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  • Mitosis  (11)
  • Crane-fly spermatocytes  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 170 (1992), S. 22-33 
    ISSN: 1615-6102
    Keywords: Mitosis ; Chromosome movement ; In vitro ; Permeabilization ; Prometaphase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary We have attempted to reactivate chromosome activity in dividing, permeabilized animal cells with the aim of analysing the physiology of chromosome movements, particularly during prometaphase. We achieved reactivation on numerous occasions, but it was limited in extent and unreliable in that many cells did not respond and spindles frequently collapsed irreversibly. Of the three cell lines used, newt lung cells gave the best examples of oscillating chromosome movement resuming upon addition of ATP to permeabilised cells. Saltatory movement, severely inhibited or stopped completely during permeabilization, was reactivated considerably by addition of ATP. Only a few of the chromosomes in any spindle moved; while this activity was an ATP-dependent reactivation, it is at present too unreliable for us to experimentally distinguish between the physiology of polar and anti-polar movement. Permeabilized metaphase LLC cells underwent some interesting transformations. Upon exposure to digitonin, many metaphase spindles partially collapsed, creating a prometaphase-like rearrangement of chromosomes; when ATP was added, the spindle in many of these cells grew and reformed until a fairly normal metaphase plate was reconstituted. Less frequently, these spindles continued to elongate, drawing the chromosomes apart into two irregular masses during “pseudoanaphase”. While our techniques are still too unreliable to permit analysis of prometaphase at the level desired, they demonstrate that the motility systems of prometaphase can survive permeabilization, as can the intrinsic ability of spindle to shorten and elongate in a manner reminiscent of anaphase elongation. Throughout all manipulations, chromosomes seemingly maintained their attachment to spindle fibres although the pseudoanaphase transformations suggested that some kinetochore fibre connections were weakened enough to be broken by spindle regrowth.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1615-6102
    Keywords: Mitosis ; ATP, Microtubules ; Spindle ; Metabolic inhibitors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary At telophase in the diatomPinnularia, the two half spindles that comprise the central spindle, separate and then disassemble unidirectionally from the end formerly in the central overlap, back to the pole (Soranno andPickett-Heaps 1982). The metabolic inhibitors dinitrophenol plus deoxyglucose were applied to cells at telophase, depleting their ATP levels at the early stages of half-spindle disassembly; the cells were maintained in this state for 5 minutes, before the inhibitors were washed out. Disassembly of the half spindles, as judged from their birefringence, ceased in ATP-depleted conditions, and recommenced soon after the inhibitors were removed, going to completion quite rapidly. We conclude that disassembly of these MTsin vivo requires energy, probably in the form of ATP.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1615-6102
    Keywords: Microtubules ; Basal bodies ; Flagellar apparatus ; Prymnesiophyceae ; Mitosis ; Pleurochrysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Immunofluorescence microscopy, conventional and high voltage transmission electron microscopy were used to describe changes in the flagellar apparatus during cell division in the motile, coccolithbearing cells ofPleurochrysis carterae (Braarud and Fagerlund) Christensen. New basal bodies appear alongside the parental basal bodies before mitosis and at prophase the large microtubular (crystalline) roots disassemble as their component microtubules migrate to the future spindle poles. By prometaphase the crystalline roots have disappeared; the flagellar axonemes shorten and the two pairs of basal bodies (each consisting of one parental and one daughter basal body) separate so that each pair is distal to a spindle pole. By late prometaphase the pairs of basal bodies bear diminutive flagellar roots for the future daughter cells. The long flagellum of each daughter cell is derived from the parental basal bodies; thus, the basal body that produces a short flagellum in the parent produces a long flagellum in the daughter cell. We conclude that each basal body in these cells is inherently identical but that a first generation basal body generates a short flagellum and in succeeding generations it produces a long flagellum. At metaphase a fibrous band connecting the basal bodies appears and the roots and basal bodies reorient to their interphase configuration. By telophase the crystalline roots have begun to reform and the rootlet microtubules have assumed their interphase appearance by early cytokinesis.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1615-6102
    Keywords: Kinetochore ; Microtubules ; Mitosis ; Pac-Man ; Tensegrity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The “Pac-Man” model for explaining chromosome movement is based on three main tenets: (i) the force that moves chromosomes is generated at the kinetochore; (ii) disassembly of the microtubules (MTs) of the kinetochore fibre generates poleward movement; and (iii) the energy required for this movement comes from MT disassembly. We show that these tenets are not valid in some and perhaps many situations. Thus, the Pac-Man model is inadequate and misleading as the central basis for explaining chromosomal motion generally. We argue that multiple mechanisms are involved in mitotic function and that a contractile/elastic spindle matrix is likely involved not only in anchoring kinetochore fibres, but also by exerting force on them. This view of the spindle matrix shares some features with the “tensegrity” model already formulated as a basis for understanding interphase cell behaviour.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1615-6102
    Keywords: Mitosis ; ATP ; Metabolic inhibitors ; Spindle ; Microtubule
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary To examine the effects exerted on the microtubule (MT) cytoskeleton by dinitrophenol/deoxyglucose (DNP/DOG) and nocodazole, live PtK1 cells were treated with the drugs and then fixed and examined by immunofluorescence staining and electronmicroscopy. DNP/DOG had little effect on interphase MTs. In mitotic cells, kinetochore and some astral fibers were clearly shortened in metaphase figures by DNP/DOG. Nocodazole rapidly broke down spindle MTs (except those in the midbody), while interphase cells showed considerable variation in the susceptibility of their MTs. Nocodazole had little effect on MTs in energy-depleted (DNP/DOG-treated) cells. When cytoplasmic MTs had all been broken down by prolonged nocodazole treatment and the cells then released from the nocodazole block into DNP/DOG, some MT reassembly occurred in the ATP-depleted state. MTs in permeabilized, extracted cells were also examined with antitubulin staining; the well-preserved interphase and mitotic arrays of MTs showed no susceptibility to nocodazole. In contrast, MTs suffered considerable breakdown by ATP, GTP and ATPγS; AMPPNP had little effect. This susceptibility of extracted MT cytoskeleton to nucleotide phosphates was highly variable; some interphase cells lost all MTs, most were severely affected, but some retained extensive MT networks; mitotic spindles were diminished but structurally coherent and more stable than most interphase MT arrays. We suggest that: 1. in the living cell, ATP or nucleotide triphosphates (NTPs) are necessary for normal and nocodazole-induced MT disassembly; 2. the NTP requirement may be for phosphorylation; 3. shortening of kinetochore fibers may be modulated by compression and require ATP; 4. many of these results cannot be accomodated by the dynamic equilibrium theory of MT assembly/disassembly; 5. the use and role of ATP on isolated spindles may have to be reevaluated due to the effects ATP has on the spindle cytoskeleton of permeabilized cells.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1615-6102
    Keywords: Mitosis ; ATP ; Metabolic inhibitors ; Spindle ; Nocodazole
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Dinitrophenol and deoxyglucose (DNP/DOG) were used to investigate the effects of ATP depletion on mitotic PtK1 cells. Direct determination of cellular ATP levels showed that the drop of ATP induced by DNP/DOG was rapid; recovery to normal ATP levels was equally rapid once DNP/DOG was removed. On addition of DNP/DOG to live cells, cytoplasmic activity ceased; interphase and prophase cells showed little other response to DNP/DOG. During prometaphase, DNP/DOG induced a pronounced movement of oscillating, monopolar chromosomes towards the spindle poles. As chromosomes became bipolarly attached, DNP/DOG caused the spindle poles themselves to move together. By metaphase, DNP/DOG-treatment led to significant shortening of the spindle which remained intact. DNP/DOG rapidly stopped anaphase chromosome movement and cytokinesis. Nocodazole (NOC) caused the rapid breakdown of the mitotic spindle; prometaphase chromosomes clustered at the poles and in metaphase cells, the poles were drawn towards the chromosomes as the spindle became disorganized. When cells were pretreated with DNP/DOG and then NOC/DNP/DOG, nocodazole did not break down the spindle. When nocodazole was applied first to break down spindle MTs then DNP/DOG was added to the nocodazole, a second contraction was often induced by the DNP/DOG in the absence of spindle microtubules (MTs). Chromosomes expanded appreciably outwards from the poles when the DNP/DOG was removed, even when the cells remained in nocodazole.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1615-6102
    Keywords: Newt cells ; PtK1 cells ; Diazepam ; Mitosis ; Microtubule ; Spindle
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The effects of diazepam (DZP) on mitosis and the microtubule (MT) cytoskeleton were examined using live and fixed PtK1 and newt (Taricha granulosa) epithelial lung cells. DZP treatment caused rapid shortening of spindle MTs at prometaphase and metaphase, inducing movement of the poles together while chromosome oscillations continued. DZP treatment slowed the rate of anaphase A but did not detectably affect anaphase B, cell cleavage or interphase cells. Our results suggest that DZP inhibits mitosis by affecting prometaphase and metaphase MTs. Its action is not equivalent to that of common anti-MT drugs, since only a small subpopulation of MTs are significantly susceptible. Likewise, its effects are not equivalent to those generated by metabolic inhibitors. The related benzodiazepines, medazepam and oxazepam, induce effects equivalent to those of DZP.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 137 (1987), S. 29-44 
    ISSN: 1615-6102
    Keywords: Kinetochore fiber ; Microtubules ; Mitosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The microtubule (MT) arrangement in three kinetochore fibers in the acentric spindles of the green algaOedogonium cardiacum were reconstructed from serial sections of prometaphase and metaphase cells. The majority of the MTs attached to the kinetochore (kMTs) are relatively short, extending less than a third of the distance to the putative spindle pole region, and none extended the full distance. Fine filaments and a matrix described earlier (Schibler andPickett-Heaps 1980) were associated with the MTs all along the fibers. Live cells ofOedogonium were also studied by time lapse cinematography for correlation with the ultrastructural observations. Late prometaphase and metaphase kinetochore fibers appear to move independently as if unattached at their poleward ends. These observations suggest that kinetochore fibers inOedogonium are not attached to a specific pole structure from late prometaphase until the inception of anaphase. The results are discussed with reference to spindle structure and function in general.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1615-6102
    Keywords: Mitosis ; Ultraviolet microbeam
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary We describe the assembly of a UV microbeam microscope based on a Zeiss IM35 inverted microscope. The important UV transmitting elements are standard UV epifluorescence attachments available from Zeiss; the main modification involves fitting an adjustable slit in place of the field diaphragm. We describe how to align and focus the UV source for optimal irradiations. Our current version of this machine is also fitted with a monochromator and using monochromatic UV light, we can reproduceably create Areas of Reduced Birefringence in spindle fibres with ca. 2–3 s irradiations, while continually observing the fibres. The microscope is stable and easy to set up, allowing many consecutive experiments to be done, including multiple irradiations on the one cell. In conjunction with video image processing techniques, the cells can be observed continuously using polarising, Nomarski or other optical systems. Some preliminary observations demonstrating the versatility of the machine are described.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 192 (1996), S. 130-144 
    ISSN: 1615-6102
    Keywords: Actin ; Cytochalasin ; Microtubules ; Mitosis ; Spindle
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Mitosis in living cells ofOedogonium observed by time-lapse, was blocked by cytochalasin D (CD; 25–100 μg/ml). Normal prometaphase to anaphase takes 10–15 min; blockage of entry into anaphase by CD was reversible up to 2–2.5 h in CD and washout was followed within 10–20 min by normal anaphase and cytokinesis. After 3–6 h in CD, unseparated chromatids segregated randomly into two groups as the spindle slowly elongated considerably, becoming distorted and twisted. During this “pseudoanaphase”, chromatids sometimes split irregularly and this was stimulated by late washout of CD. CD affected chromosomal attachment to the spindle. If applied at prophase and prometaphase, spindle fibres entered the nucleus; chromosomes moved vigorously and irregularly. A few achieved metaphase only briefly. Treatment at metaphase caused chromosomes to irregularly release and after random movement, all slowly gathered at either pole. Upon removal of CD, chromosomes rapidly achieved metaphase and anaphase A and B soon followed. If CD took effect during anaphase, chromatids detaching from the spindle oscillated rapidly along it; anaphase and cytokinesis (phycoplast formation) were delayed as the cell attempted to correct for abnormal chromosomal behaviour. Thus, CD prevents normal kinetochore attachment to the spindle and actin may be the target for this response.
    Type of Medium: Electronic Resource
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