One of the key factors in cell differentiation and development is the intracellular synthesis of macromolecules specific to the differentiated cells. The chick embryo lens is widely used as a model system in the study of cell differentiation. Its morphology and cytoplasmic protein composition are simple and it is accessible at all stages of development. Considerable effort has been focused on the protein chemistry of the lens using molecular genetic techniques in relation to cataract. We have recently developed a technique of microscopic laser light scattering spectroscopy that allows observation of the Brownian motion of macromolecules within the cytoplasm of a single, live cell. From the amplitude and relaxation time of the fluctuations of light scattered from the macromolecules, it is possible to determine their intracellular concentration and size distribution. With this non-invasive technique, we have succeeded in determining the time course of intracellular accumulation of Delta-crystallin within the chick embryo lens during development. The technique is sensitive and quantitative for the study of the state of cytoplasmic proteins as was demonstrated in a study of hemoglobin aggregation inside human normal and sickle red blood cells. Based on our preliminary data we propose t study the in vivo development of the chick embryo lens, in vitro differentiation of retinal pigmented epithelium into lens cells upon clonal cell culture. Using the technique, the intracellular composition of crystallin proteins will be determined during the differentiation processes. Comparative studies using biochemical techniques will also be carried out. The technique will also be used to study the aggregation process of crystallins associated with osmotic swelling of the lens cells. The studies as proposed will lead to quantitatively better understanding of the development and transdifferentiation of the eye, and shed light on the physical basis for cytoplasmic abnormalities.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY005272-03
Application #
3260237
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1985-07-01
Project End
1988-06-30
Budget Start
1987-07-01
Budget End
1988-06-30
Support Year
3
Fiscal Year
1987
Total Cost
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Type
Schools of Arts and Sciences
DUNS #
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Peetermans, J A; Foy, B D; Tanaka, T (1987) Accumulation and diffusion of crystallin inside single fiber cells in intact chicken embryo lenses. Proc Natl Acad Sci U S A 84:1727-30
Peetermans, J A; Nishio, I; Ohnishi, S T et al. (1987) Single cell laser light scattering spectroscopy in a flow cell: repeated sickling of sickle red blood cells. Biochim Biophys Acta 931:320-5
Peetermans, J; Nishio, I; Ohnishi, S T et al. (1986) Light-scattering study of depolymerization kinetics of sickle hemoglobin polymers inside single erythrocytes. Proc Natl Acad Sci U S A 83:352-6