Palevitz B A, Hepler P K
J Cell Biol. 1975 Apr;65(1):29-38. doi: 10.1083/jcb.65.1.29.
Using a glycerination procedure designed to avoid excessive plasmolysis or disruption of the ectoplasm, microfilaments in bundles at the ectoplasm-endoplasm interface of Nitella internode cell segments were found to bind rabbit heavy meromyosin (HMM) in situ. All HMM arrowheads in a bundle seem to have the same polarity and many lie in register as judged from the electron micrographs; the arrowhead periodicity is approximately 380 . The decorated microfilaments are thus similar to those seen in negatively stained cytoplasmic suspensions of internode cells. In glycerinated material, as well as in suspensions, the microfilaments are closely associated with chloroplasts. The microfilaments lie adjacent to or are attached to the chloroplast envelope. The results provide further evidence that the microfilaments thought to play a role in cytoplasmic streaming in vivo in Nitella consist of actin and suggest that they may be anchored to the chloroplasts.
通过采用一种旨在避免过度质壁分离或外质破坏的甘油化程序,发现在丽藻节间细胞段的外质-内质界面处成束的微丝能够在原位结合兔重酶解肌球蛋白(HMM)。从电子显微镜照片判断,一束中的所有HMM箭头似乎都具有相同的极性,并且许多箭头排列整齐;箭头的周期性约为380 。因此,这些被标记的微丝与在节间细胞的负染细胞质悬浮液中看到的微丝相似。在甘油化材料以及悬浮液中,微丝都与叶绿体紧密相关。微丝位于叶绿体包膜附近或附着于叶绿体包膜。这些结果进一步证明,在丽藻体内被认为在细胞质流动中起作用的微丝由肌动蛋白组成,并表明它们可能锚定在叶绿体上。