A diffuse,invaginating cone bipolar cell in primate retina

A bipolar cell type forming invaginating contacts with many cones was found by light and electron microscopy of Golgi preparations of the rhesus monkey retina. This diffuse, invaginating cone bipolar cell resembles, superficially, rod (“mop”) bipolars, and so may correspond to Polyak's “brush” bipolar. However, it differs from rod bipolars in that its dendrites are finer and they end in a single stratum containing cone pedicles in the outer plexiform layer (OPL). In the inner plexiform layer (IPL) its axon terminal is located sclerad (S₄) to those of rod bipolars (S₅), is thinner, and also more branched, and wider in span than rod bipolar axon terminals. Resectioning of Golgi-impregnated diffuse, invaginating cone bipolars to study their connections in the OPL shows that their dendrites invaginate as many as seven cone pedicles, and terminate as central elements at the ribbon synaptic complex. Thus, the primate retina has multiple (diffuse) and single (midget) cone-contacting bipolar cell pathways in both invaginating as well as flat varieties.     

Uniqueness of the S-cone pedicle in the human retina and consequences for color processing

The purpose of this study was to investigate more fully the shape and content of ribbons and synapses to second-order neurons in the short-wavelength cone (S-cone, blue cone) pedicle and to learn more concerning the uniqueness of the S-cone system in the primate retina. A piece of well-fixed peripheral human retina (10 mm, 35° nasal to the fovea) was serially thick sectioned in the tangential plane from the level of the outer segments to the tops of the cone pedicles. Then serial electron microscope (EM) sections were collected through the whole depth of the pedicle-occupying region into the neuropil of the outer plexiform layer (OPL). The resultant EM micrograph montages of a large field of cone pedicles were perused, and S-cone pedicles were identified. Serial micrographs of a single S-cone pedicle, picked out of the montages, were digitized and reconstructed by computer three-dimensional methods. The S-cone pedicle arose from a slightly oblique axon and projected 0.5-1 μm more vitread in the OPL than other cone pedicles. It was bilobed in shape, with synaptic invaginations and ribbons in both lobes. No cone-contacting telodendria projected from the S-cone pedicle itself, but a small number of neighboring cones sent telodendria to its surface to make small gap junctions. Neighboring rod spherules also made small gap junctions. Four robust bipolar cell dendrites, most likely from S-cone-specific bipolar cells, made synapses at ribbons and basal (distal) junctions. A small number of other bipolar cell dendrites made narrow-cleft basal junction only. The majority of lateral elements were thought to be from HII horizontal cells, and a minority from HI horizontal cells. We conclude that the S-cone pedicle has a unique morphology and connectivity to second-order neurons that makes it quite different from the other two longer wavelength cone systems, and we speculate on the consequences for color processing in the visual system in general. J. Comp. Neurol. 386:443-460, 1997. © 1997 Wiley-Liss, Inc.     

An ultrastructural study of interplexiform cell synapses in the human retina

Using serial sections and electron microscopy, we have found several morphological types of synapses within the outer plexiform layer (OPL) of the human retina. The most conspicuous of these is described in this paper. They have a unique morphology and form synapses with rod and cone bipolar cells in the OPL and onto bipolar and amacrine cell bodies in the inner nuclear layer (INL). Because they occur in processes that extend across the INL, we believe these synapses are made by interplexiform cells (IPCs). These same processes also contact cone pedicles with specialized cell junctions like those made between cones and flat bipolars. These junctions have densification of both cell membranes and widening of the extracellular cleft, but no accumulation of synaptic vesicles. Similar-appearing processes in the inner plexiform layer are thought to belong to IPCs but their contacts were less completely identified. Possible circuitry for these IPCs is described and the possibility that there are different classes of IPCs in the human retina is discussed. The OPL forms in the posterior retina during the tenth fetal week. Our observations suggest that different types of synapses including those of the IPCs are present in this layer from the time of its first appearance.     

Synaptic contacts between bipolar and photoreceptor cells in the retina of Callionymus lyra L

A combined light and electron microscopic study of Golgi-impregnated retinas of the marine teleost Callionymus lyra L. revealed mixed bipolar cells (M types) contacting rods and cones and pure cone bipolar cells (C types). Five types of mixed bipolar cells can be differentiated on the basis of their synaptic contacts. Two out of the five mixed bipolar cell types contact double cones, single cones, and rods (mixed, dark, pale, single [Mdps and midget-Mdps]). Their endbuds make narrow cleft junctions, with each type of photoreceptor, and in addition, two endbuds end centrally in the synaptic ribbon complexes of the dark and pale double-cone pedicles. Three types of mixed bipolar cells contact only double cones and rods. The endbuds of one type (mixed, dark, pale, ribbon [Mdpr]) end centrally in the synaptic ribbon complexes of the dark and pale double-cone pedicles as well as of the rod spherules. The endbuds of two types (Mdp and midget-Mdp) make wide cleft junctions in dark and pale double-cone pedicles and in rod spherules. All pure cone bipolar cell types contact cones exclusively with narrow cleft junctions. Four types are seen: a type that contacts predominantly pale double-cone pedicles but also a few dark double-cone pedicles (Cp), a type that is connected with dark and pale double-cone pedicles in about equal numbers (Cdp), a type that makes synaptic contacts with pale double-cone pedicles and single-cone pedicles (Cps), and a type that is connected with both types of double cones and to single-cone pedicles (Cdps). A resemblance between the ultrastructural features of mixed bipolar cell synapses in Callionymus and in Carassius auratus is noted.     

Connections of two types of flat cone bipolars in the rabbit retina

The synaptic connections of two types of cone bipolar cells in the rabbit retina were studied with the electron microscope after labeling in vitro with 4′,6-diamidino-2-phenylindole (DAPI), intracellular injection with Lucifer Yellow, and photooxidation (Mills and Massey [1992] J. Comp. Neurol. 321:133). Both types of bipolars belong to the flat variety, because they make basal junctions with a group of four to ten neighboring cone pedicles. One cell type has an axonal arborization that occupies strata 1 through 3 of the inner plexiform layer (IPL). At ribbon synaptic junctions, it is presynaptic to ganglion cell dendrites and to reciprocal dendrites belonging to narrow-field bistratified (AII) amacrine cells. In addition, it contacts and is contacted by other amacrine cell processes of unknown origin. The other cell type has an axonal arborization entirely confined to stratum 2 of the IPL; it is pre- or postsynaptic to a pleomorphic population of amacrine cell processes, and, in particular, it receives input from the lobular appendages of AII. Thus, these two bipolar types probably belong to the off-variety because they make basal junctions with cone photoreceptors and send their axon to sublamina α of the IPL, which is occupied by the dendrites of off-ganglion cells. They are also part of the rod pathway because they receive input from AII amacrine cells. © 1996 Wiley-Liss, Inc.     

Bipolar cells specific for blue cones in the macaque retina.

A distinct subpopulation of bipolar cells in macaque monkey retina was labeled with antisera that recognize glycine-extended cholecystokinin precursors. The labeled bipolar cells were found throughout the retina and had dendrites contacting a subpopulation of cone pedicles and axons ramifying in the fifth stratum of the inner plexiform layer. Several lines of evidence indicate that the labeled bipolar cells are a single type despite some variations in their morphology. First, the density of perikarya and their diameters varied continuously as a function of eccentricity. Second, the positions of perikarya within the inner nuclear layer and the level at which the axons branched in the inner plexiform layer were constant at all eccentricities. Bipolar cells with similar morphology have been described previously as "blue cone bipolar cells" (Mariani, 1984b), but there was no direct evidence that this was the case. In this study, we show by light microscopy that labeled bipolar cells have dendrites ending exclusively upon presumptive blue cones labeled by Procion black dye. All blue cones were contacted by labeled bipolar cells, and virtually all bipolar cells contacted blue cones, the only exceptions being in regions where blue cones had been lost. Approximately 20% more labeled bipolar cells than blue cones were found at every eccentricity; thus, connections between blue cones and labeled bipolar cells were not strictly one to one. The mean number of cones presynaptic to each bipolar cell was 1.2, and the mean number of bipolar cells postsynaptic to each cone was 1.8. By an electron microscopic study of labeled bipolar cell dendrites, we determined that they became central elements of ribbon synapses in blue cones. Some of their ribbon synapses were unusual: in one type, a single, large labeled dendrite was postsynaptic to two or more ribbons, while in the other type, ribbons had two or more central elements. The presence of these invaginating contacts and the axonal terminals in the proximal inner plexiform layer suggest that the labeled bipolar cells depolarize to short-wavelength stimuli and function to relay information from blue cones to the inner plexiform layer. There were also other, unlabeled bipolar cell dendrites that received inputs from blue cones at basal junctions and triad-associated flat contacts, which suggests that there are additional types of bipolar cells conveying information from short-wavelength cones in the primate retina.     

Ectopic retinal ON bipolar cell synapses in the OFF inner plexiform layer: Contacts with dopaminergic amacrine cells and melanopsin ganglion cells

A key principle of retinal organization is that distinct ON and OFF channels are relayed by separate populations of bipolar cells to different sublaminae of the inner plexiform layer (IPL). ON bipolar cell axons have been thought to synapse exclusively in the inner IPL (the ON sublamina) onto dendrites of ON‐type amacrine and ganglion cells. However, M1 melanopsin‐expressing ganglion cells and dopaminergic amacrine (DA) cells apparently violate this dogma. Both are driven by ON bipolar cells, but their dendrites stratify in the outermost IPL, within the OFF sublamina. Here, in the mouse retina, we show that some ON cone bipolar cells make ribbon synapses in the outermost OFF sublayer, where they costratify with and contact the dendrites of M1 and DA cells. Whole‐cell recording and dye filling in retinal slices indicate that type 6 ON cone bipolars provide some of this ectopic ON channel input. Imaging studies in dissociated bipolar cells show that these ectopic ribbon synapses are capable of vesicular release. There is thus an accessory ON sublayer in the outer IPL. J. Comp. Neurol. 517:226‐244, 2009. © 2009 Wiley‐Liss, Inc.     

Localization of kainate receptors at the cone pedicles of the primate retina.

In the macaque monkey retina cone pedicles, the output synapses of cone photoreceptors, contain between 20 and 45 ribbon synapses (triads), which are the release sites for glutamate, the cone transmitter. Several hundred postsynaptic dendrites contact individual cone pedicles, and we studied the glutamate receptors expressed and clustered at these contacts, particularly the kainate receptor subunits GluR5, GluR6/7, and KA2. Pre- and postembedding immunocytochemistry and electron microscopy were used to localize GluR5 and GluR6/7 to specific synaptic contacts at the cone pedicle base. The GluR5 subunit was aggregated at bipolar cell flat contacts. The GluR6/7 subunit was aggregated at bipolar cell flat contacts and at the desmosome-like junctions formed by horizontal cell processes underneath the cone pedicles. KA2 immunoreactivity was observed at the invaginating dendritic tips of ON-cone and rod bipolar cells, which we interpret as a cross-reactivity of the KA2 antiserum with some other, unknown protein of the monkey retina. Kainate receptors are preferentially expressed by OFF-cone bipolar cells and to a lesser extent by horizontal cells. We also performed double-labeling experiments with the ribbon-specific marker bassoon and with antibodies against GluR5 and GluR6/7 in order to define the position of the flat bipolar cell contacts with respect to the triads. There was a tendency of GluR6/7 clusters to represent triad-associated contacts, whereas GluR5 clusters represented non-triad-associated contacts. The GluR5 and GluR6/7 subunits were clustered at different bipolar cell contacts. We studied a possible cone-selective expression of the kainate receptor subunits by double labeling cone pedicles for the S-cone opsin and for the different receptor subunits. We observed a reduced expression of both GluR5 and GluR6/7 at the S-cone pedicles. The reduced expression of GluR6/7 was analyzed in more detail and it appears to be a consequence of a horizontal cell-specific expression: H1 horizontal cells express GluR6/7, whereas H2 horizontal cells, which preferentially innervate S-cones, show no expression of GluR6/7.     

Retinal structure in the smooth dogfish Mustelus canis: electron microscopy of serially sectioned bipolar cell synaptic terminals

Portions of axons of bipolar cells in the retina of the smooth dogfish Mustelus canis were sectioned serially and examined by electron microscopy. The studied axons generally could be related to a bipolar cell sub-type identified by light microscopy. Bipolar cell axons make ribbon synapses onto amacrine processes and ganglion cell dendrites, and onto ganglion cell perikarya. Bipolar cell ribbon synaptic complexes varied as to the number of post-synaptic processes (1–3) and the orientation of the ribbon with respect to the post-synaptic membrane. Amacrine processes made numerous conventional synapses onto bipolar cell axons, but reciprocal synapses between amacrine and bipolar cells constituted only 3–25% of all synapses observed. The number of ribbon synapses per unit area of bipolar cell axon membrane differed little among bipolar cell sub-classes. However, the density of amacrine cell conventional synapses was markedly lower for thin, horizontally-oriented bipolar cell axons than for axons of other bipolar cell types. Gap junctions were noted between bipolar cell axons of the same sub-type. They are structurally similar to gap junctions between horizontal cells in Mustelus retina and to those found elsewhere in the nervous system.     

Electron microscopic analysis of the rod pathway of the rat retina

Two immunocytochemical markers were used to label the rod pathway of the rat retina. Rod bipolar cells were stained with antibodies against protein kinase C and AII-amacrine cells with antibodies against parvalbumin. The synaptic circuitry of rod bipolars in the inner plexiform layer (IPL) was studied. Rod bipolar cells make approximately 15 ribbon synapses (dyads) in the IPL. Both postsynaptic members of the dyads are amacrine cells; one is usually the process of an AII-amacrine cell and the other one frequently provides a reciprocal synapse. No direct output from rod bipolar cells into ganglion cells was found. AII-amacrine cells make chemical output synapses with cone bipolar cells and ganglion cells in sublamina a of the IPL. They make gap junctions with cone bipolar cells and other AII-amacrine cells in sublamina b of the IPL. The rod pathway of the rat retina is practically identical to that of the cat and of the rabbit retina. It is very likely that this circuitry is a general feature of mammalian retinal organization. © Wiley-Liss, Inc.     

Development of cone photoreceptors and their synapses in the human and monkey fovea

During retinal development, ribbon synapse assembly in the photoreceptors is a crucial step involving numerous molecules. While the developmental sequence of plexiform layers in human retina has been characterized, the molecular steps of synaptogenesis remain largely unknown. In the present study, we focused on the central rod-free region of primate retina, the fovea, to specifically investigate the development of cone photoreceptor ribbon synapses. Immunocytochemistry and electron microscopy were utilized to track the expression of photoreceptor transduction proteins and ribbon and synaptic markers in fetal human and Macaca retina. Although the inner plexiform layer appears earlier than the outer plexiform layer, synaptic proteins, and ribbons are first reliably recognized in cone pedicles. Markers first appear at fetal week 9. Both short (S) and medium/long (M/L) wavelength-selective cones express synaptic markers in the same temporal sequence; this is independent of opsin expression which takes place in S cones a month before M/L cones. The majority of ribbon markers, presynaptic vesicular release and postsynaptic neurotransduction-related machinery is present in both plexiform layers by fetal week 13. By contrast, two crucial components for cone to bipolar cell glutamatergic transmission, the metabotropic glutamate receptor 6 and voltage-dependent calcium channel α1.4, are not detected until fetal week 22 when bipolar cell invagination is present in the cone pedicle. These results suggest an intrinsically programmed but nonsynchronous expression of molecules in cone synaptic development. Moreover, functional ribbon synapses and active neurotransmission at foveal cone pedicles are possibly present as early as mid-gestation in human retina.     

Horizontal cells and cone photoreceptors in human retina: A Golgi-electron microscopic study of spectral connectivity

Connections of the three human horizontal cell (HC) types with overlying cone pedicles have been studied via electron microscopy (EM). Because blue cones (B-cones) can be recognized on distinctive morphological criteria, we could determine their presence by light microscopy (LM) in the mosaic overlying HC dendritic trees. Then we could confirm the presence or absence of dendritic contacts to B-cone pedicles by examining EM serial sections and making reconstructions of examples of the three HC types. Three HI cells have been reconstructed. Their dendritic terminals ended as lateral elements of ribbon synapses in green and red cone pedicles (G- and R-cones) primarily. B-cones pedicles in HI cell dendritic fields received no more than one or two contacts. Six reconstructed HII cells were found to contact all the pedicles within their dendritic field. However, their dendritic reached especially for B-cones pedicles and innervated them with disproportionately large number of terminals compared with G- and R-cines. HII axons appeared to contact B-cones exclusively. The four reconstructed HIII cells were found to avoid completely B-cones in their dendritic fields. Data have been collected on synaptic ribbon lengths at HII and HIII lateral elements in the B-cone as compared with G- and R-cone pedicles. HIII dendritic terminals end almost exclusively at the smaller ribbons and HI dendrites at the large ribbons. The number of dendritic terminals provided by the HCs to G-and R-cone pedicles as compared B-cone pedicles has been more accurately quantitated than was possible in the LM analysis (accompanying paper). New findings on the morphology of B-cone pedicles in peripheral retina have revealed that 1) B-cone pedicles end further vitread in the outer plexiform layer (OPL) than other cone pedicles, thereby forming a sublayer of the OPL neuropil, here named OPLb, in comparison to OPLa, where the G- and R-cone pedicles end; 2) B-cone pedicles have very few telodentrial connections; and 3) in peripheral retina (probably beyond 8 mm from the fovea to the ora serrata), they are bi- or trilobed, with each lobe containing separate synaptic invaginations. The vitread position and unique morphology of B-cone pedicles appear to relate directly to the unique morphology and unusual connectivity patterns of both their B-cone-specific bipolar and B-cone-related horizontal cell, the HII cell. Taken together with the LM and quantitative data of our two preceding papers, these findings provide morphological evidence that a chromatically selective weighting pattern in HCs and could play a role in color-opponent surround formation in the human retina. © 1994 Wiley-Liss, Inc.     

Synapses from bipolar cells onto dopaminergic amacrine cells in cat and rabbit retinas

Dopaminergic amacrine cells in the vertebrate retina have long been characterized as 'interamacrine' as they were only found to be pre- and postsynaptic to other amacrine cells. Immunohistochemistry with antibodies directed against tyrosine hydroxylase (TH) revealed synapses from bipolar cell axon terminals to TH-containing neuronal processes at ribbon synapses in the rhesus monkey retina. This finding challenged the notion of the dopaminergic amacrine cell phenotype as 'interamacrine'. In order to determine if the finding of synapses from bipolar cells to dopaminergic amacrine cells could be generalized to other species, we studied the synaptic organization of dopaminergic amacrine cells in the retinas of cats and rabbits with electron microscopy of TH immunoreactivity. In both species, TH-immunoreactive processes were found to be postsynaptic to bipolar axon terminals at ribbon synapses demonstrating that the original finding in the primate may be a significant feature in the retinas of many other vertebrates as well.     

The rod pathway in the rabbit retina: a depolarizing bipolar and amacrine cell

Anatomical and electrophysiological techniques were combined to study the morphology, synaptic connections, and response properties of two neurons in the rod pathway of the rabbit retina: the rod bipolar cell and the narrow-field, bistratified (NFB) amacrine cell. Rod bipolars receive synaptic input from rod cells in the outer plexiform layer (OPL), where their dendrites end as central elements in the invaginating synapse of rod spherules. Their main synaptic output in the inner plexiform layer (IPL) is onto NFB amacrine cells and at least one other type of amacrine, which in turn feeds a reciprocal synapse back onto the bipolar endings. Rod bipolars, or a variety of them, respond to diffuse, white light stimulation with a transient-sustained depolarization dominated by rods; with high-intensity flashes, they generate a secondary depolarization at off, which is homologous to the rod aftereffect of horizontal cells, although opposite in polarity. NFB amacrine cells receive synaptic input from rod bipolars, cone bipolars, and other types of amacrine cells; they are presynaptic to ganglion cell dendrites and communicate via gap junctions with other processes, whose parent neuron has not yet been identified. They respond to light with a triphasic potential, characterized by a depolarizing transient at on, followed by a sustained plateau phase, and finally by a hyperpolarizing transient at off. Threshold of their responses is the same as in the depolarizing rod bipolars and saturation is reached with nearly the same stimulus intensity in both neurons. Furthermore, NFB amacrine cells exhibit a depolarizing rod aftereffect at the termination of high-intensity flashes. Thus, this amacrine cell type is inserted in series along the rod pathway in the rabbit retina and modulates the transfer of scotopic signals from rod bipolars to ganglion cells.     

Morphological Classification of Bipolar Cells of the Primate Retina

Bipolar cells were studied in Golgi - Colonnier-stained whole mounts of macaque monkey retinae. A piece of retina, at 6 - 7 mm eccentricity, was particularly well stained for the analysis of the different bipolar cell types. Many midget bipolar cells were encountered and the dichotomy into flat and invaginating midget bipolars was confirmed. Six types of diffuse cone bipolar cell are distinguished. They differ in their dendritic branching pattern, in the number of cones contacted-usually between five and ten-and in the shape and branching level of their axons. The size, shape and stratification of the axons were found to be the most reliable distinguishing features for classifying diffuse cone bipolar cells. The stratification of the axons in the inner plexiform layer (IPL), whether closer to the amacrine or ganglion cells, was used to name diffuse cone bipolar cells in the order DB1 to DB6. Blue cone and rod bipolar cells were confirmed as distinct types. Axon terminals of diffuse cone bipolars were found to tile their sublamina of the IPL in a territorial manner. From this the density of each type could be estimated, and it is shown that a single cone is likely to be in contact with as many as 15 individual diffuse bipolar cells, as well as two midget bipolars. The diffuse bipolar cells observed contact all the cone pedicles in their dendritic fields. It is, therefore, unlikely that they carry a chromatic signal into the inner retina. The presence of many midget bipolar cells, which make contact with one cone pedicle only, suggests that midget bipolars provide chromatic input to ganglion cells in peripheral retina as well as in the fovea. The data show that the P- and M-cell pathways of the primate visual system are, to a significant extent, already anatomically discrete at the photoreceptor synapse.     

Accumulation of (3H)glycine by cone bipolar neurons in the cat retina

Cone bipolar neurons in the cat retina were studied in serial sections prepared as electron microscope autoradiograms following intravitreal injection of (3H)glycine. The goal was to learn whether the cone bipolar types that accumulate glycine correspond to the types thought on other grounds to be inhibitory. About half of the cone bipolars in a given patch of retina showed specific accumulation of silver grains. The specificity of accumulation was similar to that shown by glycine-accumulating amacrines. All of the cone bipolars arborizing in sublamina b accumulated glycine but none of the cone bipolars arborizing in sublamina a did so. The types of cone bipolars accumulating glycine did not match the types thought to be inhibitory. Cone bipolar types CBb1 and CBb2 both form gap junctions with the glycine-accumulating AII amacrine, thus raising the possibility that glycine might accumulate in these cone bipolars by diffusion from the AII cell or vice versa. Thus it is logically impossible to tell which of these three cells contains a high-affinity uptake mechanism for glycine and consequently which of the three might actually use glycine as a neurotransmitter.     

The connections between bipolar cells and photoreceptors in the retina of the domestic cat

An invaginating bipolar cell that has dendritic terminals forming the central elements of the cone triads is described for the retina of the cat. This type of bipolar contacts a minimum of four or five and a maximum of nine or ten cones. There is no evidence for a bipolar cell which contacts only one cone, i.e., a midget bipolar cell as in simians. There are flat bipolar cells that make superficial contacts with the bases of the cone pedicles and are postsynaptic to between 8 and 14 cones. One cone can be in contact with both an invaginating and a flat bipolar cell. There is evidence suggestive of two kinds of flat bipolars. A comparison is made between the bipolar connections in simians and the cat. The comparison is summarized in figures 29 and 30.     

Localization of glycine-containing neurons in the Macaca monkey retina

Autoradiography following 3H-glycine (Gly) uptake and immunocytochemistry with a Gly-specific antiserum were used to identify neurons in Macaca monkey retina that contain a high level of this neurotransmitter. High-affinity uptake of Gly was shown to be sodium dependent whereas release of both endogenous and accumulated Gly was calcium dependent. Neurons labeling for Gly included 40-46% of the amacrine cells and nearly 40% of the bipolars. Synaptic labeling was seen throughout the inner plexiform layer (IPL) but with a preferential distribution in the inner half. Bands of labeled puncta occurred in S2, S4, and S5. Both light and postembedding electron microscopic (EM) immunocytochemistry identified different types of amacrine and bipolar cell bodies and their synaptic terminals. The most heavily labeled Gly+ cell bodies typically were amacrine cells having a single, thick, basal dendrite extending deep into the IPL and, at the EM level, electron-dense cytoplasm and prominent nuclear infoldings. This cell type may be homologous with the Gly2 cell in human retina (Marc and Liu: J. Comp. Neurol. 232:241-260, '85) and the AII/Gly2 of cat retina (Famiglietti and Kolb: Brain Res. 84:293-300, '75; Pourcho and Goebel: J. Comp. Neurol. 233:473-480, '85a). Gly+ amacrines synapse most frequently onto Gly- amacrines and both Gly- and Gly+ bipolars. Gly+ bipolar cells appeared to be cone bipolars because their labeled dendrites could be traced only to cone pedicles. The pattern of these labeled dendritic trees indicated that both diffuse and midget types of biopolars were Gly+. The EM distribution of labeled synapses showed Gly+ amacrine synapses throughout the IPL, but these composed only 11-23% of the amacrine population. Most of the Gly+ bipolar terminals were in the inner IPL, where 70% of all bipolar terminals were labeled. These findings are consistent with previous data from cats and humans and suggest that both amacrine and bipolar cells contribute to glycine-mediated neurotransmission in the monkey retina.     

Goalpha labels ON bipolar cells in the tiger salamander retina

By using double-label immunocytochemistry and confocal microscopy, we studied rod and cone synaptic contacts, photoreceptor-bipolar cell convergence, and patterns of axon terminal ramification of ON bipolar cells in the tiger salamander retina. An antibody to recoverin, a calcium-binding protein found in photoreceptors and other retinal neurons in various vertebrates, differentially labeled rods and cones by lightly staining rod cell bodies, axons, and synaptic pedicles and heavily staining cone cell bodies and pedicles. An antibody to G(oalpha) labeled most ON bipolar cells, with axon terminals ramified mainly in strata 6-9 and a minor band in stratum 3 of the inner plexiform layer (IPL). Stratum 10 of the IPL was G(oalpha) negative, and previous studies showed that axon terminals of rod-dominated ON bipolar cells are monostratified in that stratum. The axonal morphology of G(oalpha)-positive cells resembled that of the cone-dominated (DBC(C)) or mixed rod and cone ON (DBC(M)) bipolar cells. The G(oalpha)-positive dendritic processes made close contact with all cone pedicles and superficial contact with some rod pedicles, consistent with the idea that G(oalpha) subunits are present in DBC(C)s and DBC(M)s. The size and density of these cells were analyzed, and their spatial distributions were determined. To our knowledge, this is the first study to characterize photoreceptor inputs and axon terminal morphology of a population of ON bipolar cell with the use of a G(oalpha) antibody as an immunomarker in the salamander retina.