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Overview
editBiological systems exist as a complex interplay of countless cellular components interacting across four dimensions to produce the phenomenon called life. While it is common to reduce living organisms to non-living samples to accommodate traditional static imaging tools, the further the sample deviates from the native conditions the more likely the delicate processes in question will exhibit perturbations.[1] The onerous task of capturing the true physiological identity of living tissue, therefore, requires high-resolution visualization across both space and time within the parent organism.[2] The technological advances of live-cell imaging, designed to provide spatiotemporal images of subcellular events in real-time, serves an important role for corroborating the biological relevance of physiological changes observed during experimentation. Due to their contiguous relationship with physiological conditions, live-cell assays are considered the standard for probing complex and dynamic cellular events.[3] As dynamic processes such as migration, cell development, and intracellular trafficking increasingly become the focus of biological research, techniques capable of capturing 3-dimensional data in real-time for cellular networks (in situ) and entire organisms (in vivo) will become indispensable tools in understanding biological systems. The general acceptance of live-cell imaging has led to a rapid expansion in the number of practitioners and established a need for increased spatial and temporal resolution without compromising the health of the cell.[4]
Instrumentation and Optics
editLive-cell imaging represents a careful compromise between acquiring the highest-resolution image and keeping the cells alive for as long as possible. [5] As a result, live-cell microscopists face a unique set of challenges that are often overlooked when working with fixed-specimens. Moreover, live-cell imaging often employs special optical system and detector specifications. For example, ideally the microscopes used in live-cell imaging would have high signal-to-noise ratios, fast image acquisition rates to capture time-lapse video of extracellular events, and maintaining the long-term viability of the cells.[6] However, optimizing even a single facet of image acquisition can be resource intensive and should be considered on a case by case basis.
Live-cell Imaging Lens Designs
edit
Low Magnification "Dry" Lenses
editIn cases where extra space between the objective and the specimen is required to work with the sample, a dry lens can be used, potentially requiring additional adjustments of the correction collar to account for differences in imaging chambers. Special objective lenses are designed with correction collars that correct for spherical aberrations while accounting for the cover slip thickness. In high numerical aperture (NA) dry objective lenses, the correction collar adjustment ring will change the position of a movable lens group to account for differences in the way the outside of the lens focuses light relative to the center. Although lens aberrations are inherent in all lens designs, they become more problematic in dry lenses where resolution retention is key.[7]
Oil Immersion High NA Lenses
editOil immersion is a technique that can increase image resolution by immersing the lens and the specimen in oil with a high refractive index. Since light bends when it passes between mediums with different refractive indexes, by placing oil with the same refractive index as glass between the lens and the slide, two transitions between refractive indices can be avoided.[8] However, for most applications it is recommended that oil immersion be used with fixed (dead) specimens because live cells require an aqueous environment and the mixing of oil and water can cause severe spherical aberrations. For some applications silicone oil can be used to produce more accurate image reconstructions. Silicone oil is an attractive media because it has a refractive index that is close to that of living cells, allowing it to produce high resolution images while minimizing spherical aberrations.[7]
Water Immersion Lenses
editLive-cell imaging requires a sample in an aqueous environment that is often 50 to 200 micrometers away from the cover glass. Therefore, water immersion lenses can help achieve a higher resolving power due to the fact that both the environment and the cells themselves will be close to the refractive index of water. Water immersion lenses are designed to be compatible with the refractive index of water and usually have a corrective collar which allows for adjustment of the objective. Additionally, because of the higher refractive index of water, water immersion lenses have a high numerical aperture and can produce images superior to oil immersion lens when resolving planes deeper than 10µm.[7]
Dipping Lenses
editAnother solution for live-cell imaging is the dipping lens. These lenses are a subset of water immersion lenses that do not require a cover slip and can be dipped directly into the aqueous environment of the sample. One of the main advantages of the dipping lens is that it has a long effective working distance.[9] Since a cover slip is not required, this type of lens can approach the surface of the specimen and as a result, the resolution is limited by the restraints imposed by spherical aberration rather than the physical limitations of the cover slip. Although dipping lenses can be very useful, they are not ideal for all experiments since the act of "dipping" the lens can disturb the cells in the sample. Additionally, since the incubation chamber must be open to the lens, changes in the sample environment due to evaporation must be closely monitored.[7]
Phototoxicity and Photobleaching
editThe rise of confocal microscopy is closely correlated with accessibility of high power lasers, which are able to achieve high intensities of light excitation. However, the high power output can damage sensitive fluorophores and are usually run significantly below their maximum power output.[10] Over exposure to light can result in photodamage due to photobleaching or phototoxicity. The effects of photobleaching can significantly reduce the quality of fluorescent images and in recent years there has been a significant demand for longer-lasting commercial fluorophores. One solution, the Alexa Fluor series, show little to no fading even at high laser intensities.[11]
Under physiological conditions, many cells and tissue types are exposed to only low levels of light.[12] As a result, it is import to minimize the exposure of live cells to high doses of ultraviolet (UV), infrared (IR), or fluorescence exciting wavelengths of light, which can damage DNA, raise cellular temperatures, and cause photo bleaching respectively.[13] High energy photons absorbed by the fluorophores and the sample are emitted at longer wavelengths proportional to the Stokes shift.[14] However, cellular organelles can be damaged when the photon's energy produces chemical and molecular changes rather than being re-emitted.[15] It is believe that the primary culprit in the light induced toxicity experienced by live cells is a result of free radicals produced by the excitation of fluorescent molecules.[12] These free radicals are highly reactive and will result in the destruction of cellular components, which can result in non-physiological behavior.
One method of minimizing photo-damage is to lower the oxygen concentration in the sample to avoid the formation of reactive oxygen species.[16] However, this method is not allows possible in live-cell imaging and may require additional intervention. Another method for reducing the effects of free radicals in the sample is the use of antifade reagents. Unfortunately, most commercial antifade reagents cannot be used in live-cell imaging because of their toxicity.[17] Instead, natural free-radical scavengers such as vitamin C or vitamin E can be used without substantially altering physiological behavior on shorter time scales.[18]
References
edit- ^ Petroll, W. M.; Jester, J. V.; Cavanagh, H. D. (1994-5). "In vivo confocal imaging: general principles and applications". Scanning. 16 (3): 131–149. ISSN 0161-0457. PMID 8038913.
{{cite journal}}: Check date values in:|date=(help) - ^ "Methods for Cell and Particle Tracking". Methods in Enzymology. 504: 183–200. 2012-01-01. doi:10.1016/B978-0-12-391857-4.00009-4. ISSN 0076-6879.
- ^ Allan, Victoria J.; Stephens, David J. (2003-04-04). "Light Microscopy Techniques for Live Cell Imaging". Science. 300 (5616): 82–86. doi:10.1126/science.1082160. ISSN 1095-9203. PMID 12677057.
- ^ DanceMar. 27, Amber; 2018; Pm, 2:10 (2018-03-27). "Live-cell imaging: Deeper, faster, wider". Science | AAAS. Retrieved 2018-12-17.
{{cite web}}:|last2=has numeric name (help)CS1 maint: numeric names: authors list (link) - ^ Jensen, Ellen C. (2012-08-21). "Overview of Live-Cell Imaging: Requirements and Methods Used". The Anatomical Record: Advances in Integrative Anatomy and Evolutionary Biology. 296 (1): 1–8. doi:10.1002/ar.22554. ISSN 1932-8486.
- ^ Waters, Jennifer C. (2013). "Live-cell fluorescence imaging". Methods in Cell Biology. 114: 125–150. doi:10.1016/B978-0-12-407761-4.00006-3. ISSN 0091-679X. PMID 23931505.
- ^ a b c d R., Hibbs, Alan (2004). Confocal microscopy for biologists. New York: Kluwer Academic/Plenum Publishers. ISBN 0306484684. OCLC 54424872.
{{cite book}}: CS1 maint: multiple names: authors list (link) - ^ Mansfield, S. M.; Kino, G. S. (1990-12-10). "Solid immersion microscope". Applied Physics Letters. 57 (24): 2615–2616. doi:10.1063/1.103828. ISSN 0003-6951.
- ^ Keller, H. Ernst (2006), "Objective Lenses for Confocal Microscopy", Handbook Of Biological Confocal Microscopy, Springer US, pp. 145–161, doi:10.1007/978-0-387-45524-2_7, ISBN 9780387259215, retrieved 2018-10-23
- ^ "How the Confocal Laser Scanning Microscope entered Biological Research". Biology of the Cell. 95 (6): 335–342. 2003-09-01. doi:10.1016/S0248-4900(03)00078-9. ISSN 0248-4900.
- ^ "Improved fluoroimmunoassays using the dye Alexa Fluor 647 with the RAPTOR, a fiber optic biosensor". Journal of Immunological Methods. 271 (1–2): 17–24. 2002-12-20. doi:10.1016/S0022-1759(02)00327-7. ISSN 0022-1759.
- ^ a b Frigault, Melanie M.; Lacoste, Judith; Swift, Jody L.; Brown, Claire M. (2009-03-15). "Live-cell microscopy – tips and tools". J Cell Sci. 122 (6): 753–767. doi:10.1242/jcs.033837. ISSN 0021-9533. PMID 19261845.
- ^ Magidson, Valentin; Khodjakov, Alexey (2013), "Circumventing Photodamage in Live-Cell Microscopy", Methods in Cell Biology, Elsevier, pp. 545–560, doi:10.1016/b978-0-12-407761-4.00023-3, ISBN 9780124077614, PMC 3843244, PMID 23931522, retrieved 2018-09-29
{{citation}}: CS1 maint: PMC format (link) - ^ D., Rost, F. W. (1992–1995). Fluorescence microscopy. Cambridge: Cambridge University Press. ISBN 052123641X. OCLC 23766227.
{{cite book}}: CS1 maint: date format (link) CS1 maint: multiple names: authors list (link) - ^ Laissue, P Philippe; Alghamdi, Rana A; Tomancak, Pavel; Reynaud, Emmanuel G; Shroff, Hari (2017-06-29). "Assessing phototoxicity in live fluorescence imaging". Nature Methods. 14 (7): 657–661. doi:10.1038/nmeth.4344. ISSN 1548-7091.
- ^ Ettinger, Andreas; Wittmann, Torsten (2014). "Fluorescence Live Cell Imaging". Methods in cell biology. 123: 77–94. doi:10.1016/B978-0-12-420138-5.00005-7. ISSN 0091-679X. PMC 4198327. PMID 24974023.
{{cite journal}}: CS1 maint: PMC format (link) - ^ Handbook of biological confocal microscopy. Pawley, James B. (3rd ed ed.). New York, NY: Springer. 2006. ISBN 9780387455242. OCLC 663880901.
{{cite book}}:|edition=has extra text (help)CS1 maint: others (link) - ^ Watu, Aswani; Metussin, Nurzaidah; Yasin, Hartini M.; Usman, Anwar (2018). "The total antioxidant capacity and fluorescence imaging of selected plant leaves commonly consumed in Brunei Darussalam". Author(s). doi:10.1063/1.5023935.
{{cite journal}}: Cite journal requires|journal=(help)
Category:Microscopy Category:Microscopes Category:Cell imaging Category:Microbiology techniques Category:Laboratory techniques Category:Laboratory equipment Category:Articles containing video clips