The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Live-cell microscopy – tips and tools
Abstract
Imaging of living cells and tissue is now common in many fields of the life and physical sciences, and is instrumental in revealing a great deal about cellular dynamics and function. It is crucial when performing such experiments that cell viability is at the forefront of any measurement to ensure that the physiological and biological processes that are under investigation are not altered in any way. Many cells and tissues are not normally exposed to light during their life cycle, so it is important for microscopy applications to minimize light exposure, which can cause phototoxicity. To ensure minimal light exposure, it is crucial that microscope systems are optimized to collect as much light as possible. This can be achieved using superior-quality optical components and state-of-the-art detectors. This Commentary discusses how to set up a suitable environment on the microscope stage to maintain living cells. There is also a focus on general and imaging-platform-specific ways to optimize the efficiency of light throughput and detection. With an efficient optical microscope and a good detector, the light exposure can be minimized during live-cell imaging, thus minimizing phototoxicity and maintaining cell viability. Brief suggestions for useful microscope accessories as well as available fluorescence tools are also presented. Finally, a flow chart is provided to assist readers in choosing the appropriate imaging platform for their experimental systems.
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Citations
Cites
Mitochondrial dynamics and apoptosis
Suen, D.-F., Norris, K. L., & Youle, R. J. (2008) · Genes & Development · doi:10.1101/gad.1658508 · Cited by 1,270 · cited 1×
“During apoptosis, this network collapses into more numerous, enlarged and isolated mitochondria (Suen et al., 2008).”
BackgroundChoi, C. K., Vicente-Manzanares, M., Zareno, J., Whitmore, L. A., Mogilner, A., & Horwitz, A. R. (2008) · Nature Cell Biology · doi:10.1038/ncb1763 · Cited by 797
Actions of ultraviolet light on cellular structures
Pattison, D. I., & Davies, M. J. (2006) · Experientia Supplementum · doi:10.1007/3-7643-7378-4_6 · Cited by 283
Cited by
Phototoxicity in live fluorescence microscopy, and how to avoid it
Icha, J., Weber, M., Waters, J. C., & Norden, C. (2017) · BioEssays · doi:10.1002/bies.201700003 · Cited by 622
An optogenetic toolbox designed for primates
Diester, I., Kaufman, M. T., Mogri, M., Pashaie, R., Goo, W., Yizhar, O., Ramakrishnan, C., Deisseroth, K., & Shenoy, K. V. (2011) · Nature Neuroscience · doi:10.1038/nn.2749 · Cited by 443
Tutorial: guidance for quantitative confocal microscopy
Jonkman, J., Brown, C. M., Wright, G. D., Anderson, K. I., & North, A. J. (2020) · Nature Protocols · doi:10.1038/s41596-020-0313-9 · Cited by 401
Self-citationGradient light interference microscopy for 3D imaging of unlabeled specimens
Nguyen, T. H., Kandel, M. E., Rubessa, M., Wheeler, M. B., & Popescu, G. (2017) · Nature Communications · doi:10.1038/s41467-017-00190-7 · Cited by 259
Present Application and Perspectives of Organoid Imaging Technology
Fei, K., Zhang, J., Yuan, J., & Xiao, P. (2022) · Bioengineering · doi:10.3390/bioengineering9030121 · Cited by 65
Metadata
- Authors
- Frigault, M. M., Lacoste, J., Swift, J. L., & Brown, C. M.
- Venue
- Journal of Cell Science
- Publisher
- The Company of Biologists
- Published
- 2009-03-15
- Volume
- 122
- Issue
- 6
- Pages
- 753-767
- ISSN
- 0021-9533 (ISSN-L)
- 1477-9137
- OpenAlex
- W1978372216
- Cited by
- 304
- References
- 3
- FWCI
- 10.12
- Type
- journal article
- Language
- en
- Open access
- closed
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