Scanning electron microscopy of the third ventricle of sheep

Summary Scanning electron microscopy of the third ventricle of sheep demonstrates areas of ciliated ependymal cells at the dorsal and middle third. The cilia of the dorsal portion of the ventricle have biconcave discs that are attached to each cilium by a slender stalk. The lower third and floor of the ventricular wall, as well as the pineal recess, are largely covered by ependymal cells that possess numerous microvilli with only a few isolated cilia scattered along cell surfaces. The infundibular recess is papillated with apical blebs of the ependymal cells that project into the lumen of the recess. Measurements of these surface elements indicate an average diameter of 0.28 for cilia, 0.10 for microvilli and 0.50 for the apical blebs of the infundibular recess. The functional significance of the regional differences in surface structures is discussed in relation to cerebrospinal fluid movement, ependymoabsorption and ependymosecretion.Supported by U.S.P.H.S. Grant NS 08171.Career Development Awardee KO4 GM 70001.     

Localization of gamma-tubulin to the basal foot associated with the basal body extending a cilium

The human oviduct epithelium primarily consists of ciliated cells and secretory cells. Solitary cilia usually extend from the apical surface of the secretory cells. We investigated the localization of -tubulin in the ciliary basal apparatus of both cell types by fluorescence immunohistochemistry and immunoelectron microscopy. In addition to basal bodies, -tubulin was identified in the lateral basal foot, especially the basal foot cap. This observation is consistent with previous observations that microtubules radiate from the basal foot and the basal foot serves as the microtubule organizing centre.     

The bovine oviduct epithelium and its secretory process as studied with the electron microscope and histochemical tests

Summary The epithelium of the bovine oviduct was studied with respect to its ultrastructural organization and histochemical features.The ciliated cells seem to undergo no changes during the sexual cycle. The nucleus is regular, the mitochondria are small and frequent. Particles resembling lysosomes are present. Except for the free surface, containing alkaline phosphatase, these cells do not present any particular histochemical characteristics.The secretory cells contain more ribonucleic acid than the ciliated cells, and the endoplasmic reticulum is better developed. This also shows changes correlated with the sexual phases, thus the cisternae are much larger during the follicular phase than during the luteal phase. The nucleus is deeply fissured, the cisternae of the ergastoplasm dipping into these fissures. The mitochondria are larger and less frequent than in the ciliated cells. Secretion granules are frequently present. They are basophilic and periodic acid-Schiff reactive. They seem not to contain glycogen. The granules undergo characteristic changes and are subsequently discharged. This process is not paralleled by any changes in the histochemical reactions studied.Tests for the demonstration of lipids, non-specific esterase, and acid phosphatase did not give information that could be correlated to the ultrastructural organization.This investigation was supported by a grant from the foundation Therése och Johan Anderssons Minne     

A light and electron microscope study of some opisthobranch eyes

Summary The retina of nudibranch eyes contains two types of large cells; pigment cells which comprise about two-thirds of the total, with unpigmented sensory cells making up the remainder. Both pigment and receptor cells carry microvilli on their distal borders, but no traces of cilia were observed among them. The cornea of the eyes of aeolid and dendronotid nudibranchs is composed of a single layer of small cells, unlike the dorids where the cornea is made up of one of more large cells. The latter contain nuclei comparable in size with those of the pigment cells in the retina, but are themselves unpigmented.The elliptical eyes ofAplysia contain three types of retinal cell; the pigment cells and two kinds of receptor cells. The ciliary receptor cells bear equal numbers of cilia (9+2) and microvilli, while the microvillous receptor cells carry long tufts of microvilli with only an occasional cilium among them. The proximal cytoplasm of the receptor cells inAplysia and the nudibranchs contains large quantities of the small spherical vesicles (averaging 660 Å in diameter) which appear to be characteristic of gastropod eyes.     

Ultrastructure of the osphradium of Aplysia californica

Summary The osphradium of Aplysia californica, a sensory organ, is a small yellow-brown epithelial patch located in the mantle cavity immediately anterior to the rostral attachment of the gill. Scanning electron microscopy reveals a round ellipsoid structure of 0.6–1 mm in diameter with a central, occasionally folded, sensory epithelium. The central area is covered with microvilli and surrounded by a densely ciliated epithelium. Transmission electron micrographs show that the columnar supporting cells in the sensory epithelium contain an abundance of apical pigment granules and microvilli. Between the epithelial-supporting cells, the putative sensory elements consist of thin neurites (0.4–1.5 m in diameter) that reach the sea-water side of the osphradium. The neurites contain many neurotubules, mitochondria, vesicles and cilia in their apices. The nerve endings originate from cell bodies up to 40 m below the epithelium or in the osphradial ganglion itself, as revealed by electron microscopy and retrograde labeling with Lucifer yellow. There appear to be two populations of putative sensory cells, a large population of heavily stained cell bodies 4–10 m in diameter and a few scattered cells of large diameter (25–60 m). Following lanthanum impregnation, septate junctions can be seen between all types of cells in the epithelium, 3–5 m below the sea-water surface. This study provides new information for further investigation of osmo- and mechanosensation in Aplysia californica.     

Sensory cells in the head skin of pond snails

Summary Several types of receptor endings were identified with scanning electron microscopy and silver-impregnation techniques in the skin of the tentacles, lips, dorsal surface of the head and mouth region of the pond snails Lymnaea stagnalis and Vivipara viviparus. Sensory endings at the tips of dendrites of primary receptor neurones, scattered below the epithelium, differ in structure, i.e., the endings exposed to the surface of the skin possess different proportions of cilia and microvilli, which vary in number, length, and packing. Type-I endings have microvilli and a few (1–5) cilia, 5–12 m in length. Type-2 endings have abundant (20–40), interwoven long (9–12 m) cilia and random microvilli. Type-3 endings show typical packing of 10–25 cilia in the form of bundles or brushes. They may be composed either of long (9–18 m) or short (2–7 m) cilia, or of both long and short ones. Microvilli here are absent. Type-4 endings have only microvilli. Two other types of skin receptors do not extend their sensory endings to the surface and can be indentified only in silver-stained preparations. Type-5 endings are branching dendrites of skin receptors cells that terminate among epithelial cells. In type-6, the sensory endings also terminate among epithelial cells but their cell bodies are located outside of the skin. In both species all skin regions examined possess the receptors of all six types differing only in their relative proportion. Possible functional roles of different receptors are discussed.     

Fine structural localization of acid and alkaline phosphatase activities in the absorbing cells of the duodenum of rodents

Summary The morphology of the absorbing cells of the duodenal villi in the mouse, the rat, the hamster and the guinea-pig is described. The polymorphism of the dense bodies is pointed out. The fine localization of acid and alkaline phosphatase is investigated and compared. In all the species, acid phosphatase activity is observed in the dense bodies, Golgi vesicles and rare smooth endoplasmic profiles. Alkaline phosphatase is localized on the microvilli, Golgi apparatus, some smooth endoplasmic cisternae and numerous dense bodies. The presence of an alkaline phosphatase reaction in the dense bodies, probably lysosomes, of the absorbing cells is discussed. It is assumed that this enzyme follows a catabolic pathway and is finally degraded in the lysosomes.Abbreviations used AlPase alkaline phosphatase - AcPase acid phosphatase This work was done thanks to the contract C.E.N./A.I.E.A. N 347/RB and thanks to grants from the Fonds de la Recherche scientifique fondamentale collective.     

A quantitative immunoelectronmicroscopic study on soluble, membrane-associated and membrane-bound lysosomal enzymes in human intestinal epithelial cells

Summary We have used quantitative immunoelectronmicroscopy to compare thein situ localization of acid -glucosidase, lysosomal acid phosphatase, -hexosaminidase and glucocerebrosidase in intestinal epithelial cells of the human duodenum. Differences between these four lysosomal enzymes were observed with respect to their presence at the apical cell surface. Transport to the apical membrane seems to be a more important intracellular route for lysosomal acid phosphatase and acid -glucosidase than it is for -hexosaminidase. The membrane associated lysosomal enzyme glucocerebrosidase is not transported to the microvilli. The studies emphasize that lysosomal enzyme transport pathways are enzyme and cell type specific.     

Structure and histochemistry of the normal intestine of the fowl. I. The mature absorptive cell

Synopsis The fine structure and cytochemistry of the intestinal epithelial cell of the fowl have been investigated. The fine structure of the mature absorptive cell of the fowl duodenum was very similar to that described for man and other mammals. Minor differences were the thinner microvillous glycocalyx, the unusual length of the cells and their microvilli, and the wide distribution of lysosomal bodies. The membrane-associated enzymes alkaline phosphatase, ATPase (pH 7.2) and leucine naphthylamidase were mainly associated with the brush border; this organelle also gave positive reactions for mucopolysaccharides and phospholipids. No enzyme activities were found in the terminal web.The distribution of lysosomes between the terminal web and the Golgi apparatus was correlated with the granular localization of the lysosomal enzymes acid phosphatase, -glucuronidase and non-specific esterase. The mitochondrial enzyme succinate dehydrogenase was seen to be localized in rod-like dots which marked the distribution of mitochondria in the absorptive cell. The localization of mitochondrial ATPase (pH 9.4) was not clearly demonstrated because of diffusion artifacts. The region of the Golgi apparatus gave a strong reaction for thiamine pyrophosphatase, together with weak reactions for acid and alkaline phosphatases after extensive overincubation.The endoplasmic reticulum-associated enzymes glucose-6-phosphatase and nonspecific esterase were distributed throughout the absorptive cell, with a maximum activity apical to the Golgi apparatus. Additionally, the jejunal absorptive cells showed endoplasmic reticulum-as well as lysosomal-associated -glucuronidase.     

Fine structural localization of alkaline phosphatase in the fracture callus of the rat

Summary The fine structural localization of nonspecific alkaline phosphomonoesterase in the different cells constituting the fracture callus in the rat was studied by incubating sections of glutaraldehyde-fixed callus tissue of variable age in media containing -glycerophosphate and either lead or calcium ions. The specificity of the reactions were tested by exposing the tissues to inhibitors of alkaline phosphatase.The results showed presence of final product on the plasma membranes and associated structures (subplasmalemmal endocytotic vesicles) of fibroblasts, pre-osteoblasts, osteoblasts, and cartilaginous cells in the callus. With the calcium method, reaction product was demonstrated in vesicular elements of the Golgi apparatus in osteoblasts and chondrocytes. Precipitates indicating presence of alkaline phosphatase activity were also observed on the membranes bordering cytoplasmic projections and fragments of cytoplasm located adjacent to enzyme-containing cells. Furthermore, the globule-shaped bodies in the matrix (Bonucci-bodies) showed evidence of alkaline phosphatase activity.The evidence obtained supported the view that alkaline phosphatase plays a role in calcification. It is suggested that transfer of cellular alkaline phosphatase to the sites of initial calcification in the extracellular matrix occurs by way of pinched off vesicular fragments of the cytoplasm and plasma membrane of osteogenic enzyme-producing cells; these structures appear to move awy from their cells of origin to form the Bonucci bodies in the matrix.     

Effects of Bone Morphogenetic Protein-2 and Transforming Growth Factor-β1 on Gene Expression of Decorin and Biglycan by Cultured Osteoblastic Cells

The influence of bone morphogenetic protein-2 (BMP-2) and transforming growth factor (TGF-) on the expression of small proteoglycans, decorin and biglycan was investigated in a clonal rat osteoblastic cell line, ROS-C26 (C26) cells, which is a potential osteoblast precursor cell line and capable of differentiating into mature osteoblasts after treatment with recombinant BMP-2 (rhBMP-2). Following the culture of C26 cells for 3, 6, and 9 days in the presence or absence of rhBMP-2, alkaline phosphatase activity increased in the rhBMP-2 treated cells in direct proportion to their differentiation into more mature osteoblastic cells, whereas decorin mRNA decreased in the cells, when compared to control cells without rhBMP-2 treatment. These results were evident 6 days after treatment. However, rhBMP-2 treatment had no effect on biglycan mRNA expression in the cells. Subsequently, after removal of rhBMP-2 from the culture media, the cells were further cultured for 24h with graded concentrations of TGF-1 (0, 0.1, 1.0, 5.0, and 10ng/ml). TGF-1 decreased decorin mRNA expression in the cells dose dependently, but did not affect their biglycan mRNA expression. Furthermore, either removal of rhBMP-2 from the culture media or addition of TGF-1 significantly decreased alkaline phosphatase activity of rhBMP-2-induced cells. These results indicate that osteoblastic differentiation is accompanied by increased alkaline phosphatase activity and decreased expression of decorin mRNA, but continuous expression of biglycan mRNA. Both rhBMP-2 and TGF-1 inhibit decorin mRNA expression in osteoblasts at varying stages of differentiation, but their effects on biglycan mRNA expression and alkaline phosphatase are different.     

Fine structural analysis of the basal epidermal receptor cells in the earthworm (Lumbricus terrestris L.)

Summary A fine structural investigation was performed on receptor cells lying at the base of the epidermis in the earthworm, Lumbricus terrestris. Two types of receptor cells with many similarities, but also with major differences, were discriminated.One receptor is of the microvillar receptor type, that appears to be identical with the photoreceptor cell described earlier by Röhlich et al. (1970). Proximal to the nucleus is a large vacuole (phaosome, Binnenkörper) with many daughter cavities containing a large number of microvilli and several cilia with the 9 × 2 + 0 microtubular pattern. The intracellular cavity has no connection with the surface membrane, in contrast to that in hirudineans (White and Walther, 1969) and pogonophores (Nørrevang, 1974).The other receptor is the ciliated receptor type, that is presently described for the first time. This receptor also has a comparatively large uniform cavity, few microvilli and about 20 cilia with the 9 × 2 + 2 microtubular pattern. The cilia leave the cell in the proximal part through a wide opening, make a turn of 180 °, and proceed toward the epidermal surface. Receptors of a similar type have been described by Golding and Whittle (1975) in the cerebral ganglion of four limicole oligochaete annelids; they presumed that these cells have an osmoreceptor function. The new epidermal receptor type described in the present investigation probably has a chemoreceptor function of hitherto unknown kind.This investigation was supported by the Royal Physiographic Society at Lund, Sweden. The author would like to express his thanks to Mrs. Lena Sandell for skilful technical assistance     

Freeze-fracture study of the receptor membranes in the olfactory organ of Alburnus alburnus (Teleostei)

Summary Olfactory receptor molecules are assumed to be integral membrane proteins which may be visualized on fracture faces of the membrane as intramembrane particles (IMPs). In the present study, the plasma membrane of the receptor dendrites and ciliated epithelial cells in the teleost fish Alburnus alburnus were studied by freeze-fracture electron microscopy. The IMP diameters on the membrane P-faces of both receptor dendrites and ciliated epithelial cells ranged from 5 nm to 11 nm. The average IMP densities on membrane fracture faces of the ciliated and microvillous sensory dendrites were 3130±780 for the cilia, 2070±550 for the microvilli, 2390±1190 on the knob regions and 3050±1130/m on the lateral dendrite membranes. The IMP densities on the P fracture faces of the cilia and knob regions were compared with the densities found on the lateral membranes of each individual dendrite. The ratios ranged from 0.5 to 0.96 in the case of the cilia/lateral membrane and from 0.5 to 0.90 in that of the knob/lateral membrane, indicating that, in contrast to the average densities, it is the lateral membrane which has the higher IMP densities and not the cilia. The great variations in the average IMP densities, as well as the considerable variety of the ratios, may be explained by the maturation and turnover of the olfactory sensory neurons.     

The fine structure of the eye of the mollusc Pecten maximus

Summary The retina of Pecten maximus is divided into two light sensitive layers forming the distal and proximal retinae. The cells from these layers have different electrophysiological responses, the distal cells giving primary off responses, and the proximal cells giving on responses. The receptor surfaces of the distal retinal cells are formed from lamellae produced by the outer membranes of flattened cilia. These cilia have a basal body, basal foot, no root system and a 9 + 0 internal filament content. Each cell gives rise to an axon from its distal side, and this process goes up to the basement membrane, which is present below the cellular lens, passes along beneath it, and joins the distal optic nerve. The receptor part of the proximal retinal cells is formed from a vast array of microvilli. Each of these cells also bears one or two cilia with a probable 9 + 0 internal filament complement and no roots. The proximal cells give rise to axons, forming the proximal optic nerve. Below the proximal retina is a reflecting layer, the argentea, and below this is a pigment cell layer.We would like to acknowledge the advice and encouragement of Professor A. F. Huxley, Professor J. Z. Young and Dr. E. G. Gray. — We would like to thank Mrs. J. I. Astafiev for drawing Fig. 1, Mr. S. Waterman for photographic help and Miss C. Martin for clerical assistance.     

Untersuchungen an der Regio olfactoria des Aals,Anguilla anguilla L.

Zusammenfassung Das Flimmerepithel von Anguilla anguilla besteht aus 4 Zellarten: Flimmerzellen, Stützzellen, Basalzellen und Schleimbecherzellen. Flimmerzellen enthalten im oberen Zelldrittel zahlreiche Mitochondrien und tragen an ihrer Oberfläche bis zu 140 Kinocilien. Die Basalkörper dieser Kinocilien haben lange Wurzelfilamente, von denen ein Teil ins Zellinnere zieht; der andere Teil verläuft parallel zur Oberfläche und verbindet benachbarte Basalapparate. — Ein Übergangsepithel verknüpft das Flimmerepithel mit dem Riechepithel. Im Riechepithel finden sich außer den Zellarten des Flimmerepithels die Rezeptoren. Bei einheitlichem Aufbau des Zellkörpers lassen sich aufgrund rein morphologischer Unterschiede der Vesiculae olfactoriae 3 Rezeptortypen unterscheiden: 1. Cilien-Rezeptor, 2. Mikrovilli-Rezeptor und 3. Pfriem-Rezeptor. — Der Cilien-Rezeptor trägt unterhalb der Vesicula olfactoria in einer Einschnürung 4–8 sensorische Cilien, die alle auf gleicher Höhe entspringen. Zwei gegenüberliegende sensorische Cilien schließen einen konstanten Winkel von 60° ein. — Der Mikrovilli-Rezeptor trägt auf seiner abgerundeten Vesicula olfactoria 30 bis 60 Mikrovilli von 0,1 m Dicke und bis zu 5 m Länge. Der Mikrovillus wird von einem zentralen, 160 Å weiten, Tubulus durchzogen. Unterhalb der Vesicula olfactoria liegen mehrere Centriolen. Die Rezeptornatur dieser Zellen wird durch ein Axon unterstrichen. — Der Pfriem-Rezeptor besitzt eine 0,8 m breite und bis zu 4 m lange Vesicula olfactoria ohne sensorische Cilien und ohne Mikrovilli. Im Lumen der Vesicula olfactoria befinden sich neben Neurotubuli auch Fibrillen von 40–50 Å Durchmesser, die gebündelt auftreten. An der Basis des Köpfchens liegen mehrere Centriolen.

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Studies of the regio olfactoria in the eel, Anguilla anguilla I. Fine structure of the olfactory epithelium

Summary The ciliary and olfactory epithelia of the olfactory folds in Anguilla anguilla were studied with the electron microscope. The ciliary epithelium is composed of ciliary cells, supporting cells, basal cells, and mucous cells. The ciliary cells contain numerous mitochondria in their apical portion and bear up to 140 cilia. The ciliary basal bodies have rootlets, some of which project towards the central part of the cell, and others parallel to the cell surface thereby connecting neighbouring basal bodies. A transitional epithelium is located between the ciliary and olfactory epithelia. The olfactory epithelium is composed of the same 4 cell types of the ciliary epithelium and besides contains three morphologically different receptor cell types: ciliary receptor cells, microvillous receptor cells, and receptors with a single rodshaped free appendage. The ciliary receptors have 4 to 8 sensory cilia which project from below the vesicula olfactoria, each forming a constant angle of about 30° with the vertical cell axis. The vesicula olfactoria of the microvillous receptors bears from 30 to 60 microvilli, each of 0.1 m diameter and up to 5 m length. Each microvillus of this receptor type contains a central tubulus of 160 Å diameter. Few centrioles are located closely to the vesicula olfactoria. The third receptor type, which has neither cilia nor microvilli, is characterised by a single rod-shaped appendage of 0.8 m diameter which projects up to 4 m above the epithelial surface. This appendage contains neurotubules and fibril bundles; some centrioles lie close to the base of the appendage.

     

Electron microscope observations on chemo- and mechano-receptor cells of fishes

Summary This paper reports on the fine structure of chemo and mechano-receptor cells found in three species of fishes (Corydoras paleatus, Cnesterodon decemmaculatus, Fitzroyia lineata).Taste cells were studied in the food-finding barbels of adult species belonging to the Genus Corydoras. They are characterized by the presence of a great amount of vesicular material concentrated at the level of the apical and medial region. Most of these cells terminate at the barbel surface by means of a cylindrical or tapered extremity devoid of sensory hairs. It was possible to observe, in some cases, the existence of short and ill defined microvilli. The basal pole of each sensory cell contacts with several sensory nerve fibers. These fibers contain mitochondria and a few vesicles.The fine structure of the olfactory neurons was studied in full-developed embryos of Cnesterodon and Fitzroyia. The olfactory sensory hairs consist of long cilia which project into the lumen of the olfactory pit. Cilia arise from the olfactory knob which is merely an apical swelling of the dendrite. The dendrite of the olfactory neuron shows profiles of small tubules, aligned parallel to its length. Near the basement membrane of the epithelium groups of axons are seen encased in the surface of the sustentacular cells.The mechano-receptor cells studied were: 1.) The sensory cells existing in the neuromasts of the lateral line system of Cnesterodon and Fitzroyia, and 2.) the receptor cells of the ampullar crests of the same species.Neuromast receptor-cells have well developed sensory hairs which consist of cilia and microvilli. It is highly probable that each receptor cell, like those of the vestibular epithelium, bears only one cilium asymmetrically located in relation to the units of the sensory process. One of the most striking characteristics of this type of cell is the existence of a high amount of vesicular material accumulated in the cytoplasm of the basal region; it is at this level that the nerve fibers take contact with the receptor cell membrane.Three main types of neuroepithelial junction are described in the neuromasts (nerve fiber deeply recessed in the cytoplasm, calyx type and knob-like ending). In these junctions the vesicular material is almost exclusively concentrated in the cytoplasm of the receptor cell, while only few vesicles are seen within the neuroplasm of the sensory fibers.The receptor cells occuring in the ampullar crests of Cnesterodon and Fitzroyia show many structural characteristics similar to those present in neuromasts' receptor cells. Like these, they bear sensory hairs consisting of several microvilli and only one cilium which is always asymmetrically located within the group of hairs. The basal region of the cell is filled with a large amount of small vesicles. Nerve endings also show vesicles but they are less in number than inside the cytoplasm of the receptor cell.Comments are made on the apparent significance of the sensory hairs. These structures are considered (in chemo-receptor cells) as devices serving to enlarge the active surface of the cell and increasing by this way the effectiveness of the whole receptive system. In mechano-receptor cells cilia and microvilli may act as levers of different mechanical characteristics which convey stimuli to the receptor-cell cytoplasm.In this paper three main types of neuroepithelial junctions connecting receptor cells with the central nervous system are described.     

Observations on the cytolemma of the olfactory receptor cell in the newt

Summary The fine structure of the cytolemma of olfactory receptor cells in the newt was studied by the freeze-fracture replica method. Two kinds of receptor cells were recognized, namely ciliated cells (ciliary type) and non-ciliated cells (microvilli type). The cytolemma of olfactory knobs as well as their processes from both types of receptor cells showed an abundance of large membrane particles 80110Å in diameter. The large square aggregation of membrane particles, 0.1×0.1 m to 0.2×0.3 m in size, consisting of 50100 cuboidal subunits, were found in the cytolemma of the dendrite. A structural model of aggregation is presented. The soma of the receptor cell revealed large pitted membrane particles about 140Å in diameter. These particles are possibly the morphologic counterpart to ionophores which have been proposed by electrophysiological studies.     

Der Feinbau des Auges der Mehlmotte,Ephestia kuehniella Zeller (Lepidoptera,Pyralididae)

Zusammenfassung Die Retinula im Ommatidium der Mehlmotte besteht aus einer wechselnden Anzahl (9–12, meist 11) langgestreckter, prismatischer Sinneszellen. Außerdem enthält jede Retinula nahe der Basalmembran im Zentrum zwischen diesen distalen Retinulazellen noch eine basale Retinulazelle. Die Längsachse der Retinula wird von der Achsenstruktur eingenommen, die aus Mikrovilli besteht. Ihr distaler Teil ist der Achsenfaden, der breitere, proximale Teil bildet das Rhabdom. Dieses erscheint im Querschnitt meist vierstrahlig gelappt, da seine Außenseite in Längsrichtung tief gekehlt ist. Der Rhabdomquerschnitt gliedert sich in mehrere Schöpfe parallel angeordneter Mikrovilli (Rhabdomsektoren); jeder Rhabdomsektor besteht aus 1 oder 2 Rhabdomeren. Die basale Retinulazelle entsendet einen kleinen Schopf von Mikrovilli in die proximale Spitze des Rhabdoms. Die distalen Retinulazellen setzen sich proximal in Neuriten fort, welche sich in Einkehlungen der basalen Retinulazelle bzw. der Tracheenendzelle einschmiegen. Jeweils eine Tracheole durchbricht zusammen mit dem Neuritenstrang einer Retinula die Basalmembran; sie verzweigt sich distal zu ca. 30 Tracheolen, die die Retinula umhüllen.Die Kristallkegelzellen grenzen distal an die Cornea; proximal laufen die Kristallkegelzellen eines Ommatidiums in einen gemeinsamen Fortsatz aus, der zwischen den Retinulazellen unmittelbar am Achsenfaden endet. — Nur das helladaptierte Auge wurde untersucht. Hierbei erscheint im distalen Teil der Retinula nur der Achsenfaden lichtdurchlässig, das Cytoplasma der Retinulazellen hingegen von Pigmentgrana durchsetzt und für Licht undurchlässig.

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Fine structure of the eye of the meal moth, Ephestia kuehniella Zeller (Lepidoptera, Pyralididae)

Summary In each ommatidium of the meal moth a retinula is formed from a varying number (9–12, mostly 11) of elongated, prismatic sense cells. In addition, a basal retinular cell is situated near the basement membrane in the center of the other (distal) retinular cells. The axis of the retinula is occupied by many microvilli forming the axial structure, the distal section of which is the slender axial thread. Proximally, the axial structure widens (to 8.5 m instead of 1 m in diameter) and is now called rhabdom. Cross sections of the rhabdom mostly look like a petaloid with four petals; this figure is due to longitudinal infoldings along the length of the rhabdom surface. The rhabdom cross section is subdivided into several brushes of microvilli (rhabdom sectors), each one being characterized by an approximately parallel arrangement of its microvilli. One rhabdom sector may be composed of one or two rhabdomeres respectively.The basal retinular cell participates in rhabdom formation through a small brush of microvilli at the proximal end of the rhabdom. Proximally, the distal retinular cells taper into slender neurites which are embedded in grooves at the surface of the basal retinular cell and the tracheal end cell respectively. One tracheole piercing the basement membrane together with the neurites of one retinula branches into about 30 tracheoles surrounding the retinula.The crystalline cone cells touch the cornea; proximally, their cytoplasm forms a point which eventually terminates amongst the distal tips of the retinular cells, immediately at the axial thread.—Our work was restricted to light adapted eyes; in this condition, light transmission in the distal part of the retinula seems to be blocked by retinular cell pigment except inside the axial thread.

Mit Unterstützung durch die Deutsche Forschungsgemeinschaft.     

Isolation,culture, and preliminary characterization of ellipsoids (sheathed capillaries of Schweigger-Seidel) of the pig spleen

Summary Whole isolated ellipsoids (sheathed capillaries of Schweiger-Seidel) of the pig spleen were explanted in Medium 199 containing 20% fetal calf serum or horse serum respectively. Cultures were kept in a gas phase of 5% carbon dioxide in air at 37°C. After about 4 days in culture the outgrowth of two morphologically different cell types was apparent. Small cells of fusiform or stellate morphology disalayed high activity of acid phosphatase. N-acetyl--glucosaminidase and -glucuronidase activity were also detectable. Furthermore these cells were highly reactive for unspecific esterase and -glutamyl transpeptidase activity. Endogenous peroxidase activity was present in the cytoplasm and in the perinuclear space. Stellate cells therefore are thought of as ellipsoid macrophages. Additional observations reported are the expression of Fc-receptors on stellate cells. They triggered the phagocytosis of opsonized test particles. The second cell type showed fibroblastic morphology. The large well spread cells did exhibit low activities of acid phophatase and N-acetyl--glucosaminidase. The other enzyme activities examined were not detectable. The nature of these cells is not well understood at present. Most likely they are constituents of the framework of the ellipsoids. No transitions between stellate cells and fibroblastic cells were found.     

The surface fine structure of the walls of cerebral ventricles and of choroid plexus in cat

Summary The surface of ependymal cells bordering the brain ventricles, and that of the epithelial cells of choroid plexuses of the cat have been investigated by means of the scanning electron microscope. The ventricle walls are entirely covered with very long and numerous cilia and no regional differences have been observed regarding their number and disposition. Among the ciliated cells dome-shaped structures are present, possibly containing nervous elements. The ependymal cells of the third ventricle floor are mainly non ciliated but the surface thereof shows numerous small microvilli. Numerous round formations are present among these cells, their nature being difficult to interpret. Also present on the floor are small cells of triangular shape with long and tortuous protrusions, tentatively identified as small neurons. The choroid plexuses have a typical sinuous structure of long tortuous villi rich in cavities and convolutions. Details of the epithelial cells covering the plexus and their surface organization are also reported.Part of these results were presented to the Septième Congrès International de Microscopie Electronique, Grenoble 1970.