Ultrastructural and time-lapse observations of intraepithelial lymphocytes in the small intestine of the guinea pig: their possible role in the removal of effete enterocytes

In previous ultrastructural studies we have shown that at the tip of intestinal villi in guinea pigs, effete enterocytes are separated into two portions: a thin apical cytoplasm to be exfoliated into the lumen and a major basal portion to be ingested by lamina propria macrophages. During this process, intraepithelially disposed, large granular lymphocytes interdigitate with enterocytes in a complex manner. In the present study, the relation between the enterocytes and the lymphocytes in the villous epithelium of the guinea pig small intestine is described by use of transmission and scanning electron microscopy in an attempt to visualize the roles and activities of the lymphocytes more clearly. The lymphocytes project numerous pointed processes into effete enterocytes, even piercing them. Enterocytes are deeply indented or perforated, probably as a result of the encroaching lymphocyte processes. Some enterocytes are separated into apical and basal portions by numerous large excavations in the cytoplasm. These findings indicate that repeated perforating penetration of the lymphocytes induces cell cleavage. Supporting this supposition, our microcinematographic observations demonstrate the alternate protrusion and withdrawal of processes of lymphocytes. The processes advance with a pointed end, and subsequently, retract with a rounded end in a cycle of 8–18 seconds.     

Protoplasmic streaming in the giant unicellular green algaAcetabularia mediterranea

Summary Protoplasmic Streaming inAcetabularia mediteranea has been studied by microcinematography in 1. germinating zygotes, 2. germlings before the differentiation of rhizoids and apices, 3. young cells with rhizoids and apices, 4. vegetative cells-several centimeters in length, 5. cells with a maximum sized cap, containing secondary nuclei, and 6. cells after cyst formation. Intracellular transport is found to occur at a network-system of thin filaments and at a different system of headed streaming bands. At the network of filaments chloroplasts are found to move at a velocity of 1–2 m/sec. Headed streaming bands move along the filaments and may lead without interruption from the rhizoid to the apex of the cell andvice versa. The front zone of the streaming bands is occupied by a leading cytoplasmic head-structure. Small vesicles, polyphosphate granula and secondary nuclei are the predominant moving structures in headed streaming bands. The velocity of these particles is found to be 3–11 m/sec. The filament system is found during all developmental stages. Headed streaming bands are undetectable in germinating zygotes and develop from small cytoplasmic droplets in germlings to broad heavily loaded bands in the huge vegetative cell.Transport of secondary nuclei by headed streaming bands is not observed during mitotic divisions and after cyst formation, though moving bands are still present for several weeks after cyst formation.     

Role of three basic light reactions in photomovement of desmids

Photoaccumulations in light trap experiments have been studied in the desmids, Cosmarium, Micrasterias and Euastrum. Dependence of accumulation density on exposure time follows saturation curves, while dose response curves show optima. Time-lapse microcinematography and population methods have revealed that all three basic light-induced motor responses known in microorganisms participate in producing photoaccumulations in desmids. During the initial phase the cells are phototactically attracted towards the trap by scattered light. In low light intensity traps photokinetic reactions may play only a minor role, since photokinesis could be evoked only by light intensities100 lx in Cosmarium cucumis. True photophobic reactions have been demonstrated for the first time in desmids. There are two types of phobic responses in desmids: either the cell reverses its movement or it swings sidewise into the new direction. Behaviour of partially shadowed cells suggests that perception of light direction is brough about by simultaneous intensity measurement at two or more sites within the cell.     

Rapid exocytosis of stenotele nematocysts in Hydra vulgaris

Each cnidarian nematocyte includes a vesicular organelle, called nematocyst, which discharges its content when the cell receives appropriate stimuli. Extracellular electrical stimuli induced discharge of in situ stenoteletype nematocysts in Hydra vulgaris when the apical membrane of nematocytes was depolarized by about 25 mV or more (threshold). Stimuli hyperpolarizing the apical membrane induced discharge only at high amplitudes, adding about 80 mV or more to the resting membrane potential of the nematocyte (resulting in a voltage that may permeabilize the apical membrane). In order to determine the speed of the initiating (exocytotic) process, the delay between stimulus and a clearly visible sign of discharge (i.e., protrusion of the nematocyst's stylets) was measured using video microscopy with triggered flash illumination. The minimal delay was 330–450 s and 230–350 s for depolarizing and large hyperpolarizing stimuli, respectively. With depolarizing stimuli, all discharges of stenoteles occurred between 330 and 950 s after the stimulus. The deviation was caused by differences in the physiological state of the animals tested rather than by variance in the responsiveness of different stenoteles in the same tentacle.Voltage dependence, short latency and Ca/Mg-antagonism are similar to those characterizing exocytosis of synaptic vesicles. This correspondence suggests that discharge of nematocysts is initiated by a similar exocytotic process preceding the ejection of the nematocyst's content.