ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Inc
    The @journal of eukaryotic microbiology 52 (2005), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: We have induced the resorption of the micronucleus in living conjugants of Tetrahymena. After pairing, but prior to meiosis, the micronucleus undergoes an extraordinary elongation, expanding from a sphere of about 1-μm diameter to a ribbon-shaped structure whose length is greater than that of the cell. Previous EM studies showed an organized basket of microtubules subjacent to the nuclear envelope in the elongating micronucleus. We exposed early pairs to colchicines (1–5 mM), a microtubule inhibitor, and found that micronuclear elongation was prevented. Further, colchicine caused the collapse of already elongated micronuclei. Unexpectedly, with increased time of exposure to colchicine, micronuclei gradually disappeared from view; by 5 h ∼60% of cells in pairs lost their micronuclei. Direct observation ruled out ejection from the cell. We present evidence that microcnuclei are degraded by the lysosmally mediated process of autophagy. Degrading micronuclei in living pairs exposed to both Hoescht 33342 and Acridine Orange stain yellow—blue (for DNA) and orange (for acidification)—as expected for an autophagic vacuole. Further, 3-methyladenine, an inhibitor of autophagy, blocked acidification and prevented degradation. Also, based on the requirement of actin filaments to form autophagosomes, we tested Cytochalasin B, an actin inhibitor. Cytochalasin prevented acidification and blocked micronuclear degradation. Finally, degrading micronuclei, uniquely, fluoresced red in cells whose lysosomes were pre-loaded with Texas Red Dextran, indicate that material was transferred from lysosomes to nuclei-containing vacuoles. These data suggest that nuclear degradation is achieved by autophagy. The mechanism by which colchicine triggers micronuclear autophagy remains to be explored.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 50 (2003), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: . During conjugation in the binucleate ciliate, Tetrahymena thermophila, the old macronucleus is eliminated as new macronuclei and micronuclei are ontogenetically derived from the zygote nucleus. The mechanism of programmed nuclear elimination in ciliates may be related to the mechanism of apoptosis in higher organisms since its chromatin undergoes major condensation, its DNA is digested into nucleosome-sized fragments, and it stains positively for TUNEL. The present study explores whether caspases are involved in programmed macronuclear degradation in Tetrahymena. We show here that caspase-like activity is detectable using two specific colorimetric substrates, and that the activity is reduced with specific caspase inhibitors. In addition, using the fluorigenic substrate PhiPhiLux, active caspase-like activity is detected in living cells, localized to cytoplasmic vesicles; activity is not detected in pre- or post-condensed macronuclei. Finally, three different inhibitors of caspase activity cause a block to macronuclear chromatin condensation and elimination. Therefore, a caspase-like enzyme activity is necessary for regulating macronuclear elimination in Tetrahymena. These data support the possibility that macronuclear elimination is related, evolutionarily, to regulated cell death in multicellular organisms.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 47 (2000), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: . During sexual conjugation in Tetrahymena the micronucleus divides meiotically, producing four haploid nuclei. While one of these nuclei divides mitotically to yield two genetically identical gametic pronuclei, a stationary pronucleus and a migratory pronucleus, the remaining three haploid nuclei degenerate and disappear. Typically, they migrate to the posterior end of the cell where they remain as residual bodies until they disappear. In the present study we asked whether degenerating haploid nuclei share any properties with apoptotic nuclei. Specifically, we wondered whether they would be stained by “apofluor”, a combination of vital fluorescent indicators that differentially stains apoptotic nuclei in living cells. “Apofluor” includes acridine orange, which becomes trapped in acidic compartments and stains lysosomal bodies a brilliant orange-red, and Hoechst 33342, which binds to DNA and stains nuclei bright blue. With this dye combination, while ordinary nuclei stain blue, the apoptotic macronucleus stains first blue-green, then yellow, and finally orange. The progression in color is presumed to be due to the accumulation of protons in the apoptotic nucleus compartment. We found that three of the four post-meiotic haploid nuclei, those that are eliminated, were stained differentially green, then yellow, and then come to be indistinguishable from the orange lysosomal bodies. Differential staining can occur even while the nuclei are located at the anterior ends of the cells, and before the “viable” nucleus divides to form pronuclei. These results indicate that haploid nuclei in the process of degradation are differentially stained in living cells by “apofluor”, and that the differential staining occurs early in the elimination process. Further, since the degenerating haploid nuclei are stained by “apofluor” it is likely that they are degraded by a mechanism similar to the elimination of the apoptotic macronucleus.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 35 (1988), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: . There are numerous mucocysts in Tetrahymena; however, little is known about their composition, organization, biosynthesis, or function. Mucocysts of Tetrahymena are membrane-bounded vesicles located at the cell cortex. They are torpedo-shaped structures (0.9 μm x 0.3 μm) lined up in longitudinal rows along the surface. It is estimated here that each cell contains about 5000 mucocysts. Mucocyst contents are organized in a crystalline manner, but when that material is released by exocytosis, it swells and forms a gel. Using fluorescence microscopy, we demonstrate that mucocysts contain concanavalin A (Con A)-binding material. First, intracellular fluorescent particles in fixed cells incubated with fluorescein-derivatized Con A (F-Con A) have the same distribution, shape, and orientation as mucocysts in living cells. Also, mucocysts were induced to undergo synchronous exocytosis, and the released material formed a capsule around the cell. The capsule was fluorescent after incubation with F-Con A. In both cases fluorescence was abolished by competition with α methyl mannoside, indicating that Con A is binding specifically to a glycosidic component of the mucocyst. Mucocyst capsules also bind wheat germ agglutinin but not soybean agglutinin, pea lectin, or lentil lectin. Preparations of mucocyst material were analyzed by SDS-PAGE. Silver stain revealed a high molecular weight band that had not previously been detected by Coomassie blue staining. That band also stained with Alcian blue, indicating that it is a mucopolysaccharide. Finally, that same band was shown to be Con A binding. Thus the Con A-binding and Alcian blue-staining properties of mucocysts can be attributed to the same high molecular weight mucopolysaccharide component. This study indicates that it may be possible to purify a specific carbohydrate component of mucocysts which may be helpful in analyzing their function, biogenesis, and structural organization.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 27 (1980), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: SYNOPSIS. Simple media for Tetrahymena, using rat gut or soybean as the nutrient source are described. Cultures can be maintained in these media up to one year at room temperature.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 26 (1979), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: SYNOPSIS.In Tetrahymena thermophila subline B, a morphogenic alteration of the anterior end of cells of mating types III and VII results from a cellular interaction which precedes and is a prerequisite for pairing. Cell pairing begins 1 h after starved cells of complementary mating type are mixed. The 1 h-long lag period is characterized by an actinomycin D-sensitive inductive interaction in the first 30 min, followed by a maturation period. Tip transformation begins during the maturation period and continues after pairing. Scanning electron microscopy of deciliated cells reveals ridges which form a chevron meeting in a midline seam between the oral apparatus and the anterior tip. During transformation, the seam broadens until the ridged surface is completely smooth. Melding of the ridges also occurs at the tip of the cell resulting in its blunted appearance. Cells of complementary mating types join in the region of this modified surface, which eventually becomes a specialized cell junction perforated by cytoplasmic bridges. Thus, pursuant to an inductive interaction the structure of the tip of cells is modified in anticipation of the pairing event. Rate of cell pairing might be limited by rate of tip transformation.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 274 (1978), S. 54-55 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Figure 1 shows that when the starved mating types are washed and suspended in fresh buffer before mixing, pairing is delayed for 〉3 h. By this time control cells have already reached their plateau value. A mock wash control showed the effects of centrifugation and resuspension can be ruled out as a ...
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Thin sections show the macronuclei of Paramecium aurelia and Tetrahymena pyriformis to contain two types of bodies. The smaller, measuring 0.1–0.2 μ in diameter, have been resolved in the light microscope by first removing the macronuclei from the cells in the presence of Mg++, then chelating that divalent cation with EDTA, resulting in expansion of the nuclear material. By staining with methyl green, Azure B, and the Feulgen procedure, the small bodies were shown to contain DNA. In whole mounts these small bodies appear to be joined to one another producing a complex network suspended in which are the larger bodies, or nucleoli. — Macronuclei from both ciliates were isolated in large quantities and purified for spreading on an air-water interface. When the nuclei burst from surface tension forces and are examined with the electron microscope, the DNA containing bodies remain attached to one another by means of 100 Å fibrils. The pattern of attachment is non-linear. Occasionally individual DNA-containing bodies “loosen” revealing a coil resembling both in shape and dimensions the 250 Å coil characteristic of eucaryotic chromatin. The substructure of the 250 Å coil has not been directly observed. However, the frequent association of pairs of 100 Å fibrils makes it likely that two such fibrils are tightly complexed in the 250 Å coil. The 100 Å fibril, in turn, contains two 20 Å strands, each presumably a DNA double helix. — In Paramecium each small body of the macronucleus contains approximately one chromosome-equivalent of DNA. The fact that these small bodies are joined to form large structured masses of chromatin within the macronucleus indicates that the distribution of genetic material is not random. It is possible that, similar to bacteria, entire genomes segregate as units, thus accounting for successful amitotic division.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Chromosoma 55 (1976), S. 289-308 
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Micronuclear elongation is the first major event in a series of nuclear changes occurring during the sexual stage of the life cycle of Tetrahymena. Beginning at about one hour after cells of complementary mating types have conjugated, the micronucleus leaves its recess in the macronucleus and swells slightly. This is accompanied by a reorganization of its chromatin from a reticular to a solid body. In the next stage the micronucleus assumes an egg shape, a development concomitant with the appearance of microtubules. While the chromatin “spins out” from the dense body, and microtubules increase in number, the nucleus assumes a spindle shape. During the elongation, which increases the length of the nucleus some fifty fold, microtubules are prominent in clusters just internal to the nuclear membrane, and parallel to the longitudinal axis of the nucleus. When elongation is completed the nucleus is curved around the macronucleus. Internally, partially condensed strands of chromatin are located off-center, towards the macronuclear side, and the density of the microtubules is diminished. At all the stages, DNA is located throughout the nucleus; neither discrete chromosomes nor synaptonemal complexes are seen. Occasionally cytoplasmic membrane systems are seen fused to the nuclear envelope which retains the typical appearance of a double membrane with pores.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 172 (1982), S. 159-178 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The conjugation junction of Tetrahymena has been examined by thin sections, freeze fracture preparations, and by scanning electron microscopy. The junction is formed where the anterior tips of the pairing cells attach to one another. The structure is essentially a large disk composed of two face-to-face plasma membranes separated by a gap of extracellular space measuring about 50 nm. Rows of intramembrane particles are present at the boundary between the junction and ordinary cell cortex. These particles form a ring around the junction. Subjacent to each membrane is a thick mottled layer of material. Pores form in the junction at sites of membrane fusion. Though wider than long, these structures are actually bridges of cytoplasm that connect the conjugating cells. Pores fall into certain size and shape classes, indicating that membrane fusion is highly controlled in this system. At the level of the cytoplasmic bridge the submembrane material is compact and electron-dense. Changes in the structure of the epiplasmic layer have been monitored as the normal cortex is modified during tip transformation and through formation of the mature conjugation junction. Evidence is provided that the submembrane layer plays a significant role in the regulation of pore formation. This cytoskeletal structure may also limit the extent of membrane fusion, thus controlling the size of the cytoplasmic channels.
    Additional Material: 17 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...