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PubMed1988

Phagosome formation in Paramecium: effects of solid particles.

Digestive vacuole (DV) formation in Paramecium can be separated into four steps: sequestration and recycling of the spent DV membrane, sweeping and concentrating of particles into the nascent DV, vacuole growth, and the release of the nascent DV. How the size, load and surface charge of solid particles affected formation and subsequently the digestive processes in log-phase cells were investigated. Pulsing cells continuously with beads resulted in an initial linear increase, followed by a steady state, of labelled DVs. Above a certain threshold concentration, the rate of formation and the size of the DVs formed (as well as the steady state) all increased with increasing bead load, so that for a 16-fold increase in bead load, a corresponding fourfold increase in the incorporation of the recycled membrane into the DVs was observed. The threshold values, which depended on the sensitivity of the technique used to score these DVs, were lowered as bead size increased. The steady state of labelled DVs was shown to correspond to a strict balance between the formation and defecation rates as shown by efflux measurements and pulse-chase protocols using two consecutive labels. The duration of the pulse required to reach these steady states was inversely proportional to the logarithm of the bead number at low bead loads but remained constant at higher bead loads. The formation rates and the DV size were similar when cells were pulsed with beads from 0.5 to 3 microns, but DV size increased using beads of 4.5 and 5.7 microns. The maximal bead size that could be ingested was approximately 10 microns.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1988

Characterization of monoclonal antibodies to trichocyst antigens in Paramecium.

Ten mouse monoclonal antibodies (mAbs) were raised against trichocyst contaminants present in crude or enriched lysosome fractions of Paramecium multimicronucleatum. Using an indirect immunofluorescence assay (IFA) and immunogold labelling on frozen thin sections, epitopes were located on the outer edge, cortex and the core of the trichocyst body, as well as the sheath covering the tip. Except for the two on the tip, epitopes were reactive after SDS-PAGE under non-reducing conditions. Four mAbs (131C1E8, A1-3, A16-2, D7) were directed to a trio of bands of 37, 34 and 29 (x 10(3] Mr from the beaded or meshlike trichocyst body sheath. A fifth mAb (135B9E7), directed to epitopes on the cortex inside the beaded body sheath, reacted strongly with the 37 and 34 bands, but weakly with the 29 x 10(3) Mr band. The last three mAbs (270D5, 22D7F2, D8) were reactive with one or more of three families of antigens found on the trichocyst core. mAb 270D5 reacted mainly with the 34 and 29 (x 10(3] Mr bands of the family containing the above trio, while mAb 22C7F2 reacted consistently with the 47 x 10(3) band of the higher Mr family but variably with both the trio of bands and the 17 x 10(3) band of the lower Mr family. mAb D8, which was directed to epitopes on the trichocyst core and small vesicles in the endoplasm, reacted only with the 29 x 10(3) Mr band. The mAbs were cross-reactive with the trichocysts of P. primaurelia, P. tetraurelia, P. caudatum and P. calkinsi with some small variation in blotting patterns.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1989

Properties of microtubule-free cortical residues isolated from Paramecium tetraurelia.

We have found that shape-preserving residues devoid of microtubules can be prepared from Paramecium using Triton X-100 at high ionic strength. These residues contain many proteins, including one showing antigenic relationship to chicken alpha-spectrin, and three showing antigenic relationship to Tetrahymena cortical proteins. These antigens have been localized by immunofluorescence microscopy, and the isolated cortical residues have been characterized ultrastructurally. These preparations should be useful in detailed studies of the structure, development and evolutionary relationships of cortical architecture in ciliated protozoa.

Animals↗
PubMed1989

Biochemical characterization of the proteins of Paramecium secretory granules.

The proteins of trichocysts (secretory granules) from Paramecium tetraurelia have been biochemically characterized. Two-dimensional electrophoresis revealed 34 major components and at least 120 minor components, most with molecular weights ranging from 14,000 to 21,000 and isoelectric points ranging from 4.8 to 5.2. Comparison of two-dimensional electrophoretic patterns of trichocysts before and after exocytosis revealed only minor changes in these patterns, although the protein matrix undergoes a striking change in morphology. To clarify the interrelationships among trichocyst proteins, two proteins from extruded trichocyst matrix were purified to homogeneity and sequenced at their N termini. Their sequences are distinct, but they share limited homology.

Amino Acid Sequence↗
PubMed1990

Monoclonal antibody study of the decorated spongiome of contractile vacuole complexes of Paramecium.

A monoclonal antibody (mAb) has been developed and selected by immunofluorescence for the radial canals of the contractile vacuole complex (CVC) of Paramecium multimicronucleatum. By applying indirect immunogold labeling to thin frozen sections this mAb has been shown at the electron microscopic level to be specific for the decorated spongiome. We have used the mAb to study the normal interfission appearance as well as developmental stages of the decorated spongiomes. Two decorated spongiomes, presumably involved in water sequestration, radiate as 5-10 bands from unlabeled, circular, 25 microns diameter centers. Two new CVCs arise just anterior to the space occupied by the old spongiomes, the new anterior CVC appearing slightly before the posterior one. Development of the new spongiomes around a 10 microns unlabeled central zone is accompanied by a regression of old spongiome bands until the lengths of these bands in both old and new CVCs are equal just before cell division. After division both old and new spongiome bands grow at equal rates to the same length. Exceptions to the above general scheme, both in number of CVCs in interfission, as well as in position of the new relative to the old CVCs, are also observed.

Animals↗
PubMed1991

Analysis of Ni(2+)-induced arrest of Paramecium axonemes.

This study examines the molecular basis for paralysis of ciliary motility by Ni2+. At concentrations above 0.1 mM, Ni2+ slowed and subsequently stopped swimming of living, axenically grown Paramecium tetraurelia. However, some cilia still beat in the presence of 0.1 mM Ni2+. When permeabilized and reactivated with 4 mM ATP at pCa greater than 7, cells resumed ciliary beat and swam forward at approximately 170 +/- 28 microns s-1; swimming speed increased in the presence of 10 microM cyclic AMP. Addition of Ni2+ (pNi less than 5) caused rapid arrest of all ciliary beat in a single position. This was fully reversible when EGTA was added to raise the pNi. Axonemes were then isolated and sliding was observed in the presence of trypsin and ATP. When pNi was lowered to about 5, sliding was reduced dramatically. This too was reversible with EGTA. Dynein was then extracted from the axonemes and used for in vitro translocation assays. At concentrations of Ni2+ where microtubule-sliding and axonemal beat were greatly inhibited or absent, microtubule translocation in vitro by 22 S dynein was only slightly affected. However, translocation by 14 S dynein was stopped completely. When pNi was raised by repeated washing with solutions containing EGTA, microtubule translocation by 14 S dynein resumed. We conclude that Ni2+ induces a reversible paralysis by a direct effect on 14 S dynein while 22 S dynein is not a primary target.

Adenosine Triphosphatases↗
PubMed1991

Photoreception of Paramecium cilia: localization of photosensitivity and binding with anti-frog-rhodopsin IgG.

Paramecium bursaria is photosensitive and accumulates in a lighted area. The cells can be deciliated by a brief suspension in dilute ethanol. Both intact and deciliated cells showed depolarization in response to light stimulation by a step-increase from dark to above 0.7 mW cm-2 (550 nm). On the other hand, after a step-increase to below 0.4 mW cm-1, intact cells showed hyperpolarization, while the deciliated cells showed no change in membrane potential. This difference in membrane potential response between ciliated and deciliated cells suggests that both somatic and ciliary structures are photosensitive. In our search for the photoreceptive molecules, a polyclonal antibody induced in rabbits against frog rhodopsin was found to cross-react with a 63x10(3) Mr protein of P. bursaria, by immunoelectrophoresis. Immunocytochemical studies showed that the antibody labeling was localized on both the ciliary and the somatic membranes. These results raise the possibility that P. bursaria may contain a rhodopsin-like protein as a photoreceptor molecule.

Animals↗
PubMed2003

Photolysis of caged calcium in cilia induces ciliary reversal in Paramecium caudatum.

Intracellular Ca(2+) concentration controls both the pattern and frequency of ciliary and flagellar beating in eukaryotes. In Paramecium, it is widely accepted that the reversal of the direction of ciliary beating (ciliary reversal) is induced by an increase in intra-ciliary Ca(2+) levels. Despite this, the Ca(2+)-sensitive region of the cilium that initiates ciliary reversal has not been clearly identified. We injected caged calcium into living P. caudatum cells and applied ultraviolet (UV) light to portions of the injected cells to raise artificially the intracellular Ca(2+) level ([Ca(2+)](i)). UV application to the upper ciliary region above the basal body induced ciliary reversal in injected cells. Furthermore, UV application to the tips of cilia induced weak ciliary reversal. Larger areas of photolysis in the cilium gave rise to greater angles of ciliary reversal. These results strongly suggest that the Ca(2+)-sensitive region for ciliary reversal is distributed all over the cilium, above the basal body.

Animals↗
PubMed2005

Cell volume control in Paramecium: factors that activate the control mechanisms.

A fresh water protozoan Paramecium multimicronucleatum adapted to a given solution was found to swell until the osmotic pressure difference between the cytosol and the solution balanced the cytosolic pressure. The cytosolic pressure was generated as the cell swelled osmotically. When either one or both of these pressures was somehow modified, cell volume would change until a new balance between these pressures was established. A hypothetical osmolyte transport mechanism(s) was presumably activated when the cytosolic pressure exceeded the threshold value of approximately 1.5 x 10(5) Pa as the cell swelled after its subjection to a decreased osmolarity. The cytosolic osmolarity thereby decreased and the volume of the swollen cell resumed its initial value. This corresponds to regulatory volume decrease (RVD). By contrast, another hypothetical osmolyte transport mechanism(s) was activated when the cell shrank after its subjection to an increased osmolarity. The cytosolic osmolarity thereby increased and volume of the shrunken cell resumed its initial value. This corresponds to regulatory volume increase (RVI). The osmolyte transport mechanism responsible for RVD might be activated again when the external osmolarity decreases further, and the cytosolic osmolarity thereby decreases to the next lower level. Similarly, another osmolyte transport mechanism responsible for RVI might be activated again when the external osmolarity increases further, and the cytosolic osmolarity thereby increases to the next higher level. Stepwise changes in the cytosolic osmolarity caused by a gradual change in the adaptation osmolarity found in P. multimicronucleatum is attributable to these osmolyte transport mechanisms. An abrupt change in the amount of fluid discharged from the contractile vacuole seen immediately after changing the external osmolarity reduces an abrupt change in cell volume and thereby protects the cell from the disruption of the plasma membrane by excessive stretch or dehydration during shrinkage.

Adaptation, Physiological↗
PubMed2005

Electrical properties and fusion dynamics of in vitro membrane vesicles derived from separate parts of the contractile vacuole complex of Paramecium multimicronucleatum.

The contractile vacuole complex of Paramecium multimicronucleatum transforms into membrane-bound vesicles on excision from the cell. The I-V relationship was linear in a voltage range of -80 to +80 mV in all vesicles, despite being derived from different parts of the contractile vacuole complex. No voltage-gated unit currents were observed in membrane patches from the vesicles. Vesicles derived from the radial arm showed a membrane potential of >10 mV, positive with reference to the cytosol, while those derived from the contractile vacuole showed a residual (<5 mV) membrane potential. The electrogenic V-ATPases in the decorated spongiome are responsible for the positive potential, and Cl- leakage channels are responsible for the residual potential. The specific resistance of the vesicle membrane (approximately 6 kOmega cm2) increased, while the membrane potential shifted in a negative direction when the vesicle rounded. An increase in the membrane tension (to approximately 5 x 10(-3) N m(-1)) is assumed to reduce the Cl- leakage conductance. It is concluded that neither voltage- nor mechano-sensitive ion channels are involved in the control of the fluid segregation and membrane dynamics that govern fluid discharge cycles in the contractile vacuole complex. The membrane vesicles shrank when the external osmolarity was increased, and swelled when the osmolarity was decreased, implying that the contractile vacuole complex membrane is water permeable. The water permeability of the membrane was 4-20 x 10(-7) microm s(-1) Pa(-1). The vesicles containing radial arm membrane swelled after initially shrinking when exposed to higher external osmolarity, implying that the V-ATPases energize osmolyte transport mechanisms that remain functional in the vesicle membrane. The vesicles showed an abrupt (<30 ms), slight, slackening after rounding to the maximum extent. Similar slackening was also observed in the contractile vacuoles in situ before the opening of the contractile vacuole pore. A slight membrane slackening seems to be an indispensable requirement for the contractile vacuole membrane to fuse with the plasma membrane at the pore. The contractile vacuole complex-derived membrane vesicle is a useful tool for understanding not only the biological significance of the contractile vacuole complex but also the molecular mechanisms of V-ATPase activity.

Animals↗
PubMed2006

Correlation between thermotolerance and membrane properties in Paramecium aurelia.

The relationship between thermotolerance and membrane properties was studied by using a ciliated protozoan, Paramecium aurelia. P. aurelia is a complex of sibling species termed ;syngens' whose cell morphology appear similar on microscopic examination. From the comparison of tolerance to increasing temperature among 14 syngens of P. aurelia, we selected syngens 2 and 3 as low thermotolerant examples, and syngens 8 and 10 as high thermotolerant examples. The membrane resistance of high thermotolerant syngens measured by injection of a constant inward current was greater than that of low thermotolerant syngens. Membrane fluidity measurements of living cells using the fluorescent dye, 6-lauroyl-2-dimethylaminonaphtalene (laurdan) showed that the fluidity at the cultured temperature was decreased in high thermotolerant syngens compared to that of low thermotolerant syngens. However, when the temperature was increased to the killing temperature of each syngens, the fluidity was increased to almost the same level irrespective of syngen. Furthermore, analysis of fatty acids extracted from whole cells showed that the ratios of unsaturated to saturated fatty acids was smaller in high thermotolerant syngens than in low thermotolerant syngens. These results suggest that the thermotolerance of P. aurelia syngens is determined by the membrane fluidity which is related to the fatty acids composition.

Acclimatization↗
PubMed2007

Genetic dissection of attractant-induced conductances in Paramecium.

Paramecium tetraurelia is attracted to acetate and biotin by swimming smoothly and fast up gradients of these attractants, and turning immediately and slowing down when leaving these stimuli. We use a group of mutants, each with a different defect in an identified ion conductance, to show that these two stimuli open different ion channels, and the behaviors that occur upon application of stimulus (on-response) and removal of stimulus (off-response) have different roles in attraction to these two stimuli. The most important parameters for successful attraction to acetate are the on-response behaviors of fast swimming with few turns, and the mutants' behavior suggests that I(K(Ca,h)) is the conductance involved that initiates this behavior. I(K(Ca,h or d)) appears to be important to the on-response in biotin; the results with mutants suggest that the biotin off-response depolarization is initiated by an I(Ca), which can be large enough or close enough to channels to open I(K(Ca,d)), I(Na(Ca)) and I(Mg(Ca)).

Acetates↗
PubMed1994

The effects of altering extracellular potassium ion concentration on the membrane potential and circadian clock of Paramecium bursaria.

In some neural models of circadian rhythmicity, membrane potential and transmembrane flux of potassium and calcium ions appear to play important roles in the entrainment and central mechanisms of the biological clock. We wondered whether these cellular variables might be generally involved in circadian clocks, even non-neural clocks. Therefore, we tested the impact of changing extracellular potassium level on the circadian rhythm of photoaccumulation of Paramecium cells, whose membrane potential responds to changes of extracellular potassium in a manner similar to that of neurones. We found that pulse or step changes of extracellular potassium concentration did not phase-shift the circadian clock of P. bursaria cells in a phase-specific manner. Furthermore, modifying the extracellular concentration of calcium did not affect the magnitude of light-induced phase resetting. Therefore, while membrane potential and calcium fluxes may be crucial components of the circadian clock system in some organisms, especially in neural systems that involve intercellular communication, the P. bursaria data indicate that membrane potential changes are not necessarily an intrinsic component of circadian organization at the cellular level.

Animals↗
PubMed1998

Long-term adaptation of Ca2+-dependent behaviour in Paramecium tetraurelia.

Prolonged exposure to KCl has long been recognized to modify swimming behaviour in Paramecium tetraurelia, a phenomenon known as 'adaptation'. In this study, we have investigated behavioural adaptation systematically. A 24 h exposure to 30 mmol l-1 KCl deprived cells of the ability to respond behaviourally to two established chemoeffectors. We also explored the effects of 30 mmol l-1 KCl on the duration of backward swimming induced by Ba2+ and Mg2+. A brief (60 min) exposure prevented cells from swimming backwards in response to either cation, but recovery was rapid (<60 min) following a return to control medium. Prolonged (48 h) exposure caused a more persistent loss of response to Ba2+, so that several hours was now required for recovery. Surprisingly, responses to Mg2+ reappeared during 6-8 h in KCl, with backward swimming durations increasing to more than 300 % of control values after 26 h. Thus, we can distinguish two phases to adaptation. The short-term phase is characterized by an inability to respond behaviourally to most stimuli and might be adequately explained in terms of Ca2+ channel inactivation and K+-induced shifts in membrane potential. The long-term phase is characterized by enhanced responses to Mg2+ (and also to Na+), suggesting that a more extensive reprogramming of membrane excitability may occur during chronic K+-induced depolarization.

Adaptation, Physiological↗
PubMed1998

Relaxation and activation of graviresponses in Paramecium caudatum.

The kinetics of gravitaxis and gravikinesis in Paramecium caudatum were investigated by employing (1) step transitions from normal gravity (1 g) to weightlessness (microgravity) and (2) turns of the experimental chambers from the horizontal to the vertical position at 1 g. The transition to microgravity left existing cell orientations unchanged. Relaxation of negative gravitaxis under microgravity took longer than 10 s and may be described by the time constant of the decay of orientation coefficients. Gravitaxis was started at 1 g by turning the experimental chamber from a horizontal to a vertical position. Gravitaxis activated rapidly during the turning procedure and relaxed to an intermediate level after the turning had stopped. Gravity-induced regulation of swimming speed (gravikinesis) at 1 g had reached a steady state after 1 min; at this point, gravikinesis counteracted the effects of sedimentation (negative gravikinesis). A step transition to microgravity initially reversed the sign of the gravikinesis (positive gravikinesis). The relaxation of this kinetic response was not completed during 10 s of microgravity. The data suggest that gravikinesis is functionally unrelated to gravitaxis and is strongly affected by the rate of change in acceleration. We present a model explaining why gravikinesis reverses sign upon the onset of a step from 1 g to microgravity.

Animals↗
PubMed2000

Periodic tension development in the membrane of the in vitro contractile vacuole of Paramecium multimicronucleatum: modification by bisection, fusion and suction.

The contractile vacuole of the freshwater protozoan Paramecium multimicronucleatum is a membrane-bound exocytotic vesicle that expels excess cytosolic water. The in vitro contractile vacuole isolated from P. multimicronucleatum along with a small amount of cytosol and confined under mineral oil showed periodic rounding and slackening at fairly regular intervals. Activity lasted for over 30 min at room temperature (24-27 degrees C). The rounding of the in vitro contractile vacuole corresponded to the increased membrane tension of the in vivo contractile vacuole that occurs immediately before fluid expulsion. Unlike the in vivo contractile vacuole, the in vitro contractile vacuole did not expel fluid, since it lacked a mechanism to form a pore. The subsequent slackening of the in vitro contractile vacuole corresponded to the fluid-filling phase of the in vivo contractile vacuole that occurs at decreased membrane tension. Fluid filling occurred in the in vitro contractile vacuole only when it was isolated together with its radial arms. In vitro membrane-bound vesicles obtained by 'bisecting' (although the two parts were not always identical in size) an in vitro contractile vacuole established their own independent rounding-slackening cycles. In vitro contractile vacuole vesicles could fuse again when the vesicles slackened. The fused vesicle then showed a rounding-slackening cycle with a period closer to that of the vesicle that exhibited the shorter cycle period. An additional rounding phase of the in vitro contractile vacuole could be induced by applying suction to a portion of its membrane with a micropipette when the contractile vacuole was in its slackened phase. This suggests that maximum tension development in the contractile vacuole membrane can be triggered when tension is increased in any part of the contractile vacuole membrane. The time from the start of an extra rounding phase to the next spontaneous rounding and for subsequent rounding-slackening cycles was nearly the same as that before the extra rounding phase. This implies that there is no master pacemaker to control the rounding-slackening cycle in the contractile vacuole membrane. Severed radial arms also became vesiculated and, like contractile vacuole membranes, these in vitro vesicles showed independent rounding-slackening cycles and vesicle-vesicle fusions. Thus, membrane derived from the radial arm seems to be identical in its tension-developing properties with the contractile vacuole membrane. ATP was found to be required for contractile vacuole rounding but inhibitors of actin or tubulin polymerization, such as cytochalasin B and Nocodazole, had no effect on the in vitro contractile vacuole's rounding-slackening cycle.

Actins↗
PubMed2000

Physical and physiological components of the graviresponses of wild-type and mutant Paramecium Tetraurelia.

Wild-type and the morphological mutant kin 241 of Paramecium tetraurelia showed improved orientation away from the centre of gravity (negative gravitaxis) when accelerations were increased from 1 to 7 g. Gravitaxis was more pronounced in the mutant. A correlation between the efficiency of orientation and the applied g value suggests a physical basis for gravitaxis. Transiently enhanced rates of reversal of the swimming direction coincided with transiently enhanced gravitaxis because reversals occurred more often in downward swimmers than in upward swimmers. The results provide evidence of a physiological modulation of gravitaxis by means of the randomizing effect of depolarization-dependent swimming reversals. Gravity bimodally altered propulsion rates of wild-type P. tetraurelia so that sedimentation was partly antagonized in upward and downward swimmers (negative gravikinesis). In the mutant, only increases in propulsion were observed, although the orientation-dependent sensitivity of the gravikinetic response was the same as in the wild-type population. Observed swimming speed and sedimentation rates in the wild-type and mutant cells were linearly related to acceleration, allowing the determination of gravikinesis as a linear (and so far non-saturating) function of gravity.

Animals↗
PubMed2001

Synthesis of the signal molecule acetylcholine during the developmental cycle of Paramecium primaurelia (Protista, Ciliophora) and its possible function in conjugation.

We recently discovered, in mating-competent Paramecium primaurelia, the presence of functionally related molecules of the cholinergic system: the neurotransmitter acetylcholine (ACh), both its nicotinic and muscarinic receptors and its lytic enzyme acetylcholinesterase (AChE). Our results on the inhibition of mating-cell pairing in vivo in mating-competent cells treated with cholinomimetic drugs support the hypothesis that the cholinergic system plays a role in cell-to-cell adhesion. To investigate the possible function of the signal molecule ACh in conjugation in P. primaurelia, we attempted to detect the intracellular sites of ACh synthesis by localizing the ACh biosynthetic enzyme choline acetyltransferase (ChAT). Using immunocytochemical and histochemical methods, we have demonstrated the presence and activity of ChAT principally on the surface membrane of mating-competent cells and of mature but non-mating-competent cells. No evidence for ChAT activity was found in immature cells. Immunoblot analysis revealed the presence of immunoreactive bands, ranging in molecular mass from 42 to 133 kDa, as reported for ChAT isolated from higher organisms. In vivo experiments showed that inhibition of ChAT activity by Congo Red, known to be a potent competitive inhibitor of acetyl coenzyme A, did not affect mating-cell pairing. Conversely, inhibition of AChE with BW 284c51 or eserine, which block enzyme activity by reacting with a specific serine within the catalytic centre, significantly inhibited mating-cell pairing. Our results suggest that ACh has a negative modulating effect on conjugation in P. primaurelia.

Acetylcholine↗