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PubMed1978

[Relationship between the environment and pyramidal neuron differentiation in the hippocampus (CA 1) of the rat. Differentiation of apical lateral and basal dendrites].

A total of 60 newborn Wistar-rats was divided into three groups, each of which was exposed to a different environmental situation. The first group was reared in complete darkness while the second one was subjected to permanent noise. The third group (controls) was reared under normal laboratory conditions. The animals of all three groups were sacrificed on postnatal day 15 and prepared according to the Golgi-Kopsch technique. Apical oblique dendrites and basal dendrites of hippocampal pyramidal cells (CA 1 region) were ranked in a centrifugal ordering system for measurements of dendritic length and for spine counts. In the successive dendritic orders as well as in the dendritic field (all branches of a dendrite arising from the cell body or main apical shaft) no statistically significant differences between the groups were found with regard to dendritic length. The spine counts, however, revealed significant changes. In the dark reared group, the number of spines on oblique dendrites as well as on basal dendrites is significantly decreased in comparison with the controls. On the contrary, animals subjected to permanent noise exhibit significantly more spines on oblique and basal dendrites when compared with the controls (mean number of spines in the apical dendritic field: controls 30.1 +/- 26.9, dark reared animals 17l1 +/- 15.4 (-43.2%), animals subjected to noise 36.4 +/- 31.4 (+ 20.9%); basal dendritic field: controls 82.2 +/- 70.1, dark reared animals 47.3 +/- 35.1 (-42.5%), animals exposed to noise 114,1 +/- 94.6 (+ 38.8%)). These results confirm previous studies on the number of spines along the main apical shaft of CA 1 pyramidal cells (Frotscher et al. 1975) and on the number of synapses in the stratum radiatum of CA 1 (Frotscher et al. 1977) in rats reared under identical experimental conditions. On the basis of these results it seems to be obvious that synaptogenesis in the hippocampus is influenced by the environmental conditions used though this region is not directly involved in the optic or in the acoustic pathway.

Acoustic Stimulation↗

PubMed1994

TTX-sensitive dendritic sodium channels underlie oscillatory discharge in a vertebrate sensory neuron.

Immunocytochemical and electrophysiological techniques were used to localize TTX-sensitive sodium channels (NaChs) over the soma-dendritic axis of basilar and nonbasilar pyramidal cells of the electrosensory lateral line lobe (ELL) of weakly electric fish (Apteronotus leptorhynchus). Dense NaCh-like immunolabel was detected on the membranes of basilar and nonbasilar pyramidal cell somata. Punctate regions of immunolabel (approximately 15 microns) were separated by nonlabeled expanses of membrane over the entire extent of basal dendrites. Similar punctate immunolabel was observed over the apical dendrites, and frequently on membranes of afferent parallel fiber boutons in the distal apical dendritic region. Intracellular recordings from pyramidal cell somata or proximal apical dendrites (75-200 microns) were obtained using an in vitro ELL slice preparation. TTX-sensitive potentials were identified by focal pressure ejection of TTX. Somatic recordings demonstrated both TTX-sensitive fast spike discharge and a slow prepotential; similar but lower amplitude potentials were recorded in apical dendrites. Dendritic spikes were composed of at least two active components triggered by a fast prepotential (FPP) generated by the somatic spike. TTX-sensitive spikes propagated in a retrograde fashion over at least the proximal 200 microns of the apical dendrites, as determined by the conduction of an antidromic population spike and focal TTX ejections. Somatic spikes were followed by a depolarizing afterpotential (DAP) that was similar in duration and refractory period to that of proximal dendritic spikes. During repetitive spike discharge, the DAP could increase in amplitude and attain somatic spike threshold, generating a high-frequency spike doublet and a subsequent hyperpolarization that terminated spike discharge. Repetition of this process gave rise to an oscillatory burst discharge (2-6 spikes/burst) with a frequency of 40-80 Hz. Both the DAP and oscillatory discharge were selectively blocked by TTX ejections restricted to the proximal apical dendritic region. The present study demonstrates an immunolocalization of NaChs over somatic and dendritic membranes of a vertebrate sensory neuron that correlates with the distribution of TTX-sensitive potentials. The interaction of somatic and dendritic action potentials is further shown to underlie an oscillatory discharge believed to be important in electrosensory processing.

Animals↗

PubMed1993

Basal versus apical dendritic long-term potentiation of commissural afferents to hippocampal CA1: a current-source density study.

Current-source density analysis was used to estimate the magnitude of the synaptic excitation at the basal and apical dendritic synapses of CA1 following commissural stimulation in the urethane-anesthetized rat, before and after a theta-frequency patterned primed burst tetanus. Stimulation of the contralateral CA3 or the contralateral CA1 stratum oriens excited both the basal and apical dendrites in CA1 about equally. However, primed burst tetanization of the contralateral CA3 or CA1 stratum oriens resulted in significant long-term potentiation (LTP) only at the basal dendrites and not at the apical dendrites. Stimulation of the contralateral CA1 stratum radiatum excited the apical dendrites more than the basal dendrites of CA1, but tetanization of this contralateral site gave little change in the apical or basal dendritic excitation. Tetanization of the contralateral CA1 stratum radiatum after an intraventricular administration of bicuculline, a GABAA antagonist, however, resulted in significant LTP at both the apical and basal dendrites. It was concluded that, in the intact hippocampus in vivo, the threshold for LTP at the commissural apical dendritic synapse was high in comparison to that at the basal dendritic synapse and this high threshold may be partly caused by inhibitory interneurons that predominantly synapsed on the apical dendrites. Thus, the basal and apical dendrites of the CA1 pyramidal cells are not equal in their propensity for long-term plasticity.

Animals↗

PubMed2006

Principles of self-assembly of helical pores from dendritic dipeptides.

The self-assembly of the dendritic dipeptides (4-3,4-3,5)nG2-CH2-Boc-L-Tyr-L-Ala-OMe and their achiral dendritic alcohol (4-3,4-3,5)nG2-CH2OH precursors, both with n = 1-16, where n represents the number of methylenic units in the alkyl groups of the dendron, are reported. All chiral dendritic dipeptides and achiral dendritic alcohols self-assemble into helical porous columns that are stable in both solution and solid state. The pore diameter (D(pore)) of the columns self-assembled from dendritic dipeptides is approximately 10 A larger than that of structures assembled from dendritic alcohols. The increase of the D(pore) at the transition from dendritic alcohol to dendritic dipeptide is accompanied by a decreased solid angle of the building block. This trend is in agreement with previous pore size-solid angle dependences observed with different protective groups of the dipeptide and primary structures of the dendron. However, within the series of dendritic alcohols and dendritic dipeptides with various n, the D(pore) increases when the solid angle increases. The results of these investigations together with those of previous studies on the role of dipeptide stereochemistry and protective groups on this self-assembly process provide the molecular principles required to program the construction of supramolecular helical pores with diameter controlled at the A level from a single dendritic dipeptide architecture. These principles are expected to be valid for libraries of dendritic dipeptides based on dendrons and dipeptides with various primary structures.

Circular Dichroism↗

PubMed1992

Simulation of the Effect of Synapses: the Significance of the Dendritic Diameter in Impulse Propagation.

The effectiveness of synapses at various sites of the dendritic tree was studied using a segmental cable model with a program developed by Hines (Int. J. Biomed. Comput., 24, 55 - 68, 1989). The model rendered possible a high-fidelity simulation of the dendritic geometry of a frog motoneuron described in the accompanying paper (Birinyi et al., Eur. J. Neurosci., 1003 - 1012, 1992). The model was used in the passive membrane mode and the synaptic activity was simulated with current injections into large and small diameter dendrites at proximal and distal locations. Synaptic efficiency was defined by the charge transfer ratio expressed as the proportion of the injected current which appeared at the soma. The charge transfer ratio was determined with uniform and non-uniform distribution of specific membrane resistance over the soma - dendrite surface while the diameter of selected dendrite segments changed. The best charge transfer ratio was found with the largest dendrite membrane resistance, and the maximum efficiency of synaptic activity appeared at the original size of the dendrite segment stimulated. The amount of current that flowed in the proximal and distal directions from the segment stimulated depended on the diameter of that segment. The increase in diameter of proximal dendrites increased synaptic efficiency on distal dendrites, whereas the reverse caused a decline in synaptic efficiency on proximal dendrites. In addition to the diameter of dendrites, the arborization pattern also played a significant role in this mechanism. It is concluded that the cellulipetal increase in dendrite diameter greatly increases synaptic efficiency.

Journal Article↗

PubMed1995

Regenerative properties of pyramidal cell dendrites in area CA1 of the rat hippocampus.

1. Intracellular recordings were obtained from 184 distal apical dendrites and twenty-six somata of CA1 pyramidal neurones in the rat hippocampal slice preparation. In the presence of 3.25 mM K+ 200 ms suprathreshold current pulses evoked three different types of firing patterns in the apical dendrites, all of which were distinct from regular somatic firing. Fast tetrodotoxin (TTX)-sensitive spiking was evoked in 38.8% of the dendrites. Compound spiking, consisting of an initial fast spike followed by one or more secondary slow spikes of variable amplitude and duration, was seen in 44.1% of dendrites. 'Classical' burst firing, resembling intrinsic somatic bursts, was evoked in 17.1% of the dendrites. 2. In fast spiking dendrites, the spikes evoked by long depolarizing pulses were rarely overshooting, showed prominent accommodation and declined progressively to about one-third of the initial amplitude. The amplitude of single dendritic fast spikes (50.6 +/- 1.5 mV; mean +/- S.E.M.) was smaller than that of somatic spikes (82.2 +/- 1.9 mV) and their rate of rise (81.3 +/- 4.3 V s-1) was markedly slower than that of somatic spikes (291.5 +/- 17.8 V s-1). However, the thresholds were not significantly different (dendrites, -49.8 +/- 0.8 mV; somata, -50.8 +/- 1.3 mV). These results indicate that fast spikes in the distal parts of apical dendrites are generated by a local regenerative Na+ current. 3. 4-Aminopyridine (4-AP, 0.1-0.5 mM) caused a dose-dependent slowing of the repolarization of the fast spikes, while tetraethylammonium (TEA, 2 mM) and Co2+ (2 mM) induced a slowing of the late phase of the repolarization. These results indicate that the transient outward K+ current, IA, and the Ca(2+)-activated K+ current, IC, are involved in the repolarization of dendritic Na(+)-dependent spikes. 4. Compound spiking was completely blocked by TTX (0.5-1 microM). The secondary slow spikes within the complex were blocked by Co2+ (2 mM), nifedipine (10 microM) and high concentrations (> 50 microM) of verapamil, while Ni2+ (100-300 microM) had no effect. Thus, compound spiking consists of an initial Na(+)-dependent spike followed by one or more slow Ca(2+)-dependent spikes mediated by L-type Ca2+ channels located in the apical dendrites. 5. In fast spiking dendrites, 4-AP (0.5-2.5 mM) changed the firing pattern from regular fast spiking to compound spiking. In the presence of 4-AP (0.1-0.5 mM), the single fast spike evoked by a short (20 ms), threshold current pulse, was followed by secondary slow spikes of variable amplitude and duration.(ABSTRACT TRUNCATED AT 400 WORDS)

4-Aminopyridine↗

PubMed2004

Dynamic regulation of spine-dendrite coupling in cultured hippocampal neurons.

We investigated the role of dendritic spine morphology in spine-dendrite calcium communication using novel experimental and theoretical approaches. A transient rise in [Ca2+]i was produced in individual spine heads of Fluo-4-loaded cultured hippocampal neurons by flash photolysis of caged calcium. Following flash photolysis in the spine head, a delayed [Ca2+]i transient was detected in the parent dendrites of only short, but not long, spines. Delayed elevated fluorescence in the dendrite of the short spines was also seen with a membrane-bound fluorophore and fluorescence recovery from bleaching of a calcium-bound fluorophore had a much slower kinetics, indicating that the dendritic fluorescence change reflects a genuine diffusion of free [Ca2+]i from the spine head to the parent dendrite. Calcium diffusion between spine head and the parent dendrite was regulated by calcium stores as well as by a Na-Ca exchanger. Spine length varied with the recent history of the [Ca2+]i variations in the spine, such that small numbers of calcium transients resulted in elongation of spines whereas large numbers of calcium transients caused shrinkage of the spines. Consequently, spine elongation resulted in a complete isolation of the spine from the dendrite, while shrinkage caused an enhanced coupling with the parent dendrite. These studies highlight a dynamically regulated coupling between a dendritic spine head and its parent dendrite.

Animals↗

PubMed1998

Theta oscillations in somata and dendrites of hippocampal pyramidal cells in vivo: activity-dependent phase-precession of action potentials.

Theta frequency field oscillation reflects synchronized synaptic potentials that entrain the discharge of neuronal populations within the approximately 100-200 ms range. The cellular-synaptic generation of theta activity in the hippocampus was investigated by intracellular recordings from the somata and dendrites of CA1 pyramidal cells in urethane-anesthetized rats. The recorded neurons were verified by intracellular injection of biocytin. Transition from non-theta to theta state was characterized by a large decrease in the input resistance of the neuron (39% in the soma), tonic somatic hyperpolarization and dendritic depolarization. The probability of pyramidal cell discharge, as measured in single cells and from a population of extracellularly recorded units, was highest at or slightly after the negative peak of the field theta recorded from the pyramidal layer. In contrast, cyclic depolarizations in dendrites corresponded to the positive phase of the pyramidal layer field theta (i.e. the hyperpolarizing phase of somatic theta). Current-induced depolarization of the dendrite triggered large amplitude slow spikes (putative Ca2+ spikes) which were phase-locked to the positive phase of field theta. In the absence of background theta, strong dendritic depolarization by current injection led to large amplitude, self-sustained oscillation in the theta frequency range. Depolarization of the neuron resulted in a voltage-dependent phase precession of the action potentials. The voltage-dependent phase-precession was replicated by a two-compartment conductance model. Using an active (bursting) dendritic compartment spike phase advancement of action potentials, relative to the somatic theta rhythm, occurred up to 360 degrees. These data indicate that distal dendritic depolarization of the pyramidal cell by the entorhinal input during theta overlaps in time with somatic hyperpolarization. As a result, most pyramidal cells are either silent or discharge with single spikes on the negative portion of local field theta (i.e., when the somatic region is least polarized). However, strong dendritic excitation may overcome perisomatic inhibition and the large depolarizing theta rhythm in the dendrites may induce spike bursts at an earlier phase of the extracellular theta cycle. The magnitude of dendritic depolarization is reflected by the timing of action potentials within the theta cycle. We hypothesize that the competition between the out-of-phase theta oscillation in the soma and dendrite is responsible for the advancement of spike discharges observed in the behaving animal.

Action Potentials↗

PubMed2002

Morphometric analysis of dendritic remodeling in an identified motoneuron during postembryonic development.

A detailed quantitative description of modifications in neuronal architecture is an important prerequisite to investigate the signals underlying behaviorally relevant changes in neuronal shape. Extensive morphological remodeling of neurons occurs during the metamorphosis of holometabolous insects, such as Manduca sexta, in which new adult behaviors develop postembryonically. In this study, a morphometric analysis of the structural changes of an identified Manduca motoneuron, MN5, was conducted by sampling its metric parameters at different developmental stages. The remodeling of MN5 is divided into three main phases. The regression of most larval dendrites (1) is followed by the formation of dendritic growth-cones (2), and subsequently, adult dendrite formation (3). In contrast, the cell body and link segment surface increase during dendritic regression and regrowth, indicating that different cell compartments receive different signals, or respond differently to the same signal. During dendritic growth-cone formation, the growth of the cell body and the link segment are arrested. Sholl and branch frequency analysis suggest two different modes of dendritic growth. During a first growth-cone-dependent phase, new branch formation occurs at all dendrites. The maximum path length of the major dendritic tree changes little, whereas branch order increases from 20 to 45. Changes in total dendritic length are correlated with strong changes in the number of nodes but with minor changes in the average dendritic segment length, indicating a mode of growth similar to that induced by steroid hormone application to cultured motoneurons. The second phase is growth-cone-independent, and branching is limited to high order dendrites.

Animals↗

PubMed2005

Distribution of contacts from vestibulospinal axons on the dendrites of splenius motoneurons.

Current descriptions of the organization of synapses on the dendritic trees of spinal motoneurons indicate that the inputs are arranged in several patterns: some are widely distributed; some are distributed to proximal dendrites; others are distributed based on the trajectory of the dendrites. However, the principles governing the organization of synapses on spinal motoneurons remain poorly defined. Our goal was to extend the descriptions of the distribution of synapses, identified by their source, on the dendritic trees of spinal motoneurons. We combined anterograde and intracellular staining techniques in cats to determine the distribution of contacts between excitatory axons from the rostral aspect of the descending vestibular nucleus and the dendrites of motoneurons supplying a dorsal neck muscle, splenius. In five of five motoneurons, the contacts were preferentially distributed on dendrites medial to the soma. This qualitative observation was confirmed by using Monte Carlo methods. The results from this analysis showed that the distribution of contacts can be explained not by the overall distribution of the dendritic membrane area but rather by a systematic innervation of the medial regions of the dendritic trees (P < 0.02). Despite this selectivity, there was no additional bias in the distribution of contacts to proximal vs. distal dendrites. By concentrating excitatory synapses in a restricted region of the dendritic tree, the actions of vestibulospinal connections on neck motoneurons may be increased as a result of a greater probability of activating persistent inward currents on the dendrites.

Animals↗

PubMed1981

Ruffed cell: a new type of neuron with a distinctive initial unmyelinated portion of the axon in the olfactory bulb of the goldfish (Carassius auratus). III. Three-dimensional structure of the ruffed cell dendrite.

The three-dimensional structure of the ruffed cell dendrite in the olfactory bulb of the goldfish (Carassius auratus) was studied by means of light and high-voltage electron microscopy of Golgi-impregnated material, combined Golgi-electron microscopy, and electron microscopy of serial thin sections. Ruffed cell dendrites ramify in the glomerular area with tufted branching patterns. They give rise to many appendages of various shapes and sizes: sheetlike processes, fingerlike projections, or small tuftlike appendages. These appendages, singly or together, appear to entwine or cover other neuronal processes. In thin sections ruffed cell dendritic appendages frequently look like glial processes; that is, they appear to conform in shape to the contours of surrounding neuronal elements, such as mitral and granule cell dendrites. Ruffed cell dendrites display intimate relationships with mitral cell dendrites. The former appear to coil around and cover the latter. Nothwithstanding the intimate relationship between ruffed cell dendrites and mitral cell dendrites, there seem to be no synaptic connection between them. Ruffed cell dendrites bear a rather small number of presynaptic and postsynaptic sites, most of which area with granule cell dendrites. Ruffed cell dendrites seem to receive no synapses from olfactory nerve terminals.

Animals↗

PubMed1984

Afferent influences on brain stem auditory nuclei of the chicken: time course and specificity of dendritic atrophy following deafferentation.

The time course and specificity of the changes in dendritic morphology following deafferentation were examined in nucleus laminaris of young chickens. The dendrites of nucleus laminaris neurons are segregated into dorsal and ventral domains, which are innervated separately from the ipsilateral and contralateral nucleus magnocellularis, respectively. Transection of the crossed dorsal cochlear tract deafferents the ventral dendrites of nucleus laminaris bilaterally without interrupting the matching input to the dorsal dendrites. In 10-day-old chicks, atrophy of the ventral dendrites began immediately after transecting the tract; the ventral dendrites were 10% shorter by 1 hour and 16% shorter by 2 hours after deafferentation. The length of the ventral dendrites progressively decreased over the next 2 weeks, resulting in at least a 60% loss of ventral dendrite 16 days after surgery. The dorsal dendrites of the same cells, whose afferents remained intact, did not change in length during the time course of this study. However, 16 days after the lesion, spines appeared on the normally smooth dorsal and ventral dendrites. The time course of dendritic atrophy and its restriction to the deafferented postsynaptic surface are related to possible mechanisms by which afferents regulate and maintain their target neurons.

Afferent Pathways↗

PubMed1985

Dendrite distribution of identified motoneurons in the lumbar spinal cord of the turtle Pseudemys scripta elegans.

Motoneurons in the turtle lumbar spinal cord were injected with HRP by electrophoresis after being electrophysiologically identified as innervating a muscle belonging to a functional group. The distribution of dendrites was studied in transverse reconstructions of 45 motoneurons, including 11 motoneurons identified as innervating knee extensor muscles, eight motoneurons innervating hip retractor and knee flexor muscles, 14 motoneurons innervating ankle and/or toe extensors and 12 motoneurons innervating ankle and/or toe flexor muscles. The dorsal dendritic tree of motoneurons innervating distally positioned musculature (ankle and/or toe extensors and flexors) was observed to contain significantly less terminal dendritic branches compared to the dorsal dendritic trees of motoneurons innervating proximally situated (hip and knee) muscles. The distribution of dendrites within the white matter was studied by measuring the total projected length of the dendritic branches within empirically defined sectors in the transverse plane. This kind of analysis also revealed differences between the dorsal dendrites of motoneurons innervating distally and proximally positioned muscles conforming to the counts of terminal dendritic branches. It is suggested that these apparent differences in the size of the dorsal dendrite may be related to the number of synapses made by primary afferents. In the white matter, the highest dendritic density for all four groups of mononeurons was found within the central part of the lateral funiculus. However, only in the ventral funiculus could slight indications be found that the dendritic density of functionally different motoneuron groups may bear some relation to the locations of the terminations of the descending pathways known to establish monosynaptic contacts with lumbar mononeurons.

Animals↗

PubMed1987

Three-dimensional architecture of dendritic trees in type-identified alpha-motoneurons.

We have studied the spatial distribution of dendrites of type-identified triceps surae alpha-motoneurons, labeled intracellularly with HRP, using a variety of analytical approaches that were designed to quantify the ways in which dendrites occupy three-dimensional space. All of the methods indicated a strong tendency for motoneuron dendrites to project radially. However, regions dorsal and ventral to the somata contained fewer dendritic elements, and less membrane area, than expected for complete radial symmetry. Individual dendrites projecting into these regions tended to be smaller than those projecting rostrocaudally or mediolaterally. Nevertheless, the center of mass of membrane area for five of six fully analyzed cells was within 100 micron of the soma and, in all six cells, was located in the same dorsoventral plane as the cell soma. Maps of the projection of dendritic branches onto concentric shells at various radial distances from the soma showed that some regions have high concentrations of branches, sometimes with considerable overlap between branches arising from different stem dendrites, while other regions have relatively few branches, or none at all. Each motoneuron exhibited a different pattern of projection and there were no systematic differences between fast-twitch (type F, including both types FF and FR units) and slow-twitch (type S) motoneurons evident in the patterns of dendritic concentration. Assessment of the three-dimensional territories of individual dendrites showed that dendrites with larger numbers of terminal branches tended to have larger spatial territories. Despite considerable scatter, the results suggest that the density of branches tends to be approximately the same in large and small dendrites, and in F and S cell groups. The results are discussed in relation to the spatial location of synaptic input to motoneurons.

Animals↗

PubMed1988

Postnatal development of dendrites of relay neurons in the lateral geniculate nucleus of the marmoset (Callithrix jacchus): a quantitative Golgi study.

Dendrites of multipolar relay neurons in the lateral geniculate nucleus of the marmoset (Callithrix jacchus), at various ages from birth to adulthood, were studied in rapid Golgi preparations. The dendrites were analyzed by means of three-dimensional computer reconstructions and decomposed into intermediate and terminal segments, both of which were further classified according to their centrifugal order. Measurements were made of the number of segments per dendrite, the total length of dendrites, and the mean length of intermediate and terminal segments. In adult marmosets, there are four stem dendrites on average per neuron, and each dendrite divides into a mean of 14 segments. Between birth and 6 weeks of age, the mean dendritic length doubles, mainly because of changes in terminal segments. There is a significant decrease in dendritic length into adulthood. The total number of stem dendrites does not change after birth, but during the first postnatal week dendrites lose distal segments, after which there is a significant increase in the number of segments of orders 3 to 7. The mean length of intermediate segments does not change with age, nor with order, whereas the length of terminal segments increases from 50 to 120 microns from birth to 6 weeks of age, and then decreases to the adult value of 80 microns. In conclusion, during the period of most rapid visual development, important morphological changes occur in geniculate relay-cell dendrites, involving essentially terminal segments. These observations correlate well with changes of geniculate volume and neuronal density.

Animals↗

PubMed1989

Golgi study of the mouse striatum: age-related dendritic changes in different neuronal populations.

The Van der Loos modification of the Golgi-Cox method and morphometric analyses were used to study the neuronal types in the striatum of adult (3, 6, and 10 months) and aged (20, 25, and 30 months) C57BL/6N mice. In adult mice six types of striatal neurons were distinguished primarily on the basis of the morphology of their cell body and dendrites. Each of these types was compared with morphologically similar neurons from previous Golgi classifications in other species and discussed within the framework of recent immunocytochemical work. With similar methods the age-related changes occurring on the dendrites of three of the six striatal types were also analyzed. In the medium-sized neuron with spine-laden dendrites, various dendritic tree shapes and sizes were distinguished in all age groups studied. Qualitative observations as well as measurements of total dendritic length per cell suggested that the dendrites in this type may both grow and regress throughout the life span, although signs of dendritic atrophy and regression were observed only in the aged groups. In the other two types of neuron, one a medium aspiny cell with thin varicose dendrites and the other a large spiny neuron with many dendrites, measurements of total dendritic lengths revealed sustained growth of the tree well into advanced age, followed by moderate regression in the oldest groups. The present findings also indicate that the dendrites of each type of striatal neuron follow unique temporal patterns of growth and regression during the life span of the mouse.

Aging↗

PubMed1990

Early development of retinal ganglion cell dendrites in the marsupial Setonix brachyurus, quokka.

The dendritic morphology of retinal ganglion cells was studied in flat-mounted retinae of the marsupial Setonix brachyurus, quokka. In the adults, horseradish peroxidase (HRP) was applied to the vitread surface of flattened retinae. Wide-, large-, medium-, and small-field classes appeared to correspond to gamma, alpha, delta, and beta cells, respectively, in the cat (Boycott and Wässle, J. Physiol. 249:397-419, 1974). To reveal the early stages of dendritic development, HRP was placed on the optic nerve of isolated eye cups from the day of birth to postnatal day (P) 63 when the area centralis is beginning to form (Dunlop and Beazley, Dev. Brain Res. 23:81-90, 1985). Youngest cells lacked dendrites and had an elongate soma in the cytoblastic layer with an endfoot contacting the ventricular surface. Once in the ganglion cell layer, the soma was rounded and dendrites appeared as short, unbranched processes. Most cells were asymmetric or "polarised" with the axon arising from the side nearest the optic disk and dendrites from the opposite side. Polarity was maintained in cells with longer, branched dendrites. A small proportion of cells exhibited a reversed polarity in which the axon arose from the side nearest the retinal edge and dendrites towards the disk. Cells appeared to acquire an approximately symmetric, adult-like tree by the addition of new primary dendrites between the existing ones and the axon hillock. Wide-, large-, medium-, and small-field cells were evident from P6, P25, P31, and P40, respectively. Spines were observed on dendrites and axons during development but were rare in the adult. Some dendro-axons were seen at all ages examined. The existence of an initial axodendritic polarity in retinal ganglion cells supports the hypothesis that the axon hillock is the determinant of dendritic geometry (Maffei and Perry, Dev. Brain Res. 41:185-194, 1988). Polarity may also contribute to the establishment of "radial orientation" in which the long axis of the elliptical dendritic tree of cells outside the area centralis points towards central retina and the weighted centre is displaced towards the retinal periphery (Leventhal and Schall, J. Comp. Neurol. 220:465-475, 1983).

Animals↗

PubMed1992

Dendritic sampling across processing streams in monkey striate cortex.

Cytochrome oxidase (CO) dense blobs in primate striate cortex provide a striking example of parallel processing of visual information. The level of isolation of the blobs from the surrounding interblob tissue was investigated in the present study by combining CO staining with Golgi impregnation of dendritic arbors in the same tissue sections. The data are based on material from two marmoset and three squirrel monkeys. The analysis was conducted on two types of Golgi preparations. In the first preparation, dense networks of overlapping dendrites were impregnated over blob margins. The results of analyzing these networks with transmission and confocal microscopy revealed that dendritic arbors penetrate freely through blob margins. Statistical analysis revealed that the density of dendritic crossings at blob margins was similar to that found at blob and interblob centers. In the second type of Golgi preparation, single, isolated neurons were impregnated. Studies of such neurons revealed occasional examples of dendritic arbors that appeared to reflect back from blob margins, but counter examples were equally abundant. Bias index analysis indicated that dendritic arbors were generally unaffected by the presence of a nearby blob margin. Scanning a large number of impregnated arbors indicated that at least half of the population of blob-related neurons had dendrites in both blob and interblob territory. Under the conditions of free dendritic penetration of blob margins, the sole factor that determines the level of blob/interblob mixing appears to be the relationship between blob size and the dendritic spread of blob neurons. Interestingly, in both the marmoset and squirrel monkeys this size ratio is similar despite a large difference in their cortical surface area. Thus, it is hypothesized that blob size is optimally matched to the dendritic span so as to create a smooth transition of dendritic sampling from blob to interblob-related processing streams.

Animals↗