The influence of microinjected phalloidin on locomotion, protoplasmic streaming and cytoplasmic organization in Amoeba proteus and Physarum polycephalum.

Cytobiologie Pub Date : 1978-10-01
W Stockem, K Weber, J Wehland
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Abstract

Microinjected phalloidin induces both time and concentration-dependent changes in morphology and motility of amoebae and acellular slime moulds. In A. proteus injection of a 10(-3)M solution of the drug causes a separation of cortical hyaline plasma from central granular plasma. Simultaneously protoplasmic streaming and cellular locomotion are lost irreversibly. Lowering the concentration of phalloidin to 2 x 10(-4)M results in a reversible disturbance; amoebae recover after 30 to 60 minutes and show normal movement. In Ph. polycephalum the injection of a 10(-3)M solution of phalloidin into single veins induces a local gelation of the protoplasm followed by the separation of hyalo- and granuloplasm. In semi-thin and ultrathin sections the hyaline plasma regions contain a fine granular groundplasm rich in ribosomes but free of cellular organelles. The central granular plasma consists mainly of membrane-surrounded cellular compartments. The two morphologically distinct plasma regions are separated by a 0.5 to 1.0 micrometer layer of filamentous material. In A. proteus the filamentous layer is found shortly after phalloidin injection in close proximity to the plasma membrane, and consists of thin 5 to 6 nm filaments. With increasing time this layer contracts, separates from the inner plasma membrane and moves to the interior of the cell. During contraction thicker filaments with diameters of 10 to 30 nm and lengths of 300 to 500 nm are formed. The results indicate that the display and contraction of the phalloidin-induced filament layer can account for the changes observed in cellular movement and cytoplasmic organization. The resulting phenomena i.e. separation of hyaline plasma from granular plasma and changes in both the protoplasmic streaming pattern and locomotory activity of the cells, are discussed in terms of a general understanding of amoeboid movement.

微注射phalloidin对变形变形虫和多头绒泡菌运动、原生质流动和细胞质组织的影响。
微注射phalloidin诱导变形虫和脱细胞黏菌形态和运动的时间和浓度依赖性变化。在变形杆菌中,注射10(-3)M的药物溶液会导致皮质透明质浆与中央颗粒浆分离。原生质流动和细胞运动同时不可逆转地丧失。将phalloidin的浓度降低到2 × 10(-4)M会导致可逆的干扰;变形虫在30 ~ 60分钟后恢复正常活动。在polycephalum中,将10(-3)M的phalloidin溶液注射到单静脉中会引起原生质的局部凝胶化,然后是透明质和颗粒质的分离。在半薄和超薄切片上,透明质区含有富含核糖体但不含细胞器的细颗粒质。中央颗粒质主要由膜包围的细胞室组成。两个形态不同的等离子体区域被0.5至1.0微米的丝状物质层隔开。在A. proteus中,在注射phalloidin后不久,在靠近质膜的地方发现丝状层,由5至6 nm的细丝组成。随着时间的增加,这一层收缩,从内质膜分离并移动到细胞内部。在收缩过程中,形成直径为10至30纳米、长度为300至500纳米的较粗细丝。结果表明,phalloidin诱导的丝层的显示和收缩可以解释细胞运动和细胞质组织的变化。由此产生的现象,如透明等离子体与颗粒等离子体的分离,以及原生质流模式和细胞运动活性的变化,根据对变形虫运动的一般理解进行了讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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