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  • 1
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Physiology 28 (1966), S. 267-310 
    ISSN: 0066-4278
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Medicine , Biology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Plant Physiology 38 (1987), S. 119-137 
    ISSN: 0066-4294
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Medicine 15 (1964), S. 315-334 
    ISSN: 0066-4219
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Planta 164 (1985), S. 439-447 
    ISSN: 1432-2048
    Keywords: Cytoskeleton ; Ethylene (microtubule reorientation) ; Helix (microtubule) ; Microtubule ; Pisum (microtubule, ethylene) ; Vigna (microtubule, ethylene)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Entire microtubule arrays, within outer cortical and epidermal cells of pea epicotyl and mung-bean hypocotyl, have been visualized by indirect immunofluorescence. In all cells the microtubule arrangement can be interpreted as being a single multistart helix of variable pitch. In control cells the predominant pattern is a tightly compressed helix with the microtubules consequently in a net transverse direction with respect to the cell axis. Occasionally some cells show an oblique helix and rare cells show a longitudinal array which may be interpreted as a steeply pitched helix. By contrast in ethylene treated tissue, many cells show net longitudinal and oblique arrays of microtubules and few show transverse arrays. Similar effects can be induced by high osmolality. It is suggested that the plant cortical cytoskeleton is an integral unit, capable of wholesale reorientation in response to environmental signals.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1615-6102
    Keywords: Intermediate filaments ; Cytoskeleton ; Monoclonal antibody
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary In previous studies on plant cells, antibodies directed against intermediate filaments (IFs) have shown that IF antigens are distributed in one of two quite distinct forms. The first co-distributes with each of the four microtubule arrays (cortical, preprophase band, spindle and phragmoplast), while the second form is associated with cytoplasmic paracrystalline fibrillar bundles (FBs) of 10 nm filaments. Conditions allowing one form to be labelled with antibody have generally proved unsuitable for labelling of the other; this has prevented the simultaneous visualization of the two forms of IF antigen in plants and the study of any possible physical relationships between them at the electron microscopic level. In this paper, we show that ME 101, which recognizes an epitope in the N-terminal portion of all classes of intermediate filaments, stains both forms of plant IF antigen simultaneously in tobacco suspension cells using immunofluorescence or immunogold labelling techniques. These cells contain in their cortex short (ca. l μm) fibrillar bundles which stain with ME 101. These bundles appear to be independent of the microtubule-associated epitope which stains in a continuous linear manner with ME 101. When protoplasts are either cleaved open on grids or sequentially extracted with detergents prior to critical point drying, the short fibrillar bundles are specifically labelled by ME 101 tagged with colloidal gold. ME 101 also co-distributed with underlying linear filaments, which appeared to be microtubules. In addition to these structures, the cortex also contains a meshwork of variably-sized fine filaments but these are not labelled with ME 101 nor with an antibody raised against the plant cytoskeleton, which recognizes cytokeratin 8. These results confirm that the fibrillar bundles and the microtubule-associated form of plant IF antigens are present simultaneously rather than experimentally-interconvertible, and that they appear to be physically unconnected.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 157 (1990), S. 92-101 
    ISSN: 1615-6102
    Keywords: Tradescantia ; Epidermis ; Division plane ; Actin filaments ; Wounding
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary This paper describes the role of actin filaments in setting up the phragmosome — the transvacuolar device that anticipates the division plane — and in forming a supracellular system that seems to override cell boundaries. Tradescantia leaf epidermal cells were induced to divide by wounding the leaf. New division planes formed parallel to slits, and encircled puncture wounds — the new division planes lining up across cells, instead of the joints being off-set as in normal, unwounded tissue. Within 30 min after wounding, rhodamine phalloidin staining showed that a belt of fine, cortical actin filaments formed parallel to the wound. In the next stage, migration of nuclei to a wall adjacent to the wound, involved pronounced association of actin filaments with the nucleus. Migration could be inhibited with cytochalasin D, confirming the role of actin in traumatotaxis. Later still, actin strands were seen to line up from cell to cell, parallel to the wound, anticipating the future division plane. Next, actin filaments accumulated in this anticlinal plane, throughout the depth of the cell, thereby contributing to the formation of the phragmosome. The phragmosome has been shown in previous work (Flanders et al. 1990) to contain microtubules that bridge nucleus to cortex, and is now found to contain actin filaments. Actin filaments are therefore involved in the key stages of nuclear migration and division plane alignment. The supracellular basis of actin alignment is discussed.
    Type of Medium: Electronic Resource
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