发布: 2017年04月20日第7卷第8期 DOI: 10.21769/BioProtoc.2225 浏览次数: 9565
评审: Jihyun KimFilipa VazAnonymous reviewer(s)
Abstract
In this protocol, we provide an experimental procedure that perform time-lapse observation of intra-cellular structures such as chromosomes, cytoskeletons and cell organelles during meiotic cell divisions in Drosophila males. As primary spermatocyte is the largest dividing diploid cell in Drosophila, which is equivalent in size to mammalian cultured cells, one can observe dynamics of cellular components during division of the model cells more precisely. Using this protocol, we have showed that a microtubule-associated protein plays an essential role in microtubule dynamics and initiation of cleavage furrowing through interaction between microtubules and actomyosin filaments. We have also reported that nuclear membrane components are required for a formation and/or maintenance of the spindle envelope essential for cytokinesis in the Drosophila cells.
Keywords: Drosophila (果蝇)Background
In Drosophila, good cultured cell lines that proliferate well in a standard culture condition are also available. However, their cell size, particularly cytoplasmic volume, is much smaller than that of mammalian cells. This compromises the examination of cellular components during cell division. Spermatocytes, on the other hand, achieve distinct cell growth before initiation of first meiotic division. The primary spermatocytes are the largest diploid cells among proliferative cells to appear in Drosophila development. Thus, one can easily perform detailed observation of cellular structures in dividing cells using optical microscopes. In Drosophila melanogaster, well-advanced and sophisticated genetic techniques are available (Ashburner et al., 2004). Meiotic defects in chromosome segregation and in cytokinesis appear in cellular organization of spermatids just after completion of 2nd meiotic division. By observation of such early spermatids, one can easily find out even subtle meiotic abnormalities (Giansanti et al., 2012; Inoue et al., 2012). Furthermore, if a loss of microtubule integrity or dynamics would have occurred in normal cultured cells, their cell cycle progression should be arrested before metaphase. Therefore, it is hard to examine how microtubules would influence later processes of cell divisions in the somatic cells. Spermatocytes, on the other hand, are less sensitive to microtubule abnormalities at microtubule assembly checkpoint before metaphase. One can, therefore, examine a role of microtubule-related genes in cytokinesis without arresting cell cycle. We and other groups have established systems to facilitate dynamics of chromosomes or microtubules by expression of proteins fused with GFP fluorescence tag (Clarkson and Saint, 1999; Inoue et al., 2004; Rebollo and Gonzalez, 2004; Kitazawa et al., 2012).
Previous protocols can trap the male meiotic cells in a narrow space sandwiched between a coverslip and a slide glass, ensured by a small cushion materials and observe chromosome segregation under an upright microscope (Savoian et al., 2000; Inoue et al., 2004; Savoian, 2015). These protocols allowed us to collect clear images of microtubules. However, a preparation that makes the cells flattened often prevents initiation and/or progression of cytokinesis. In addition, it was difficult to add drugs or inhibitors to the living cells while time-lapse observation.
Therefore, we have established a new method that allows us to observe a whole meiosis I from prophase I to end of cytokinesis in an open chamber under an inverted microscope. We can add drugs in the cell culture in any timing of the imaging. We also improved the protocol so that we can perform a simultaneous observation of chromosomes and other cellular components such as microtubules, actin filaments, endoplasmic reticulum, Golgi apparatuses or mitochondria during male meiosis I. It can be achieved by a simultaneous expression of proteins fused with different fluorescent tags showing spectrally separable colors. As most aspects of division process seen in Drosophila meiotic cells are shared among higher eukaryotes, this protocol should be useful for studying cell division processes of other organisms as well as Drosophila somatic cell mitosis.
Materials and Reagents
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文章信息
版权信息
© 2017 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Tanabe, K., Okazaki, R., Kaizuka, K. and Inoue, Y. H. (2017). Time-lapse Observation of Chromosomes, Cytoskeletons and Cell Organelles during Male Meiotic Divisions in Drosophila. Bio-protocol 7(8): e2225. DOI: 10.21769/BioProtoc.2225.
分类
细胞生物学 > 细胞成像 > 活细胞成像
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