Yaginuma T, Kai H, Happ G M
Department of Zoology, University of Vermont, Burlington 05405.
Dev Biol. 1988 Mar;126(1):173-81. doi: 10.1016/0012-1606(88)90251-5.
The cells of the bean-shaped accessory glands of mealworms proliferate through the first 7 days of the 9-day pupal stage. Immediately after larval-pupal ecdysis, 25-27% of the cells were in the G1 phase, 60-65% were in the G2 phase, and the balance were in S phase. Over the first 4 days of normal development, the S fraction gradually increased, to reach its highest level in the mid-pupa at the time of the major ecdysteroid peak (Delbecque et al., 1978). Thereafter, the S fraction declined until over 95% of the cells had accumulated in G2 on Day 8. When 0-day pupal glands were explanted into Landureau's S-20 medium for 6 days, the G1 fraction remained fairly constant (25-30%) while S and the G2 fractions fluctuated. On the first day in vitro, the G2 fraction declined and the S fraction rose. On the second day in basal media, the S fraction fell and G2 rose correspondingly until 70% of the cells reached G2 when cycling stopped on the third day. With addition of 20-hydroxyecdysone to 0-day cultures, the S fraction increased quite sharply. It remained large for all 6 days of the experiment in the continuing presence of hormone. A 1-day pulse of hormone produced a transient increase in S. We blocked cell cycling with hydroxyurea in a stathmokinetic experiment and showed that 20-hydroxyecdysone accelerated the flow of cells from the G2 phase to the G1 phase by 2.5-fold. An increase in the G1 fraction was detected within 10 hr of hormone administration and the effect was dose-dependent with an ED50 of 5 X 10(-7) M for 20-hydroxyecdysone. We conclude that 20-hydroxyecdysone acts at a control point in the G2 phase. Incubation of the glands with 20-hydroxyecdysone for only 30-60 min followed by washout stimulated the flow from G2 to G1 and the effect persisted after transfer of the tissues to hormone-free media. Dose-dependent stimulation also occurred with ponasterone A (ED50 3 X 10(-9] but not with cholesterol.
黄粉虫豆形附腺的细胞在9天蛹期的前7天进行增殖。幼虫-蛹蜕皮后立即观察到,25%-27%的细胞处于G1期,60%-65%处于G2期,其余处于S期。在正常发育的前4天,S期细胞比例逐渐增加,在蛹中期蜕皮甾类激素达到峰值时达到最高水平(德尔贝克等人,1978年)。此后,S期细胞比例下降,直到第8天超过95%的细胞积累在G2期。将0日龄蛹的腺体在朗迪厄的S-20培养基中培养6天,G1期细胞比例保持相当恒定(25%-30%),而S期和G2期细胞比例则波动。在体外培养的第一天,G2期细胞比例下降,S期细胞比例上升。在基础培养基中培养的第二天,S期细胞比例下降,G2期细胞比例相应上升,直到第三天细胞停止循环时70%的细胞进入G【2期。在0日龄培养物中添加20-羟基蜕皮甾酮后,S期细胞比例急剧增加。在激素持续存在的情况下,整个6天的实验中该比例都保持在较高水平。1天的激素脉冲使S期短暂增加。我们在一个静止动力学实验中用羟基脲阻断细胞周期,结果表明20-羟基蜕皮甾酮使细胞从G2期进入G1期的速度加快了2.5倍。在给予激素后10小时内检测到G1期细胞比例增加,且该效应呈剂量依赖性,20-羟基蜕皮甾酮的半数有效剂量(ED50)为5×10-7 M。我们得出结论,20-羟基蜕皮甾酮作用于G2期的一个控制点。将腺体与20-羟基蜕皮甾酮孵育仅30-60分钟后冲洗,刺激了细胞从G2期向G1期的流动,并且在将组织转移到无激素培养基后该效应仍然存在。波那甾酮A(ED50 3×10-9)也出现剂量依赖性刺激,但胆固醇没有这种作用。