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  • 1
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 1990
    In:  Protoplasma Vol. 157, No. 1-3 ( 1990-2), p. 92-101
    In: Protoplasma, Springer Science and Business Media LLC, Vol. 157, No. 1-3 ( 1990-2), p. 92-101
    Type of Medium: Online Resource
    ISSN: 0033-183X , 1615-6102
    RVK:
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 1990
    detail.hit.zdb_id: 1463033-3
    SSG: 12
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  • 2
    In: Development, The Company of Biologists, Vol. 113, No. 3 ( 1991-11-01), p. 931-939
    Abstract: In epidermal cells of the plant Nautilocalyx lynchii, induced to divide by explantation, the nucleus undergoes a series of movements, on cytoplasmic strands, leading to construction of a division plane across the vacuole. In the early stage, the nucleus separates from the cortex, occupying an eccentric position in the cell, suspended across the vacuole by few thin strands. In the central stage, the nucleus occupies a central position anchored to the cortex by more numerous, thicker strands. Finally, the phragmosome forms as a coalescence of cytoplasmic strands across the cell, constituting the division plane within which mitosis and cytokinesis take place. The behaviour and alignment of these strands is therefore important since some are precursors of the division plane. In a previous paper (Flanders et al (1990)J. Cell Biol. 110,1111 – 1122), it was pointed out that the alignment of cytoplasmic strands showed features common to a variety of elements under tension. That is, provided they are free to move relative to the cortex, strands radiating from the nucleus should tend to seek short rather than long routes to the cortex. In this way, strands under tension would move away from distant cell corners where two of the cell’s edges make a three-way junction with a neighbouring wall. This provides a basis for the avoidance of four-way junctions and the maintenance of three-way junctions which are a characteristic feature of most plant tissues. In addition, tensile elements such as soap bubble walls contact rigid surfaces perpendicularly. Perpendicular attachment of the cell plate to the side wall is embodied in Sachs’ rule of cell division and the existence of the premitotic strands in a state of tension would provide a basis for this rule. In this study, laser microsurgery has been used to confirm that strands connecting the premitotic nucleus to the cortex are under tension since the severed ends retract immediately upon severance. However,. the response of the nucleus to the breaking of a cytoplasmic strand by laser depends upon the particular stage. The nucleus is most likely to move during the early stage when it is eccentrically placed and has few cytoplasmic strands. In the middle and phragmosomal stages the nucleus is more resistant. Computer-aided image reconstruction of anti-tubulin-labelled confocal sections indicates that the middle stage is characterised by thick microtubule (MT) bundles, which radiate from the nucleus and which seem to account for. the increasing stabilization of the nucleus. Although such strands are more difficult to sever with the laser, their ends still display elastic properties when cut. It is proposed that tension is likely to influence the alignment of strands as well as the position of the nucleus during division plane formation in vacuolated cells.
    Type of Medium: Online Resource
    ISSN: 0950-1991 , 1477-9129
    Language: English
    Publisher: The Company of Biologists
    Publication Date: 1991
    detail.hit.zdb_id: 2007916-3
    SSG: 12
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  • 3
    Online Resource
    Online Resource
    The Company of Biologists ; 1989
    In:  Journal of Cell Science Vol. 93, No. 3 ( 1989-07-01), p. 427-438
    In: Journal of Cell Science, The Company of Biologists, Vol. 93, No. 3 ( 1989-07-01), p. 427-438
    Abstract: Intermediate filament antigens are known to coalign, patchily, with cortical microtubules in plant cells, but nothing else is established about this relationship or the form the antigens take. This was studied further using cell suspensions, instead of root tip cells, since their cortex is accessible to antibodies without the rigours of cell separation. Both carrot and sweetcorn suspension cells were labelled with three antibodies known to recognize animal intermediate filaments. The mitotic and cytokinetic apparatus could be stained with these antibodies, which, in interphase cells, also labelled cortical microtubule-like arrays. One antibody (AFB), raised against cytoplasmic bundles of 7nm fibrils from carrot cells, immunostained the bundles but only under conditions of fixation that did not allow the finer, microtubule-associated staining pattern to be seen. By exploring various preparatory conditions it was concluded that these two forms of antigen co-exist: they are not experimentally interconvertible but require different conditions for exposure to different antibodies. Double immunofluorescence established that the intermediate filament antigens do not parallel the actin network, nor did cytochalasin D affect their distribution. Taxol, however, bundled the intermediate filament antigens, whereas they are dispersed when microtubules are depolymerized, rather than collapsing in perinuclear whorls. Under conditions permitting the microtubule-associated antigens to be stained by immunofluorescence, carrot protoplasts were cleaved on grids, exposing the cortical microtubules. Immunogold labelling then showed that the antibody raised against fibrillar bundles recognizes patches of electron-dense material, along and between the microtubules, rather than individual filaments. To confirm that the plant antigens are capable of forming filaments, a high salt, detergent-insoluble fraction was prepared from the maize line. By dialysing from urea, intermediate-sized filaments could be reconstituted and they immunoblotted with the broadly cross-reactive antibody to intermediate filament antigens (anti-IFA). These studies underline the problems of visualizing in plants, conformations of intermediate filament antigens that are not directly comparable to the extensively studied animal models, and that appear to be sensitive to the way in which cells are manipulated.
    Type of Medium: Online Resource
    ISSN: 0021-9533 , 1477-9137
    Language: English
    Publisher: The Company of Biologists
    Publication Date: 1989
    detail.hit.zdb_id: 219171-4
    detail.hit.zdb_id: 1483099-1
    SSG: 12
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  • 4
    In: The Plant Journal, Wiley, Vol. 4, No. 4 ( 1993-10), p. 631-641
    Type of Medium: Online Resource
    ISSN: 0960-7412 , 1365-313X
    Language: English
    Publisher: Wiley
    Publication Date: 1993
    detail.hit.zdb_id: 2020961-7
    SSG: 12
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  • 5
    In: Journal of Microscopy, Wiley, Vol. 166, No. 1 ( 1992-04), p. 99-109
    Type of Medium: Online Resource
    ISSN: 0022-2720
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 1992
    detail.hit.zdb_id: 2007259-4
    SSG: 11
    SSG: 12
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  • 6
    In: Journal of Cell Science, The Company of Biologists, Vol. 92, No. 3 ( 1989-03-01), p. 371-378
    Abstract: Carrot suspension cells contain cytoplasmic bundles of fibrils that are distinct from F-actin and microtubules and have some of the characteristics of intermediate filaments. In characterizing these fibrillar bundles further, we have raised a monoclonal antibody against them. This anti-fibrillar bundle antibody (AFB) immunoblots vimentin from a range of animal cells and tissues, as well as glial fibrillary acidic protein in brain and desmin in BHK fibroblasts, which are representatives of the type III intermediate filaments. Immunofluorescence staining of PtK2 cells indicates that AFB recognizes a network co-distributing with cytoplasmic microtubules. When this co-alignment is disturbed with the anti-microtubule agent, colcemid, the AFB staining segregates with the collapsed perinuclear whorls of vimentin. In carrot, AFB immunoblots the major bundle proteins but not plant tubulin. In plant as in animal cells, AFB immunofluorescently labels antigens that co-distribute with microtubules. In onion cells (which, unlike carrot, do not possess paracrystalline arrays of fibrils) AFB labels all four microtubule arrays throughout the cell cycle. The antigens do not, however, collapse around the spindle poles during mitosis. Double immunofluorescence, using anti-dog brain tubulin, indicates that the FB antigen is more diffusely distributed than tubulin; it is patchy and co-alignment is not exact, particularly during early preprophase band formation. Antigens in detergent-insoluble fibrils of carrot cells therefore exist both in animal type III intermediate filaments (IF), and in a more dispersed, microtubule-associated manner in onion meristematic cells. This constitutes an independent line of evidence for the existence of IF antigens in plants.
    Type of Medium: Online Resource
    ISSN: 0021-9533 , 1477-9137
    Language: English
    Publisher: The Company of Biologists
    Publication Date: 1989
    detail.hit.zdb_id: 219171-4
    detail.hit.zdb_id: 1483099-1
    SSG: 12
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