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PubMed1979

Organization and development of brain stem auditory nuclei of the chicken: dendritic gradients in nucleus laminaris.

Nucleus laminaris (NL) is a third-order auditory nucleus in the avian brain stem which receives spatially-segregated binaural inputs from the second-order magnocellular nuclei. The organization of dendritic structure in NL was examined in Golgi-impregnated brains from hatchling chickens. Quantitative analyses of dendritic size and number were made from camera lucida drawings of 135 neurons sampled from throughout the nucleus. The most significant results of this study may be summarized as follows: (1) The preponderant neuron in n. laminaris may be characterized as having a cylindrical-to-ovoid cell body, about 20 micrometer in diameter. The neurons comprising NL were found to be nearly completely homogeneous in issuing their dendrites in a bipolar fashion: one group of dendrites is clustered on the dorsal surface of the cells, the other group on the ventral. The dendrites of NL are contained within the glia-free neuropil surrounding the nucleus. From the rostromedial to the caudolateral poles of NL there is a gradient of increasing extension of the dendrites, increasing number of tertiary and higher-order dendrites, and increasing distance from the somata of the occurrence of branching. (2) The total dendritic size (sum of the dorsal) and ventral dendritic lengths of the cells) increases 3-fold from the rostromedial to the caudolateral poles of NL. About 50% of the variance in dendritic size is accounted for by the position of the cells in NL, and the gradient of dendritic size increase has the same orientation across NL as the tonotopic gradient of decreasing characteristic frequency in NL. (3) From the rostromedial pole to the caudolateral pole of NL there is an 11-fold decrease in the number of primary dendrites along a gradient coinciding with the length and frequency gradients. Sixty-six percent of the variance in dendrite number is accounted for by position in the nucleus. (4) The correlation of dorsal and ventral dendritic size on a cell-by-cell basis is not high (r = 0.47), indicating a fair amount of variability on the single-cell level. On the other hand, the average dorsal dendritic length within an isofrequency band in NL correlates very highly with the average ventral dendritic length. Thus, on an areal basis, the amount of dendritic surface area offered to the dorsal and ventral afferents is tightly regulated. (5) The dorsal and ventral dendrites have separate gradients of increasing length and number across NL. The dorsal gradients are skewed toward the rostrocaudal axis, while the ventral dendritic gradients are skewed mediolaterally. (6) There was no correlation between either dendritic size or number of primary dendrites and the size of the somata in NL, which remains relatively constant throughout the nucleus. Several hypotheses about the ontogenetic control of dendritic structure are examined in light of the above data. Of these, the hypotheses that the ontogeny of dendritic size and number is largely under afferent control receives a great deal of circumstantial support.

Animals↗
PubMed1994

Dendritic architecture of rat somatosensory thalamocortical projection neurons.

This study examines dendrites from physiologically characterized and intracellularly labelled thalamocortical projection (TCP) neurons from the rat ventrobasal complex (VB) and posterior nucleus (POm). The goals were to provide quantitative descriptions of TCP neuron dendrites, examine underlying design principles of dendritic morphology, and determine correlations between dendritic size parameters. Forty-four dendrites from seven VB neurons and 21 dendrites from three POm TCP neurons that responded to low-threshold mechanical stimuli were reconstructed and quantitatively analyzed at the light microscopic level. The dendritic architecture of the neurons was remarkably similar in most parameters studied, including the percentage of dichotomous branching, contribution of terminal branches to total dendritic length, and branching symmetry. There was a positive correlation between stem dendrite diameter and the length of the entire dendrite arbor, making it possible to estimate the total length of a dendritic arbor by measuring the stem dendrite diameter. The correlations of the VB and POm dendrites had different slopes. The path distance (the distance from the soma to a dendritic end point) of individual dendrites showed only a small variation with large differences in the total dendritic length of an arbor. The constant diameter of distal dendrites shows that dendrite diameter is a poor predictor of synaptic location on the dendritic tree. Although the morphology of neurons and their individual dendrites varied considerably in overall size and qualitative appearance, when examined qualitatively, many aspects of dendritic structure were similar within and between groups. We suggest that the rat somatosensory TCP neurons have a stereotyped dendritic architecture and present data which provide a base for future comparative, developmental, and plasticity studies.

Animals↗
PubMed1982

Dendritic organization of the human spinal cord: the motoneurons.

The dendritic organization of motoneurons was analyzed with the Golgi stain and a morphometric method in the immature and adult human spinal cord. Each motoneuronal column was found to be characterized by a specific orientation of dendritic trees and by a distinct pattern of dendritic bundling. Ventromedial motoneurons have a pyramidal dendritic tree with numerous, short longitudinal branches and elongated dorsal branches. The latter form thick bundles oriented toward the ventral gray commissure. Longitudinal dendrites form a narrow-meshed dendritic plexus, containing abundant microbundles. Motoneurons of the ventromedial column have fewer primary dendrites and a lower ramification index than other motoneurons. Central motoneurons are predominantly oriented longitudinally. The meshes of the rostrocaudal dendritic plexus are looser and the microbundles are finer. Most transverse dendrites run laterally and participate in dendritic bundles which penetrate into the ventrolateral funiculus. The rostrocaudal dendritic domain of ventrolateral motoneurons is the largest dendritic domain of all spinal neurons. The longitudinal dendritic network contains fine microbundles and appears wide-meshed. Transverse dendrites form lateral or medial dendritic bundles depending upon the position of their perikaryon. Dorsolateral motoneurons differ from other motoneurons by their multipolar organization with a slight preponderance of dorsoventral dendritic spread. Rudimentary lateral dendrite bundles are restricted to marginal neurons. The longitudinal plexuses of motoneuronal dendrites and the verticotransverse dendrite bundles of the ventromedial column are well developed in the 26-28-week-old fetus. In contrast, the horizontotransverse dendrite bundles of central and ventrolateral motoneurons can only be recognized from 36 weeks on. The possible specific functions of the various types of dendrites bundles are examined and a laminar dendroarchitectonic schema of the human cord is proposed.

Adult↗
PubMed2006

The level and integrity of synaptic input regulates dendrite structure.

How localized synaptic input regulates dendritic branch structure is not well understood. For these experiments, we used single-cell electroporation, live cell imaging, in vitro deafferentation, pharmacology, and electrophysiological stimulation to study how local alterations in synaptic input affect dendritic branch structure in nucleus laminaris (NL). We found that interrupting or modulating synaptic input to distinct sets of NL dendrites can regulate their structure on a very short timescale. Specifically, eliminating synaptic input by deafferenting only one set of the bitufted NL dendrites caused a selective reduction in the total dendritic branch length of the deafferented dendrites but relatively few changes in the normally innervated dendrites on the same cell. An analysis of individual dendritic branch changes demonstrated that both control and deafferented NL dendrites exhibit branch extension and retraction. However, the presence of intact synaptic inputs balanced these changes, maintaining the total dendritic branch length of control dendrites. When glutamate receptor signaling was blocked (DNQX and AP-5), NL neurons exhibited significant dendrite retraction, demonstrating that NL dendrite maintenance depends in part on presynaptic glutamatergic input. Electrophysiological experiments further confirmed that modulating the level of synaptic input regulates NL dendrite structure. Differential stimulation of the two sets of dendrites resulted in a selective reduction in the total dendritic branch length of the unstimulated dendrites and a selective increase in the total dendritic branch length of the stimulated dorsal dendrites. These results suggest that balanced activation of the two sets of NL dendrites is required to maintain the relative amount of dendritic surface area allotted to each input.

Animals↗
PubMed1990

Dendritic transport: quantitative analysis of the time course of somatodendritic transport of recently synthesized RNA.

We have previously reported that recently synthesized RNA is selectively transported into the dendrites of hippocampal neurons grown in culture (Davis et al., 1987). The present study provides further details about this transport process, focusing especially on the velocity of transport, by comparing the velocity of dendritic transport of RNA in neurons of different ages and in the branched and unbranched dendrites of individual neurons. In our previous study, we recognized that calculations of transport velocity could be compromised because transport was being evaluated in a population of dendrites of varying lengths. The present study uses a mathematical modeling approach to determine how the morphology of the population of dendrites would affect the analysis of transport velocity. Focusing first on a simple model, we compared the distribution of transported material at various times when all dendrites were of the same length and when the population included dendrites of different lengths. We found that the distance of labeling increased linearly over time when all dendrites were of the same length, but increased with a negatively accelerating curve when dendrites were of different lengths. We then determined the actual distribution of dendritic lengths in cultured hippocampal neurons, based on immunostaining with an antibody directed against the selective dendritic marker, microtubule-associated protein 2 (MAP2). Using a computer model, we calculated the mean distance of transport as a function of time in this population of dendrites, assuming different velocities of transport. The velocity that best fit the measured distances of RNA transport in both 7- and 15-d-old neurons was 11 microns/hr (0.26 mm/d). However, for the dendrites exhibiting the longest distance of labeling, the best-fitting curve assumed a velocity of 21 microns/hr in both 7- and 15-d-old neurons (0.50 mm/d). Comparisons of transport in branched and unbranched dendrites revealed that the distance of labeling over branched dendrites was consistently longer than over unbranched dendrites of individual neurons. However, neurons with a larger proportion of branched dendrites did not exhibit a greater mean distance of transport. The density of silver grains was higher over branched than over unbranched dendrites, suggesting that a greater amount of recently synthesized RNA may be transported into branched dendrites. Taken together, these results suggest that RNA transport into dendrites is regulated differentially in the dendrites of individual neurons.

Animals↗
PubMed1999

Dendritic cells with immature phenotype and defective function in the peripheral blood from patients with hepatocellular carcinoma.

BACKGROUND/AIMS: Defects and dysfunctions in antigen-presenting dendritic cells have been shown during carcinogenesis. The phenotype and function of dendritic cells have been studied in patients with hepatocellular carcinoma to explore the possibility of dendritic cell-based immune therapy in hepatocellular carcinoma. METHODS: The stimulatory capacity of dendritic cells in allogenic mixed leukocytes reaction, the expression of surface makers on dendritic cells, the production of cytokines and nitric oxide by dendritic cells and the levels of maturation of dendritic cells from 17 patients with hepatocellular carcinoma, 10 patients with liver cirrhosis and 10 normal controls were compared. RESULT: Dendritic cells from hepatocellular carcinoma had significantly lower capacity to stimulate allogenic T cells in allogenic mixed leukocytes reaction compared with dendritic cells from liver cirrhosis and normal controls (p<0.05). Dendritic cells from hepatocellular carcinoma expressed significantly lower levels of HLA DR and induced decreased amounts of interleukin-12 compared with dendritic cells from normal controls (p<0.05). On the other hand, dendritic cells from hepatocellular carcinoma produced significantly higher levels of nitric oxide and tumor necrosis factor-a compared with dendritic cells from liver cirrhosis and normal controls (p<0.05). The uptake of fluorescein isothiocyanate-labeled dextran revealed an immature phenotype of dendritic cells from hepatocellular carcinoma compared with dendritic cells from liver cirrhosis (p<0.05). CONCLUSION: The results of this study on the function of dendritic cells in hepatocellular carcinoma, and the prevalence of immature dendritic cells in hepatocellular carcinoma in the microenvironment of high levels of inflammatory cytokines indicate a specific defect of dendritic cell maturation during hepatocarcinogenesis. These data show that induction of dendritic cell maturation might be an approach to dendritic cell-based immune therapy during hepatocellular carcinoma.

Biomarkers↗
PubMed1976

[Development of neuronal structure in the hippocampus during pre- and post-natal ontogenesis in the albino rat. III. Morphometric determination of ontogenetic changes in dendrite structure and spine distribution on pyramidal neurons (CA1) of the hippocampus].

Following GOLGI impregnation pyramidal neurons of the rat hippocampus (CA1) from four stages of age (E21, P5, P10, P20) were investigated by morphometric methods with regard to their dendritic structure and amount and distribution of spines. The daesults show, that during the ontogenesis until reaching adult values the determined parameters are strongly following in their expression the sequence: degree of ramification, length of dendrites, amount of spines, and in the development of the certain dendritic parts of the pyramid the sequence: main apical dendrite with end ramifications, basal dendrites, apical lateral dendrites. Along the main apical dendrite the pattern of spine distribution develops proceeding from the form of a reverse nearly plain parabola (P5, P10) to the curve known from other adult pyramides (P20) with a spine poor initial segment, then the rapid increase in the number of spines (maximum of spine density in the middle of the whole distance), followed by a subsequent slow decrease in the number of spines. The apical end ramifications are mostly developed in the degree of ramification and length of dendrites during the prenatal period and show postnatal only significant changes in the spine density without reaching the values of the other dendritic fields. At basal dendrites no further increase in the number of dendrites can be found after P10. In dendritic length and spine density they are reaching adult level about the 20th postnatal day. In comparison with that, apical lateral dendrites show at P20 their definitive amount and a further increase of the spine density must be expected. The single dendritic fields of apical lateral dendrites are in length and total amount of spines sometimes smaller than those of basal dendrites, but more abundant. In both cases the spine densities increase until the stage P20 but they are not differing. Caused by the further development of apical lateral dendrites to adultness a predominance of the spine density of this part of the neuron is known. The total length of the dendrites of one pyramidal neuron (CA1) increases from 1000 mum (E21) to 5600 mum (P20), while the total amount of visible spines and the spine density increase from 20 to 3000 spines resp. from 0,02 to 0,55 spines/mum. It is important that the portion of the apical lateral dendrites grows from 2 to 40%, the portion of basal dendrites only from 20 to 33%, while the importance of the apical end ramifications decreases from 60 to 20%. In the presented paper the comparisons of developmental stages of the most pyramidalized hippocampal neurons (CA1) with adult pyramids of this region and with cortical pyramidal neurons of different phylogenetic ages are discussed.

Age Factors↗
PubMed2002

How voltage-gated ion channels alter the functional properties of ganglion and amacrine cell dendrites.

The present study compares the structure and function of retinal ganglion and amacrine cell dendrites. Although a superficial similarity exists between amacrine and ganglion cell dendrites, a comparison between the branching pattern of the two cell types reveals differences which can only be appreciated at the microscopic level. Whereas decremental branching is found in ganglion cells, a form of non-decremental or "trunk branching" is observed in amacrine cell dendrites. Physiological differences are also observed in amacrine vs ganglion cells in which many amacrine cells generate dendritic impulses which can be readily distinguished from those of the soma, while separate dendritic impulses in ganglion cell dendrites have not been reported. Despite these differences, both amacrine and ganglion cell dendrites appear to contain voltage-gated ion channels, including TTX-sensitive sodium channels. One way to account for separate dendritic impulses in amacrine cells is to have a higher density of sodium channels and we generally find in modeling studies that a dendritic sodium channel density that is more than about 50% of that in the soma is required for excitatory, synaptic currents to give rise to local dendritic spike activity. Under these conditions, impulses can be generated in the dendrites and propagate for some distance along the dendritic tree. When the soma generates impulse activity in amacrine cells, it can activate, antidromically, the entire dendritic tree. Although ganglion cell dendrites do not appear to generate independent impulses, the presence of voltage-gated ion channels in these structures appears to be important for their function. Modeling studies demonstrate that when dendrites lack voltage-gated ion channels, impulse activity evoked by current applied to the cell body is generated at rates that are much higher than those observed physiologically. However, by placing ion channels in the dendrites at a reduced density compared to those of amacrine cells, the firing rate of ganglion cells becomes more physiological and the relationship between frequency and current (F/I relationship) can be precisely matched with physiological data. Recent studies have demonstrated the presence of T-type calcium channels in ganglion cells and our analysis suggests that they are found in higher density in the dendrites compared to the soma. This is the first voltage-gated ion channel which appears more localized to the dendrites than other cell copartments and this difference alone cries for an interpretation. The presence of a significant T-type calcium channel density in the dendrites can influence their integrative properties in several important ways. First, excitatory synaptic currents can be augmented by the activation of T-type calcium channels, although this is more likely to occur for transient rather than sustained synaptic currents because T-type currents show strong inactivation properties. In addition, T-type calcium channels may serve to limit the electrical load which dendrites impose on the spike initiation process and thus enhance the speed with which impulses can be triggered by the impulse generation site. This role whill enhance the safety factor for impulses traveling in the orthograde direction.

Action Potentials↗
PubMed1997

In vitro generation of CD83+ human blood dendritic cells for active tumor immunotherapy.

There is increasing clinical interest in dendritic cells that are capable of initiating antitumor immune responses. Dendritic cells cultured from human blood mononuclear cells using granulocyte/macrophage colony-stimulating factor (GM-CSF) and interleukin-4 (IL-4) are competent for antigen uptake but express relatively low levels of costimulatory molecules and thus correspond to immature resident tissue dendritic cells. In this study we took advantage of the new dendritic cell-specific marker CD83, which is expressed by mature dendritic cells, to delineate the maturation of cultured human blood dendritic cells. Although dendritic cells cultured with GM-CSF and IL-4 contained transcripts for CD83 as determined by reverse transcription PCR, CD83 protein was barely detectable by flow cytometry, confirming that dendritic cells obtained with this system are immature. However, treatment of dendritic cells with tumor necrosis factor-alpha (TNF-alpha) significantly increased the levels of CD83 transcripts and induced CD83 protein expression in dendritic cells. In contrast to the initiation of dendritic cell culture, which was facilitated by high cell density (5 x 10(6) cells/mL), differentiation into CD83+ dendritic cells required a low cell concentration (0.5 x 10(6) cells/mL). At higher cell density (1 x 10(6) cells/mL), CD83 expression was suppressed and was almost completely prevented at 2 x 10(6) cells/mL. Induction of CD83 expression was accompanied by a strong upregulation of the costimulator B7-2 (CD86) on dendritic cells. While untreated CD83(-) dendritic cells efficiently internalized fluoresceinated Dextran, TNF-alpha treated CD83+ dendritic cells excluded these molecules, confirming that maturation of dendritic cells was associated with the silencing of the antigen-capturing machinery. Morphologically, CD83+ dendritic cells presented with pronounced cytoplasmic projections (veils) characteristic of mature dendritic cells. In summary, we show that cell density critically regulates dendritic cell development. Knowledge of the appropriate conditions for dendritic cell generation and maturation will be important in clinical immunotherapy settings.

Antigens, CD↗
PubMed1980

Normal dendritic morphology of frog spinal motoneurons: a Golgi study.

Normal dendritic morphology of frog (Rana pipiens) lumbar motoneurons was studied using Golgi silver impregnation. Branching characteristics and quantitative measurements of dendrites were obtained using computer-aided serial reconstruction of a typical lumbar motoneuron over seven adjacent 80-micrometer transverse sections. Dendrites were classified based upon site of dendrite origin from the soma and distribution of the dendritic array within the spinal cord. Eight possible sites of dendritic origin from the soma were identified. Two dendrites, D1 and D2, are planar dendrites which arise from the dorsal aspect of the soma. They are moderately complex, reaching branch order 5-6, and are oriented predominantly in the transverse plane. Input to these dendrites is primarily segmental via dorsal root projections. Three dendrites, D3, D4, and D5, arise laterally from the soma and extend through the lateral funiculus toward the subpial region. Two dendrites, D6 and D7, arise ventrally. D6 extends ventrolaterally and is a simple dendrite reaching branch order 3-4. D7 aborizes extensively in the ventral funiculus and in the central gray, reaching a branch order of 8-9. This dendrite extends rostrally and caudally over a distance of at lest 560 micrometer. Another dendrite (D8) arises from the medial aspect of the soma and projects toward the central canal. Four sites (D1, D2, D6, and D7) almost invariably give rise to dendrites. Dendrites arise at D4 in 66% of the cells examined. Dendrites are found at D3, D5, and D8 much less frequently (6-21%). Total dendritic length (12,043 micrometer) and lengths of the individual dendrites, branch length versus branch order, and number of branches at increasing radii were examined, and Sholl analysis was performed.

Animals↗
PubMed1981

A quantitative light microscopic study of the dendrites of cat spinal alpha-motoneurons after intracellular staining with horseradish peroxidase.

The cell bodies and dendrites of cat spinal alpha-motoneurons were studied after intracellular staining with horseradish peroxidase. The mean diameter of the soma was positively correlated to both the mean diameter and the combined diameter of the first-order dendrites, but not to the number of first-order dendrites. On the average, 11.2 dendrites originated from the soma. The dendritic trees were more extensive than has been described previously. The mean value for the combined length of a whole dendrite was 4.7 mm, while the mean values for the total surface area and volume of a dendrite were 33.0 x 10(3) micron (2) and 27.2 x 10(3) micron (3), respectively. The diameter of the first-order dendrite was positively correlated to the combined length of the entire dendrite, the number of dendritic branching points, and the number of dendritic end branches. The diameter of the first-order dendrite was also directly proportional to the volume and the surface area of the entire dendrite. About 75% of the dendritic surface area and 55% of the dendritic volume was located more than 300 micron away from the soma. The dendrites constituted about 97% of the surface area and about 75% of the volume of the entire motoneuron (excluding the axon). The dendritic tapering was moderate. On the average, the distal decrease in dendritic diameters caused a reduction in the combined dendritic parameter (sigma d 3/2) by 1.5% and 15% at 500 micron and 800 micron distance, respectively, from the soma.

Animals↗
PubMed1985

Quantitative analysis of the dendrites of cat phrenic motoneurons stained intracellularly with horseradish peroxidase.

All the dendrites (N = 37) generated by four phrenic motoneurons were analyzed following intracellular injection of horseradish peroxidase. The dendritic arbors produced from each of these stem dendrites were studied in detail. The mean number of stem dendrites produced by a phrenic motoneuron was 9.7, their mean diameter was 6.0 micron, and their mean combined diameter was 58.3 micron. The length at which a phrenic motoneuronal dendrite terminated was 1,236 micron, with several end terminals extending more than 2 mm from the cell body. The mean value for the combined lengths of all segments originating from a single stem dendrite was 5.3 mm. A full spectrum of dendritic branching patterns was observed from simple (five unbranched) to complex, the latter producing up to ninth-order branches. Most terminal and nonterminal dendritic segments tapered, producing a mean diameter reduction of 34%, or approximately 9% per 100-micron length. All phrenic motoneurons exhibited a steady decrease in the combined dendritic parameter (sigma d3/2) with distance from the soma as a result of tapering and end-branch termination. The mean surface area and volume of a phrenic motoneuronal dendrite were 35.3 X 10(3) micron 2 and 25.9 X 10(3) micron 3, respectively. The dendrites constituted greater than 97% of the total phrenic motoneuronal surface area, with 75% of this area lying outside of a 300-micron radius from the cell body. The diameter of a stem dendrite was positively correlated with its combined dendritic length, number of terminal branches, dendritic surface area, and volume. Despite this strong correlation, the value of total dendritic surface area calculated using the power equation derived from the dendritic surface area versus stem dendritic diameter plot was not a consistent estimator of the total dendritic surface area directly measured for these four phrenic motoneurons. It is suggested that this inconsistency may be the result of a heterogeneity in the phrenic motoneuronal population and/or in the dendrites projecting to the different terminal fields.

Animals↗
PubMed2002

Inter-ictal- and ictal-like epileptic discharges in the dendritic tree of neocortical pyramidal neurons.

Dendritic mechanisms have been implied to play a key role in the formation of epileptic discharges. However, presently only a handful of direct dendritic recordings have been reported during epileptic discharges. In this study, I performed simultaneous voltage recordings from the soma and apical dendrite of the same neuron combined with calcium-imaging measurements to investigate inter-ictal- and ictal-like epileptic discharges in dendrites of layer 5 pyramidal neurons. Neocortical brain slices treated with bicuculline (BCC) produced both isolated "inter-ictal" paroxysymal depolarization shift (PDS) responses and electrographic seizures. Concomitant voltage recordings from the soma and apical dendrite revealed that PDS responses developed in both the apical dendrites and soma. However, the two responses differed from one another. In apical dendrites, the PDS was significantly higher in amplitude and shorter in duration compared with the somatic PDS. The PDS response in dendrites had a peak amplitude of 68.9 +/- 2.2 (SD) mV, peak voltage value of 9.3 +/- 2.7 mV, and half-width of 203.8 +/- 38.4 ms. In contrast, the somatic PDS had a peak amplitude of 48.7 +/- 2.7 mV, peak voltage value of -11.9 +/- 3.1 mV, and half-width of 247.8 +/- 57.3 ms (P < 0.01, n = 18). In addition the apical dendritic PDS always preceded the somatic counterpart in all 18 neurons examined. Concomitant calcium-imaging measurements showed the PDS evoked large calcium influx into the entire dendritic tree including the apical tuft, basal, and oblique dendrites. The PDS evoked [Ca(2+)](i) were not uniform along the dendritic tree, being highest in the oblique dendrites (71.3 +/- 14.5 microM) and lowest at the distal tuft branches (9.3 +/- 0.7 microM). The PDS responses persisted after blockade of voltage-gated sodium channels by intracellular QX-314 but became narrower (by 69.6 +/- 9.7%) following intracellular administration of the voltage-gated calcium channel blocker D600. Electrographic seizures recorded in the soma and apical dendrites were composed of recurrent bursts. The initial bursts represented PDS responses. During the seizure the amplitude of bursts gradually attenuated and reached an average value of 26 +/- 13% of the initial ictal PDS burst. Double recordings during electrographic seizures revealed the initial one to four ictal bursts appeared first at the apical dendrite while later ictal bursts were always observed first at the soma. In conclusion, the results of this study show "inter-ictal" PDS responses originated in the apical dendritic tree, were partially mediated by voltage-gated calcium channels and spread throughout the dendritic tree including the fine tuft, basal, and oblique dendrites. During electrographic seizures the origin of epileptic bursts shifted from the apical dendritic tree to the soma-basal region.

Animals↗
PubMed1982

A quantitative anatomical study of the granule cell dendritic fields of the rat dentate gyrus using a novel probabilistic method.

The granule cell dendritic fields of the adult rat dentate gyrus were analyzed quantitatively using a probabilistic method developed to correct dendritic length and segment number for dendrites cut during sectioning. Golgi-impregnated, linearized hippocampi were sectioned serially in one of the three hippocampal planes. Three dendritic field parameters were quantified from camera lucida drawings of these dendritic fields: dendritic field spread, dendritic length, and the branching and termination patterns of dendritic segments. Granule cell dendritic fields resembled cones, their maximal extent occurring in the distal third of the molecular layer. The ratio of transverse to longitudinal dendritic field spread was greater than 1:1 for the dorsal leaf and crest regions, but close to or less than 1:1 for the ventral leaf. The probabilities of segment branching and termination were highly similar for transversely and longitudinally sectioned tissue. The probability of branching varied among dendritic orders and across the molecular layer for the same order. The probability of termination did not vary greatly across orders. Most nonbranching segments terminated adjacent to the hippocampal fissure. On the average, a granule cell had 2.23 first-order dendrites that branched into a dendritic field containing seventh-order dendrites. Total dendritic length, corrected for cut dendrites and projection errors, averaged 3,662 +/- 88 microns. The somatic layer and proximal third of the molecular layer contained approximately 35% of this total length. The remainder, ca. 60%, was restricted to the distal two-thirds of the molecular layer, the predominant termination zone of perforant path axons. These data provide a quantitative characterization of the rat granule cell dendritic fields. Implementation of the probabilistic correction method overcomes methodological problems common to quantitative Golgi studies. These data permit a more precise relationship to be drawn between dendritic architecture and granule cell physiology.

Animals↗
PubMed1988

Postnatal development of cat hind limb motoneurons. I: Changes in length, branching structure, and spatial distribution of dendrites of cat triceps surae motoneurons.

The postnatal development of length, branching structure, and spatial distribution of dendrites of triceps surae motoneurons, intracellularly stained with horseradish peroxidase, was studied from birth up to 44-46 days of postnatal (d.p.n.) age in kittens and compared with corresponding data from adult cats. The number of dendrites of a triceps surae motoneuron was about 12, and the arborization of each dendrite generated an average of 12-15 terminal branches. There was no net change in the number of dendrites of a neuron or in the degree of branching of the dendrites despite the occurrence of both a transient remodeling of the dendritic branching structure and changes of the spatial distribution of the dendritic branches during postnatal development. The perisomatic territory in the transverse plane occupied by the dendritic branches of a motoneuron increased in parallel with the overall growth of the spinal cord. Thus, the relative size of the dendritic territory in this plane was kept almost constant, whereas dendritic branches projecting in the rostrocaudal direction grew much faster than the spinal cord and also became more numerous. At birth the rostro-caudal dendritic span of individual motoneurons bridged 1:6 to 1:5 of the L7 spinal cord segment length; this figure was 1:3 at 22-24 d.p.n. Hence, in this direction, the growing dendritic branches invaded novel dendritic territories. The change in dendritic branch length from birth to 6 weeks of age corresponded to an average growth rate of 2 to 4 microns per dendritic branch and day, which implies that the total increase in length of the dendrites of a neuron could amount to 1 mm/day. The increase in branch length did not occur in a uniform or random manner; instead, it followed a spatiotemporal pattern with three phases: From birth to 22-24 d.p.n., growth was particularly prominent in greater than or equal to 3rd order preterminal and 2nd through 6th order terminal branches. From 22-24 to 44-46 d.p.n., a large increase in branch length confined to terminal branches of greater than or equal to 3rd branch orders was observed. As indicated by topological analysis, this length increase was probably due in part to a resorption of peripheral dendritic branches during this stage of development. From 44-46 d.p.n. to maturity, the increase of dendritic branch length was restricted to preterminal branches of low (less than or equal to 4th) branch order.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1990

Quantitative, three-dimensional analysis of granule cell dendrites in the rat dentate gyrus.

The three-dimensional organization of dentate granule cell dendritic trees has been quantitatively analyzed with the aid of a computerized microscope system. The dendrites were visualized by iontophoretic injection of horseradish peroxidase into individual granule cells in the in vitro hippocampal slice preparation. Selection criteria insured that the analyzed cells were completely stained and that only neurons with two or fewer cut dendrites in the distal portion of the molecular layer were analyzed. Twenty-nine of the 48 sampled granule cells had no cut dendrites. The granule cells had between one and four primary dendrites. Granule cell dendritic branches were covered with spines and most extended to the hippocampal fissure or pial surface. The mean total dendritic length was 3,221 microns with a range from 2,324 microns to 4,582 microns. The dendrites formed an elliptical plexus with the transverse spread averaging 325 microns and the spread in the septotemporal axis averaging 176 microns. On individual neurons, the maximum branch order ranged from four to eight and the number of dendritic segments ranged from 22 to 40. Approximately 63% of the dendritic branch points occurred in a zone that included the granule cell layer and the inner one-third of the molecular layer. The dendritic tree was organized so that, on average, 30% of the length was in the granule cell layer and proximal third of the molecular layer, 30% was in the middle third, and 40% was in the distal third. Comparisons were made between the dendrites of granule cells in the suprapyramidal and infrapyramidal blades of the dentate gyrus. Suprapyramidal cells had a significantly greater total dendritic length than infrapyramidal cells, their transverse spread was higher, and they had a greater number of dendritic segments. When neurons in the suprapyramidal blade were further subdivided on the basis of somal position within the depth of the cell body layer, superficial neurons were found to have a greater number of primary dendrites, more elliptical trees, and larger transverse spreads of their dendrites. There were no significant differences in dendritic segment number or total dendritic length between superficial and deep cells.

Animals↗
PubMed1995

A quantitative analysis of the dendritic organization of pyramidal cells in the rat hippocampus.

The three dimensional organization of the dendritic trees of pyramidal cells in the rat hippocampus was investigated using intracellular injection of horseradish peroxidase in the in vitro hippocampal slice preparation and computer-aided reconstruction. The total dendritic length, dendritic length in each of the hippocampal laminae, and the number of dendritic branches were measured in 20 CA1 pyramidal cells, 7 neurons in CA2 and 20 CA3 pyramidal cells. The total dendritic length of CA3 pyramidal cells varied in a consistent fashion depending on their position within the field. Cells located close to the dentate gyrus had the smallest dendritic trees which averaged 9,300 microns in total length. Cells in the distal part of CA3 (near CA2) had the largest dendritic trees, averaging 15,800 microns. The CA2 field contained cells which resembled CA3 pyramidal cells in most respects except for the absence of thorny excrescences on their proximal dendrites. There were also smaller pyramidal cells that resembled CA1 neurons. CA1 pyramidal cells tended to be more homogeneous. Pyramidal neurons throughout the transverse extent of CA1 had a total dendritic length on the order of 13,500 microns. The quantitative analysis of the laminar distribution of dendrites demonstrated that the stratum oriens and stratum radiatum contained significant portions of the pyramidal cell dendritic trees. In Ca3, for example, 42-51% of the total dendritic length was located in stratum oriens; about 34% of the dendritic tree was located in stratum radiatium. The amount of dendritic length in stratum lacunosum-moleculare of CA3 varied depending on the location of the cell. Many CA3 cells located within the limbs of the dentate gyrus, for example, had no dendrites extending into stratum lacunosum-moleculare whereas those located distally in CA3 had about the same percentage of their dendritic tree in stratum lacunosum-moleculare as in stratum radiatum. In CA1, nearly half of the dendritic length was located in stratum radiatum, 34% was in stratum oriens and 18% was in stratum lacunosum-moleculare. These studies identified distinctive dendritic branching patterns, in the stratum radiatum and stratum lacunosum-moleculare, which clearly distinguished CA3 from CA1 neurons.

Animals↗
PubMed1990

Anatomy of soleus alpha-motoneurone dendrites in normal cats and in cats subjected to chronic postnatal tenotomy or overload of the soleus muscle.

The anatomy of intracellularly HRP-labeled soleus alpha-motoneurone dendrites was studied both in normal adult cats ("normal soleus", NS) and in adult cats which at a postnatal age of 5-7 days had been subjected to chronic tenotomy of either the soleus muscle ("tenotomized soleus", TS), or all the soleus synergists contributing to the achilles tendon ("overloaded soleus", OS). A set of "structural rules" seemed to govern the architecture of normal soleus alpha-motoneurone dendrites. Thus, the dendrites branched dichotomously and the number of daughter branches originating from a preterminal branch was proportional to the diameter of that parent branch. Branch diameter decreased across branching points according to the "3/2 power rule" of Rall (1959). Branching occurred down to a preterminal branch diameter of about 0.8 micron. Through all branch orders there existed a quite precise relation between the diameter of a preterminal branch and the membrane area of its distal dendritic arborization. The average dendritic path distance from soma to termination was not closely related to the diameter of the stem dendrite, since thick stem dendrites rather generated more profusely branched arborizations than thin stem dendrites. As a corollary of these characteristics close relations existed between the dendritic stem diameter on one hand, and the total number of branches, combined dendritic length, total dendritic membrane area and total volume, on the other. In the OS material, the dendrites were not different from those of normal soleus motoneurone dendrites. In the TS material, the dendrites were less branched and had greater dendritic path lengths, although the relations between various size-parameters within the dendrites were not significantly altered compared with normal dendrites. It was concluded that the change in branching pattern was due to a net elimination of dendritic branches following the muscle tenotomy.

Achilles Tendon↗