Schalkoff Mary Ellen, Hart Nathan H
Department of Biology, Boston College, 02167, Chestnut Hill, MA, USA.
Department of Biological Sciences, Rutgers University - Busch Campus, Nelson Biological Laboratories, 08903, New Brunswick, NJ, USA.
Rouxs Arch Dev Biol. 1986 Jan;195(1):39-48. doi: 10.1007/BF00444040.
The effects of the divalent ionophore A23187 upon unfertilized eggs of the freshwater teleost fish, Brachydanio rerio, have been examined by light, scanning (SEM) and transmission (TEM) electron microscopy. Treatment of eggs with micromolar amounts (1 μM, 10 μM) of A23187 triggers cortical granule exocytosis and elevation of the chorion. However, the exocytosis of cortical granules in ionophore-activated eggs is explosive and occurs more rapidly than in eggs naturally activated in conditioned tap water. Eggs treated with A23187 in a medium lacking extra-cellular calcium also show cortical granule exocytosis, suggesting strongly that egg activation in Brachydanio results from release of calcium primarily from intracellular stores; however, there is a distinct delay in the onset of cortical granule breakdown. Unfertilized eggs exposed to A23187 for 1-5 min show noticeable disturbances in cell surface topography, including loss of microplicae and the appearance of prominent membrane-limited blebs.To determine if cortical granule exocytosis is self-propagating once initiated, A23187 was applied to a localized portion of the unfertilized egg surface, using either a G-50 sephadex gel bead or a 1 mm glass capillary tube. Eggs placed in continuous contact for 15 min with a bead coated with 10 μM A23187 show neither exocytosis of cortical granules nor elevation of the chorion. All eggs exhibit exocytosis when positioned against a glass rod coated with 1 μM A23187. The cortical granule breakdown is partial and restricted to less than 50% of the egg surface in most cells. The complete exocytosis of cortical granules in the zebra danio egg appears to require the stimulation and release of calcium from multiple sites over the cortex.
通过光学显微镜、扫描电子显微镜(SEM)和透射电子显微镜(TEM)研究了二价离子载体A23187对淡水硬骨鱼斑马鱼未受精卵的影响。用微摩尔量(1μM、10μM)的A23187处理卵会引发皮质颗粒胞吐作用和卵膜升高。然而,离子载体激活的卵中皮质颗粒的胞吐作用是爆发性的,并且比在经处理的自来水中自然激活的卵中发生得更快。在缺乏细胞外钙的培养基中用A23187处理的卵也显示出皮质颗粒胞吐作用,这强烈表明斑马鱼的卵激活主要是由于钙从细胞内储存库释放;然而,皮质颗粒分解的开始有明显延迟。暴露于A23187 1 - 5分钟的未受精卵在细胞表面形貌上显示出明显的扰动,包括微褶消失和出现突出的膜限制泡。为了确定皮质颗粒胞吐作用一旦启动是否会自我传播,使用G - 50葡聚糖凝胶珠或1毫米玻璃毛细管将A23187应用于未受精卵表面的局部区域。与涂有10μM A23187的珠子连续接触15分钟的卵既没有皮质颗粒的胞吐作用也没有卵膜升高。当靠在涂有1μM A23187的玻璃棒上时,所有卵都表现出胞吐作用。在大多数细胞中,皮质颗粒分解是部分性的,并且局限于卵表面不到50%的区域。斑马鱼卵中皮质颗粒的完全胞吐作用似乎需要皮质上多个位点的钙刺激和释放。