The mammalian midbody is an enigmatic structure in that while it is a constant feature of mitosis and cytokinesis, its exact relationship to these important cellular events is not understood. The proposed work is directed toward answering some of the questions regarding the composition of the midbody and its possible functional roles in cell division. Large populations of post-telophase mitotic cells will be used to isolate the midbodies, and to examine their composition by polyacrylidme gel electrophoresis. Midbody components will be used to prepare antibodies for immunofluorescence to determine distribution of these components prior to late anaphase, when they are first seen by electron microscopy. Midbodies will be freeze fractured to examine the plasma membrane overlying the midbody matrix for differences in particle distribution indicating association between the membrane and the matrix.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM026802-06
Application #
3274252
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Project Start
1979-09-28
Project End
1988-03-31
Budget Start
1985-04-01
Budget End
1988-03-31
Support Year
6
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Catholic University of America
Department
Type
Schools of Arts and Sciences
DUNS #
City
Washington
State
DC
Country
United States
Zip Code
20064
Snyder, J A; Mullins, J M (1993) Analysis of spindle microtubule organization in untreated and taxol-treated PtK1 cells. Cell Biol Int 17:1075-84
Hoffman, J C; Mullins, J M (1990) Nuclear and mitotically enhanced epitope. Cell Motil Cytoskeleton 16:68-79
Leonard, P J; Mullins, J M (1987) D2O induced alterations of mitosis in PtK1 cells. Exp Cell Res 172:204-11
Wolf, K M; Mullins, J M (1987) Cytochalasin B-induced redistribution of cytokeratin filaments in PtK1 cells. Cell Motil Cytoskeleton 7:347-60
Mullins, J M; Wolf, K M; Snyder, J A (1986) Immunofluorescence analysis of sucrose-induced changes in spindle morphology. Eur J Cell Biol 39:333-40