Refractive index measurement in viable cells using quantitative phase‐amplitude microscopy and confocal microscopy

Claire L. Curl1, Catherine J. Bellair2, Trudi Harris3, B. E. Allman4, P. Harris1, Alastair G. Stewart3, Ann Roberts2, K. Nugent2, Lea M.D. Delbridge1
1Department of Physiology, University of Melbourne, Parkville, Victoria, Australia
2School of Physics, University of Melbourne, Parkville, Victoria, Australia
3Department of Pharmacology, University of Melbourne, Parkville, Victoria, Australia
4Imaging Division, Iatia Ltd., Box Hill, Victoria, Australia

Tóm tắt

AbstractBackground

The refractive index (RI) of cellular material provides fundamental biophysical information about the composition and organizational structure of cells. Efforts to describe the refractive properties of cells have been significantly impeded by the experimental difficulties encountered in measuring viable cell RI. In this report we describe a procedure for the application of quantitative phase microscopy in conjunction with confocal microscopy to measure the RI of a cultured muscle cell specimen.

Methods

The experimental strategy involved calculation of cell thickness by using confocal optical sectioning procedures, construction of a phase map of the same cell using quantitative phase microscopy, and selection of cellular regions of interest to solve for the cell RI.

Results

Mean cell thickness and phase values for six cell regions (five cytoplasmic and one nuclear) were determined. The average refractive index calculated for cytoplasmic and nuclear regions was 1.360 ± 0.004. The uncertainty in the final RI value represents the technique measurement error.

Conclusions

The methodology we describe for viable cell RI measurement with this prototype cell has broad generic application in the study of cell growth and functional responses. The RI value we report may be used in optical analyses of cultured cell structure and morphology. © 2005 Wiley‐Liss, Inc.

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Tài liệu tham khảo

10.1364/AO.38.003651

10.1364/OL.19.002062

10.1117/12.231370

10.1117/1.1463043

10.1083/jcb.82.3.767

10.1088/0031-9155/41/3/002

10.1364/JOSA.47.000545

Ross KFA, 1967, Phase contrast and interference microscopy for cell biologists

10.1364/OL.23.000817

10.1103/PhysRevLett.80.2586

10.1046/j.1365-2818.2002.01027.x

10.1364/OL.27.002061

10.1111/j.0022-2720.2004.01302.x

10.1038/sj.bjp.0701128

10.1016/S0006-3495(96)79711-4

Visser TD, 1992, Refractive index and axial distance measurements in 3‐D microscopy, Optik, 90, 17

10.1046/j.1365-2818.1997.d01-627.x

Roper Scientific. Available at:www.roperscientific.com.

10.1007/s00424-004-1248-7

10.1364/AO.28.002297

Olympus Microscopy Resource Center. Available at:www.olympusmicro.com/primer/techniques/fluorescence/tirf/tirfintro.html.

Delbridge LMD, 2002, Quantitative phase imaging—a new way to ‘see’ cells, Today Life Sci, 14, 28

Iatia Ltd. Available at:www.iatia.com.au/applications/apps_confocal.asp.

10.1111/j.1440-1681.2004.04100.x