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Notes: Summary In sympathectomized cats the innervation of the Achilles tendon by fine afferent nerve fibers was studied with semithin and ultrathin sections. Several different types of sensory endings of group III and group IV nerve fibers were identified. Of the five different types of endings in the group III range (T III endings), two are located within vessel walls. One of them ends in the circumference of the venous vessels (T III/VV). Its lanceolate terminals have characteristic receptor areas at their edges. The second type ends in the adventitia of lymphatic vessels (T III/LV). Its receptive areas are scattered along their terminal course. Two further group III endings ramify within the connective tissue compartments of the vessel-nerve-fascicles of the peritenonium externum and internum. One type is tightly surrounded by collagen fibrils (T III/PTic); the other terminates between the collagen fiber bundles (T III/PTgc). The latter arrangement recalls the ultrastructural relation between nerve terminals and collagen tissue in Golgi tendon organs. The fifth type innervates the endoneural connective tissue of small nerve fiber bundles (T III/EN). At least some of them come into close contact with bundles of collagen fibers which penetrate the perineural sheath to terminate within the endoneurium. The endings of group IV afferents (T IV endings) show a striking topographic relationship to the blood and lymphatic vessels of all connective tissue compartments of the Achilles tendon. They form penicillate endings which may contain granulated vesicles. In any event, they can easily be discriminated from the T III endings in the vessel walls. In close neighborhood to Remak bundles, a cell has been regularly found which fulfilled all ultrastructural criteria for mast cells. But this cell is not a mast cell proper because it is surrounded by a basal lamina (pseudo mast cell).

Notes: Summary In cats the time course of degeneration following lumbal sympathectomy was studied in the ramus communicans griseus (reg) and in the nerves to the triceps surae muscle using light and electron microscopic methods. The left lumbar sympathetic trunk including its rami communicantes was removed from L2 to S1 using a lateral approach. The animals were sacrificed between 2 and 48 days after the sympathectomy. Tissue samples were taken (a) one cm proximal to the entrance of the rcg into the spinal nerve, and (b) one cm proximal to the entrance of the nerve into the muscle belly. In the reg signs of degeneration can already be recognized in the myelinated as well as in the unmyelinated axons 48h after sympathectomy. The degenerative processes in the axons reach their peak activity at about 4 days p.o. They end a weck later. Signs of the reactions of the Schwann cells and of the endoneural cells can first be seen 2 days p.o. They are most pronounced around the 8th day p.o., and last at least up to the third week. Thereafter the cicatrization processes settled to a rather steady state (total observation period 7 weeks). In the muscle nerves the first signs of an axonal degeneration of the sympathetic fibers can be recognized 4 days after surgery. The signs of axonal degeneration are most striking about 8 days p.o. They have more or less disappeared another week later. The reactions of the Schwann cells also start on the fourth day but outlast the degenerative processes by some 8 days. Thus the degenerative and reactive processes in the reg precede those in the muscle nerves by 2 days early after surgery and by 6 days 3 weeks later. Seven weeks after surgery, fragments of folded basement lamella and Remak bundles with condensed cytoplasm and numerous flat processes are persisting signs of the degeneration. In addition to the differences in time course between the proximal and the distal site of observation, it was also noted that both the axonal degeneration and the reactions of the Schwann cells are more pronounced in the rcg than in the muscle nerve. For example there was abundant mitotic activity in the central endoneural and Schwann cells whereas we could not detect such activity in the periphery. It is concluded that the time course of degeneration and the intensity of the degenerative and reactive processes is, to a considerable extent, determined by the distance between the site of nerve section and the site from which the specimen is taken. Many of the conflicting data in the literature can be explained by this finding.

Notes: Summary Two types of electroreceptors, the ampullary and the tuberous electroreceptor (silurid knollenorgan) in the epidermis of the catfish, Pseudocetopsis spec., were investigated with semithin and ultrathin serial sections. The ampullary organ contains one or two sensory cells which are embedded in supporting cells at the base of open epithelial canals. They bear some slender microvilli on their apical surface and form several synaptic bars. The afferent myelinated nerve fiber arborizes in the connective tissue papilla and looses its myelin sheath about 30 μm below the supporting cell layer. A second thin myelinated axon occur up to the supporting cell layer. The tuberous electroreceptor organ contains one large receptor cell. Most of the cell body is exposed to the lumen of a specialized proximal canal segment and is closely covered with microvilli. A single myelinated axon looses its myelin sheath within the supporting cell layer about 1 μm before terminating as a flat calyx at the base of the sensory cell. A functional significance of the two types of receptors will be discussed.

Notes: Summary The dura mater encephali of the rat is richly supplied by myelinated (A-axons) and unmyelinated (C-axons) nerve fibres. For the supratentorial part the main nerve supply stems from all three branches of the trigeminal nerve. Finally, 250 myelinated and 800 unmyelinated nerve fibres innervate one side of the supratentorial part. The vascular bed of the dura mater exhibits long postcapillary venules up to 200 μm in length with segments of endothelial fenestration. Lymphatic vessels occur within the dura mater. They leave the cranial cavity through the openings of the cribriform plate, rostral to the bulla tympani together with the transverse sinus, and the middle meningeal artery. The perineural sheath builds up a tube-like net containing the A- and C-axons. It is spacious in the parietal dura mater and dense at the sagittal sinus along its extension from rostral to caudal and at the confluence of sinuses. Terminals of both the A- and C-axons are of the unencapsulated type. Unencapsulated Ruffini-like receptors stemming from A-axons are found in the dural connective tissue at sites where superficial cerebral veins enter the sagittal sinus and at the confluence of sinuses. The terminations of single A-axons together with C-fibre bundles mix up in their final course in one Schwann cell to build up multiaxonal units or terminations (up to 15 axonal profiles). A morphological differentiation is made due to the topography of these terminations; firstly, in different segments of the vascular bed: postcapillary venule, venule, the sinus wall, lymphatic vessel wall, and secondly, within the dura mater: inner periosteal layer, collagenous fibre bundles of the meningeal layer and at the mesothelial cell layer of the subdural space.

Notes: Summary New results as revealed by scanning and transmission electron microscopy have given us further knowledge about the structure of the olfactory region of vertebrates. With comparative studies we are now able to discuss the functional relationship of this region. In all vertebrates the olfactory cell is a primary sensory cell. The apical segment of the olfactory cell with its olfactory vesicle is involved in the formation of the olfactory border. As a rule the receptor possesses cilia or cilia-like processes. These are absent in the olfactory receptor of the shark, the microvillus receptor of the fish and the olfactory cell of Jabonsons organ of amphibians, reptiles and mammals. The odorous substances in the fish are brought to the receptor membrane by the water flow. In air breathing vertebrates a terminal film is present. This film is a product of secretion from the Bowmans glands. Gasous odorous substances must first be dissolved in the terminal film and penetrate it before reaching the receptor membrane. The cilia-like olfactory process of the fish in the proximal segment is not essentially different from the kinocilia of the supporting cell, except that they are shorter. In contrast the olfactory cell of air-breathing vertebrates form cilia-like processes with a short cilia-like proximal segment and a long and very thin distal end piece. In the amphibians and sauropsidians the end pieces can have a lenght of up to 150 μ and up to 80 μ in mammals. The olfactory vesicles with its processes undergo continuous regeneration. The olfactory epithelium of man show the same structural formation as observed in other mammals. Regressive changes in the adult can lead to a reduction in the number of sensory cells and also to a flattening of the epithelium. Morphological criteria for regenerative processes in the sensory cell structures are present. A specialized olfactory cell type has been found in some teleosts. This cell is characterized by a small pit below the olfactory border in which the cilia of the olfactory cell are redrawn. There is some evidence that this olfactory cell type may be compared with the olfactory cells in the parafollicular tubes of lamprey. The so called rod-shaped receptor in the olfactory mucosa of fishes has no axon and is therefore no olfactory cell. The same kind of cell is also present in the olfactory mucosa of airbreathing animals. We classify this cell as brush cell. Comparative electron microscopic studies reveal identical ultrastructural organization of the olfactory bulb in all classes of vertebrates, including cyclostomes and man. The size and structure of synapses in the olfactory bulb are specific for each connection type. The dark endings of the olfactory receptor cells have small axo-dendritic contacts to the bright mitral or tufted cell processes within the glomeruli. Granule cells, periglomerular cells and mitral cells interact by dendro-dendritic, dendro-axonic and somato-dendritic synaptic complexes which often have “reciprocal” arrangements. Presynaptic endings on the granule cell dendrites and somata contain a large number of small synaptic vesicles and have membrane complexes more than 0.5 μm in diameter. In the periventricular or central zone of the olfactory bulb excitatory synapses with interdigitation between the pre- and postsynaptic processes are present. We are able to give schematic representations of postulated nerve circuits with the aid of the different morphological appearances of the different synapses. The cellular composition of the taste buds of different mammals can be described from electron microscopical studies. As a rule 5 cell types which regenerate through mitosis from the basal or marginal cells can be differentiated. Only the active sensory cell forms synaptic membrane complexes. It sends rod-shaped processes into the taste pores. Growing and dying sensory cells do not possess these processes. The supporting cells surround the single sensory cell. The apical pole of the supporting cell enters the taste pore by a bundle of microvilli. Secretory granules accumulate in the apical part of the supporting cell and empty their contents into the taste pore. The terminal processes of the myelinated afferent nerve fibres form a plexus in the lamina propria and penetrate the taste bud with numerous itraepithelial branchings.

Notes: Abstract We report the first measurements of the magnetic-field penetration depth λ in the heavy electron superconductor UBe13, performed using a SQUID magnetometer. We find the temperature dependence of λ(T)-λ(0) to follow aT 2 law at low temperatures, giving further evidence of extreme gap anisotropy in this compound. We calculate the temperature dependence expected for a variety of anisotropic states, including those representing certain classes of “exotic” pairing. In general situations, the supercurrent is not parallel to the vector potential, and a more complicated field penetration takes the place of the normal Meissner effect. We argue that the data are consistent with an energy gap with point nodes on the Fermi surface but inconsistent with the large value of the Landau parameterF 1 S expected for a translationally invariant Fermi liquid with large effective mass.

Notes: Abstract Measurements of the γ-ray anisotropy of recoil-implanted52Mn ions in pure Au down to 3 mK indicate marked deviations from free-ion behavior in low applied fields. The effective hyperfine field that explains the anisotropy is found to decrease below 10 mK. Although this behavior could be a signature of a “bound” Kondon state with a lower effective hyperfine coupling constant, it is better explained as arising from a combination of Kondo and relaxation effects. The data indicate that the Mn local moment relaxation timeT 1 is comparable to or larger than the Larmor precession time of the Mn nuclei at 3 mK. Other possible reasons for an attenuated γ-ray anisotropy, such as nuclear quadrupole and second-order crystal field effects, are also considered.

Notes: Summary Scintigraphic experiments and radioactivity measurements of tissues have shown that the radioactivity of 51Cr-labelled and neuraminidase-treated rabbit erythrocytes is rapidly accumulated in liver and spleen. Sequestration of these erythrocytes by liver and spleen was demonstrated by light and electron microscopy of these tissues after perfusion of the rabbits with solutions for tissue fixation. In liver the phagocytic activity of Kupffer cells was increased after injection of desialylated erythrocytes, while in spleen a significantly enhanced number of erythrocytes was found attached to the sinusoidal walls and in the reticulum of the red pulp. It was shown by scanning electron microscopy that neuraminidasetreatment did not influence the shape of erythrocytes. Desialylated and 51Cr-labelled erythrocytes from the cow are rapidly cleared from the blood-stream with a half-life time of about 3 h. It was shown in an in-vitro test that they adsorb to surviving slices from liver and spleen derived from the same animal. The amount of radioactivity adsorbed is appreciably enhanced in the presence of homologous serum when compared with buffer only. Human neuraminidase-treated erythrocytes are agglutinated in the direct and especially in the indirect Coombs-tests. The involvement of T-antigen in this phenomenon was largely excluded. The in vitro experiments and antibody consumption tests suggest that immunoglobulins (IgG) and complement from serum may be involved in recognition and sequestration of desialylated erythrocytes by macrophages in vivo.