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  • Articles  (25)
  • Articles: DFG German National Licenses  (25)
  • Life and Medical Sciences  (20)
  • Plasmodesmata  (5)
  • EARTH RESOURCES AND REMOTE SENSING
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  • Articles  (25)
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  • Articles: DFG German National Licenses  (25)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 174 (1993), S. 36-44 
    ISSN: 1615-6102
    Keywords: Cell-to-cell communication ; Plasmodesmata ; Setcreasea purpurea ; Transport ; Intercellular
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Diffusion coefficients for FITC-molecular probes in intercellular pores (D) and rate of molecular probe loss into the vacuole (k1) have been obtained for FITC molecular probes in staminal hairs ofSetcreasea purpurea. The kinetic curves of FITC-Gly, -Ala, -Leu,-Ser, -Thr, -Cys, -Met, -Tyr, -Asp, -Glu, -Asn, -Gln, -Lys, -His,-Arg, -(Asp)2, -(Glu)2, -(Lys)2, -(Asp)3, -(Glu)3, -(Gln)2, -(Gln)3, -(Gln)4, and carboxyfluorescein (group I probes) matched the curves calculated for simple diffusion through a chain of cells, while the majority of kinetic curves of FITC-Phe, and -Try (group II probes) did not. None of the kinetic curves for FITC-(Met)2 and -(His)2 (group III probes) matched. Average Ds for group I probes ranged from 0.77× 10−8cm2/s to 3.75× 10−8cm2/s and for group II probes were 0.50× 10−8cm2/s. A meaningful average D for group III probes could not be calculated. Average k1 for group I probes ranged from 1.62× 10−7/μm2/s to 13.21× 10−7/μm2/s, and for group II probes were 5.42 and 11.54× 10−7/μm2/s. Average k1s for group III probes could not be calculated. Symplastic transport occurred by cell-to-cell diffusion for most of the probes (e.g., group I probes) but not always for some (e.g., group II probes) and never for others (group III probes). The rate of cell-to-cell diffusion and loss within the vacuole depended upon the molecule's specific structure, molecular weight and charge. We concluded that plasmodesmata select for molecules that are hydrophilic, small and have a charge of from — 2 to — 4, and against molecules that contain either Phe, Try, Met or His groups.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 113 (1982), S. 193-201 
    ISSN: 1615-6102
    Keywords: Intercellular communication ; Plasmodesmata ; Symplastic transport ; Setcreasea purpurea
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Investigations into plant intercellular communication were initiated through an examination of plasmodesmata and cell-to-cell passage of molecular probes in the staminal hairs ofSetcreasea purpurea. Plasmodesmata connecting staminal hair cells of small buds are filled with an electron-opaque homogenous material. To examine the permeation selectivity of plasmodesmata, molecular probes made up of fluorescein isothiocyanate (FITC) complexed with amino acids and peptides were injected into the staminal hair cells and the spread of these fluorescent molecules through the symplast, was monitored. Molecules composed of FITC complexed to single amino acids with polar and aliphatic R groups travel rapidly, while those which include peptides travel slowly. Dye molecules composed of an amino acid with an aromatic side group do not pass from cell to cell at all. It is hypothesized that the material occluding the plasmodesmata constitutes the diffusion barrier, by presenting a hydrophilic environment which allows passage of molecules with maximum molecular weights of 700–800 daltons, but which retains those with aromatic side groups.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 128 (1985), S. 167-172 
    ISSN: 1615-6102
    Keywords: Intercellular transport ; Plasmodesmata ; Setcreasea purpurea ; Symplastic transport
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Previously reported studies of cell ultrastructure and molecular probe passage in immature staminal hairs were extended to kinetic studies. The rate of transport of carboxyfluorescein into the cytoplasm in individual cells was monitored with a video analyzer and transport coefficients were determined. Carboxyfluorescein was found to traverse 5 cells in less than 5 minutes. The values of transport coefficients differed between cells and this was taken to mean that some cells are more closely coupled than others.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 174 (1993), S. 45-49 
    ISSN: 1615-6102
    Keywords: Cell-to-cell communication ; Plasmodesmata ; Setcreasea purpurea ; Azide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The effect of azide on the diffusion of fluorescent molecular probes was examined in staminal hairs ofSetcreasea purpurea. Staminal hairs were treated with azide before being microinjected with fluorescent molecular probes of different size, charge, and structure. The cell-to-cell movement of these fluorescent molecules was videotaped, analyzed, and coefficients of diffusion through plasmodesmata (D) and coefficients of diffusion across the tonoplast (k1) were calculated and compared to those of untreated cells. The D was larger and the k1 was smaller for many fluorescent probes in azide treated cells compared to normal, untreated cells. In addition, the cell-to-cell diffusion selectivity based on molecule structure, size and charge no longer existed in azide treated cells. An average D of 3.3×10−8cm2/s and an average k1 of 2.9×10−7/μm2/s was calculated for the molecular probes tested. New size limits for permeation were observed indicating that the plasmodesmata had become enlarged.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 137 (1987), S. 140-144 
    ISSN: 1615-6102
    Keywords: Intercellular transport ; Cell-to-cell communication ; Plasmodesmata ; Cytoplasmic streaming ; Setcreasea purpurea
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The effect of inhibition of cytoplasmic streaming on intercellular passage of carboxyfluorescein (CF) in staminal hairs ofS. purpurea was examined. Tip cells of staminal hairs were microinjected with buffered-CF. Cytoplasmic streaming was then inhibited by addition of KCN or NaN3 to the external bathing solution. In separate experiments, cytoplasmic streaming was inhibited by microinjection of cytochalasin D along with the buffered-CF. CF passage over a 5 minutes treatment period was monitored by video fluorescence microscopy and video intensity analysis. Cytoplasmic streaming ceased within 1 minute of inhibitor agent treatment, however, little change in the kinetics of intercellular passage was noted over the 5 minute experimental period. Th us, cytoplasmic streaming plays no major role in the regulation of intercellular passage of the hydrophilic, negatively charged molecule CF.
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  • 6
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Additional Material: 5 Tab.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 168 (1981), S. 51-71 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The topography and histology of the skin of the naked mole (Heterocephalus glaber) have been correlated with its behavior. The integument is exceptionally loose, thereby reducing integumentary stresses when the animal is digging and moving in narrow tunnels. It also allows the position of the nasolabial sensory patch to change. This patch is exposed to mechanical stimuli when Heterocephalus moves along the tunnel, but becomes partially shielded by a transient buccal evagination, the formation and function of which are here described. Most of the differentiated patches of the skin lie in the cranial and anogenital regions. The eyes are microphthalmic and nearly completely closed by the nonmobile eyelids; there is no pinna, hair-coat or sweat glands.The epidermis is of variable thickness; in some places it has only one layer of cells. The detached epidermal cells penetrate the dermis irregularly.The epidermis of Heterocephalus is specialized by modifications of its germinative stratum, equivalent to an epidermosis, the syndrome of which consists of reduction of all types of epidermal buddings - pilogenetic and adenogenetic - as well as those which have a mechanical significance.
    Additional Material: 45 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 5 (1985), S. 225-237 
    ISSN: 0886-1544
    Keywords: neural crest ; migratory behavior ; microfilaments ; stress fibers ; tractional force ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: We have investigated one aspect of the migratory behavior of quail neural crest (NC) cells by comparing the organization of microfilament bundles and the ability to distort migratory substrata by NC, somite, and notochord cells in vitro. In contrast to the numerous cytoplasmic stress fibers in somite-derived fibroblasts and notochord cells revealed by rhodamine-phalloidin staining and thin-section electron microscopy, microfilaments in NC cells are restricted to the cell cortex. To test the relative degrees of tension generated by these cell types on the underlying substratum, cells were cultured in collagen gels and on distortable silicone rubber sheets. Explanted somites and notochords produced dramatic radial alignment of 750 μg/ml collagen gels, whereas neural crest cells only aligned gels of lower concentrations. Fibroblasts did not migrate individually from explanted somites and notochords into 250 μg/ml collagen gels as readily as into higher concentration collagen lattices. In contrast, neural crest cells migrated into matrices of low concentration as well as into higher concentration collagen gels. Neural crest cells and their pigmented derivatives did not distort silicone rubber sheets, whereas somite and notochord-derived fibroblasts wrinkle this substratum after 4 days in culture. Thus, the differences in organization of the actin cytoskeleton reflect the tractional force exerted by these cells on their substratum. We hypothesize that the migratory behavior of NC cells in vivo may be related to their ability to translocate through embryonic extracellular matrices while generating relatively weak adhesions with the substratum, whereas the stronger forces generated by other embryonic cell types upon the delicate extracellular matrix may restrict their migration and may be associated with other morphogenetic events.
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 6 (1986), S. 305-313 
    ISSN: 0886-1544
    Keywords: cytoplasmic streaming ; Setcreasea purpurea ; intracellular particle movements ; intercellular transport ; azide ; low temperature ; calcium ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Cytoplasmic streaming and its response to azide and low temperature were examined by using high-resolution video-enhanced light microscopy in Setcreasea purpurea staminal hair cells of immature flowers. Particles and organelles examined moved along well-defined pathways, in repeated and unequal saltatory steps, at different rates and sometimes against the main direction of flow (bidirectionally) in both transvacuolar strand and peripheral cytoplasm. Particle movements were reversibly inhibited with azide. Low temperatures caused transvacuolar strands to shift or break. This cytoplasm accumulated in areas outside of the vacuole where spherosomes continued to saltate, but not along well-defined pathways. In the peripheral cytoplasm, however, the spherosomes continued to move normally, amyloplasts became swollen, and they plus the other organelles (except spherosomes) were stationary. Normal particle movements were obtained when chilled cells were rewarmed to 27°C for ca 15 min.
    Additional Material: 8 Ill.
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  • 10
    ISSN: 0886-1544
    Keywords: microtubule bending ; cytoskeletal assembly ; cochlea ; mouse ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Mature inner pillar cells in the mammalian organ of Corti are curved through about 60°, where they arch over adjacent epithelial cells and the apex of an intercellular space called the tunnel of Corti. This report deals with changes in microtubule organization that are associated with cell bending and tunnel formation during morphogenesis of the mouse organ of Corti.A large bundle of up to 3,000 microtubules assembles in each inner pillar cell. Microtubule rearrangement occurs about 5 days after bundle assembly begins. The lumen of each initially straight hollow tube-shaped microtubule bundle is occluded as the bundle becomes more compact and elliptical in cross section. This event anticipates the once-only bending which subsequently occurs between particular levels (abut 9-19 μm) below the top of a bundle as it curves into its final shape about 2 days later. Microtubule rearrangement presumably facilitates bending which is effected in the plane of lest mechanical resistance parallel to the short axis of a bundle's elliptical cross-sectional profile.Precocious bending of bundles has been induced about 1.5 days in advance of the natural event. Abnormal positioning of these prematurely curved bundles indicates that bending is effected by a contractile mechanism located within bundles rather than being a response to externally applied forces. The potential importance of such microtubule-associated contractions for active modulation of the vibratory response in the cochlea during hearing is considered. © 1993 Wiley-Liss, Inc.
    Additional Material: 8 Ill.
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