Title :
Optical scatter imaging of programmed cell death
Author :
Joiner, W.M. ; Boustany, N.N. ; Thakor, N.V.
Author_Institution :
Dept. of Biomed. Eng., Johns Hopkins Univ., USA
Abstract :
Optical Scatter Imaging (OSI) was recently developed in our laboratory to study subcellular morphological changes in viable cells. The process utilizes Fourier filtering and the ratio of wide-to-narrow angle scatter intensity (OSIR) to detect alterations in the size of particles with wavelength-scale dimensions. In the present study, we utilize OSI to track subcellular changes during programmed cell death. OSI showed an average 21% decrease in OSIR. The OSIR initial was 183.8±7.2 and the OSIR final was 145.9±4.3, p<0.001, n=57 (mean ±95% confidence interval of the mean) upon induction of cell death by 1 μM of the kinase inhibitor staurosporine. This decrease was not observed in cells that over expressed Bcl-x, an antiapoptotic protein localized on the mitochondria. Combining OSI with genetic manipulations provides a novel approach and tool, with which to study apoptosis, a fundamental biological process
Keywords :
biological techniques; cellular biophysics; genetics; laboratory techniques; light scattering; optical images; particle size measurement; Bcl-x; antiapoptotic protein; apoptosis; biophysical research technique; fundamental biological process; genetic manipulations; kinase inhibitor staurosporine; mitochondria; optical scatter imaging; programmed cell death; subcellular changes tracking; wavelength-scale dimensions; wide-to-narrow angle scatter intensity; Biomedical optical imaging; Filtering; Inhibitors; Laboratories; Open systems; Optical filters; Optical imaging; Optical scattering; Particle scattering; Proteins;
Conference_Titel :
Bioengineering Conference, 2002. Proceedings of the IEEE 28th Annual Northeast
Conference_Location :
Philadelphia, PA
Print_ISBN :
0-7803-7419-3
DOI :
10.1109/NEBC.2002.999498