Milner M J, Sang J H
J Embryol Exp Morphol. 1977 Feb;37(1):119-31.
The theory that beta-ecdysone initiates developmental changes during insect metamorphosis by causing an increase in intranuclear levels of potassium, together with a concomitant decrease in sodium levels, has been investigated by two methods. First, imaginal discs from late third instar larvae have been cultured with 0-2 microng/ml of beta-ecdysone together with inhibitors of active ion transport. Non-specific inhibitors, which may have general effects on sulphydryl groups, such as iodoacetic acid, N-ethylmaleimide ethacrinic acid and furosemide, inhibit both eversion and differentiation at concentrations of from 10(-3) M to 2 X 10(-3) M. Ouabain, the only specific inhibitor of the active transport of Na+ and K+ across membranes, had no effect on development even at a concentration of 10(-2) M. Second, a medium containing raised levels of K+, and reduced concentrations of Na+, neither initiated disc development in the absence of beta-ecdysone, nor stimulated development induced by suboptimal levels (0-02 microng/ml) of beta-ecdysone, either in the presence or absence of ouabain. These results suggest that beta-ecdysone induced morphogenesis is not dependent upon Na+ and K+ concentrations, or on the activity of an ouabain-sensitive ion pump.
β-蜕皮激素通过引起细胞核内钾水平升高以及伴随的钠水平降低来启动昆虫变态发育过程中的发育变化这一理论,已通过两种方法进行了研究。首先,将三龄晚期幼虫的成虫盘与0 - 2微克/毫升的β-蜕皮激素以及活性离子转运抑制剂一起培养。非特异性抑制剂,如碘乙酸、N - 乙基马来酰亚胺、依他尼酸和速尿,它们可能对巯基有一般影响,在浓度为10⁻³ M至2×10⁻³ M时会抑制外翻和分化。哇巴因是唯一一种特异性抑制Na⁺和K⁺跨膜主动转运的抑制剂,即使在浓度为10⁻² M时对发育也没有影响。其次,一种含有升高水平的K⁺和降低浓度的Na⁺的培养基,在没有β-蜕皮激素的情况下既不能启动成虫盘发育,在存在或不存在哇巴因的情况下,也不能刺激由次优水平(0 - 02微克/毫升)的β-蜕皮激素诱导的发育。这些结果表明,β-蜕皮激素诱导的形态发生不依赖于Na⁺和K⁺浓度,也不依赖于哇巴因敏感离子泵的活性。