Shimizu T
Graduate School of Science, Hokkaido University, Sapporo, 060, Japan.
Dev Biol. 1997 Aug 1;188(1):110-21. doi: 10.1006/dbio.1997.8606.
Tubifex eggs undergo a drastic reorganization of the cortical actin cytoskeleton during metaphase of the second meiosis. At the end of the first meiosis, the egg cortex displays only scattered actin filaments and tiny dots of F-actin; during the following 90 min, cortical F-actin gradually increases in amount, becomes organized into foci that are interlinked by actin bundles, and generates a geodesic dome-like organization. In this study, we have characterized this reorganization of the cortical actin cytoskeleton. In living eggs injected with rhodamine-phalloidin at the beginning of the second meiosis, cortical actin assembly (i.e., formation of actin foci and bundles) proceeds normally, but labeled F-actin is not found to be included significantly in the formed cortical actin network, suggesting that the increase in cortical F-actin is not simply ascribable to the recruitment of preexisting actin filaments. Cortical actin assembly can be induced precociously not only by calcium ionophore A23187 but also by a phorbol ester PMA, an agonist of protein kinase C (PKC). Conversely, the formation of actin foci and bundles is inhibited by PKC antagonists, although cortical F-actin increases to some extent in the presence of these inhibitors. Similar inhibition of the cortical reorganization is elicited in eggs whose intracellular free calcium level ([Ca2+]i) has been clamped low by microinjection of a calcium chelator BAPTA. The treatment of BAPTA-injected eggs with PMA results in the formation of actin foci and bundles. An experiment with eggs injected with fluo-3 shows that [Ca2+]i increases during metaphase of the second meiosis. These results suggest that the reorganization of cortical actin during metaphase of the second meiosis requires activation of PKC, which depends on increases in [Ca2+]i.
颤蚓卵在第二次减数分裂中期经历皮质肌动蛋白细胞骨架的剧烈重组。在第一次减数分裂结束时,卵皮质仅显示出分散的肌动蛋白丝和微小的F-肌动蛋白点;在接下来的90分钟内,皮质F-肌动蛋白的量逐渐增加,形成由肌动蛋白束相互连接的焦点,并产生类似测地线穹顶的组织。在本研究中,我们对皮质肌动蛋白细胞骨架的这种重组进行了表征。在第二次减数分裂开始时注射罗丹明-鬼笔环肽的活卵中,皮质肌动蛋白组装(即肌动蛋白焦点和束的形成)正常进行,但未发现标记的F-肌动蛋白显著包含在形成的皮质肌动蛋白网络中,这表明皮质F-肌动蛋白的增加不仅仅归因于预先存在的肌动蛋白丝的募集。皮质肌动蛋白组装不仅可以由钙离子载体A23187早熟诱导,还可以由佛波酯PMA(蛋白激酶C(PKC)的激动剂)诱导。相反,PKC拮抗剂抑制肌动蛋白焦点和束的形成,尽管在这些抑制剂存在的情况下皮质F-肌动蛋白在一定程度上增加。通过显微注射钙螯合剂BAPTA将细胞内游离钙水平([Ca2+]i)钳制在低水平的卵中也引发了类似的皮质重组抑制。用PMA处理注射了BAPTA的卵会导致肌动蛋白焦点和束的形成。用fluo-3注射卵的实验表明,[Ca2+]i在第二次减数分裂中期增加。这些结果表明,第二次减数分裂中期皮质肌动蛋白的重组需要PKC的激活,而PKC的激活依赖于[Ca2+]i的增加。