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  • 1
    Electronic Resource
    Electronic Resource
    Mechanisms of Microsporidial Cell Division: Ultrastructural Study on Encephalitozoon hellem (1998)
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 45 (1998), S. 0 
    Details
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The mitotic process in microsporidian Encephalitozoon hellem. a known human pathogen, has been studied with the aim of elucidating some ultrastructural aspects of its nuclear division. The presence of a nuclear spindle, of “electrondense spindle plaques” associated with the nuclear envelope and of cytoplasmic double walled vesicles are reported. We suggest that these “electrondense spindle plaques” serve as foci for intranuclear and cytoplasmic microtubule arrangements, similar to the microtubule organizing centers within the centrosomes of animal cells. The extent to which the microsporidial division process is comparable with that of more familiar eukaryotes such as yeast cells is discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1111/j.1550-7408.1998.tb04547.x
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  • 2
    Electronic Resource
    Electronic Resource
    Evidence of Actin in the Cytoskeleton of Microsporidia (1999)
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 46 (1999), S. 0 
    Details
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Using transmission electron microscopy, fluorescence microscopy, immuno-electron microscopy, and biochemical techniques such as 2-D electrophoresis and immunoblotting, actin was found in all biological stages of the microsporidia Encephalitozoon hellem and Encephalitozoon cuniculi.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1111/j.1550-7408.1999.tb04621.x
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  • 3
    Electronic Resource
    Electronic Resource
    Cytoskeleton of the Drosophila egg chamber: New observations on microfilament distribution during oocyte growth (1995)
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 31 (1995), S. 298-306 
    Details
    ISSN: 0886-1544
    Keywords: Drosophila ; nurse cells ; oocyte ; microfilaments ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The distribution of microfilaments in Drosophila egg chambers stained with rhodamine (Rh)-conjugated phallcidin was studied by laser scanning confocal microscopy and transmission electron microscopy. These techniques revealed new details in the pattern of microfilament localization. We observed in stage 1-3 egg chambers accumulation of filamentous actin in the oocyte cytoplasm between the ring canals connecting the oocyte with adjacent nurse cells. Starting from stages 6-7 short microfilament bundles arranged in basket-like structures were associated with the side of the ring canals facing the nurse cell cytoplasm. We also observed a dramatic decrease in the actin network associated with the cortex of the oocyte in stage 10. During stage 10B the nurse cell cytoplasm was crossed by radial actin bundles that showed a sarcomeric-like cross striation after Rh-phalloidin staining. The ring canals also did not uniformly stain but showed a punctate labeling. The implications of the actin cytoskeleton during oocyte growth are discussed. © 1995 Wiley-Liss, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cm.970310406
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  • 4
    Electronic Resource
    Electronic Resource
    A monoclonal antibody recognizing a common antigen on Drosophila embryos and human fibroblasts (1991)
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 19 (1991), S. 1-8 
    Details
    ISSN: 0886-1544
    Keywords: anti-vimentin antibody ; nuclear envelope ; centrosomes ; Drosophila early embryogenesis ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: We used a monoclonal antibody specific for vimentin from human fibroblasts to stain whole mounts of Drosophila embryos. In immunofluorescence observations this antibody cross-reacts with an antigenic determinant localized throughout mitosis at the nuclear boundary. Double fluorescence observations with the Rb188 antibody that specifically recognizes a centrosomal protein of the Drosophila embryo [Whitfield et al., 1988] showed that the anti-vimentin antibody cross-reacts with an antigen localized in the centrosomal region.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cm.970190102
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  • 5
    Electronic Resource
    Electronic Resource
    Monoclonal antibody raised against murine IL-1 α peptide cross-reacts with a 60-kDa antigen in early Drosophila melanogaster embryo (1995)
    Springer
    Cell & tissue research 282 (1995), S. 269-275 
    Details
    ISSN: 1432-0878
    Keywords: Key words: Mitosis ; Nuclear envelope ; Interleukin ; Development ; ontogenetic ; Drosophila melanogaster (Insecta)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract. Whole-mounts of Drosophila embryos were stained with the monoclonal antibody Vmp 18, raised against the peptide 199–208 of murine interleukin 1/α. Immunofluorescence observations showed that the antibody cross-reacted with an antigenic determinant that changed in localization during Drosophila development. In syncytial Drosophila embryos, the antibody recognized an epitope localized on the nuclear envelope throughout mitotic division. As cellularization occurred, the fluorescence was mainly concentrated in the apical region of the blastoderm cells. Western blot analysis of whole Drosophila embryo extracts showed that the antibody recognized a 60-kDa protein in syncytial embryos and during germ band elongation. This suggests that the 60-kDa antigen undergoes dynamic redistribution during embryogenesis.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/s004410050478
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  • 6
    Electronic Resource
    Electronic Resource
    Surface cap modifications in cold-treatedDrosophila melanogaster embryos (1992)
    Springer
    Cell & tissue research 270 (1992), S. 553-558 
    Details
    ISSN: 1432-0878
    Keywords: Development, ontogenetic ; Cold exposure ; Microfilaments ; Microtubules ; Centrioles ; Drosophila melanogaster (Insecta)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary When earlyDrosophila embryos were allowed to develop at 0°C, several abnormalities in the surface cap organization were observed. Scanning electron microscopy showed that exposure to cold mainly lead to the deformation of the cortical caps and to their partial fusion with adjacent caps. The process of cellularization was presumably affected and large uncellularized areas were observed. Rhodamine-phalloidin staining showed that cap deformation was closely related to the altered microfilament distribution, which was presumably responsible for the failure of large syncytial areas to cellularize. During the process of cellularization, F-actin localization did not depend on the microtubules forming the baskets around the elongating nuclei, but was related to the subpopulation of mictotubules radiating from the centrosomes toward the plasma membrane. Only these microtubules seemed to be affected by cold treatment.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00645058
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  • 7
    Electronic Resource
    Electronic Resource
    The cytoskeleton of the ventral nephrocytes of Ceratitis capitata larva (1994)
    Springer
    Cell & tissue research 275 (1994), S. 529-536 
    Details
    ISSN: 1432-0878
    Keywords: Nephrocytes, insect ; Microfilaments ; Microtubules ; Junctional structures ; Ceratitis capitata (Insecta)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Nephrocytes are cells involved in the regulation of the composition of the hemolymph and are characterized by peripheral finger-like projections delimiting a labyrinthine channel system. We have combined structural and immunological methods to examine the spatial distribution of microtubules and microfilaments in disseminated nephrocytes of Ceratitis capitata larva; the nephrocytes are scattered among the fat-body cells, close to the salivary glands. Actin filaments are localized in two discrete peripheral domains and microtubules are mostly concentrated in the cortical region. We discuss the possibility that these cytoskeletal elements, localized in the finger-like processes of the plasma membrane, are involved in maintaining the spatial architecture of the cell periphery and in modifying the junctional complexes that represent the entrance to the labyrinthine channel system.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00318821
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  • 8
    Electronic Resource
    Electronic Resource
    Monoclonal antibody raised against murine IL-1 α peptide cross-reacts with a 60-kDa antigen in early Drosophila melanogaster embryo (1995)
    Springer
    Cell & tissue research 282 (1995), S. 269-275 
    Details
    ISSN: 1432-0878
    Keywords: Mitosis ; Nuclear envelope ; Interleukin ; Development, ontogenetic ; Drosophila melanogaster (Insecta)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Whole-mounts of Drosophila embryos were stained with the monoclonal antibody Vmp 18, raised against the peptide 199–208 of murine interleukin 1/α. Immunofluorescence observations showed that the antibody cross-reacted with an antigenic determinant that changed in localization during Drosophila development. In syncytial Drosophila embryos, the antibody recognized an epitope localized on the nuclear envelope throughout mitotic division. As cellularization occurred, the fluorescence was mainly concentrated in the apical region of the blastoderm cells. Western blot analysis of whole Drosophila embryo extracts showed that the antibody recognized a 60-kDa protein in syncytial embryos and during germ band elongation. This suggests that the 60-kDa antigen undergoes dynamic redistribution during embryogenesis.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00319117
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