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  • Cell plate  (3)
  • High pressure freezing  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 157 (1990), S. 182-192 
    ISSN: 1615-6102
    Keywords: Caffeine ; Cell plate ; Phragmoplast ; Endoplasmic reticulum ; Golgi vesicles ; Microtubules ; Calcium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Caffeine is a potent inhibitor of cell plate formation in dividing plant cells. Previous studies living cells reveal that the drug always permits the cell plate to arise and grow normally until about 80% complete, but then causes it to break down. In the present investigation we examine this formation/degradation cycle at the ultrastructure level. Our results show that during the formation phase the caffeine treated plate is indistinguishable from untreated controls. Phragmoplast microtubules arise and align in the interzone, Golgi vesicles are produced and aggregate in a line that defines the young cell plate, and considerable fusion of these vesicles occurs to form islands of plate material. However, under the influence of caffeine these islands do not fuse to form the enlarged lamellar expanses characteristic of maturing cell plates. Instead, the partially fused material reverts to small vesicles which appear to become resorbed by the cellular membrane systems. The resorption process continues leaving no evidence of the previously developing plate, although occasionally we observe a stub of fused vesicles attached to the parent wall. Following cell plate disintegration the reformed nuclei move close together and occupy the central region of the cell. These observations focus attention on the consolidation phase of cell plate formation as the one being maximally affected by caffeine.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 155 (1990), S. 116-126 
    ISSN: 1615-6102
    Keywords: Actin ; Cytoplasmic streaming ; Drosera ; Endoplasmic reticulum ; Freeze fixation ; Freeze substitution ; Hyperbaric freezing ; High pressure freezing ; Immunogold localization ; Microfilaments ; Plasmalemma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract In epidermal cells ofDrosera tentacles that have been preserved for ultrastructural analysis through high pressure freeze fixation and freeze substitution we describe the frequent occurrence of microfilament (MF)-endoplasmic reticulum (ER) complexes. These are found throughout the cytoplasm where they are observed in close association with the plasmalemma (PL), the tonoplast, nuclei, mitochondria, chloroplasts, and microbodies. The MF component of the complexes is identified as actin based on immunogold labelling with actin antibodies. The actin-ER complexes are prominent in the cortical cytoplasm. In this region a network of predominantly tubular ER occupies an intermediary position in which it associates closely with both the PL and the actin MFs. We suggest that the ER, especially those elements adjacent to the PL in the cortical cytoplasm, stabilizes the actin MFs and provides the necessary anchor against which the forces for cytoplasmic streaming are generated.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1615-6102
    Keywords: High pressure freezing ; Plunge freezing ; Freeze substitution ; Phytophthora ; Sporangia ; Immunogold labelling
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The effects of high pressure on the ultrastructure of sporangia ofPhytophthora cinnamomi andP. palmivora have been examined by comparing sporangia frozen in a Balzers hyperbaric freezer or pressurized in a French pressure cell with sporangia plunge frozen at ambient pressure. Both freeze fixation methods provided excellent preservation of most cell structures, but one organelle type seen in plunge frozen material, the large peripheral vesicle (LPV), was not observed in high pressure frozen sporangia. Instead, these sporangia contained large irregularly shaped structures which exhibit the patterns of spatial distribution and, forP. cinnamomi, the monoclonal antibody binding characteristic of LPVs. These findings suggest that some factor of the hyperbaric freezing process causes LPVs to be degraded. Sporangia ofP. cinnamomi that had been pressurized in a French pressure cell also exhibited large structures with the spatial distribution and monoclonal antibody binding characteristic of LPVs. The apparent expansion of LPVs that follows from both pressurizing treatments causes considerable passive disruption of sporangial structure. This is the first report of a major disturbance of cell structure from use of the Balzers hyperbaric freezer, and reflects the lability, noted in previous work, of LPVs inPhytophthora.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 111 (1982), S. 121-133 
    ISSN: 1615-6102
    Keywords: Cell plate ; Endoplasmic reticulum ; Dictyosome vesicles ; Plasmodesmata
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The association of endoplasmic reticulum (ER) with the developing cell plate has been analyzed in lettuce roots fixed in glutaraldehyde and post-fixed in a mixture of osmium tetroxide-potassium ferricyanide (OsFeCN). Electron microscopic observations show that elements of ER, which are selectively stained by the OsFeCN reagent, become loosely associated with aggregating dictyosome vesicles at the onset of plate formation. Subsequently the ER, in a tubular reticulate network, surrounds the vesicular aggregates creating a three dimensional membrane matrix. It is suggested that the ER (1) provides a structural framework that holds the vesicles in position and directs their fusion within the plane of the plate and/or (2) regulates the local release of calcium ions required for vesicle fusion. OsFeCN post-fixation also provides new information about the cell plate vesicles themselves. The results demonstrate that vesicles derived from dictyosomes undergo an abrupt increase in staining as they fuse at the plate. Finally the ER associated with developing and mature plasmodesmata has been examined. Electron micrographs reveal that the OsFeCN staining, seen traversing the cell plate in early stages, later becomes restricted from that portion of the ER extending through the plasmodesmatal canal. These structural observations support the idea that during formation of the plasmodesma a tubular element of ER is tightly furled upon itself and that its inner leaflet is compressed into a rod. The ER cisternal space appears occluded and thus it is argued that intercellular transport occurs through the cytoplasmic annulus of the plasmodesmata.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1615-6102
    Keywords: BAPTA ; Cell plate ; Cytokinesis ; Free Ca2+ gradient
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Five BAPTA buffers with differential affinities for Ca2+ have been examined for their effects on cell plate formation in stamen hair cells ofTradescantia. The five include 5,5′-dimethyl BAPTA (Kd=0.15 μM), BAPTA (Kd=0.22 μM), 5,5′-dibromo BAPTA (Kd=1.5 μM), 5-methyl,5′-nitro BAPTA (Kd=22 μM), and 5-nitro BAPTA (Kd=40 μM). At a concentration of 5 mM and 25 mM in the pipette, the buffers were iontophoretically microinjected into dividing stamen hair cells (2 nA for 1 min) prior to or at the onset of cell plate formation. At the lowest concentration (5 mM), only one buffer, 5,5′-dibromo BAPTA, inhibits cell plate formation, and is most effective if delivered at the moment of cell plate vesicle aggregation. The inhibitory effects appear as a slowing of cell plate expansion, the formation of distorted plates, or the complete dissolution of plates that might have initiated normally. When the pipette tip concentration is elevated to 25 mM, the effects of 5,5′-dibromo BAPTA become more profound. At these levels 5,5′-dimethyl BAPTA, BAPTA, and 5-nitro BAPTA also modulate cell plate formation, producing effects similar to that of 5,5′-dibromo BAPTA at the lower concentration. Independent studies using fura-2 as a fluorescent analogue of the BAPTA buffers, indicate that the apparent effective concentration for 5,5′-dibromo BAPTA is between 1.0–1.4 mM; its threshold concentration is not known but expected to be somewhat lower. For the other buffers the threshold concentration is between 1.5–2.2 mM. The concentration dependence supports the idea that the buffers facilitate diffusion of Ca2+ away from regions of elevated concentration. The results thus provide evidence that local Ca2+ gradients may be present in the vicinity of the cell plate and that they participate in the cytokinetic process.
    Type of Medium: Electronic Resource
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