Nakamura S, Tamm S L
J Cell Biol. 1985 May;100(5):1447-54. doi: 10.1083/jcb.100.5.1447.
Previous work showed that ctenophore larvae swim backwards in high-KCl seawater, due to a 180 degrees reversal in the direction of effective stroke of their ciliary comb plates (Tamm, S. L., and S. Tamm, 1981, J. Cell Biol., 89: 495-509). Ion substitution and blocking experiments indicated that this response is Ca2+ dependent, but comb plate cells are innervated and presumably under nervous control. To determine whether Ca2+ is directly involved in activating the ciliary reversal mechanism and/or is required for synaptic triggering of the response, we (a) determined the effects of ionophore A23187 and Ca2+ on the beat direction of isolated nerve-free comb plates dissociated from larvae by hypotonic, divalent cation-free medium, and (b) used permeabilized ATP-reactivated models of comb plates to test motile responses to known concentrations of free Ca2+. We found that 5 microM A23187 and 10 mM Ca2+ induced dissociated comb plate cells to beat in the reverse direction and to swim counterclockwise in circular paths instead of in the normal clockwise direction. Detergent/glycerol-extracted comb plates beat actively in the presence of ATP, and reactivation was reversibly inhibited by micromolar concentrations of vanadate. Free Ca2+ concentrations greater than 10(-6)M caused reversal in direction of the effective stroke but no significant increase in beat frequency. These results show that ciliary reversal in ctenophores, like that in protozoa, is activated by an increase in intracellular free Ca2+ ions. This allows the unique experimental advantages of ctenophore comb plate cilia to be used for future studies on the site and mechanism of action of Ca2+ in the regulation of ciliary motion.
先前的研究表明,栉水母幼虫在高氯化钾海水中向后游动,这是由于其纤毛栉板有效摆动方向发生了180度反转(Tamm, S. L., 和S. Tamm, 1981, 《细胞生物学杂志》, 89: 495 - 509)。离子置换和阻断实验表明,这种反应依赖于Ca2+,但栉板细胞有神经支配,推测受神经控制。为了确定Ca2+是否直接参与激活纤毛反转机制和/或是否是该反应突触触发所必需的,我们(a)通过低渗、无二价阳离子培养基从幼虫中分离出无神经的栉板,测定离子载体A23187和Ca2+对其摆动方向的影响,(b)使用经通透处理的ATP再激活的栉板模型来测试对已知浓度游离Ca2+的运动反应。我们发现,5微摩尔的A23187和10毫摩尔的Ca2+诱导解离的栉板细胞反向摆动,并沿逆时针方向呈圆形路径游动,而不是正常的顺时针方向。去污剂/甘油提取的栉板在ATP存在下能积极摆动,微摩尔浓度的钒酸盐可可逆地抑制再激活。游离Ca2+浓度大于10(-6)M会导致有效摆动方向反转,但摆动频率无显著增加。这些结果表明,栉水母中的纤毛反转与原生动物一样,是由细胞内游离Ca2+离子增加激活的。这使得栉水母栉板纤毛具有独特的实验优势,可用于未来关于Ca2+在调节纤毛运动中的作用位点和作用机制的研究。