The effect of antiserum against nerve-ending membranes from cat cerebral cortex on the ultrastructure of isolated nerve endings and mollusc neurons.
Explore the source record for details and available documents.
SEARCH · Search PubMed
Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.
Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.
Explore the source record for details and available documents.
Nerve fibres and their connections with chromaffin cells in the carp head kidney were studied by light and electron microscopy. Some nerve bundles entered the head kidney from the dorsal aspect along veins. Many unmyelinated axons emerged from the nerve bundles to invade the clusters of chromaffin cells, the distribution of which was restricted to the neighbourhood of the venous trunks and their tributaries. Most of the nerve endings were attached to a chromaffin cell by synaptic junctions and were generally invaginated into the cell. Some nerve endings were flattened in shape and connected with two chromaffin cells. Occasional exocytotic figures of synaptic vesicles opening into the intercellular space, or synaptic junctions along the course of the nerve fibre were observed. The percentage of the chromaffin cells supplied by nerve endings in the head kidney as a whole was similar to that in primitive amphibians. The distribution of the chromaffin cells and the frequency of their innervation suggest that carp chromaffin cells are phylogenetically similar to those of amphibians. The frequencies of synaptic connections in the carp head kidney showed regional differences. The number in dorsal portion was significantly higher than that in two ventral portions. It is suggested that chromaffin cells in the head kidney are separable into two populations: one (in the dorsal portion) shows closer and the other (in the ventral portions) less contact with nerve fibres. The fine structure of the nerve endings indicates that catecholamine secretion of carp chromaffin cells is partially modulated by nerve fibres (probably preganglionic cholinergic fibres). However, the low frequency of synaptic connections on the chromaffin cells and their distribution suggest that carp chromaffin cells are mainly modulated by the endocrine system via the bloodstream.
In addition to annulospiral sensory endings and fusimotor endings, multiaxonal nerve endings consisting of a bundle of naked axons were frequently found in the muscle spindles of the adult Chinese hamster. The multiaxonal endings were mainly distributed in the equatorial region of the nuclear bag fibers, adjacent to the annulospiral sensory endings. Terminal axons composing the endings were less than 1.5 microns in diameter and contained a significant number of clear synaptic vesicles and large granulated vesicles. Some axons formed synaptic contacts with each other and with the muscle cell surface. These structural features suggest that the multiaxonal endings are efferent in nature. They may possibly represent a temporal structure of fusimotor endings, or belong to the autonomic nerves.
In the neurosecretory nerve endings of the neurohypophysis depolarization-induced exocytosis is followed by endocytosis of vacuole-like structures with diameter similar to that of neurosecretory granules. However, it remains unknown whether the membrane of the endocytotic vacuoles is comprised primarily of retrieved secretory granule membrane, plasma membrane or of a mixture of the granule and plasma membrane. In the present paper membrane retrieval following depolarization-induced exocytosis has been studied in isolated neurosecretory nerve endings from the rat neurohypophysis. The origin of the retrieved membrane was assessed by pre-labeling the plasma membrane with an antibody against neural cell adhesion molecule, a plasma membrane specific protein. Horseradish peroxidase was used as an index of fluid endocytosis and secretion of vasopressin was measured by radioimmunoassay. Following potassium-induced depolarization, endocytotic vacuoles showed labeling with the fluid phase marker horseradish peroxidase but never showed significant neural cell adhesion molecule labeling. The time-course of endocytosis following closely that of exocytosis as endocytotic vacuoles labeled with horseradish peroxidase were only observed when the fluid phase marker was present in the extracellular medium during the period of evoked exocytosis. Our results are consistent with a model in which in neurosecretory nerve endings, after transient exocytotic fusion of the granule membrane with the plasma membrane, the granule membrane is rapidly and selectively retrieved into the nerve endings in the form of vacuoles similar in size to that of the neurosecretory granules.
Nerve cells with their very long axons and dendrites have an effective system of anterograde and retrograde transport. In the retrograde direction there is, in addition to endogeneous cell constituents, a substantial transport of exogenous material like e.g. trophic factors like NGF. We have found that molecules which bind with high affinity to receptors in the nerve teminal surface membranes (e.g. NGF, tetanus and cholera toxin, lectins) are selectively internalized and transported retrogrdely to the cell body. Although most of them are incorporated into lysosomes in the cell body, they can nevertheless exert specific signal functions in the cell (NGF). Tetanus toxin, however, is released by the dendrites and transferred trans-synaptically to higher order neurons. We suggest that this retrograde and trans-synaptic transport represents an important pathway for "trophic" signal molekules, which convey information from the target cells to the innervating neurons. The same pathways can be used by neurotoxins *tetanus toxin) and neurotrophic viruses for entering the nervous system.
Isolated nerve endings have been demonstrated to undergo saturable, covalent interactions with [3H]-dopamine under physiological conditions; and the reaction is greatly accelerated by flash photolysis with ultraviolet light. With intact nerve endings, under conditions where dopamine reuptake occurs, benztropine and cocaine (inhibitors of dopamine reuptake), but not atropine or haloperidol (a postsynaptic antagonist), prevent the reaction. The reaction also occurs in vivo following the intraventricular administration of [3H]-dopamine, the reaction being greatest with mitochondria, followed by the nerve ending and myelin. With the use of sodium dodecylsulfate-gel electrophoresis, a number of proteins of varying molecular weight were labeled, and the pattern of labeling was similar in vitro and in vivo. One protein, with a MW of about 60,000 was labeled to an exceptionally high degree. A number of protein bands showed decreased radiolabeling in the presence of benztropine, a finding which suggests that they may be associated with the reuptake site. Both the addition of ascorbic acid and unlabeled dopamine inhibited the reactivity of [3H]-dopamine, and the effects were concentration dependent. In the absence of photolysis, the reaction (3H]-dopamine to synaptic membranes attained saturation within 10 min, but with photolysis and reaction continued at a constant rate even after 20 min. The results are discussed in relation to the use of [3H]-dopamine as a photoaffinity label of the dopamine reuptake site and in relation to the nature of the reactions with and without photolysis.
Normal nociceptors are sensitized by hyperalgesic mediators such as eicosanoids and tachykinins. The possibility that these mediators contribute to hyperalgesic pain associated with neural injury was investigated by examining their effects on the excitability of injured afferent nerve endings. In amounts that sensitize normal nociceptors and are hyperalgesic in normal skin, the eicosanoids prostaglandin I2 (PGI2), and 8(R),15(S)-dihydroxyicosatetraenoic acid (8(R),15(S)-diHETE) both excited some C-fibers in chronic neuromas of rat sciatic nerve. In contrast, the selective tachykinin-receptor agonists septide and senktide did not excite C-fibers. None of the mediators affected A-fibers. We conclude that PGI2 and 8(R),15(S)-diHETE may contribute to post-injury pain and hyperalgesia by an action on injured afferent endings.
Ultrastructure of tibial nerve receptor endings was studied in two rat lines different in the threshold of the nerve excitation after decapitation and euthanasia with diethyl ether use. Interlinear diversities of shape and parameters of receptor endings and their mitochondria were established. The results obtained indicate different reactivity of rats varying in genetically determined nervous system excitation threshold to tissue respiration decrease and oxygen insufficiency on ultramicroscopic levels.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
The distribution of low molecular weight phosphotyrosine protein phosphatase (LMW-PTP) in subcellular fractions of rat brain tissue was investigated by immunoblotting analysis using anti-LMW-PTP antibody. The enzyme was detected in the 105000 g precipitate in addition to the supernatant of brain homogenate, even after the precipitate was extensively washed, and was abundant in the particulate fraction of nerve endings. Nerve ending LMW-PTP was effectively solubilized by 1% Triton X-100 or 1% deoxycholate, though the enzyme was solubilized by thorough sonication. Two forms of LMW-PTP, designated as LMW-PTP-I and -II, were separated from the nerve ending-rich fraction by chromatofocusing. Nerve endings PTP-I and -II were different in molecular weight, isoelectric point and susceptibility to activators and inhibitors. The properties of nerve endings LMW-PTP-I and -II were similar to those of cytosolic LMW-PTP-I and -II. The abundance of LMW-PTP in nerve endings as well as in the cytosol suggests that this enzyme plays an important role in synaptic function.
The enterotoxin of Clostridium perfringens type A, a channel-pore forming protein toxin, inhibited neuromuscular transmission in isolated mouse phrenic nerve-diaphragm preparation at low concentrations of calcium. We investigated immunohistochemically the localization of the binding sites of the enterotoxin in the preparation under the conditions in which the enterotoxin reduced maximally the amplitudes of the twitch tension elicited by electrical stimulations to the phrenic nerve. Under the conditions, double immunohistochemical staining of the preparation with (1) rabbit anti-enterotoxin IgG-rhodamine-labeled goat anti-rabbit IgG and (2) mouse anti-synaptophysin (one of the synaptic vesicle-specific membrane proteins)-fluorescein isothiocyanate (FITC)-labeled goat anti-mouse IgG showed that the enterotoxin binds specifically to most of the sites which were stained with anti-synaptophysin exactly in the same configurations having the shapes of the nerve endings in the endplates. The thin section electron micrographs of the enterotoxin-intoxicated preparation showed no alterations in the ultrastructure of the neuromuscular junction and the nerve endings filled with numerous synaptic vesicles. The present results, together with our previous electrophysiological findings, indicate that the enterotoxin binds specifically to the presynaptic nerve endings and inhibits neurotransmitter release at the neuromuscular junction.
Explore the source record for details and available documents.
The nerve endings of the human acetabular labrum were investigated. Twenty-three acetabular labra were obtained from 24 fresh human cadavers, stained with Suzuki's silver impregnation and an immunohistochemical technique for neurogenic specific protein S-100, and examined by light and electron microscopy. Ramified free nerve endings were seen in all specimens by silver staining, and also were observed by the immunohistochemical technique for S-100 protein. Sensory nerve end organs, such as a Vater-Pacini corpuscle, Golgi-Mazzoni corpuscle, Ruffini corpuscle, and articular corpuscle (Krause corpuscle), were observed by silver staining. Collagen fibers were scattered sparsely in the superficial layer of the labrum, and nerve endings were observed mostly in this region. Collagen fibers were sparse, and nerve endings also were observed in some regions among the collagen fiber bundles in the inner layer. Innervation of the acetabular labrum was confirmed in this study, suggesting that nerve endings in the labrum may be involved in nociceptive and proprioceptive mechanisms.
Explore the source record for details and available documents.
To discuss the significance of laryngeal sensation on various disorders of the horse, we studied the morphological and topographical characteristics of sensory structures in the laryngeal mucosa using immunohistochemistry and immunoelectron microscopy. Various sensory structures, i.e. glomerular endings, taste buds and intraepithelial free nerve endings, were found in the laryngeal mucosa by immunohistochemistry for protein gene product 9.5 (PGP 9.5) and neurofilament 200kD (NF200). Glomerular nerve endings were distributed mainly in the epiglottic mucosa; some endings were also found in the arytenoid region arising from thick nerve fibres running through the subepithelial connective tissue. Some terminals directly contacted the epithelial cells. Taste buds were distributed in the epithelium of the epiglottis and aryepiglottic fold. In the whole mount preparation, the taste buds were supplied by the terminal branching of the thick nerve fibres. In some cases, the taste buds were arranged around the opening of the duct of the epiglottic glands. The intraepithelial free nerve endings were found to be immunoreactive for substance P (SP) and calcitonin gene-related peptide (CGRP). These nerve endings were surrounded by the polygonal stratified epithelial cells in the supraglottic region, and by the ciliated cells in the subglottic region. The density of the intraepithelial free nerve endings was highest in the corniculate process of the arytenoid region and lowest in the vocal cord mucosa. The densities of CGRP- and SP-immunoreactive nerve endings in the arytenoid region were (mean +/- s.d.) 30.6+/-12.0 and 10.0+/-4.9 per unit epithelial length (1 mm), respectively and in the vocal fold mucosa, 1.1+/-0.9 and 0.8+/-0.7, respectively. Approximately one half of the CGRP immunoreactive nerve endings were immunoreactive for SP, and most SP-immunoreactive nerve endings were also immunoreactive for CGRP. Well-developed subepithelial plexus with numerous intraepithelial fibres were observed in flat or round mucosal projections that existed on the corniculate process of the arytenoid region. In conclusion, the laryngeal mucosa of the horse seems to have morphology- and/or location-dependent sensory mechanisms against various endo-and exogenious stimuli.
The occurrence and distribution of intraepidermal nerve endings in hairy and glabrous skin of the rat foot was examined in normal cases and three months after sciatic neurotomy/suture or a crush lesion. The nerve endings were visualized in cryostate sections with antibodies against protein gene product 9.5. Normal glabrous skin exhibited 23.3 endings/mm length. Neurotomy/suture cases had 6.1 endings/mm. In rats with nerve crush injury the occurrence was normal, but the intraepidermal nerve endings tended to be abnormally short and occurred mainly in the basal layer of the epidermis. In sections from hairy skin countings were not possible. Subjective evaluation indicated that the occurrence of dermal and epidermal axon profiles usually was very deficient after neurotomy/suture and essentially normal after crush. Skin samples from the contralateral side of operated animals showed a normal occurrence and distribution of nerve endings. We also noted that cases subjected to neurotomy/suture showed increased numbers of protein gene product 9.5-immunoreactive intraepidermal cells and an abnormally thin epidermis. We suggest that a highly deficient occurrence of intraepidermal nerve endings may be one factor behind the unsatisfactory restitution of the sensory function of the hand typically seen in patients subjected to neurotomy and suture.
Myotendinous nerve endings in extraocular muscles of some mammals consist exclusively of palisade nerve endings incorporated in myotendinous cylinders. There is evidence for a similar form in man, some doubt remains. The objectives of the present study were to examine the structure and distribution of nerve endings in extraocular muscles of infant and adult human material. Muscles from five infants and six adults aged 3 days to 90 years were prepared for light and electron microscopy. Nerve endings were sparse in a 4-year-old and none were present in the muscles of younger donors. They were present in all adult samples. One group of nerve endings branched from single recurrent nerve fibers and were distributed in the encapsulated tendon of single Felderstruktur muscle fibers. Terminals were varicose and shared certain characteristics of known sensory endings and were similar to those of myotendinous cylinders except that none formed neuromuscular junctions. In other myotendinous complexes capsules were fragmented and nerve endings were dispersed in tendon common to two or more muscle fibers. In the myotendon of two adult donors, a further group of endings issuing from non-recurrent nerves were unencapsulated and distributed randomly in tendon. The frequency of nerve endings varied across myotendon and in some instances, most marked in one case, large areas lacked nerve endings. Golgi tendon organs were not present. The terminals having features characteristic of sensory endings suggest a proprioceptive function, which is apparently unavailable in infancy. In mature muscles, the irregular distribution and variety of terminal form cannot be equated with those found in extraocular muscles of animals. We suggest that these features reflect an aberrant development and conclude that their capacity to fulfil an effective proprioceptive role is open to question.