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At least 415 records · Page 23Linked to original sources
PubMed1983

Co-operative dynamics in organelles.

Some organelles produce elementary life phenomena which are characterized by the spontaneous formation and/or maintenance of ordered macroscopic dynamics like e.g. the shortening of sarcomeres in striated muscle and the transmission of electrical impulses in an axon. It has been widely accepted that such organelles are organized molecular systems where molecular elements work independently under constraint of a more or less rigid and regular structure of the system. On the other hand, such organelles should be regarded as self-organizing systems if the ordered macroscopic dynamics are self-organized. As the macroscopic dynamics gradually emerge, the microscopic dynamics of its elements become linked to each other through a feedback loop. It is crucial for the feedback loop to operate that the macroscopic dynamics are "free" in their behavior. In the present paper, it is pointed out that the traditional view of independent molecular elements has been obtained from experiments in which, by means of external constraint, the macroscopic dynamics is "clamped". Under such conditions, the self-organizing system may behave as an organized one. Based on synergetics we propose criterions for proving self-organizing systems, and, by applying the criterions, we conclude that skeletal muscle actomysin is a co-operative element in the sense of self-organization.

Actins↗
PubMed1995

Cytoplasmic motility reflects phagocytic activity in alveolar macrophages from dog lungs.

To determine whether cytoplasmic motility relates to phagocytic activity of alveolar macrophages (AM), we measured the remanent field strength (RFS) from the AM containing Fe3O4 particles (5 x 10(6) cells) and the number of phagocytized fluorescent latex spheres in the AM without having Fe3O4 particles (10(6) cells) harvested by broncho-alveolar lavage from dog lungs in vitro. Cytoplasmic motility was estimated from the relaxation rate (lambda o; min-1) calculated from the decay curve of RFS and the number of phagocytized latex spheres was counted using fluorescent microscopy after the addition of latex spheres (5 x 10(7)). The tumor necrosis factor increased both lambda o and the number of phagocytized latex spheres, and cytochalasin D and colchicine decreased them in a concentration-dependent fashion. Increases and decreases in lambda o induced by drugs paralleled the number of phagocytized latex spheres. These results suggest that cytoplasmic motility reflects phagocytic activity of AM and both cytoplasmic movement and phagocytosis may be regulated by a similar mechanism in the cytoskeletal system.

Animals↗
PubMed1982

Cell morphological, ontogenic, and genetic reactions to 0-g simulation and hyper-g.

Organisms use gravity for spatial orientation, and differentiation into species during evolution follows geological processes which are caused by gravity. On the other hand, the task of most organismic functions which have or may have a relation to gravity is to compensate gravity. Furthermore, today it is very obvious that organisms do not disintegrate under the conditions of weightlessness, at least for the currently tested durations. These previous statements indicate a large field of still unknown regulation and adaptation mechanisms. Experiments to simulate weightlessness on the fast clinostat and with hyper-g show a highly developed ability of the genetic chain and of differentiating cells in being autonomous against mechanical stresses caused by outer accelerations. Nevertheless, different strong and slight changes of different tested end points were found. The question remains if the cells react actively or only passively.

Animals↗
PubMed1983

Influence of zero gravity simulation on time course of mitosis in microplasmodia of Physarum polycephalum.

Detrimental effects of weigntlessness are no longer expected to hinder successful mitosis. Experiments in space and on the fast clinostat give no hints of this. Nevertheless we are thinking of a g sensitivity during the process of chromosome condensation and distribution. The time course of nuclear division in microplasmodia of the slime mold Physarum polycephalum was investigated under 0 g simulation on the fast rotating clinostat in comparison to 1 g controls. The result of this experiment is: A significant shortening of mitosis under 0 g simulation compared to 1 g controls.

Animals↗
PubMed1989

Subcellular components of the amphibian egg: insights provided by gravitational studies.

Most cytoplasmic regions of fertilized amphibian eggs move with respect to the gravity vector in experimentally gravity oriented eggs. The pattern and extent of this movement varies among different batches of eggs. This variation in apparent cytoplasmic viscosity (or, conversely, cytoplasmic mobility) can be correlated with variations in subsequent morphogenesis of experimental, gravitationally manipulated eggs. Therefore, the proper interpretation of gravity experiments with amphibian eggs requires that one understand the subcellular basis for this variation on cytoplasmic mobility. Variation in the packing of the major cytoplasmic organelle, the yolk platelets, or the organization and amount of cytoskeletal components may explain the variation in cytoplasmic mobility. Evidence is presented that the variation in yolk volume density (fraction of total cytoplasmic volume occupied by yolk platelets) does not account for the variation in cytoplasmic mobility in Xenopus laevis eggs. Experimental evidence from cold-shocked inverted eggs indicates that microtubules may be involved in determining cytoplasmic mobility. However, quantitative evidence that the microtubule levels and state of the microtubules (polymerized vs. non-polymerized) in the whole Xenopus laevis egg does not correlate directly with cytoplasmic mobility is presented. The apparent conflict these data represent regarding the role of the cytoskeleton in determining cytoplasmic mobility is discussed.

Animals↗
PubMed1992

Physical effects at the cellular level under altered gravity conditions.

Several modifications of differentiated functions of animal cells cultivated in vitro have been reported when cultures have been exposed to increased or decreased inertial acceleration fields by centrifugation, clinorotation, and orbital space flight. Variables modified by clinorotation conditions include inertial acceleration, convection, hydrostatic pressure, sedimentation, and shear stress, which also affect transport processes in the extracellular chemical environment. Autocrine, paracrine and endocrine substances, to which cells are responsive via specific receptors, are usually transported in vitro (and possibly in certain embryos) by convection and in vivo by a circulatory system or ciliary action. Increased inertial acceleration increases convective flow, while microgravity nearly abolishes it. In the latter case the extracellular transport of macromolecules is governed by diffusion. By making certain assumptions it is possible to calculate the Peclet number, the ratio of convective transport to diffusive transport. Some, but not all, responses of cells in vitro to modified inertial environments could be manifestations of modified extracellular convective flow.

Acceleration↗
PubMed1994

Gravitational response of the slime mold Physarum.

The acellular slime mold Physarum polycephalum is used as a model system to investigate the graviresponse of single cells which possess no receptors specialized for the perception of gravity. To obtain insights into the gravity-signal transduction mechanism the light response of the cell is used: Macroplasmodia of the slime mold show clear geo- and phototaxes. Gravity increases and white light decreases transiently the contraction frequency of plasmodial strands whereby both responses follow the same time pattern. Since mitochondria play a major role in changing the contraction rhythm in response to light and gravity stimuli, the simultaneous and subsequent inductions of the opposing light and gravity responses and their mutual influences on one another were investigated. The experiments were performed in weightlessness (0 g)--simulated on the fast-rotating clinostat as well as in actual weightlessness during the IML-1 Space Shuttle mission. The results indicate that mitochondria (chondriome) are part of the acceleration-stimulus reaction chain in Physarum. Two models for a direct gravireceptor mechanism are discussed.

Animals↗
PubMed1978

Oscillating contractions in protoplasmic strands of Physarum: infared reflexion as a non-invasive registration technique.

An inexpensive electronic device employing a miniaturised infrared reflection detector is described which enables the automatic registration of intrinsic radial contraction activities of protoplasmic strands of Physarum growing on their original substrate. Advantages and shortcoming of the new registration technique are discussed in relation to recent tensiometric techniques applied to protoplasmic strands for analysing the contraction physiology of cytoplasmic actomyosins, the force generating substrate of the contraction automaticity in the Physarum system.

Cytoplasm↗
PubMed1979

Oscillating contractions in protoplasmic strands of Physarum: effects of externally applied ouabain, sodium-, potassium- and calcium-ions.

1. Concentrations of 0.1-10 mM Ouabain do not affect oscillating contractions, when applied externally in physiological solutions. 2. Ouabain has no effect, when applied in solutions of increased sodium- (100 mM) and lowered potassium-concentration (0.1 or zero mM). 3. De novo generation of oscillating contractions in protoplasmic drops is not suppressed in Ouabain-solutions. 4. Biochemical studies of Na-K-ATPase did not show any Ouabain sensitive ATPase-activity. 5. Reaction of veins on high concentrations (300 mosm) is discussed as to be a physical effect. 6. It is concluded that no Na-K-ATPase is engaged in triggering oscillating contraction automaticity.

Adenosine Triphosphatases↗
PubMed1983

Cell-substrate interactions in amoeboid locomotion - a matched reflexion interference and transmission electron microscopy study.

Cell-substrate separation distance were measured on Naegleria gruberi amoebae moving in deionized H2O on an untreated glass substratum (weakly adhesive) and on a polylysine treated glass surface (strongly adhesive). The values obtained by transmission electron microscopy on fixed cells and reflexion interference microscopy on live cells were in broad agreement.

Amoeba↗