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水蛭卵中极性细胞质区域(端质)的形成是一个三步分离过程。

Formation of polar cytoplasmic domains (teloplasms) in the leech egg is a three-step segregation process.

作者信息

Fernandez J, Olea N, Ubilla A, Cantillana V

机构信息

Departamento de Biología, Facultad de Ciencias, Universidad de Chile, Santiago.

出版信息

Int J Dev Biol. 1998 Mar;42(2):149-62.

PMID:9551860
Abstract

Segregation and proliferation of mitochondria, leading to formation of the teloplasms (pole plasms), were studied in eggs of the leech T. rude by immunocytochemistry, fluorescent time lapse video imaging, confocal and electron microscopy. The translocation of mitochondria was analyzed after loading the egg with either Rhodamine 123 or a Mitotracker. Mitochondrial proliferation was assessed after pulse labeling with BrdU. The involvement of the cytoskeleton in the segregation process was determined by drug action. The teloplasms form during the first interphase as consequence of a 3-step sequential process of mitochondrial redistribution throughout the egg cytoplasm. The first step is a microtubule dependent process of ectoplasm thickening due to centrifugal mitochondrial transportation from the neighboring endoplasm. During the second step mitochondria move in the plane of the ectoplasm to become concentrated at the wall of rings (polar rings) and bands of contraction. This process appears to mostly depend on actin. The furrowing pattern of the egg during this step can be modified by cold treatment and seems to be determined during oogenesis. During the third step the ectoplasm flows to either of the poles in conjunction with bipolar displacement of the polar rings and shortening of the contraction bands. This step depends on both microtubules and microfilaments. Mitochondria of first interphase eggs have three special features: (1) they move in clusters, (2) their movement depends on both microtubules and microfilaments and (3) they proliferate continuously. During the first interphase the polarized meiotic egg becomes a bipolar cell.

摘要

通过免疫细胞化学、荧光延时视频成像、共聚焦显微镜和电子显微镜,研究了水蛭T. rude卵中线粒体的分离和增殖,这导致了端质(极质)的形成。在用罗丹明123或线粒体追踪染料加载卵后,分析线粒体的转运。在用BrdU脉冲标记后,评估线粒体的增殖。通过药物作用确定细胞骨架在分离过程中的参与情况。端质在第一次间期形成,这是线粒体在整个卵细胞质中进行三步连续重分布过程的结果。第一步是一个依赖微管的外质增厚过程,这是由于线粒体从邻近的内质进行离心运输所致。在第二步中,线粒体在外质平面内移动,集中在环(极环)壁和收缩带处。这个过程似乎主要依赖于肌动蛋白。在此步骤中,卵的沟纹模式可通过冷处理改变,且似乎在卵子发生过程中就已确定。在第三步中,外质与极环的双极移位和收缩带的缩短一起流向两极。这一步依赖于微管和微丝。第一次间期卵的线粒体有三个特殊特征:(1)它们成簇移动,(2)它们的移动依赖于微管和微丝,(3)它们持续增殖。在第一次间期,极化的减数分裂卵变成一个双极细胞。

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