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Displaced small amacrine cells in the retina of the marine teleost Callionymus lyra L.

The displaced small amacrine cells (DSA cells) in the dorsal pure cone part of the retina of the marine teleost Callionymus lyra have been analysed in a combined light and electron microcopical study. These unistratified cells have their dendritic arborization at 70% of the depth of the inner plexiform layer (P5 level). The DSA cells constitute a dense population and have variable dendritic field sizes. The bipolar input occurs in the P5,1 and the P5,2 pattern layer. The short, central DSA dendrites make ribbon synapses with midget mixed di-cone bipolar cells and with two types of pure cone bipolar cells. The amacrine input and output occurs in the fibrous layer that separates both pattern layers. The dendritic arborization is most extensive and the dendrites of neighbouring DSA cells are interconnected. The thick, central DSA dendrites are presynaptic to adjacent DSA cells and possibly to large bistratified and diffuse ganglion cells. The fine, peripheral DSA dendrites receive input from neighbouring DSA cells and probably from large uni- and bistratified and diffuse amacrine cells. A matching population of regularly placed small amacrine cells (RSA cells) has been observed. Their unistratified dendritic arborization is situated at 20% of the depth of the inner plexiform layer. The synaptic relations of RSA cells have not yet been completely analysed in detail. However, results up till now indicate that they most probably receive input from two bipolar cell types, one of which may be a pure cone type. In addition, the large bistratified amacrine and ganglion cells may be synaptically connected to the RSA cells as well as to the DSA cells.

Animals↗

Topographic organization of the ganglion cell layer and intraocular vascularization in the retinae of two reef teleosts.

The retinae of two species of teleosts, the rippled blenny Istiblennius edentulus and the blue tusk fish Choerodon albigena are examined in wholemount. The retinal topography of Nissl-stained cells within the ganglion cell layer in each species reveals a temporal (4.32 x 10(4) cells per mm2) and a nasal (3.83 x 10(4) cells per mm2) area centralis in the rippled blenny and two temporal areae centrales (8.30 x 10(4) and 8.00 x 10(4) cells per mm2) and a horizontal streak (5.00 x 10(4) cells per mm2) in the tusk fish. These areas are thought to subserve higher spatial resolution. Transcardial perfusions of indian ink reveal an extensive network of vitreal blood vessels which are supplied by the hyaloid artery and overlie the retina in each species. This rich network of vitreal vessels supplies areas of increased ganglion cell density although areas of maximum cell density are devoid of vessels to preserve the high spatial resolving power of the eye within this region. Unique blood vessel plexuses overlying the optic disc and falciform process in the tusk fish are also described. The diameter of the overlying vitreal vessels is compared to the soma sizes of cells within the ganglion cell layer.

Animals↗

The spectral transmission of freshwater teleost ocular media--an interspecific comparison and a guide to potential ultraviolet sensitivity.

Based on their spectral transmission, the lenses of 50 teleost species can be classified into three categories: "type 1" colourless lenses with 50% transmission points between 315 and 354 nm, "type 2" lenses which also appear colourless but have 50% cut-off points around 362-405 nm, and "type 3" lenses which are visibly yellow (50% transmission 425-450 nm). Most corneas transmit all wavelengths down to around 300 nm, with only 3 species showing a distinct yellow colouration. This distribution of ocular media transmission is related both to the phylogenetic group of the fish and to their photic environment.

Animals↗

Release pattern of endogenous dopamine in teleost retinae during light adaptation and pharmacological stimulation.

The release of endogenous dopamine from teleost retinae was studied using high-performance-liquid-chromatography and electrochemical detection. Dopamine was measured in superfusates of isolated retinae after stimulation with flickering light as well as in the presence of GABA, L-glutamate, kainate or taurine. The effect of the receptor antagonists bicuculline, picrotoxin and kynurenic acid was also tested in retinae kept in the dark. We report a low level, basal release of dopamine in the dark (20 pg x 10 min-1/retina), which is transiently increased by stimulation with flickering light. This light evoked release of dopamine is inhibited by GABA and L-glutamate, whilst antagonists of these retinal transmitters stimulate release in the dark.

Adaptation, Ocular↗

Characteristics of single-channels activated by quisqualate and kainate in teleost retinal horizontal cells.

There is increasing evidence in the teleost retina that the excitatory amino acid glutamate is the neurotransmitter used by some photoreceptors. Single kainate and quisqualate channels were recorded on isolated white bass horizontal cells using patch-clamp techniques. Two categories of channels were observed. The first, labelled a slow-channel, exhibited conductance and open time averages for channels activated by quisqualate of 8.5 pS and 8.8 msec, and for kainate 8.5 pS and 4.5 msec. The closed times of these channels could be described by two time constants. The second channel category was termed a fast-channel. Quisqualate and kainate activated channels in this category with two prominent conductances in the range of about 10 pS and 20-30 pS and open times of 1-2 msec. These channels demonstrated closed times with only a single time constant. Openings of slow-channels elicited by the agonists tended to occur in bursts. Activity of the fast-channels was noisy and no bursting behavior could be seen. Both channels exhibited multiple conductance states.

Animals↗

Characterization of a GABAergic population of interstitial amacrine cells in the teleost retina.

We used postembedding immunocytochemistry with an antiserum against BSA-conjugated GABA to study the inner plexiform layer of a cyprinid teleost, the roach. In this part of the retina, we observed a distinct banding pattern of GABA-positive material. There was a narrow unstained region separating the distal sublamina a from the proximal sublamina b; each sublamina was further subdivided into four (a) and two (b) sublayers of heavier staining, respectively. Using three-dimensional reconstruction of series of half-micron tangential sections, we were able to characterize a population of interstitial amacrine cells which contained GABA-like immunoreactive material. These cells had elliptical dendritic fields (area: about 0.04 mm2) and conspicuous, thick processes (dia. 4-5 microns). In tangential sections, the dendrites of individual cells appeared to be in close contact, occasionally resulting in difficulties in defining the boundaries of a single dendritic field. Two sub-populations of these cells were observed, one in each sublamina. By comparison with a catalogue of Golgi impregnated amacrine cells and cells microinjected with Lucifer Yellow or HRP, the identity of this type of interstitial amacrine cell is established and its possible physiological properties discussed. Apart from this GABA positive type, a second population of interstitial amacrine cell was observed which did not show positive reaction to the GABA antiserum used.

Animals↗

Lymphoid organs of teleost fish. III. Splenic lymphoid tissue of Rutilus rutilus and Gobio gobio.

The ultrastructure of splenic lymphoid tissue of two teleost fish, Rutilus rutilus and Gobio gobio, constitutes discrete foci around the small arteries and "melano-macrophage" centres. It contains small and medium lymphocytes, lymphoblasts, macrophages and plasma cells. Plasmacytopoiesis and macrophage-lymphocyte clusters have been described and the significance of "melano-macrophage" centres and macrophage-lymphocyte clusters is discussed.

Animals↗

Effects of gamma-irradiation on the rejection of transplanted scale melanophores in the teleost, Oryzias latipes.

The effects of gamma-irradiation on allograft rejection in the teleost, Oryzias latipes, were examined at 25 degrees C. The survival of melanophores in the transplanted scale was observed as an index of rejection. Allografts were rejected in non-irradiated fish within 7 days. In the gamma-irradiated recipients (2kR), the grafts were rejected more slowly, but still within 20 days. The gamma-ray effects, however, disappeared almost completely within 25 days after the irradiation. If the same recipient again received transplants, the secondary response occurred clearly and the melanophores were rejected very rapidly. The secondary response was suppressed by gamma-rays if the fish was irradiated just before the second transplantation. Immunologic memory against the first transplants disappeared within 30 days, a period shorter than that of mammals.

Animals↗

Ontogeny of the lymphoid organs in an Antarctic teleost, Harpagifer antarcticus (Notothenioidei: Perciformes).

The effect of an evolutionary adaptation to low environmental temperature on the development of lymphoid organs was examined in Harpagifer antarcticus from Signy Island (South Orkney Islands; 60 degrees 43'S, 45 degrees 38'W). Thymus, pronephric kidney and spleen were typical, both in position and structural development, of those observed in warmer-water teleosts. The pronephric kidney was the first organ to be infiltrated by leucocytes, at 1 h post-hatch, though the infiltration of the thymic epithelia and the development of the splenic anlage were not observed until 4 weeks post-hatch. Full development of the lymphoid organs was not achieved until the juvenile stage. Although an increased infiltration of the thymus, by subepithelial connective tissues and epithelial mucous cells, occurred in the juvenile and adult stages, there was no evidence of an advanced stage of thymic regression or involution in the adult Harpagifer. Thus, a suppressive influence of the low temperature environment, on the onset and degree of lymphoid organ development and thymic involution, was indicated in this species.

Acclimatization↗

Leukocyte proliferation mediated by protein kinase C in the marine teleost fish, Sciaenops ocellatus.

A major route of signal transduction in mammalian lymphocytes is the phosphatidyl inositol (PI) pathway. As previously demonstrated in the channel catfish, and confirmed in the present work with the red drum, modulators of the PI pathway such as phorbol ester and calcium ionophore acted synergistically to stimulate proliferation of teleost peripheral blood leukocytes (PBL). Red drum PBL also proliferated strongly in response to phorbol ester alone, at doses which were not mitogenic for catfish PBL. Cell depletion studies suggested that macrophage-derived cytokines probably played a role in supporting the mitogenic response to phorbol ester alone. Dose titration studies with a panel of kinase inhibitors suggested that mitogenic and synergistic doses of phorbol ester primarily targeted an enzyme activity similar to protein kinase C (PKC). However, in the same inhibitor studies, the target enzyme was insensitive to staurosporine, suggesting the involvement of an unusual form of PKC. Similarly, cell proliferation stimulated by phorbol ester was suppressed, but not eliminated by a calcium channel blocker Verapamil. Thus, while the synergistic action of phorbol ester and calcium ionophore appeared to be mediated by a PI pathway, these studies have suggested that PKC isoforms and membrane ion pumps unique to the lower vertebrates may participate in regulation of the cell cycle.

1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine↗

Effect of cupric chloride on oxidative metabolism in the freshwater teleost, Tilapia mossambica.

The freshwater teleost Tilapia mossambica was subjected to lethal (6.0 mg X liter-1 = LC50/48 hr) and sublethal (1.5 mg X liter-1 copper treatment for 1, 7, and 14 days. The whole animal oxygen consumption and the activity levels of succinate dehydrogenase and lactate dehydrogenase in liver and muscle were studied. The decrease in oxygen consumption and succinate dehydrogenase activity and significant increase in lactate dehydrogenase activity suggest that the stressed fish is meeting its energy requirements through anaerobic oxidation and these enzymes can be used as indicators in monitoring metal-induced toxicity in fish.

Animals↗

Methyl parathion (O-O-dimethyl O-4-nitrophenyl thiophosphate) effects on whole-body and tissue respiration in the teleost, Tilapia mossambica (Peters).

The respiratory parameters of a freshwater teleost, Tilapia mossambica Peters, were studied under sublethal intoxication of methyl parathion. The rate of oxygen consumption by whole fish and selected tissues decreased during a 48-hr time-course study. The activities of the respiratory enzymes succinate dehydrogenase, malate dehydrogenase, and cytochrome-c oxidase also decreased considerably under methyl parathion exposure in muscle, gill, liver, and brain tissues. These results suggest that methyl parathion has a profound effect on the oxidative metabolism of the fish which results in low ATP turnover, possibly due to its influence on the respiratory center of the brain.

Animals↗

Histopathological alterations in the liver of freshwater teleost Tilapia mossambica in response to cadmium toxicity.

The effects of lethal (50 ppm) and sublethal (5 ppm) concentrations of CdCl2 on the liver of the freshwater teleost Tilapia mossambica were studied by routine histological techniques. Engorged blood vessels, congestion, vacuolar degeneration of hepatocytes, necrosis of pancreatic cells, and fatty changes in the peripancreatic hepatocytes were the pathological alterations observed in liver.

Animals↗

The release of neuronal 5-HT from the intestine of a teleost fish, Platycephalus bassensis.

The superfused, isolated intestine of a teleost fish which lacks enterochromaffin cells spontaneously released 5-hydroxytryptamine (5-HT) and 5-hydroxyindoleacetic acid (5-HIAA), presumably from enteric neurons. The release of 5-HT, but not 5-HIAA, increased on transmural electrical stimulation. Addition of tetrodotoxin or omission of Ca2+ from the superfusate prevented the increase in 5-HT release on electrical stimulation. Fluoxetine added to the superfusate increased the amount of 5-HT released spontaneously but also prevented the increase in 5-HT release on stimulation. Pretreatment of fish with reserpine markedly reduced tissue levels of 5-HT and 5-HIAA and led to an almost complete loss of the spontaneous release of 5-HT and an elimination of the stimulated release of 5-HT.

Animals↗

Neurogenesis in tissue cultures of adult teleost spinal cord.

[3H]Thymidine autoradiography of explant cultures from the spinal cord of an adult teleost, Sternarchus albifrons, reveals the presence of thymidine-labeled cells with neuronal morphology. These cells have also been identified as neurons by positive staining with two monoclonal antibodies against neurofilaments. Thymidine labeling occurs in cultured neurons derived from both normal (histologically and functionally mature) and regenerating spinal cord of adult Sternarchus albifrons. These results provide evidence that some cells in spinal cord of adult Sternarchus retain the ability to incorporate thymidine and undergo neuronal differentiation in vitro.

Animals↗

Development of tectal neurons in the perciform teleost Haplochromis burtoni. A Golgi study.

The differentiation of the tectum mesencephali of Haplochromis burtoni (Teleostei, Cichlidae) was studied using a modified Golgi rapid impregnation. The analysis concentrated on the gradient of differentiation of four neuronal types, type I, IIIu, VI and XII, in 15-day-old larvae. The following developmental steps taken by these neuronal types are identified: (1) morphogenesis and growth are largely independent developmental events. Tectal neurons first develop their typical dendritic morphology. The tectal lamination, as indicated by the spatial relationships of the dendrites of tectal neurons, is acquired already in 15-day-old larvae. Subsequently the neurons grow to their adult size. Intersegments of dendrites elongate considerably. Dendritic and axonal reorganization and/or intersegmental growth may take place. (2) The teleost cell types I and VI show variable positions of their perikaryon in 15-day-old larvae, but not in adults. It is suggested that they translocate their perikaryon inside their stem dendrite, while their dendrites are already well developed.

Animals↗

Ontogeny of gonadotropin releasing hormone-containing neurons in the teleost brain.

We investigated changes in two gonadotropin releasing hormone (GnRH)-containing neuronal populations during juvenile development in the African teleost, Haplochromis burtoni. Juveniles were sampled at weekly intervals and GnRHir neurons were identified through immunocytochemistry (ICC), then counted and measured on computer-captured video images. Soma size of GnRH neurons in the preoptic area (POA), which regulate gonadotropin release from the pituitary, is socially modulated in adults. Here we show that in juveniles the soma size of these neurons increases as a linear function of body weight. Terminal nerve (TN) GnRHir neurons, in contrast, are not involved in pituitary regulation and their soma size is not socially modulated in adults. In juveniles, soma size of these neurons is a quadratic function of body size and the covariance of soma size and body size is much less than in the POA GnRHir neurons. In both populations, GnRHir neuronal number covaries with body size or age only in the earliest juvenile stages. Analysis of the development of these two distinct GnRHir neuronal populations provides insight into their functional differentiation in adults.

Aging↗

C-reactive protein and serum amyloid P component in the plaice (Pleuronectes platessa L.), a marine teleost, are homologous with their human counterparts.

C-reactive protein and serum amyloid P component were isolated from serum of the plaice (Pleuronectes platessa L.), a murine teleost. The isolation was based on their calcium-dependent binding affinity for pneumococcal C-polysaccharide and for agarose, respectively. These specificities are the same as those of human C-reactive protein and serum amyloid P component, respectively, and we have previously reported that the plaice molecules resemble human C-reactive protein and serum amyloid P component in their electron microscopic appearance. We describe here estimation of the molecular weights of plaice C-reactive protein and serum amyloid P component and their subunits, and analysis of their amino acid composition, glycosylation and partial amino-terminal amino acid sequences. The results establish that plaice C-reactive protein and serum amyloid P component are homologous with each other and with their human counterparts and indicate that there has been stable conservation of this protein family throughout vertebrate evolution.

Amino Acid Sequence↗