The fine structure of the kidney of Achatina achatina (L.)

Summary The kidney sac of Achatina achatina, the site of primary urine formation, seems to contain no direct structural analogue of the vertebrate glomerular podocytes. The nephrocytes which line the kidney sac and separate the blood from the primary urine are supported by a basal lamina which is permeable to ferritin but impermeable to colloidal gold particles (ca. 100 Å, and 80–240 Å respectively). The blood capillaries within the kidney sac are of two types, fenestrated and unfenestrated. The basal lamina which surrounds them is impermeable to haemocyanin. The nephrocytes are then, bathed apically by primary urine and basally by an ultrafiltrate of the blood. It is proposed that fluid enters the urinary space from the connective tissue by passing between the nephrocytes, perhaps through pores in the septate junctions. Other possible mechanisms of primary urine formation are discussed. The nephrocytes contain peroxisomes which may be involved in urate metabolism.The cells of the ureteral epithelium bear a lumenal microvillous border. Their lateral and basal plasma membranes are elaborately folded. These cytoplasmic folds enclose extracellular channels through which fluid is transported from the urine back into the blood.     

Die Ultrastruktur des Juxtaglomerulären Apparates des Meerschweinchens

Zusammenfassung Der Beweis für das Vorkommen von Sekretgranula in den epitheloiden Zellen des Meerschweinchens ist bisher von keinem Autor erbracht worden. Ihre Abwesenheit ist um so erstaunlicher, als die Renin-Aktivität in der Niere dieses Tieres etwa 1/10 der der Ratte mit ihren stark granulierten Epitheloidzellen beträgt und die des Menschen sogar übertrifft. In unserem Untersuchungsgut finden wir hin und wieder einige wenige, wahrscheinlich Renin enthaltende Granula (Abb. 1–4). Anscheinend erfolgen Synthese und Ausscheidung des Enzyms im gleichen Rhythmus; zu einer geringgradigen Speicherung kommt es offenbar nur unter bestimmten funktionellen Bedingungen.Die Goormaghtighschen Zellen (Abb. 5) zeigen kein besonderes auffälliges artspezifisches Verhalten.An der Macula densa wird erstmals eine starke Erweiterung sowohl der intracytoplasmatischen Einfaltungen des basalen Plasmalemms — des basalen Labyrinthes — als auch der Interzellularspalten beschrieben (Abb. 6–9). Diese oberhalb der Basalmembran gelegenen Pseudovakuolen sind somit extrazellulär und möglicherweise als morphologisches Äquivalent einer starken Reabsorptionstätigkeit zu deuten. Es ist zur Zeit noch nicht entschieden, ob sie mit der von uns angewandten Präparationstechnik auch bei anderen Tieren und beim Menschen darstellbar sind.

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Summary The presence of secretory granules in the epithelioid (juxtaglomerular) cells in the media of the preglomerular portion of the afferent arterioles in the kidney of the Guinea pig has not been proven by any author until now. The absence of these granules is all the more astonishing in view of the fact that the renin activity of this animal is about 1/10 of that of the rat — with its highly granulated cells — and even surpasses that of humans. In our inbread strain rare granules likely containing renin can be found from time to time (Fig. 1–4). Apparently, the synthesis and extrusion of the enzyme takes place with the same rhythm; a very low degree of accumulation occurs probably only under certain functional conditions.The Goormaghtigh Cells (Fig. 5) show no noticeable differences specific for the Guinea pig. In the Macula densa highly developed enlargements of the basal infoldings of the plasma membrane — basal labyrinthe — as well as of the intercellular spaces are described for the first time (Fig. 6–9). These enlargements (Pseudovacuoles), situated above the basement membrane, are extracellular and can possibly be interpreted as the morphological equivalent of a high degree of absorption activity. At the present time it has not been decided, if, using the authors' technique, these enlargements can be demonstrated in other animals and humans.

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In Zusammenarbeit mit dem Pharmakologischen Institut der Universität Lausanne und mit Unterstützung durch die Fritz Hoffmann-La Roche-Stiftung zur Förderung wissenschaftlicher Arbeitsgemeinschaften in der Schweiz.     

Neurosecretion in the basommatophoran snail Bulinus truncatus (Gastropoda,Pulmonata)

Summary The neurosecretory system of the freshwater snail Bulinus truncatus was investigated. With the Alcian blue-Alcian yellow (AB/AY) staining method at least 10 different types of neurosecretory cells (NSC) were distinguished in the ganglia of the central nervous system. The differences in staining properties of the NSC — with AB/AY the cells take on different shades of green and yellow — are borne out at the ultrastructural level: the NSC types contain different types of neurosecretory elementary granules.The neurosecretory system of B. truncatus is compared to that of Lymnaea stagnalis, the species which has received the most attention among the pulmonates. It appears from the comparison that the systems of both species show many similarities, although some differences are also apparent.     

Monoamine precursor uptake in ganglia of a mollusc Anodonta cygnea L. (Bivalvia)

Summary In vitro-uptake and localization of ³H-5-hydroxytryptophan and ³H-dihydroxyphenylalanine have been investigated by means of light microscopic autoradiography in the central nervous system of the freshwater mussel, Anodonta cygnea L. Accumulation of the labelled monoamine precursors could be observed both over neuronal perikarya and neuropil in the ganglia. ³H-5-hydroxytryptophan and ³H-dihydroxyphenylalanine were taken up by neurons characterized by a small size (10–20 m), a polygonal form and an intense staining with toluidine blue. Labelled axon branches situated either in the neuropil or between nerve cells in the cortex exhibited only a moderate activity, frequently of a diffuse character.After pretreatment for 24 h with colchicine, silver grains were also seen over the neuronal perikarya and some axon profiles. This shows that local uptake of the monoamine precursors and, presumably, the synthesis of the monoamines takes place both at perikaryal and axonal/terminal level.The nerve cells accumulating the monoamine precursors contain a nucleus with rich chromatin content and a deeply invaginated nuclear envelope. Further ultrastructural characteristics of these neurons are their well-developed rough endoplasmic reticulum system, a great number of mitochondria and glycogen granules, and the presence of dense-cored vesicles of different types. All these features are responsible for the electron-dense appearance of the cytoplasm.     

Über die Neubildung von Mitochondrien: Elektronenmikroskopische Untersuchungen an Spermatiden von Eisenia foetida (Annelidae)

Zusammenfassung Elektronenmikroskopische Befunde sprechen für die de novo — Biogenese von Mitochondrien in den Spermatiden des Regenwurms (Eisenia foetida) zu Beginn der Spermiohistogenese. Es lassen sich zwei Entstehungsorte und -arten unterscheiden: An der Kernmembran — und zwar im Bereich des prospektiven Schwanzendes — bilden sich die künftigen sechs Mittelstücksmitochondrien aus, im Grundcytoplasmaohne erkennbare Bevorzugung bestimmter Regionen— differenzieren sich die übrigen Mitochondrien. Die Mitochondrienmatrix entsteht offenbar unter Mitwirkung eines granulären, aus dem Kernraum in das Cytoplasma gelangenden Materials. Hierbei löst sich die Kernmembran temporär und lokal begrenzt auf oder zerfällt in Fragmente. In einer diffus begrenzten, relativ elektronendichten Matrix, der Mitochondrien-Anlage, kommt es zur Neubildung von Mitochondrienmembranen, die eine Substruktur aus 45–60 Å messenden Untereinheiten erkennen lassen. Wider Erwarten treten zunächst die Membranen der Cristae und erst anschließend die der Hülle in Erscheinung. Eine Membransynthese aus einem vorgegebenen rimer wird diskutiert.

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On the de novo biogenesis of mitochondria: Electronmicroscopical observations on spermatids of Eisenia foetida (Annelidae)

Summary Electronmicroscopical observations on spermatids of Eisenia foetida demonstrate a de novo biogenesis of mitochondria in cytoplasm. There are two kinds of differentiation: The later mitochondria of the middlepiece originate in the prospective tailside attached to the outer nuclear membrane; the other mitochondria differentiate in the cytoplasm without obvious preference of particular regions. The mitochondrial matrix is formed in connection with a granular material, which is transferred from the nucleus to the cytoplasm. At the places of transference the nuclear membrane breaks up into fragments. In a matrix which is diffused in the beginning new membranes originate, in which a substructure of subunits of 45–60 Å can be discerned. The outer mitochondrial membrane is built up after the cristae. A synthesis of membrane in connection with a given primer is discussed.

     

Acute treatment with tumour necrosis factor-α induces changes in protein metabolism in rat skeletal muscle

Acute treatment of rats with recombinant tumour necrosis factor (TNF-) caused an enhanced proteolytic rate —measured as tyrosine released in the presence of cycloheximide — insoleus muscle (34%). The cytokine treatment also decreased the rate of protein synthesis in this muscle (22%) while it had no effect upon the same parameter inextensor digitorum longus (EDL) (26%) muscle. In addition, treatment of rats with TNF- increased amino acid uptake by transport system A in the incubated muscles both insoleus (45%) andEDL (99%) in the presence of insulin in the incubating medium. This effect was not associated with a direct action of TNF on muscle since the addition of different concentrations of the cytokine to the preparations did not alter the uptake of -(methyl)-aminoisobutyric acid by the incubated muscles. It can be concluded that acute TNF- treatment causes changes in protein metabolism in red-type muscles — suchsoleus — while little effects are seen in white-type muscles — such as EDL. The results presented may, to some extent, be related to the cachectic response associated with cancer and inflammation.     

Histochemische Studien an den Plexus chorioidei,an der Paraphyse und am Ependym von Rana temporaria L.

Zusammenfassung Die Epithelzellen der Plexus chor. ventr. III und IV, das Paraphysenepithel und das Ventrikelependym von Rana temporaria L. zeigen eine deutliche — wenn auch quantitativ unterschiedliche — Aktivität von SDH, -HBDH und LDH. Der Nachweis einer UDPGGT-Aktivität fällt dagegen nur im Plexusepithel positiv aus. In der Plexusepithelzelle sind die Formazangranula gleichmäßig über das gesamte Plasma verteilt, während sie in den Ependymzellen vorwiegend im apikalen, lumenwärtigen Teil der Zelle angeordnet sind. Die Ependymzellen lassen im Reaktionsausfall Typenunterschiede erkennen. Bei einigen Tieren wird die Auswirkung einer Adrenalininjektion auf das Enzymmuster der Plexusepithelzellen untersucht; die funktionellen Zusammenhänge mit einer gleichzeitigen Entspeicherung ihres Glykogenvorrats werden erörtert. Die Verteilung und der Lamellierungstyp der Mitochondrien im Plexus- und Paraphysenepithel werden mit elektronenmikroskopischen Aufnahmen illustriert. Einige Komentare sind dem histochemischen Verhalten des Wundrandes gewidmet.

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Histochemical studies on the choroid plexuses, the paraphysis cerebri, and the ependyma of Rana temporaria L.

Summary The epithelium of the choroid plexuses of the IIIrd and IVth ventricles as well as the paraphyseal epithelium and the ventricular ependyma cells of Rana temporaria L. show distinct activities of SDH, -HBDH and LDH, that differ quantitatively. The UDPGGT-reaction is positive in the plexus epithelium. In the epithelium of the choroid plexus, the formazan granules are evenly distributed in the cytoplasm. In the ependyma cells an apical accumulation of this material can be demonstrated. The various morphological types of the ependyma cells differ in the intensity of the SDH, -HBDH and LDH-reactions. In the plexus cells of some animals the effect of epinephrine was studied on the histochemically-detectable activity of these enzymes with respect to the simultaneous depletion of the glycogen depot. The distribution and ultrastructure of mitochondria is described in the choroid plexus and paraphyseal epithelial cells. A comment is made in reference to some histochemical pecularities of stab wound areas.

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Teil einer medizinischen Doktorarbeit.

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Mit Unterstützung durch die Deutsche Forschungsgemeinschaft.     

The fine structure of the mesonephros of the lamprey,Entosphenus japonicus Martens

Summary The fine structure of the mesonephric kidney of the lamprey, Entosphenus japonicus Martens, has been investigated with the electron microscope and discussed from the viewpoint of comparative morphology of the mesonephros.The structure of the capillary wall of the glomerulus essentially coincides with that of higher vertebrates, though its basement membrane is remarkably thick (300–400 m) because of a dense accumulation of fibrillar material between the endothelium and the basal lamina of epithelial cell. No obvious fenestration of the endothelial cell has been observed in the glomerulus or capillaries in any part of this organ.The kidney tubule is divided into three segments: 1. neck segment composed of ciliated cells with numerous mitochondria and glycogen particles, 2. proximal tubule composed of brush bordered cells provided with extensive pinocytotic vesicles and lysosomal granules in the apical cytoplasm and with lamellar membranes in the basal, and 3. distal tubule characterized by cells which, with their abundant mitochondria and branched tubular endoplasmic reticulum (about 500 Å diameter) with a central core, closely resemble the chloride cells in the gill filament of some teleosts. The possibility that the lamellar membranes in the proximal tubule cells correspond to basal infoldings is discussed.The extensive development of the tubular reticulum and of the mitochondria in the distal tubule cells is believed to reflect the active absorption of urine chloride in the urinary tubule of lamprey mesonephric kidney evidenced by physiologists. The proximal tubule is suggested to take a part also in the urinary transport of water and ions, as the lamellar membranes found in the cells of this portion likely correspond to the basal infoldings in more advanced forms of the kidney.The epithelial cells of the ureteric duct are characterized by granules suggesting a mucous secretion. No fine structure implying an absorptive activity in this duct has been observed.     

Granulated folliculo-stellate cells and growth hormone cells immunostained with anti-S 100 protein serum in the pituitary glands of the goat

Summary Goat pituitary glands were immunohistochemically studied with antisera for bovine S-100 protein, rat LH, FSH, TSH, prolactin, ovine GH, and porcine ACTH^1–39 by use of the superimposition technique on adjacent sections. Folliculo-stellate (F-S) cells were divided into two categories on the basis of ultrastructural properties: One consisted of a mass of agranular cells in which the pseudolumina were equipped with microvilli and cilia. Elongate gap junctions were often observed among these cells. The other was a group of granulated cells with or without pseudolumina. In this group the gap junctions were shown to be disintegrated. The dense granules 150–250 nm in diameter began to accumulate in the cells. However, neither type of these F-S cells was immunostained for S-100 protein. On the other hand, numerous polygonal, elongate, irregular or stellate cells containing S-100 protein were distributed throughout the gland. Most of them were immunohistochemically identical with the GH cells laden with the secretory granules 250–450 nm in diameter, but some of them were identical to TSH and prolactin cells which immunostained faintly for S-100 protein. This appears to be the first demonstration of GH cells intensely immunostained for S-100 protein.     

Food dependent color patterns inThamnocephalus platyurus Packard (Branchiopoda: Anostraca); a laboratory study

Coloration of phyllopods varies from place to place and from one life stage to another. It ranges from translucent or whitish through gray, blue, green, orange, and reddish. Here, we present experimental evidence for a food- dependent color pattern inThamnocephalus platyurus Packard. The presence or absence of the synthetic pigment trans — — carotene in a baker's yeast diet was the controlling factor. All the 24 old larvae used in the experiment were whitish in color. From day 6 until the end the experiment (day 11), 100% of the shrimps under a diet with synthetic trans — — carotene (treatment 1) exhibited a characteristic color pattern which consisted of an orange color in the cercopods, and in all theracopods; the rest of the body exhibited no particular color. In comparison, 100% of the shrimps under a diet without synthetic trans — — carotene (treatment 2) were whitish throughout the body. In females from treatment 1, the ovaries and oocytes were green-bluish, while in females from treatment 2 the ovaries and oocytes were whitish. No significant differences in survival and growth were found, except that at day 9, there was a significant difference in growth, the females with the synthetic trans — — carotene group growing faster.     

Corynebacterium glutamicum: morphological and ultrastructural changes of l-lysine producing cells in continuous culture

Summary Corynebacterium glutamicum was observed to undergo several morphological and ultrastructural changes during a shift in dilution rate when grown in phosphate-limiting continuous culture. At 0.1 h^–1 the cell culture appeared homogeneous and the average diameter of cells and the cell length was approximately 0.7 m and 1–1.5 m respectively. At 0.04 h^–1 there was essentially no change in these readings, but at this dilution rate there was a significant proportion of cells that measured three times the original length. At six residence times the elongated cells were increasing in number, but these changes occurred without diminishing the system's performance. Some changes in cell ultrastructure were observed during the shift in dilution rate. Thus, the presence of polyphosphate granules and of glycogen appeared in the cytoplasm of producing cells (0.04 h^–1). We have confirmed by mass spectrometry the absence of poly--hydroxybutyrate (PHB) in C. glutamicum.Correspondence to: N. Coello     

Small-sized euryhaline fish as intermediate hosts of the digenetic trematodeCryptocotyle concavum

Cercariae of the trematodeCryptocotyle concavum, which encyst in skin and/or kidney of sticklebacks and gobies, were studied in the Schlei Fjord (western Baltic Sea). Mean incidence of dermal cysts was 48 % inGasterosteus aculeatus and 37 % inPungitius pungitius. No cysts were found in the kidneys of sticklebacks. While 97 % ofPomatoschistus microps had encysted metacercariae in the kidneys, only 2 % had cysts in the skin.Pomatoschistus minutus, however, showed hardly any cyst infestation of either skin or kidney. InP. microps the intensity of infestation by metacercariae was frequently more than 50 cysts; in contrast, sticklebacks rarely exhibited more than 5 dermal cysts. Infested fish were larger than 10 mm in total length, the incidence rate increasing with growth. Parasitic infestation depends on ambient salinity:C. concavum was not found at salinities below 4 . In contrast to the high incidence in fish, the first hosts — the snailsHydrobia stagnalis andH. neglecta — showed remarkably low infection rates (3 to 5 %). The findings reported are related to the distribution ofC. concavum, the mode of life of infested fish, the feeding habits of the final hosts and the infestation ofP. microps by other parasites. Evidently,P. microps represents an optimal second host forC. concavum.     

Effect of Exogenous Glucose on Photosynthesis in the Diatom Thalassiosira weissflogii Depending on Nitrate Nitrogen Supply and Illumination

The rate of photosynthetic carbon fixation (P) in the diatom Thalassiosira weissflogii cultivated in the presence of exogenous glucose in the medium (0–10.56 g C/l) at different levels of illumination—25, 50, and 100 E/(m² s)—was studied as a function of nitrate nitrogen supply. In the diatoms limited in nitrogen and assimilating exogenous glucose, P was found to decrease or increase depending on the light intensity, glucose concentration, and the duration of exposure. In the diatoms assimilating both nitrate nitrogen and glucose, compared to those supplied with nitrates alone, P was higher at the medium and high light intensities and lower at the low light intensity. The interrelation of the processes of carbon and nitrogen metabolism in mixotrophic algae and the ecological role of glucose uptake by phytoplankton are discussed.     

Cell multiplication and ultrastructure ofMicrasterias denticulata (Desmidiaceae) grown under salt stress

Cells ofMicrasterias denticulata Bréb. were kept in nutrient solution of high osmolality (salt stress) for four weeks. In a special cell multiplication test it was established that cell division is gradually inhibited at increasing salt concentrations and totally arrested at the highest concentration (26 mosm/kg). Recovery studies proved that even cells from the highest concentration range start dividing immediately after being placed in aqua bidest. thus indicating the full reversibility of the inhibiting effect. — Cells of the highest concentration range show marked ultrastructural changes. Besides an enormous accumulation of starch and oil bodies and a condensed appearance of the ground plasma, a reduction of mitochondria, ER and the Golgi-system is found. The most striking effect occurs on the vacuolar system which appears extremely reduced and condensed. The cell wall is thickened by the formation of an additional cell wall layer with a spongy electron microscopical appearance. Through the cell wall many droplets of a probably fat-like substance are excreted. — In summary, salt stress induces growth-inhibited akinete cells in the sense ofFritsch; these can be reactivated by decreasing the salt concentration. The salt-induced akinete state seems to be an ecological adaption to unfavourable conditions rather than a degeneration of the cells.Dedicated to Prof. DrLothar Geitler on the occasion of his 90th birthday.23. 12. 1988     

Ultrastructure and potential significance of cerebral light-refracting bodies of Stenostomum virginianum (Turbellaria,Catenulida)

Summary Light-refracting bodies, possibly photoreceptors, occurring in the posterior lobes of the brain are considered characteristic for most species of catenulid turbellarians of the freshwater genus Stenostomum. In S. virginianum, each of two light-refracting bodies consists of a single cup-shaped granule (3–4 m) situated in the perikaryon of a single nerve cell (the clear vesicle of earlier papers). TEM reveals each granule as an enlarged and folded mitochondrion with a dense matrix inclusion of undetermined composition. Cristae are well-developed and there is a dense granular extramito-chondrial layer of uniform thickness (100 nm) along the posteromedial surface of the mitochondrion. The perikaryon is packed with ribosomes, -glycogen granules and 60–100 nm dense-cored vesicles. A neurite extends from the perikaryon into the neuropile of the brain. Experimental data indicate an absence of phototaxis and photokinesis and an absence of ultrastructural modifications with light- and dark-adaptation. An ultrastructural comparison is made of the light-refracting bodies of S. virginianum with those of a second species. Hypotheses regarding the role of light-refracting bodies as photoperiodic receptors and/or specialized neurosecretory cells are advanced.This study was supported in part by a National Science Foundation grant DEB-7823395 and a Clemson University Faculty Research Grant to E. Ruppert     

Specific binding of kainic acid to purified subcellular fractions from rat brain

The subcellular distribution of kainic acid (KA) binding sites in rat brain has been studied using a microcentrifugation assay. KA did not bind to myelin or brain cytosol and had few or no binding sites in the nuclear fraction. However, it bound to microsomal components (K _d =128–136 nM; 2.5–4.8 pmol/mg protein), purified synaptic plasma membranes (SPM) (K _d =45–71 nM; 5.8–6.5 pmol/mg), and purified cell-body and intraterminal mitochondria (K _d =11–31 nM; 0.4–1.1 pmol/mg). Bound KA could be totally displaced byl-glutamate orl-aspartate, but several putative antagonists of these amino acids (nuciferin, compound HA-966, 2-amino-4-phosphonobutyrate, and 2-amino-3-phosphonoproprionate) failed to displace KA or did so at very high concentrations (4 mM). Glutamic acid diethyl ester (GDEE) andd,l--aminoadipate (-AA) were more effective (IC₅₀, 0.2–0.8 mM) and showed differential effects in their capacity to displace KA bound to the various subcellular fractions. Thus, GDEE only displaced 40–60% of the KA bound by SPM or mitochondria and did not prevent the binding of KA to microsomes. -AA, on the other hand, was more effective in preventing the binding of KA at high concentrations and displaced between 80 and 100% of the drug. Both compounds showed biphasic curves of KA displacement from synaptic plasma membranes and mitochondria. The overall results indicate the presence of multiple binding sites for KA in brain cells and suggest that KA does not act exclusively at synaptic glutamate receptors. The mechanism of KA action is most likely quite complex, and the drug probably acts at multiple binding sites affecting a number of processes.     

Structural organization of two fast,rhythmically active crustacean muscles

Summary The organization of the flagellum abductor muscle and of a scaphognathite levator muscle of the green crab, Carcinus maenas, has been compared quantitatively using light and electron microscopy. These muscles are rhythmically active at relatively high frequencies and for long durations. Fibers of both muscles are interconnected to form fascicles of 50 or more fibers within which there is cytoplasmic continuity. A single muscle is made up of 8–12 fascicles. Individual fibers consist of a peripheral rind of densely packed mitochondria, a thick region of glycogen granules, and myofibrils arranged into scattered central islands. Less than half the volume-density of these muscles is contractile material, the balance being largely mitochondria and glycogen. The fibers within a muscle are structurally similar. They have short sarcomeres (about 2 m), thin to thick filament ratios of about 3:1, and junctions between the sarcoplasmic reticulum and the transverse tubules at the M line. Sarcoplasmic reticulum occupies about 10% of the myofibrillar volume-density. A well developed sarcoplasmic reticulum appears to underlie the capacities of these two muscles for high frequency contraction; extensive mitochondria and glycogen stores should confer fatigue resistance under both aerobic and anaerobic conditions.     

An ultrastructural examination of developing and mature paraspermatozoa in Pyrazus ebeninus (Mollusca,Gastropoda, Potamididae)

Summary The mesogastropod Pyrazus ebeninus, produces true spermatozoa (here termed euspermatozoa) and multi-flagellate, mobile cells (here termed paraspermatozoa). The mature paraspermatozoon consists of an elongateconical head (6.5–8.5 m in length), constructed of an electron-dense mosaic sheath surrounding a similarly dense, rod-shaped nuclear core (which runs almost the full length of the head). An acrosome-like structure forms the apex of the head. Five to eight axonemes are fixed to the posterior extremity of the nuclear core, each by means of an attachment complex (dense attachment rod, centriolar cap and centriole). A short (3–4 m) midpiece zone follows the head and consists of the multiple axonemes interspersed with very elongate mitochondria. A tuft of short (20 m) tails (termed minor tails) emerges from the midpiece in addition to one very long tail (termed the major tail) ensheathed in dense granules which resemble glycogen granules. A single membrane surrounds head, midpiece and tails whilst the nuclear core retains the original double nuclear membrane.Developmentally, the multiple axonemes arise from one of a pair of wheel-shaped arrangements of centrioles and attach to posterior indentations in the nucleus prior to its transformation into the nuclear core. Dense vesicles, derived apparently from the endoplasmic reticulum, accumulate along and around the developing nuclear core and (in the presence of microtubules) condense into the mosaic head sheath. Cytoplasmic mitochondria elongate and collect at the posterior axis of the cell, where, together with the axonemes, they form the midpiece.Features not previously reported in other ultrastructural studies of paraspermatozoa include the acrosome-like structure of the head, the structure of the midpiece zone, the glycogen sheath of the major tail, the dense annular structure at the junction of the midpiece and major tail and the presence of microtubules in the final phase of head and midpiece maturation. Some features of the euspermatozoon are also described and the comparative ultrastructure of mature and developing paraspermatozoa and their possible functions in the Gastropoda, are reviewed.Abbreviations ac euspermatozoon acrosomal cone - ar euspermatozoon axial rod - ax axoneme - b dense block of mosaic sheath - c centriole - cc centriolar cap - co cone of acrosome-like structure - dr dense attachment rod - dv dense vesicle - g glycogen granules - G Golgi complex - GER granular endoplasmic reticulum - H head of paraspermatozoon - m mitochondrion - M midpiece (euspermatozoon, paraspermatozoon) - maj major tail - min minor tails - mt microtubules - n nucleus - nc nuclear core - p dense plug of acrosome-like structure - pm plasma membrane - sGv small Golgi vesicles - Z transition of centriole to centriolar cap of attachment complex     

Choline stimulates synthesis of extracellular proteins in Trichoderma reesei QM 9414

A correlation between intracellular phospholipid levels and the rate of exoprotein synthesis was investigated in the filamentous fungus Trichoderma reesei QM 9414 during growth on cellulose. When the incubation temperature was varied between 20 and 37°C, the exoprotein synthesis rate correlated with the total cellular amount of phospholipids, but not with an individual phospholipid component. In contrast, when phospholipid bases were added exogenuously, a significant stimulation of exoprotein synthesis was observed with choline. The addition of the surfactant Tween 80—which also stimulates exoprotein secretion in T. reesei QM 9414—prevented choline stimulation. Optimal stimulation occurred around 20 mM choline. Choline stimulated exoprotein synthesis in general as shown by increased activities of several extracellular enzymes. Mycelia required preincubation for at least 20 h before stimulation of choline could be seen. Mycelia pregrown in the absence or presence of choline were equally effective in formation of -glucosidase upon induction with methyl--d-glucoside, and the addition of choline to the induction medium had no effect. Choline did not alter the osmotic stability of protoplasts of T. reesei. Electron microscopic examinations and analysis of chemical constituents as well as marker enzymes from choline grown and non-choline grown mycelia revealed higher contents of mitochondria and endoplasmic reticula in choline grown mycelia. The possibility is discussed that choline may stimulate exoprotein synthesis by increasing the cellular content of endoplasmic reticula.     

Mucosubstances in the normal human oesophageal epithelium

Summary Normal human oesophageal epithelium was investigated with the periodic acid — silver methenamine technique and its variations to demonstrate neutral mucosubstances at the ultrastructural level. The results were compared with the acid phosphotungstic acid method. Neutral mucosubstances were shown in the cell coat and membrane coating granules by both techniques. The silver methods also demonstrated glycogen, the Golgi apparatus and dense bodies. The periodic acid — silver methenamine technique outlined positive material in the intercellular space of the prickle cell layer, but the other silver methods did not.