Biomedical subjects
C F Bardele
Publications and source records attributed to C F Bardele.
Organization and control of microtubule pattern in centrohelidan heliozoa.
Comparative studies of axopodial microtubule pattern in 10 different centrohelidan Heliozoa belonging to the genera Acanthocystis, Raphidiophrys and Heterophrys suggest that 2 basic principles govern pattern formation in centrohelidan Heliozoa. While the larger "open" arrays with unspecified number of microtubules, e.g. in A. aculeata and R. ambigua, may result from self-linkage of additional microtubules around centroplast-nucleated "starter microtubules," the smaller "closed" arrays with specified microtubule number, e.g. in A. pectinata and H. marina, favor a template-driven linkage mechanism. The centroplast is a highly complex microtubule organizing center involved in the control of orientation, number, and diameter of the axonemes. Its shell may serve as a surface upon which the microtubule nucleating sites assemble, but how the precise positioning of these sites occurs is still open to debate. Some of the unsolved problems of microtubule pattern formation may be explained by the "linker nucleation hypothesis" which is an extension of the "gradion hypothesis" by Roth et al. It is shown how both the formation of closed arrays and the balanced lateral growth of open arrays may result from linker-induced microtubule nucleation.
Comparative study of axopodial microtubule patterns and possible mechanisms of pattern control in the centrohelidian heliozoa Acanthocystis, Raphidiophrys and Heterophrys.
The axopodial microtubule pattern of 9 centrohelidians belonging to the genera Acanthocystis, Raphidiophrys and Heterophrys, as well as the fine structure of their microtubule organizing centre, the centroplast, was studied to determine the rules which govern their patterns. Microtubules capable of binding a xamimum of 4 linkers are arranged in regularly distorted hexagons and equilateral triangles. The number of microtubules present in each axoneme ranges from some 140 in Acanthocystis turfacea to as few as 6 in Heterophrys marina (Stock I). In the later species each axoneme contains a single hexagon of microtubules only. In other Heterophrys species, the central hexagon is surrounded by closely packed microtubules or by microtubules arranged in pentagons; only the central hexagon is anchored in the centroplast shell, whereas additional microtubules seem to originate from secondary nucleation sites somewhat distal to the centroplast. It is argued that the distortion of the basic unit hexagon (with alternate angles close to 134 degrees and 106 degrees) indicates that the microtubules are composed of 13 protofilaments. While in the larger Acanthocystis and Raphidiophrys species, the pattern may result from self-linkage, the arrays found in the Heterophrys species seem to favour a template-determined linkage. To explain the formation of the central hexagon in Heterophrys and balanced lateral growth in the larger microtubule arrays, a 'linker-nucleation hypothesis' is proposed. The assumption is made that graded conformational changes in the microtubule subunits not only specify the position where the next linker will bind, but that this linker, through linkage, becomes able to induce secondary microtubule nucleation, which will result in balanced lateral growth of the array. The application of this hypothesis to other microtubule systems, e.g. basal body formation, is discussed.
The fine structure of the centrohelidian heliozoan Heterophrys marina.
The fine structure of Heterophrys marina (Centrohelidia, Heliozoa) is described with special reference to centroplast structure, morphogenesis and "behavior" of kinetocysts (= axopodial granules which perform saltatory movement), and formation of organic spicules in a new type of organelle located in the plasma membrane. A low calcium pretreatment and fixation was used to improve preservation of highly labile axopodia which near their distal end contain a single microtubule (MT) only. Two varieties of H. marina with a respective maximum of 6 and 12 MTs per axopodium, and 2 hitherto undescribed species, H. elati and H. multipoda, were found among 9 stocks collected in Europe and North America. In all species only the central 6 MTs of each axoneme originate from a scaffolding layer of electron dense material which surrounds the central granule. Evidence is presented which indicates that in Heterophrys self-linkage is not the only principle of MT pattern generation but that instead precisely localized MT nucleation and specific linkage of MTs within the cortex of the centroplast lead to the MT patterns observed. Prekinetocysts originate from vesicles found in the neighborhood of the dictyosomes. After maturation the kinetocysts become attached to the plasma membrane which seems to play an important role both in selection of particles transported in the axopodia and particle movement as well.
Particle movement in heliozoan axopods associated with lateral displacement of highly ordered membrane domains.
Freeze-fracture studies reveal that extrusive organelles displaying saltatory particle movements in centrohelidian axopod are attached to highly ordered domains within the plasma membrane. It is postulated that the motive force for lateral displacement of these membrane domains with the adhering organelle is located immediately underneath the plasma membrane being either part of the peripheral membrane proteins or attached filaments alined parallel to the axopodial microtubules. The attachment domain is interpreted as a "frozen" membrane area preventing untimely organelle discharge by membrane fusion.