Correlating light scattering with internal cellular structures

The origins of side scattering from a fibroblast and cervical cell line were determined by comparing side-scatter images with images stained for lysosomes, nuclei, and mitochondria on a cell by cell basis. Lysosomes or nuclei are the most efficient type of scatterer depending on the cell type and incident light polarization. The relative scattering efficiencies of lysosomes and mitochondria were the same for both cell lines, while the scattering efficiencies of the nuclei differed. The percent of 90° scattering from the nucleus, mitochondria, and lysosomes as well as the group of other internal cellular objects was estimated. The nucleus was the largest contributor to side scatter in the cervical carcinoma cells. The contributions of lysosomes, mitochondria, the nucleus, and particles unstained by either Hoechst, LysoSensor or MitoTracker ranges from ∼20% to ∼30% in fibroblast cells. The contribution of lysosomes to side scatter was much stronger when the incident light was polarized perpendicular to the scattering plane than when the polarization of the side scatter laser was parallel to the scattering plane. This dependence on side scatter polarization indicates that lysosomes contain scattering structures that are much smaller than the wavelength of light used in the measurements (785 nm). In conclusion, mitochondria were not found to be either the most efficient scatterer or to have the largest contribution to scattering in either cell line, in contrast to previous reports. Rather lysosomes, nuclei and unknown particles all have significant contributions to 90° scattering and the contributions of some of these particles can be modulated by changing the polarization of the incident light.

[1]  David A Basiji,et al.  Sensitivity measurement and compensation in spectral imaging , 2006, Cytometry. Part A : the journal of the International Society for Analytical Cytology.

[2]  Cahir J. O'Kane,et al.  Lysosomal positioning coordinates cellular nutrient responses , 2011, Nature Cell Biology.

[3]  Irving Itzkan,et al.  Confocal light absorption and scattering spectroscopic microscopy monitors organelles in live cells with no exogenous labels , 2007, Proceedings of the National Academy of Sciences.

[4]  Stephen Chad Kanick,et al.  Integration of single-fiber reflectance spectroscopy into ultrasound-guided endoscopic lung cancer staging of mediastinal lymph nodes. , 2010, Journal of biomedical optics.

[5]  N. Demaurex pH Homeostasis of cellular organelles. , 2002, News in physiological sciences : an international journal of physiology produced jointly by the International Union of Physiological Sciences and the American Physiological Society.

[6]  T. Kitai,et al.  Contribution of the mitochondrial compartment to the optical properties of the rat liver: a theoretical and practical approach. , 1994, Biophysical journal.

[7]  Nada N Boustany,et al.  Optical scatter changes at the onset of apoptosis are spatially associated with mitochondria. , 2010, Journal of biomedical optics.

[8]  Judith R Mourant,et al.  Detection of Cervical Intraepithelial Neoplasias and Cancers in Cervical Tissue by In Vivo Light Scattering , 2009, Journal of lower genital tract disease.

[9]  J. Mourant,et al.  Polarized wavelength-dependent measurements of turbid media. , 1999, Optics express.

[10]  Michele Follen,et al.  Model-based analysis of reflectance and fluorescence spectra for in vivo detection of cervical dysplasia and cancer. , 2008, Journal of biomedical optics.

[11]  T. Foster,et al.  Mie theory interpretations of light scattering from intact cells. , 2005, Optics letters.

[12]  R. Richards-Kortum,et al.  Light scattering from normal and dysplastic cervical cells at different epithelial depths: finite-difference time-domain modeling with a perfectly matched layer boundary condition. , 2003, Journal of biomedical optics.

[13]  M. Murphy,et al.  Altered mitochondrial function in fibroblasts containing MELAS or MERRF mitochondrial DNA mutations. , 1996, The Biochemical journal.

[14]  Thomas H Foster,et al.  Index-of-refraction-dependent subcellular light scattering observed with organelle-specific dyes. , 2007, Journal of biomedical optics.

[15]  E R Weibel,et al.  Distribution of Organelles and Membranes between Hepatocytes and Nonhepatocytes in a Stereological Study , 2022 .

[16]  Rebecca Richards-Kortum,et al.  Autofluorescence and diffuse reflectance spectroscopy of oral epithelial tissue using a depth-sensitive fiber-optic probe. , 2008, Applied optics.

[17]  J. Schmitt,et al.  Optical scattering properties of soft tissue: a discrete particle model. , 1998, Applied optics.

[18]  Torre M Bydlon,et al.  Optical Assesssment of Tumor Resection Margins in the Breast , 2010, IEEE Journal of Selected Topics in Quantum Electronics.

[19]  Judith R. Mourant,et al.  Light scattering from cells: the contribution of the nucleus and the effects of proliferative status , 2000, BiOS.

[20]  Thomas H Foster,et al.  Characterization of lysosomal contribution to whole-cell light scattering by organelle ablation. , 2007, Journal of biomedical optics.

[21]  L. S. Cram,et al.  Fluorescence and light-scattering measurements on hog cholera-infected PK-15 cells. , 1973, Experimental cell research.

[22]  D. Stojanovski,et al.  Mitochondrial morphology and distribution in mammalian cells , 2006, Biological chemistry.

[23]  J. Heuser Changes in lysosome shape and distribution correlated with changes in cytoplasmic pH , 1989, The Journal of cell biology.

[24]  G. Salzman Light Scatter: Detection and Usage , 1999, Current protocols in cytometry.

[25]  J P Freyer,et al.  Polarized angular dependent spectroscopy of epithelial cells and epithelial cell nuclei to determine the size scale of scattering structures. , 2002, Journal of biomedical optics.

[26]  P. K. Kennady,et al.  Variation of mitochondrial size during the cell cycle: A multiparameter flow cytometric and microscopic study , 2004, Cytometry. Part A : the journal of the International Society for Analytical Cytology.

[27]  P. Marchand,et al.  Elastic light scattering from single cells: orientational dynamics in optical trap. , 2004, Biophysical journal.

[28]  Tom Fearn,et al.  Elastic scattering spectroscopy for detection of cancer risk in Barrett's esophagus: experimental and clinical validation of error removal by orthogonal subtraction for increasing accuracy. , 2009, Journal of biomedical optics.

[29]  G C Salzman,et al.  Cell classification by laser light scattering: identification and separation of unstained leukocytes. , 1975, Acta cytologica.