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  • Microtubule  (3)
  • Ultraviolet microbeam  (2)
  • 1
    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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  • 2
    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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  • 3
    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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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 176 (1993), S. 14-16 
    ISSN: 1615-6102
    Keywords: Axoneme ; Flagella ; Historical ; Microtubule
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary An early paper demonstrating the existence of fibrils (microtubules) within the flagellum is summarised. The paper appears the first to have demonstrated the existence of flagellar microtubules using electron microscopy, and it has been neglected in the literature.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1615-6102
    Keywords: Mitosis ; Ultraviolet microbeam ; Spindle fibres ; Microtubules ; Crane-fly spermatocytes ; Newt epithelial cells
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary In order to resolve apparent differences in reported experiments, we directly compared the effects of ultraviolet (UV) microbeam irradiations on the behaviour of spindle fibres in newt epithelial cells and crane-fly spermatocytes, using the same apparatus for both cell types. This work represents the first time that irradiated crane-fly spermatocytes have been followed using a high-NA objective and video-enhancement of images. In both cell types, irradiation of a kinetochore fibre in metaphase produced an area of reduced birefringence (ARB), known to be devoid of spindle microtubules (MTs). Subsequently the kinetochore-ward edge of the ARB moved poleward with average velocities of 0.5 μm/min (n=20) in spermatocytes and 1.1 μm/min (n=6) in epithelial cells. The poleward edge of the ARB rapidly disappeared when viewed using a ×100, high-NA objective but generally remained visible when viewed with a ×32, low-NA objective; this difference suggests that MTs poleward from the ARB disperse vertically out of the narrow depth of field of the ×100 objective but that many remain encompassed by that of the ×32 objective. The primary difference in response between the two cell types was in the behaviour of the spindle poles after an ARB formed. In spermatocytes the spindle maintained its original length whereas in epithelial cells the pole on the irradiated side very soon moved towards the chromosomes, after which the other pole did the same and a much shortened functional metaphase spindle was formed.
    Type of Medium: Electronic Resource
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