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  • 1
    ISSN: 1615-6102
    Keywords: Chloramphenicol ; Cell proliferation ; Cellular ATP content ; Mitochondrial substructure ; Tetrahymena pyriformis GL
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary A time-dependent loss of tubular infolding of the inner mitochondrial membrane was reported recently as an effect of the cytostatic drug, methotrexate (MTX), onTetrahymena (Nilsson 1983); this finding was interpreted as an inhibition of mitochondrial protein synthesis. In the present study, the cells were exposed to chloramphenicol (CAP), an inhibitor of mitochondrial translation, at the same concentrations (1–25 mM) as MTX; the question asked was whether the two drugs acted similarly. CAP affected cell proliferation by causing a dose-dependent prolongation of the generation time, but at 10–25 mM permitted only a limited number of cell doublings, whereas 1 mM MTX inhibits growth after 5 cell doublings. With CAP the inner mitochondrial membrane diminished gradually in accordance with the number of cell doublings at 10–25 mM, but in 2 mM CAP, for example, some tubular infoldings were still present after 17 cell doublings. The gradual loss of the inner mitochondrial membrane correlated with a gradual decrease in the cellular ATP content, irrespective of the concentration of the drug but dependent on the progress of the cells through their first cycle when exposed to the drug; in cells which continued to proliferate, the ATP content remained at a value corresponding to 80% of the control value. With respect to cell proliferation, the two drugs act differently. CAP is less toxic than MTX, reflected in a 10 times shorter recovery time for cell proliferation after removal of CAP. Hence, although the structural manifestation of the action of the two drugs on mitochondria is identical, their target site may differ.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1615-6102
    Keywords: Nickel ; Endocytosis ; Motility ; Proliferation ; Cellular nickel content ; Adaptation ; Tetrahymena pyriformis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary At concentrations above 1 mM, nickel has a dose-dependent effect on the rate of food vacuole formation in cells in the growth medium, proteose peptone (PP); total inhibition of endocytosis occurs within 10 minutes in 6mM nickel. However, only a 10 times lower concentration of nickel is tolerated by starved cells in an inorganic salt medium, a difference which may be ascribed to the high binding property of nickel to organic material. In the PP medium, nickel affects cell motility by increasing the rate of movement at a concentration of 1 mM, and by causing immobilization after 30 minutes in 6mM nickel; a spontaneous, partial recovery of cell motility is seen after 3 hours in 6 mM nickel. The effects of nickel on endocytosis and cell motility are reversible after removal of nickel. Cell proliferation continues at a reduced rate in 1 mM nickel, while only 1 1/2 cell doublings are achieved in 3 mM nickel during a 72-hour exposure, and no proliferation occurs in 6mM nickel, where an increasing cell mortality is observed after 12 hours. The cell content of nickel relates initially to the external concentration of the metal; however, cells in 1 mM nickel are capable of maintaining a constant content of the metal, whereas in 3 mM, the rate of accumulation is reduced after 3 hours, and cells in 6mM nickel accumulate the metal at a constant rate. All nickel-treated cells contain small refractive granules, previously proposed as representing an ion-regulating system, and the apparent adaption ofTetrahymena to the effects of nickel may be ascribed to such a regulation of the intracellular concentration of the metal.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 132 (1986), S. 99-106 
    ISSN: 1615-6102
    Keywords: Continuous flow cultivation system ; Growth characteristics ; Tetrahymena pyriformis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary A completely liquid-filled culture chamber with gas exchange across a synthetic membrane (Larsen andNilsson 1985) was incorporated into an automatic continuous flow system. The absence of an airliquid interface in the system permits removal of cell samples, and addition of fresh medium, under strictly sterile conditions. In this system,Tetrahymena pyriformis can be kept under optimal growth conditions in a rich nutrient medium and any defined cell density may be maintained for extended periods of time by varying the dilution rate of the culture. Furthermore, it has been possible to demonstrate, in the slope of the growth curve, even small changes which are difficult to detect in batch cultures since the duration of these changes is short. In the continuous flow system, the relative cell volume distribution and the food vacuole forming capacity of the cells were unaltered; however, all cells contained small refractive granules. The system permits the culture volume to be varied, but a standard volume of 20 ml was maintained in most experiments. Since the culture volume is small, the system requires less than one liter of fresh medium per week to maintain the cells in the exponentially multiplying growth phase.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 95 (1978), S. 163-173 
    ISSN: 1615-6102
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The ciliateTetrahymena pyriformis was exposed to lead acetate. Cell proliferation in the presence of 0.1% lead salt (with or without EDTA) equaled, after a variable lag period, that of the control cells. The lead (550 ppm) forms a “fluffy” precipitate with the organic growth medium; this was in part prevented by addition of EDTA. The cells primarily ingested the “fluffy” precipitate whereby they became exposed to large amounts of lead. Within the digestive vacuole, the “fluffy” precipitate became converted into refractile structures (3 μm in diameter) which were egested and accumulated at the bottom of the culture flask. The lead content of these defecation balls was higher than that of the “fluffy” precipitate. In addition to the lead-containing vacuoles, the cells contained small, refractile granules. The apparent, high tolerance ofTetrahymena towards lead is believed to be due in part to the low ionic concentration of lead under the present conditions and in part to a “detoxication mechanism” consisting of retention of lead within the digestive vacuoles and perhaps of accumulation of lead within the small, refractile granules.
    Type of Medium: Electronic Resource
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