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PubMed1998

Dendritic arborization and spines of the neurons of the cat and human periaqueductal gray: a light, confocal laser scanning, and electron microscope study.

Neurons of the periaqueductal gray (PAG) have an extensive dendritic tree which plays an important role in the neuronal circuits supporting the functional activities of this region. The complexity of the local circuits is increased by the occurrence of dendritic spines. We have compared the dendritic and spine organization in the cat with that of man in order to verify whether an inverse relationship exists between dendritic tree extension and spine density and complexity. Sections of cat and human PAG prepared according to the Golgi-Cox method were studied with the conventional light microscope (LM) and the confocal laser scanning microscope (CLSM). The cat PAG was also studied at the electron microscopic level. The light microscopic study provided the morphoquantitative characteristics of the dendritic arborization and spines of the multipolar and fusiform neurons of the human and cat PAG. The CLSM methodology, thanks to the three-dimensional reconstruction of the neurons and the rotation of the reconstructed images, brought into view dendritic branches and spines that could not have been observed at the LM, thereby showing a wider dendritic tree and more numerous spines. The data combined from LM and CLSM demonstrate that in both species most spiny neurons are multipolar and probably projection neurons. In man, the multipolar neurons show a more extensive dendritic tree due to a wider secondary ramification, which would seem to be balanced by more numerous spines in cat. At the electron microscopic level, axo-dendritic synapses are numerous and show symmetrical and asymmetrical junctions in equal proportions; furthermore, the great majority of the spines are in contact with synaptic boutons which contain round vesicles and make predominantly asymmetrical contacts features which indicate excitatory activity. The combined use of different techniques gave a complete picture of the dendritic tree and spines of the neurons of human and cat PAG and showed a wider dendritic surface available for the receipt of the synaptic contacts than had been reported previously. Furthermore, our findings demonstrate that the PAG dendritic spines are important and specific structures in the synaptic complex of the neuropil, suggesting that they might create a local device to modulate and integrate the afferent inputs, probably in an excitatory way. The differences observed in the two species suggest that afferent information might be handled in different ways in human and cat PAG.

Adult↗

PubMed1996

Human renal-cell carcinoma tissue contains dendritic cells.

Immune surveillance of cancer requires antigen-presenting cells which activate T cells specific for tumor-associated antigens. We show here that substantial numbers of dendritic cells, which are the most potent antigen-presenting cells, emigrate from renal-tumor explants in organ culture. Tumor-derived dendritic cells presented with all characteristics of mature dendritic cells. Dendritic cells could be identified by typical cytoplasmic projections (=veils). They expressed high levels of MHC products and of the co-stimulator CD86 (B7-2). Dendritic cells expressed the CD45RO isoform but not CD45RA. The most important point was that up to 9% of the emigrating leukocytes expressed the CD83 antigen, a specific marker for mature dendritic cells. CD83+ cells were approximately 40-fold enriched in the tumor tissue as compared to the peripheral blood. In contrast to cultured blood dendritic cells, tumor-emigrant dendritic cells had a reduced potential to capture soluble antigen, as shown by the exclusion of fluoresceinated Dextran molecules. Finally, in mixed leukocyte reactions, tumor-derived dendritic cells were able to stimulate naive T cells from cord blood, which is a unique feature of dendritic cells. This study demonstrates that genuine dendritic cells reside in or infiltrate renal-cell carcinoma tissue. The failure of patients with renal-cell carcinoma to mount an anti-tumor immune response despite the presence of professional antigen-presenting cells in the tumor tissue suggests that tumor-associated dendritic cells are suppressed in situ, in a similar way to that described for tumor-infiltrating lymphocytes.

Antigens, CD↗

PubMed2001

Quantitative analysis of the dendrites of sacral preganglionic neurons in the cat.

Quantitative analyses were performed on the dendrites and somata of 25 electrophysiologically identified preganglionic neurons (PGN) obtained from the sacral spinal cord of the cat by intracellular injection of Neurobiotin or horseradish peroxidase. Total dendritic length and surface area were measured for each dendrite. The sizes of the stem dendrites measured at their base were positively correlated with the sizes of the entire tree and numbers of end branches. Total surface area of somata and dendrites averaged 39,138 microm(2); 90.7% of that was from the dendrites. To obtain measurements of the relative contributions of PGN dendrites to specific regions of the spinal cord, the percentage of each dendrite occupying eight spinal cord regions was recorded. Sixty-three percent of the dendrites projected dorsal to their somata, whereas an average of 33.3% of dendrites were located in the white matter, most of them in the lateral and dorsolateral funiculi. The neurons within this sample formed a continuum with some neurons having a large percentage of dendrites in lamina I but little in the white matter, whereas at the other end of the continuum were cells with the reverse configuration. The intermediate neurons had dendrites in both locations. Taken together, these data indicate a heterogeneous population of PGN in the lateral band of the sacral parasympathetic nucleus.

Animals↗

PubMed1987

Relationships between ganglion cell dendritic structure and retinal topography in the cat.

The morphology of ganglion cell dendritic trees varies across the cat retina. Evidence is presented that the variation in two attributes of ganglion cell dendritic structure can be accounted for by specific aspects of the topography of the adult and developing retina. The first attribute considered was the displacement of the center of the dendritic field from the cell body in the plane of the retina. The results of this study provide evidence that most ganglion cell dendritic fields are displaced away from neighboring cells, i.e., down the retinal ganglion cell density gradient. Because of the systematic dendritic displacement locally, the centers of the dendritic fields are arranged in a more precise mosaic than are their cell bodies. The second attribute considered was the elongation and orientation of the dendritic fields. From approximately embryonic day 50 to postnatal day 10 the cat retina undergoes a process of maturation (reviewed by Rapaport and Stone: Neuroscience 11:289-301, '84) that begins at the area centralis and spreads over the retina in a horizontally elongated wave. We found that the elongation and orientation of retinal ganglion cell dendritic fields is significantly correlated with the shape of the wave of maturation. The orientation of a dendritic field is not predicted by the direction of its displacement nor is it directly related to the distribution of neighboring retinal ganglion cells. These results indicate that the displacement of a ganglion cell's dendritic field from its cell body results from mechanisms different from those responsible for the orientation of the dendritic field. Factors that may be responsible for these two attributes of ganglion cell dendritic morphology are discussed.

Animals↗

PubMed1990

Anatomy of the rat medial geniculate body: II. Dendritic morphology.

The medial geniculate body (MGB) of the rat was studied with Golgi methods to determine the distribution of neurons identified by dendritic morphology. These findings were compared with major divisions and constituent nuclei established by somatic and fiber architectonics, and by connections with temporal neocortex (Clerici et al.: Society of Neuroscience Abstracts 12:1272, 1986; 13:325, 1987; Anatomical Record 218:23, 1987; Winer and Larue: Journal of Comparative Neurology 257:282-315, 1987; Clerici and Coleman: Journal of Comparative Neurology 297:14-31, 1990). It was found that an elaboration of the prototypical scheme proposed by Morest (Journal of Anatomy 98:611-630, 1964) for partitioning the mammalian MGB is valid for characterizing the rat MGB. Two predominant categories of principal neuron dendritic patterning were identified: a bushy cell having tufted dendritic fields and a stellate cell with a radiate dendritic domain. Tufted neurons have large caliber dendritic trunks that divide profusely into daughter branches close to the soma with intertwining higher order branches that maintain a relatively restricted dendritic field. Stellate neurons typically emit primary dendrites in all directions that then divide dichotomously at wide angles at subsequent orders of branching to produce a somewhat spheroidal dendritic field. In the present study, the rat MGB is found to be a tripartite structure composed of ventral (MGv), dorsal (MGd), and medial (MGm) divisions, each uniquely characterized by constituent dendritic morphology. The paramount neuronal class of the MGv is the tufted principal cell. In the ventral and ovoid nuclei of the MGv the neuronal orientation of highly oriented bitufted cells is in register with afferent brachial axons. In the ventral nucleus, this arrangement approximates vertical with a dorsomedial tilt most prominent rostrally; in the ovoid nucleus, tufted cells adhere to the double spiraled course of afferent axons. The transition zone between ventral and ovoid nuclei contains tufted neurons that align with radially oriented fibers issuing from the junction of the ovoid and midgeniculate bundles. Bitufted neurons of the marginal zone parallel fibers at the lateral margin of the geniculate. Within the MGd the dorsal and caudodorsal nuclei are characterized by stellate cells with extensive dendritic arbors and busy neurons with dendritic branches less tufted than those observed in the MGv. The deep dorsal nucleus contains bitufted neurons that polarize with the long axis of the midgeniculate bundle and intermingle with stellate neurons. The suprageniculate nucleus includes neurons with large somata and long, sparsely branched and dorsoventrally oriented dendrites orthagonal to corticothalamic axons, as well as smaller neurons and classical stellate cells.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

PubMed1995

Morphology and dendritic domains of neurons in the lateral parabrachial nucleus of the rat.

The present study provides a description of the dendritic morphology and the dendritic domains of neurons in the lateral parabrachial nucleus (PB) of the rat. The cells were intracellularly stained in vitro with Lucifer yellow. A subpopulation of these cells was characterized beforehand as neurons projecting to the amygdaloid complex by retrograde transport with rhodamine beads. With respect to their dendritic arborization, different types of "spatially" organized PB neurons were discriminated. One major cell type in the external lateral PB (PBel) is characterized by long, elongated dendritic trees that are preferentially oriented parallel to the superior cerebellar peduncle. The majority of their dendrites appears to respect subnuclear boundaries, yet their distal dendrites often exceed the limits of the PBel to encroach upon adjacent subnuclei located dorsally and ventrolaterally to the PBel. Another prominent cell type in the PBel has fairly small and locally restricted dendritic trees that are also elongated, running with their main axis from ventrolateral to dorsomedial. The dendrites of the majority of these neurons apparently stay within the confines of the PBel. A distinct group of neurons is found in the ventral portion of the PBel. The majority of their dendrites is mediolaterally oriented and not confined to the PBel subnucleus. In addition, we found a smaller number of neurons scattered within the lateral PB whose dendrites do not show a preferential orientation but travel across subnuclear boundaries into several different PB subnuclei. Our data show that the dendrites of a large proportion of neurons in the lateral PB either stay within the confines of a particular subnucleus or slightly extend across subnuclear limits. In any case, they appear to match with terminal territories of afferent axons and, thus, maintain the functional specificity of inputs by their relay through the PB. In contrast, PB neurons that extend their dendrites across subnuclear boundaries or known terminal territories are likely to receive inputs of different qualities from a variety of sources and therefore transmit a more general, integrated signal to the forebrain.

Animals↗

PubMed2006

GABA(B) receptors inhibit backpropagating dendritic spikes in hippocampal CA1 pyramidal cells in vivo.

Spike backpropagation has been proposed to enhance dendritic depolarization and synaptic plasticity. However, relatively little is known about the inhibitory control of spike backpropagation in vivo. In this study, the backpropagation of the antidromic spike into the dendrites of CA1 pyramidal cells was studied by extracellular recording in urethane-anesthetized rats. The population antidromic spike (pAS) in CA1 following stimulation of the alveus was recorded simultaneously with a 16-channel silicon probe and analyzed as current source density (CSD). The pAS current sink was shown to sequentially invade the soma and then the apical and basal dendrites. When the pAS was preceded <400 ms by a conditioning orthodromic CA3 stimulus, the apical and basal dendritic spike sinks were reduced and delayed. Dendritic spike suppression was large after a high-intensity CA3 conditioning stimulus that evoked a population spike, small after a low-intensity CA3 conditioning stimulus, and weak after conditioning by another pAS. The late (150-400 ms latency) inhibition of the backpropagating pAS at the apical and basal dendrites was partially relieved by a GABA(B) receptor antagonist, CGP35348 or CGP56999A, given intracerebroventricularly (icv). CGP35348 icv also decreased the latency of the antidromic spike sinks at all depths. A compartment cable model of a CA1 pyramidal cell with excitable dendrites, combined with a model of extracellular potential generation, confirms that GABA(B) receptor activation delays a backpropagating spike and blocks distal dendritic spikes. GABA(B) receptor-mediated conductance increase and hyperpolarization, amplified by removing dendritic I(A) inactivation, contribute to conditioned dendritic spike suppression. In addition, the model shows that slow Na(+) channel inactivation also participates in conditioned spike suppression, which may partly explain the small dendritic spike suppression after conditioning with a weak orthodromic stimulus or another antidromic spike. Thus, both theory and experiment confirm an important role of the GABA(B) receptors in controlling dendritic spike backpropagation.

Animals↗

PubMed1992

Cytoskeletal events underlying dendrite formation by cultured pigment cells.

In contrast to neurite outgrowth, pigment cell dendrite formation is relatively unstudied. Keratinocyte-conditioned medium (KCM) induces a striking dendricity in human melanocytes and B16 melanoma cells that is detectable within 30 min, maximal in 24-48 hr, and quantifiable by computerized image analysis. Cytochalasin B (CB), known to disrupt actin microfilaments, completely blocks dendrite formation if added to cultures before or with KCM. This effect is rapidly reversible, and dendrites appear within 1 hr after refeeding with KCM alone. In contrast, CB treatment fails to disrupt existing dendrites previously induced by KCM. Agents known to cause microtubule disassembly (colchicine, nocodazole, or vinblastine) do not inhibit dendrite formation if added before or with KCM. In contrast, these agents disrupt established dendrites. Inhibition of protein synthesis with cycloheximide or actinomycin D completely blocks dendrite formation, but if cultures are provided fresh KCM lacking protein synthesis inhibitors, dendrites reappear within 24 hr. Actin microfilaments visualized with a monoclonal antibody or rhodamine-phalloidin are poorly organized in untreated cells, but form numerous fibers localized along dendrites in KCM-treated cells. Microtubules visualized with a monoclonal anti-tubulin antibody are localized in the center of dendrites. These cytoskeletal changes occur without altering beta actin or beta tubulin mRNA levels. Taken together, these data implicate actin microfilaments in dendrite outgrowth, but not in maintenance, and conversely microtubules in dendrite maintenance but not in formation. These keratinocyte-induced changes involving beta actin and beta tubulin polymerization appear to require both new protein synthesis and post-translational regulation. The observed similarities between melanocytes and other neural crest-derived cells suggest that cutaneous pigment cells might serve as an alternative model for studies of neurite outgrowth.

Actins↗

PubMed2002

Dendritic cell susceptibility to hepatitis C virus genotype 1 infection.

In vitro infection of human monocyte-derived dendritic cells was carried out to study their susceptibility to hepatitis C virus (HCV) infection. Immature dendritic cells and mature dendritic cells were incubated overnight at 37 degrees C with HCV-positive (genotype 1) serum samples; the presence of the viral genome associated with the production of its replicative intermediate was used as evidence of infection. In immature dendritic cells, HCV RNA was detectable from days 1-10 post-infection (p.i.), and de novo synthesis of negative-strand HCV RNA could be demonstrated by a strand-specific rTth reverse transcription-polymerase chain reaction at day 2. In mature dendritic cells, the positive-strand form was detectable from days 1-5 p.i., while the negative-strand HCV RNA appeared at days 1 and 2 p.i. Quasispecies present in the inoculum and 6 days p.i. were analyzed by sequencing hypervariable region 1 of the E2 protein. Only two of seven HVR variants present in the inoculum were found in HCV-infected immature dendritic cells. Another two HVR variants not found in the inoculum were recovered from infected immature dendritic cells, suggesting serum minor variants selection or virus evolution during in vitro replication. Analysis by single-strand conformation polymorphism assay of 5' untranslated region of HCV sequences showed that the patterns obtained from the inoculum and infected immature dendritic cells and mature dendritic cells differed slightly. These findings indicate that both immature dendritic cells and mature dendritic cells are susceptible to HCV genotype 1 infection, supporting at least HCV RNA replication. This model should be a valuable tool for the study of modulation of dendritic cell functions in HCV infection.

Amino Acid Sequence↗

PubMed1990

Distribution patterns of dendrites in motor neuron pools of lumbosacral spinal cord of the chicken.

The morphology of dendritic trees (dendroarchitecture) of motor neurons innervating specific hindlimb muscles (motoneuron pools, MNP) was studied in the chick spinal cord. Motoneurons were labelled by intramuscular injections of horseradish peroxidase conjugated with cholera toxin subunit B. MNPs of posterior iliotibial and femorotibial muscles were located at the dorsolateral part of lateral motor column of lumbosacral segments (LS) 1-4 and 1-3, respectively. Although the dendritic profiles of femorotibialis motoneurons were fewer than those of posterior iliotibialis, these two MNPs had a similar distribution pattern of dendrites. Dendritic profiles were about equally distributed in the gray and white matter. Dendrites from the MNP of posterior iliotibialis radiated in all directions. A large number of dendrites penetrated into the white matter, and some even reached to the subpial regions of the lateral funiculus. One array of dendrites that projected dorsomedialwards extended to the base of the posterior horn. MNPs of both the iliofibularis (LS 4-7) and caudilioflexorius (LS 6-8) had dendritic trees with similar distribution patterns. There were two main arrays of dendritic extensions; one along the dorsal, and another along the ventral border of the lateral motor column. Dendrites from the iliofibularis and caudilioflexorius motoneurons were located more frequently in the white matter than in the gray matter. A large number of dendrites extended in all directions from the MNP of the adductor muscle, which was located in the medial region of lateral motor column of LS 1-2. The distribution of dendrites from a few other MNPs was also examined.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

PubMed2002

Antigen-presenting dendritic cells in ulcerative colitis.

BACKGROUND: Antigen-presenting dendritic cells are the inducers and regulators of immune responses. Here, we have discussed the phenotype and function of dendritic cells in situ and their alteration during lymphocytapheresis in patients with ulcerative colitis. METHODS: Dendritic cells were enriched from the peripheral blood mononuclear cells by culturing with granulocyte-macrophage colony-stimulating factors and interleukin 4 for 8 days. The function of dendritic cells was evaluated in an allogenic mixed leukocyte reaction. Flow cytometry was employed to study the phenotype of dendritic cells. Lymphocytapheresis was done by a continuous flow centrifugation technique using a CS-3000 separator. Immunohistochemical methodology was employed to detect dendritic cells at the colonic mucosa. RESULTS: Peripheral blood dendritic cells had increased functional capacity, and these cells were matured and activated compared to dendritic cells from normal controls. CD83-positive activated and mature dendritic cells were found at the colonic mucosa from patients with ulcerative colitis. Lymphocytapheresis induced decreased function of peripheral blood dendritic cells in patients with ulcerative colitis. Also, the levels of inflammatory cytokines were reduced by lymphocytapheresis. CONCLUSIONS: Increased function of dendritic cells may be related to the inflammatory mucosal milieu found in patients with ulcerative colitis. Depletion of dendritic cells during lymphocytapheresis may downregulate the exacerbated immune response in patients with ulcerative colitis.

Antigen-Presenting Cells↗

PubMed1975

Purkinje cell dendritic alterations after transient developmental injury of theexternal granular layer.

To examine the influence of granule cell axons on morphogenesis of their major synaptic target, the Purkinje cell dendrites, a transient injury of the external granular layer of developing rat cerebellum was induced by injecting 10 mg/kg methylazoxymethanol acetate on postnatal days 1, 2, 3 and 4. The antiproliferative action of the drug resulted in a diminution of the mitotic population which slowed the expansion of the internal granular and molecular layers. This was followed by a reconstitution of a thicker than normal external granular layer and a late phase of extensive growth. Perturbations of Purkinje cell dendritic morphology induced by this altered timing of granule cell accumulation were studied with Golgi-Cox impregnation techniques. Systematic observation were made of a number of defined abnormalities of Purkinje cells which included somas positioned below the normal monolayer; elongated dendrites; multiple somatic dendrites; S-shaped dendrites; dendrites disoriented away from the radial direction; and portions of dendrites below the soma of origin. The results indicated that most of these 'abnormalities' occur to a small extent in normal cerebellum but that these experimental conditions induced a bias in favor of their appearance. Some dendritic abnormalities, i.e., dendrites tilted out of the sagittal plane, dendrites directed toward the white matter, and apical dendrites growing vertically between cells of the external granular layer, were not noted in normal cerebellum and we attribute these particular changes to unique developmental possibilities occuring only after a more or less severe injury. This analysis of bias in dendritic morphology subsequent to subtle developmental injury provides informat on on processes of normal development and on the genesis of phylogenetic variants of Purkinje cell morphology.

Abnormalities, Drug-Induced↗

PubMed1976

Morphological characteristics of dendrite bundles in the lumbar spinal cord of the rat.

The finding of motoneuron dendrites organized into small compact bundles in cats, monkeys and pigs suggested that a study of this phenomenon in rats should be undertaken. An analysis was performed with electron microscopy, light microscopy and Golgi methods. An extensive dendrite bundle organization was found in the sixth lumbar segment of the spinal cord. Two discrete bundles were localized bilaterally: a lateral bundle in the ventrolateral gray substance, and a medial bundle in the ventral funiculus. The lateral bundle was found to consist of longitudinally oriented dendrites, neurocytons, glial cells and capillaries. As many as 1678 closely packed dendrites were observed in the lateral bundle. The medial bundle contained dendrites directed across the midline and also longitudinally oriented dendrites. Neurocytons in the medial dendrite bundle were found singly or in clusters, and many radiating bundles of dendrites were observed projecting toward the lateral bundle. Golgi analysis confirmed that neurons in the lateral bundle had most of their dendrites oriented longitudinally. It was possible to trace several dendrites into the lateral bundle from dorsally and medially lying neurons. Electron microscopy substantiated the fact that the bundles were composed of dendrites. It also revealed numerous dendrodendritic and dendrosomatic contacts which were desmosomal in type as well as an abundance of small unidentified processes. Various functions which have been attributed to the dendrite bundles are discussed.

Animals↗

PubMed1994

Cell body and dendritic tree size of intracellularly labeled thalamocortical projection neurons in the ventrobasal complex of cat.

Fifteen thalamocortical projection (TCP) neurons from the adult cat ventrobasal complex (VB) were intracellularly labeled with horseradish peroxidase or neurobiotin and examined quantitatively. We find that cat TCP neurons share key morphological features and form one neuronal type. Previously reported variations in dendritic appearance cannot be supported by the present quantitative data. The number of dendrites varied between 4 and 13 (mean 9.1; +/- 4.0) and the total dendritic length of adult cat VB neurons varied between 9,421 and 19,646 microns (mean 13,120 microns; +/- 2,605). Linear regression analyses showed that soma diameter or cross-sectional area measurements provide a poor estimate for total dendritic length in TCP neurons. In contrast, the number of first order dendrites or the sum of first order dendrite diameters do provide a good estimate of overall TCP neuron size. This relationship is useful in predicting total dendritic length when it is not possible to reconstruct the entire dendritic tree. The mean dendritic path distance (distance from soma to the dendritic tip measured along the dendrite) was relatively constant for all neurons regardless of differences in total dendritic length or the number of branches that form the path distance.

Animals↗

PubMed1988

Morphological differentiation of embryonic rat sympathetic neurons in tissue culture. II. Serum promotes dendritic growth.

In the preceding paper, we reported that embryonic rat sympathetic neurons formed axons, but not dendrites, when they were maintained in the absence of serum and nonneuronal cells. To assess the effects of serum-derived factors on cellular morphology, cultures were initially maintained in serum-free medium while nonneuronal cells were eliminated. Subsequently some cultures were chronically exposed either to fetal calf serum (10%) or to a high-molecular-weight ammonium sulfate fraction of serum (P40 material, 500 micrograms/ml). Phase-contrast microscopy revealed that serum and P40 material did not alter neuronal survival, but did cause flattening of the somata and fasciculation of processes. When neurons exposed to serum or P40 material were injected with Lucifer Yellow, it was found that the majority (greater than or equal to 90%) had local, tapered processes that could be identified as dendrites by light microscopic criteria. These local processes also exhibited other dendritic characteristics in that (1) they reacted with monoclonal antibodies to nonphosphorylated forms of the M and H neurofilament subunits and to microtubule-associated protein 2; and (2) they had substantial amounts of RNA as determined by [3H]uridine autoradiography. Quantitative measurements of the effects of serum and P40 material on dendritic morphology revealed that (1) an 8-day exposure caused most neurons (greater than 80%) to form dendrites; (2) neurons typically had more than one dendrite (mean of 4.1 +/- 0.2 dendrites/cell after a 28-day exposure); and (3) the dendrites were relatively short with the maximum extent of the dendritic arbor being 110 +/- 13 micron after 4 weeks. Serum and P40 material did not routinely cause the formation of supernumerary axons, did not alter radial axonal outgrowth from ganglion explants, and did not significantly increase [3H]leucine incorporation. Thus, serum contains a factor (or factors) which selectively stimulates the extension of dendrites, but not axons. If such a factor were operative in situ, it could play an important role in determining the morphology of sympathetic neurons. In examining the mechanism of serum-induced dendritic growth, we found that even high concentrations (5 micrograms/ml) of nerve growth factor failed to promote dendritic growth in the absence of serum; thus, nerve growth factor by itself is not a sufficient condition for the extension of dendrites.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

PubMed1981

Development of the brain stem reticular core: an assessment of dendritic state and configuration in the perinatal rat.

The brain stems of normal newborn, 11- and 20-day-old rats were examined using Golgi techniques in the light and electron microscope. Patterns of dendritic branching and growth of brain stem reticular core neurons were analyzed by projection drawing and quantitative methods. The number of protospines and dendritic varicosities was counted on proximal and distal dendritic segments. The amount of DNA and protein in the brain stem was determined using colorimetric methods. During the course of early development, the sparsely branched reticular core dendrites extend rapidly into the neuropil. The dendritic branching of these neurons increases slightly but the number of primary dendrites remains constant. Protospine development follows a regular progression increasing in number to 11 days, then declining to 20 days as protospines are resorbed onto the dendritic surface. Dendritic varicosities often contain additional vesicles as a source of dendritic membrane and subsequent preterminal dendritic growth. The gradual decline of dendritic varicosities, first proximally then distally, indicates a shift of growth toward the distal extreme of the dendrite.

Aging↗

PubMed1984

Alterations in the postnatal development of the cerebellar cortex due to zinc deficiency. III. Impaired dendritic differentiation of basket and stellate cells.

The effects of zinc deficiency and undernutrition on the dendritic differentiation of basket and stellate cells were studied in 21-day-old rats. A morphometric analysis of the dendritic branching of basket and stellate neurons was used that took into account the cell's position in the molecular layer. Zinc deficiency and undernutrition during the suckling period impaired the dendritic differentiation of cerebellar basket and stellate cells. The effects of zinc deficiency were not due totally to the reduced food intake of lactating dams. In the lower 65-75% of the molecular layer of zinc-deficient (ZD) pups, the dendritic field area, the total dendritic length and the number of branches per interneuron were reduced by 45-61%. In the lower 50-60% of the molecular layer, undernutrition reduced the dendritic field area, the total dendritic length and the number of branches per neuron by 32-44%. A comparison of ZD and undernourished (pair-fed) pups indicated that the dendritic field area and total dendritic length of neurons of ZD animals were 43% and 30% smaller in the lower half of the molecular layer. The number of branches per neuron was not significantly different between ZD and undernourished animals. The area of the soma was unaffected by dietary treatment. A delay in the onset of dendritic differentiation and a retarded rate of dendritic growth were considered possible mechanisms for the impaired dendritic differentiation.

Aging↗

PubMed1990

Differentiation of apical, basal and mixed dendrites of fusiform cells in the cochlear nucleus.

Many studies suggest that the details of morphogenesis (e.g. the length and number of dendrites) are determined by factors extrinsic to the cell, while the basic form of the neuron (e.g. the shape of the soma and the placement of the primary dendritic trunks) is determined by intrinsic factors. The following study describes the development of the dendrites of fusiform cells in the dorsal cochlear nucleus of the hamster using Golgi-stained brains from hamsters of various ages. Two basic types of dendrites are described--apical and basal--which emanate from opposite ends of the cell body and differ in their morphology. A third type of dendrite that exits the cell laterally can create a deflection in the perimeter of the cell body altering its shape. The morphology of these dendrites is described and compared to the apical and basal dendrites. Segments of laterally extending dendrites that are near apical dendrites are qualitatively and quantitatively identical to apical dendrites (that is they branch frequently and are spine-laden) and the converse is true of the segments near basal dendrites. The results suggest that during development, whether a dendritic will be apical-like or basal-like is determined by the location of its distal segment. Thus, extrinsic factors influence the overall form of these neurons.

Animals↗