6533b85ffe1ef96bd12c2559

RESEARCH PRODUCT

Variability of ecdysteroid-induced cell cycle alterations in Drosophila Kc sublines.

G. CordierM. T. BessonAndré QuennedeyBrigitte QuennedeyJean Delachambre

subject

Programmed cell deathCellClone (cell biology)MitosisCell CountBiologyCell Linechemistry.chemical_compoundmedicineAnimalsInterphaseEcdysteroidCell CycleCell BiologyGeneral MedicineAnatomyDNACell cycleCell countingFlow CytometryMolecular biologyCulture Mediamedicine.anatomical_structureEcdysteronechemistryCell cultureDrosophilaMoulting

description

. The cell cycle of two lines isolated from Drosophila Kc cells was followed by flow cytofluorometry and cell counting. The first line is the 8-9K clone which grew in a medium supplemented with 5% serum; the second, named subline Kc0, grew in a serum-free medium. The stationary phase is characterized by a G2 cell accumulation: 73% in the 8-9K clone and 50% in the Kc0 subline. When the medium was supplemented with the steroid moulting hormone 20-hydroxyecdysone, more than 90% of 8-9K cells and 65% of Kc0 cells were progressively arrested in G2. In the continuous presence of 20-hydroxyecdysone, most of the 8-9K cells remain G2-arrested; no massive G2 release into M was observed and only a few cells were able to divide. When treated for only 3 or 7 days, a transient release into M and proliferation occurred after hormone-free medium renewal, largely masked by G2 cell death. These results are discussed in comparison with other reports on cell cycle alteration induced by ecdysteroids.

10.1111/j.1365-2184.1987.tb01326.xhttps://pubmed.ncbi.nlm.nih.gov/3427605