the white perch and the hybrid bass were similar. However, the hybrid bass retina showed much lower levels of dopamine than did the white perch retina.

Adaptation, Ocular↗
PubMedDate not supplied

Identification and localization of connexin26 within the photoreceptor-horizontal cell synaptic complex.

Connexin26 (Cx26) is a member of the family of integral membrane proteins that normally form intercellular gap junctional channels. We have used Western blotting, immunofluorescence, immunoelectron microscopy, and single-cell reverse-transcriptase polymerase chain reaction amplification (RT-PCR) to analyze the expression and cellular localization of Cx26 in the carp retina. In the outer plexiform layer, strong clustered Cx26 immunolabeling was concentrated at and restricted to the terminal dendrites of horizontal cells. Single-cell RT-PCR confirmed the expression of Cx26 in carp retinal horizontal cells. 248-bp fragments amplified from cDNAs of four different horizontal cells were cloned and each nucleotide sequence encodes a protein fragment (AA 104-185) with highly significant homology to rat and mouse Cx26. Immunoelectron microscopy revealed that only the invaginating dendrites of horizontal cells in intimate lateral association with the presynaptic ribbon complex were labeled. No labeling was found at the photoreceptor membrane and there was no septalaminar structure, indicative of gap junctions, between photoreceptors and horizontal cells. The focal location of Cx26 at the membrane of the dendritic tips of horizontal cells and the lack of gap junctional morphology suggests that Cx26 might form hemichannels.

Amino Acid Sequence↗
PubMedDate not supplied

Dynamic changes in the receptive fields of L1-type horizontal cells in the retina of the turtle Mauremys caspica.

The resistances of the horizontal cell syncytium in the vertebrate retina are modulated in a time-dependent fashion during light stimulation. Therefore, the spatial properties of horizontal cells are expected to change with time after the illumination conditions are altered. This study was designed to investigate time- and intensity-dependent changes in the receptive-field properties of L1-type horizontal cells in the turtle Mauremys caspica. Photoresponses were elicited by monochromatic (650 nm) light stimuli of 2-s duration covering retinal spots of different radii. The length constants were derived from the relationships between amplitude and spot radius that were constructed for different time intervals after onset of the light stimulus. For a given stimulus intensity, the length constant transiently increased to a peak value and then slowly recovered to a plateau level. When the length constant was compared to the amplitude of the response to full-field illumination for the entire duration of the light stimulus, an ellipse-like curve was obtained indicating that for a given membrane potential, two different values of the length constant could be obtained. Dopamine considerably reduced the size of the receptive fields but did not affect the time-dependent changes in the length constant. These results indicate that changes in the membrane resistance underlie short-term modulation of the receptive-field properties of turtle L1-type horizontal cells after onset of a light stimulus.

Animals↗
PubMedDate not supplied

Co-localization of neurotensin-like immunoreactivity and 3H-glycine uptake system in sustained amacrine cells of turtle retina.

Amacrine cells are axonless intrinsic neurones of the vertebrate retina which have cell bodies in the proximal inner nuclear layer and processes contributing to the synaptic network of the inner plexiform layer. They receive input from bipolar, interplexiform and other amacrine cells, and synapse onto these and ganglion cells. Amino acid and monoamine transmitters are found in most retinal neurones, but peptide transmitters are exclusively located in amacrine cells. Only one neuropeptide, amino acid or monoamine transmitter exists in any single amacrine cell population. Coexistence of neuropeptides with classical transmitters has been demonstrated histologically in many neurones of the central nervous system, but the physiological relevance of these findings is unknown. We report here evidence of such coexistence in retinal amacrine cells of the turtle, Pseudemys scripta elegans. Using combined immunocytochemistry and autoradiography, we have localized both neurotensin-like immunoreactivity and a high affinity uptake system for 3H-glycine to the same amacrine cell, implying that this cell type may use both substances as neurotransmitters. We also present electrophysiological evidence that this type of amacrine cell responds to photic stimulation with a sustained and graded membrane depolarization.

Animals↗