Henson J H, Schatten G
Cell Motil. 1983;3(5-6):525-34. doi: 10.1002/cm.970030519.
Coelomocytes from several echinoderm species undergo an actin-mediated cytoskeletal transformation once subjected to hypotonic shock. In this study, coelomocytes from the sea urchins Lytechinus variegatus and Arbacia punctulata were induced to "transform" by treatment with greater than 5 microM of the calcium ionophore A23187 in the presence of external Ca++. The dependence of ionophore transformation on external Ca++ and the lack of chlorotetracycline staining indicates that these cells rely on external Ca++ sources. NBD-phallacidin (7-Nitrobenz-2-oxa-1,3-diazole-phallacidin) staining of lysolecithin permeabilized cells and whole-mount transmission electron microscopy (TEM) show that similar reorganizations of the actin cytoskeleton take place during hypotonic shock and ionophore transformation, although actin filament bundling is less apparent in A23187-treated cells. As has been shown with hypotonic shock transformation, the ionophore elicited shape change is inhibited by anticalmodulin drugs. Greater than 10 microM concentrations of W 13 inhibit filopod formation, while this drug's less active structural analogue, W 12, exhibits no effects. W 13 also appears to disrupt actin filament-membrane associations in the cells. Fluorescent localization of calmodulin using a photooxidized derivative of trifluoperazine indicates a general cytoplasmic distribution with some concentration in filopod core bundles. Coelomocyte transformation may be an example of a cellular shape change regulated by Ca++ through the action of calmodulin modulation of actin-membrane interactions.
几种棘皮动物的体腔细胞一旦受到低渗休克,就会经历肌动蛋白介导的细胞骨架转变。在本研究中,用大于5微摩尔的钙离子载体A23187在外部Ca++存在的情况下处理来自海胆Lytechinus variegatus和Arbacia punctulata的体腔细胞,诱导其“转变”。离子载体转变对外部Ca++的依赖性以及缺乏氯四环素染色表明这些细胞依赖外部Ca++来源。用NBD-鬼笔环肽(7-硝基苯-2-恶唑-1,3-二氮杂环戊二烯-鬼笔环肽)对溶血卵磷脂通透化细胞进行染色以及进行整装透射电子显微镜(TEM)观察表明,在低渗休克和离子载体转变过程中肌动蛋白细胞骨架会发生类似的重组,尽管在A23187处理的细胞中肌动蛋白丝束集没那么明显。正如低渗休克转变所显示的那样,离子载体引发的形状变化受到抗钙调蛋白药物的抑制。大于10微摩尔浓度的W 13抑制丝状伪足的形成,而该药物活性较低的结构类似物W 12则无此作用。W 13似乎还会破坏细胞中肌动蛋白丝与膜的结合。使用三氟拉嗪的光氧化衍生物对钙调蛋白进行荧光定位表明其在细胞质中普遍分布,在丝状伪足核心束中有一定浓度。体腔细胞转变可能是Ca++通过钙调蛋白对肌动蛋白-膜相互作用的调节作用来调控细胞形状变化的一个例子。