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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 433 (1996), S. 351-356 
    ISSN: 1432-2013
    Keywords: Key words Cell proliferation ; Wound repair ; Arachidonic acid mobilization ; PDGF ; Prostaglandins ; Cyclooxygenase ; Phospholipase A2 ; Fibroblasts
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abtract  Foetal calf serum (FCS) and platelet-derived growth factor (PDGF) induced arachidonate release in subconfluent murine 3T6 fibroblast cultures. However, the magnitude of this effect decreased significantly as the cell culture became confluent. Wound-induced injury of the fibroblast monolayer initiated a repair process that was potentiated by FCS or PDGF and which restored the integrity of cell monolayer. Under these experimental conditions, FCS and PDGF induced phospholipase A2 activity and subsequent arachidonic acid mobilization and production of eicosanoids in wounded fibroblast cultures. Finally, it is demonstrated that prostanoids, specifically prostaglandin E2, play an important role in cell proliferation induced by FCS and PDGF during wound repair.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 432 (1996), S. 655-662 
    ISSN: 1432-2013
    Keywords: Key words Cell proliferation ; Arachidonic acid mobilization ; Prostaglandins ; Phospholipase A2 ; Fibroblasts
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract When we stimulated 3T6 fibroblasts, we observed a mobilization of arachidonic acid (AA) from phospholipids. The magnitude of this response decreased as the cells became confluent and the change coincided with a decrease in the percentage of cells in growth phases (G2 + M); this was not a consequence of the time in culture or a factor in the growth medium. Preconfluent fibroblasts incubated with the calcium ionophore A23187 (1 μM), 4β-phorbol-12-myristate acetate (PMA, 10 μM), bradykinin (10 μM) or fetal calf serum (20%) released 38.8%, 62.5%, 11.2% and 45.6% [3H]AA, respectively. Confluent cells stimulated under the same conditions released only 16.9%, 1.5%, 0.5% and 18.5% [3H]AA, respectively. This decreasing mobilization of AA was demonstrated using metabolic labelling and measurement of prostaglandin PGE2. The decrease was not due to a changing pool of AA. [3H]AA release from each phospholipid decreased with confluence. Conversion of confluent cells to the proliferative phenotype by mechanical wounding of the monolayer increased the release of [3H]AA. This effect is consistent with regulated, growth-dependent changes in the activity of phospholipase A2, a process regulated by changes in phosphorylation of the enzyme. The increased release of [3H]AA from preconfluent, actively dividing cells may have important physiological implications and may help elucidate mechanisms regulating release of AA.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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