Zoologisches Forschungsmuseum Alexander Koenig, Adenauerallee 160, 53113 Bonn, Germany.
Toxicon. 2012 Nov;60(6):1108-16. doi: 10.1016/j.toxicon.2012.08.003. Epub 2012 Aug 14.
The sequestration of nematocysts (a special group of cnidocysts) from cnidarian prey with subsequent use in defence is described for few metazoan phyla. Members of the taxon Aeolidoidea (Nudibranchia, Gastropoda) are well-known for this. Questions regarding the reasons some nematocysts do not discharge when the gastropod feeds and how these same nematocysts can be transported along the digestive tract into specialized morphological structures called cnidosacs, remain unanswered. Within the cnidosac, nematocysts are incorporated in cells and finally be used for defence against predators. The most plausible explanation for this phenomenon suggests there are immature and therefore non-functional nematocysts in the food. A recent study by Berking and Herrmann (2005) on cnidarians suggested that the nematocysts mature by acidification via proton transfer into the nematocyst capsule. According to this hypothesis only immature nematocysts are transported into the cnidosac where they are then made functional through an accumulation of protons. In this study we present a fluorescence staining method that tests the hypothesis by Berking and Herrmann (2005) and detects changes in the pH values of incorporated nematocysts, interpreted as changes in maturation stages. This marker, the fluorescent dye Ageladine A, stains nematocyst capsules according to their pH values. With Ageladine A we were able to show that kleptocnides indeed change their pH value after incorporation into the aeolidoidean cnidosac.
从刺胞动物猎物中隔离(一种特殊的刺细胞)并用其进行防御的现象仅在少数几个后生动物门中被描述过。 分类群 Aeolidoidea(腹足纲,软体动物)的成员就是这种现象的典型代表。 一些刺胞动物在进食时为什么有些刺细胞不排出以及这些相同的刺细胞如何沿着消化道被输送到专门的形态结构称为刺丝囊,这些问题仍然没有答案。 在刺丝囊中,刺细胞被包裹在细胞内,最终用于防御捕食者。 对于这种现象最合理的解释是食物中存在不成熟且因此功能不健全的刺细胞。 最近由 Berking 和 Herrmann(2005 年)对刺胞动物进行的一项研究表明,刺细胞通过质子转移到刺细胞囊中酸化来成熟。 根据这一假设,只有不成熟的刺细胞才会被输送到刺丝囊中,在那里通过质子的积累使它们变得具有功能。 在本研究中,我们提出了一种荧光染色方法,通过该方法可以测试 Berking 和 Herrmann(2005 年)的假设,并检测到所包含的刺细胞的 pH 值变化,这些变化被解释为成熟阶段的变化。 这种标记物,荧光染料 Ageladine A,根据 pH 值对刺细胞囊进行染色。 通过 Ageladine A,我们能够证明 kleptocnides 在被纳入 Aeolidoidea 刺丝囊后确实会改变其 pH 值。