Intracellular injections of lucifer yellow into lightly fixed mitral cells reveal neuronal dye-coupling in the developing rat olfactory bulb.

We report that intracellular injections of Lucifer Yellow into lightly fixed mitral cells revealed dye-coupling between mitral cells and between mitral and granule cells in the form of discrete, radially oriented cell clusters. Dye-coupling was observed in animals as early as postnatal day 10 (P10) and at least until P30. In P10 rats, a mean of 2.5 dye-coupled mitral cells and 27 granule cells were observed per column. Mean column depth and width were 169 microns and 86 microns respectively. Most of the dye-filled granule cells were found within 150 microns of the mitral cell layer. No significant changes were found at P20. By P30, the mean number of granule cells per column increased to 42 and the addition of granule cells occurred in areas proximal to the mitral cell layer. Immunocytochemical results indicate that the developing bulb contains a large concentration of the gap junction protein Connexin 43 (Cx43). Cx43-like immunoreactivity was found at all ages examined, with the most intense staining in the nerve and glomerular layers. Less intense Cx43-like immunoreactivity was found in both the mitral and granule cell layers, with Cx43-like immunoreactive puncta observed between and around cell body profiles. Freeze-fracture analysis revealed the presence of gap junction-like plaques on mitral cells, further suggesting that the dye-coupling occurred across interneuronal gap junctions. Neuronal coupling during development could provide an inter-cellular pathway for the passage of relevant developmental signals which could influence the formation and/or strengthening of synaptic contacts. The coupling could also be involved in the synchronization of neuronal activity, which may be important for olfactory coding.

Olfactory bulb granule cell aggregates: morphological evidence for interperikaryal electrotonic coupling via gap junctions.

Anaxonic interneurons of the granule cell type in the mammalian main olfactory bulb (MOB) are characterized by prominent membrane specializations, which include reciprocal, interdendritic chemical and electrical synapses; however, the latter are thought to be restricted to the external plexiform layer (EPL) and connect granule-mitral- and granule-tufted-cell dendrites (Landis et al., 1974). The present study focuses on interperikaryal membrane specializations between tangentially oriented aggregates of granule microneurons in the lamina granularis interna (IGL). Both infraprimate (Rattus norvegicus, Gerbillus perpallidus) and primate species (Callithrix jacchus) were studied using the following methods: (1) transmission electron microscopy (TEM), (2) freeze-fracture analysis, (3) light and TEM immunohistochemistry using affinity-purified antibodies directed against the connexin-32 or connexin-43 carboxy tail fragment of the gap-junction protein (GJP), and (4) intracellular Lucifer yellow injections in fixed tissue (LYF technique). Freeze-fracture replicas of the MOB-IGL showed that adjacent granule cell perikarya have numerous particle aggregates on the cytoplasmic membrane; in terms of their structure and arrangement, such particles are characteristic of gap junctions. The existence of junctional membranes was substantiated by application of antibodies against GJP demonstrating punctate immunoreactivity, frequently confined to the interperikaryal plasmalemmae of granule cells in the IGL and their dendritic processes in the EPL. Upon TEM analysis, GJP-like immunoreactivity was additionally found in membranous organelles, including Golgi apparati and associated vesicular components. In order to test the permeability of identified membrane specializations, the LYF technique was used, which resulted in bright fluorescence of the perikaryal and dendritic components of the transsomatically injected neuron and staining of neighboring neurons with similar morphology. These findings imply that small molecules can diffuse across the interperikaryal membrane specializations. The existence of gap junctions between granule cell perikarya suggests that there is a significant, low-resistance electrical transmission between aggregated granule cells. This coupling might permit synchronization of neural discharge among small aggregates of these neurons. Gap junctions between granule cells may also serve signaling functions associated with the protracted period of granule cell development.

Chemoanatomical organization of the noradrenergic input from locus coeruleus to the olfactory bulb of the adult rat.

The locus coeruleus contains noradrenergic neurons which project widely throughout the CNS. A major target of locus coeruleus projections in the rat is the olfactory bulb (Shipley et al.: Brain Res. 329:294-299, '85) but the organization of the projections within the bulb has not been systematically examined. In this study, the laminar distribution and densities of locus coeruleus-noradrenergic fibers in the main and accessory olfactory bulbs were determined with anterograde tracing and immunocytochemical techniques. Following iontophoretic injections of 1% wheat germ agglutinin-horseradish peroxidase into the locus coeruleus, the densest anterograde label in the accessory olfactory bulb was observed in the external plexiform layer, granule cell layer, and especially in the internal part of the mitral cell layer. Virtually no label was observed in the glomerular layer. In the main olfactory bulb, labelled axons were observed in the granule cell layer, in the internal and external plexiform layers, occasionally in the mitral cell layer, and least often in the glomerular layer. Noradrenergic fibers in the olfactory bulb were identified by using immunocytochemistry with an antibody to dopamine-beta-hydroxylase. Laminar patterns and densities of noradrenergic innervation were determined with quantitative image analysis. In the accessory olfactory bulb, the densest innervation was in the innermost portion of the mitral cell layer followed by the granule cell layer, the superficial part of the mitral cell layer, and the external plexiform layer. The density of fibers in the glomerular layer was least. The laminar pattern of noradrenergic fiber distribution in the main olfactory bulb was similar to that in accessory olfactory bulb. The present studies demonstrate that locus coeruleus-noradrenergic fibers terminate preferentially in the internal plexiform, granule cell, and external plexiform layers. This suggests that the major influence of the locus coeruleus input to both the main and accessory the olfactory bulbs is on the predominant neuronal element in those layers, the granule cells. Additional studies are needed to resolve how this input influences specific olfactory bulb circuits.

Persistence of the pars externa system of the anterior olfactory nucleus in a microsmatic primate, Callithrix jacchus.

The pars externa (PE) system of the anterior olfactory nucleus (AON) in a primate, Callithrix jacchus, was defined by its architecture and by its connection patterns with the main olfactory bulb (MOB) as revealed by tracing techniques. Focal, unilateral injections of wheat germ agglutinin-conjugated horseradish peroxidase into the MOB yielded ipsilaterally labelled afferent neurons in all subdivisions of the AON, with the exception of a clearly circumscribed area in the ventrolateral retrobulbar field of the basocaudal frontal lobe; in the contralateral hemisphere, this same area contained intensely stained neurons forming a horizontal flat plate of small neurons. This unique commissural connection pattern parallels the organization of the PE to MOB connection in sub-primates (Schoenfeld and Macrides, 1984, J. Comp. Neurol., 227: 121-135). Thus, despite earlier controversy (Crosby and Humphrey, 1939, J. Comp. Neurol., 71: 121-213), there appears to be a PE system in a microsmatic primate whose organization is quite similar to that in sub-primates.

Interbulbar axonal collateralization and morphology of anterior olfactory nucleus neurons in the rat.

The organizational patterns of the bilateral projections of the anterior olfactory nucleus (AON) to the main olfactory bulb (MOB) were defined in the rat with Golgi staining, HRP tracing-methods and fluorescent dyes. Three issues were addressed: (1) description of the morphology of the AON-neurons projecting to the MOB, (2) quantitative analysis of the bilateral pathways arising in different AON subdivisions and (3) ultrastructural identification of AON to MOB channels. The cytoarchitectural features of the AON as recognized in Golgi preparations were correlated with its neural architecture as revealed by retrograde HRP-tracing from the MOB. The following cell types were determined: (1) pyramidal like neurons typified by a lack of basal dendrites and a sparse covering with long spines (pars externa), (2) fusiform shaped cells with bipolar dendritic arborisations (pars medialis) and (3) densely spined fusiform, pyramidal, and polygonal neurons (pars ventroposterior, lateralis and dorsalis) with a tendency of radial orientation of their apical dendrites. In addition, in the more caudal parts of the pars ventroposterior there were neurons with tertiary dendritic processes oriented nearly parallel to the molecular layer. Quantitative analysis of AON neurons projecting to the MOB showed that the pars externa neurons project exclusively to the contralateral MOB while pars medialis neurons project almost exclusively to the ipsilateral MOB. All subdivisions of the AON which establish specific termination patterns within the MOB, participated in about equal portion in the ipsilateral projections to the MOB. The highest proportion of the bilaterally projecting neurons were found in the dorsal subdivision, followed by the lateral and ventroposterior subdivisions. The postsynaptic targets of the AON to MOB channel are the spinous processes and varicosities of the proximal and distal-most dendrites of granule cells. The boutons derived from AON projection neurons contained clear spherical vesicles and established exclusively asymmetric synaptic junctions.