Abstract
The coherent phase microscopy (CPM) provides a convenient and non-invasive tool for imaging cells and intracellular organelles. In this article, we consider the applications of the CPM method to imaging different cells and energy-transducing intracellular organelles (mitochondria and chloroplasts). Experimental data presented below demonstrate that the optical path length difference of the object, which is the basic optical parameter measured by the CPM method, can serve as an indicator of metabolic states of different biological objects at cellular and subcellular levels of structural organization.
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Abbreviations
- CPM:
-
Coherent phase microscopy
- DPM:
-
Dynamic phase microscopy
- OPLD:
-
Optical path length difference
- h(x):
-
The OPDL profile along a certain scan line
- Δh :
-
The height of the OPDL profile
- Δn :
-
Refractivity
- ATP:
-
Adenosine triphosphate
- CCCP:
-
Carbonylcyanide-3-chlorophenyl hydrazone
- DCMU:
-
3-(3,4-dichloro-phenyl)-1,1-dimethylurea.
- DBMIB:
-
2,5-dibromo-3-methyl-6-isopropyl-p-benzoquinone
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Acknowledgments
The authors consider their pleasant duty to express a lot of thanks to the MIREA Laboratory staff and to list our collaborators, A.V. Kretushev and T.V. Vyshenskaja, who made a principal contribution to CPM measurements reviewed above. Fruitful discussions and cooperation were with A.A. Shtil, L.S. Yaguzhinsky, O.V. Zatsepina and G.I. El’Registan. We thank the anonymous referees for critical reading of the manuscript. This work was partly supported by grants 06-04-48620 and 09-04-00978 from the Russian Foundation for Basic Researches.
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Tychinsky, V.P., Tikhonov, A.N. Interference Microscopy in Cell Biophysics. 2. Visualization of Individual Cells and Energy-Transducing Organelles. Cell Biochem Biophys 58, 117–128 (2010). https://doi.org/10.1007/s12013-010-9115-y
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DOI: https://doi.org/10.1007/s12013-010-9115-y