An ultrastructural study of the synaptic densities,nematosomes, neurotubules,neurofilaments and of a further three-dimensional filamentous network as disclosed by the E-PTA staining procedure

Summary After the staining of nervous tissue with phosphotungstic acid in absolute ethanol (E-PTA), a selective opacification occurs at certain specific sites, while other structures, especially the plasma and intra-cellular membranes, remain electron-lucent. Among those selectively stained sites, our studies have been focussed on: (1) The dense synaptic material consisting of several presynaptic clumps, termed projections, an intrasynaptic dense line and a subsynaptic web from which fine fibrillar wisps extend into the surrounding ground substance; (2) Neurofilaments and neurotubules, the surface of which is bristled by numerous side-arms; (3) A microfilamentous network intertwines the neurotubules, the neurofilaments and the mitochondria in the dendrites and axon, and is also connected to the E-PTA dense undercoating delineating the inner aspect of the plasma membrane and to the fine wisps emanating from the subsynaptic web. A three-dimensional microfilamentous latticework is thus formed in the nerve cell processes; (4) Dense cytoplasmic inclusions, termed nematosomes, which are usually located in the ground substance of the perikaryon among or in the vicinity of clusters of ribosomes. Tiny microfilaments emanate from the peripheral strands of these bodies. The presence of basic residues in the chains of structural proteins of which consist the subsynaptic web and the nematosome is plausible, since the specificity of the E-PTA staining procedure for the detection of basic residues has previously been put forth. The occurrence of a three-dimensional microfilamentous network in the nerve cell processes led us to hypothesize that it plays a role in translocation of materials. It may provide the motive force for the axoplasmic transport, for instance, with the neurotubules, as well as, plausibly, with the neurofilaments, serving as attachment sites and guideways.Supported by grant MA-3448 from The Medical Research Council of Canada.     

THE RESPONSE OF VENTRAL HORN NEURONS TO AXONAL TRANSECTION

The morphological changes induced in the frog ventral horn neurons by axonal transection have been studied with the electron microscope. During the first 2 wk after axotomy the neuronal nucleus becomes more translucent and the nucleolus becomes enlarged and less compact. The cisternae of the granular endoplasmic reticulum vesiculate and ribosomes dissociate from membranes. Free ribosomes and polysomes are dispersed in the cytoplasmic matrix. Neurofilaments and neurotubules are increased in number. These structures appear to be important in the regeneration of the axon. It is proposed that neurotubules, neurofilaments, and axoplasmic matrix are synthesized by the free polyribosomes in the chromatolytic neuron. By the fourth postoperative week, the neurons show evidence of recovery. The cytoplasm is filled with profiles of granular endoplasmic reticulum and many intercisternal polysomes. The substances being manufactured by the newly formed granular endoplasmic reticulum are not clearly defined, but probably include elements essential to electrical and chemical conduction of impulses. The significance of these observations in respect to recent studies of axoplasmic flow is discussed.     

Flagellar elongation and shortening in Chlamydomonas. III. structures attached to the tips of flagellar microtubules and their relationship to the directionality of flagellar microtubule assembly

Two structures on the distal ends of Chlamydomonas flagellar microtubules are described. One of these, the central microbutule cap, attaches the distal ends of the central pair microtubules to the tip of the flagellar membrane. In addition, filaments, called distal filaments, are observed attached to the ends of the A-tubules of the outer doublet microtubules. Inasmuch as earlier studies suggested that flagellar elongation in vivo occurs principally by the distal addition of sublnits and because it has been shown that brain tubulin assembles in vitro primarily onto the distal ends of both central and outer doublet microtubules, the presence of the cap and distal filaments was quantitated during flagellar resorption and elongation. The results showed that the cap remains attached to the central microtubules throughout flagellar resorption and elongation. The cap was also found to block the in vitro assembly of neurotubules onto the distal ends of the central microtubules. Conversely, the distal filaments apparently do not block the assembly of neurotubules onto the ends of the outer doublets. During flagellar elongation, the distal ends of the outer doublets are often found to form sheets of protofilaments similar to those observed on the elongating ends of neurotubules being assembled in vitro. These results suggest that the outer doublet microtubules elongate by the distal addition of subunits, whereas the two central microtubules assemble by the addition of subunits to the proximal ends.     

Effect of colchicine and lumicolchicine on the ultrastructure of non-myelinated axons in autonomic nerves in cat in vitro]

The effects of colchicine and lumicolchicine on the ultrastructure of non-myelinated axons in cat autonomic nerves were studied using in vitro preparations of inferior mesenteric ganglion/hypogastric nerves. After 24 hrs of in vitro incubation with colchicine added to the medium (10 microng/ml) a significant decrease in number of neurotubules per 1 axon was observed. In the presence of a solution of alpha-beta and gamma-lumicolchicine (10 microng/ml) severe degenerative changes occured in axons and Schwann cells. At a lower dose of lumicolchicine (3 microng/ml) these changes were less frequent and the number of neurotubules per 1 axon did not differ from that in control nerves.     

The periodic association of MAP2 with brain microtubules in vitro

Several high molecular weight polypeptides have been shown to quantitatively copurify with brain tubulin during cycles of in vitro assembly-disassembly. These microtubule-associated proteins (MAPs) have been shown to influence the rate and extent of microtubule assembly in vitro. We report here that a heat-stable fraction highly enriched for one of the MAPs, MAP2 (mol wt approximately 300,000 daltons), devoid of MAP1 (mol wt approximately 350,000 daltons), has been purified from calf neurotubules. This MAP2 fraction stoichiometrically promotes microtubule assembly, lowering the critical concentration for tubulin assembly to 0.05 mg/ml. Microtubules saturated with MAP2 contain MAP2 and tubulin in a molar ratio of approximately 1 mole of MAP2 to 9 moles of tubulin dimer. Electron microscopy of thin sections of the MAP2-saturated microtubules fixed in the presence of tannic acid demonstrates a striking axial periodicity of 32 +/- 8 nm.     

On degeneration of peptidergic neurosecretory fibres in the albino rat

Three types of degenerating peptidergic neurosecretory fibres have been found in the posterior pituitary of chronically dehydrated albino rats. "Dark" neurosecretory fibres and their swellings contain neurosecretory granules, neurotubules, shrunken mitochondria and diffusely distributed fine dense material. Some swellings are filled with synaptic vesicles and/or conglomerations of dense membranes. The transitional forms exist between these fibres and extracellular accumulations of electron dense material. Synaptic vesicles, single neurosecretory granules, lipid-like droplets and lamellar bodies occur in the latter. Some neurosecretory fibres and swellings have numerous polymorphous inclusions arising due to degradation of secretory inclusions and organelles, mitochondria and neurotubules in particular. "Dark" neurosecretory elements and those with numerous polymorphous inclusions are enveloped by pituicyte cytoplasm. Sometimes the plasma membranes both of the pituicytes and neurosecretory fibres are destroyed or transformed into a multi-membrane complex. It is assumed that pituicytes may phagocytize degenerating neurosecretory elements. N urosecretory fibres with a locally dissolved neuroplasm and/or large lucent vacuoles seem to be due to axonal degeneration by the "light" type. These neurosecretory elements, the largest of them in particular, may transform into large cavities bordered by a membrane and containing flake-like material and single-membrane vacuoles. Degeneration of neurosecretory elements seems to occur mainly due to hyperfunction of the hypothalamo-hypophysial neurosecretory system.     

Fine structure of the receptors at the myotendinous junction of human extraocular muscles

The myotendinous junction of the human extraocular muscles was studied by electron microscopy. Some peculiar receptorial structures have been found in the majority of the samples examined. These structures are very small and consist of 1) the terminal portion of one muscle fibre, 2) the tendon into which it inserts and 3), within the tendon, a rich nerve arborization, whose branches are always very close to the muscle component. Only one discontinuous layer, made up of flat cells, which lack a basal lamina and often show pinocytotic vesicles, encapsules every musculo-tendinous complex. The tendinous component consists of amorphous ground substance of different electron density, of collagen and elastic fibres and is divided in compartments by ramified cells, which make an inner capsular-like covering to the nerve fibres. Three types of afferent nerve endings can be identified. One type is usually more frequent than the others, possesses a large number of neurotubules and neurofilaments and few mitochondria and is always surrounded by a Schwann cell which forms finger-like processes penetrating into the axoplasm. The second type is only partially enveloped by the Schwann cell. The axoplasm is devoid of neurotubules and contains few neurofilaments, several mitochondria and groups of small clear vesicles placed in the areas uncovered by the glial sheath. The third one is completely surrounded by the Schwann cell, but is devoid of neurotubules and neurofilaments and full of mitochondria. These morphological features correspond well with the probable role of these receptorial structures, which is to ensure very exact and precise ocular movements.     

Colchicine-binding activity and neurotubule integrity in a rat sympathetic ganglion

The colchicine-binding activity of rat superior cervical ganglia was examined. Ganglia were cooled and re-warmed in the presence of either Cu²⁺ or of metabolic inhibitors. Electronmicroscopy showed that these treatments depolymerized the neurotubules. This depolymerization of neurotubules did not affect the colchicine-binding activity of ganglion homogenates but caused a two-fold increase in colchicine-binding by whole ganglia. This suggests that colchicine binds only to depolymerized neurotubule subunits and that colchicine-binding by whole ganglia can be used as a measure of polymerization of the neurotubule protein.The major part of the colchicine-binding activity of ganglion homogenates was found in the soluble fraction and was unstable. In the absence of divalent cations, 10⁻⁴ M vinblastine stabilised the soluble colchicine-binding activity.     

Ultrastructural changes in an unciliated sensory receptor during activation of the metacestode of Hymenolepis microstoma.

The fine structure of an unciliated sensory receptor of the metacestode of Hymenolepis microstoma is described. Each receptor contains a basal body inserted into an electron dense matrix; a terminal cilium is lacking. At this stage of development neurotubules were lacking, but rapidly appeared following excystation. It is suggested that neurotubules play a role in the functioning of the putative proprioceptor.     

Electron microscope demonstration of tubulin in cilia and basal bodies of rat tracheal epithelium by the use of an antitubulin antibody

It has been previously demonstrated that both cytoplasmic microtubules and the microtubules of cilia, flagella, and sperm tail contain tubulin. Although the morphology of cytoplasmic microtubules and that of axonemes differs in cells from which they have been isolated, the tubulin of the two structures shares physical and chemical properties. In some mammalian tissues, such as tracheal epithelium, cilia and basal bodies are difficult to isolate and characterize. The use of an enzyme- labeled immunoglobulin probe would facilitate identification and in situ localization of such proteins. Tubulin prepared from porcine brain by ion-exchange chromatography and from rat brain by the method of cyclic polymerization and depolymerization with subsequent disk gel electrophoresis with SDS were injected intravenously into rabbits. The animals were intermittently bled and the antisera extracted. The specificity of the antisera was proved by indirect immunofluorescence staining of the mitotic spindle, specific blocking of spindle staining by purified tubulin and not by other proteins, staining of 3T3 cytoplasmic microtubules, single line on immunoelectrophoresis, failure of control antisera to show any of these, and precipitation of antibody with all tubulin preparations and not with actin. We have shown by electron microscopy of ciliated cells of the tracheal epithelium stained with antitubulin by the indirect enzyme-labeled antibody method that the basal bodies, outer doublets, and central pair of the cilia contain tubulin. This indicates that tubulin in microtubules of cilia and basal bodies of rat tracheal epithelium is antigenically similar to tubulin extracted from cytoplasmic neurotubules of brains from the same species and from a different mammalian species. No other axonemal structures stained with the antitubulin. Three different preparations of tubulin from pigs and rats were used to immunize rabbits. All elicited similar antisera which gave identical staining patterns. The specificity of the staining was demonstrated by the absence of staining with immune serum absorbed with purified tubulin, the absence of staining with preimmune serum, and the absence of staining if any of the reagents were omitted during the staining reaction.     

Neurotubule assembly at substoichiometric nucleotide levels using a GTP regenerating system

Tubulin derived from cold depolymerized bovine microtubules has been gel filtered to obtain a tubulin preparation with only 3% of the tubulin dimers containing exchangeable [³H]-guanine nucleotide. In the presence of acetyl-P and bacterial acetate kinase, this preparation polymerizes to form microtubules which are morphologically indistinguishable from microtubules formed in the presence of excess GTP. The extent of microtubule formation at substoichiometric nucleotide levels using the GTP regenerating system exceeds the extent of assembly obtained with excess GTP. It is concluded that the exchangeable guanine nucleotide site can be virtually unoccupied in intact neurotubules and this finding indicates that GDP can “catalyze” tubule assembly in the presence of a GTP regenerating system.     

The fine structure of a nauplius eye

Summary The nauplius eye of the cyclopoid copepod Macrocyclops albidus has been studied by means of the electron microscope. It is composed of 1 ventral and 2 dorsal ocelli. Each dorsal ocellus consists of a large, pigmented cell, 2 tapetal cells which form a hemispherical cup and are tightly packed with crystals, 9 retinula cells and 5 conjunctival cells. The retinula cells have large masses of endoplasmic reticulum, which can be found in two distinct distributional states, also numerous bodies composed of variously coiled membranes, large amounts of glycogen, mitochondria and scattered neurotubules. The light-sensitive brush borders of these cells are closely coapted and form the irregularly shaped rhabdome. Each of the 9 retinula cells sends an axon by one of three routes to the protocerebrum. In addition, a dendrite emerges from the protocerebrum, enters the ocellus and ends blindly in immediate vicinity to the rhabdome. The observations concerning the structure of the eye made in the present study have been compared to those of light microscopical investigations. Comparison of structure and probable function of the nauplius eye and other arthropod eyes has led to consideration of the probable mode of synaptic transmission between primary and secondary sensory neurons in the ocellus, i.e. between retinula cells and eccentric cell dendrite, and various morphological features that might be of importance in this connection.Supported in part by Postdoctoral Fellowship 41044 and Research Grant G-23972 from the National Science Foundation, and Research Grant HE-005129-04 from the National Institutes of Health to the Oregon Regional Primate Research Center.     

The neurotubular system of the axon and the origin of granulated and non-granulated vesicles in regenerating nerves

Summary Electronmicroscope observations have been made on compressed sciatic nerves and preganglionic afferents to the superior cervical ganglia of rats. After 6 hours, the proximal regenerating stumps of both myelinated and unmyelinated axons become filled with enlarged neurotubules and vesicles. Granulated vesicles of 750–900 Å, having a dense core become abundant in all types of regenerating axons and they increase in number after 24 hours. The vesicular material is formed by dilatation and pinching off from neurotubules. The existence of a neurotubular system within the axon, connected with the Golgi complex at the perikaryon and involved in the formation of vesicles, is postulated. The presence of granulated vesicles in all types of regenerating axons and nerve terminals is discussed in relation with their possible functional significance. The distal stumps of compressed sciatic nerves show, after 6 hours, a considerable increase in membranous material within the axoplasm mainly represented by multivesicular and lamellar bodies. This reaction, which is interpreted as being autolytic, is compared with the regenerative reaction of the proximal stump.This paper was supported by Grants of the Consejo Nacional de Investigaciones Cientificas y Técnicas and U.S. Air Force (AF-AFOSR 963—67).     

Effects of colchicine and vinblastine on neurotubules of the sciatic nerve and cholinesterases in the developing myoneural junction of the rat

Summary Colchicine (0.1 M) or vinblastine (0.01 M) was locally applied on the sciatic nerves of newborn rats. Both colchicine and vinblastine caused reversible disappearance of axonal neurotubules and appearance of increased amounts of neurofilaments at the site of application. Subsequent morphogenesis of myoneural junctions in the tibialis anterior muscle was studied after histochemical demonstration of acetylcholinesterase (AChE; E.C. 3.1.1.7) and non-specific cholinesterase (Ns. ChE; E.C. 3.1.1.8) activity in the myoneural area.Development of the postsynaptic muscle plasma membrane of the myoneural junction was arrested in the ipsilateral, but not in the contralateral control side, for a period of about three weeks following treatment with the test substances. After this delay the myoneural morphogenesis continued normally and neurotubules were seen in the axoplasm.Since disruption of neurotubules is likely to cause blockage of the intratubular axoplasmic transport system, it seems possible that the neurotrophic influence responsible for the development of the postsynaptic muscle membrane is mediated through a secretory product transported along axons intratubularly to the nerve endings.     

Studies on the transport of secretory granules in the magnocellular hypothalamic neurons

Summary The axonal flow of neurosecretory elementary granules has been studied in the paraventricular neurons of the rat (PVN), with the help of three techniques: light microscopy, radioautography after labelling with ³⁵S-L-cysteine, and electron microscopy.Colchicine treatment does not alter the uptake of ³⁵S cysteine in the PVN but the flow of labelled neurosecretory material towards the neurohypophysis is interrupted. Interruption of the axonal flow is also evidenced by the stagnation of neurosecretory granules at the periphery of the neuronal cytoplasm and by the presence of numerous axonal swellings, heavily loaded with neurosecretory granules and often containing abnormal elongated granules, surrounded by a single membrane, oriented more or less parallely to the long axis of the axons. Other cell organelles and neurotubules are not altered. The present experiments bring further evidence of the arrest by colchicine of the axonal flow of secretory granules without apparent changes of the neurotubules.This work was supported by a grant (1970/1971) from the Belgian National Fund for Scientific Research (J. F.-D), and by grant No 1120 from the Belgian National Fund for Medical Research (P. D).The authors wish to thank Mrs. A.-M. Hunninck-Couck for her devoted and skillful technical assistance, and are endebted to Dr. J. C. Heuson for kindly supplying the rats.     

Ultrastructural localization of the high molecular weight proteins associated with in vitro-assembled brain microtubules

Microtubules isolated from brain extracts by in vitro assembly (1, 19, 23) are composed principally of two tubulins and two high molecular weight proteins (microtubule-associated proteins [MAPS] 1 and 2) (2,5,7,20). Recently, it was demonstrated that in vitro-assembled brain microtubules (neurotubules) are coated with filaments (5, 7) which are similar to the filaments attached to neurotubules in situ (4, 15, 21, 24, 25), and it was suggested that the filaments are composed of the higher molecular weight MAPs (5, 7, 12). In this study, microtubules were assembled in the presence and absence of the MAPs, and thin sections of the microtubules were examined by electron microscopy. The results show that the filaments only occur on microtubules assembled in the presence of the MAPs and it is therefore concluded that the filaments are composed of the high molecular weight MAP's.     

Ultrastructure of synapses in the nucleus of the trapezoid body of the bat]

The subsynaptic structure of the synapses in the medial nucleus of the trapezoid body was studied in the bat Myotis oxygnatus. The synaptic endings in the nucleus are represented by large-cup-shaped and small loop-shaped terminations. The cup-shaped terminations are formed of large branches originating from a thick myelinated fibre after loss of myelin from it. Each branch forms a series of contacts alternating with vast enlargements of extracellular space, on the body of the cell and its processes. Large branches are filled with synaptic vesicles, neurofilaments and neurotubules, mitochondria; all these components are distributed rather regularly along the branch diameter. In fine branches of the cup the synaptic vesicles are the main and often the only component. The pattern of the cup branch changes as the distance from the main fibre increases, namely the amount of neurofilaments and neurotubules diminishes up to their disappearance, while the amount and the density of synaptic vesicles increases. The small loop-shaped treminals are different from the cup-shaped ones by the composition of the synaptic vesicles and the structure of the contact zone. In addition to agranular vesicles there are also granular ones. Both types of terminations--cup-shaped and loop-shaped ones -- are found both on the bodies and dendrites. On distal portions of dendrites the terminations are disposed in nests.     

Further ultrastructural data on the cytoplasmic nucleolus resembling bodies or nematosomes. Their relationship with the subsynaptic web and a cytoplasmic filamentous network

Summary An electron microscope study of the rat supraoptic nucleus, substantia nigra, neostriatum and periventricular preoptic area demonstrates that nematosomes are present within the perikaryon of neurons located in these structures. The latter structure may be found in close association with the subsynaptic web of axosomatic synapses. Numerous micro-filaments fan out from the nematosome and link the latter organelle to the ribosomes, the cytoplasmic membranes and the plasma membrane thus establishing an interwoven filamentous cytoplasmic network. A possible close relationship between the nematosomes and the neurofilaments and neurotubules is discussed.This work was supported by research grant MA-3448 from the Medical Research Council of Canada. The skillful technical assistance of Miss Marjolaine Thiffeault is gratefully acknowledged.     

Interaction between embryonic rat superior cervical ganglion and syngeneic heart fragments in a confronting culture

Freshly dissected 17-19 days embryonic superior cervical ganglia are confronted with 0.5 mm diameter heart fragments of the same Wistar rat. Incubation in vitro at 37 degrees C of confronting heart-ganglion pairs is carried out in Dulbecco's medium on a gyratory shaker. Fixation and staining followed after 2 hr, 1, 3 and 6 days of incubation. Histological analysis with light and electron microscopy revealed the interaction between the sympathetic ganglion and its target organ. Ingrowth of axons rich in neurofilaments and neurotubules and containing light and dense core vesicles, is observed.     

EFFECTS OF COLCHICINE ON AXONAL TRANSPORT IN PERIPHERAL NERVES

—Colchicine injected intracisternally markedly inhibited the rapid migration (300-400 mm/day) of labelled proteins in the hypoglossal and vagus nerve of the rabbit. The transport of acetylcholinesterase (EC 3.1.1.7) and choline acetyltransferase (EC 2.3.1.6) previously shown to move with the slow (5-26 mm/day) phase of axoplasmic transport in these nerves, was only partially blocked. In view of this differential effect on axonal flow, we suggest that the neurotubules, on which colchicine acts preferentially, are primarily involved in the rapid (300-400 mm/day) axoplasmic flow. After local injection of colchicine into the nerves both the rapidly migrating labelled proteins and the enzymes (AChE and ChAc) accumulated above the site of injection to the same degree as they accumulate above a nerve ligation. Since this blockage of enzyme transport occurred after concentrations of colchicine much higher than those used for intracisternal injections these findings after local injection may represent more severe effects on axonal transport systems.