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Long-term live cell cycle imaging of single Cyanidioschyzon merolae cells
Live cell imaging by fluorescence microscopy is a useful tool for elucidating the localization and function of proteins and organelles in single cells. Especially, time-lapse analysis observing the same field sequentially can be used to observe cells of many organisms and analyze the dynamics of int...
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Published in: | Protoplasma 2021-05, Vol.258 (3), p.651-660 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Live cell imaging by fluorescence microscopy is a useful tool for elucidating the localization and function of proteins and organelles in single cells. Especially, time-lapse analysis observing the same field sequentially can be used to observe cells of many organisms and analyze the dynamics of intracellular molecules. By single-cell analysis, it is possible to elucidate the characteristics and fluctuations of individual cells, which cannot be elucidated from the data obtained by averaging the characteristics of an ensemble of cells. The primitive red alga
Cyanidioschyzon merolae
has a very simple structure and is considered a useful model organism for studying the mechanism of organelle division, since the division is performed synchronously with the cell cycle. However,
C. merolae
does not have a rigid cell wall, and environmental changes such as low temperature or high pH cause morphological change and disruption easily. Therefore, morphological studies of
C. merolae
typically use fixed cells. In this study, we constructed a long-term time-lapse observation system to analyze the dynamics of proteins in living
C. merolae
cells. From the results, we elucidate the cell division process of single living cells, including the function of intracellular components. |
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ISSN: | 0033-183X 1615-6102 |
DOI: | 10.1007/s00709-020-01592-z |