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  • Na+, K+-ATPase  (1)
  • Percoll gradient  (1)
  • Ultraviolet light  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Archives of dermatological research 278 (1986), S. 382-385 
    ISSN: 1432-069X
    Keywords: DNA polymerase ; Epidermis ; Percoll gradient ; Hyperkeratosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary DNA polymerase activity was determined in hyperkeratotic epidermis of the guinea pig by topical application of n·hexadecane. Epidermal cells were separated by Percoll gradient centrifugation. DNA polymerase α activity was higher in the basal cells, but polymerase β activity was higher in granular cells than in cells from the other layers. The hyperkeratosis was accompanied by an increase in polymerase α activity in both the squamous and basal cells. However, polymerase β activity decreased in the granular cells and was distributed almost uniformly across the epidermis. The distribution pattern of polymerase activities in the hyperkeratotic epidermis was not simply an enhancement of the pattern in normal epidermis.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Archives of dermatological research 280 (1988), S. 29-32 
    ISSN: 1432-069X
    Keywords: Electron spin resonance ; Epidermis ; Percoll density centrifugation ; Membrane fluidity ; Na+, K+-ATPase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The dynamic properties of plasma membrane in epidermal cells were determined by means of electron spin resonance using two kinds of doxyl stearic acid spin labeling agents: 5-DSA and 12-DSA. 5-DSA and 12-DSA are stearic acid analogues with a nitroxide radical ring at the 5th and 12th carbon positions, and these motions reflect molecular motion of lipid bilayer surrounding the hydrophilic region and the hydrophobic region, respectively. Guinea pig epidermal cells were separated into three regions of keratinocytes by Percoll density gradient centrifugation; the upper, middle, and lower epidermal cells. The order parameter S values for 5-DSA and 12-DSA incorporated into the isolated keratinocytes increased, suggesting a decrease in the plasma membrane fluidity, as cells approached the upper epidermal cell layer. The Na+, K+-ATPase activity as a plasma membrane-bound enzyme was determined in each epidermal cell region, and was found to decrease gradually as the cells approached the upper layer. Accordingly, the differentiation of epidermal cells in the keratinization process was found to be assiciated with a decrease in plasma membrane fluidity and with a decline of Na+, K+-ATPase activity.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Archives of dermatological research 280 (1989), S. 481-486 
    ISSN: 1432-069X
    Keywords: Electron spin resonance ; Ultraviolet light ; B-16 Melanoma cells ; Membrane fluidity ; Phospholipase A2
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Electron spin resonance spectroscopy using the spin probe (5-, 12-and 16-deoxylstearic acid) was employed to analyze the changes in membrane fluidity in B-16 melanoma cells following UV-B exposure. The UV exposure resulted in the immediate accumulation of lipid peroxide, being accompanied by a change in membrane fluidity. The 12-DSA is the most sensitive to the changes in membrane organization caused by UV light. Na+,K+-ATPase activity was regulated by a change in membrane fluidity. Following UV exposure, the release of the prelabeled arachidonic acid from the cells was observed immediately. Ca2+-dependent calmodulin-dependent phospolipase A2-like activity was involved in the UV-stimulated arachidonic acid release from phospholipid.
    Type of Medium: Electronic Resource
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