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Biophys J, April 2002, p. 2256-2264, Vol. 82, No. 4

*G. R. Harrison Spectroscopy Laboratory, Massachusetts
Institute of Technology, Cambridge Massachusetts 02139 and
Department of Pathology,
Children's Hospital and Harvard Medical School, Boston, Massachusetts
02115 USA
We measure the organization and substructure of HT29
epithelial cells in a monolayer using angle-resolved low-coherence
interferometry. This new technique probes cellular structure by
measuring scattered light, as in flow cytometry, but offers an
advantage in that the structure can be examined in situ, avoiding the
need to disrupt the cell monolayer. We determine the size distribution
of the cell nuclei by fitting measured light-scattering spectra to the predictions of Mie theory. In addition, we obtain information about the
cellular organization and substructure by examining the spatial
correlations within the monolayer. A remarkable finding is that the
spatial correlations over small length scales take the form of an
inverse power law, indicating the fractal nature of the packing of the
subcellular structures. We also identify spatial correlations on a
scale large compared with the size of a cell, indicating an overlying
order within the monolayer.
Biophys J, April 2002, p. 2256-2264, Vol. 82, No. 4
© 2002 by the Biophysical Society 0006-3495/02/04/2256/09 $2.00
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